Antarctica is experiencing significant ecological and environmental change, which may facilitate the establishment of non‐native marine species. Non‐native marine species will interact with other anthropogenic stressors affecting Antarctic ecosystems, such as climate change (warming, ocean acidification) and pollution, with irreversible ramifications for biodiversity and ecosystem services. We review current knowledge of non‐native marine species in the Antarctic region, the physical and physiological factors that resist establishment of non‐native marine species, changes to resistance under climate change, the role of legislation in limiting marine introductions, and the effect of increasing human activity on vectors and pathways of introduction. Evidence of non‐native marine species is limited: just four marine non‐native and one cryptogenic species that were likely introduced anthropogenically have been reported freely living in Antarctic or sub‐Antarctic waters, but no established populations have been reported; an additional six species have been observed in pathways to Antarctica that are potentially at risk of becoming invasive. We present estimates of the intensity of ship activity across fishing, tourism and research sectors: there may be approximately 180 vessels and 500+ voyages in Antarctic waters annually. However, these estimates are necessarily speculative because relevant data are scarce. To facilitate well‐informed policy and management, we make recommendations for future research into the likelihood of marine biological invasions in the Antarctic region.
ABSTRACTThe zebra mussel, Dreissena polymorpha, is a major biofouling pest of water treatment works, irrigation systems and power stations in Europe and North America. This paper documents current problems associated with zebra mussels in English waterworks. Questionnaires and manual surveys conducted between 2001 and 2003 have revealed that over 30 water treatment works in England suffer problems associated with zebra mussels. Hundreds of tonnes of mussels are being removed each year from raw water intakes, pipelines and reservoirs. Problems have increased in. the last five years, due to a spread in the range of zebra mussels around England and the cessation of chemical treatment at the intakes of many treatment facilities during the 1990s. The importance of taking control of zebra mussels into account in planning new water supply schemes is highlighted.
AbstractThe substantial filtration capacity of freshwater mussels makes them attractive tools for environmental management. In this study, we applied a central composite design to estimate independent variables and establish optimal conditions of filtration rate and faeces production that enhance filtration of suspended organic matter by the freshwater mussel Sinanodonta woodiana. The results indicated that statistical design methodology offers an efficient and feasible approach for identifying optimal conditions for high filtration and low faeces production, using just a small number (30) of individuals. The proposed model equation takes into account the quantitative effect of variables and also the influence of interactions among variables on mussel filtration rate. Under the optimal experimental conditions (mussel size, 13.0 ± 0.2 cm; flow rate, 17.5 L/h), the experimental filtration rate of 4.47 ± 1.82 L/mussel/h showed a degree of correspondence with the predicted value of 8.4 L/mussel/h, which verified the practicability of this optimum strategy. Our findings contribute to our understanding of the context‐specific ecosystem engineering provided by mussels in natural systems, and also provides a framework for optimizing conditions for the applied use of mussels as biological filters.
Unprecedented rates of introduction and spread of non-native species pose burgeoning challenges to biodiversity, natural resource management, regional economies, and human health. Current biosecurity efforts are failing to keep pace with globalization, revealing critical gaps in our understanding and response to invasions. Here, we identify four priority areas to advance invasion science in the face of rapid global environmental change. First, invasion science should strive to develop a more comprehensive framework for predicting how the behavior, abundance, and interspecific interactions of non-native species vary in relation to conditions in receiving environments and how these factors govern the ecological impacts of invasion. A second priority is to understand the potential synergistic effects of multiple co-occurring stressors— particularly involving climate change—on the establishment and impact of non-native species. Climate adaptation and mitigation strategies will need to consider the possible consequences of promoting non-native species, and appropriate management responses to non-native species will need to be developed. The third priority is to address the taxonomic impediment. The ability to detect and evaluate invasion risks is compromised by a growing deficit in taxonomic expertise, which cannot be adequately compensated by new molecular technologies alone. Management of biosecurity risks will become increasingly challenging unless academia, industry, and governments train and employ new personnel in taxonomy and systematics. Fourth, we recommend that internationally cooperative biosecurity strategies consider the bridgehead effects of global dispersal networks, in which organisms tend to invade new regions from locations where they have already established. Cooperation among countries to eradicate or control species established in bridgehead regions should yield greater benefit than independent attempts by individual countries to exclude these species from arriving and establishing.
Identification of ecosystem services, i.e. the contributions that ecosystems make to human well-being, has proven instrumental in galvanising public and political support for safeguarding biodiversity and its benefits to people. Here we synthe-sise the global evidence on ecosystem services provided and disrupted by freshwater bivalves, a heterogenous group of >1200 species, including some of the most threatened (in Unionida) and invasive (e.g. Dreissena polymorpha) taxa globally. Our systematic literature review resulted in a data set of 904 records from 69 countries relating to 24 classes of provision-ing (N = 189), cultural (N = 491) and regulating (N = 224) services following the Common International Classification of Ecosystem Services (CICES). Prominent ecosystem services included (i) the provisioning of food, materials and medicinal products, (ii) knowledge acquisition (e.g. on water quality, past environments and historical societies), ornamental and other cultural contributions, and (iii) the filtration, sequestration, storage and/or transformation of biological and physico-chemical water properties. About 9% of records provided evidence for the disruption rather than provision of ecosystem services. Synergies and trade-offs of ecosystem services were observed. For instance, water filtration by freshwater bivalves can be beneficial for the cultural service 'biomonitoring', while negatively or positively affecting food consumption or human recreation. Our evidence base spanned a total of 91 genera and 191 species, dominated by Unionida (55% of records, 76% of species), Veneroida (21 and 9%, respectively; mainly Corbicula spp.) and Myoida (20 and 4%, respectively; mainly Dreissena spp.). About one third of records, predominantly from Europe and the Amer-icas, related to species that were non-native to the country of study. The majority of records originated from Asia (35%), with available evidence for 23 CICES classes, as well as Europe (29%) and North America (23%), where research was largely focused ...
Identification of ecosystem services, i.e. the contributions that ecosystems make to human well-being, has proven instru-mental in galvanising public and political support for safeguarding biodiversity and its benefits to people. Here we synthe-sise the global evidence on ecosystem services provided and disrupted by freshwater bivalves, a heterogenous group of>1200 species, including some of the most threatened (in Unionida) and invasive (e.g.Dreissena polymorpha) taxa globally.Our systematic literature review resulted in a data set of 904 records from 69 countries relating to 24 classes of provision-ing (N=189), cultural (N=491) and regulating (N=224) services following the Common International Classification ofEcosystem Services (CICES). Prominent ecosystem services included (i) the provisioning of food, materials and medicinalproducts, (ii) knowledge acquisition (e.g. on water quality, past environments and historical societies), ornamental andother cultural contributions, and (iii) thefiltration, sequestration, storage and/or transformation of biological andphysico-chemical water properties. About 9% of records provided evidence for the disruption rather than provision ofecosystem services. Synergies and trade-offs of ecosystem services were observed. For instance, waterfiltration by fresh-water bivalves can be beneficial for the cultural service'biomonitoring', while negatively or positively affecting food consumption or human recreation. Our evidence base spanned a total of 91 genera and 191 species, dominated byUnionida (55% of records, 76% of species), Veneroida (21 and 9%, respectively; mainlyCorbiculaspp.) and Myoida(20 and 4%, respectively; mainlyDreissenaspp.). About one third of records, predominantly from Europe and the Amer-icas, related to species that were non-native to the country of study. The majority of records originated from Asia (35%),with available evidence for 23 CICES classes, as well as Europe (29%) and North America (23%), where research waslargely focused on'biomonitoring'. ...
Freshwater mussels are a critically imperiled group of mollusks that play key ecological roles and provide important services to humans. The Ambleminae is the only subfamily of these mussels, endemic to North America. Complete mitogenomes have only been sequenced for two of five tribes of the subfamily. Pleurobema oviforme, Amblema plicata, and Popenaias popeii each belong to tribes Pleurobemini, Amblemini, and Popenaidini, respectively, and have not had published mitogenomes. Thus, this study aims to present the complete mitogenomes for these species, to provide a phylogeny of the Ambleminae and confirm the gene arrangements with representation from each of its tribes. The newly sequenced mitogenomes range from 15,852 to 15,993 nucleotides, are composed of 13 PCGs, 22 tRNAs, and two rRNAs and all share the same (UF1) gene order. ; This work was supported by Portuguese Foundation for Science and Technology (FCT) [grant number ConBioMics/BI-Lic/2019-037 (JTT), grant number SFRH/BD/137935/2018 (AGS)]; COMPETE 2020, Portugal 2020 and the European Union through the ERDF, and by Portuguese Foundation for Science and Technology (FCT) through national funds [UID/Multi/04423/2019] under project ConBiomics: the missing approach for the Conservation of Bivalves Project, and [project number NORTE-01- 0145-FEDER-030286]. Fieldwork in Texas was funded by the U.S. Fish and Wildlife Service, and Texas Parks and Wildlife Department (TPWD) as a Joint Traditional Section 6 Project 407348. ; info:eu-repo/semantics/publishedVersion
Using a new fossil-calibrated mitogenome-based approach, we identified macroevolutionary shifts in mitochondrial gene order among the freshwater mussels (Unionoidea). We show that the early Mesozoic divergence of the two Unionoidea clades, Margaritiferidae and Unionidae, was accompanied by a synchronous split in the gene arrangement in the female mitogenome (i.e., gene orders MF1 and UF1). Our results suggest that this macroevolutionary jump was completed within a relatively short time interval (95% HPD 201–226 Ma) that coincided with the Triassic–Jurassic mass extinction. Both gene orders have persisted within these clades for ~200 Ma. The monophyly of the so-called "problematic" Gonideinae taxa was supported by all the inferred phylogenies in this study using, for the first time, the M- and F-type mitogenomes either singly or combined. Within Gonideinae, two additional splits in the gene order (UF1 to UF2, UF2 to UF3) occurred in the Mesozoic and have persisted for ~150 and ~100 Ma, respectively. Finally, the mitogenomic results suggest ancient connections between freshwater basins of East Asia and Europe near the Cretaceous–Paleogene boundary, probably via a continuous paleo-river system or along the Tethys coastal line, which are well supported by at least three independent but almost synchronous divergence events. ; The authors wish to thank the Editor and the three anonymous reviewers for helpful remarks and suggestions that improved the quality of the manuscript. This research was developed under ConBiomics: the missing approach for the Conservation of freshwater Bivalves Project N° NORTE-01-0145-FEDER-030286, cofinanced by COMPETE 2020, Portugal 2020 and the European Union through the ERDF, and by FCT through national funds (UID/Multi/04423/2019). FCT also supported MLL (SFRH/BD/115728/2016). The Russian Ministry of Education and Science (project no. 6.2343.2017/4.6), the Federal Agency for Scientific Organizations (project no. 0409-2015-0143), the Presidium of the Russian Academy of Sciences (scientific program no. 52), and the Russian Foundation for Basic Research, RFBR (project no. 17-45-290066) supported INB. Permits for fieldwork and sampling in Malaysia were issued by the Malaysian Ministry of Higher Education (FRGS/1/2015/WAB13/UNIM//1). ; info:eu-repo/semantics/publishedVersion
The European Union (EU) has recently published its first list of invasive alien species(IAS) of EU concern to which current legislation must apply. The list comprises speciesknown to pose great threats to biodiversity and needs to be maintained and updated.Horizon scanning is seen as critical to identify the most threatening potential IAS thatdo not yet occur in Europe to be subsequently risk assessed for future listing. Accord-ingly, we present a systematic consensus horizon scanning procedure to derive a rankedlist of potential IAS likely to arrive, establish, spread and have an impact on biodiversityin the region over the next decade. The approach is unique in the continental scaleexamined, the breadth of taxonomic groups and environments considered, and themethods and data sources used. International experts were brought together to addressfive broad thematic groups of potential IAS. For each thematic group the experts firstindependently assembled lists of potential IAS not yet established in the EU but poten-tially threatening biodiversity if introduced. Experts were asked to score the specieswithin their thematic group for their separate likelihoods of i) arrival, ii) establishment,iii) spread, and iv) magnitude of the potential negative impact on biodiversity within theEU. Experts then convened for a 2‐day workshop applying consensus methods to com-pile a ranked list of potential IAS. From an initial working list of 329 species, a list of 66species not yet established in the EU that were considered to be very high (8 species),high (40 species) or medium (18 species) risk species was derived. Here, we presentthese species highlighting the potential negative impacts and the most likely biogeo-graphic regions to be affected by these potential IAS.
The complete mitogenomes of one (M-)ale (North America), one Hermaphroditic (Europe), and two (F-)emale (North America and Europe) individuals of the freshwater pearl mussel Margaritifera margaritifera were sequenced. The M-type and F-type (Female and Hermaphroditic) mitogenomes have 17,421 and 16,122 nucleotides, respectively. All with the same content: 13 protein-coding genes, 22 transfer RNA, two ribosomal RNA genes, and one sex-related ORF. The M-type is highly divergent (37.6% uncorrected p-distance) from the F-type mitogenomes. North American and European F-type mitogenomes exhibit low genetic divergence (68 nt substitutions), and the Female and Hermaphroditic European mitogenomes are almost identical, and matching sex-related ORFs. ; This work was supported by Portuguese Foundation for Science and Technology (FCT) [grant number SFRH/BD/115728/2016 (MLL), grant number SFRH/BD/137935/2018 (AGS)]; Russian Foundation for Basic Research [grant number 18-34-20033 (IVV)]; Dawson Fellowship at St. Catharine's College, Cambridge (DCA); Life Margal Ulla [number LIFE09 NAT/ES/000514 (RA and PO)]; COMPETE 2020, Portugal 2020 and the European Union through the ERDF, and by Portuguese Foundation for Science and Technology (FCT) through national funds [UID/Multi/04423/2019] under project ConBiomics: the missing approach for the Conservation of freshwater Bivalves Project, and [project number NORTE-01-0145-FEDER-030286]; Federal Agency for Scientific Organizations under Grants [grant number 0409-2015-0143 (INB and IVV)] ; info:eu-repo/semantics/publishedVersion
The complete mitogenomes of one (M-)ale (North America), one Hermaphroditic (Europe), and two (F-)emale (North America and Europe) individuals of the freshwater pearl mussel Margaritifera margaritifera were sequenced. The M-type and F-type (Female and Hermaphroditic) mitogenomes have 17,421 and 16,122 nucleotides, respectively. All with the same content: 13 protein-coding genes, 22 transfer RNA, two ribosomal RNA genes, and one sex-related ORF. The M-type is highly divergent (37.6% uncorrected p-distance) from the F-type mitogenomes. North American and European F-type mitogenomes exhibit low genetic divergence (68 nt substitutions), and the Female and Hermaphroditic European mitogenomes are almost identical, and matching sex-related ORFs. ; This work was supported by Portuguese Foundation for Science and Technology (FCT) [grant number SFRH/BD/115728/2016 (MLL), grant number SFRH/BD/137935/2018 (AGS)]; Russian Foundation for Basic Research [grant number 18-34-20033 (IVV)]; Dawson Fellowship at St. Catharine's College, Cambridge (DCA); Life Margal Ulla [number LIFE09 NAT/ES/000514 (RA and PO)]; COMPETE 2020, Portugal 2020 and the European Union through the ERDF, and by Portuguese Foundation for Science and Technology (FCT) through national funds [UID/Multi/04423/2019] under project ConBiomics: the missing approach for the Conservation of freshwater Bivalves Project, and [project number NORTE-01-0145-FEDER-030286]; Federal Agency for Scientific Organizations under Grants [grant number 0409-2015-0143 (INB and ...
In: Ricciardi , A , Iacarella , J C , Aldridge , D C , Blackburn , T M , Carlton , J T , Catford , J A , Dick , J T A , Hulme , P E , Jeschke , J M , Liebhold , A M , Lockwood , J L , MacIsaac , H J , Meyerson , L A , Pyšek , P , Richardson , D M , Ruiz , G M , Simberloff , D , Vilà , M & Wardle , D A 2021 , ' Four priority areas to advance invasion science in the face of rapid environmental change ' , Environmental Reviews , vol. 29 , no. 2 , pp. 119-141 . https://doi.org/10.1139/er-2020-0088
Unprecedented rates of introduction and spread of non-native species pose burgeoning challenges to biodiversity, natural resource management, regional economies, and human health. Current biosecurity efforts are failing to keep pace with globalization, revealing critical gaps in our understanding and response to invasions. Here, we identify four priority areas to advance invasion science in the face of rapid global environmental change. First, invasion science should strive to develop a more comprehensive framework for predicting how the behavior, abundance, and interspecific interactions of non-native species vary in relation to conditions in receiving environments and how these factors govern the ecological impacts of invasion. A second priority is to understand the potential synergistic effects of multiple co-occurring stressors— particularly involving climate change—on the establishment and impact of non-native species. Climate adaptation and mitigation strategies will need to consider the possible consequences of promoting non-native species, and appropriate management responses to non-native species will need to be developed. The third priority is to address the taxonomic impediment. The ability to detect and evaluate invasion risks is compromised by a growing deficit in taxonomic expertise, which cannot be adequately compensated by new molecular technologies alone. Management of biosecurity risks will become increasingly challenging unless academia, industry, and governments train and employ new personnel in taxonomy and systematics. Fourth, we recommend that internationally cooperative biosecurity strategies consider the bridgehead effects of global dispersal networks, in which organisms tend to invade new regions from locations where they have already established. Cooperation among countries to eradicate or control species established in bridgehead regions should yield greater benefit than independent attempts by individual countries to exclude these species from arriving and establishing.
Dreissenid mussels (including the zebra mussel Dreissena polymorpha and the quagga mussel D. rostriformis) are among the world's most notorious invasive species, with large and widespread ecological and economic effects. However, their long-term population dynamics are poorly known, even though these dynamics are critical to determining impacts and effective management. We gathered and analyzed 67 long-term (>10 yr) data sets on dreissenid populations from lakes and rivers across Europe and North America. We addressed five questions: (1) How do Dreissena populations change through time? (2) Specifi- cally, do Dreissena populations decline substantially after an initial outbreak phase? (3) Do different measures of population performance (biomass or density of settled animals, veliger density, recruitment of young) follow the same patterns through time? (4) How do the numbers or biomass of zebra mussels or of both species combined change after the quagga mussel arrives? (5) How does body size change over time? We also considered whether current data on long-term dynamics of Dreissena populations are adequate for science and management. Individual Dreissena populations showed a wide range of temporal dynamics, but we could detect only two general patterns that applied across many populations: (1) Populations of both species increased rapidly in the first 1-2 yr after appearance, and (2) quagga mussels appeared later than zebra mussels and usually quickly caused large dedines in zebra mussel populations. We found little evidence that combined Dreissena populations declined over the long term. Different measures of population performance were not congruent; the temporal dynamics of one life stage or population attribute cannot generally be accurately inferred from the dynamics of another. We found no consistent patterns in the long-term dynamics of body size. The long-term dynamics of Dreissena populations probably are driven by the ecological characteristics (e.g., predation, nutrient inputs, water temperature) and their temporal changes at individual sites rather than following a generalized time course that applies across many sites. Existing long-term data sets on dreissenid populations, although dearly valuable, are inadequate to meet research and management needs. Data sets could be improved by standardizing sampling designs and methods, routinely collecting more variables, and increasing support. ; Deutsche Forschungsgemeinschaft (DFG) [JE 288/8-1]; G.E. Hutchinson Chair at the Cary Institute of Ecosystem Studies (DLS); NSF-LTREB grants [DEB-1556246]; NSF-OPUS grant [DEB-1456532]; DFG [JE 288/9-1, JE 288/9-2]; USGS [G14AC000263]; US EPA [GL00E01184]; Cornell Agricultural Experiment Station [NYC-0226747]; New York State Department of Environmental Conservation grants; NSF [1517823]; Belarusian Republican Foundation for Fundamental Research; Mercator Fellowship; [TaMOP-4.2.2.A-11/1/KONV-2012-0038]; [GINOP-2.3.2-15-2016-00019] ; This study is a contribution of the Invasion Dynamics Network (InDyNet), funded by the Deutsche Forschungsgemeinschaft (DFG; JE 288/8-1) including a Mercator Fellowship to DLS. Additional support came from the G.E. Hutchinson Chair at the Cary Institute of Ecosystem Studies (DLS), NSF-LTREB grants (most recently DEB-1556246), and NSF-OPUS grant DEB-1456532 to DLS; DFG projects JE 288/9-1 and JE 288/9-2 to JMJ; TaMOP-4.2.2.A-11/1/KONV-2012-0038 and the GINOP-2.3.2-15-2016-00019 to CSB and LG-T; USGS G14AC000263 and US EPA GL00E01184 to LEB and AYK; Cornell Agricultural Experiment Station NYC-0226747 and New York State Department of Environmental Conservation grants to LGR and ALH, and NSF grant 1517823 (ALH); and the Belarusian Republican Foundation for Fundamental Research to BA and OM. We thank Krzysztof Lewandowski for his help with data from Polish lakes; Mike Davis, the Minnesota Department of Natural Resources, and the United States Army Corps of Engineers for the Lake Pepin data; Kristen Holeck and Ed Mills for help with Oneida Lake data; the Onondaga County Department of Water Environment Protection; Ulrike Scharfenberger for her advice on the statistical analyses; Jaclyn McGuire for helping to gather information for the supplementary materials; Maggie Oudsema; and Juergen Geist, other InDyNet members, and Ladd Johnson, Alex Latzka, and Teresa Newton for helpful comments and suggestions. Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
Multiple national and international trends and drivers are radically changing what biological security means for the United Kingdom (UK). New technologies present novel opportunities and challenges, and globalisation has created new pathways and increased the speed, volume and routes by which organisms can spread. The UK Biological Security Strategy (2018) acknowledges the importance of research on biological security in the UK. Given the breadth of potential research, a targeted agenda identifying the questions most critical to effective and coordinated progress in different disciplines of biological security is required. We used expert elicitation to generate 80 policy-relevant research questions considered by participants to have the greatest impact on UK biological security. Drawing on a collaboratively-developed set of 450 questions, proposed by 41 experts from academia, industry and the UK government (consulting 168 additional experts) we subdivided the final 80 questions into six categories: bioengineering; communication and behaviour; disease threats (including pandemics); governance and policy; invasive alien species; and securing biological materials and securing against misuse. Initially, the questions were ranked through a voting process and then reduced and refined to 80 during a one-day workshop with 35 participants from a variety of disciplines. Consistently emerging themes included: the nature of current and potential biological security threats, the efficacy of existing management actions, and the most appropriate future options. The resulting questions offer a research agenda for biological security in the UK that can assist the targeting of research resources and inform the implementation of the UK Biological Security Strategy. These questions include research that could aid with the mitigation of Covid-19, and preparation for the next pandemic. We hope that our structured and rigorous approach to creating a biological security research agenda will be replicated in other countries and regions. The world, not just the UK, is in need of a thoughtful approach to directing biological security research to tackle the emerging issues.