Volume 20, Issue 12
Primary Research Article

Vulnerability of coastal ecosystems to changes in harmful algal bloom distribution in response to climate change: projections based on model analysis

Patricia M. Glibert

Corresponding Author

Horn Point Laboratory, University of Maryland Center for Environmental Science, P.O. Box 775, Cambridge, MD, 21613 USA

Correspondence: Patricia M. Glibert, tel. +1 410 221 8422, fax +1 410 221 8290, e‐mail: glibert@umces.eduSearch for more papers by this author
J. Icarus Allen

Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, PL1 3DH UK

Search for more papers by this author
Yuri Artioli

Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, PL1 3DH UK

Search for more papers by this author
Arthur Beusen

PBL Netherlands Environmental Assessment Agency, PO Box 303, Bilthoven, 3720 AH The Netherlands

Search for more papers by this author
Lex Bouwman

PBL Netherlands Environmental Assessment Agency, PO Box 303, Bilthoven, 3720 AH The Netherlands

Department of Earth Sciences, Geochemistry, Faculty of Geosciences, Utrecht University, P.O. Box 80.021, Utrecht, 3508 TA The Netherlands

Search for more papers by this author
James Harle

Natural Environmental Research Council, National Oceanography Centre, Joseph Proudman Building, 6 Brownlow St., Liverpool, L3 5DA UK

Search for more papers by this author
Robert Holmes

Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, PL1 3DH UK

Search for more papers by this author
Jason Holt

Natural Environmental Research Council, National Oceanography Centre, Joseph Proudman Building, 6 Brownlow St., Liverpool, L3 5DA UK

Search for more papers by this author
First published: 18 June 2014
Citations: 87

Abstract

Harmful algal blooms (HABs), those proliferations of algae that can cause fish kills, contaminate seafood with toxins, form unsightly scums, or detrimentally alter ecosystem function have been increasing in frequency, magnitude, and duration worldwide. Here, using a global modeling approach, we show, for three regions of the globe, the potential effects of nutrient loading and climate change for two HAB genera, pelagic Prorocentrum and Karenia, each with differing physiological characteristics for growth. The projections (end of century, 2090–2100) are based on climate change resulting from the A1B scenario of the Intergovernmental Panel on Climate Change Institut Pierre Simon Laplace Climate Model (IPCC, IPSL‐CM4), applied in a coupled oceanographic‐biogeochemical model, combined with a suite of assumed physiological ‘rules’ for genera‐specific bloom development. Based on these models, an expansion in area and/or number of months annually conducive to development of these HABs along the NW European Shelf‐Baltic Sea system and NE Asia was projected for both HAB genera, but no expansion (Prorocentrum spp.), or actual contraction in area and months conducive for blooms (Karenia spp.), was projected in the SE Asian domain. The implications of these projections, especially for Northern Europe, are shifts in vulnerability of coastal systems to HAB events, increased regional HAB impacts to aquaculture, increased risks to human health and ecosystems, and economic consequences of these events due to losses to fisheries and ecosystem services.

Number of times cited according to CrossRef: 87

  • Quantifying Nutrient Budgets for Sustainable Nutrient Management, Global Biogeochemical Cycles, 10.1029/2018GB006060, 34, 3, (2020).
  • Algal toxins in Alaskan seabirds: Evaluating the role of saxitoxin and domoic acid in a large-scale die-off of Common Murres, Harmful Algae, 10.1016/j.hal.2019.101730, 92, (101730), (2020).
  • Combined Effects of Temperature, Irradiance, and pH on Teleaulax amphioxeia (Cryptophyceae) Physiology and Feeding Ratio For Its Predator Mesodinium rubrum (Ciliophora)1, Journal of Phycology, 10.1111/jpy.12977, 56, 3, (775-783), (2020).
  • Climate-induced interannual variability and projected change of two harmful algal bloom taxa in Chesapeake Bay, USA, Science of The Total Environment, 10.1016/j.scitotenv.2020.140947, 744, (140947), (2020).
  • Projecting global mariculture diversity under climate change, Global Change Biology, 10.1111/gcb.14974, 26, 4, (2134-2148), (2020).
  • Using Copernicus Sentinel-2 and Sentinel-3 data to monitor harmful algal blooms in Southern Chile during the COVID-19 lockdown, Marine Pollution Bulletin, 10.1016/j.marpolbul.2020.111722, 161, (111722), (2020).
  • Microalgae harvesting using colloidal gas aphrons generated from single and mixed surfactants, Chemosphere, 10.1016/j.chemosphere.2020.128568, (128568), (2020).
  • Copernicus Marine Service Ocean State Report, Issue 4, Journal of Operational Oceanography, 10.1080/1755876X.2020.1785097, 13, sup1, (S1-S172), (2020).
  • Further Evidence of the Haber-Bosch—Harmful Algal Bloom (HB-HAB) Link and the Risk of Suggesting HAB Control Through Phosphorus Reductions Only, Just Enough Nitrogen, 10.1007/978-3-030-58065-0, (255-282), (2020).
  • Spatially Explicit Inventory of Sources of Nitrogen Inputs to the Yellow Sea, East China Sea, and South China Sea for the Period 1970–2010, Earth's Future, 10.1029/2020EF001516, 8, 10, (2020).
  • Effects of HABs and a dystrophic event on zooplankton community structure in a Mediterranean lagoon (W Greece), Estuarine, Coastal and Shelf Science, 10.1016/j.ecss.2020.106985, 245, (106985), (2020).
  • Nutrient mitigation under the impact of climate and land-use changes: A hydro-economic approach to participatory catchment management, Journal of Environmental Management, 10.1016/j.jenvman.2020.110976, 271, (110976), (2020).
  • Barriers and facilitators to shellfish cultivation, Reviews in Aquaculture, 10.1111/raq.12325, 12, 1, (406-437), (2019).
  • Assessing risks and mitigating impacts of harmful algal blooms on mariculture and marine fisheries, Reviews in Aquaculture, 10.1111/raq.12403, 12, 3, (1663-1688), (2019).
  • Assimilating multi-source data into a three-dimensional hydro-ecological dynamics model using Ensemble Kalman Filter, Environmental Modelling & Software, 10.1016/j.envsoft.2019.03.028, (2019).
  • Influence of salinity on growth and cell volume in three strains of Prorocentrum cordatum (Dinophyceae), Aquatic Biology, 10.3354/ab00704, 28, (1-12), (2019).
  • Turn the potential greenhouse gases into biomass in harmful algal blooms waters: A microcosm study, Science of The Total Environment, 10.1016/j.scitotenv.2018.11.262, 655, (520-528), (2019).
  • The Effects of Climate Change on Disease Spread in Wildlife, Fowler's Zoo and Wild Animal Medicine Current Therapy, Volume 9, 10.1016/B978-0-323-55228-8.00036-9, (247-254), (2019).
  • Climate Change and Harmful Algal Blooms: Insights and perspective, Harmful Algae, 10.1016/j.hal.2019.101731, (101731), (2019).
  • Harmful algal blooms: A climate change co-stressor in marine and freshwater ecosystems, Harmful Algae, 10.1016/j.hal.2019.03.008, (2019).
  • Mapping of climate vulnerability of the coastal region of Bangladesh using principal component analysis, Applied Geography, 10.1016/j.apgeog.2018.12.011, 102, (47-57), (2019).
  • Meta‐analysis reveals enhanced growth of marine harmful algae from temperate regions with warming and elevated CO2 levels, Global Change Biology, 10.1111/gcb.14678, 25, 8, (2607-2618), (2019).
  • The harmful algae, Cochlodinium polykrikoides and Aureococcus anophagefferens, elicit stronger transcriptomic and mortality response in larval bivalves (Argopecten irradians) than climate change stressors, Ecology and Evolution, 10.1002/ece3.5100, 9, 8, (4931-4948), (2019).
  • Assessing uncertainty of hydrological and ecological parameters originating from the application of an ensemble of ten global-regional climate model projections in a coastal ecosystem of the lagoon of Venice, Italy, Ecological Engineering, 10.1016/j.ecoleng.2019.04.011, 133, (121-136), (2019).
  • A model predicting the PSP toxic dinoflagellate Alexandrium minutum occurrence in the coastal waters of the NW Adriatic Sea, Scientific Reports, 10.1038/s41598-019-40664-w, 9, 1, (2019).
  • Simulating Water Residence Time in the Coastal Ocean: A Global Perspective, Geophysical Research Letters, 10.1029/2019GL085097, 46, 23, (13910-13919), (2019).
  • Modeling harmful algal blooms in a changing climate, Harmful Algae, 10.1016/j.hal.2019.101729, (101729), (2019).
  • Biological aspects of the marine crab Plagusia depressa (Fabricius, 1775) on the northeast coast of Brazil , Marine Biology Research, 10.1080/17451000.2019.1612070, (1-10), (2019).
  • Future Extreme Event Risk in the Rural Northeastern United States, Annals of the American Association of Geographers, 10.1080/24694452.2018.1540920, (1-21), (2019).
  • Warming Amplifies the Frequency of Harmful Algal Blooms with Eutrophication in Chinese Coastal Waters, Environmental Science & Technology, 10.1021/acs.est.9b03726, (2019).
  • Rapid screening fluorescence method applied to detection and quantitation of paralytic shellfish toxins in invertebrate marine vectors, Food Additives & Contaminants: Part A, 10.1080/19440049.2019.1615645, (1-20), (2019).
  • Marine Dinoflagellate Assemblage in the Galápagos Marine Reserve, Frontiers in Marine Science, 10.3389/fmars.2019.00235, 6, (2019).
  • Inter-species variability of okadaic acid group toxicity in relation to the content of fatty acids detected in different marine vectors, Food Additives & Contaminants: Part A, 10.1080/19440049.2019.1569265, (1-19), (2019).
  • Differential Mortality of North Atlantic Bivalve Molluscs During Harmful Algal Blooms Caused by the Dinoflagellate, Cochlodinium (a.k.a. Margalefidinium) polykrikoides, Estuaries and Coasts, 10.1007/s12237-018-0445-0, 42, 1, (190-203), (2018).
  • Hurricane storm surge in Volusia County, Florida: evidence of a tipping point for infrastructure damage, Disasters, 10.1111/disa.12296, 43, 1, (157-180), (2018).
  • Multiple stressors and benthic harmful algal blooms (BHABs): Potential effects of temperature rise and nutrient enrichment, Marine Pollution Bulletin, 10.1016/j.marpolbul.2018.04.012, 131, (552-564), (2018).
  • Mixotrophy in Harmful Algal Blooms: By Whom, on Whom, When, Why, and What Next, Global Ecology and Oceanography of Harmful Algal Blooms, 10.1007/978-3-319-70069-4_7, (113-132), (2018).
  • Changing Land-, Sea-, and Airscapes: Sources of Nutrient Pollution Affecting Habitat Suitability for Harmful Algae, Global Ecology and Oceanography of Harmful Algal Blooms, 10.1007/978-3-319-70069-4_4, (53-76), (2018).
  • Key Questions and Recent Research Advances on Harmful Algal Blooms in Relation to Nutrients and Eutrophication, Global Ecology and Oceanography of Harmful Algal Blooms, 10.1007/978-3-319-70069-4_12, (229-259), (2018).
  • Advancements and Continuing Challenges of Emerging Technologies and Tools for Detecting Harmful Algal Blooms, Their Antecedent Conditions and Toxins, and Applications in Predictive Models, Global Ecology and Oceanography of Harmful Algal Blooms, 10.1007/978-3-319-70069-4_18, (339-357), (2018).
  • The Baltic Sea as a time machine for the future coastal ocean, Science Advances, 10.1126/sciadv.aar8195, 4, 5, (eaar8195), (2018).
  • Recent Advances in Modelling of Harmful Algal Blooms, Global Ecology and Oceanography of Harmful Algal Blooms, 10.1007/978-3-319-70069-4_19, (359-377), (2018).
  • Dinoflagellaten – ein Dauerexperiment der Evolution?, Biologie in unserer Zeit, 10.1002/biuz.201810650, 48, 4, (228-238), (2018).
  • Harmful algal blooms and climate change: exploring future distribution changes, ICES Journal of Marine Science, 10.1093/icesjms/fsy113, 75, 6, (1882-1893), (2018).
  • Modelling climate change impacts on nutrients and primary production in coastal waters, Science of The Total Environment, 10.1016/j.scitotenv.2018.02.131, 628-629, (919-937), (2018).
  • Thermal acclimation affects growth and lipophilic toxin production in a strain of cosmopolitan harmful alga Dinophysis acuminata, Harmful Algae, 10.1016/j.hal.2018.02.004, 73, (119-128), (2018).
  • Life histories of microalgal species causing harmful blooms: Haploids, diploids and the relevance of benthic stages, Harmful Algae, 10.1016/j.hal.2018.01.006, 73, (44-57), (2018).
  • Development and analysis of spring plant phenology products: 36 years of 1-km grids over the conterminous US, Agricultural and Forest Meteorology, 10.1016/j.agrformet.2018.06.028, 262, (34-41), (2018).
  • Risk Perception of Coastal Communities and Authorities on Harmful Algal Blooms in Ecuador, Frontiers in Marine Science, 10.3389/fmars.2018.00365, 5, (2018).
  • Toxic algal bloom induced by ocean acidification disrupts the pelagic food web, Nature Climate Change, 10.1038/s41558-018-0344-1, (2018).
  • Modeling sources of nutrients in rivers draining into the Bay of Bengal—a scenario analysis, Regional Environmental Change, 10.1007/s10113-017-1176-7, 17, 8, (2495-2506), (2017).
  • Novel method to delimitate and demarcate coastal zone boundaries, Ocean & Coastal Management, 10.1016/j.ocecoaman.2017.04.021, 144, (105-119), (2017).
  • Mass mortality of marine birds in the Northeast Pacific caused by Akashiwo sanguinea, Marine Ecology Progress Series, 10.3354/meps12253, 579, (111-127), (2017).
  • Analysis of phytoplankton assemblage structure in the Mediterranean Sea based on high-throughput sequencing of partial 18S rRNA sequences, Marine Genomics, 10.1016/j.margen.2017.06.001, 36, (49-55), (2017).
  • Effects of fertilizers used in agricultural fields on algal blooms, The European Physical Journal Special Topics, 10.1140/epjst/e2017-70031-7, 226, 9, (2119-2133), (2017).
  • Effects of elevated CO2 on phytoplankton during a mesocosm experiment in the southern eutrophicated coastal water of China, Scientific Reports, 10.1038/s41598-017-07195-8, 7, 1, (2017).
  • Evaluation of phytoplankton quality and toxicity risk based on a long-term time series previous to the implementation of a bivalve farm (Basque coast as a case study), Regional Studies in Marine Science, 10.1016/j.rsma.2016.12.012, 10, (10-19), (2017).
  • Which ocean colour algorithm for MERIS in North West European waters?, Remote Sensing of Environment, 10.1016/j.rse.2016.11.012, 189, (132-151), (2017).
  • Nitrate uptake of the red tide dinoflagellate Prorocentrum micans measured using a nutrient repletion method: effect of light intensity, ALGAE, 10.4490/algae.2017.32.5.20, 32, 2, (139-153), (2017).
  • Ocean warming since 1982 has expanded the niche of toxic algal blooms in the North Atlantic and North Pacific oceans, Proceedings of the National Academy of Sciences, 10.1073/pnas.1619575114, 114, 19, (4975-4980), (2017).
  • Long-term variations in sediment heavy metals of a reservoir with changing trophic states: Implications for the impact of climate change, Science of The Total Environment, 10.1016/j.scitotenv.2017.04.041, 609, (242-250), (2017).
  • Species’ traits influenced their response to recent climate change, Nature Climate Change, 10.1038/nclimate3223, 7, 3, (205-208), (2017).
  • Prevalence, Variability and Bioconcentration of Saxitoxin-Group in Different Marine Species Present in the Food Chain, Toxins, 10.3390/toxins9060190, 9, 6, (190), (2017).
  • Nitrogen transformations along a shallow subterranean estuary, Biogeosciences, 10.5194/bg-14-3321-2017, 14, 13, (3321-3336), (2017).
  • Showcasing metabolomic applications in aquaculture: a review, Reviews in Aquaculture, 10.1111/raq.12152, 10, 1, (135-152), (2016).
  • The relative availability of inorganic carbon and inorganic nitrogen influences the response of the dinoflagellate Protoceratium reticulatum to elevated CO2, Journal of Phycology, 10.1111/jpy.12463, 53, 2, (298-307), (2016).
  • Responses of Phytoplankton Communities to Environmental Variability in the East China Sea, Ecosystems, 10.1007/s10021-016-9970-5, 19, 5, (832-849), (2016).
  • Ecological impacts of parasitic chytrids, syndiniales and perkinsids on populations of marine photosynthetic dinoflagellates, Fungal Ecology, 10.1016/j.funeco.2015.03.007, 19, (47-58), (2016).
  • Effect of nitrogen/phosphorus concentration on algal organic matter generation of the diatom Nitzschia palea : Total indicators and spectroscopic characterization, Journal of Environmental Sciences, 10.1016/j.jes.2016.02.002, 47, (130-142), (2016).
  • Ecological niche partitioning of the invasive dinoflagellate Prorocentrum minimum and its native congeners in the Baltic Sea, Harmful Algae, 10.1016/j.hal.2016.09.006, 59, (100-111), (2016).
  • The dinoflagellate Prorocentrum cordatum at the edge of the salinity tolerance: The growth is slower but cells are larger, Estuarine, Coastal and Shelf Science, 10.1016/j.ecss.2015.11.013, 168, (71-79), (2016).
  • Temperature controls the toxicity of the ichthyotoxic dinoflagellate Cochlodinium polykrikoides, Marine Ecology Progress Series, 10.3354/meps11590, 545, (63-76), (2016).
  • Transcriptomic profiles reveal the genome-wide responses of the harmful dinoflagellate Cochlodinium polykrikoides when exposed to the algicide copper sulfate, BMC Genomics, 10.1186/s12864-015-2341-3, 17, 1, (2016).
  • Coastal Ecosystem Modeling in the Context of Climate Change, Ecological Model Types, 10.1016/B978-0-444-63623-2.00011-6, (227-260), (2016).
  • Range expansion of the invasive lionfish in the Northwest Atlantic with climate change, Marine Ecology Progress Series, 10.3354/meps11638, 546, (225-237), (2016).
  • Phycotoxins by Harmful Algal Blooms (HABS) and Human Poisoning: An Overview, International Clinical Pathology Journal, 10.15406/icpjl.2016.02.00062, 2, 6, (2016).
  • ERSEM 15.06: a generic model for marine biogeochemistry and the ecosystem dynamics of the lower trophic levels, Geoscientific Model Development, 10.5194/gmd-9-1293-2016, 9, 4, (1293-1339), (2016).
  • Marine Nitrogen and Climate Change, Nitrogen and Climate Change, 10.1057/9781137286963, (125-143), (2015).
  • The sxt Gene and Paralytic Shellfish Poisoning Toxins as Markers for the Monitoring of Toxic Alexandrium Species Blooms , Environmental Science & Technology, 10.1021/acs.est.5b03298, 49, 24, (14230-14238), (2015).
  • Modelling the combined impacts of climate change and direct anthropogenic drivers on the ecosystem of the northwest European continental shelf, Journal of Marine Systems, 10.1016/j.jmarsys.2015.07.006, 152, (51-63), (2015).
  • Warm temperature acclimation impacts metabolism of paralytic shellfish toxins from Alexandrium minutum in commercial oysters, Global Change Biology, 10.1111/gcb.12952, 21, 9, (3402-3413), (2015).
  • A framework for examining climate-driven changes to the seasonality and geographical range of coastal pathogens and harmful algae, Climate Risk Management, 10.1016/j.crm.2015.03.002, 8, (16-27), (2015).
  • Study of Adsorption and Flocculation Properties of Natural Clays to Remove Prorocentrum lima, Toxins, 10.3390/toxins7103977, 7, 10, (3977-3988), (2015).
  • EMPOWER-1.0: an Efficient Model of Planktonic ecOsystems WrittEn in R, Geoscientific Model Development, 10.5194/gmd-8-2231-2015, 8, 7, (2231-2262), (2015).
  • ERSEM 15.06: a generic model for marine biogeochemistry and the ecosystem dynamics of the lower trophic levels, Geoscientific Model Development Discussions, 10.5194/gmdd-8-7063-2015, 8, 8, (7063-7187), (2015).
  • The Haber Bosch–harmful algal bloom (HB–HAB) link, Environmental Research Letters, 10.1088/1748-9326/9/10/105001, 9, 10, (105001), (2014).
  • iMarNet: an ocean biogeochemistry model intercomparison project within a common physical ocean modelling framework, Biogeosciences, 10.5194/bg-11-7291-2014, 11, 24, (7291-7304), (2014).

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.