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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"><channel rdf:about="http://onlinelibrary.wiley.com/rss/journal/10.1111/(ISSN)1948-7134" xmlns="http://purl.org/rss/1.0/"><title>Journal of Vector Ecology</title><description> Wiley Online Library : Journal of Vector Ecology</description><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2F%28ISSN%291948-7134</link><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc</dc:publisher><dc:language xmlns:dc="http://purl.org/dc/elements/1.1/">en</dc:language><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/">Copyright © 2013 Society for Vector Ecology</dc:rights><prism:issn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1081-1710</prism:issn><prism:eIssn xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1948-7134</prism:eIssn><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-12-01T00:00:00-05:00</dc:date><prism:coverDisplayDate xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">December 2012</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">37</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">2</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">269</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">480</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/jvec.2012.37.issue-2/asset/cover.gif?v=1&amp;s=79d251207854101eeb28c644bc22e213136e50e6"/><items><rdf:Seq><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00257.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00258.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00227.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00228.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00229.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00230.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00231.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00232.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00233.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00234.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00235.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00236.x"/><rdf:li 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rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00255.x"/><rdf:li rdf:resource="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00256.x"/></rdf:Seq></items></channel><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00257.x" xmlns="http://purl.org/rss/1.0/"><title>Cover</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00257.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cover</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00257.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.1948-7134.2012.00257.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00257.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">i</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">i</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.1948-7134.2012.00258.x" xmlns="http://purl.org/rss/1.0/"><title>Table of contents</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00258.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Table of contents</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00258.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.1948-7134.2012.00258.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00258.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">ii</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">iii</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.1948-7134.2012.00227.x" xmlns="http://purl.org/rss/1.0/"><title>Comparison of different trapping methods for surveillance of mosquito vectors of West Nile virus in Rhône Delta, France</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00227.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparison of different trapping methods for surveillance of mosquito vectors of West Nile virus in Rhône Delta, France</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Grégory L'Ambert, Jean-Baptiste Ferré, Francis Schaffner, Didier Fontenille</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00227.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.1948-7134.2012.00227.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00227.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">269</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">275</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>Five trapping methods were compared for monitoring potential vectors of the West Nile virus in four areas in the Camargue Plain of France: carbon dioxide traps, bird-baited traps, gravid traps, resting boxes, and human landing catches. A total of 73,721 specimens, representing 14 species, was trapped in 2006. Results showed significant differences in species and abundance between the type of traps. Many more specimens were collected using CO<sub>2</sub> traps than any other method, with an average of 212 specimens per night per trap (p&lt;0.05). <em>Culex pipiens</em> was the most abundant species collected (36.8% of total with CO<sub>2</sub> traps), followed by <em>Aedes caspius</em> (22.7%), <em>Anopheles hyrcanus</em> (18.3%), <em>Culex modestus</em> (18.3%), and <em>Aedes detritus</em> (3.2%). Bird-baited traps captured only eight specimens per night per trap on average, mainly <em>Cx. pipiens</em> (89.9%). The species collected and their abundance are influenced by the trap location, at ground or canopy level. <em>Culex pipiens</em> was twice as abundant in the canopy as on the ground, whereas it was the opposite for <em>Ae. caspius</em>, <em>An. hyrcanus</em>, and <em>Ae. detritus. Culex modestus</em> was equally abundant at both levels. Resting boxes and gravid traps were much less efficient, capturing around 0.3 specimens per night per trap. Results are discussed in relation to West Nile virus surveillance.</p></div>
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Five trapping methods were compared for monitoring potential vectors of the West Nile virus in four areas in the Camargue Plain of France: carbon dioxide traps, bird-baited traps, gravid traps, resting boxes, and human landing catches. A total of 73,721 specimens, representing 14 species, was trapped in 2006. Results showed significant differences in species and abundance between the type of traps. Many more specimens were collected using CO2 traps than any other method, with an average of 212 specimens per night per trap (p&lt;0.05). Culex pipiens was the most abundant species collected (36.8% of total with CO2 traps), followed by Aedes caspius (22.7%), Anopheles hyrcanus (18.3%), Culex modestus (18.3%), and Aedes detritus (3.2%). Bird-baited traps captured only eight specimens per night per trap on average, mainly Cx. pipiens (89.9%). The species collected and their abundance are influenced by the trap location, at ground or canopy level. Culex pipiens was twice as abundant in the canopy as on the ground, whereas it was the opposite for Ae. caspius, An. hyrcanus, and Ae. detritus. Culex modestus was equally abundant at both levels. Resting boxes and gravid traps were much less efficient, capturing around 0.3 specimens per night per trap. Results are discussed in relation to West Nile virus surveillance.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00228.x" xmlns="http://purl.org/rss/1.0/"><title>Spatiotemporal dynamics of Puumala hantavirus in suburban reservoir rodent populations</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00228.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Spatiotemporal dynamics of Puumala hantavirus in suburban reservoir rodent populations</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alexandre Dobly, Chloé Yzoard, Christel Cochez, Geneviève Ducoffre, Marc Aerts, Stefan Roels, Paul Heyman</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00228.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.1948-7134.2012.00228.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00228.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">276</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">283</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 transmission of pathogens to susceptible hosts is dependent on the vector population dynamics. In Europe, bank voles (<em>Myodes glareolus</em>) carry Puumala hantavirus, which causes nephropathia epidemica (NE) in humans. Fluctuations in bank vole populations and epidemics in humans are correlated but the main factors influencing this relationship remain unclear. In Belgium, more NE cases are reported in spring than in autumn. There is also a higher incidence of human infections during years of large vole populations. This study aimed to better understand the link between virus prevalence in the vector, vole demography, habitat quality, and human infections. Three rodent populations in different habitats bordering Brussels city, Belgium, were studied for two years. The seroprevalence in voles was influenced first by season (higher in spring), then by vole density, vole weight (a proxy for age), and capture site but not by year or sex. Moreover, voles with large maximal distance between two captures had a high probability for Puumala seropositivity. Additionally, the local vole density showed similar temporal variations as the number of NE cases in Belgium. These results showed that, while season was the main factor influencing vole seroprevalence, it was not sufficient to explain human risks. Indeed, vole density and weight, as well as the local habitat, were essential to understanding the interactions in these host-pathogen dynamics. This can, in turn, be of importance for assessing the human risks.</p></div>
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The transmission of pathogens to susceptible hosts is dependent on the vector population dynamics. In Europe, bank voles (Myodes glareolus) carry Puumala hantavirus, which causes nephropathia epidemica (NE) in humans. Fluctuations in bank vole populations and epidemics in humans are correlated but the main factors influencing this relationship remain unclear. In Belgium, more NE cases are reported in spring than in autumn. There is also a higher incidence of human infections during years of large vole populations. This study aimed to better understand the link between virus prevalence in the vector, vole demography, habitat quality, and human infections. Three rodent populations in different habitats bordering Brussels city, Belgium, were studied for two years. The seroprevalence in voles was influenced first by season (higher in spring), then by vole density, vole weight (a proxy for age), and capture site but not by year or sex. Moreover, voles with large maximal distance between two captures had a high probability for Puumala seropositivity. Additionally, the local vole density showed similar temporal variations as the number of NE cases in Belgium. These results showed that, while season was the main factor influencing vole seroprevalence, it was not sufficient to explain human risks. Indeed, vole density and weight, as well as the local habitat, were essential to understanding the interactions in these host-pathogen dynamics. This can, in turn, be of importance for assessing the human risks.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00229.x" xmlns="http://purl.org/rss/1.0/"><title>A comparison of adult mosquito trapping regimes across seasons and ecosystems in Darwin, Australia</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00229.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A comparison of adult mosquito trapping regimes across seasons and ecosystems in Darwin, Australia</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Susan P. Jacups, Peter I. Whelan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00229.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.1948-7134.2012.00229.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00229.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">284</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">288</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>Mosquitoes are problematic as vectors and pests in many tropical cities, including Darwin, the principal city in the Northern Territory of Australia. To monitor peaks in mosquito populations, the Medical Entomology unit of the Health Department sets overnight CO<sub>2</sub>-baited traps weekly. Trap setting and retrieving, followed by mosquito counting and identification, are labor intensive. Aiming to reduce this workload, we tested the hypothesis that fortnightly trapping is as effective as weekly trapping across seasons and ecologically distinct systems in Darwin. We applied cross-sectional negative binomial mixed effects models, which adjusted for rain and calendar month, to existing historical data. <em>Culex annulirostris</em> peaks were effectively identified using fortnightly trapping across all three ecological systems, during wet/dry and build-up seasonal patterns. For <em>Aedes vigilax</em>, fortnightly trapping was adequate in identifying peaks during wet and dry season months, but inadequate during build-up months across all three ecological systems. Therefore, weekly trapping should continue during build-up months, but trapping could be reduced to fortnightly for wet and dry season months for all ecological systems. Trapping for <em>Cx. annulirostris</em> monitoring could be reduced to fortnightly in all areas and seasons. Evaluation of programs can maximize staff efficiency and improve service delivery by reducing the need for unnecessary tasks.</p></div>
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Mosquitoes are problematic as vectors and pests in many tropical cities, including Darwin, the principal city in the Northern Territory of Australia. To monitor peaks in mosquito populations, the Medical Entomology unit of the Health Department sets overnight CO2-baited traps weekly. Trap setting and retrieving, followed by mosquito counting and identification, are labor intensive. Aiming to reduce this workload, we tested the hypothesis that fortnightly trapping is as effective as weekly trapping across seasons and ecologically distinct systems in Darwin. We applied cross-sectional negative binomial mixed effects models, which adjusted for rain and calendar month, to existing historical data. Culex annulirostris peaks were effectively identified using fortnightly trapping across all three ecological systems, during wet/dry and build-up seasonal patterns. For Aedes vigilax, fortnightly trapping was adequate in identifying peaks during wet and dry season months, but inadequate during build-up months across all three ecological systems. Therefore, weekly trapping should continue during build-up months, but trapping could be reduced to fortnightly for wet and dry season months for all ecological systems. Trapping for Cx. annulirostris monitoring could be reduced to fortnightly in all areas and seasons. Evaluation of programs can maximize staff efficiency and improve service delivery by reducing the need for unnecessary tasks.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00230.x" xmlns="http://purl.org/rss/1.0/"><title>Variation in energy reserves and role of body size in the mating system of Anopheles gambiae</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00230.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Variation in energy reserves and role of body size in the mating system of Anopheles gambiae</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hamidou Maïga, Roch K. Dabiré, Tovi Lehmann, Frédéric Tripet, Abdoulaye Diabaté</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00230.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.1948-7134.2012.00230.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00230.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">289</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">297</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><em>Anopheles gambiae</em> mates in flight. Males gather at stationary places at sunset and compete for incoming females. Factors that account for male mating success are not known but are critical for the future of any genetic control strategy. The current study explored variations in nutritional reserves (sugars, glycogen, lipids, and proteins) in wild-caught swarming and resting males and evaluated the effect of body size and wing symmetry on male mating success. Our results showed that glycogen and sugar reserves are mobilized for flight. Males consume proportionally 5.9-fold as much energy derived from sugars in swarming activities than when they are at rest. Mated males were on average bigger than unmated ones (P&lt;0.0001). A strong correlation between the left and right wings in both mated and unmated males was found and additional analysis on fluctuating asymmetry did not show any indication of mated males being more symmetrical than unmated ones. The distribution of wing size of mated males was focused around a central value, suggesting that intermediate size of males is advantageous in the <em>An. gambiae</em> mating system. The results are discussed in the context of sexual selection.</p></div>
]]></content:encoded><description>

Anopheles gambiae mates in flight. Males gather at stationary places at sunset and compete for incoming females. Factors that account for male mating success are not known but are critical for the future of any genetic control strategy. The current study explored variations in nutritional reserves (sugars, glycogen, lipids, and proteins) in wild-caught swarming and resting males and evaluated the effect of body size and wing symmetry on male mating success. Our results showed that glycogen and sugar reserves are mobilized for flight. Males consume proportionally 5.9-fold as much energy derived from sugars in swarming activities than when they are at rest. Mated males were on average bigger than unmated ones (P&lt;0.0001). A strong correlation between the left and right wings in both mated and unmated males was found and additional analysis on fluctuating asymmetry did not show any indication of mated males being more symmetrical than unmated ones. The distribution of wing size of mated males was focused around a central value, suggesting that intermediate size of males is advantageous in the An. gambiae mating system. The results are discussed in the context of sexual selection.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00231.x" xmlns="http://purl.org/rss/1.0/"><title>Development and evaluation of methods to assess populations of black flies (Diptera: Simuliidae) at nests of the endangered whooping crane (Grus americana)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00231.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Development and evaluation of methods to assess populations of black flies (Diptera: Simuliidae) at nests of the endangered whooping crane (Grus americana)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Richard S. King, Peter H. Adler</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00231.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.1948-7134.2012.00231.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00231.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">298</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">306</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>Hematophagous insects can negatively affect the reproductive success of their vertebrate hosts. To determine the influence of hematophagous insects on endangered vertebrates requires specially designed programs that minimize disturbance to the hosts and address problems associated with their small populations. We developed and evaluated a surveillance program for black flies potentially affecting a population of whooping cranes (<em>Grus americana</em>) introduced to central Wisconsin, U.S.A. In one of the few studies to survey host-seeking female black flies and their immature stages concurrently, we processed nearly 346,000 specimens and documented 26 species, of which only two, <em>Simulium annulus</em> and <em>Simulium johannseni</em>, were attracted to nesting whooping cranes. Attempts to assess black fly populations with artificial nests and real crane eggs were unsuccessful. Carbon-dioxide traps performed well in describing black fly taxa on the landscape. However, the number of black flies at whooping crane nests was consistently higher than the number captured in carbon-dioxide traps. The carbon-dioxide traps poorly described the presence/absence, population fluctuations, and periodicity of black flies at whooping crane nests. The weak performance of the carbon-dioxide traps might have resulted from microhabitat differences between trap locations and nests or from <em>Simulium annulus</em> and <em>Simulium johannseni</em> using sensory cues in addition to carbon dioxide to find hosts. Choice of trapping techniques, therefore, depends on the information required for the particular study objectives.</p></div>
]]></content:encoded><description>

Hematophagous insects can negatively affect the reproductive success of their vertebrate hosts. To determine the influence of hematophagous insects on endangered vertebrates requires specially designed programs that minimize disturbance to the hosts and address problems associated with their small populations. We developed and evaluated a surveillance program for black flies potentially affecting a population of whooping cranes (Grus americana) introduced to central Wisconsin, U.S.A. In one of the few studies to survey host-seeking female black flies and their immature stages concurrently, we processed nearly 346,000 specimens and documented 26 species, of which only two, Simulium annulus and Simulium johannseni, were attracted to nesting whooping cranes. Attempts to assess black fly populations with artificial nests and real crane eggs were unsuccessful. Carbon-dioxide traps performed well in describing black fly taxa on the landscape. However, the number of black flies at whooping crane nests was consistently higher than the number captured in carbon-dioxide traps. The carbon-dioxide traps poorly described the presence/absence, population fluctuations, and periodicity of black flies at whooping crane nests. The weak performance of the carbon-dioxide traps might have resulted from microhabitat differences between trap locations and nests or from Simulium annulus and Simulium johannseni using sensory cues in addition to carbon dioxide to find hosts. Choice of trapping techniques, therefore, depends on the information required for the particular study objectives.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00232.x" xmlns="http://purl.org/rss/1.0/"><title>Woodland biodiversity management as a tool for reducing human exposure to Ixodes ricinus ticks: A preliminary study in an English woodland</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00232.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Woodland biodiversity management as a tool for reducing human exposure to Ixodes ricinus ticks: A preliminary study in an English woodland</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J.M. Medlock, H. Shuttleworth, V. Copley, K.M. Hansford, S. Leach</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00232.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.1948-7134.2012.00232.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00232.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">307</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">315</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 paper presents preliminary findings towards developing a UK-specific approach to reducing public exposure to woodland questing <em>Ixodes ricinus</em> tick populations by harnessing existing biodiversity-enhancing woodland ride (i.e., linear non-wooded herbaceous habitat either side of track within woodland) management strategies. This preliminary study in an English woodland firstly assesses whether ecological and environmental factors determine presence and density of questing <em>Ixodes ricinus</em> along woodland rides. Secondly, it sets these findings in the context of woodland ride management guidelines in England in order to understand what impact ride management strategies might have on numbers of questing ticks and tick survival. Nymph and adult <em>I. ricinus</em> presence and abundance were modelled in relation to relevant microclimate and ecological parameter variables. Predictor variables for increased questing nymph abundance included ride orientation, mat depth, occurrence of bracken/bramble and animal tracks, ride/path width, and sward height. Ticks thrive in the ecotonal habitat of a woodland ride, therefore we urge woodland managers to consider the impact of their ride management on ticks and human exposure to ticks. Possible recommendations for mitigating questing <em>I. ricinus</em> in line with biodiversity management guidelines rides are discussed in this paper and include seasonal mowing regimes, management of mulch/mat, and bracken/bramble management through use of scalloped ride edges.</p></div>
]]></content:encoded><description>

This paper presents preliminary findings towards developing a UK-specific approach to reducing public exposure to woodland questing Ixodes ricinus tick populations by harnessing existing biodiversity-enhancing woodland ride (i.e., linear non-wooded herbaceous habitat either side of track within woodland) management strategies. This preliminary study in an English woodland firstly assesses whether ecological and environmental factors determine presence and density of questing Ixodes ricinus along woodland rides. Secondly, it sets these findings in the context of woodland ride management guidelines in England in order to understand what impact ride management strategies might have on numbers of questing ticks and tick survival. Nymph and adult I. ricinus presence and abundance were modelled in relation to relevant microclimate and ecological parameter variables. Predictor variables for increased questing nymph abundance included ride orientation, mat depth, occurrence of bracken/bramble and animal tracks, ride/path width, and sward height. Ticks thrive in the ecotonal habitat of a woodland ride, therefore we urge woodland managers to consider the impact of their ride management on ticks and human exposure to ticks. Possible recommendations for mitigating questing I. ricinus in line with biodiversity management guidelines rides are discussed in this paper and include seasonal mowing regimes, management of mulch/mat, and bracken/bramble management through use of scalloped ride edges.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00233.x" xmlns="http://purl.org/rss/1.0/"><title>Mosquitoes in degraded and preserved areas of the Atlantic Forest and potential for vector-borne disease risk in the municipality of São Paulo, Brazil</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00233.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Mosquitoes in degraded and preserved areas of the Atlantic Forest and potential for vector-borne disease risk in the municipality of São Paulo, Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andressa Francisca Ribeiro, Paulo Roberto Urbinatti, Ana Maria Ribeiro de Castro Duarte, Marcia Bicudo de Paula, Diego Mendes Pereira, Luís Filipe Mucci, Aristides Fernandes, Maria Helena Silva Homem de Mello, Marco Otávio de Matos Júnior, Rosane Correa de Oliveira, Delsio Natal, Rosely dos Santos Malafronte</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00233.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.1948-7134.2012.00233.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00233.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">316</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">ABSTRACT: </h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>In order to assess the epidemiological potential of the Culicidae species in remaining areas of the Brazilian Atlantic Forest, specimens of this family were collected in wild and anthropic environments. A total of 9,403 adult mosquitoes was collected from May, 2009 to June, 2010. The most prevalent among species collected in the wild environment were <em>Anopheles (Kerteszia) cruzii</em>, the Melanoconion section of <em>Culex</em> (<em>Melanoconion</em>), and <em>Aedes serratus</em>, while the most common in the anthropic site were <em>Coquillettidia chrysonotum/albifera, Culex (Culex)</em> Coronator group, and <em>An. (Ker.) cruzii</em>. Mosquito richness was similar between environments, although the abundance of individuals from different species varied. When comparing diversity patterns between environments, anthropic sites exhibited higher richness and evenness, suggesting that environmental stress increased the number of favorable niches for culicids, promoting diversity. Increased abundance of opportunistic species in the anthropic environment enhances contact with culicids that transmit vector-borne diseases.</p></div>
]]></content:encoded><description>

In order to assess the epidemiological potential of the Culicidae species in remaining areas of the Brazilian Atlantic Forest, specimens of this family were collected in wild and anthropic environments. A total of 9,403 adult mosquitoes was collected from May, 2009 to June, 2010. The most prevalent among species collected in the wild environment were Anopheles (Kerteszia) cruzii, the Melanoconion section of Culex (Melanoconion), and Aedes serratus, while the most common in the anthropic site were Coquillettidia chrysonotum/albifera, Culex (Culex) Coronator group, and An. (Ker.) cruzii. Mosquito richness was similar between environments, although the abundance of individuals from different species varied. When comparing diversity patterns between environments, anthropic sites exhibited higher richness and evenness, suggesting that environmental stress increased the number of favorable niches for culicids, promoting diversity. Increased abundance of opportunistic species in the anthropic environment enhances contact with culicids that transmit vector-borne diseases.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00234.x" xmlns="http://purl.org/rss/1.0/"><title>Pyrethroid resistance in Aedes aegypti and Aedes albopictus from Port-au-Prince, Haiti</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00234.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Pyrethroid resistance in Aedes aegypti and Aedes albopictus from Port-au-Prince, Haiti</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Janet C. McAllister, Marvin S. Godsey, Mariah L. Scott</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00234.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.1948-7134.2012.00234.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00234.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/">332</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>In Port-au-Prince, Haiti, the status of insecticide resistance has not recently been evaluated for <em>Aedes aegypti</em> (L) and <em>Aedes albopictus</em> (Skuse) populations. No prophylactics exist for dengue, so prevention is only through vector control methods. An earthquake occurred in Haiti on January 12, 2010, with a magnitude of 7.0 Mw that devastated the area. Dengue became a major concern for the humanitarian relief workers that entered the country. Bottle bioassays were conducted in the field on adult mosquitoes reared from larvae collected from the grounds of the U.S. Embassy and from an adjacent neighborhood in eastern Port-au-Prince, Haiti. At the CDC, Fort Collins, CO, bioassays, molecular, and biochemical assays were performed on mosquitoes reared from field-collected eggs. A small percentage of the population was able to survive the diagnostic dose in bioassays run in Haiti. Mosquitoes tested at the CDC demonstrated no phenotypic resistance. A variety of factors could be responsible for the discrepancies between the field and lab data, but temperature and larval nutrition are probably most important. Knowledge of localized resistance and underlying mechanisms helps in making rational decisions in selection of appropriate and effective insecticides in the event of a dengue outbreak.</p></div>
]]></content:encoded><description>

In Port-au-Prince, Haiti, the status of insecticide resistance has not recently been evaluated for Aedes aegypti (L) and Aedes albopictus (Skuse) populations. No prophylactics exist for dengue, so prevention is only through vector control methods. An earthquake occurred in Haiti on January 12, 2010, with a magnitude of 7.0 Mw that devastated the area. Dengue became a major concern for the humanitarian relief workers that entered the country. Bottle bioassays were conducted in the field on adult mosquitoes reared from larvae collected from the grounds of the U.S. Embassy and from an adjacent neighborhood in eastern Port-au-Prince, Haiti. At the CDC, Fort Collins, CO, bioassays, molecular, and biochemical assays were performed on mosquitoes reared from field-collected eggs. A small percentage of the population was able to survive the diagnostic dose in bioassays run in Haiti. Mosquitoes tested at the CDC demonstrated no phenotypic resistance. A variety of factors could be responsible for the discrepancies between the field and lab data, but temperature and larval nutrition are probably most important. Knowledge of localized resistance and underlying mechanisms helps in making rational decisions in selection of appropriate and effective insecticides in the event of a dengue outbreak.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00235.x" xmlns="http://purl.org/rss/1.0/"><title>Geographical distribution of bat flies (Diptera: Nycteribiidae and Streblidae), including two new records, Nycteribia allotopa and N. formosana, collected from bats (Chiroptera: Rhinolophidae and Vespertilionidae) in the Republic of Korea</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00235.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Geographical distribution of bat flies (Diptera: Nycteribiidae and Streblidae), including two new records, Nycteribia allotopa and N. formosana, collected from bats (Chiroptera: Rhinolophidae and Vespertilionidae) in the Republic of Korea</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Heung Chul Kim, Sang Hoon Han, Carl W. Dick, Yong Gun Choi, Sung Tae Chong, Terry A. Klein, Leopoldo M. Rueda</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00235.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.1948-7134.2012.00235.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00235.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">333</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">ABSTRACT: </h3>
<div class="para" xmlns="http://www.w3.org/1999/xhtml"><p>As part of the 65<sup>th</sup> Medical Brigade, U.S. Army, arthropod-borne disease surveillance program and in collaboration with the Korea National Institute of Biological Resources (NIBR), bats were captured from caves and abandoned mines in the Republic of Korea. A total of 39 adult bat flies including five species of Nycteribiidae [<em>Penicillidia jenynsii</em>, <em>Nycteribia parvula</em>, <em>N. formosana</em>, <em>N. allotopa mikado</em>, and an unidentified species of <em>Nycteribia</em> (<em>N</em>. cf. <em>formosana</em>)], and one species of Streblidae, Brachytarsina kanoi, were collected from bats belonging to two families, Rhinolophidae and Vespertilionidae. This is the first report of <em>N. allotopa mikado</em> and <em>N. formosana</em> from the Republic of Korea.</p></div>
]]></content:encoded><description>

As part of the 65th Medical Brigade, U.S. Army, arthropod-borne disease surveillance program and in collaboration with the Korea National Institute of Biological Resources (NIBR), bats were captured from caves and abandoned mines in the Republic of Korea. A total of 39 adult bat flies including five species of Nycteribiidae [Penicillidia jenynsii, Nycteribia parvula, N. formosana, N. allotopa mikado, and an unidentified species of Nycteribia (N. cf. formosana)], and one species of Streblidae, Brachytarsina kanoi, were collected from bats belonging to two families, Rhinolophidae and Vespertilionidae. This is the first report of N. allotopa mikado and N. formosana from the Republic of Korea.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00236.x" xmlns="http://purl.org/rss/1.0/"><title>Modeling the influence of Peromyscus leucopus body mass, sex, and habitat on immature Dermacentor variabilis burden</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00236.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Modeling the influence of Peromyscus leucopus body mass, sex, and habitat on immature Dermacentor variabilis burden</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tad A. Dallas, Stephanie A. Foré, Hyun-Joo Kim</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00236.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.1948-7134.2012.00236.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00236.x</prism:url><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/">341</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>Immature (larvae and nymph) tick burden on rodents is an important determinant of adult tick population size and understanding infectious disease dynamics. The objective of this research was to build a descriptive model for immature <em>Dermacentor variabilis</em> burden on <em>Peromyscus leucopus</em>. Mice were live-trapped on two permanent grids in an old field and an early successional forest every other month between April and October, 2006–2009. Negative binomial regression was used to examine the association between immature <em>D. variabilis</em> burden and the host related variables of host habitat, body mass, and/or sex. The model containing all three variables had the lowest Akaike's Information Criterion (AIC), corrected AIC (AICc), and greatest AICc weight. Immature <em>D. variabilis</em> burden was positively associated with mice with higher body mass, male mice, and those captured in the field habitat. These data are consistent with studies from other tick-rodent systems and suggest that single factor models do not describe host burden. Variables other than those that are related to the host may also be important in describing the tick burden on rodents. The next step is to examine variables that affect tick development rate and questing behavior.</p></div>
]]></content:encoded><description>

Immature (larvae and nymph) tick burden on rodents is an important determinant of adult tick population size and understanding infectious disease dynamics. The objective of this research was to build a descriptive model for immature Dermacentor variabilis burden on Peromyscus leucopus. Mice were live-trapped on two permanent grids in an old field and an early successional forest every other month between April and October, 2006–2009. Negative binomial regression was used to examine the association between immature D. variabilis burden and the host related variables of host habitat, body mass, and/or sex. The model containing all three variables had the lowest Akaike's Information Criterion (AIC), corrected AIC (AICc), and greatest AICc weight. Immature D. variabilis burden was positively associated with mice with higher body mass, male mice, and those captured in the field habitat. These data are consistent with studies from other tick-rodent systems and suggest that single factor models do not describe host burden. Variables other than those that are related to the host may also be important in describing the tick burden on rodents. The next step is to examine variables that affect tick development rate and questing behavior.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00237.x" xmlns="http://purl.org/rss/1.0/"><title>Feeding patterns of mosquitoes (Diptera: Culicidae) in six Brazilian environmental preservation areas</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00237.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Feeding patterns of mosquitoes (Diptera: Culicidae) in six Brazilian environmental preservation areas</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Júlia dos Santos Silva, Jeronimo Alencar, Janira Martins Costa, Elias Seixas-Lorosa, Anthony Érico Guimarães</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00237.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.1948-7134.2012.00237.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00237.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">342</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">350</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>Feeding patterns of mosquitoes in six Brazilian environmental preservation areas were analyzed by the precipitin technique. The mosquito populations were captured using Shannon traps during different time periods. Bird, cow, dog, horse, opossum, human, and rodent antisera diagnostic tests were employed and results were analyzed by calculating the Sørensen similarity index and using the null-model test. Of the 647 analyzed specimens, 443 reacted to the utilized antisera, of which 331 reacted to one blood source, with the most frequent being birds (49.4%); and 112 specimens reacted to two blood sources, with the most frequent combination from birds + rodents (14.3%). The feed profiles demonstrated that <em>Anopheles albitarsis</em>, <em>An. evansae</em>, <em>Aedes fulvus</em>, <em>Psorophora albigenu</em>, <em>Ps. albipes</em>, <em>Ps. ferox</em>, and <em>Mansonia titillans</em> fed predominantly on birds. The similarity index showed that in some localities <em>An. cruzii</em>, <em>Chagasia fajardi</em>, <em>Ae. scapularis</em>, <em>Ae. serratus</em>, <em>Haemagogus leucocelaenus, Ps. albigenu</em>, and <em>Ps. ferox</em> presented similar dietary habits. The null-models test indicated that species from SMSP, INP, CGNP, and THP demonstrated an aggregate pattern, while species from SONP and SBNP showed a random pattern. The mosquitoes fed predominantly on birds, but from an epidemiological standpoint, the eclectic feeding habits were found to be constant among the mosquitoes analyzed.</p></div>
]]></content:encoded><description>

Feeding patterns of mosquitoes in six Brazilian environmental preservation areas were analyzed by the precipitin technique. The mosquito populations were captured using Shannon traps during different time periods. Bird, cow, dog, horse, opossum, human, and rodent antisera diagnostic tests were employed and results were analyzed by calculating the Sørensen similarity index and using the null-model test. Of the 647 analyzed specimens, 443 reacted to the utilized antisera, of which 331 reacted to one blood source, with the most frequent being birds (49.4%); and 112 specimens reacted to two blood sources, with the most frequent combination from birds + rodents (14.3%). The feed profiles demonstrated that Anopheles albitarsis, An. evansae, Aedes fulvus, Psorophora albigenu, Ps. albipes, Ps. ferox, and Mansonia titillans fed predominantly on birds. The similarity index showed that in some localities An. cruzii, Chagasia fajardi, Ae. scapularis, Ae. serratus, Haemagogus leucocelaenus, Ps. albigenu, and Ps. ferox presented similar dietary habits. The null-models test indicated that species from SMSP, INP, CGNP, and THP demonstrated an aggregate pattern, while species from SONP and SBNP showed a random pattern. The mosquitoes fed predominantly on birds, but from an epidemiological standpoint, the eclectic feeding habits were found to be constant among the mosquitoes analyzed.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00238.x" xmlns="http://purl.org/rss/1.0/"><title>Multiple blood meals in Anopheles darlingi (Diptera: Culicidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00238.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Multiple blood meals in Anopheles darlingi (Diptera: Culicidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Caroline Dantas de Oliveira, Wanderli Pedro Tadei, Fábio Camargo Abdalla, Paulo Filemon Paolucci Pimenta, Osvaldo Marinotti</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00238.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.1948-7134.2012.00238.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00238.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">351</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">358</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><em>Anopheles darlingi</em> is an important vector of human malaria in the Amazon. Adult females of this mosquito species require a blood meal to develop eggs, preferring humans to other blood sources. Although gonotrophic concordance has been described as the norm for <em>An. darlingi</em>, here we report <em>An. darlingi</em> female mosquitoes taking two or more blood meals within their first gonotrophic cycle. Only half of field-captured adult females fed one blood meal developed follicles to Christophers' stage V. This outcome is dependent on larval nutrition, as 88% of laboratory-raised well-nourished females completed the first gonotrophic cycle with only one blood meal, while less nourished females needed additional blood meals. Half of the field-captured blood-seeking <em>An. darlingi</em> females had follicles in intermediate (IIIa and IIIb) and final (V) stages of the gonotrophic cycle, supporting the conclusion that <em>An. darlingi</em> blood feed more than once during a gonotrophic cycle. Additionally, we observed females attempting to blood feed a second time during the same day. Additional studies of <em>An. darlingi</em> biting behavior are necessary to accurately estimate <em>Plasmodium sp</em>. entomologic inoculation rates throughout the <em>An. darlingi</em> vast geographical distribution.</p></div>
]]></content:encoded><description>

Anopheles darlingi is an important vector of human malaria in the Amazon. Adult females of this mosquito species require a blood meal to develop eggs, preferring humans to other blood sources. Although gonotrophic concordance has been described as the norm for An. darlingi, here we report An. darlingi female mosquitoes taking two or more blood meals within their first gonotrophic cycle. Only half of field-captured adult females fed one blood meal developed follicles to Christophers' stage V. This outcome is dependent on larval nutrition, as 88% of laboratory-raised well-nourished females completed the first gonotrophic cycle with only one blood meal, while less nourished females needed additional blood meals. Half of the field-captured blood-seeking An. darlingi females had follicles in intermediate (IIIa and IIIb) and final (V) stages of the gonotrophic cycle, supporting the conclusion that An. darlingi blood feed more than once during a gonotrophic cycle. Additionally, we observed females attempting to blood feed a second time during the same day. Additional studies of An. darlingi biting behavior are necessary to accurately estimate Plasmodium sp. entomologic inoculation rates throughout the An. darlingi vast geographical distribution.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00239.x" xmlns="http://purl.org/rss/1.0/"><title>Cues used by the black fly, Simulium annulus, for attraction to the common loon (Gavia immer)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00239.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cues used by the black fly, Simulium annulus, for attraction to the common loon (Gavia immer)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Meggin L. Weinandt, Michael Meyer, Mac Strand, Alec R. Lindsay</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00239.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.1948-7134.2012.00239.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00239.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">359</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[
<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 parasitic relationship between a black fly, <em>Simulium annulus</em>, and the common loon (<em>Gavia immer</em>) has been considered one of the most exclusive relationships between any host species and a black fly species. To test the host specificity of this blood-feeding insect, we made a series of bird decoy presentations to black flies on loon-inhabited lakes in northern Wisconsin, U.S.A. To examine the importance of chemical and visual cues for black fly detection of and attraction to hosts, we made decoy presentations with and without chemical cues. Flies attracted to the decoys were collected, identified to species, and quantified. Results showed that <em>S. annulus</em> had a strong preference for common loon visual and chemical cues, although visual cues from Canada geese (<em>Branta canadensis)</em> and mallards (<em>Anas platyrynchos</em>) did attract some flies in significantly smaller numbers.</p></div>
]]></content:encoded><description>

The parasitic relationship between a black fly, Simulium annulus, and the common loon (Gavia immer) has been considered one of the most exclusive relationships between any host species and a black fly species. To test the host specificity of this blood-feeding insect, we made a series of bird decoy presentations to black flies on loon-inhabited lakes in northern Wisconsin, U.S.A. To examine the importance of chemical and visual cues for black fly detection of and attraction to hosts, we made decoy presentations with and without chemical cues. Flies attracted to the decoys were collected, identified to species, and quantified. Results showed that S. annulus had a strong preference for common loon visual and chemical cues, although visual cues from Canada geese (Branta canadensis) and mallards (Anas platyrynchos) did attract some flies in significantly smaller numbers.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00240.x" xmlns="http://purl.org/rss/1.0/"><title> Aedes (Stegomyia) aegypti and Aedes (Howardina) cozumelensis in Yucatán State, México, with a summary of published collection records for Ae. cozumelensis</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00240.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/"> Aedes (Stegomyia) aegypti and Aedes (Howardina) cozumelensis in Yucatán State, México, with a summary of published collection records for Ae. cozumelensis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Julián E. García-Rejón, Mildred P. López-Uribe, María Alba Loroño-Pino, Roger Arana-Guardia, Maria Puc-Tinal, Genny M. López-Uribe, Carlos Coba-Tún, Carlos M. Baak-Baak, Carlos Machain-Williams, Guadalupe C. Reyes-Solis, Saul Lozano-Fuentes, Karla Saavedra-Rodriguez, William C. Black, Barry J. Beaty, Lars Eisen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00240.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.1948-7134.2012.00240.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00240.x</prism:url><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/">372</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 collected mosquito immatures from artificial containers during 2010–2011 from 26 communities, ranging in size from small rural communities to large urban centers, located in different parts of Yucatán State in southeastern México. The arbovirus vector <em>Aedes</em> (<em>Stegomyia</em>) <em>aegypti</em> was collected from all 26 examined communities, and nine of the communities also yielded another container-inhabiting <em>Aedes</em> mosquito: <em>Aedes (Howardina) cozumelensis</em>. The communities from which <em>Ae. cozumelensis</em> were collected were all small rural communities (&lt;6,000 inhabitants) in the north-central part of Yucatán State. These new collection records for <em>Ae. cozumelensis</em> demonstrate that this mosquito has a far broader geographic range in the Yucatán Peninsula than previously known. <em>Ae. cozumelensis</em> immatures were collected from both residential premises and cemeteries, with specimens recovered from rock holes as well as various artificial containers including metal cans, flower vases, buckets, tires, and a water storage tank. The co-occurrence with <em>Ae. aegypti</em> in small rural communities poses intriguing questions regarding linkages between these mosquitoes, including the potential for direct competition for larval development sites. Additional studies are needed to determine how commonly <em>Ae. cozumelensis</em> feeds on human blood and whether it is naturally infected with arboviruses or other pathogens of medical or veterinary importance. We also summarize the published records for <em>Ae. cozumelensis</em>, which are restricted to collections from México's Yucatán Peninsula and Belize, and uniformly represent geographic locations where <em>Ae. aegypti</em> can be expected to occur.</p></div>
]]></content:encoded><description>

We collected mosquito immatures from artificial containers during 2010–2011 from 26 communities, ranging in size from small rural communities to large urban centers, located in different parts of Yucatán State in southeastern México. The arbovirus vector Aedes (Stegomyia) aegypti was collected from all 26 examined communities, and nine of the communities also yielded another container-inhabiting Aedes mosquito: Aedes (Howardina) cozumelensis. The communities from which Ae. cozumelensis were collected were all small rural communities (&lt;6,000 inhabitants) in the north-central part of Yucatán State. These new collection records for Ae. cozumelensis demonstrate that this mosquito has a far broader geographic range in the Yucatán Peninsula than previously known. Ae. cozumelensis immatures were collected from both residential premises and cemeteries, with specimens recovered from rock holes as well as various artificial containers including metal cans, flower vases, buckets, tires, and a water storage tank. The co-occurrence with Ae. aegypti in small rural communities poses intriguing questions regarding linkages between these mosquitoes, including the potential for direct competition for larval development sites. Additional studies are needed to determine how commonly Ae. cozumelensis feeds on human blood and whether it is naturally infected with arboviruses or other pathogens of medical or veterinary importance. We also summarize the published records for Ae. cozumelensis, which are restricted to collections from México's Yucatán Peninsula and Belize, and uniformly represent geographic locations where Ae. aegypti can be expected to occur.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00241.x" xmlns="http://purl.org/rss/1.0/"><title>Relationship between habitat type, fire frequency, and Amblyomma americanum populations in east-central Alabama</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00241.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Relationship between habitat type, fire frequency, and Amblyomma americanum populations in east-central Alabama</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Damien Willis, Robert Carter, Chris Murdock, Benjie Blair</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00241.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.1948-7134.2012.00241.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00241.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">373</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">381</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>Ticks were collected from 20 sites in the Calhoun, Cherokee, and Cleburne Counties in east-central Alabama areas to determine the relationship between plant physiognomy, environmental variables, and tick populations. Sites investigated included various burning regimes, wildland-urban–interface (WUI), a college campus, and an unmanaged area. <em>Amblyomma americanum</em> (L.) (Acari: Ixodidae) dominated the tick population while <em>Ixodes scapularis</em> Say was not encountered. There were complex differences in tick populations among site conditions. After prescribed burning, the tick population size was small but was larger in subsequent 2- and 5-year post-burn sites. An increase in <em>Odocoileus virginianus</em> foraging in recently burned sites is likely responsible for this phenomenon. WUI areas had the largest tick populations likely due to <em>Odocoileus virginianus</em> activity in an area that provides cover, forage, and a connection to a wildlife refuge. It is possible that the likelihood of humans coming in contact with ticks and tick-borne diseases is greater in WUI areas than in unbroken contiguous forest. <em>A. americanum</em> showed a positive correlation with percent cover of grass and leaf litter mass and a negative relationship with pine sapling density. Variables expected to be strongly correlated with <em>A. americanum</em> populations such as soil moisture, canopy closure, and tree density were found to have weak correlations.</p></div>
]]></content:encoded><description>

Ticks were collected from 20 sites in the Calhoun, Cherokee, and Cleburne Counties in east-central Alabama areas to determine the relationship between plant physiognomy, environmental variables, and tick populations. Sites investigated included various burning regimes, wildland-urban–interface (WUI), a college campus, and an unmanaged area. Amblyomma americanum (L.) (Acari: Ixodidae) dominated the tick population while Ixodes scapularis Say was not encountered. There were complex differences in tick populations among site conditions. After prescribed burning, the tick population size was small but was larger in subsequent 2- and 5-year post-burn sites. An increase in Odocoileus virginianus foraging in recently burned sites is likely responsible for this phenomenon. WUI areas had the largest tick populations likely due to Odocoileus virginianus activity in an area that provides cover, forage, and a connection to a wildlife refuge. It is possible that the likelihood of humans coming in contact with ticks and tick-borne diseases is greater in WUI areas than in unbroken contiguous forest. A. americanum showed a positive correlation with percent cover of grass and leaf litter mass and a negative relationship with pine sapling density. Variables expected to be strongly correlated with A. americanum populations such as soil moisture, canopy closure, and tree density were found to have weak correlations.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00242.x" xmlns="http://purl.org/rss/1.0/"><title>Fatty acids in anopheline mosquito larvae and their habitats</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00242.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fatty acids in anopheline mosquito larvae and their habitats</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dana Komínková, Eliška Rejmánková, John Grieco, Nicole Achee</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00242.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.1948-7134.2012.00242.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00242.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">382</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">395</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>Larvae of the three important Central American malaria vectors, <em>Anopheles albimanus, An. vestitipennis</em>, and <em>An. darlingi</em>, are found in distinctly different habitats broadly defined by hydrology and aquatic vegetation, but little is known about the actual food quality and quantity of these habitats. Polyunsaturated fatty acids (PUFA) are of special interest, because mosquitoes require 20:5ω3 (EPA), 20:4ω6 (ARA), and 22:6ω3 (DHA) and without an adequate supply of these PUFAs they are not able to complete their life cycle. We collected samples of larvae and their corresponding habitats and analyzed their fatty acid (FA) composition to reveal if there are any species-specific and habitat-specific differences in FA composition, and if habitat FA differences can be linked to differences in the mosquito FA pattern and, ultimately, mosquito performance. We also assessed how FA of wild larvae compare to the laboratory-reared larvae. Habitats were generally low in essential PUFAs and there were no significant differences among the FA composition of habitat samples. There were significant differences in FA composition of larvae. <em>An. darlingi</em> contained significantly higher amounts of FA, specifically a higher content of ω-6 PUFA, represented mainly by the linoleic acid (18:2ω-6). Large differences were found between field-collected and laboratory-reared <em>An. vestitipennis</em> larvae, especially in the content of PUFAs. The laboratory-reared larvae contained significantly more of the total FA, ω3 PUFA, and MUFA. The laboratory-reared larvae contained three to five times more essential PUFAs, EPA, and DHA. However, there were no differences in the total dry weight of the 4<sup>th</sup> instar larvae between the wild vs laboratory-reared larvae. Total FA in both larvae and habitats of <em>An. albimanus</em> and <em>An. darlingi</em> were positively correlated with the concentration of particulate organic carbon and nitrogen (POC, PON) in their respective habitats, but no such correlation was found for <em>An. vestitipennis</em>. PUFA are a good indicator of nutritional quality, although factors controlling the success of anopheline development from larval habitats are likely to be more complex and would include the presence of predators, pathogens, and toxins as interacting factors.</p></div>
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Larvae of the three important Central American malaria vectors, Anopheles albimanus, An. vestitipennis, and An. darlingi, are found in distinctly different habitats broadly defined by hydrology and aquatic vegetation, but little is known about the actual food quality and quantity of these habitats. Polyunsaturated fatty acids (PUFA) are of special interest, because mosquitoes require 20:5ω3 (EPA), 20:4ω6 (ARA), and 22:6ω3 (DHA) and without an adequate supply of these PUFAs they are not able to complete their life cycle. We collected samples of larvae and their corresponding habitats and analyzed their fatty acid (FA) composition to reveal if there are any species-specific and habitat-specific differences in FA composition, and if habitat FA differences can be linked to differences in the mosquito FA pattern and, ultimately, mosquito performance. We also assessed how FA of wild larvae compare to the laboratory-reared larvae. Habitats were generally low in essential PUFAs and there were no significant differences among the FA composition of habitat samples. There were significant differences in FA composition of larvae. An. darlingi contained significantly higher amounts of FA, specifically a higher content of ω-6 PUFA, represented mainly by the linoleic acid (18:2ω-6). Large differences were found between field-collected and laboratory-reared An. vestitipennis larvae, especially in the content of PUFAs. The laboratory-reared larvae contained significantly more of the total FA, ω3 PUFA, and MUFA. The laboratory-reared larvae contained three to five times more essential PUFAs, EPA, and DHA. However, there were no differences in the total dry weight of the 4th instar larvae between the wild vs laboratory-reared larvae. Total FA in both larvae and habitats of An. albimanus and An. darlingi were positively correlated with the concentration of particulate organic carbon and nitrogen (POC, PON) in their respective habitats, but no such correlation was found for An. vestitipennis. PUFA are a good indicator of nutritional quality, although factors controlling the success of anopheline development from larval habitats are likely to be more complex and would include the presence of predators, pathogens, and toxins as interacting factors.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00243.x" xmlns="http://purl.org/rss/1.0/"><title>Synanthropy of mosquitoes and sand flies near the Aimorés hydroelectric power plant, Brazil</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00243.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Synanthropy of mosquitoes and sand flies near the Aimorés hydroelectric power plant, Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R.A. Barata, R.L. Ursine, F.P. Nunes, D.H. Morais, H.S. Araújo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00243.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.1948-7134.2012.00243.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00243.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">397</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">401</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 environmental changes resulting from the construction of hydroelectric dams may affect the fauna of insect vectors and consequently the epidemiology of the diseases they transmit. This work examined the mosquito and sand fly fauna in the area of the Aimorés hydroelectric power plant, analyzing the seasonal distribution and the degree of species synanthropy in different ecotopes. Between November, 2008 and September, 2009, entomological captures were performed with the help of HP light traps in the rural, urban, and forest areas of Aimorés, Ituêta, Resplendor, and Baixo Guandu counties. The fauna proved to be quite diversified. Twenty-two species of mosquitoes and 11 species of sand flies were found. <em>Culex quinquefasciatus</em> was predominant among mosquitoes (76.7%), while <em>Lutzomyia intermedia</em> prevailed among sand flies (34.5%). Some of the captured species have medical interest. Supported by the high degree of synanthropy, those species reinforce the need for epidemiological surveillance.</p></div>
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The environmental changes resulting from the construction of hydroelectric dams may affect the fauna of insect vectors and consequently the epidemiology of the diseases they transmit. This work examined the mosquito and sand fly fauna in the area of the Aimorés hydroelectric power plant, analyzing the seasonal distribution and the degree of species synanthropy in different ecotopes. Between November, 2008 and September, 2009, entomological captures were performed with the help of HP light traps in the rural, urban, and forest areas of Aimorés, Ituêta, Resplendor, and Baixo Guandu counties. The fauna proved to be quite diversified. Twenty-two species of mosquitoes and 11 species of sand flies were found. Culex quinquefasciatus was predominant among mosquitoes (76.7%), while Lutzomyia intermedia prevailed among sand flies (34.5%). Some of the captured species have medical interest. Supported by the high degree of synanthropy, those species reinforce the need for epidemiological surveillance.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00244.x" xmlns="http://purl.org/rss/1.0/"><title>Modification of Anopheles gambiae distribution at high altitudes in Madagascar</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00244.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Modification of Anopheles gambiae distribution at high altitudes in Madagascar</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Michaël Luciano Tantely, Jean-Claude Rakotoniaina, Etienne Tata, Lala Andrianaivolambo, Didier Fontenille, Nohal Elissa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00244.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.1948-7134.2012.00244.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00244.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">402</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">406</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>In Madagascar, <em>Anopheles gambiae</em> has been found below altitudes of 1,000 m. We sampled <em>An. gambiae sensu lato</em> (<em>sl</em>) between 2008 and 2010 in the Central Highlands of Madagascar at altitudes over 1,200 m. The study site consists of rainforest, rainforest edge, and an open savanna biotope. <em>Anopheles gambiae</em> and <em>An. arabiensis</em>, as well as molecular forms of <em>An. gambiae</em>, were identified molecularly. <em>An. gambiae</em> accounted for 26.7% at the edge of the rainforest and 2.3% in the open savanna biotope. One specimen of this species was caught in the forest. <em>An. arabiensis</em> accounted for 66.3% at the edge of the rainforest and 97.7 % in the open savanna biotope. All <em>An. gambiae</em> adults tested belonged to the S molecular form. <em>An. gambiae</em> is present at high altitudes in Madagascar, with a high prevalence at the rainforest edge. Several factors, including the appearance of new favorable biotopes, recolonization after a reduction of indoor vector control, and climate change, may contribute to its distribution. The changing distribution of <em>An. gambiae</em> may have consequences for the distribution and incidence of malaria in the Malagasy Highlands.</p></div>
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In Madagascar, Anopheles gambiae has been found below altitudes of 1,000 m. We sampled An. gambiae sensu lato (sl) between 2008 and 2010 in the Central Highlands of Madagascar at altitudes over 1,200 m. The study site consists of rainforest, rainforest edge, and an open savanna biotope. Anopheles gambiae and An. arabiensis, as well as molecular forms of An. gambiae, were identified molecularly. An. gambiae accounted for 26.7% at the edge of the rainforest and 2.3% in the open savanna biotope. One specimen of this species was caught in the forest. An. arabiensis accounted for 66.3% at the edge of the rainforest and 97.7 % in the open savanna biotope. All An. gambiae adults tested belonged to the S molecular form. An. gambiae is present at high altitudes in Madagascar, with a high prevalence at the rainforest edge. Several factors, including the appearance of new favorable biotopes, recolonization after a reduction of indoor vector control, and climate change, may contribute to its distribution. The changing distribution of An. gambiae may have consequences for the distribution and incidence of malaria in the Malagasy Highlands.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00245.x" xmlns="http://purl.org/rss/1.0/"><title>Fine scale spatial urban land cover factors associated with adult mosquito abundance and risk in Tucson, Arizona</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00245.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fine scale spatial urban land cover factors associated with adult mosquito abundance and risk in Tucson, Arizona</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Katheryn I. Landau, Willem J.D. van Leeuwen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00245.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.1948-7134.2012.00245.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00245.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">407</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">418</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>It is currently unclear what role microhabitat land cover plays in determining the seasonal spatial distribution of <em>Aedes aegypti</em> and <em>Culex quinquefasciatus</em>, disease vectors of dengue and West Nile Virus, respectively, in Tucson, AZ. We compared mosquito abundance to sixteen land cover variables derived from 2010 NAIP multispectral data and 2008 LiDAR height data. Mosquitoes were trapped with 30–9 traps from May to October of 2010 and 2011. Variables were extracted for five buffer zones (10–50 m radii at 10 m intervals) around trapping sites. Stepwise regression was performed to determine the best scale for observation and the influential land cover variables. The 30 m radius buffer was determined to be the best for observing the land cover-mosquito abundance relationship. <em>Ae. aegypti</em> presence was positively associated with structure and medium height trees and negatively associated with bare earth; <em>Cx. quinquefasciatus</em> presence was positively associated with pavement and medium height trees and negatively associated with shrubs. These findings emphasize vegetation, impervious surfaces, and soil influences on mosquito presence in an urban setting. Lastly, the land cover-mosquito abundance relationships were used to produce risk maps of seasonal presence that highlight high risk areas in Tucson, which may be useful for focusing mosquito control program actions.</p></div>
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It is currently unclear what role microhabitat land cover plays in determining the seasonal spatial distribution of Aedes aegypti and Culex quinquefasciatus, disease vectors of dengue and West Nile Virus, respectively, in Tucson, AZ. We compared mosquito abundance to sixteen land cover variables derived from 2010 NAIP multispectral data and 2008 LiDAR height data. Mosquitoes were trapped with 30–9 traps from May to October of 2010 and 2011. Variables were extracted for five buffer zones (10–50 m radii at 10 m intervals) around trapping sites. Stepwise regression was performed to determine the best scale for observation and the influential land cover variables. The 30 m radius buffer was determined to be the best for observing the land cover-mosquito abundance relationship. Ae. aegypti presence was positively associated with structure and medium height trees and negatively associated with bare earth; Cx. quinquefasciatus presence was positively associated with pavement and medium height trees and negatively associated with shrubs. These findings emphasize vegetation, impervious surfaces, and soil influences on mosquito presence in an urban setting. Lastly, the land cover-mosquito abundance relationships were used to produce risk maps of seasonal presence that highlight high risk areas in Tucson, which may be useful for focusing mosquito control program actions.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00246.x" xmlns="http://purl.org/rss/1.0/"><title>Malaria and the Anopheles mosquitoes of Tajikistan</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00246.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Malaria and the Anopheles mosquitoes of Tajikistan</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zamonidin Habirov, Dilshod Kadamov, Firuz Iskandarov, Saodat Komilova, Shelley Cook, Erica McAlister, Ralph E. Harbach</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00246.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.1948-7134.2012.00246.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00246.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">419</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">427</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>Surveys of <em>Anopheles</em> mosquitoes were conducted in urban, rural, and natural areas of Tajikistan to obtain updated information on their distributions, especially in southern districts of the country where malaria is a prevalent disease. Nine species of <em>Anopheles</em> are found in Tajikistan. <em>Anopheles superpictus</em>, <em>An. claviger</em>, <em>An. hyrcanus</em>, and <em>An. pulcherrimus</em> are the most widespread and abundant species. Investigations in northern Tajikistan confirmed the presence of <em>An. artemievi</em> and the absence of <em>An. martinius</em>, both members of the <em>An. maculipennis</em> complex of malaria vectors. <em>Anopheles barianensis, An. lindesayi</em>, and <em>An. marteri sogdianus</em>, species previously recorded in the country, were not encountered during our surveys. The history of <em>Anopheles</em> and malaria research in Tajikistan is reviewed and bionomical and distributional information is provided for each of the nine species.</p></div>
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Surveys of Anopheles mosquitoes were conducted in urban, rural, and natural areas of Tajikistan to obtain updated information on their distributions, especially in southern districts of the country where malaria is a prevalent disease. Nine species of Anopheles are found in Tajikistan. Anopheles superpictus, An. claviger, An. hyrcanus, and An. pulcherrimus are the most widespread and abundant species. Investigations in northern Tajikistan confirmed the presence of An. artemievi and the absence of An. martinius, both members of the An. maculipennis complex of malaria vectors. Anopheles barianensis, An. lindesayi, and An. marteri sogdianus, species previously recorded in the country, were not encountered during our surveys. The history of Anopheles and malaria research in Tajikistan is reviewed and bionomical and distributional information is provided for each of the nine species.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00247.x" xmlns="http://purl.org/rss/1.0/"><title>The influence of local environment on the aging and mortality ofAedes aegypti (L.): Case study in Fortaleza-CE, Brazil</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00247.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The influence of local environment on the aging and mortality ofAedes aegypti (L.): Case study in Fortaleza-CE, Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nicolas Degallier, Jacques Servain, Paulo Sérgio Lucio, Alexis Hannart, Bruno Durand, Raimundo Nonato de Souza, Zolyde Mota Ribeiro</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00247.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.1948-7134.2012.00247.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00247.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">428</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">441</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>It is generally assumed that the daily probability of survival of mosquitoes is independent of age. To test this assumption we have conducted a three-year experimental fieldwork study (2005–2007) at Fortaleza-CE in Brazil, determining daily survival rates of the dengue vector <em>Aedes aegypti</em> (L.). Survival rates of adult <em>Ae. aegypti</em> may be age-dependent and the statistical analysis is a sensitive approach for comparing patterns of mosquito survival. The mosquito survival data were better fit by a Weibull survival function than by the more traditionally used Gompertz or logistic survival functions. Gompertz, Weibull, or logistic survival functions often fit the survival, and the tails of the survival curves usually appear to fall between the values predicted by the three functions. We corroborate that the mortality of <em>Ae. aegypti</em> in semi-natural conditions may no more be considered as a constant phenomenon during the life of adult mosquitoes but varies according to the age and environmental conditions under a tropical climate. This study estimates the variability in the survival rate of <em>Ae. aegypti</em> and environmental factors that are related to such variability. The statistical analysis shows that the fitting ability, concerning the hazard function, was in decreasing order: Seasonal Cox, the three-parameter Gompertz, and the three-parameter Weibull, that was similar to the three-parameter logistic. The advantage of using the Cox model is that it is convenient for exploring the relationship between survival and several explanatory variables. The Cox model has the advantage of preserving the variable in its original quantitative form and of using a maximum of information. The survival analyses indicate that mosquito mortality is both age- and environment-dependent.</p></div>
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It is generally assumed that the daily probability of survival of mosquitoes is independent of age. To test this assumption we have conducted a three-year experimental fieldwork study (2005–2007) at Fortaleza-CE in Brazil, determining daily survival rates of the dengue vector Aedes aegypti (L.). Survival rates of adult Ae. aegypti may be age-dependent and the statistical analysis is a sensitive approach for comparing patterns of mosquito survival. The mosquito survival data were better fit by a Weibull survival function than by the more traditionally used Gompertz or logistic survival functions. Gompertz, Weibull, or logistic survival functions often fit the survival, and the tails of the survival curves usually appear to fall between the values predicted by the three functions. We corroborate that the mortality of Ae. aegypti in semi-natural conditions may no more be considered as a constant phenomenon during the life of adult mosquitoes but varies according to the age and environmental conditions under a tropical climate. This study estimates the variability in the survival rate of Ae. aegypti and environmental factors that are related to such variability. The statistical analysis shows that the fitting ability, concerning the hazard function, was in decreasing order: Seasonal Cox, the three-parameter Gompertz, and the three-parameter Weibull, that was similar to the three-parameter logistic. The advantage of using the Cox model is that it is convenient for exploring the relationship between survival and several explanatory variables. The Cox model has the advantage of preserving the variable in its original quantitative form and of using a maximum of information. The survival analyses indicate that mosquito mortality is both age- and environment-dependent.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00248.x" xmlns="http://purl.org/rss/1.0/"><title>West Nile virus cluster analysis and vertical transmission in Culex pipiens complex mosquitoes in Sacramento and Yolo Counties, California, 2011</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00248.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">West Nile virus cluster analysis and vertical transmission in Culex pipiens complex mosquitoes in Sacramento and Yolo Counties, California, 2011</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ethan Fechter-Leggett, Brittany M. Nelms, Christopher M. Barker, William K. Reisen</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00248.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.1948-7134.2012.00248.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00248.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">442</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">449</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>West Nile virus (WNV) is now endemic in California, with annual transmission documented by the statewide surveillance system. Although much is known about the horizontal avian-mosquito transmission cycle, less is known about vertical transmission under field conditions, which may supplement virus amplification during summer and provide a mechanism to infect overwintering female mosquitoes during fall. The current study identified clusters of WNV-infected mosquitoes in Sacramento and Yolo Counties, CA, during late summer 2011 and tested field-captured ovipositing female mosquitoes and their progeny for WNV RNA to estimate the frequency of vertical transmission. Space-time clustering of WNV-positive <em>Culex pipiens</em> complex pools was detected in the northern Elk Grove area of Sacramento County between July 18 and September 18, 2011 (5.22 km radius; <em>p</em>&lt;0.001 and RR=7.80). Vertical transmission by WNV-infected females to egg rafts was 50% and to larvae was 40%. The estimated minimal filial infection rate from WNV-positive, ovipositing females was 2.0 infected females/1,000. The potential contribution of vertical transmission to WNV maintenance and amplification are discussed.</p></div>
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West Nile virus (WNV) is now endemic in California, with annual transmission documented by the statewide surveillance system. Although much is known about the horizontal avian-mosquito transmission cycle, less is known about vertical transmission under field conditions, which may supplement virus amplification during summer and provide a mechanism to infect overwintering female mosquitoes during fall. The current study identified clusters of WNV-infected mosquitoes in Sacramento and Yolo Counties, CA, during late summer 2011 and tested field-captured ovipositing female mosquitoes and their progeny for WNV RNA to estimate the frequency of vertical transmission. Space-time clustering of WNV-positive Culex pipiens complex pools was detected in the northern Elk Grove area of Sacramento County between July 18 and September 18, 2011 (5.22 km radius; p&lt;0.001 and RR=7.80). Vertical transmission by WNV-infected females to egg rafts was 50% and to larvae was 40%. The estimated minimal filial infection rate from WNV-positive, ovipositing females was 2.0 infected females/1,000. The potential contribution of vertical transmission to WNV maintenance and amplification are discussed.
</description></item><item rdf:about="http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00249.x" xmlns="http://purl.org/rss/1.0/"><title>Species composition of the mosquito Anopheles hyrcanus (Diptera, Culicidae) Group in the Russian Far East</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00249.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Species composition of the mosquito Anopheles hyrcanus (Diptera, Culicidae) Group in the Russian Far East</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Natalia V. Khrabrova, Valery P. Perevozkin, Yulia V. Andreeva, Anuarbek K. Sibataev, Vladimir N. Stegniy</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00249.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.1948-7134.2012.00249.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00249.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">450</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">452</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.1948-7134.2012.00250.x" xmlns="http://purl.org/rss/1.0/"><title>Distance from the stable affects trapping of biting midges (Diptera, Ceratopogonidae)</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00250.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Distance from the stable affects trapping of biting midges (Diptera, Ceratopogonidae)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Renke Lühken, Ellen Kiel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00250.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.1948-7134.2012.00250.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00250.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">453</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">457</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.1948-7134.2012.00251.x" xmlns="http://purl.org/rss/1.0/"><title>First laboratory culture of Phortica variegata (Diptera, Steganinae), a vector of Thelazia callipaeda</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00251.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">First laboratory culture of Phortica variegata (Diptera, Steganinae), a vector of Thelazia callipaeda</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Domenico Otranto, Cinzia Cantacessi, Riccardo P. Lia, Ilona C. Grunwald Kadow, Siju K. Purayil, Filipe Dantas-Torres, Jan Máca</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00251.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.1948-7134.2012.00251.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00251.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">458</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">461</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.1948-7134.2012.00252.x" xmlns="http://purl.org/rss/1.0/"><title>Status of the invasive species Aedes japonicus japonicus (Diptera: Culicidae) in southwest Germany in 2011</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00252.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Status of the invasive species Aedes japonicus japonicus (Diptera: Culicidae) in southwest Germany in 2011</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Katrin Huber, Björn Pluskota, Artur Jöst, Klaus Hoffmann, Norbert Becker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00252.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.1948-7134.2012.00252.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00252.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">462</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">465</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.1948-7134.2012.00253.x" xmlns="http://purl.org/rss/1.0/"><title>Alteration in frequency of sand flies in domiciles after changes in the peridomicile area, State of Paraná, Brazil</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00253.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Alteration in frequency of sand flies in domiciles after changes in the peridomicile area, State of Paraná, Brazil</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Herintha C. Neitzke-Abreu, Demilson R. Santos, Allan M. Silva, Kárin R. Reinhold-Castro, Thaís G. V. Silveira, Maria V. C. Lonardoni, Ueslei Teodoro</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00253.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.1948-7134.2012.00253.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00253.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">466</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">470</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.1948-7134.2012.00254.x" xmlns="http://purl.org/rss/1.0/"><title>Pre-imaginal development of Aedes aegypti in brackish and fresh water urban domestic wells in Sri Lanka</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00254.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Pre-imaginal development of Aedes aegypti in brackish and fresh water urban domestic wells in Sri Lanka</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sinnathamby N. Surendran, Pavilupillai J. Jude, Veluppillai Thabothiny, Selvarajah Raveendran, Ranjan Ramasamy</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00254.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.1948-7134.2012.00254.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00254.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">471</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">473</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.1948-7134.2012.00255.x" xmlns="http://purl.org/rss/1.0/"><title>Bionomics of populations of Meccus pallidipennis (Stål), 1872 (Hemiptera: Reduviidae) from Mexico</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00255.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Bionomics of populations of Meccus pallidipennis (Stål), 1872 (Hemiptera: Reduviidae) from Mexico</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">José Alejandro Martínez-Ibarra, Benjamín Nogueda-Torres, Gerardo García-Benavídez, Víctor Vargas-Llamas, Rafael Bustos-Saldaña, Oziel Dante Montañez-Valdez</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00255.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.1948-7134.2012.00255.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00255.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">474</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">477</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.1948-7134.2012.00256.x" xmlns="http://purl.org/rss/1.0/"><title>Ticks on northward migrating birds in southern Spain during Spring, 2011</title><link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00256.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ticks on northward migrating birds in southern Spain during Spring, 2011</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Foley-Fisher, P. Phipps, J.M. Medlock, P. Atkinson, B. Atkinson, R. Hewson, P. Gale</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-11-26T13:57:01.138978-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1948-7134.2012.00256.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.1948-7134.2012.00256.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1111%2Fj.1948-7134.2012.00256.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">478</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">480</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item></rdf:RDF>