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and temporal analysis of killer whale (Orcinus orca) strandings in the North Pacific Ocean and the benefits of a coordinated stranding response protocol</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12044</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Spatial and temporal analysis of killer whale (Orcinus orca) strandings in the North Pacific Ocean and the benefits of a coordinated stranding response protocol</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michelle M. Barbieri, Stephen Raverty, M. Bradley Hanson, Stephanie Venn-Watson, John K. B. Ford, Joseph K. Gaydos</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-22T01:27:02.13597-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12044</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12044</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12044</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Killer whales (<em>Orcinus orca</em>) are widely distributed throughout the world's oceans, yet little has been documented about their stranding patterns. Knowledge of stranding patterns improves our ability to examine and sample carcasses and provides a foundation for understanding killer whale natural history, diet, reproduction, anthropogenic stressors, emerging diseases, and patterns of unusual mortality. We compiled published and unpublished killer whale stranding data to describe stranding patterns in the North Pacific Ocean. Between 1925 and 2011, 371 stranded killer whales were reported in Japan (20.4%), Russia (3.5%), Alaska (32.0%), British Columbia (27.4%), Washington (4.0%), Oregon (2.7%), California (5.1%), Mexico (3.8%), and Hawaii (0.8%). Strandings occurred at all times of year, but regionally specific seasonal differences were observed. Mortality and annual census data from Northern and Southern Resident populations were extrapolated to estimate that across the North Pacific, an average of 48 killer whales die annually. However, over the last two decades, an average of only 10 killer whale carcasses were recovered annually in this ocean, making each event a rare opportunity for study. Publication of a standardized killer whale necropsy protocol and dedicated funding facilitated the number of complete postmortem necropsies performed on stranded killer whales from 1.6% to 32.2% annually.</p></div>
]]></content:encoded><description>

Killer whales (Orcinus orca) are widely distributed throughout the world's oceans, yet little has been documented about their stranding patterns. Knowledge of stranding patterns improves our ability to examine and sample carcasses and provides a foundation for understanding killer whale natural history, diet, reproduction, anthropogenic stressors, emerging diseases, and patterns of unusual mortality. We compiled published and unpublished killer whale stranding data to describe stranding patterns in the North Pacific Ocean. Between 1925 and 2011, 371 stranded killer whales were reported in Japan (20.4%), Russia (3.5%), Alaska (32.0%), British Columbia (27.4%), Washington (4.0%), Oregon (2.7%), California (5.1%), Mexico (3.8%), and Hawaii (0.8%). Strandings occurred at all times of year, but regionally specific seasonal differences were observed. Mortality and annual census data from Northern and Southern Resident populations were extrapolated to estimate that across the North Pacific, an average of 48 killer whales die annually. However, over the last two decades, an average of only 10 killer whale carcasses were recovered annually in this ocean, making each event a rare opportunity for study. Publication of a standardized killer whale necropsy protocol and dedicated funding facilitated the number of complete postmortem necropsies performed on stranded killer whales from 1.6% to 32.2% annually.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12040" xmlns="http://purl.org/rss/1.0/"><title>Hydrodynamic performance of the flippers of large-bodied cetaceans in relation to locomotor ecology</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12040</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hydrodynamic performance of the flippers of large-bodied cetaceans in relation to locomotor ecology</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paul W. Weber, Laurens E. Howle, Mark M. Murray, Joy S. Reidenberg, Frank E. Fish</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-21T22:49:53.414457-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12040</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12040</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12040</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Cetaceans evolved flippers that are unique in both size and shape probably due to selection pressures associated with foraging and body size. Flippers function as control surfaces for maneuverability and stability. Flippers of cetaceans and engineered hydrofoils are similar with streamlined cross-sections and wing-like planforms, which affect lift, drag and hydrodynamic efficiency. Scale models of the flippers from large-bodied (body length &gt; 6 m) cetaceans (fin whale, killer whale, sperm whale) were constructed from computed tomography (CT) scans of flippers. Flipper planforms were highly tapered for the fin whale, a rounded, paddle-like design for the killer whale, and a square geometry for the sperm whale. Hydrodynamic properties of the models at varying angles of attack (−40º to 40<sup>o</sup>) were determined in a water tunnel with a multi-axis load cell. The flippers were found to have hydrodynamic characteristics similar to engineered wings. Differences in flipper morphology of large-bodied cetaceans and their hydrodynamic performance are associated with the requirements of aquatic locomotion involved with ecology of the whales. The flippers of the killer whale provided the greatest maneuverability, whereas the flippers of the fin whale had low drag for lunging and the flippers of the sperm whale provided lift for diving.</p></div>
]]></content:encoded><description>

Cetaceans evolved flippers that are unique in both size and shape probably due to selection pressures associated with foraging and body size. Flippers function as control surfaces for maneuverability and stability. Flippers of cetaceans and engineered hydrofoils are similar with streamlined cross-sections and wing-like planforms, which affect lift, drag and hydrodynamic efficiency. Scale models of the flippers from large-bodied (body length &gt; 6 m) cetaceans (fin whale, killer whale, sperm whale) were constructed from computed tomography (CT) scans of flippers. Flipper planforms were highly tapered for the fin whale, a rounded, paddle-like design for the killer whale, and a square geometry for the sperm whale. Hydrodynamic properties of the models at varying angles of attack (−40º to 40o) were determined in a water tunnel with a multi-axis load cell. The flippers were found to have hydrodynamic characteristics similar to engineered wings. Differences in flipper morphology of large-bodied cetaceans and their hydrodynamic performance are associated with the requirements of aquatic locomotion involved with ecology of the whales. The flippers of the killer whale provided the greatest maneuverability, whereas the flippers of the fin whale had low drag for lunging and the flippers of the sperm whale provided lift for diving.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12042" xmlns="http://purl.org/rss/1.0/"><title>Behavioral impacts of disentanglement of a right whale under sedation and the energetic cost of entanglement</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12042</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Behavioral impacts of disentanglement of a right whale under sedation and the energetic cost of entanglement</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Julie Hoop, Michael Moore, Andreas Fahlman, Alessandro Bocconcelli, Clay George, Katharine Jackson, Carolyn Miller, David Morin, Thomas Pitchford, Teri Rowles, Jamison Smith, Barb Zoodsma</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-21T04:28:48.07829-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12042</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12042</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12042</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Protracted entanglement in fishing gear often leads to emaciation through reduced mobility and foraging ability, and energy budget depletion from the added drag of towing gear for months or years. We examined changes in kinematics of a tagged entangled North Atlantic right whale (Eg 3911), before, during, and after disentanglement on 15 January 2011. To calculate the additional drag forces and energetic demand associated with various gear configurations, we towed three sets of gear attached to a load-cell tensiometer at multiple speeds. Tag analyses revealed significant increases in dive depth and duration; ascent, descent and fluke stroke rates; and decreases in root mean square fluke amplitude (a proxy for thrust) following disentanglement. Conservative drag coefficients while entangled in all gear configurations (mean ± SD <em>C</em><sub><em>d,e,go</em></sub> = 3.4 × 10<sup>−3</sup> ± 0.0003, <em>C</em><sub><em>d,e,gb</em></sub> = 3.7 × 10<sup>−3</sup> ± 0.0003, <em>C</em><sub><em>d,e,sl</em></sub> = 3.8 × 10<sup>−3</sup> ± 0.0004) were significantly greater than in the nonentangled case (<em>C</em><sub><em>d,n</em></sub> = 3.2 × 10<sup>−3</sup> ± 0.0003; <em>P </em>=<em> </em>0.0156, 0.0312, 0.0078, respectively). Increases in total power input (including standard metabolism) over the nonentangled condition ranged from 1.6% to 120.9% for all gear configurations tested; locomotory power requirements increased 60.0%–164.6%. These results highlight significant alteration to swimming patterns, and the magnitude of energy depletion in a chronically entangled whale.</p></div>
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Protracted entanglement in fishing gear often leads to emaciation through reduced mobility and foraging ability, and energy budget depletion from the added drag of towing gear for months or years. We examined changes in kinematics of a tagged entangled North Atlantic right whale (Eg 3911), before, during, and after disentanglement on 15 January 2011. To calculate the additional drag forces and energetic demand associated with various gear configurations, we towed three sets of gear attached to a load-cell tensiometer at multiple speeds. Tag analyses revealed significant increases in dive depth and duration; ascent, descent and fluke stroke rates; and decreases in root mean square fluke amplitude (a proxy for thrust) following disentanglement. Conservative drag coefficients while entangled in all gear configurations (mean ± SD Cd,e,go = 3.4 × 10−3 ± 0.0003, Cd,e,gb = 3.7 × 10−3 ± 0.0003, Cd,e,sl = 3.8 × 10−3 ± 0.0004) were significantly greater than in the nonentangled case (Cd,n = 3.2 × 10−3 ± 0.0003; P = 0.0156, 0.0312, 0.0078, respectively). Increases in total power input (including standard metabolism) over the nonentangled condition ranged from 1.6% to 120.9% for all gear configurations tested; locomotory power requirements increased 60.0%–164.6%. These results highlight significant alteration to swimming patterns, and the magnitude of energy depletion in a chronically entangled whale.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12037" xmlns="http://purl.org/rss/1.0/"><title>Nitric oxide in the breath of bottlenose dolphins: Effects of breath hold duration, feeding, and lung disease</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12037</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Nitric oxide in the breath of bottlenose dolphins: Effects of breath hold duration, feeding, and lung disease</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laura C. Yeates, Kevin P. Carlin, Mark Baird, Stephanie Venn-Watson, Sam Ridgway</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-14T03:31:53.985756-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12037</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12037</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12037</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Breath analysis, including measurement of nitric oxide (NO), is a noninvasive diagnostic tool that may help evaluate cetacean health. This is the first report on the effects of breath hold duration, feeding, and lung disease on NO in dolphin exhaled breath. Three healthy dolphins were trained to hold their breath for 30, 60, 90, and 120 s and then exhale into an underwater funnel. Exhaled NO values from 157 breath samples were compared among three healthy dolphins by breath hold time and after fasting and feeding. Exhaled NO values were also measured in two dolphins with pulmonary disease. NO in dolphin breath was higher compared to ambient air; healthy dolphins had higher NO concentrations in their breath after feeding compared to after overnight fasting; and there were no significant differences in exhaled NO levels by breath hold duration. A dolphin with <em>Mycoplasma</em>-associated pneumonia and chronic gastrointestinal disease had higher postprandial exhaled NO levels compared to healthy controls. This study demonstrates, contrary to previous publications, that dolphins exhale NO. Given the high standard deviations present in exhaled breath NO values, future studies are needed to further standardize collection methods or identify more reliable samples (<em>e.g</em>., blood).</p></div>
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Breath analysis, including measurement of nitric oxide (NO), is a noninvasive diagnostic tool that may help evaluate cetacean health. This is the first report on the effects of breath hold duration, feeding, and lung disease on NO in dolphin exhaled breath. Three healthy dolphins were trained to hold their breath for 30, 60, 90, and 120 s and then exhale into an underwater funnel. Exhaled NO values from 157 breath samples were compared among three healthy dolphins by breath hold time and after fasting and feeding. Exhaled NO values were also measured in two dolphins with pulmonary disease. NO in dolphin breath was higher compared to ambient air; healthy dolphins had higher NO concentrations in their breath after feeding compared to after overnight fasting; and there were no significant differences in exhaled NO levels by breath hold duration. A dolphin with Mycoplasma-associated pneumonia and chronic gastrointestinal disease had higher postprandial exhaled NO levels compared to healthy controls. This study demonstrates, contrary to previous publications, that dolphins exhale NO. Given the high standard deviations present in exhaled breath NO values, future studies are needed to further standardize collection methods or identify more reliable samples (e.g., blood).
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12041" xmlns="http://purl.org/rss/1.0/"><title>Improving population estimates by quantifying diving and surfacing patterns: A dugong example</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12041</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Improving population estimates by quantifying diving and surfacing patterns: A dugong example</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rie Hagihara, Rhondda E. Jones, Alana Grech, Janet M. Lanyon, James K. Sheppard, Helene Marsh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T22:55:27.703587-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12041</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12041</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12041</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Diving animals are available for detection from above the water when environmental conditions are favorable and the animals are near the surface. The number of animals that are unavailable for detection needs to be estimated to obtain unbiased population estimates. The current availability correction factors used in aerial surveys for the dugong (<em>Dugong dugon</em>) allow for variation in environmental conditions but use the average time dugongs spend near the surface (<em>i.e</em>., constant availability corrections). To improve availability estimates, we examined location and dive data from nine dugongs fitted with satellite telemetry units and time-depth recorders (TDRs) in eastern Australia. The effects of water depth, tidal conditions, and habitat types on dugong surfacing time were examined using generalized linear mixed models (GLMMs). We found that availability for detection differed with water depth, and depth-specific availability estimates were often lower than the constant estimates. The habitat effect was less influential, and there was no tidal effect. The number of dugongs estimated using depth-specific availabilities were higher than those obtained using constant availabilities across water depth. Hence, information on water depth can refine availability estimates and subsequent abundance estimates from dugong aerial surveys. The methodology may be applicable to other aquatic wildlife.</p></div>
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Diving animals are available for detection from above the water when environmental conditions are favorable and the animals are near the surface. The number of animals that are unavailable for detection needs to be estimated to obtain unbiased population estimates. The current availability correction factors used in aerial surveys for the dugong (Dugong dugon) allow for variation in environmental conditions but use the average time dugongs spend near the surface (i.e., constant availability corrections). To improve availability estimates, we examined location and dive data from nine dugongs fitted with satellite telemetry units and time-depth recorders (TDRs) in eastern Australia. The effects of water depth, tidal conditions, and habitat types on dugong surfacing time were examined using generalized linear mixed models (GLMMs). We found that availability for detection differed with water depth, and depth-specific availability estimates were often lower than the constant estimates. The habitat effect was less influential, and there was no tidal effect. The number of dugongs estimated using depth-specific availabilities were higher than those obtained using constant availabilities across water depth. Hence, information on water depth can refine availability estimates and subsequent abundance estimates from dugong aerial surveys. The methodology may be applicable to other aquatic wildlife.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12038" xmlns="http://purl.org/rss/1.0/"><title>Social structure of Atlantic spotted dolphins, Stenella frontalis, following environmental disturbance and demographic changes</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12038</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Social structure of Atlantic spotted dolphins, Stenella frontalis, following environmental disturbance and demographic changes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cindy R. Elliser, Denise L. Herzing</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-05-07T04:17:38.157309-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12038</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12038</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12038</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Extreme environmental events and demographic changes can have variable effects on the social structure of animal populations. This study compared the social structure of a community of Atlantic spotted dolphins in the Bahamas before and after two hurricanes. Approximately 36% of the individuals were lost, with no subsequent increase in immigration. The majority of the social structure characteristics were consistent with results from a long-term study covering the previous 12 yr, including community structure with definitive social clusters, sex preferences and overall association patterns. However some changes occurred, though still constrained within sex preferences. Posthurricane there was a decrease in social differentiation and increased cohesion within clusters and across age class. Males retained or made new first order alliances, however, only one second order alliance was evident, revealing a simplified alliance structure. Juvenile individuals made alliance level associations, unprecedented from long-term analysis. Although other studies have shown stark restructuring, this study showed that less drastic changes within overall social structure stability can occur. Persistence and evolutionary changes in populations through environmental and/or demographic perturbations may depend on the social structure of a population or community. Understanding the processes involved in social development is paramount for conservation of diverse populations.</p></div>
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Extreme environmental events and demographic changes can have variable effects on the social structure of animal populations. This study compared the social structure of a community of Atlantic spotted dolphins in the Bahamas before and after two hurricanes. Approximately 36% of the individuals were lost, with no subsequent increase in immigration. The majority of the social structure characteristics were consistent with results from a long-term study covering the previous 12 yr, including community structure with definitive social clusters, sex preferences and overall association patterns. However some changes occurred, though still constrained within sex preferences. Posthurricane there was a decrease in social differentiation and increased cohesion within clusters and across age class. Males retained or made new first order alliances, however, only one second order alliance was evident, revealing a simplified alliance structure. Juvenile individuals made alliance level associations, unprecedented from long-term analysis. Although other studies have shown stark restructuring, this study showed that less drastic changes within overall social structure stability can occur. Persistence and evolutionary changes in populations through environmental and/or demographic perturbations may depend on the social structure of a population or community. Understanding the processes involved in social development is paramount for conservation of diverse populations.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12036" xmlns="http://purl.org/rss/1.0/"><title>Bryde's whale calls recorded in the Gulf of Mexico</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12036</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bryde's whale calls recorded in the Gulf of Mexico</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ana Širović, Hannah R. Bassett, Sarah C. Johnson, Sean M. Wiggins, John A. Hildebrand</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-25T04:30:40.039341-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12036</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12036</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12036</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12033" xmlns="http://purl.org/rss/1.0/"><title>Brain size in neonatal and adult Weddell seals: Costs and consequences of having a large brain</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12033</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Brain size in neonatal and adult Weddell seals: Costs and consequences of having a large brain</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Regina Eisert, Charles W. Potter, Olav T. Oftedal</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-25T01:51:04.046858-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12033</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12033</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12033</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Little is known about the ontogeny of brain size in pinnipeds despite potential functional implications of brain substrate (glucose, oxygen) requirements for diving, fasting, growth, and lactation strategies. We measured brain mass (brM) and cranial capacity (CC) in newborn and adult Weddell seals. Neonatal Weddell seals had brM that represented ~70% of adult brM. Weddell seals have the largest neonatal brain, proportional to adult brain, reported for any mammal to date, which is remarkable considering the relatively small size of Weddell seal pups at birth (6%–7% of maternal body mass) compared to neonates of other highly precocial mammals. Provision of sufficient glucose to maintain the large, well-developed brain of the neonatal Weddell seal has a nontrivial metabolic cost to both pup and mother. We therefore hypothesize that this phenomenon must have functional significance, such as allowing pups to acquire complex under-ice navigation skills during the period of maternal attendance.</p></div>
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Little is known about the ontogeny of brain size in pinnipeds despite potential functional implications of brain substrate (glucose, oxygen) requirements for diving, fasting, growth, and lactation strategies. We measured brain mass (brM) and cranial capacity (CC) in newborn and adult Weddell seals. Neonatal Weddell seals had brM that represented ~70% of adult brM. Weddell seals have the largest neonatal brain, proportional to adult brain, reported for any mammal to date, which is remarkable considering the relatively small size of Weddell seal pups at birth (6%–7% of maternal body mass) compared to neonates of other highly precocial mammals. Provision of sufficient glucose to maintain the large, well-developed brain of the neonatal Weddell seal has a nontrivial metabolic cost to both pup and mother. We therefore hypothesize that this phenomenon must have functional significance, such as allowing pups to acquire complex under-ice navigation skills during the period of maternal attendance.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12035" xmlns="http://purl.org/rss/1.0/"><title>Body growth in Hawaiian monk seals</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12035</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Body growth in Hawaiian monk seals</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jason D. Baker, Thea C. Johanos, Tracy A. Wurth, Charles L. Littnan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-25T01:50:48.919025-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12035</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12035</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12035</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Body length and axillary girth measurements of more than 600 free-ranging Hawaiian monk seals from 1 to 20 yr old were analyzed. Comparison of fitted von Bertalanffy growth models confirmed there is no evidence of sexual dimorphism in this species. Substantial differences in growth patterns were detected among seven subpopulations representing the species entire geographic range. The age at which seals would be expected to attain a reference length of 180 cm ranged from just over 3 yr up to almost 7 yr at the various sites. Subpopulations exhibiting slower growth have previously been found to also exhibit lower age-specific reproductive rates. Differences in growth of seals among sites likely indicate varying environmental conditions determining growth during the time periods represented in the sampled data.</p></div>
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Body length and axillary girth measurements of more than 600 free-ranging Hawaiian monk seals from 1 to 20 yr old were analyzed. Comparison of fitted von Bertalanffy growth models confirmed there is no evidence of sexual dimorphism in this species. Substantial differences in growth patterns were detected among seven subpopulations representing the species entire geographic range. The age at which seals would be expected to attain a reference length of 180 cm ranged from just over 3 yr up to almost 7 yr at the various sites. Subpopulations exhibiting slower growth have previously been found to also exhibit lower age-specific reproductive rates. Differences in growth of seals among sites likely indicate varying environmental conditions determining growth during the time periods represented in the sampled data.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12034" xmlns="http://purl.org/rss/1.0/"><title>Prey preferences of sympatric fin (Balaenoptera physalus) and humpback (Megaptera novaeangliae) whales revealed by stable isotope mixing models</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12034</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Prey preferences of sympatric fin (Balaenoptera physalus) and humpback (Megaptera novaeangliae) whales revealed by stable isotope mixing models</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Conor Ryan, Simon D. Berrow, Brendan McHugh, Ciarán O'Donnell, Clive N. Trueman, Ian O'Connor</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-25T01:50:39.545783-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12034</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12034</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12034</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Over-exploitation of top predators and fish stocks has altered ecosystems towards less productive systems with fewer trophic levels. In the Celtic Sea (CS), discards and bycatch levels have prompted concern about some fisheries, while fin and humpback whales are recovering from centuries of over-exploitation. A lack of empirical evidence on the preferred diet of some predators such as whales in the CS has hindered the implementation of effective conservation measures using an ecosystem-based approach to fisheries management. Using a Bayesian framework (SIAR), stable carbon (<em>δ</em><sup>13</sup>C) and nitrogen (<em>δ</em><sup>15</sup>N) isotope mixing models were used to assign proportionate diet solutions to fin and humpback whales (skin biopsies) and putative prey items: herring (<em>Clupea harengus</em>), sprat (<em>Sprattus sprattus</em>), and krill (<em>Meganyctiphanes norvegica</em> and <em>Nyctiphanes couchii</em>) in the CS. Krill was the single most important prey item in the diet of fin whales, but one of the least important for humpback whales (albeit based on a small sample of humpback whale samples). Age 0 sprat and herring comprised a large proportion of the diet of both species, followed by older sprat (age 1–2) and older herring (age 2–4). An ecosystem based approach to fisheries management will be required in the CS if we seek effective conservation of both fin and humpback whales, and sustainable fisheries.</p></div>
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Over-exploitation of top predators and fish stocks has altered ecosystems towards less productive systems with fewer trophic levels. In the Celtic Sea (CS), discards and bycatch levels have prompted concern about some fisheries, while fin and humpback whales are recovering from centuries of over-exploitation. A lack of empirical evidence on the preferred diet of some predators such as whales in the CS has hindered the implementation of effective conservation measures using an ecosystem-based approach to fisheries management. Using a Bayesian framework (SIAR), stable carbon (δ13C) and nitrogen (δ15N) isotope mixing models were used to assign proportionate diet solutions to fin and humpback whales (skin biopsies) and putative prey items: herring (Clupea harengus), sprat (Sprattus sprattus), and krill (Meganyctiphanes norvegica and Nyctiphanes couchii) in the CS. Krill was the single most important prey item in the diet of fin whales, but one of the least important for humpback whales (albeit based on a small sample of humpback whale samples). Age 0 sprat and herring comprised a large proportion of the diet of both species, followed by older sprat (age 1–2) and older herring (age 2–4). An ecosystem based approach to fisheries management will be required in the CS if we seek effective conservation of both fin and humpback whales, and sustainable fisheries.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12030" xmlns="http://purl.org/rss/1.0/"><title>Eastern South Pacific southern right whale photo-identification catalog reveals behavior and habitat use patterns</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12030</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Eastern South Pacific southern right whale photo-identification catalog reveals behavior and habitat use patterns</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bárbara Galletti Vernazzani, Elsa Cabrera, Robert L. Brownell</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-25T01:06:05.67729-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12030</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12030</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12030</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12032" xmlns="http://purl.org/rss/1.0/"><title>Fin whale (Balaenoptera physalus) target strength measurements</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12032</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fin whale (Balaenoptera physalus) target strength measurements</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Matteo Bernasconi, Ruben Patel, Leif Nøttestad, Andrew S. Brierley</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-15T03:33:57.873996-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12032</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12032</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12032</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Active acoustic techniques can be used to detect whales. The ability to detect whales from a moving vessel or stationary buoy could reduce conflicts between hazardous human activities and whales, enabling implementation of mitigation procedures. In order to identify acoustic targets correctly as whales, knowledge of whale target strength (<em>TS</em>) is required. Active acoustic detections of fin whales (<em>Balaenoptera physalus</em>) were made in the Norwegian Sea; acoustic data were collected using calibrated omnidirectional sonar, operating at a discrete frequency of 110 kHz. Three fin whales of similar size (estimated between 16 and 18 m total length) had an overall average TS for all insonified body aspects of −11.4 dB [95% CI −12.05, −10.8] at 110 kHz, with a total spread of nearly 14 dB. As expected, the received signals were stronger when the fin whales were insonified at broadside (−5.6 dB). Individual fin whale <em>TS</em> varied by approximately 12 dB, probably due to variation in lung volume with breathing, and to dynamic swimming kinematics. Our <em>TS</em> values are consistent with values reported previously for other large whales. All data together pave the way for development of automated acoustic whale detection protocols that could aid whale conservation.</p></div>
]]></content:encoded><description>

Active acoustic techniques can be used to detect whales. The ability to detect whales from a moving vessel or stationary buoy could reduce conflicts between hazardous human activities and whales, enabling implementation of mitigation procedures. In order to identify acoustic targets correctly as whales, knowledge of whale target strength (TS) is required. Active acoustic detections of fin whales (Balaenoptera physalus) were made in the Norwegian Sea; acoustic data were collected using calibrated omnidirectional sonar, operating at a discrete frequency of 110 kHz. Three fin whales of similar size (estimated between 16 and 18 m total length) had an overall average TS for all insonified body aspects of −11.4 dB [95% CI −12.05, −10.8] at 110 kHz, with a total spread of nearly 14 dB. As expected, the received signals were stronger when the fin whales were insonified at broadside (−5.6 dB). Individual fin whale TS varied by approximately 12 dB, probably due to variation in lung volume with breathing, and to dynamic swimming kinematics. Our TS values are consistent with values reported previously for other large whales. All data together pave the way for development of automated acoustic whale detection protocols that could aid whale conservation.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12029" xmlns="http://purl.org/rss/1.0/"><title>Remote biopsy darting and marking of polar bears</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12029</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Remote biopsy darting and marking of polar bears</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anthony M. Pagano, Elizabeth Peacock, Melissa A. McKinney</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-09T05:38:16.156725-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12029</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12029</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12029</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Remote biopsy darting of polar bears (<em>Ursus maritimus</em>) is less invasive and time intensive than physical capture and is therefore useful when capture is challenging or unsafe. We worked with two manufacturers to develop a combination biopsy and marking dart for use on polar bears. We had an 80% success rate of collecting a tissue sample with a single biopsy dart and collected tissue samples from 143 polar bears on land, in water, and on sea ice. Dye marks ensured that 96% of the bears were not resampled during the same sampling period, and we recovered 96% of the darts fired. Biopsy heads with 5 mm diameters collected an average of 0.12 g of fur, tissue, and subcutaneous adipose tissue, while biopsy heads with 7 mm diameters collected an average of 0.32 g. Tissue samples were 99.3% successful (142 of 143 samples) in providing a genetic and sex identification of individuals. We had a 64% success rate collecting adipose tissue and we successfully examined fatty acid signatures in all adipose samples. Adipose lipid content values were lower compared to values from immobilized or harvested polar bears, indicating that our method was not suitable for quantifying adipose lipid content.</p></div>
]]></content:encoded><description>

Remote biopsy darting of polar bears (Ursus maritimus) is less invasive and time intensive than physical capture and is therefore useful when capture is challenging or unsafe. We worked with two manufacturers to develop a combination biopsy and marking dart for use on polar bears. We had an 80% success rate of collecting a tissue sample with a single biopsy dart and collected tissue samples from 143 polar bears on land, in water, and on sea ice. Dye marks ensured that 96% of the bears were not resampled during the same sampling period, and we recovered 96% of the darts fired. Biopsy heads with 5 mm diameters collected an average of 0.12 g of fur, tissue, and subcutaneous adipose tissue, while biopsy heads with 7 mm diameters collected an average of 0.32 g. Tissue samples were 99.3% successful (142 of 143 samples) in providing a genetic and sex identification of individuals. We had a 64% success rate collecting adipose tissue and we successfully examined fatty acid signatures in all adipose samples. Adipose lipid content values were lower compared to values from immobilized or harvested polar bears, indicating that our method was not suitable for quantifying adipose lipid content.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12031" xmlns="http://purl.org/rss/1.0/"><title>Reestablishment of former wintering grounds by New Zealand southern right whales</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12031</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reestablishment of former wintering grounds by New Zealand southern right whales</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emma L. Carroll, William J. Rayment, Alana M. Alexander, C. Scott Baker, Nathalie J. Patenaude, Debbie Steel, Rochelle Constantine, Rosalind Cole, Laura J. Boren, Simon Childerhouse</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-03T02:09:54.503729-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12031</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12031</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12031</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Historically, the range of the southern right whale (SRW) included winter calving grounds around the North and South Islands (mainland) of New Zealand (NZ) and in the NZ subantarctic Auckland and Campbell Islands. Due to extensive whaling in the 19th and 20th centuries, no SRW was seen around mainland NZ for nearly four decades (1928–1963). Here we present evidence for the regular use of the mainland NZ wintering ground, presumably from a remnant population that persisted in the NZ subantarctic Auckland and Campbell Islands. SRWs have been sighted every year around mainland NZ since 1988, with 125 sightings during the focus of this work: from 2003 to 2010. There were 28 cow-calf pairs sighted around mainland NZ from 2003 to 2010, compared with 11 sightings from 1991 to 2002. Furthermore, two females, identified by DNA profiles, were sighted with calves around mainland at 4 yr intervals: the first evidence of female site fidelity to the mainland NZ calving ground. Individual identification from photographs of natural markings and DNA profiles provided information on within-year movements and residency around the mainland, and further evidence for exchange between the mainland and subantarctic wintering grounds. Despite these promising signs, the distribution of NZ SRWs remains primarily concentrated in the NZ subantarctic.</p></div>
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Historically, the range of the southern right whale (SRW) included winter calving grounds around the North and South Islands (mainland) of New Zealand (NZ) and in the NZ subantarctic Auckland and Campbell Islands. Due to extensive whaling in the 19th and 20th centuries, no SRW was seen around mainland NZ for nearly four decades (1928–1963). Here we present evidence for the regular use of the mainland NZ wintering ground, presumably from a remnant population that persisted in the NZ subantarctic Auckland and Campbell Islands. SRWs have been sighted every year around mainland NZ since 1988, with 125 sightings during the focus of this work: from 2003 to 2010. There were 28 cow-calf pairs sighted around mainland NZ from 2003 to 2010, compared with 11 sightings from 1991 to 2002. Furthermore, two females, identified by DNA profiles, were sighted with calves around mainland at 4 yr intervals: the first evidence of female site fidelity to the mainland NZ calving ground. Individual identification from photographs of natural markings and DNA profiles provided information on within-year movements and residency around the mainland, and further evidence for exchange between the mainland and subantarctic wintering grounds. Despite these promising signs, the distribution of NZ SRWs remains primarily concentrated in the NZ subantarctic.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12028" xmlns="http://purl.org/rss/1.0/"><title>Analysis of a Blainville's beaked whale's movement response to playback of killer whale vocalizations</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12028</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Analysis of a Blainville's beaked whale's movement response to playback of killer whale vocalizations</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ann N. Allen, Julian J. Schanze, Andrew R. Solow, Peter L. Tyack</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-01T00:04:39.375277-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12028</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12028</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12028</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Increasing evidence links exposure to Navy sonar with certain mass stranding events of deep diving beaked whales. Although the cause of these strandings is unknown, one theory suggests that the animals confuse the sonar signals with vocalizations of killer whales, a known predator. Here we analyze the movement patterns of a tagged female Blainville's beaked whale in reaction to playback of killer whale predation calls. During a deep foraging dive, the whale was exposed to a playback of killer whale vocalizations with the source level slowly increased until the whale prematurely ceased foraging. The heading data from the tag were analyzed using a rotation test with a likelihood ratio calculated for a nonparametric kernel density estimate. We found a significant difference (<em>P </em>&lt;<em> </em>0.005) in the distribution of Δheading (the change in heading averaged over 200 s) after the cessation of the killer whale playback. A test of the angular standard deviation (SD) of the Δheading showed that after the playback, the SD was significantly reduced (<em>P </em>=<em> </em>0.0064), which indicates that the animal maintained a straighter than normal course for an extended period of time. The prolonged directed avoidance response observed here suggests a behavioral reaction that could pose a risk factor for stranding.</p></div>
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Increasing evidence links exposure to Navy sonar with certain mass stranding events of deep diving beaked whales. Although the cause of these strandings is unknown, one theory suggests that the animals confuse the sonar signals with vocalizations of killer whales, a known predator. Here we analyze the movement patterns of a tagged female Blainville's beaked whale in reaction to playback of killer whale predation calls. During a deep foraging dive, the whale was exposed to a playback of killer whale vocalizations with the source level slowly increased until the whale prematurely ceased foraging. The heading data from the tag were analyzed using a rotation test with a likelihood ratio calculated for a nonparametric kernel density estimate. We found a significant difference (P &lt; 0.005) in the distribution of Δheading (the change in heading averaged over 200 s) after the cessation of the killer whale playback. A test of the angular standard deviation (SD) of the Δheading showed that after the playback, the SD was significantly reduced (P = 0.0064), which indicates that the animal maintained a straighter than normal course for an extended period of time. The prolonged directed avoidance response observed here suggests a behavioral reaction that could pose a risk factor for stranding.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12027" xmlns="http://purl.org/rss/1.0/"><title>Population genetic structure and taxonomy of the common dolphin (Delphinus sp.) at its southernmost range limit: New Zealand waters</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12027</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Population genetic structure and taxonomy of the common dolphin (Delphinus sp.) at its southernmost range limit: New Zealand waters</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Karen A. Stockin, Ana R. Amaral, Julie Latimer, David M. Lambert, Ada Natoli</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-21T03:24:01.340177-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12027</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12027</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12027</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>New Zealand is the southernmost limit of the common dolphin's (genus <em>Delphinus</em>) distribution in the Pacific Ocean. In this area, common dolphins occur in both coastal and oceanic habitats, exhibit seasonal and resident occurrence, and present high morphological variability. Here we investigated the population structure and the taxonomic identity of common dolphins (<em>Delphinus</em> sp.) within New Zealand waters using 14 microsatellite loci, 577 bp of the mtDNA control region, and 1,120 bp of the mtDNA cytochrome <em>b</em> gene across 90 individuals. We found high genetic variability and evidence of population expansion. Phylogenetic analyses conducted to clarify the taxonomic status of New Zealand common dolphins did not show any clustering reflecting geographic origin or morphotypes. The microsatellite analysis showed genetic differentiation between <em>Coastal</em> and <em>Oceanic</em> putative populations, while mtDNA revealed significant genetic differentiation only between the <em>Hauraki Gulf</em> and other putative groups. Our results suggest that differences in habitat choice and possible female site fidelity may play a role in shaping population structure of New Zealand common dolphins.</p></div>
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New Zealand is the southernmost limit of the common dolphin's (genus Delphinus) distribution in the Pacific Ocean. In this area, common dolphins occur in both coastal and oceanic habitats, exhibit seasonal and resident occurrence, and present high morphological variability. Here we investigated the population structure and the taxonomic identity of common dolphins (Delphinus sp.) within New Zealand waters using 14 microsatellite loci, 577 bp of the mtDNA control region, and 1,120 bp of the mtDNA cytochrome b gene across 90 individuals. We found high genetic variability and evidence of population expansion. Phylogenetic analyses conducted to clarify the taxonomic status of New Zealand common dolphins did not show any clustering reflecting geographic origin or morphotypes. The microsatellite analysis showed genetic differentiation between Coastal and Oceanic putative populations, while mtDNA revealed significant genetic differentiation only between the Hauraki Gulf and other putative groups. Our results suggest that differences in habitat choice and possible female site fidelity may play a role in shaping population structure of New Zealand common dolphins.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12026" xmlns="http://purl.org/rss/1.0/"><title>Long-range movement by Hector's dolphins provides potential genetic enhancement for critically endangered Maui's dolphin</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12026</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Long-range movement by Hector's dolphins provides potential genetic enhancement for critically endangered Maui's dolphin</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rebecca M. Hamner, Rochelle Constantine, Marc Oremus, Martin Stanley, Phillip Brown, C. Scott Baker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T02:21:07.479123-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12026</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12026</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12026</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>For endangered populations with low genetic diversity, low levels of immigration could lead to genetic rescue, reducing the risk of inbreeding depression and enhancing chances of long-term species survival. Our genetic monitoring of Maui's dolphins revealed the first contemporary dispersal of their sister subspecies, Hector's dolphin, from New Zealand's South Island into the Maui's dolphin distribution along ~300 km of the North Island's northwest coast. From 2010 to 2012, 44 individuals were sampled within the Maui's dolphin distribution, four of which were genetically identified as Hector's dolphins (two living females, one dead female, one dead male). We also report two Hector's dolphins (one dead female neonate, one living male) sampled along the North Island's southwest coast, outside the presumed range of either subspecies. Together, these records demonstrate long-distance dispersal by Hector's dolphins (≥400 km) and the possibility of an unsampled Hector's dolphin population along the southwest coast of the North Island. Although two living Hector's dolphins were found in association with Maui's dolphins, there is currently no evidence of interbreeding between the subspecies. These results highlight the value of genetic monitoring for subspecies lacking distinctive physical appearances as such discoveries are not detected by other means, but have important conservation implications.</p></div>
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For endangered populations with low genetic diversity, low levels of immigration could lead to genetic rescue, reducing the risk of inbreeding depression and enhancing chances of long-term species survival. Our genetic monitoring of Maui's dolphins revealed the first contemporary dispersal of their sister subspecies, Hector's dolphin, from New Zealand's South Island into the Maui's dolphin distribution along ~300 km of the North Island's northwest coast. From 2010 to 2012, 44 individuals were sampled within the Maui's dolphin distribution, four of which were genetically identified as Hector's dolphins (two living females, one dead female, one dead male). We also report two Hector's dolphins (one dead female neonate, one living male) sampled along the North Island's southwest coast, outside the presumed range of either subspecies. Together, these records demonstrate long-distance dispersal by Hector's dolphins (≥400 km) and the possibility of an unsampled Hector's dolphin population along the southwest coast of the North Island. Although two living Hector's dolphins were found in association with Maui's dolphins, there is currently no evidence of interbreeding between the subspecies. These results highlight the value of genetic monitoring for subspecies lacking distinctive physical appearances as such discoveries are not detected by other means, but have important conservation implications.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12025" xmlns="http://purl.org/rss/1.0/"><title>Lifetime survival rates and senescence in northern elephant seals</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12025</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Lifetime survival rates and senescence in northern elephant seals</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Richard Condit, Joanne Reiter, Patricia A. Morris, Ryan Berger, Sarah G. Allen, Burney J. Boeuf</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-07T02:21:02.35247-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12025</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12025</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12025</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The aim of this study was to extend 40 yr of prior demographic work on northern elephant seals (<em>Mirounga angustirostris</em>) at Año Nuevo, California, by including the oldest animals. We used a Bayesian mark-recapture analysis to estimate lifelong survival and lifespan of a cohort of 372 weaned pups branded in 1985–1987 and resighted until 2008. Annual survival probability of females averaged 86.3%/yr at ages 5–16, then declined until age 21, the age of the oldest female. Male survival was lower, averaging 67.7%/yr from age 1 to age 15, the age of the oldest male. Northern elephant seal females in the expanding population at Año Nuevo live longer than southern elephant seal females (<em>M. leonina</em>) at colonies whose populations are declining. This comparison suggests that high survival of females is a key factor in population growth.</p></div>
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The aim of this study was to extend 40 yr of prior demographic work on northern elephant seals (Mirounga angustirostris) at Año Nuevo, California, by including the oldest animals. We used a Bayesian mark-recapture analysis to estimate lifelong survival and lifespan of a cohort of 372 weaned pups branded in 1985–1987 and resighted until 2008. Annual survival probability of females averaged 86.3%/yr at ages 5–16, then declined until age 21, the age of the oldest female. Male survival was lower, averaging 67.7%/yr from age 1 to age 15, the age of the oldest male. Northern elephant seal females in the expanding population at Año Nuevo live longer than southern elephant seal females (M. leonina) at colonies whose populations are declining. This comparison suggests that high survival of females is a key factor in population growth.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12021" xmlns="http://purl.org/rss/1.0/"><title>False killer whales (Pseudorca crassidens) from Japan and South Africa: Differences in growth and reproduction</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12021</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">False killer whales (Pseudorca crassidens) from Japan and South Africa: Differences in growth and reproduction</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Inês M. Ferreira, Toshio Kasuya, Helene Marsh, Peter B. Best</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T02:59:28.040969-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12021</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12021</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12021</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Age and reproductive information for 65 false killer whales stranded in South Africa in 1981 are compared with similar material from 156 animals examined from drive fisheries in Japan in 1979 and 1980. Sizes at birth, sexual maturation, and physical maturity all indicated that both sexes were 10%–20% larger in Japan than South Africa. Females reached sexual maturation at similar ages (8–10.5 yr) in both populations, and although sample sizes were too small to establish male ages at puberty precisely the ranges in Japan (10.5–18.5 yr) and South Africa (5.25–17.5 yr) were not inconsistent. The initial ovulation rate for females from South Africa was 65% lower (and the apparent pregnancy rate 82% lower) than those from Japan and there were fewer animals ≤2 yr old within the school, but the magnitude of these differences suggests that the stranded school's reproductive performance was probably impaired. Collectively these comparisons and the literature indicate substantive size differences between false killer whales in different populations, although the patterns of growth appear similar. Firm conclusions about any geographical differences in reproduction require additional data.</p></div>
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Age and reproductive information for 65 false killer whales stranded in South Africa in 1981 are compared with similar material from 156 animals examined from drive fisheries in Japan in 1979 and 1980. Sizes at birth, sexual maturation, and physical maturity all indicated that both sexes were 10%–20% larger in Japan than South Africa. Females reached sexual maturation at similar ages (8–10.5 yr) in both populations, and although sample sizes were too small to establish male ages at puberty precisely the ranges in Japan (10.5–18.5 yr) and South Africa (5.25–17.5 yr) were not inconsistent. The initial ovulation rate for females from South Africa was 65% lower (and the apparent pregnancy rate 82% lower) than those from Japan and there were fewer animals ≤2 yr old within the school, but the magnitude of these differences suggests that the stranded school's reproductive performance was probably impaired. Collectively these comparisons and the literature indicate substantive size differences between false killer whales in different populations, although the patterns of growth appear similar. Firm conclusions about any geographical differences in reproduction require additional data.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12023" xmlns="http://purl.org/rss/1.0/"><title>Agonistic intraspecific behavior in free-ranging bottlenose dolphins: Calf-directed aggression and infanticidal tendencies by adult males</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12023</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Agonistic intraspecific behavior in free-ranging bottlenose dolphins: Calf-directed aggression and infanticidal tendencies by adult males</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kevin P. Robinson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T02:59:23.344396-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12023</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12023</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12023</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12022" xmlns="http://purl.org/rss/1.0/"><title>Pleistocene sea level fluctuations and the phylogeography of the dugong in Australian waters</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12022</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Pleistocene sea level fluctuations and the phylogeography of the dugong in Australian waters</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David Blair, Adrian McMahon, Brenda McDonald, Daniela Tikel, Michelle Waycott, Helene Marsh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T02:59:20.434767-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12022</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12022</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12022</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We investigated phylogeography, demography, and population connectivity of the dugong (<em>Dugong dugon</em>) in Australian waters using mitochondrial control region DNA sequences from 177 Australian dugongs and 11 from elsewhere. The dugong is widespread in shallow Indo-West Pacific waters suitable for growth of its main food, seagrass. We hypothesized that the loss of habitat and creation of a land barrier (the Torres Strait landbridge) during low sea level stands associated with Pleistocene glacial cycles have left a persisting genetic signature in the dugong. The landbridge was most recently flooded about 7,000 yr ago. Individual dugongs are capable of traveling long distances, suggesting an alternative hypothesis that there might now be little genetic differentiation across the dugong's Australian range. We demonstrated that Australian dugongs fall into two distinct maternal lineages and exhibit a phylogeographic pattern reflecting Pleistocene sea-level fluctuations. Within each lineage, genetic structure exists, albeit at large spatial scales. We suggest that these lineages diverged following the last emergence of the Torres Strait landbridge (<em>ca</em>. 115 kya) and remained geographically separated until after 7 kya when passage through Torres Strait again became possible for marine animals. Evidence for population growth in the widespread lineage, especially after the last glacial maximum, was detected.</p></div>
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We investigated phylogeography, demography, and population connectivity of the dugong (Dugong dugon) in Australian waters using mitochondrial control region DNA sequences from 177 Australian dugongs and 11 from elsewhere. The dugong is widespread in shallow Indo-West Pacific waters suitable for growth of its main food, seagrass. We hypothesized that the loss of habitat and creation of a land barrier (the Torres Strait landbridge) during low sea level stands associated with Pleistocene glacial cycles have left a persisting genetic signature in the dugong. The landbridge was most recently flooded about 7,000 yr ago. Individual dugongs are capable of traveling long distances, suggesting an alternative hypothesis that there might now be little genetic differentiation across the dugong's Australian range. We demonstrated that Australian dugongs fall into two distinct maternal lineages and exhibit a phylogeographic pattern reflecting Pleistocene sea-level fluctuations. Within each lineage, genetic structure exists, albeit at large spatial scales. We suggest that these lineages diverged following the last emergence of the Torres Strait landbridge (ca. 115 kya) and remained geographically separated until after 7 kya when passage through Torres Strait again became possible for marine animals. Evidence for population growth in the widespread lineage, especially after the last glacial maximum, was detected.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12024" xmlns="http://purl.org/rss/1.0/"><title>Can gray seals maintain heading within areas of high tidal current? Preliminary results from numerical modeling and GPS observations</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12024</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Can gray seals maintain heading within areas of high tidal current? Preliminary results from numerical modeling and GPS observations</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Damien Chevaillier, Mikhail Karpytchev, Bernie J. Mcconnell, Simon Moss, Cecile Vincent</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-03-01T02:59:13.240245-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12024</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12024</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12024</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12018" xmlns="http://purl.org/rss/1.0/"><title>An evaluation of lipid extraction techniques for interpretation of carbon and nitrogen isotope values in bottlenose dolphin (Tursiops truncatus) skin tissue</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12018</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">An evaluation of lipid extraction techniques for interpretation of carbon and nitrogen isotope values in bottlenose dolphin (Tursiops truncatus) skin tissue</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rachel Marie Wilson, Jeffrey P. Chanton, Brian C. Balmer, Douglas P. Nowacek</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-15T05:32:44.731449-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12018</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12018</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12018</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We studied the effects of two common chemical extraction techniques on bottlenose dolphin (<em>Tursiops truncatus</em>) skin tissues with the intent to develop a mathematical lipid correction for dolphin skin δ<sup>13</sup>C. One method employs a hot solvent mixture (chloroform and methanol) while the other method requires washing the samples with cold solvent followed by water. The water wash method resulted in significant alteration of tissue δ<sup>15</sup>N. We found no correlation between change in sample mass and C/N or between change in sample mass and the change in δ<sup>13</sup>C (Δδ<sup>13</sup>C) following lipid extraction. Although Δδ<sup>13</sup>C was positive following lipid extraction (mean = 1.6‰ and 1.2‰, for the two methods), there was no correlation between C/N and Δδ<sup>13</sup>C for either method. Cumulatively, these results prevented us from applying a mathematical lipid normalization. Based on our findings and consideration of previously reported results, we suggest that applying these extraction techniques to dolphin skin with C/N &lt; 4.5 introduces greater uncertainty than is warranted. We recommend against lipid correction for dolphin skins with C/N &lt; 4.5, but stress that the resulting uncertainty in δ<sup>13</sup>C needs to be accounted for when implementing isotope mixing models to assess diet or organic matter sources.</p></div>
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We studied the effects of two common chemical extraction techniques on bottlenose dolphin (Tursiops truncatus) skin tissues with the intent to develop a mathematical lipid correction for dolphin skin δ13C. One method employs a hot solvent mixture (chloroform and methanol) while the other method requires washing the samples with cold solvent followed by water. The water wash method resulted in significant alteration of tissue δ15N. We found no correlation between change in sample mass and C/N or between change in sample mass and the change in δ13C (Δδ13C) following lipid extraction. Although Δδ13C was positive following lipid extraction (mean = 1.6‰ and 1.2‰, for the two methods), there was no correlation between C/N and Δδ13C for either method. Cumulatively, these results prevented us from applying a mathematical lipid normalization. Based on our findings and consideration of previously reported results, we suggest that applying these extraction techniques to dolphin skin with C/N &lt; 4.5 introduces greater uncertainty than is warranted. We recommend against lipid correction for dolphin skins with C/N &lt; 4.5, but stress that the resulting uncertainty in δ13C needs to be accounted for when implementing isotope mixing models to assess diet or organic matter sources.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12017" xmlns="http://purl.org/rss/1.0/"><title>Reversible immobilization of free-ranging adult male California sea lions (Zalophus californianus)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12017</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reversible immobilization of free-ranging adult male California sea lions (Zalophus californianus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sharon R. Melin, Martin Haulena, William Bonn, Mathew J. Tennis, Robin F. Brown, Jeffrey D. Harris</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-15T05:30:41.038243-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12017</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12017</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12017</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12013" xmlns="http://purl.org/rss/1.0/"><title>Estimation of calf:cow ratios of Pacific walruses for use in population modeling and monitoring</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12013</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Estimation of calf:cow ratios of Pacific walruses for use in population modeling and monitoring</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">John J. Citta, Lori T. Quakenbush, Brian D. Taras</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-05T02:12:30.613556-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12013</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12013</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12013</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We report on a method of visually classifying Pacific walruses (<em>Odobenus rosmarus</em>) to sex and age class with the goal of estimating calf:cow ratios. Development of this method began in 1958 by Dr. F. H. Fay and was used during six surveys in the Chukchi Sea between 1981 and 1999. We estimate calf:cow ratios using beta-binomial models to allow for overdispersion and use Monte Carlo simulations to assess the reliability of prior surveys and quantify sample sizes required for future surveys. Calf:cow ratios did not vary by region, date, or by the number of cows in a group. However, higher ratios were observed in the morning and evening than during the day, indicating haul out behavior of cows varies by reproductive status. Adjusted for solar noon, few calves were observed in 1981 (3:100), 1984 (6:100), and 1998 (5:100), while substantially more were observed in 1982 (15:100) and 1999 (13:100). Classifying between 200 and 300 groups with cows (~1,600–2,300 individual cows) will yield calf:cow ratios with ~20%–30% relative precision. Tagging studies that examine hauling-out behavior of cows with and without calves relative to time-of-day are necessary to better understand how to interpret calf:cow ratios.</p></div>
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We report on a method of visually classifying Pacific walruses (Odobenus rosmarus) to sex and age class with the goal of estimating calf:cow ratios. Development of this method began in 1958 by Dr. F. H. Fay and was used during six surveys in the Chukchi Sea between 1981 and 1999. We estimate calf:cow ratios using beta-binomial models to allow for overdispersion and use Monte Carlo simulations to assess the reliability of prior surveys and quantify sample sizes required for future surveys. Calf:cow ratios did not vary by region, date, or by the number of cows in a group. However, higher ratios were observed in the morning and evening than during the day, indicating haul out behavior of cows varies by reproductive status. Adjusted for solar noon, few calves were observed in 1981 (3:100), 1984 (6:100), and 1998 (5:100), while substantially more were observed in 1982 (15:100) and 1999 (13:100). Classifying between 200 and 300 groups with cows (~1,600–2,300 individual cows) will yield calf:cow ratios with ~20%–30% relative precision. Tagging studies that examine hauling-out behavior of cows with and without calves relative to time-of-day are necessary to better understand how to interpret calf:cow ratios.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12016" xmlns="http://purl.org/rss/1.0/"><title>Nocturnal feeding of Atlantic spotted dolphins (Stenella frontalis) in the Bahamas</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12016</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Nocturnal feeding of Atlantic spotted dolphins (Stenella frontalis) in the Bahamas</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Denise L. Herzing, Cindy R. Elliser</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-05T02:12:27.224191-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12016</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12016</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12016</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12015" xmlns="http://purl.org/rss/1.0/"><title>Patterns and trends in the diet of long-finned pilot whales (Globicephala melas) in the northeast Atlantic</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12015</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Patterns and trends in the diet of long-finned pilot whales (Globicephala melas) in the northeast Atlantic</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Begoña Santos, Silvia S. Monteiro, José V. Vingada, Marisa Ferreira, Alfredo López, José A. Martínez Cedeira, Robert J. Reid, Andrew Brownlow, Graham J. Pierce</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-05T02:12:23.371747-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12015</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12015</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12015</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>There is little previous information on feeding habits of long-finned pilot whales (<em>Globicephala melas</em>) in the northeast Atlantic. The present study analyzed stomach contents of pilot whales stranded in Portugal (<em>n </em>=<em> </em>6), Galicia (northwest Spain) (<em>n </em>=<em> </em>32), and Scotland (United Kingdom) (<em>n </em>=<em> </em>10), from 1990 to 2011. These animals ranged from 213 to 555 cm in length (24 females, 19 males and 5 of unknown sex). The main prey identified were cephalopods of the families Octopodidae and Ommastrephidae, the former being numerically more important in Iberia (Portugal and Galicia) and the latter more important in Scotland, with Iberian whales also showing a more diverse diet. Multivariate analysis revealed evidence of geographical and seasonal variation in diet. Generalized Additive Modeling results indicated that more octopus (<em>Eledone cirrhosa</em>) were eaten in Iberia than in Scotland, more in the first half of the year, and more in larger whales. Numbers of ommastrephid squids in the stomach decreased over the study period and varied with season and whale length. This study confirms cephalopods as the main prey of pilot whales, as previously reported, although our results also suggest that, in the northeast Atlantic, ommastrephid squid are largely replaced as the main prey by octopods at lower latitudes.</p></div>
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There is little previous information on feeding habits of long-finned pilot whales (Globicephala melas) in the northeast Atlantic. The present study analyzed stomach contents of pilot whales stranded in Portugal (n = 6), Galicia (northwest Spain) (n = 32), and Scotland (United Kingdom) (n = 10), from 1990 to 2011. These animals ranged from 213 to 555 cm in length (24 females, 19 males and 5 of unknown sex). The main prey identified were cephalopods of the families Octopodidae and Ommastrephidae, the former being numerically more important in Iberia (Portugal and Galicia) and the latter more important in Scotland, with Iberian whales also showing a more diverse diet. Multivariate analysis revealed evidence of geographical and seasonal variation in diet. Generalized Additive Modeling results indicated that more octopus (Eledone cirrhosa) were eaten in Iberia than in Scotland, more in the first half of the year, and more in larger whales. Numbers of ommastrephid squids in the stomach decreased over the study period and varied with season and whale length. This study confirms cephalopods as the main prey of pilot whales, as previously reported, although our results also suggest that, in the northeast Atlantic, ommastrephid squid are largely replaced as the main prey by octopods at lower latitudes.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12014" xmlns="http://purl.org/rss/1.0/"><title>Are there biases in biopsy sampling? Potential drivers of sex ratio in projectile biopsy samples from two small delphinids</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12014</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Are there biases in biopsy sampling? Potential drivers of sex ratio in projectile biopsy samples from two small delphinids</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nicholas M. Kellar, Marisa L. Trego, Susan J. Chivers, Fredrick I. Archer, Jeremiah J. Minich, Wayne L. Perryman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-02-05T02:12:18.473757-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12014</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12014</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12014</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Molecular assays were used to determine the sex of 1,294 biopsied common dolphins (658 long-beaked common dolphins, <em>Delphinus capensis</em>, and 636 short-beaked common dolphins, <em>D. delphis</em>) in the Southern California Bight. Sex ratio differed substantially between the two species; females comprised 241 (36.6%) of <em>D. capensis</em> samples and 410 (64.5%) of <em>D. delphis</em> samples. All biopsies were taken either from a large research ship or from a small, rigid-hull inflatable boat (RHIB) launched from the larger ship. When conducting replicate biopsy effort on the same schools from each vessel/platform (“Tandem Biopsy Sampling”), we found evidence that disproportionately more female <em>D. capensis</em> were biopsied from the RHIB than from the ship but the same was not true for <em>D. delphis</em>. We suspect that these results are driven by bowriding-behavior differences between the two species. Biopsy duration, geographic location, school size, and Julian date were considered as potential covariates with sex ratio; geographic location was the only one to show strong evidence of correlation. This study also presents an alternative to the erroneous practice of comparing sex ratios to a theoretical assumption of parity (<em>i.e</em>., 50:50 sex ratio) when researchers avoid sampling animals paired with calves.</p></div>
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Molecular assays were used to determine the sex of 1,294 biopsied common dolphins (658 long-beaked common dolphins, Delphinus capensis, and 636 short-beaked common dolphins, D. delphis) in the Southern California Bight. Sex ratio differed substantially between the two species; females comprised 241 (36.6%) of D. capensis samples and 410 (64.5%) of D. delphis samples. All biopsies were taken either from a large research ship or from a small, rigid-hull inflatable boat (RHIB) launched from the larger ship. When conducting replicate biopsy effort on the same schools from each vessel/platform (“Tandem Biopsy Sampling”), we found evidence that disproportionately more female D. capensis were biopsied from the RHIB than from the ship but the same was not true for D. delphis. We suspect that these results are driven by bowriding-behavior differences between the two species. Biopsy duration, geographic location, school size, and Julian date were considered as potential covariates with sex ratio; geographic location was the only one to show strong evidence of correlation. This study also presents an alternative to the erroneous practice of comparing sex ratios to a theoretical assumption of parity (i.e., 50:50 sex ratio) when researchers avoid sampling animals paired with calves.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12008" xmlns="http://purl.org/rss/1.0/"><title>Decline in local abundance of bottlenose dolphins (Tursiops truncatus) in the Bay of Islands, New Zealand</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12008</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Decline in local abundance of bottlenose dolphins (Tursiops truncatus) in the Bay of Islands, New Zealand</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gabriela Tezanos-Pinto, Rochelle Constantine, Lyndon Brooks, Jennifer A. Jackson, Fabiana Mourão, Sarah Wells, C. Scott Baker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-24T11:30:38.357616-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12008</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12008</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12008</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Regional populations of bottlenose dolphins (<em>Tursiops truncatus</em>) around New Zealand are genetically isolated from each other and the species was recently classified as <em>nationally endangered</em> based on relatively small population sizes and reports of high calf mortality. Here, we estimate the abundance and trends in one of these regional populations, the Bay of Islands, using a photo-identification database collected from 1997 to 1999 and from 2003 to 2006, containing a total of 3,841 records of 317 individual dolphins. Estimates of abundance obtained with the robust design fluctuated widely but showed a significant decline in the number of dolphins present in the bay over time (7.5% annual rate of decline). Temporary emigration was random and fluctuated considerably (γ  =  0.18, SE = 0.07 to γ  =  0.84, SE = 0.06). Apparent survival was estimated at 0.928 (CI = 0.911–0.942). Seasonal estimates (26 seasons) obtained in POPAN also showed a significant decline in abundance (5.8% annual rate of decline). Despite the decline observed in local abundance, dolphins continue to be found regularly in the Bay of Islands, suggesting that fewer dolphins use the bay on regular basis. Consequently, it seems that a change in habitat use, mortality and possibly low recruitment could underlie the apparent local decline.</p></div>
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Regional populations of bottlenose dolphins (Tursiops truncatus) around New Zealand are genetically isolated from each other and the species was recently classified as nationally endangered based on relatively small population sizes and reports of high calf mortality. Here, we estimate the abundance and trends in one of these regional populations, the Bay of Islands, using a photo-identification database collected from 1997 to 1999 and from 2003 to 2006, containing a total of 3,841 records of 317 individual dolphins. Estimates of abundance obtained with the robust design fluctuated widely but showed a significant decline in the number of dolphins present in the bay over time (7.5% annual rate of decline). Temporary emigration was random and fluctuated considerably (γ  =  0.18, SE = 0.07 to γ  =  0.84, SE = 0.06). Apparent survival was estimated at 0.928 (CI = 0.911–0.942). Seasonal estimates (26 seasons) obtained in POPAN also showed a significant decline in abundance (5.8% annual rate of decline). Despite the decline observed in local abundance, dolphins continue to be found regularly in the Bay of Islands, suggesting that fewer dolphins use the bay on regular basis. Consequently, it seems that a change in habitat use, mortality and possibly low recruitment could underlie the apparent local decline.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12012" xmlns="http://purl.org/rss/1.0/"><title>An unusual case of care-giving behavior in wild long-beaked common dolphins (Delphinus capensis) in the East Sea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12012</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">An unusual case of care-giving behavior in wild long-beaked common dolphins (Delphinus capensis) in the East Sea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kyum J. Park, Hawsun Sohn, Yong R. An, Dae Y. Moon, Seok G. Choi, Doo H. An</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-18T04:03:12.421426-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12012</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12012</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12012</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12011" xmlns="http://purl.org/rss/1.0/"><title>Sex determination in adults of two otariid species (Neophoca cinerea and Arctophoca australis forsteri) based on osteology of the pelvis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12011</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sex determination in adults of two otariid species (Neophoca cinerea and Arctophoca australis forsteri) based on osteology of the pelvis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Maria Zammit, Rachel M. Norris</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-18T04:02:51.114137-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12011</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12011</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12011</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12009" xmlns="http://purl.org/rss/1.0/"><title>Fueling phocids: Divergent exploitation of primary energy sources and parallel ontogenetic diet switches among three species of subarctic seals</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12009</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fueling phocids: Divergent exploitation of primary energy sources and parallel ontogenetic diet switches among three species of subarctic seals</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Strahan Tucker, Garry B. Stenson, W. Don Bowen, Sara J. Iverson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-18T03:35:36.102135-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12009</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12009</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12009</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Determining how marine predators partition resources is hindered by the difficulty in obtaining information on diet and distribution. Stable isotopes (SI) of carbon (<sup>13</sup>C/<sup>12</sup>C, δ<sup>13</sup>C) and nitrogen (<sup>15</sup>N/<sup>14</sup>N, δ<sup>15</sup>N) provide a two-dimensional estimate of the dietary space of consumers; an animal's isotopic composition is directly influenced by what they consume and where they feed. Harp (<em>Pagophilus groenlandicus</em>) and hooded (<em>Cystophora cristata</em>) seals are abundant phocid species found in the North Atlantic. We measured and contrasted SI values between seals sampled at nearshore and offshore sites to test for effects of sampling location, sex, age-class, and body size to gain insight into how these species partition space and prey resources. In addition we contrasted previously published results for gray seals (<em>Halichoerus grypus</em>). Isotope values differed significantly by age class and location in harp and hooded seals. We found significant differences in SI values (mean δ<sup>13</sup>C and δ<sup>15</sup>N ± SE) between all species. Hooded seals, a continental shelf-edge, deep-diving species, exhibited low SI values (juveniles: −20.9‰ ± 0.03‰, 13.36‰ ± 0.05‰; adults: −20.41‰ ± 0.03‰, 14.81‰ ± 0.04‰) characteristic of feeding on meso- to bathypelagic prey. Harp seals, which dive to moderate depths primarily on the shelf had intermediate SI values (juveniles: −20.53‰ ± 0.01‰, 13.91‰ ± 0.01‰; adults: −20.13‰ ± 0.01‰, 14.96‰ ± 0.01‰) characteristic of feeding on epipelagic prey, whereas gray seals, which feed on or near the sea floor in shallow shelf waters, had high SI values (juveniles: −19.74‰ ± 0.04‰, 17.51‰ ± 0.05‰; adults: −18.86‰ ± 0.01‰, 17.23‰ ± 0.02‰) characteristic of feeding on demersal prey. In all species, δ<sup>13</sup>C values increased with body size and age in the same manner, indicating that seals exploit or forage in deeper habitats as they get larger and older. We hypothesize that the consistent ontogenetic shift in foraging niche, despite large differences between species in their diving behavior, geographic range and habitat use, not only reflects increased access to different prey due to increased diving capacity, but a progressive adjustment to balance energy budgets by reducing foraging costs.</p></div>
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Determining how marine predators partition resources is hindered by the difficulty in obtaining information on diet and distribution. Stable isotopes (SI) of carbon (13C/12C, δ13C) and nitrogen (15N/14N, δ15N) provide a two-dimensional estimate of the dietary space of consumers; an animal's isotopic composition is directly influenced by what they consume and where they feed. Harp (Pagophilus groenlandicus) and hooded (Cystophora cristata) seals are abundant phocid species found in the North Atlantic. We measured and contrasted SI values between seals sampled at nearshore and offshore sites to test for effects of sampling location, sex, age-class, and body size to gain insight into how these species partition space and prey resources. In addition we contrasted previously published results for gray seals (Halichoerus grypus). Isotope values differed significantly by age class and location in harp and hooded seals. We found significant differences in SI values (mean δ13C and δ15N ± SE) between all species. Hooded seals, a continental shelf-edge, deep-diving species, exhibited low SI values (juveniles: −20.9‰ ± 0.03‰, 13.36‰ ± 0.05‰; adults: −20.41‰ ± 0.03‰, 14.81‰ ± 0.04‰) characteristic of feeding on meso- to bathypelagic prey. Harp seals, which dive to moderate depths primarily on the shelf had intermediate SI values (juveniles: −20.53‰ ± 0.01‰, 13.91‰ ± 0.01‰; adults: −20.13‰ ± 0.01‰, 14.96‰ ± 0.01‰) characteristic of feeding on epipelagic prey, whereas gray seals, which feed on or near the sea floor in shallow shelf waters, had high SI values (juveniles: −19.74‰ ± 0.04‰, 17.51‰ ± 0.05‰; adults: −18.86‰ ± 0.01‰, 17.23‰ ± 0.02‰) characteristic of feeding on demersal prey. In all species, δ13C values increased with body size and age in the same manner, indicating that seals exploit or forage in deeper habitats as they get larger and older. We hypothesize that the consistent ontogenetic shift in foraging niche, despite large differences between species in their diving behavior, geographic range and habitat use, not only reflects increased access to different prey due to increased diving capacity, but a progressive adjustment to balance energy budgets by reducing foraging costs.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12010" xmlns="http://purl.org/rss/1.0/"><title>Patterns of social association in the franciscana, Pontoporia blainvillei</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12010</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Patterns of social association in the franciscana, Pontoporia blainvillei</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Randall S. Wells, Pablo Bordino, David C. Douglas</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-17T21:44:15.802642-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12010</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12010</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12010</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12001" xmlns="http://purl.org/rss/1.0/"><title>Effects of airgun sounds on bowhead whale calling rates in the Alaskan Beaufort Sea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12001</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of airgun sounds on bowhead whale calling rates in the Alaskan Beaufort Sea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Susanna B. Blackwell, Christopher S. Nations, Trent L. McDonald, Charles R. Greene, Aaron M. Thode, Melania Guerra, A. Michael Macrander</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-01-16T06:07:00.596929-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12001</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12001</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12001</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study assesses effects of airgun sounds on bowhead calling behavior during the autumn migration. In August–October 2007, 35 directional acoustic recorders (DASARs) were deployed at five sites in the Alaskan Beaufort Sea. Location estimates were obtained for &gt;137,500 individual calls; a subsample of locations with high detection probability was used in the analyses. Call localization rates (CLRs) were compared before, during, and after periods of airgun use between sites near seismic activities (median distance 41–45 km) and sites relatively distant from seismic activities (median distance &gt;104 km). At the onset of airgun use, CLRs dropped significantly at sites near the airguns, where median received levels from airgun pulses (SPL) were 116–129 dB re 1 μPa (10–450 Hz). CLRs remained unchanged at sites distant from the airguns, where median received levels were 99–108 dB re 1 μPa. This drop could result from a cessation of calling, deflection of whales around seismic activities, or both combined, but call locations alone were insufficient to differentiate between these possibilities. Reverberation from airgun pulses could have masked a small number of calls near the airguns, but even if masking did take place, the analysis results remain unchanged.</p></div>
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This study assesses effects of airgun sounds on bowhead calling behavior during the autumn migration. In August–October 2007, 35 directional acoustic recorders (DASARs) were deployed at five sites in the Alaskan Beaufort Sea. Location estimates were obtained for &gt;137,500 individual calls; a subsample of locations with high detection probability was used in the analyses. Call localization rates (CLRs) were compared before, during, and after periods of airgun use between sites near seismic activities (median distance 41–45 km) and sites relatively distant from seismic activities (median distance &gt;104 km). At the onset of airgun use, CLRs dropped significantly at sites near the airguns, where median received levels from airgun pulses (SPL) were 116–129 dB re 1 μPa (10–450 Hz). CLRs remained unchanged at sites distant from the airguns, where median received levels were 99–108 dB re 1 μPa. This drop could result from a cessation of calling, deflection of whales around seismic activities, or both combined, but call locations alone were insufficient to differentiate between these possibilities. Reverberation from airgun pulses could have masked a small number of calls near the airguns, but even if masking did take place, the analysis results remain unchanged.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12007" xmlns="http://purl.org/rss/1.0/"><title>Evaluating postintervention survival of free-ranging odontocete cetaceans</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12007</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evaluating postintervention survival of free-ranging odontocete cetaceans</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Randall S. Wells, Deborah A. Fauquier, Frances M. D. Gulland, Forrest I. Townsend, Robert A. DiGiovanni</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-30T08:22:32.357168-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12007</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12007</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12007</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Until recently, few data were available for evaluating postintervention survival of free-ranging cetaceans receiving aid from humans through: rescue from stranding, with rehabilitation and release; rescue, rehabilitation and release of debilitated or entangled individuals that had not beached; rescue of entangled animals with immediate release; and rescue, transport, and release of out-of-habitat animals. Advances in medical diagnosis, husbandry and therapy have improved survival of rehabilitation cases, and advances in radio-telemetry have improved postrelease monitoring. In total, 69 cases (1986–2010) were evaluated, involving 10 species of odontocete cetaceans with release data. Findings suggested a success criterion of surviving at least six weeks postrelease is useful in evaluating intervention strategies. No species had better success than others. Stranded beached cetaceans were less successful than free-swimming rescued animals. Rehabilitated animals were less successful than those released without rehabilitation. Mass stranded dolphins fared better than single stranded animals. Old age, diminished hearing ability, and lack of maternal care were factors in several unsuccessful cases. Success is not clearly related to rehabilitation duration. Retaining healthy individuals from mass strandings until all animals are ready for release may reduce success for some. Transport durations for unsuccessful cases were greater than for successful cases.</p></div>
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Until recently, few data were available for evaluating postintervention survival of free-ranging cetaceans receiving aid from humans through: rescue from stranding, with rehabilitation and release; rescue, rehabilitation and release of debilitated or entangled individuals that had not beached; rescue of entangled animals with immediate release; and rescue, transport, and release of out-of-habitat animals. Advances in medical diagnosis, husbandry and therapy have improved survival of rehabilitation cases, and advances in radio-telemetry have improved postrelease monitoring. In total, 69 cases (1986–2010) were evaluated, involving 10 species of odontocete cetaceans with release data. Findings suggested a success criterion of surviving at least six weeks postrelease is useful in evaluating intervention strategies. No species had better success than others. Stranded beached cetaceans were less successful than free-swimming rescued animals. Rehabilitated animals were less successful than those released without rehabilitation. Mass stranded dolphins fared better than single stranded animals. Old age, diminished hearing ability, and lack of maternal care were factors in several unsuccessful cases. Success is not clearly related to rehabilitation duration. Retaining healthy individuals from mass strandings until all animals are ready for release may reduce success for some. Transport durations for unsuccessful cases were greater than for successful cases.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12006" xmlns="http://purl.org/rss/1.0/"><title>The influence of habitat and time of day on the occurrence of odontocete vocalizations in Onslow Bay, North Carolina</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12006</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The influence of habitat and time of day on the occurrence of odontocete vocalizations in Onslow Bay, North Carolina</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lynne E. W. Hodge, Joel T. Bell, Anurag Kumar, Andrew J. Read</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T08:26:37.941681-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12006</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12006</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12006</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>To determine whether the occurrence and duration of odontocete vocal events varied by depth or time of day in Onslow Bay, North Carolina, we analyzed acoustic data collected by five underwater recorders. These recorders were deployed in July 2008 at three depths: two in shallow (64–73 m), one in medium (236 m), and two in deep (~366 m) water. We found that habitat influenced the occurrence of odontocete vocalizations, with significantly greater daily vocal activity from delphinids on recorders in deeper waters and sperm whale clicks recorded only on the medium and deep recorders. These findings suggest that a greater diversity and occurrence of animals are located in waters beyond the shelf break in this area, a conclusion supported by visual surveys. We also found an increase in the occurrence of delphinid clicks at night on the shallow and deep recorders, likely reflecting nocturnal foraging activity, and a regular nocturnal occurrence of sperm whale clicks on the medium-depth recorder located near the shelf break, suggesting that one or more sperm whales moved into that area to feed at night. These observations improve our understanding of the occurrence and behavior of odontocetes in this region of the U.S. Atlantic seaboard.</p></div>
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To determine whether the occurrence and duration of odontocete vocal events varied by depth or time of day in Onslow Bay, North Carolina, we analyzed acoustic data collected by five underwater recorders. These recorders were deployed in July 2008 at three depths: two in shallow (64–73 m), one in medium (236 m), and two in deep (~366 m) water. We found that habitat influenced the occurrence of odontocete vocalizations, with significantly greater daily vocal activity from delphinids on recorders in deeper waters and sperm whale clicks recorded only on the medium and deep recorders. These findings suggest that a greater diversity and occurrence of animals are located in waters beyond the shelf break in this area, a conclusion supported by visual surveys. We also found an increase in the occurrence of delphinid clicks at night on the shallow and deep recorders, likely reflecting nocturnal foraging activity, and a regular nocturnal occurrence of sperm whale clicks on the medium-depth recorder located near the shelf break, suggesting that one or more sperm whales moved into that area to feed at night. These observations improve our understanding of the occurrence and behavior of odontocetes in this region of the U.S. Atlantic seaboard.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12005" xmlns="http://purl.org/rss/1.0/"><title>Humpback whale song hierarchical structure: Historical context and discussion of current classification issues</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12005</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Humpback whale song hierarchical structure: Historical context and discussion of current classification issues</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Danielle M. Cholewiak, Renata S. Sousa-Lima, Salvatore Cerchio</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-21T14:01:54.764277-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12005</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12005</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12005</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Consistent and well-defined criteria for the classification and measurement of humpback whale song features are essential for robust comparisons between investigators. Song structure terminology has been well-established and used by many authors, though at times inconsistently. This review discusses the development of the nomenclature describing humpback song and explores the potential significance of the often-overlooked variation in song patterns. Within the hierarchical definition of humpback song, the most problematic issues arise from the inconsistent delineation of phrase types, and the use of the metric of song duration without regards to variability in thematic sequence. With regards to the former, a set of guidelines is suggested to facilitate consistent delineation of phrases. With regards to the latter, current research demonstrates that the “song duration” metric has resulted in the disregard of variability at this level, which is more widespread than traditionally reported. An exemplar case is used to highlight the problem inherent in defining and measuring song duration. Humpback song is evaluated within the framework of avian songbird research, and a shift in analysis paradigm is recommended, towards phrase-based analyses in which sequences of phrases are treated as a salient feature of song pattern.</p></div>
]]></content:encoded><description>

Consistent and well-defined criteria for the classification and measurement of humpback whale song features are essential for robust comparisons between investigators. Song structure terminology has been well-established and used by many authors, though at times inconsistently. This review discusses the development of the nomenclature describing humpback song and explores the potential significance of the often-overlooked variation in song patterns. Within the hierarchical definition of humpback song, the most problematic issues arise from the inconsistent delineation of phrase types, and the use of the metric of song duration without regards to variability in thematic sequence. With regards to the former, a set of guidelines is suggested to facilitate consistent delineation of phrases. With regards to the latter, current research demonstrates that the “song duration” metric has resulted in the disregard of variability at this level, which is more widespread than traditionally reported. An exemplar case is used to highlight the problem inherent in defining and measuring song duration. Humpback song is evaluated within the framework of avian songbird research, and a shift in analysis paradigm is recommended, towards phrase-based analyses in which sequences of phrases are treated as a salient feature of song pattern.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12004" xmlns="http://purl.org/rss/1.0/"><title>Hydrodynamic patterns associated with echelon formation swimming by feeding bowhead whales (Balaena mysticetus)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12004</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hydrodynamic patterns associated with echelon formation swimming by feeding bowhead whales (Balaena mysticetus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Frank E. Fish, Kimberly T. Goetz, David J. Rugh, Linda Vate Brattström</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-20T07:30:45.701403-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12004</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12004</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12004</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12003" xmlns="http://purl.org/rss/1.0/"><title>First insights into the effects of swim-with-dolphin tourism on the behavior, response, and group structure of southern Australian bottlenose dolphins</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12003</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">First insights into the effects of swim-with-dolphin tourism on the behavior, response, and group structure of southern Australian bottlenose dolphins</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Katharina J. Peters, Guido J. Parra, Pawel P. Skuza, Luciana M. Möller</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-20T07:28:18.046316-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12003</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12003</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12003</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12002" xmlns="http://purl.org/rss/1.0/"><title>Postrelease movement of rehabilitated harbor seal (Phoca vitulina richardii) pups compared with cohort-matched wild seal pups</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12002</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Postrelease movement of rehabilitated harbor seal (Phoca vitulina richardii) pups compared with cohort-matched wild seal pups</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Joseph K. Gaydos, L. Ignacio Vilchis, Monique M. Lance, Steven J. Jeffries, Austen Thomas, Vanessa Greenwood, Penny Harner, Michael H. Ziccardi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-08T05:43:54.562331-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12002</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12002</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12002</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Harbor seal (<em>Phoca vitulina richardii</em>) populations in the inland waters of Washington and British Columbia are at or near carrying capacity. Stranded pups often are collected and admitted to rehabilitation centers, and then released when they reach a weight of 22 kg and meet a variety of preestablished health and release conditions. While rehabilitation is common practice, it is unclear if rehabilitated seal pups behave like wild weaned pups. Using satellite transmitters, we compared movement patterns of 10 rehabilitated pups with 10 wild weaned pups. When released, rehabilitated seals were longer and heavier than wild pups, while wild pups had a larger mean axillary girth. No clinically different blood parameters were detected. On average, rehabilitated harbor seal pups traveled nearly twice as far cumulatively, almost three times as far daily, and dispersed over three times as far from the release site compared to wild weaned seals. Additionally, wild harbor seals transmitted nearly twice as long as did rehabilitated seals. These patterns suggest that learned behavior during the brief 3–4 wk nursing period likely enables wild harbor seal pups to move less daily and remain closer to their weaning site than rehabilitated pups.</p></div>
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Harbor seal (Phoca vitulina richardii) populations in the inland waters of Washington and British Columbia are at or near carrying capacity. Stranded pups often are collected and admitted to rehabilitation centers, and then released when they reach a weight of 22 kg and meet a variety of preestablished health and release conditions. While rehabilitation is common practice, it is unclear if rehabilitated seal pups behave like wild weaned pups. Using satellite transmitters, we compared movement patterns of 10 rehabilitated pups with 10 wild weaned pups. When released, rehabilitated seals were longer and heavier than wild pups, while wild pups had a larger mean axillary girth. No clinically different blood parameters were detected. On average, rehabilitated harbor seal pups traveled nearly twice as far cumulatively, almost three times as far daily, and dispersed over three times as far from the release site compared to wild weaned seals. Additionally, wild harbor seals transmitted nearly twice as long as did rehabilitated seals. These patterns suggest that learned behavior during the brief 3–4 wk nursing period likely enables wild harbor seal pups to move less daily and remain closer to their weaning site than rehabilitated pups.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00617.x" xmlns="http://purl.org/rss/1.0/"><title>The diets of humpback whales (Megaptera novaeangliae) on the shelf and oceanic feeding grounds in the western North Pacific inferred from stable isotope analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00617.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The diets of humpback whales (Megaptera novaeangliae) on the shelf and oceanic feeding grounds in the western North Pacific inferred from stable isotope analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Olga A. Filatova, Briana H. Witteveen, Anton A. Goncharov, Alexei V. Tiunov, Maria I. Goncharova, Alexander M. Burdin, Erich Hoyt</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-01T04:12:43.457219-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00617.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00617.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00617.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Humpback whales feed on a variety of prey, but significant differences likely occur between regional feeding grounds. In this study, the diets of humpback whales were analyzed by comparing stable isotope ratios in animal tissues at three humpback whale feeding grounds in the Russian Far East: Karaginsky Gulf, Anadyr Gulf, and the Commander Islands. Anadyr Gulf is a neritic zone far from a shelf break, Karaginsky Gulf is a neritic zone close to a shelf break, and the Commander Islands represent an open oceanic ecosystem where whales feed off the shelf break. Samples from the Commander Islands had the lowest mean δ<sup>13</sup>C and δ<sup>15</sup>N values (mean ± SE: δ<sup>13</sup>C = −18.7 ± 0.1, δ<sup>15</sup>N = 10.4 ± 0.1) compared to the samples from Karaginsky Gulf (δ<sup>13</sup>C = −17.2 ± 0.1, δ<sup>15</sup>N = 12.7 ± 0.2) and Anadyr Gulf (δ<sup>13</sup>C= −17.8 ± 0.1, δ<sup>15</sup>N = 14.0 ± 0.4). The samples from Anadyr Gulf had the highest δ<sup>15</sup>N values, while the samples from Karaginsky Gulf had the highest δ<sup>13</sup>C values. Both δ<sup>13</sup>C and δ<sup>15</sup>N values differed significantly among all three areas. Our data support the hypothesis that humpback whales tend to feed on fish in neritic areas and on plankton in deep oceanic waters.</p></div>
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Humpback whales feed on a variety of prey, but significant differences likely occur between regional feeding grounds. In this study, the diets of humpback whales were analyzed by comparing stable isotope ratios in animal tissues at three humpback whale feeding grounds in the Russian Far East: Karaginsky Gulf, Anadyr Gulf, and the Commander Islands. Anadyr Gulf is a neritic zone far from a shelf break, Karaginsky Gulf is a neritic zone close to a shelf break, and the Commander Islands represent an open oceanic ecosystem where whales feed off the shelf break. Samples from the Commander Islands had the lowest mean δ13C and δ15N values (mean ± SE: δ13C = −18.7 ± 0.1, δ15N = 10.4 ± 0.1) compared to the samples from Karaginsky Gulf (δ13C = −17.2 ± 0.1, δ15N = 12.7 ± 0.2) and Anadyr Gulf (δ13C= −17.8 ± 0.1, δ15N = 14.0 ± 0.4). The samples from Anadyr Gulf had the highest δ15N values, while the samples from Karaginsky Gulf had the highest δ13C values. Both δ13C and δ15N values differed significantly among all three areas. Our data support the hypothesis that humpback whales tend to feed on fish in neritic areas and on plankton in deep oceanic waters.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00621.x" xmlns="http://purl.org/rss/1.0/"><title>Diet of harbor porpoises along the Dutch coast: A combined stable isotope and stomach contents approach</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00621.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Diet of harbor porpoises along the Dutch coast: A combined stable isotope and stomach contents approach</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Okka E. Jansen, Loïc Michel, Gilles Lepoint, Krishna Das, Abraham S. Couperus, Peter J. H. Reijnders</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-01T04:12:39.761221-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00621.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00621.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00621.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>High stranding frequency of porpoises, <em>Phocoena phocoena</em>, along the Dutch coast since 2006 has led to increased interest in the ecology of porpoises in the North Sea. Stranded porpoises were collected along the Dutch coast (2006–2008) and their diet was assessed through stomach content and stable isotope analysis (δ<sup>13</sup>C and δ<sup>15</sup>N) of porpoise muscle and prey. Stable isotope analysis (SIAR) was used to estimate the contribution of prey species to the porpoises' diet. This was compared to prey composition from stomach contents, to analyze differences between long- and short-term diet. According to stomach contents, 90.5% of the diet consisted of gobies, whiting, lesser sandeel, herring, cod, and sprat. Stable isotope analysis revealed that 70-83% of the diet consisted of poor cod, mackerel, greater sandeel, lesser sandeel, sprat, and gobies, highlighting a higher importance of pelagic, schooling species in the porpoises' diet compared to stomach contents. This could be due to prey distribution as well as differences in behavior of porpoises and prey between the coastal zone and offshore waters. This study supports the need for multi-method approaches. Future ecological and fishery impact assessment studies and management decisions for porpoise conservation should acknowledge this difference between the long- and short-term diet.</p></div>
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High stranding frequency of porpoises, Phocoena phocoena, along the Dutch coast since 2006 has led to increased interest in the ecology of porpoises in the North Sea. Stranded porpoises were collected along the Dutch coast (2006–2008) and their diet was assessed through stomach content and stable isotope analysis (δ13C and δ15N) of porpoise muscle and prey. Stable isotope analysis (SIAR) was used to estimate the contribution of prey species to the porpoises' diet. This was compared to prey composition from stomach contents, to analyze differences between long- and short-term diet. According to stomach contents, 90.5% of the diet consisted of gobies, whiting, lesser sandeel, herring, cod, and sprat. Stable isotope analysis revealed that 70-83% of the diet consisted of poor cod, mackerel, greater sandeel, lesser sandeel, sprat, and gobies, highlighting a higher importance of pelagic, schooling species in the porpoises' diet compared to stomach contents. This could be due to prey distribution as well as differences in behavior of porpoises and prey between the coastal zone and offshore waters. This study supports the need for multi-method approaches. Future ecological and fishery impact assessment studies and management decisions for porpoise conservation should acknowledge this difference between the long- and short-term diet.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00615.x" xmlns="http://purl.org/rss/1.0/"><title>Sequential foraging of dusky dolphins with an inspection of their prey distribution</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00615.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sequential foraging of dusky dolphins with an inspection of their prey distribution</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mariana Degrati, Silvana L. Dans, Griselda V. Garaffo, Ariel G. Cabreira, Federico Castro Machado, Enrique A. Crespo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-01T04:12:33.700073-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00615.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00615.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00615.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The aim of this work was to analyze the sequential foraging behavior of dusky dolphins (<em>Lagenorhynchus obscurus</em>). Foraging sequences were defined when more than two feeding bouts occur with a traveling bout between them. We hypothesized that traveling costs of searching for prey patches were related to the time spent feeding on a patch. In addition, the distribution and seasonal variation of anchovy schools were studied in the area to better understand dolphins' behavior. We observed dolphins from a research vessel from 2001 to 2007, and recorded their location and behavior. Anchovy data were collected during two hydro-acoustic surveys. Dusky dolphin behaviors varied seasonally; they spent a greater proportion of time traveling and feeding in the warm season (Kruskal-Wallis: <em>H </em>=<em> </em>172.07, <em>P </em>&lt;<em> </em>0.01). During the cold season dolphin groups were more likely to exhibit diving behavior and less surface feeding. We found a positive correlation between searching and foraging time (<em>r </em>=<em> </em>0.88, <em>P </em>=<em> </em>0.019), suggesting that the costs associated with searching were compensated by an increase in the energy intake during the foraging bout. There was an association between dusky dolphin and anchovy distribution, in that they co-varied spatially and seasonally.</p></div>
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The aim of this work was to analyze the sequential foraging behavior of dusky dolphins (Lagenorhynchus obscurus). Foraging sequences were defined when more than two feeding bouts occur with a traveling bout between them. We hypothesized that traveling costs of searching for prey patches were related to the time spent feeding on a patch. In addition, the distribution and seasonal variation of anchovy schools were studied in the area to better understand dolphins' behavior. We observed dolphins from a research vessel from 2001 to 2007, and recorded their location and behavior. Anchovy data were collected during two hydro-acoustic surveys. Dusky dolphin behaviors varied seasonally; they spent a greater proportion of time traveling and feeding in the warm season (Kruskal-Wallis: H = 172.07, P &lt; 0.01). During the cold season dolphin groups were more likely to exhibit diving behavior and less surface feeding. We found a positive correlation between searching and foraging time (r = 0.88, P = 0.019), suggesting that the costs associated with searching were compensated by an increase in the energy intake during the foraging bout. There was an association between dusky dolphin and anchovy distribution, in that they co-varied spatially and seasonally.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00618.x" xmlns="http://purl.org/rss/1.0/"><title>Retrospective analysis of bottlenose dolphin foraging: A legacy of anthropogenic ecosystem disturbance</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00618.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Retrospective analysis of bottlenose dolphin foraging: A legacy of anthropogenic ecosystem disturbance</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sam Rossman, Nélio B. Barros, Peggy H. Ostrom, Craig A. Stricker, Aleta A. Hohn, Hasand Gandhi, Randall S. Wells</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-24T04:05:32.515376-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00618.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00618.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00618.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We used stable isotope analysis to investigate the foraging ecology of coastal bottlenose dolphins (<em>Tursiops truncatus</em>) in relation to a series of anthropogenic disturbances. We first demonstrated that stable isotopes are a faithful indicator of habitat use by comparing muscle isotope values to behavioral foraging data from the same individuals. δ<sup>13</sup>C values increased, while δ<sup>34</sup>S and δ<sup>15</sup>N values decreased with the percentage of feeding observations in seagrass habitat. We then utilized stable isotope values of muscle to assess temporal variation in foraging habitat from 1991 to 2010 and collagen from tooth crown tips to assess the time period 1944 to 2007. From 1991 to 2010, δ<sup>13</sup>C values of muscle decreased while δ<sup>34</sup>S values increased indicating reduced utilization of seagrass habitat. From 1944 to 1989 δ<sup>13</sup>C values of the crown tip declined significantly, likely due to a reduction in the coverage of seagrass habitat and δ<sup>15</sup>N values significantly increased, a trend we attribute to nutrient loading from a rapidly increasing human population. Our results demonstrate the utility of using marine mammal foraging habits to retrospectively assess the extent to which anthropogenic disturbance impacts coastal food webs.</p></div>
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We used stable isotope analysis to investigate the foraging ecology of coastal bottlenose dolphins (Tursiops truncatus) in relation to a series of anthropogenic disturbances. We first demonstrated that stable isotopes are a faithful indicator of habitat use by comparing muscle isotope values to behavioral foraging data from the same individuals. δ13C values increased, while δ34S and δ15N values decreased with the percentage of feeding observations in seagrass habitat. We then utilized stable isotope values of muscle to assess temporal variation in foraging habitat from 1991 to 2010 and collagen from tooth crown tips to assess the time period 1944 to 2007. From 1991 to 2010, δ13C values of muscle decreased while δ34S values increased indicating reduced utilization of seagrass habitat. From 1944 to 1989 δ13C values of the crown tip declined significantly, likely due to a reduction in the coverage of seagrass habitat and δ15N values significantly increased, a trend we attribute to nutrient loading from a rapidly increasing human population. Our results demonstrate the utility of using marine mammal foraging habits to retrospectively assess the extent to which anthropogenic disturbance impacts coastal food webs.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00620.x" xmlns="http://purl.org/rss/1.0/"><title>Subsurface behavior of bottlenose dolphins (Tursiops truncatus) interacting with fish trawl nets in northwestern Australia: Implications for bycatch mitigation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00620.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Subsurface behavior of bottlenose dolphins (Tursiops truncatus) interacting with fish trawl nets in northwestern Australia: Implications for bycatch mitigation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vanessa F. Jaiteh, Simon J. Allen, Jessica J. Meeuwig, Neil R. Loneragan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-24T04:05:27.085262-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00620.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00620.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00620.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Most studies of delphinid-trawler interactions have documented the surface behavior of dolphins feeding on discarded bycatch, but not their subsurface behavior around demersal trawl gear. Using video cameras mounted inside trawl nets, we recorded the subsurface behavior of common bottlenose dolphins (<em>Tursiops truncatus</em>) in a demersal fish trawl fishery in northwestern Australia. Footage from 36 trawls across the fishery was analyzed to determine the extent of dolphin-gear interactions and the behavior of dolphins inside the nets. Interaction rates were high, with dolphins present inside and outside the nets during 29 and 34 trawls, respectively, and for up to 99% of the trawl duration. The proportion of foraging behaviors exhibited inside the nets was higher than the proportions of traveling and socializing behaviors. Twenty-nine individuals were identified inside the net, seven of which returned repeatedly within and between trawls and fishing trips, but were observed primarily in the same localized areas in which they were first recorded. Our results suggest that entering trawl nets may be a frequently occurring, yet specialized behavior exhibited by a small subset of trawler-associated dolphins. We propose that gear modifications, not spatial or temporal adjustments to fishing effort, have the greatest potential to reduce dolphin bycatch.</p></div>
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Most studies of delphinid-trawler interactions have documented the surface behavior of dolphins feeding on discarded bycatch, but not their subsurface behavior around demersal trawl gear. Using video cameras mounted inside trawl nets, we recorded the subsurface behavior of common bottlenose dolphins (Tursiops truncatus) in a demersal fish trawl fishery in northwestern Australia. Footage from 36 trawls across the fishery was analyzed to determine the extent of dolphin-gear interactions and the behavior of dolphins inside the nets. Interaction rates were high, with dolphins present inside and outside the nets during 29 and 34 trawls, respectively, and for up to 99% of the trawl duration. The proportion of foraging behaviors exhibited inside the nets was higher than the proportions of traveling and socializing behaviors. Twenty-nine individuals were identified inside the net, seven of which returned repeatedly within and between trawls and fishing trips, but were observed primarily in the same localized areas in which they were first recorded. Our results suggest that entering trawl nets may be a frequently occurring, yet specialized behavior exhibited by a small subset of trawler-associated dolphins. We propose that gear modifications, not spatial or temporal adjustments to fishing effort, have the greatest potential to reduce dolphin bycatch.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00614.x" xmlns="http://purl.org/rss/1.0/"><title>Likely future extirpation of another Asian river dolphin: The critically endangered population of the Irrawaddy dolphin in the Mekong River is small and declining</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00614.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Likely future extirpation of another Asian river dolphin: The critically endangered population of the Irrawaddy dolphin in the Mekong River is small and declining</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">I. Beasley, K. Pollock, T. A. Jefferson, P. Arnold, L. Morse, S. Yim, S. Lor Kim, H. Marsh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-18T02:59:29.180572-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00614.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00614.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00614.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The population of Irrawaddy dolphins that occupies the Mekong River in southern Lao People's Democratic Republic and Cambodia is classified as <em>Critically Endangered</em> by the IUCN. Based on capture-recapture of photo-identified individuals, we estimated that the total population numbered 93 ±  SE 3.90 individuals (95% CI 86–101), as of April 2007. The combined photo-identification and carcass recovery program undertaken from 2001 to 2007 established that the Irrawaddy dolphin population inhabiting the Mekong River has reached a critical point with regards to its continued survival, where immediate research and management actions are required to greatly reduce adult mortality, and establish the cause of newborn mortality. In addition, community consultation is required to initiate, and evaluate, urgently required conservation measures. An ongoing well-designed combined program of abundance estimation (<em>i.e</em>., photo-identification) and carcass recovery is required to monitor total population size and mortality rates, to inform and evaluate management initiatives. The conclusions of this paper are likely generic to river dolphin populations, particularly where photo-identification is possible.</p></div>
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The population of Irrawaddy dolphins that occupies the Mekong River in southern Lao People's Democratic Republic and Cambodia is classified as Critically Endangered by the IUCN. Based on capture-recapture of photo-identified individuals, we estimated that the total population numbered 93 ±  SE 3.90 individuals (95% CI 86–101), as of April 2007. The combined photo-identification and carcass recovery program undertaken from 2001 to 2007 established that the Irrawaddy dolphin population inhabiting the Mekong River has reached a critical point with regards to its continued survival, where immediate research and management actions are required to greatly reduce adult mortality, and establish the cause of newborn mortality. In addition, community consultation is required to initiate, and evaluate, urgently required conservation measures. An ongoing well-designed combined program of abundance estimation (i.e., photo-identification) and carcass recovery is required to monitor total population size and mortality rates, to inform and evaluate management initiatives. The conclusions of this paper are likely generic to river dolphin populations, particularly where photo-identification is possible.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00613.x" xmlns="http://purl.org/rss/1.0/"><title>Vocal activity of tropical dolphins is inhibited by the presence of killer whales, Orcinus orca</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00613.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Vocal activity of tropical dolphins is inhibited by the presence of killer whales, Orcinus orca</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shannon Rankin, Frederick Archer, Jay Barlow</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-18T02:58:52.222424-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00613.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00613.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00613.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Research has suggested killer whale (<em>Orcinus orca</em>) predation may affect cetacean vocal behavior; however, few data exist to test this hypothesis. Data collected during 40,976 km of visual and acoustic shipboard surveys in the tropical Pacific Ocean, including 1,232 detections of 13 species, were examined to determine if changes in dolphin vocal activity could be attributed to the presence of killer whales. Generalized linear models and Random Forest analyses were used to test the hypothesis that dolphin vocal activity was related to the distance and time to the nearest killer whale sighting. Both results show that dolphin vocalizations were inversely correlated with the temporal proximity of killer whales (<em>P </em>&lt;<em> </em>0.05). Despite the relative rarity of killer whales in the tropics, they appear to influence vocal behavior of nearby dolphin schools. This disruption in communication may not significantly impact interactions necessary for survival in tropical waters where killer whale density is low. However, in temperate climates, where increased productivity supports a greater abundance of killer whales, this interruption in communication may have a greater impact. The lower incidence of whistling dolphins in temperate waters may be related to the greater abundance of killer whales in these areas.</p></div>
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Research has suggested killer whale (Orcinus orca) predation may affect cetacean vocal behavior; however, few data exist to test this hypothesis. Data collected during 40,976 km of visual and acoustic shipboard surveys in the tropical Pacific Ocean, including 1,232 detections of 13 species, were examined to determine if changes in dolphin vocal activity could be attributed to the presence of killer whales. Generalized linear models and Random Forest analyses were used to test the hypothesis that dolphin vocal activity was related to the distance and time to the nearest killer whale sighting. Both results show that dolphin vocalizations were inversely correlated with the temporal proximity of killer whales (P &lt; 0.05). Despite the relative rarity of killer whales in the tropics, they appear to influence vocal behavior of nearby dolphin schools. This disruption in communication may not significantly impact interactions necessary for survival in tropical waters where killer whale density is low. However, in temperate climates, where increased productivity supports a greater abundance of killer whales, this interruption in communication may have a greater impact. The lower incidence of whistling dolphins in temperate waters may be related to the greater abundance of killer whales in these areas.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00610.x" xmlns="http://purl.org/rss/1.0/"><title>Transience in the humpback whale population of New Caledonia and implications for abundance estimation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00610.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Transience in the humpback whale population of New Caledonia and implications for abundance estimation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bénédicte Madon, Claire Garrigue, Roger Pradel, Olivier Gimenez</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-18T02:58:41.772254-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00610.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00610.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00610.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A phenomenon of transience in the humpback whale population breeding in New Caledonia has been highlighted in recent analyses. We used these data to illustrate the risk of flawed inference when transience is not properly accounted for in abundance estimation of resident populations. Transients are commonly defined as individuals that pass through the sampling area once, <em>i.e</em>., have a null probability of being caught again, and therefore induce heterogeneity in the detection process. The presence of transients can lead to severe bias in the estimation of abundance and we demonstrate how to correct for this feature when estimating abundance of resident populations. In New Caledonia, very different conclusions about the number of resident whales in the southern lagoon between 1999 and 2005 are obtained when the abundance estimate accounts for the transient whales. Without correction, the estimates of the abundance were up to twice as high across all years compared to the estimates of the resident population when a correction for transients had been incorporated. Having reliable population estimates when assessing the status of endangered species is essential in documenting recovery and monitoring of population trends. Therefore, we encourage researchers to account for transients when reporting abundances of resident populations.</p></div>
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A phenomenon of transience in the humpback whale population breeding in New Caledonia has been highlighted in recent analyses. We used these data to illustrate the risk of flawed inference when transience is not properly accounted for in abundance estimation of resident populations. Transients are commonly defined as individuals that pass through the sampling area once, i.e., have a null probability of being caught again, and therefore induce heterogeneity in the detection process. The presence of transients can lead to severe bias in the estimation of abundance and we demonstrate how to correct for this feature when estimating abundance of resident populations. In New Caledonia, very different conclusions about the number of resident whales in the southern lagoon between 1999 and 2005 are obtained when the abundance estimate accounts for the transient whales. Without correction, the estimates of the abundance were up to twice as high across all years compared to the estimates of the resident population when a correction for transients had been incorporated. Having reliable population estimates when assessing the status of endangered species is essential in documenting recovery and monitoring of population trends. Therefore, we encourage researchers to account for transients when reporting abundances of resident populations.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00616.x" xmlns="http://purl.org/rss/1.0/"><title>A Longman's beaked whale (Indopacetus pacificus) strands in Maui, Hawaii, with first case of morbillivirus in the central Pacific</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00616.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A Longman's beaked whale (Indopacetus pacificus) strands in Maui, Hawaii, with first case of morbillivirus in the central Pacific</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kristi L. West, Susan Sanchez, David Rotstein, Kelly M. Robertson, Sophie Dennison, Gregg Levine, Nicole Davis, David Schofield, Charles W. Potter, Brenda Jensen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-10-09T00:10:17.053785-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00616.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00616.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00616.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00609.x" xmlns="http://purl.org/rss/1.0/"><title>The development of synchronous movement by bottlenose dolphins (Tursiops truncatus)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00609.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The development of synchronous movement by bottlenose dolphins (Tursiops truncatus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wendi Fellner, Gordon B. Bauer, Sarah A. Stamper, Barbara A. Losch, Adrian Dahood</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-27T02:47:22.928633-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00609.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00609.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00609.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The development of motor synchrony in dolphins has been described qualitatively, but seldom quantified. We provide a detailed description of the development of synchrony in 12 calves for periods ranging from birth to a few days up to 22 wk. We observed the presence of synchrony, relative positions, and proximity and undertook a videotape analysis of one calf for initiations/terminations of synchrony, response time to breaks in synchrony, and the development of complex behaviors by the calf relative to synchrony. Synchrony was uniformly present more than 90% of the time during month 1, then began to decline gradually. Echelon position was most frequent but calves also spent time in infant position. Initially all calves were most frequently in direct physical contact with their mothers, but by 2 wk of age, all pairs were more likely to be near each other (&lt;0.5 m) without touching. Behavioral complexity increased gradually over the study, and adults frequently performed behaviors during synchronous swimming, providing opportunities for social learning. Synchrony is a predominant behavior in mother-calf interactions, and we speculate that it may be an important mechanism through which calves learn from their mothers <em>via</em> their tandem interactions with the environment.</p></div>
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The development of motor synchrony in dolphins has been described qualitatively, but seldom quantified. We provide a detailed description of the development of synchrony in 12 calves for periods ranging from birth to a few days up to 22 wk. We observed the presence of synchrony, relative positions, and proximity and undertook a videotape analysis of one calf for initiations/terminations of synchrony, response time to breaks in synchrony, and the development of complex behaviors by the calf relative to synchrony. Synchrony was uniformly present more than 90% of the time during month 1, then began to decline gradually. Echelon position was most frequent but calves also spent time in infant position. Initially all calves were most frequently in direct physical contact with their mothers, but by 2 wk of age, all pairs were more likely to be near each other (&lt;0.5 m) without touching. Behavioral complexity increased gradually over the study, and adults frequently performed behaviors during synchronous swimming, providing opportunities for social learning. Synchrony is a predominant behavior in mother-calf interactions, and we speculate that it may be an important mechanism through which calves learn from their mothers via their tandem interactions with the environment.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00608.x" xmlns="http://purl.org/rss/1.0/"><title>Studying small purse-seine vessel fishing behavior with tuna catch data: Implications for eastern Pacific Ocean dolphin conservation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00608.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Studying small purse-seine vessel fishing behavior with tuna catch data: Implications for eastern Pacific Ocean dolphin conservation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cleridy E. Lennert-Cody, Jeremy D. Rusin, Mark N. Maunder, Edward H. Everett, Erick D. Largacha Delgado, Patrick K. Tomlinson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-27T02:45:27.475309-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00608.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00608.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00608.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Despite achievements in dolphin conservation for the tuna purse-seine fishery of the eastern Pacific Ocean, debate continues about the magnitude and importance of dolphin mortality caused by small (unobserved) vessels. In-port sampling of tuna catch size composition is a potentially cost-effective means of identifying unobserved vessels that may be catching tunas associated with dolphins because yellowfin tuna caught in association with dolphins are larger, on average, than those caught in other types of purse-seine sets. A classification algorithm to predict purse-seine set type (“dolphin” <em>vs</em>. “nondolphin”) was built from port-sampling data on yellowfin tuna length-frequencies and the date and location of fishing of large (observed) vessels. This classification algorithm was used to screen the port-sampling data of small vessels collected during 2006-2009, assuming the fishing practices of the two groups resulted in similar catch characteristics. From these results, hypothetical time series of dolphin mortality for small vessels were constructed and incorporated into a population dynamics model, along with mortalities of large vessels. Results suggest that any dolphin mortality of small vessels is unlikely to be substantially affecting trends in dolphin abundance. These results underscore the importance of in-port sampling, in combination with at-sea observation and fishery-independent surveys, to effective management.</p></div>
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Despite achievements in dolphin conservation for the tuna purse-seine fishery of the eastern Pacific Ocean, debate continues about the magnitude and importance of dolphin mortality caused by small (unobserved) vessels. In-port sampling of tuna catch size composition is a potentially cost-effective means of identifying unobserved vessels that may be catching tunas associated with dolphins because yellowfin tuna caught in association with dolphins are larger, on average, than those caught in other types of purse-seine sets. A classification algorithm to predict purse-seine set type (“dolphin” vs. “nondolphin”) was built from port-sampling data on yellowfin tuna length-frequencies and the date and location of fishing of large (observed) vessels. This classification algorithm was used to screen the port-sampling data of small vessels collected during 2006-2009, assuming the fishing practices of the two groups resulted in similar catch characteristics. From these results, hypothetical time series of dolphin mortality for small vessels were constructed and incorporated into a population dynamics model, along with mortalities of large vessels. Results suggest that any dolphin mortality of small vessels is unlikely to be substantially affecting trends in dolphin abundance. These results underscore the importance of in-port sampling, in combination with at-sea observation and fishery-independent surveys, to effective management.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00611.x" xmlns="http://purl.org/rss/1.0/"><title>Minke whale boing sound detections in the northeastern Chukchi Sea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00611.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Minke whale boing sound detections in the northeastern Chukchi Sea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Julien Delarue, Bruce Martin, David Hannay</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-27T02:45:23.090352-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00611.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00611.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00611.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00593.x" xmlns="http://purl.org/rss/1.0/"><title>Age estimates based on aspartic acid racemization for bowhead whales (Balaena mysticetus) harvested in 1998–2000 and the relationship between racemization rate and body temperature</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00593.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Age estimates based on aspartic acid racemization for bowhead whales (Balaena mysticetus) harvested in 1998–2000 and the relationship between racemization rate and body temperature</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cheryl Rosa, Judith Zeh, J. Craig George, Oliver Botta, Melanie Zauscher, Jeffrey Bada, Todd M. O'Hara</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-26T04:00:53.832012-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00593.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00593.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00593.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Fifty-two eyes were collected and analyzed to estimate ages of 42 bowhead whales using the aspartic acid racemization aging technique. Between-eye and within-eye variance components for the ratio of the D and L optical isomers (D/L ratio) were estimated <em>via</em> analysis of variance using multiple measurements from nine whales with both eyes sampled and analyzed. For whales with more than one (D/L)<sub>act</sub> value, an inverse variance weighted average of the values was used as (D/L)<sub>act</sub> for the whale. Racemization rate (<em>k</em><sub>A</sub><sub>sp</sub>) and D/L ratio at birth (D/L)<sub>0</sub> were estimated using (D/L)<sub>act</sub> from 27 bowhead whales with age estimates based on baleen or ovarian corpora data and two term fetuses. The estimates were <em>k</em><sub>A</sub><sub>sp</sub> = 0.977 × 10<sup>−3</sup>/yr and (D/L)<sub>0</sub> = 0.0250. The nonlinear least squares analysis that produced these estimates also estimated female age at sexual maturity as ASM = 25.86 yr. SE(age) was estimated via a bootstrap that took into account the SE of (D/L)<sub>act</sub> and the variances and covariance of <em>k</em><sub>A</sub><sub>sp</sub> and (D/L)<sub>0</sub>. One male exceeded 100 yr of age; the oldest female was 88. A strong linear relationship between <em>k</em><sub>A</sub><sub>sp</sub> and body temperature was estimated by combining bowhead data with independent data from studies of humans and fin whales. Using this relationship, we estimated <em>k</em><sub>A</sub><sub>sp</sub> and ASM for North Atlantic minke whales.</p></div>
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Fifty-two eyes were collected and analyzed to estimate ages of 42 bowhead whales using the aspartic acid racemization aging technique. Between-eye and within-eye variance components for the ratio of the D and L optical isomers (D/L ratio) were estimated via analysis of variance using multiple measurements from nine whales with both eyes sampled and analyzed. For whales with more than one (D/L)act value, an inverse variance weighted average of the values was used as (D/L)act for the whale. Racemization rate (kAsp) and D/L ratio at birth (D/L)0 were estimated using (D/L)act from 27 bowhead whales with age estimates based on baleen or ovarian corpora data and two term fetuses. The estimates were kAsp = 0.977 × 10−3/yr and (D/L)0 = 0.0250. The nonlinear least squares analysis that produced these estimates also estimated female age at sexual maturity as ASM = 25.86 yr. SE(age) was estimated via a bootstrap that took into account the SE of (D/L)act and the variances and covariance of kAsp and (D/L)0. One male exceeded 100 yr of age; the oldest female was 88. A strong linear relationship between kAsp and body temperature was estimated by combining bowhead data with independent data from studies of humans and fin whales. Using this relationship, we estimated kAsp and ASM for North Atlantic minke whales.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00605.x" xmlns="http://purl.org/rss/1.0/"><title>Potential vessel collisions with Southern Hemisphere humpback whales wintering off Pacific Panama</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00605.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Potential vessel collisions with Southern Hemisphere humpback whales wintering off Pacific Panama</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hector M. Guzman, Catalina G. Gomez, Carlos A. Guevara, Lars Kleivane</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-12T23:15:22.962123-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00605.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00605.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00605.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Vessel collision is a threat to many whale species, and the risk has increased with expanding maritime traffic. This compromises international conservation efforts and requires urgent attention from the world's maritime industry. Humpback whales (<em>Megaptera novaeangliae</em>) are at the top of the death toll, and although Central America is a wintering area for populations from both the Northern and Southern Hemispheres, existing efforts to reduce ship-whale collisions are meager. Herein, we evaluated the potential collisions between vessels and humpback whales wintering off Pacific Panama by following the movements of 15 whales tagged with satellite transmitters and comparing these data with tracks plotted using AIS real-time latitude-longitude points from nearly 1,000 commercial vessels. Movements of whales (adults and calves) in the Gulf of Panama coincide with major commercial maritime routes. AIS vessel data analyzed for individual whale satellite tracks showed that 53% (8 whales) of whales had 98 encounters within 200 m with 81 different vessels in just 11 d. We suggest implementing a 65 nmi Traffic Separation Scheme and a 10 kn maximum speed for vessel routing into the Gulf of Panama during the wintering season. In so doing, the area for potential whale-vessel collisions could be reduced by 93%.</p></div>
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Vessel collision is a threat to many whale species, and the risk has increased with expanding maritime traffic. This compromises international conservation efforts and requires urgent attention from the world's maritime industry. Humpback whales (Megaptera novaeangliae) are at the top of the death toll, and although Central America is a wintering area for populations from both the Northern and Southern Hemispheres, existing efforts to reduce ship-whale collisions are meager. Herein, we evaluated the potential collisions between vessels and humpback whales wintering off Pacific Panama by following the movements of 15 whales tagged with satellite transmitters and comparing these data with tracks plotted using AIS real-time latitude-longitude points from nearly 1,000 commercial vessels. Movements of whales (adults and calves) in the Gulf of Panama coincide with major commercial maritime routes. AIS vessel data analyzed for individual whale satellite tracks showed that 53% (8 whales) of whales had 98 encounters within 200 m with 81 different vessels in just 11 d. We suggest implementing a 65 nmi Traffic Separation Scheme and a 10 kn maximum speed for vessel routing into the Gulf of Panama during the wintering season. In so doing, the area for potential whale-vessel collisions could be reduced by 93%.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00590.x" xmlns="http://purl.org/rss/1.0/"><title>Diel changes in the movement patterns of Ganges River dolphins monitored using stationed stereo acoustic data loggers</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00590.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Diel changes in the movement patterns of Ganges River dolphins monitored using stationed stereo acoustic data loggers</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yukiko Sasaki-Yamamoto, Tomonari Akamatsu, Tamaki Ura, Harumi Sugimatsu, Junichi Kojima, Rajendar Bahl, Sandeep Behera, Shiro Kohshima</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-12T23:15:09.578003-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00590.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00590.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00590.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We monitored the underwater movements of Ganges River dolphins using stationed stereo acoustic data loggers. We estimated these movements using changes in the relative angle of the sound source direction (trajectory). Of the total acoustic recordings (66 h), 26.2% contained trajectories of dolphins, and 78.6% of these trajectories involved single animals, suggesting that dolphins tended to swim alone and were localized near the monitoring station. The observed trajectories were categorized as follows: staying type characterized by small changes in the sound source direction, moving type A (moving in the same direction), and moving type B (moving up and down the stream during recording). The average interpulse intervals of sounds in moving types A and B were significantly shorter than that of the staying type, suggesting that dolphins produce the former types of trajectories to echolocate across shorter distances during movement. The frequency of occurrence of moving type A increased during the night, whereas that of type B increased in the late afternoon and that of the staying type increased during the daytime. These results indicate that dolphins moving at night tended to use short-range echolocation, whereas during the day, they remained in relatively small areas and used long-range sonar.</p></div>
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We monitored the underwater movements of Ganges River dolphins using stationed stereo acoustic data loggers. We estimated these movements using changes in the relative angle of the sound source direction (trajectory). Of the total acoustic recordings (66 h), 26.2% contained trajectories of dolphins, and 78.6% of these trajectories involved single animals, suggesting that dolphins tended to swim alone and were localized near the monitoring station. The observed trajectories were categorized as follows: staying type characterized by small changes in the sound source direction, moving type A (moving in the same direction), and moving type B (moving up and down the stream during recording). The average interpulse intervals of sounds in moving types A and B were significantly shorter than that of the staying type, suggesting that dolphins produce the former types of trajectories to echolocate across shorter distances during movement. The frequency of occurrence of moving type A increased during the night, whereas that of type B increased in the late afternoon and that of the staying type increased during the daytime. These results indicate that dolphins moving at night tended to use short-range echolocation, whereas during the day, they remained in relatively small areas and used long-range sonar.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00604.x" xmlns="http://purl.org/rss/1.0/"><title>Methods of estimating marine mammal diets: A review of validation experiments and sources of bias and uncertainty</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00604.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Methods of estimating marine mammal diets: A review of validation experiments and sources of bias and uncertainty</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">W. D. Bowen, S. J. Iverson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-12T00:48:22.05548-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00604.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00604.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00604.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Diet estimation in marine mammals relies on indirect methods including recovery of prey hard parts from stomachs and feces, quantitative fatty acid signature analysis (QFASA), stable isotope mixing models, and identification of prey DNA in stomach contents and feces. Experimental evidence (9 species/13 studies) shows that digestion strongly influences the proportion and size of otoliths that can be recovered in feces. Number correction factors (NCF) and digestion coefficients have been experimentally determined to reduce the biases in fecal analysis. Correction factors and coefficients have not been determined for diet estimated from stomach contents. QFASA estimates which prey species and amounts must have been eaten to account for the fatty acid composition of the predator. Experimental studies on mammals and seabirds (9 species/10 studies) indicate that accurate estimates of diet can be determined using QFASA. Stable isotope mixing models provide rather coarse taxonomic resolution of diet composition. Prey DNA analysis shows promise as a method to estimate the species composition of diet, but further development and testing is needed to validate its use. Obtaining a representative sample from marine mammal populations is a significant challenge. Therefore, the use of complementary methods is recommended to obtain the most informative results.</p></div>
]]></content:encoded><description>

Diet estimation in marine mammals relies on indirect methods including recovery of prey hard parts from stomachs and feces, quantitative fatty acid signature analysis (QFASA), stable isotope mixing models, and identification of prey DNA in stomach contents and feces. Experimental evidence (9 species/13 studies) shows that digestion strongly influences the proportion and size of otoliths that can be recovered in feces. Number correction factors (NCF) and digestion coefficients have been experimentally determined to reduce the biases in fecal analysis. Correction factors and coefficients have not been determined for diet estimated from stomach contents. QFASA estimates which prey species and amounts must have been eaten to account for the fatty acid composition of the predator. Experimental studies on mammals and seabirds (9 species/10 studies) indicate that accurate estimates of diet can be determined using QFASA. Stable isotope mixing models provide rather coarse taxonomic resolution of diet composition. Prey DNA analysis shows promise as a method to estimate the species composition of diet, but further development and testing is needed to validate its use. Obtaining a representative sample from marine mammal populations is a significant challenge. Therefore, the use of complementary methods is recommended to obtain the most informative results.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00607.x" xmlns="http://purl.org/rss/1.0/"><title>Two genetically distinct stocks in Baird's beaked whale (Cetacea: Ziphiidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00607.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Two genetically distinct stocks in Baird's beaked whale (Cetacea: Ziphiidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shino Kitamura, Takashi Matsuishi, Tadasu K. Yamada, Yuko Tajima, Hajime Ishikawa, Shinsuke Tanabe, Hajime Nakagawa, Yoshikazu Uni, Syuiti Abe</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-12T00:47:35.542351-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00607.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00607.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00607.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00594.x" xmlns="http://purl.org/rss/1.0/"><title>Hector's dolphin diet: The species, sizes and relative importance of prey eaten by Cephalorhynchus hectori, investigated using stomach content analysis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00594.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hector's dolphin diet: The species, sizes and relative importance of prey eaten by Cephalorhynchus hectori, investigated using stomach content analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Elanor Miller, Chris Lalas, Steve Dawson, Hiltrun Ratz, Elisabeth Slooten</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-28T02:40:41.389166-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00594.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00594.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00594.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Stomach contents of 63 Hector's dolphins (<em>Cephalorhynchus hectori</em>) were collected between 1984 and 2006 from throughout New Zealand to provide the first quantitative assessment of prey composition. Twenty-nine taxa were identified. Those most commonly consumed were red cod (<em>Pseudophycis bachus</em>), ahuru (<em>Auchenoceros punctatus</em>), arrow squid (<em>Nototodarus</em> sp.), sprat (<em>Sprattus</em> sp.), sole (<em>Peltorhamphus</em> sp.), and stargazer (<em>Crapatalus</em> sp.). By mass, these six species contributed 77% of total diet. Red cod contributed the most in terms of mass (37%), while ahuru and Hector's lanternfish (<em>Lampanyctodes hectoris</em>) were consumed in large numbers. Prey ranged from &lt;1 cm to &gt;60 cm in total length, but the majority of prey items were &lt;10 cm long, indicating that for some species, juveniles were targeted. Diets of dolphins from South Island east and west coasts were significantly different, due largely to javelinfish (<em>Lepidorhynchus denticulatus</em>) being of greater importance in west coast stomachs, and a greater consumption of demersal prey species in the east. The feeding ecology of Hector's dolphin is broadly similar to that of other <em>Cephalorhynchus</em> species. Hector's dolphin is shown to feed on species from throughout the water column, and differences in diet between populations are thought to reflect prey availability.</p></div>
]]></content:encoded><description>

Stomach contents of 63 Hector's dolphins (Cephalorhynchus hectori) were collected between 1984 and 2006 from throughout New Zealand to provide the first quantitative assessment of prey composition. Twenty-nine taxa were identified. Those most commonly consumed were red cod (Pseudophycis bachus), ahuru (Auchenoceros punctatus), arrow squid (Nototodarus sp.), sprat (Sprattus sp.), sole (Peltorhamphus sp.), and stargazer (Crapatalus sp.). By mass, these six species contributed 77% of total diet. Red cod contributed the most in terms of mass (37%), while ahuru and Hector's lanternfish (Lampanyctodes hectoris) were consumed in large numbers. Prey ranged from &lt;1 cm to &gt;60 cm in total length, but the majority of prey items were &lt;10 cm long, indicating that for some species, juveniles were targeted. Diets of dolphins from South Island east and west coasts were significantly different, due largely to javelinfish (Lepidorhynchus denticulatus) being of greater importance in west coast stomachs, and a greater consumption of demersal prey species in the east. The feeding ecology of Hector's dolphin is broadly similar to that of other Cephalorhynchus species. Hector's dolphin is shown to feed on species from throughout the water column, and differences in diet between populations are thought to reflect prey availability.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00589.x" xmlns="http://purl.org/rss/1.0/"><title>Cutaneous nodular disease in a small population of Indo-Pacific bottlenose dolphins, Tursiops aduncus, from Japan</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00589.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cutaneous nodular disease in a small population of Indo-Pacific bottlenose dolphins, Tursiops aduncus, from Japan</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M.-F. Bressem, M. Shirakihara, M. Amano</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-17T01:40:33.900496-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00589.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00589.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00589.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00586.x" xmlns="http://purl.org/rss/1.0/"><title>Management reference points to account for direct and indirect impacts of fishing on marine mammals</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00586.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Management reference points to account for direct and indirect impacts of fishing on marine mammals</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jeffrey E. Moore</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-19T09:10:00.446938-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00586.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00586.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00586.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib"><span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span></h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Reference points can help implement an ecosystem approach to fisheries management (EAF), by establishing precautionary removal limits for nontarget species and target species of ecological importance. PBR (Potential Biological Removal), developed under the U.S. Marine Mammal Protection Act (MMPA), is a limit for direct mortality for marine mammals, but it does not account for indirect effects of fishing due to prey depletion. I propose a generalization of PBR (called PBR*) to account for plausible changes in marine mammal carrying capacity (ΔK) from prey biomass decline relative to two example benchmarks: SSB<sub>MSY</sub> (maximum sustainable yield biomass for all known prey species) or SSB<sub>K</sub> (unfished prey biomass). PBR* can help identify when indirect fishing effects (alone, or combination with direct mortality estimates) may stymie MMPA objectives, and could inform catch limit estimates for target species that are also important as marine mammal prey. As a case study, I applied PBR* estimates to evaluate the possible combined direct + indirect effects of fishing on cetaceans in northeastern U.S. waters. Estimated distributions for ΔK were based on fish stock assessments and meta-analysis of predator-prey relationships from the mammalian literature. Based on this analysis, increased risk of marine mammal depletion due to indirect fishing effects was not evident, although this result must be interpreted cautiously given our limited understanding of cetacean diets and marine trophic dynamics. This study is intended to illustrate a possible practical approach for incorporating indirect fisheries impacts on marine mammals into a comprehensive management framework, and it raises several scientific and policy issues that merit further investigation.</p></div>]]></content:encoded><description>Reference points can help implement an ecosystem approach to fisheries management (EAF), by establishing precautionary removal limits for nontarget species and target species of ecological importance. PBR (Potential Biological Removal), developed under the U.S. Marine Mammal Protection Act (MMPA), is a limit for direct mortality for marine mammals, but it does not account for indirect effects of fishing due to prey depletion. I propose a generalization of PBR (called PBR*) to account for plausible changes in marine mammal carrying capacity (ΔK) from prey biomass decline relative to two example benchmarks: SSBMSY (maximum sustainable yield biomass for all known prey species) or SSBK (unfished prey biomass). PBR* can help identify when indirect fishing effects (alone, or combination with direct mortality estimates) may stymie MMPA objectives, and could inform catch limit estimates for target species that are also important as marine mammal prey. As a case study, I applied PBR* estimates to evaluate the possible combined direct + indirect effects of fishing on cetaceans in northeastern U.S. waters. Estimated distributions for ΔK were based on fish stock assessments and meta-analysis of predator-prey relationships from the mammalian literature. Based on this analysis, increased risk of marine mammal depletion due to indirect fishing effects was not evident, although this result must be interpreted cautiously given our limited understanding of cetacean diets and marine trophic dynamics. This study is intended to illustrate a possible practical approach for incorporating indirect fisheries impacts on marine mammals into a comprehensive management framework, and it raises several scientific and policy issues that merit further investigation.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00585.x" xmlns="http://purl.org/rss/1.0/"><title>The founding of a southern elephant seal colony</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00585.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The founding of a southern elephant seal colony</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">
            Mariano A. Ferrari, Claudio Campagna, Richard Condit, Mirtha N. Lewis</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-16T03:23:58.837996-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00585.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00585.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00585.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib"><span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span></h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The only large mainland colony of southern elephant seals (<em>Mirounga leonina</em>) is on Península Valdés, at 42°S, in Argentine Patagonia. Censuses of pups have been carried out regularly there since 1970, and the population grew five-fold by 2010. Here we use Bayesian modeling tools to make rigorous estimates of the rate of population growth, <em>r</em>, and to estimate survival and recruitment parameters that could account for the growth, incorporating observation error across different census methods. In the 1970s, <em>r</em>= 8%/yr, but has slowed to &lt;1%/yr over the past decade. Using explicit demographic models, we established that the high growth of the 1970s was consistent with adult and juvenile survival at the upper end of published values (0.87/yr adult female survival; 0.40 juvenile survivorship to age four); the decline in the rate of population growth from 1970 to 2010 can be described by density-dependent reductions in adult and juvenile survival that fall well within published variation. Extrapolating empirical models of population growth rate backwards illustrates that the population could have been an established colony, with 100 pups born per year, between 1915 and 1945, consistent with qualitative observations prior to 1950. We conclude that the Valdés colony was founded by a few immigrants early in the 20th century and has been growing mostly by internal recruitment, with unknown density-dependent processes causing a reduction in growth and stabilization at 15,000–16,000 pups born.</p></div>]]></content:encoded><description>The only large mainland colony of southern elephant seals (Mirounga leonina) is on Península Valdés, at 42°S, in Argentine Patagonia. Censuses of pups have been carried out regularly there since 1970, and the population grew five-fold by 2010. Here we use Bayesian modeling tools to make rigorous estimates of the rate of population growth, r, and to estimate survival and recruitment parameters that could account for the growth, incorporating observation error across different census methods. In the 1970s, r= 8%/yr, but has slowed to &lt;1%/yr over the past decade. Using explicit demographic models, we established that the high growth of the 1970s was consistent with adult and juvenile survival at the upper end of published values (0.87/yr adult female survival; 0.40 juvenile survivorship to age four); the decline in the rate of population growth from 1970 to 2010 can be described by density-dependent reductions in adult and juvenile survival that fall well within published variation. Extrapolating empirical models of population growth rate backwards illustrates that the population could have been an established colony, with 100 pups born per year, between 1915 and 1945, consistent with qualitative observations prior to 1950. We conclude that the Valdés colony was founded by a few immigrants early in the 20th century and has been growing mostly by internal recruitment, with unknown density-dependent processes causing a reduction in growth and stabilization at 15,000–16,000 pups born.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00574.x" xmlns="http://purl.org/rss/1.0/"><title>Investigating the potential use of aerial line transect surveys for estimating polar bear abundance in sea ice habitats: A case study for the Chukchi Sea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00574.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Investigating the potential use of aerial line transect surveys for estimating polar bear abundance in sea ice habitats: A case study for the Chukchi Sea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ryan M. Nielson, Thomas J. Evans, Michelle Bourassa Stahl</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-16T03:10:52.496136-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00574.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00574.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00574.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib"><span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span></h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The expense of traditional capture-recapture methods, interest in less invasive survey methods, and the circumpolar decline of polar bear (<em>Ursus maritimus</em>) habitat require evaluation of alternative methods for monitoring polar bear populations. Aerial line transect distance sampling (DS) surveys are thought to be a promising monitoring tool. However, low densities and few observations during a survey can result in low precision, and logistical constraints such as heavy ice and fuel and safety limitations may restrict survey coverage. We used simulations to investigate the accuracy and precision of, DS for estimating polar bear abundance in sea ice habitats, using the Chukchi Sea subpopulation as an example. Simulation parameters were informed from a recent pilot survey. Predictions from a resource selection model were used for stratification, and we compared two ratio estimators to account for areas that cannot be sampled. The ratio estimator using predictions of resource selection by polar bears allowed for extrapolation beyond sampled areas and provided results with low bias and CVs ranging from 21% to 36% when abundance was &gt;1,000. These techniques could be applied to other DS surveys to allocate effort and potentially extrapolate estimates to include portions of the landscape that are logistically impossible to survey.</p></div>]]></content:encoded><description>The expense of traditional capture-recapture methods, interest in less invasive survey methods, and the circumpolar decline of polar bear (Ursus maritimus) habitat require evaluation of alternative methods for monitoring polar bear populations. Aerial line transect distance sampling (DS) surveys are thought to be a promising monitoring tool. However, low densities and few observations during a survey can result in low precision, and logistical constraints such as heavy ice and fuel and safety limitations may restrict survey coverage. We used simulations to investigate the accuracy and precision of, DS for estimating polar bear abundance in sea ice habitats, using the Chukchi Sea subpopulation as an example. Simulation parameters were informed from a recent pilot survey. Predictions from a resource selection model were used for stratification, and we compared two ratio estimators to account for areas that cannot be sampled. The ratio estimator using predictions of resource selection by polar bears allowed for extrapolation beyond sampled areas and provided results with low bias and CVs ranging from 21% to 36% when abundance was &gt;1,000. These techniques could be applied to other DS surveys to allocate effort and potentially extrapolate estimates to include portions of the landscape that are logistically impossible to survey.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00584.x" xmlns="http://purl.org/rss/1.0/"><title>Spatio-temporal shifts of the dynamic Cape fur seal population in southern Africa, based on aerial censuses (1972–2009)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00584.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Spatio-temporal shifts of the dynamic Cape fur seal population in southern Africa, based on aerial censuses (1972–2009)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Steve P. Kirkman, D. Yemane, W. H. Oosthuizen, M. A. Meÿer, P. G. H. Kotze, H. Skrypzeck, F. Vaz Velho, L. G. Underhill</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-12T04:21:51.648798-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00584.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00584.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00584.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib"><span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span></h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A time series of aerial censuses of Cape fur seal colonies, spanning four decades (1972–2009) and three countries (South Africa, Namibia, and Angola), was analyzed to assess spatio<em>-</em>temporal changes in population numbers. A weighted quantile regression approach was used to estimate trends in pup counts that were used as proxies for numbers of older animals at breeding colonies. There was a 74% increase in the number of breeding colonies over the study period, from 23 in 1973 to 40 in 2009. There was also a significant northward shift in the distribution of the breeding population. This was largely attributable to events in the northern part of the population's range coinciding with Namibia, where seal numbers declined at most colonies in the south of Namibia while several new breeding colonies developed in the northern part of Namibia and one in southern Angola. Despite range expansion and the development of new colonies, the overall size of the population in 2009 was similar to that of the early 1990s, according to the pup count models. Potential mechanisms for the observed changes, and their management implications, are discussed.</p></div>]]></content:encoded><description>A time series of aerial censuses of Cape fur seal colonies, spanning four decades (1972–2009) and three countries (South Africa, Namibia, and Angola), was analyzed to assess spatio-temporal changes in population numbers. A weighted quantile regression approach was used to estimate trends in pup counts that were used as proxies for numbers of older animals at breeding colonies. There was a 74% increase in the number of breeding colonies over the study period, from 23 in 1973 to 40 in 2009. There was also a significant northward shift in the distribution of the breeding population. This was largely attributable to events in the northern part of the population's range coinciding with Namibia, where seal numbers declined at most colonies in the south of Namibia while several new breeding colonies developed in the northern part of Namibia and one in southern Angola. Despite range expansion and the development of new colonies, the overall size of the population in 2009 was similar to that of the early 1990s, according to the pup count models. Potential mechanisms for the observed changes, and their management implications, are discussed.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00580.x" xmlns="http://purl.org/rss/1.0/"><title>Investigating the feasibility of using DNA from sloughed skin for individual identification and kinship analysis in humpback whales (Megaptera novaeangliae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00580.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Investigating the feasibility of using DNA from sloughed skin for individual identification and kinship analysis in humpback whales (Megaptera novaeangliae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. P. 
              Pierszalowski
            , M. 
              Ferrari
            , D. 
              Glockner-Ferrari
            , S. 
              Mizroch
            , P. J. 
              Clapham
            , B. R. 
              Dickerson
            </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-09T21:44:27.90279-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00580.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00580.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00580.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00582.x" xmlns="http://purl.org/rss/1.0/"><title>Rare observations of false killer whales (Pseudorca crassidens) cooperatively feeding with common bottlenose dolphins (Tursiops truncatus) in the Hauraki Gulf, New Zealand</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00582.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Rare observations of false killer whales (Pseudorca crassidens) cooperatively feeding with common bottlenose dolphins (Tursiops truncatus) in the Hauraki Gulf, New Zealand</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">
              Jochen R.
             
              Zaeschmar
            , 
              Sarah L.
             
              Dwyer
            , 
              Karen A.
             
              Stockin
            </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-09T03:30:23.902351-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00582.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00582.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00582.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00578.x" xmlns="http://purl.org/rss/1.0/"><title>Lipid content of blubber biopsies is not representative of blubber in situ for fin whales (Balaenoptera physalus)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00578.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Lipid content of blubber biopsies is not representative of blubber in situ for fin whales (Balaenoptera physalus)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">
              Conor
             
              Ryan
            , 
              Brendan
             
              McHugh
            , 
              Ian
             
              O’Connor
            , 
              Simon
             
              Berrow
            </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-05T22:37:44.898069-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00578.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00578.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00578.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00581.x" xmlns="http://purl.org/rss/1.0/"><title>Genetic and family structure in a group of 165 common bottlenose dolphins caught off the Japanese coast</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00581.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Genetic and family structure in a group of 165 common bottlenose dolphins caught off the Japanese coast</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yuki F. Kita, Kazuyoshi Hosomichi, Shingo Suzuki, Hidetoshi Inoko, Takashi Shiina, Mai Watanabe, Ayumi Tanaka, Taku Horie, Hiroshi Ohizumi, Sho Tanaka, Toshihide Iwasaki, Masao Ota, Jerzy K. Kulski</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-02T05:56:15.183414-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00581.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00581.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00581.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">A<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">bstract</span></h3><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The biological and genetic structure of common bottlenose dolphins (<em>Tursiops truncatus</em>) that migrate seasonally near Japan remains largely unknown. We investigated the genetic and family structure in a group of 165 common bottlenose dolphins caught off the coast of Japan using mitochondrial DNA (mtDNA) and 20 microsatellite DNA markers. Phylogenetic analysis of the mtDNA control region sequences suggested that the dolphins were related more closely to oceanic types from Chinese waters than other geographic regions. The information on sex, sexual maturation and age together with the genetic markers revealed a strong likelihood for 37 familial relationships related mostly to maternity and an under-representation of juvenile female offspring. The maternal dolphins had a similar offspring-birth interval as the coastal types from North Atlantic Ocean, but a slightly younger first-progeny age. The sex bias in the captured group was particularly marked towards an over-representation of males among the young and immature dolphins, whereas the mature adults had an equal number of males and females. These results should be useful for future comparative biological, genetic and evolutionary investigations of bottlenose dolphins from the North Pacific Ocean with those from other regions.</p></div>]]></content:encoded><description>The biological and genetic structure of common bottlenose dolphins (Tursiops truncatus) that migrate seasonally near Japan remains largely unknown. We investigated the genetic and family structure in a group of 165 common bottlenose dolphins caught off the coast of Japan using mitochondrial DNA (mtDNA) and 20 microsatellite DNA markers. Phylogenetic analysis of the mtDNA control region sequences suggested that the dolphins were related more closely to oceanic types from Chinese waters than other geographic regions. The information on sex, sexual maturation and age together with the genetic markers revealed a strong likelihood for 37 familial relationships related mostly to maternity and an under-representation of juvenile female offspring. The maternal dolphins had a similar offspring-birth interval as the coastal types from North Atlantic Ocean, but a slightly younger first-progeny age. The sex bias in the captured group was particularly marked towards an over-representation of males among the young and immature dolphins, whereas the mature adults had an equal number of males and females. These results should be useful for future comparative biological, genetic and evolutionary investigations of bottlenose dolphins from the North Pacific Ocean with those from other regions.</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00579.x" xmlns="http://purl.org/rss/1.0/"><title>A report on six cases of seagrass-associated gastric impaction in bottlenose dolphins (Tursiops sp.)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00579.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A report on six cases of seagrass-associated gastric impaction in bottlenose dolphins (Tursiops sp.)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. 
              Krzyszczyk
            , A. M. 
              Kopps
            , K. 
              Bacher
            , H. 
              Smith
            , N. 
              Stephens
            , N. A. 
              Meighan
            , J. 
              Mann
            </dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-06-26T03:24:39.37326-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00579.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00579.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00579.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2011.00553.x" xmlns="http://purl.org/rss/1.0/"><title>Behavioral responses of New Zealand fur seals (Arctophoca australis forsteri) to darting and the effectiveness of midazolam and tiletamine-zolazepam for remote chemical immobilization</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2011.00553.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Behavioral responses of New Zealand fur seals (Arctophoca australis forsteri) to darting and the effectiveness of midazolam and tiletamine-zolazepam for remote chemical immobilization</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jane McKenzie, Brad Page, Simon D. Goldsworthy, Mark A. Hindell</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-04-26T21:18:32.96055-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2011.00553.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2011.00553.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2011.00553.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">241</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">260</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We evaluated the behavioral response of 125 free-ranging New Zealand fur seals (75 females and 50 males) to darting and the effectiveness and safety of midazolam and tiletamine-zolazepam for remote chemical immobilization. Behavioral reactions to darting were minor and brief. Overall, severe reactions to darting such as long flight responses (7%) and escape to the sea (7%) were uncommon. Midazolam administered by dart failed to produce a satisfactory level of immobilization. Tiletamine-zolazepam was administered to 120 animals (35 females and 85 males), 104 of which were successfully immobilized and 16 escaped to the water following darting or attempted net capture. At least 10 of the 16 animals are known to have survived. Tiletamine-zolazepam caused moderate depression of swimming and diving behavior in the animals that escaped to the water. Data from dive loggers confirmed that seals that escaped remained near the sea surface for extended periods. Tiletamine-zolazepam administered by dart at a mean dosage of 1.87 ± 0.18 mg/kg for females and 1.49 ± 0.23 mg/kg for males provided effective and safe immobilization, reducing capture stress for both animals and personnel. Although there is still a risk of drugged animals escaping to the water and possibly drowning, this risk is much lower than previously reported for other pinnipeds.</p></div>
]]></content:encoded><description>

We evaluated the behavioral response of 125 free-ranging New Zealand fur seals (75 females and 50 males) to darting and the effectiveness and safety of midazolam and tiletamine-zolazepam for remote chemical immobilization. Behavioral reactions to darting were minor and brief. Overall, severe reactions to darting such as long flight responses (7%) and escape to the sea (7%) were uncommon. Midazolam administered by dart failed to produce a satisfactory level of immobilization. Tiletamine-zolazepam was administered to 120 animals (35 females and 85 males), 104 of which were successfully immobilized and 16 escaped to the water following darting or attempted net capture. At least 10 of the 16 animals are known to have survived. Tiletamine-zolazepam caused moderate depression of swimming and diving behavior in the animals that escaped to the water. Data from dive loggers confirmed that seals that escaped remained near the sea surface for extended periods. Tiletamine-zolazepam administered by dart at a mean dosage of 1.87 ± 0.18 mg/kg for females and 1.49 ± 0.23 mg/kg for males provided effective and safe immobilization, reducing capture stress for both animals and personnel. Although there is still a risk of drugged animals escaping to the water and possibly drowning, this risk is much lower than previously reported for other pinnipeds.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2011.00559.x" xmlns="http://purl.org/rss/1.0/"><title>Dispersal, philopatry, and the role of fission-fusion dynamics in bottlenose dolphins</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2011.00559.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Dispersal, philopatry, and the role of fission-fusion dynamics in bottlenose dolphins</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yi-Jiun Jean Tsai, Janet Mann</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-05-25T05:06:18.853034-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2011.00559.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2011.00559.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2011.00559.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">261</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">279</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In this quantitative study of locational and social dispersal at the individual level, we show that bottlenose dolphins (<em>Tursiops</em> sp.) continued to use their natal home ranges well into adulthood. Despite substantial home range overlap, mother–offspring associations decreased after weaning, particularly for sons. These data provide strong evidence for bisexual locational philopatry and mother–son avoidance in bottlenose dolphins. While bisexual locational philopatry offers the benefits of familiar social networks and foraging habitats, the costs of philopatry may be mitigated by reduced mother–offspring association, in which the risk of mother–daughter resource competition and mother–son mating is reduced. Our study highlights the advantages of high fission–fusion dynamics and longitudinal studies, and emphasizes the need for clarity when describing dispersal in this and other species.</p></div>
]]></content:encoded><description>

In this quantitative study of locational and social dispersal at the individual level, we show that bottlenose dolphins (Tursiops sp.) continued to use their natal home ranges well into adulthood. Despite substantial home range overlap, mother–offspring associations decreased after weaning, particularly for sons. These data provide strong evidence for bisexual locational philopatry and mother–son avoidance in bottlenose dolphins. While bisexual locational philopatry offers the benefits of familiar social networks and foraging habitats, the costs of philopatry may be mitigated by reduced mother–offspring association, in which the risk of mother–daughter resource competition and mother–son mating is reduced. Our study highlights the advantages of high fission–fusion dynamics and longitudinal studies, and emphasizes the need for clarity when describing dispersal in this and other species.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00564.x" xmlns="http://purl.org/rss/1.0/"><title>Anal glands of the Florida manatee, Trichechus manatus latirostris: A potential source of chemosensory signal expression</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00564.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Anal glands of the Florida manatee, Trichechus manatus latirostris: A potential source of chemosensory signal expression</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Meghan L. Bills, Don A. Samuelson, Iskande L. V. Larkin</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-06-05T04:26:38.498704-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00564.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00564.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00564.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">280</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">292</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In all vertebrate species examined, anal glands have been observed. These glands can be found anywhere along the anal canal and are generally a combination of apocrine and sebaceous adenomeres. They are used for signal expression in both terrestrial and aquatic settings. The goal of this study was to determine the morphology of the anal glands in the Florida manatee, <em>Trichechus manatus latirostris</em>, and suggest functional hypotheses through comparison to other species. Samples were collected from manatees of varying ages, during all seasons, and from both sexes (six females and five males). The glands were examined grossly and microscopically. They are present in fetal, juvenile, and adult male and female manatees and are found in clusters on each side of the anal canal within the sphincter muscles. Unlike in other species, the glands are solely apocrine without a sebaceous component. Branched tubules empty into collecting ducts and enter the anal canal at the anorectal junction. The secretion is mucus, protein, and lipid-rich. The large size and productive nature of the glands suggest that, like anal glands in other species, these may be used for signal transmission. This is the first detailed description of anal glands in a fully aquatic mammal.</p></div>
]]></content:encoded><description>

In all vertebrate species examined, anal glands have been observed. These glands can be found anywhere along the anal canal and are generally a combination of apocrine and sebaceous adenomeres. They are used for signal expression in both terrestrial and aquatic settings. The goal of this study was to determine the morphology of the anal glands in the Florida manatee, Trichechus manatus latirostris, and suggest functional hypotheses through comparison to other species. Samples were collected from manatees of varying ages, during all seasons, and from both sexes (six females and five males). The glands were examined grossly and microscopically. They are present in fetal, juvenile, and adult male and female manatees and are found in clusters on each side of the anal canal within the sphincter muscles. Unlike in other species, the glands are solely apocrine without a sebaceous component. Branched tubules empty into collecting ducts and enter the anal canal at the anorectal junction. The secretion is mucus, protein, and lipid-rich. The large size and productive nature of the glands suggest that, like anal glands in other species, these may be used for signal transmission. This is the first detailed description of anal glands in a fully aquatic mammal.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00571.x" xmlns="http://purl.org/rss/1.0/"><title>Seasonal abundance and adult survival of bottlenose dolphins (Tursiops truncatus) in a community that cooperatively forages with fishermen in southern Brazil</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00571.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Seasonal abundance and adult survival of bottlenose dolphins (Tursiops truncatus) in a community that cooperatively forages with fishermen in southern Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fábio G. Daura-Jorge, Simon N. Ingram, Paulo C. Simões-Lopes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-04T05:47:28.322923-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00571.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00571.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00571.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">293</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">311</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A subgroup of a population of <em>Tursiops truncatus</em> in southern Brazil is known for a cooperative behavior with artisanal fishermen whereby the dolphins shoal fish towards net-casting fishermen. Combining photo-identification data collected between September 2007 and 2009 with mark-recapture and Pollock's robust design models, we assessed abundance within seasons and survival and temporary emigration rates of dolphins between seasons. We also reanalyzed a previous data set collected during 1989–1991, and Cormack-Jolly-Seber models were applied to estimate survival rates for each of the study periods. The abundance of marked “cooperative” dolphins varied between seasons from 18 (CI: 17–24) to 21 (CI: 20–24). The total abundance varied from 59 in the winter of 2008 (CI: 49–72) to 50 in the autumn of 2009 (CI: 40–62). The annual adult survival was estimated to be 0.917 (CI: 0.876–0.961), close to that estimated from data collected in the 1990s (0.941; CI: 0.888–0.998). The emigration probability was low (0.031; CI: 0.011–0.084) and different capture probabilities between the “cooperative” and “noncooperative” dolphins indicated a degree of behavioral segregation. The precision of our estimates is likely to provide sufficient power to detect population change, but we recommend a precautionary management approach to protect this vulnerable dolphin community and its unique cooperative feeding tradition.</p></div>
]]></content:encoded><description>

A subgroup of a population of Tursiops truncatus in southern Brazil is known for a cooperative behavior with artisanal fishermen whereby the dolphins shoal fish towards net-casting fishermen. Combining photo-identification data collected between September 2007 and 2009 with mark-recapture and Pollock's robust design models, we assessed abundance within seasons and survival and temporary emigration rates of dolphins between seasons. We also reanalyzed a previous data set collected during 1989–1991, and Cormack-Jolly-Seber models were applied to estimate survival rates for each of the study periods. The abundance of marked “cooperative” dolphins varied between seasons from 18 (CI: 17–24) to 21 (CI: 20–24). The total abundance varied from 59 in the winter of 2008 (CI: 49–72) to 50 in the autumn of 2009 (CI: 40–62). The annual adult survival was estimated to be 0.917 (CI: 0.876–0.961), close to that estimated from data collected in the 1990s (0.941; CI: 0.888–0.998). The emigration probability was low (0.031; CI: 0.011–0.084) and different capture probabilities between the “cooperative” and “noncooperative” dolphins indicated a degree of behavioral segregation. The precision of our estimates is likely to provide sufficient power to detect population change, but we recommend a precautionary management approach to protect this vulnerable dolphin community and its unique cooperative feeding tradition.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00577.x" xmlns="http://purl.org/rss/1.0/"><title>Repeated call types in short-finned pilot whales, Globicephala macrorhynchus</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00577.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Repeated call types in short-finned pilot whales, Globicephala macrorhynchus</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laela Sayigh, Nicola Quick, Gordon Hastie, Peter Tyack</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-09T03:20:27.305626-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00577.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00577.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00577.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">312</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">324</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Four short-finned pilot whales, <em>Globicephala macrorhynchus</em>, were tagged with digital acoustic recording tags (DTAGs) for a total of 30 h in the Bahamas during 2007. Spectrograms were made of all audible sounds, which were independently categorized by three observers. Of 4,098 calls, 1,737 (42%) were placed into 173 call types, which were defined as calls that occurred more than once. Of the 173 call types, 51 contained at least 10 calls (<img alt="inline image" src="http://onlinelibrary.wiley.com/store/10.1111/j.1748-7692.2012.00577.x/asset/equation/mms577_mu1.gif?v=1&amp;s=7417e237d38766c7b85ce873da9e6cc6b6e3e6bc" class="inlineGraphic"/>= 24), and were termed predominant call types (PCTs), which comprised 1,219 (70%) of categorized calls. PCTs tended to occur in sequences of the same call, which appeared to be produced by a single animal. However, matching interactions consisting of adjacent or overlapping calls of the same type were also observed, and some call types were recorded on more than one tag, suggesting that at least some calls are shared by members of a group or subgroup. These results emphasize the importance of categorizing calls before attempting to draw conclusions about call usage and possible effects of noise on vocal behavior.</p></div>
]]></content:encoded><description>

Four short-finned pilot whales, Globicephala macrorhynchus, were tagged with digital acoustic recording tags (DTAGs) for a total of 30 h in the Bahamas during 2007. Spectrograms were made of all audible sounds, which were independently categorized by three observers. Of 4,098 calls, 1,737 (42%) were placed into 173 call types, which were defined as calls that occurred more than once. Of the 173 call types, 51 contained at least 10 calls (= 24), and were termed predominant call types (PCTs), which comprised 1,219 (70%) of categorized calls. PCTs tended to occur in sequences of the same call, which appeared to be produced by a single animal. However, matching interactions consisting of adjacent or overlapping calls of the same type were also observed, and some call types were recorded on more than one tag, suggesting that at least some calls are shared by members of a group or subgroup. These results emphasize the importance of categorizing calls before attempting to draw conclusions about call usage and possible effects of noise on vocal behavior.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00572.x" xmlns="http://purl.org/rss/1.0/"><title>New insights into the northward migration route of gray whales between Vancouver Island, British Columbia, and southeastern Alaska</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00572.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">New insights into the northward migration route of gray whales between Vancouver Island, British Columbia, and southeastern Alaska</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">John K. B. Ford, John W. Durban, Graeme M. Ellis, Jared R. Towers, James F. Pilkington, Lance G. Barrett-Lennard, Russel D. Andrews</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-11T04:35:26.133075-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00572.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00572.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00572.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">325</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">337</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The route taken by northward migrating gray whales during spring between Vancouver Island and southeastern Alaska, a distance of about 575 km, has long been uncertain. It is generally believed that the whales closely follow the western, outer coastline of Haida Gwaii (formerly the Queen Charlotte Islands), an archipelago lying between Vancouver Island and southeastern Alaska, consistent with their pattern of migrating close to shore over the majority of their northward migratory corridor. By tracking satellite-tagged individuals and surveying whales from shore bases, we provide evidence that this is not the primary migratory corridor, but instead that most whales migrate through Hecate Strait and Dixon Entrance, broad waterways that lie to the east and north of Haida Gwaii. By using this route, northbound gray whales potentially face a wider range of industrial activities and developments than they would by migrating along the outer coast.</p></div>
]]></content:encoded><description>

The route taken by northward migrating gray whales during spring between Vancouver Island and southeastern Alaska, a distance of about 575 km, has long been uncertain. It is generally believed that the whales closely follow the western, outer coastline of Haida Gwaii (formerly the Queen Charlotte Islands), an archipelago lying between Vancouver Island and southeastern Alaska, consistent with their pattern of migrating close to shore over the majority of their northward migratory corridor. By tracking satellite-tagged individuals and surveying whales from shore bases, we provide evidence that this is not the primary migratory corridor, but instead that most whales migrate through Hecate Strait and Dixon Entrance, broad waterways that lie to the east and north of Haida Gwaii. By using this route, northbound gray whales potentially face a wider range of industrial activities and developments than they would by migrating along the outer coast.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00562.x" xmlns="http://purl.org/rss/1.0/"><title>Dental erosion in South Atlantic dolphins (Cetacea: Delphinidae): A macro and microscopic approach</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00562.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Dental erosion in South Atlantic dolphins (Cetacea: Delphinidae): A macro and microscopic approach</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carolina Loch, Liliane J. Grando, Donald R. Schwass, Jules A. Kieser, R. Ewan Fordyce, Paulo C. Simões-Lopes</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-04-23T03:18:29.955758-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00562.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00562.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00562.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">338</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">347</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00568.x" xmlns="http://purl.org/rss/1.0/"><title>Parameters of growth and reproduction of white-beaked dolphins (Lagenorhynchus albirostris) from the North Sea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00568.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Parameters of growth and reproduction of white-beaked dolphins (Lagenorhynchus albirostris) from the North Sea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anders Galatius, Okka E. Jansen, Carl C. Kinze</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-03T01:07:41.543505-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00568.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00568.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00568.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">348</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">355</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00575.x" xmlns="http://purl.org/rss/1.0/"><title>Effects of fishing gear on bottlenose dolphins (Tursiops truncatus) in the Indian River Lagoon system, Florida</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00575.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of fishing gear on bottlenose dolphins (Tursiops truncatus) in the Indian River Lagoon system, Florida</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Megan Stolen, Wendy Noke Durden, Teresa Mazza, Nélio Barros, Judy St. Leger</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-08T22:31:15.140274-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00575.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00575.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00575.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">356</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">364</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12020" xmlns="http://purl.org/rss/1.0/"><title>
Polar Bears: A Complete Guide to Their Biology and Behavior. A. E. Derocher and W. Lynch. ISBN 978-1-4214-0305-2. The Johns Hopkins University Press, Baltimore, MD. 2012. 248 pp. Hardcover US$39.95.
</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12020</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">
Polar Bears: A Complete Guide to Their Biology and Behavior. A. E. Derocher and W. Lynch. ISBN 978-1-4214-0305-2. The Johns Hopkins University Press, Baltimore, MD. 2012. 248 pp. Hardcover US$39.95.
</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Karyn D. Rode</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-04T05:19:31.858343-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12020</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12020</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12020</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Books</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">365</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">367</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12019" xmlns="http://purl.org/rss/1.0/"><title>
Whales and Dolphins: Cognition, Culture, Conservation and Human Perceptions. P. Brakes and M. P. Simmonds, eds. ISBN 978-1-84971-225-5. Earthscan Ltd., London, U.K. 2011. 220 pp. Hardcover £85 and paperback £24.99.
</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12019</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">
Whales and Dolphins: Cognition, Culture, Conservation and Human Perceptions. P. Brakes and M. P. Simmonds, eds. ISBN 978-1-84971-225-5. Earthscan Ltd., London, U.K. 2011. 220 pp. Hardcover £85 and paperback £24.99.
</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bernd Würsig</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2013-04-04T05:19:31.858343-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/mms.12019</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/mms.12019</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fmms.12019</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Books</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">368</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">370</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00588.x" xmlns="http://purl.org/rss/1.0/"><title>Application of a novel method for age estimation of a baleen whale and a porpoise</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00588.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Application of a novel method for age estimation of a baleen whale and a porpoise</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nynne H. Nielsen, Eva Garde, Mads Peter Heide-Jørgensen, Christina H. Lockyer, Susanne Ditlevsen, Droplaug Òlafsdóttir, Steen H. Hansen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-21T02:18:00.826807-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00588.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00588.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00588.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E23</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Eyeballs from 121 fin whales (<em>Balaenoptera physalus</em>) and 83 harbor porpoises (<em>Phocoena phocoena</em>) were used for age estimation using the aspartic acid racemization (AAR) technique. The racemization rate (<em>k</em><sub>A</sub><sub>sp</sub>) for fin whales was established from 15 fetuses (age 0) and 15 adult whales where age was estimated by reading growth layer groups (GLGs) in the earplugs. The (<em>k</em><sub>A</sub><sub>sp</sub>) for harbor porpoises was derived from 15 porpoises (two calves and 13 &gt; 1 yr old) age-estimated by counting GLGs in the teeth and two calves classified to age based on length. The (<em>k</em><sub>A</sub><sub>sp</sub>) values were estimated by regression of GLGs against D/L ratios. For the fin whales an (<em>k</em><sub>A</sub><sub>sp</sub>) of 1.15 × 10<sup>−3</sup>/yr (SE ± 0.00005) and a D/L ratio at birth [(D/L)<sub>0</sub>] of 0.028 (SE ± 0.0012) were estimated, which is in agreement with rates for other mysticeti. For the harbor porpoises a (<em>k</em><sub>A</sub><sub>sp</sub>) of 3.10 × 10<sup>−3</sup>/yr (SE ± 0.0004) and a (D/L)<sub>0</sub> value of 0.023 (SE ± 0.0018) were estimated, which is considerably higher than found for other cetaceans. Correlation between chosen age estimates from AAR and GLG counts indicated that AAR might be an alternative method for estimating age in marine mammals.</p></div>
]]></content:encoded><description>

Eyeballs from 121 fin whales (Balaenoptera physalus) and 83 harbor porpoises (Phocoena phocoena) were used for age estimation using the aspartic acid racemization (AAR) technique. The racemization rate (kAsp) for fin whales was established from 15 fetuses (age 0) and 15 adult whales where age was estimated by reading growth layer groups (GLGs) in the earplugs. The (kAsp) for harbor porpoises was derived from 15 porpoises (two calves and 13 &gt; 1 yr old) age-estimated by counting GLGs in the teeth and two calves classified to age based on length. The (kAsp) values were estimated by regression of GLGs against D/L ratios. For the fin whales an (kAsp) of 1.15 × 10−3/yr (SE ± 0.00005) and a D/L ratio at birth [(D/L)0] of 0.028 (SE ± 0.0012) were estimated, which is in agreement with rates for other mysticeti. For the harbor porpoises a (kAsp) of 3.10 × 10−3/yr (SE ± 0.0004) and a (D/L)0 value of 0.023 (SE ± 0.0018) were estimated, which is considerably higher than found for other cetaceans. Correlation between chosen age estimates from AAR and GLG counts indicated that AAR might be an alternative method for estimating age in marine mammals.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00583.x" xmlns="http://purl.org/rss/1.0/"><title>Response of southern right whales to simulated swim-with-whale tourism at Península Valdés, Argentina</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00583.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Response of southern right whales to simulated swim-with-whale tourism at Península Valdés, Argentina</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David Lundquist, Mariano Sironi, Bernd Würsig, Victoria Rowntree, Julieta Martino, Lesley Lundquist</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-09T03:51:12.263504-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00583.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00583.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00583.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E24</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E45</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Guidelines for sustainable tourism involving swimming with large whales are not well-developed compared to those focused on programs of swimming with delphinids. From September to November 2005 and August to September 2006, we collected behavioral and movement data for southern right whales (<em>Eubalaena australis</em>) exposed to interactions with boats and swimmers at Península Valdés, Argentina. Whales were tracked from shore using a theodolite before, during, and after a series of directed interactions with swimmers and a boat. Resting, socializing, and surface active behavior decreased, traveling increased, and whales swam faster and reoriented more often during interactions. Responses were variable by age/sex class, with mother/calf pairs showing strongest responses. Increased levels of tourism activity are a concern, as reduction in resting time and disruption of socialization among adults, juveniles, and mother/calf pairs have unknown long-term consequences. Additional data should be collected for whale behavior in proposed tourism and nontourism areas to build a long-term database which can be used to determine if reactions of whales change over time. Our data suggest that swimming with whales in Chubut Province should not be legalized until further investigations are completed, especially in light of the recent southern right whale die-offs recorded in Península Valdés.</p></div>
]]></content:encoded><description>

Guidelines for sustainable tourism involving swimming with large whales are not well-developed compared to those focused on programs of swimming with delphinids. From September to November 2005 and August to September 2006, we collected behavioral and movement data for southern right whales (Eubalaena australis) exposed to interactions with boats and swimmers at Península Valdés, Argentina. Whales were tracked from shore using a theodolite before, during, and after a series of directed interactions with swimmers and a boat. Resting, socializing, and surface active behavior decreased, traveling increased, and whales swam faster and reoriented more often during interactions. Responses were variable by age/sex class, with mother/calf pairs showing strongest responses. Increased levels of tourism activity are a concern, as reduction in resting time and disruption of socialization among adults, juveniles, and mother/calf pairs have unknown long-term consequences. Additional data should be collected for whale behavior in proposed tourism and nontourism areas to build a long-term database which can be used to determine if reactions of whales change over time. Our data suggest that swimming with whales in Chubut Province should not be legalized until further investigations are completed, especially in light of the recent southern right whale die-offs recorded in Península Valdés.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00587.x" xmlns="http://purl.org/rss/1.0/"><title>Delphinid whistle production and call matching during playback of simulated military sonar</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00587.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Delphinid whistle production and call matching during playback of simulated military sonar</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stacy L. DeRuiter, Ian L. Boyd, Diane E. Claridge, Christopher W. Clark, Chuck Gagnon, Brandon L. Southall, Peter L. Tyack</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-07-19T09:15:31.581519-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00587.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00587.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00587.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E46</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E59</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">
<span class="smallCaps" xmlns="http://www.w3.org/1999/xhtml">Abstract</span>
</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In 2007 and 2008, controlled exposure experiments were performed in the Bahamas to study behavioral responses to simulated mid-frequency active sonar (MFA) by three groups of odontocetes: false killer whales, <em>Pseudorca crassidens</em>; short-finned pilot whales, <em>Globicephala macrorhynchus</em>; and melon-headed whales, <em>Peponocephala electra</em>. An individual in each group was tagged with a Dtag to record acoustic and movement data. During exposures, some individuals produced whistles that seemed similar to the experimental MFA stimulus. Statistical tests were thus applied to investigate whistle-MFA similarity and the relationship between whistle production rate and MFA reception time. For the false killer whale group, overall whistle rate and production rate of the most MFA-like whistles decreased with time since last MFA reception. Despite quite low whistle rates overall by the melon-headed whales, statistical results indicated minor transient silencing after each signal reception. There were no apparent relationships between pilot whale whistle rates and MFA sounds within the exposure period. This variability of responses suggests that changes in whistle production in response to acoustic stimuli depend not only on species and sound source, but also on the social, behavioral, or environmental contexts of exposure.</p></div>
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In 2007 and 2008, controlled exposure experiments were performed in the Bahamas to study behavioral responses to simulated mid-frequency active sonar (MFA) by three groups of odontocetes: false killer whales, Pseudorca crassidens; short-finned pilot whales, Globicephala macrorhynchus; and melon-headed whales, Peponocephala electra. An individual in each group was tagged with a Dtag to record acoustic and movement data. During exposures, some individuals produced whistles that seemed similar to the experimental MFA stimulus. Statistical tests were thus applied to investigate whistle-MFA similarity and the relationship between whistle production rate and MFA reception time. For the false killer whale group, overall whistle rate and production rate of the most MFA-like whistles decreased with time since last MFA reception. Despite quite low whistle rates overall by the melon-headed whales, statistical results indicated minor transient silencing after each signal reception. There were no apparent relationships between pilot whale whistle rates and MFA sounds within the exposure period. This variability of responses suggests that changes in whistle production in response to acoustic stimuli depend not only on species and sound source, but also on the social, behavioral, or environmental contexts of exposure.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00597.x" xmlns="http://purl.org/rss/1.0/"><title>Geographic, seasonal, and diurnal surface behavior of harbor porpoises</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00597.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Geographic, seasonal, and diurnal surface behavior of harbor porpoises</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jonas Teilmann, Casper T. Christiansen, Sanne Kjellerup, Rune Dietz, Gösta Nachman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-28T03:20:28.766761-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00597.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00597.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00597.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E60</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E76</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>During ship surveys harbor porpoises are only visible when breaking the sea surface to breathe, while during aerial surveys they may be seen down to 2 m below the surface. The fractions of time spent at these two depths can be used for correcting visual surveys to actual population estimates, which are essential information on the status and management of the species. Thirty-five free-ranging harbor porpoises (<em>Phocoena phocoena</em>) were tracked in the region between the Baltic and the North Sea for 25–349 d using Argos satellite transmitters. No differences were found in surface behavior between geographical areas or the size of the animals. Slight differences were found between the two sexes and time of day. Surface time peaked in April, where 6% was spent with the transmitter above surface and 61.5% between 0 and 2 m depth, while the minimum values occurred in February (3.4% and 42.5%, respectively). The analyses reveal that individual variation among porpoises is the most important factor in explaining variation in surface rates. However, the large number of animals documented in the present study covering a wide range of age and sex groups justifies the use of the seasonal average surface times for correcting abundance surveys.</p></div>
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During ship surveys harbor porpoises are only visible when breaking the sea surface to breathe, while during aerial surveys they may be seen down to 2 m below the surface. The fractions of time spent at these two depths can be used for correcting visual surveys to actual population estimates, which are essential information on the status and management of the species. Thirty-five free-ranging harbor porpoises (Phocoena phocoena) were tracked in the region between the Baltic and the North Sea for 25–349 d using Argos satellite transmitters. No differences were found in surface behavior between geographical areas or the size of the animals. Slight differences were found between the two sexes and time of day. Surface time peaked in April, where 6% was spent with the transmitter above surface and 61.5% between 0 and 2 m depth, while the minimum values occurred in February (3.4% and 42.5%, respectively). The analyses reveal that individual variation among porpoises is the most important factor in explaining variation in surface rates. However, the large number of animals documented in the present study covering a wide range of age and sex groups justifies the use of the seasonal average surface times for correcting abundance surveys.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00592.x" xmlns="http://purl.org/rss/1.0/"><title>Biosonar, dive, and foraging activity of satellite tracked harbor porpoises (Phocoena phocoena)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00592.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Biosonar, dive, and foraging activity of satellite tracked harbor porpoises (Phocoena phocoena)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Meike Linnenschmidt, Jonas Teilmann, Tomonari Akamatsu, Rune Dietz, Lee A. Miller</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-12T00:47:22.726036-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00592.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00592.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00592.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E77</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E97</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>This study presents bioacoustic recordings in combination with movements and diving behavior of three free-ranging harbor porpoises (a female and two males) in Danish waters. Each porpoise was equipped with an acoustic data logger (A-tag), a time-depth-recorder, a VHF radio transmitter, and a satellite transmitter. The units were programmed to release after 24 or 72 h. Possible foraging occurred mostly near the surface or at the bottom of a dive. The porpoises showed individual diversity in biosonar activity (&lt;100 to &gt;50,000 clicks per hour) and in dive frequency (6–179 dives per hour). We confirm that wild harbor porpoises use more intense clicks than captive animals. A positive tendency between number of dives and clicks per hour was found for a subadult male, which stayed near shore. It showed a distinct day-night cycle with low echolocation rates during the day, but five times higher rates and higher dive activity at night. A female traveling in open waters showed no diel rhythm, but its sonar activity was three times higher compared to the males'. Considerable individual differences in dive and echolocation activity could have been influenced by biological and physical factors, but also show behavioral adaptability necessary for survival in a complex coastal environment.</p></div>
]]></content:encoded><description>

This study presents bioacoustic recordings in combination with movements and diving behavior of three free-ranging harbor porpoises (a female and two males) in Danish waters. Each porpoise was equipped with an acoustic data logger (A-tag), a time-depth-recorder, a VHF radio transmitter, and a satellite transmitter. The units were programmed to release after 24 or 72 h. Possible foraging occurred mostly near the surface or at the bottom of a dive. The porpoises showed individual diversity in biosonar activity (&lt;100 to &gt;50,000 clicks per hour) and in dive frequency (6–179 dives per hour). We confirm that wild harbor porpoises use more intense clicks than captive animals. A positive tendency between number of dives and clicks per hour was found for a subadult male, which stayed near shore. It showed a distinct day-night cycle with low echolocation rates during the day, but five times higher rates and higher dive activity at night. A female traveling in open waters showed no diel rhythm, but its sonar activity was three times higher compared to the males'. Considerable individual differences in dive and echolocation activity could have been influenced by biological and physical factors, but also show behavioral adaptability necessary for survival in a complex coastal environment.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00591.x" xmlns="http://purl.org/rss/1.0/"><title>Rope trauma, sedation, disentanglement, and monitoring-tag associated lesions in a terminally entangled North Atlantic right whale (Eubalaena glacialis)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00591.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Rope trauma, sedation, disentanglement, and monitoring-tag associated lesions in a terminally entangled North Atlantic right whale (Eubalaena glacialis)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michael Moore, Russel Andrews, Trevor Austin, James Bailey, Alex Costidis, Clay George, Katie Jackson, Tom Pitchford, Scott Landry, Allan Ligon, William McLellan, David Morin, Jamison Smith, David Rotstein, Teresa Rowles, Chris Slay, Michael Walsh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-08-28T03:20:32.560937-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00591.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00591.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00591.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E98</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E113</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>A chronically entangled North Atlantic right whale, with consequent emaciation was sedated, disentangled to the extent possible, administered antibiotics, and satellite tag tracked for six subsequent days. It was found dead 11 d after the tag ceased transmission. Chronic constrictive deep rope lacerations and emaciation were found to be the proximate cause of death, which may have ultimately involved shark predation. A broadhead cutter and a spring-loaded knife used for disentanglement were found to induce moderate wounds to the skin and blubber. The telemetry tag, with two barbed shafts partially penetrating the blubber was shed, leaving barbs embedded with localized histological reaction. One of four darts administered shed the barrel, but the needle was found postmortem in the whale with an 80º bend at the blubber-muscle interface. This bend occurred due to epaxial muscle movement relative to the overlying blubber, with resultant necrosis and cavitation of underlying muscle. This suggests that rigid, implanted devices that span the cetacean blubber muscle interface, where the muscle moves relative to the blubber, could have secondary health impacts. Thus we encourage efforts to develop new tag telemetry systems that do not penetrate the subdermal sheath, but still remain attached for many months.</p></div>
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A chronically entangled North Atlantic right whale, with consequent emaciation was sedated, disentangled to the extent possible, administered antibiotics, and satellite tag tracked for six subsequent days. It was found dead 11 d after the tag ceased transmission. Chronic constrictive deep rope lacerations and emaciation were found to be the proximate cause of death, which may have ultimately involved shark predation. A broadhead cutter and a spring-loaded knife used for disentanglement were found to induce moderate wounds to the skin and blubber. The telemetry tag, with two barbed shafts partially penetrating the blubber was shed, leaving barbs embedded with localized histological reaction. One of four darts administered shed the barrel, but the needle was found postmortem in the whale with an 80º bend at the blubber-muscle interface. This bend occurred due to epaxial muscle movement relative to the overlying blubber, with resultant necrosis and cavitation of underlying muscle. This suggests that rigid, implanted devices that span the cetacean blubber muscle interface, where the muscle moves relative to the blubber, could have secondary health impacts. Thus we encourage efforts to develop new tag telemetry systems that do not penetrate the subdermal sheath, but still remain attached for many months.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00598.x" xmlns="http://purl.org/rss/1.0/"><title>Comparison of abundance and habitat usage for common bottlenose dolphins between sites exposed to differential anthropogenic stressors within the estuaries of southern Georgia, U.S.A</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00598.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparison of abundance and habitat usage for common bottlenose dolphins between sites exposed to differential anthropogenic stressors within the estuaries of southern Georgia, U.S.A</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Brian C. Balmer, Lori H. Schwacke, Randall S. Wells, Jeffrey D. Adams, R. Clay George, Suzanne M. Lane, William A. McLellan, Patricia E. Rosel, Kate Sparks, Todd Speakman, Eric S. Zolman, D. Ann Pabst</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-04T23:42:39.759499-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00598.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00598.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00598.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E114</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E135</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>The health of common bottlenose dolphins (<em>Tursiops truncatus)</em> within southern Georgia estuaries is of particular concern due to high levels of anthropogenic contaminants in their tissues. Dolphins in this region have the highest polychlorinated biphenyl (PCB) concentrations recorded for any marine mammal and these concentrations correlate to distance from a Superfund point-source in the Turtle/Brunswick River Estuary (TBRE). Currently, little is known about the population structure of dolphins in this region. This study identifies and compares baseline data on abundance, habitat use, site-fidelity, and ranging patterns of dolphins across two adjacent field sites; Brunswick, including the TBRE, and Sapelo, including the Sapelo Island National Estuarine Research Reserve. Sapelo is relatively undeveloped and was selected for comparison to the more contaminated TBRE. Dolphin densities increased with tributary size in both sites but dolphin density and total abundance were significantly higher in Sapelo than in Brunswick. Anthropogenic stressors within the TBRE may be an important factor contributing to the differences in abundance, density, and habitat use observed in this study.</p></div>
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The health of common bottlenose dolphins (Tursiops truncatus) within southern Georgia estuaries is of particular concern due to high levels of anthropogenic contaminants in their tissues. Dolphins in this region have the highest polychlorinated biphenyl (PCB) concentrations recorded for any marine mammal and these concentrations correlate to distance from a Superfund point-source in the Turtle/Brunswick River Estuary (TBRE). Currently, little is known about the population structure of dolphins in this region. This study identifies and compares baseline data on abundance, habitat use, site-fidelity, and ranging patterns of dolphins across two adjacent field sites; Brunswick, including the TBRE, and Sapelo, including the Sapelo Island National Estuarine Research Reserve. Sapelo is relatively undeveloped and was selected for comparison to the more contaminated TBRE. Dolphin densities increased with tributary size in both sites but dolphin density and total abundance were significantly higher in Sapelo than in Brunswick. Anthropogenic stressors within the TBRE may be an important factor contributing to the differences in abundance, density, and habitat use observed in this study.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00601.x" xmlns="http://purl.org/rss/1.0/"><title>Ocean nomads: Distribution and movements of sperm whales in the North Pacific shown by whaling data and Discovery marks</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00601.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ocean nomads: Distribution and movements of sperm whales in the North Pacific shown by whaling data and Discovery marks</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sally A. Mizroch, Dale W. Rice</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-07T07:01:27.233703-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00601.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00601.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00601.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E136</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E165</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>We investigated the distribution and movements of sperm whales (<em>Physeter macrocephalus</em>) in the North Pacific by analyzing whaling data and movement data of whales marked with Discovery marks. Prior studies suggested that there were discrete “stocks” of sperm whales, assuming that the intervals between historical areas of concentration indicated subpopulation boundaries. Our analyses clearly refute this assumption: whaling and marking data suggest no obvious divisions between separate demes or stocks within the North Pacific. Sperm whales appear to be nomadic and show widespread movements between areas of concentration, with documented movements of over 5,000 km, time spans between marking and recovery over 20 yr, and ranges that cover many thousand km<sup>2</sup>. Males appear to range more widely than females. Sperm whales likely travel in response to geographical and temporal variations in the abundance of medium- and large-sized pelagic squids, their primary prey. Our analyses demonstrate that males and females concentrated seasonally in the Subtropical Frontal Zone (<em>ca</em>. 28ºN–34ºN) and the Subarctic Frontal Zone (<em>ca</em>. 40ºN–43ºN), and males also concentrated seasonally near the Aleutian Islands and along the Bering Sea shelf edge. It appears that the sperm whales targeted by the pelagic whalers range widely across this ocean basin.</p></div>
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We investigated the distribution and movements of sperm whales (Physeter macrocephalus) in the North Pacific by analyzing whaling data and movement data of whales marked with Discovery marks. Prior studies suggested that there were discrete “stocks” of sperm whales, assuming that the intervals between historical areas of concentration indicated subpopulation boundaries. Our analyses clearly refute this assumption: whaling and marking data suggest no obvious divisions between separate demes or stocks within the North Pacific. Sperm whales appear to be nomadic and show widespread movements between areas of concentration, with documented movements of over 5,000 km, time spans between marking and recovery over 20 yr, and ranges that cover many thousand km2. Males appear to range more widely than females. Sperm whales likely travel in response to geographical and temporal variations in the abundance of medium- and large-sized pelagic squids, their primary prey. Our analyses demonstrate that males and females concentrated seasonally in the Subtropical Frontal Zone (ca. 28ºN–34ºN) and the Subarctic Frontal Zone (ca. 40ºN–43ºN), and males also concentrated seasonally near the Aleutian Islands and along the Bering Sea shelf edge. It appears that the sperm whales targeted by the pelagic whalers range widely across this ocean basin.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00602.x" xmlns="http://purl.org/rss/1.0/"><title>Movement patterns of Antillean manatees in Chetumal Bay (Mexico) and coastal Belize: A challenge for regional conservation</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00602.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Movement patterns of Antillean manatees in Chetumal Bay (Mexico) and coastal Belize: A challenge for regional conservation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. N. Castelblanco-Martínez, J. Padilla-Saldívar, H. A. Hernández-Arana, D. H. Slone, J. P. Reid, B. Morales-Vela</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-17T22:31:45.133967-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00602.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00602.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00602.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E166</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E182</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>Information from 15 satellite-tracked Antillean manatees (<em>Trichechus manatus manatus</em>) was analyzed in order to assess individual movements, home ranges, and high-use areas for conservation decisions. Manatees were captured in Chetumal Bay, Mexico, and tagged with Argos-monitored satellite transmitters. Location of the manatees and physical characteristics were assessed to describe habitat properties. Most manatees traveled to freshwater sources. The Maximum Area Size (MAS) for each manatee was determined using the observation-area method. Additional kernel densities of 95% home range and 50% Center of Activity (COA) were also calculated, with manatees having 1–3 COAs. Manatees exhibited two different movement patterns: remaining in Chetumal Bay, and long-distance (up to 240 km in 89 d). The residence time in Chetumal Bay was higher for females (89.6% of time) than for males (72.0%), but the daily travel rate (0.4–0.5 km/d) was similar for both sexes. Most of the COAs fell within Natural Protected Areas (NPA). However, manatees also travel for long distances into unprotected areas, where they face uncontrolled boat traffic, fishing activities, and habitat loss. Conservation of movement corridors may promote long-distance movements and facilitate genetic exchange.</p></div>
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Information from 15 satellite-tracked Antillean manatees (Trichechus manatus manatus) was analyzed in order to assess individual movements, home ranges, and high-use areas for conservation decisions. Manatees were captured in Chetumal Bay, Mexico, and tagged with Argos-monitored satellite transmitters. Location of the manatees and physical characteristics were assessed to describe habitat properties. Most manatees traveled to freshwater sources. The Maximum Area Size (MAS) for each manatee was determined using the observation-area method. Additional kernel densities of 95% home range and 50% Center of Activity (COA) were also calculated, with manatees having 1–3 COAs. Manatees exhibited two different movement patterns: remaining in Chetumal Bay, and long-distance (up to 240 km in 89 d). The residence time in Chetumal Bay was higher for females (89.6% of time) than for males (72.0%), but the daily travel rate (0.4–0.5 km/d) was similar for both sexes. Most of the COAs fell within Natural Protected Areas (NPA). However, manatees also travel for long distances into unprotected areas, where they face uncontrolled boat traffic, fishing activities, and habitat loss. Conservation of movement corridors may promote long-distance movements and facilitate genetic exchange.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00603.x" xmlns="http://purl.org/rss/1.0/"><title>C-reactive protein in blood plasma and serum samples of harbor seals (Phoca vitulina)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00603.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">C-reactive protein in blood plasma and serum samples of harbor seals (Phoca vitulina)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Kakuschke, D. Pröfrock, A. Prange</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-12T23:15:22.03042-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00603.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00603.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00603.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E183</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E192</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[
<h3 xhtml="http://www.w3.org/1999/xhtml" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib">Abstract</h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>C-reactive protein (CRP) belongs to the acute phase proteins. Increased levels are present in inflammatory conditions, trauma, or intoxications. In veterinary medicine CRP is used as powerful diagnostic parameter in health studies, whereas little is known about the role of CRP in Pinnipedia. Therefore, samples were collected from 131 harbor seals from the North Sea between November 2002 and November 2007. CRP blood values were measured and the physiological range was calculated. Furthermore, the influence of age and sex of the animal, geographical location and season was investigated. The CRP concentrations in plasma/serum showed a median of 33 μg/mL, a 5th percentile of 18 μg/mL, and a 95th percentile of 80 μg/mL. No significant influences of sex, season, or geographical location on CRP concentration were detected. Juveniles showed significantly higher CRP levels than adult animals, whereas CRP values in newborns appear to be lower than in juveniles and adults. Our report describes for the first time CRP plasma/serum concentrations in a large group of harbor seals. It suggests that CRP is useful to detect inflammatory conditions and may help to improve health studies of this species.</p></div>
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C-reactive protein (CRP) belongs to the acute phase proteins. Increased levels are present in inflammatory conditions, trauma, or intoxications. In veterinary medicine CRP is used as powerful diagnostic parameter in health studies, whereas little is known about the role of CRP in Pinnipedia. Therefore, samples were collected from 131 harbor seals from the North Sea between November 2002 and November 2007. CRP blood values were measured and the physiological range was calculated. Furthermore, the influence of age and sex of the animal, geographical location and season was investigated. The CRP concentrations in plasma/serum showed a median of 33 μg/mL, a 5th percentile of 18 μg/mL, and a 95th percentile of 80 μg/mL. No significant influences of sex, season, or geographical location on CRP concentration were detected. Juveniles showed significantly higher CRP levels than adult animals, whereas CRP values in newborns appear to be lower than in juveniles and adults. Our report describes for the first time CRP plasma/serum concentrations in a large group of harbor seals. It suggests that CRP is useful to detect inflammatory conditions and may help to improve health studies of this species.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00599.x" xmlns="http://purl.org/rss/1.0/"><title>An investigation of sound use and behavior in a killer whale (Orcinus orca) population to inform passive acoustic monitoring studies</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00599.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">An investigation of sound use and behavior in a killer whale (Orcinus orca) population to inform passive acoustic monitoring studies</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marla M. Holt, Dawn P. Noren, Candice K. Emmons</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-09-12T00:47:25.62633-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1748-7692.2012.00599.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1748-7692.2012.00599.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1748-7692.2012.00599.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Notes</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E193</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">E202</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item></rdf:RDF>