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3.
Proc Natl Acad Sci U S A ; 118(15)2021 04 13.
Article in English | MEDLINE | ID: mdl-33876750

ABSTRACT

The latitudinal gradient in species richness, with more species in the tropics and richness declining with latitude, is widely known and has been assumed to be stable over recent centuries. We analyzed data on 48,661 marine animal species since 1955, accounting for sampling variation, to assess whether the global latitudinal gradient in species richness is being impacted by climate change. We confirm recent studies that show a slight dip in species richness at the equator. Moreover, richness across latitudinal bands was sensitive to temperature, reaching a plateau or declining above a mean annual sea surface temperature of 20 °C for most taxa. In response, since the 1970s, species richness has declined at the equator relative to an increase at midlatitudes and has shifted north in the northern hemisphere, particularly among pelagic species. This pattern is consistent with the hypothesis that climate change is impacting the latitudinal gradient in marine biodiversity at a global scale. The intensification of the dip in species richness at the equator, especially for pelagic species, suggests that it is already too warm there for some species to survive.


Subject(s)
Aquatic Organisms/physiology , Biodiversity , Global Warming , Biomass
4.
PLoS Biol ; 18(7): e3000736, 2020 07.
Article in English | MEDLINE | ID: mdl-32634138

ABSTRACT

Lists of species underpin many fields of human endeavour, but there are currently no universally accepted principles for deciding which biological species should be accepted when there are alternative taxonomic treatments (and, by extension, which scientific names should be applied to those species). As improvements in information technology make it easier to communicate, access, and aggregate biodiversity information, there is a need for a framework that helps taxonomists and the users of taxonomy decide which taxa and names should be used by society whilst continuing to encourage taxonomic research that leads to new species discoveries, new knowledge of species relationships, and the refinement of existing species concepts. Here, we present 10 principles that can underpin such a governance framework, namely (i) the species list must be based on science and free from nontaxonomic considerations and interference, (ii) governance of the species list must aim for community support and use, (iii) all decisions about list composition must be transparent, (iv) the governance of validated lists of species is separate from the governance of the names of taxa, (v) governance of lists of accepted species must not constrain academic freedom, (vi) the set of criteria considered sufficient to recognise species boundaries may appropriately vary between different taxonomic groups but should be consistent when possible, (vii) a global list must balance conflicting needs for currency and stability by having archived versions, (viii) contributors need appropriate recognition, (ix) list content should be traceable, and (x) a global listing process needs both to encompass global diversity and to accommodate local knowledge of that diversity. We conclude by outlining issues that must be resolved if such a system of taxonomic list governance and a unified list of accepted scientific names generated are to be universally adopted.


Subject(s)
Classification , Biodiversity , Decision Making , Knowledge , Reproducibility of Results , Species Specificity
5.
Proc Natl Acad Sci U S A ; 117(23): 12891-12896, 2020 06 09.
Article in English | MEDLINE | ID: mdl-32457146

ABSTRACT

A major research question concerning global pelagic biodiversity remains unanswered: when did the apparent tropical biodiversity depression (i.e., bimodality of latitudinal diversity gradient [LDG]) begin? The bimodal LDG may be a consequence of recent ocean warming or of deep-time evolutionary speciation and extinction processes. Using rich fossil datasets of planktonic foraminifers, we show here that a unimodal (or only weakly bimodal) diversity gradient, with a plateau in the tropics, occurred during the last ice age and has since then developed into a bimodal gradient through species distribution shifts driven by postglacial ocean warming. The bimodal LDG likely emerged before the Anthropocene and industrialization, and perhaps ∼15,000 y ago, indicating a strong environmental control of tropical diversity even before the start of anthropogenic warming. However, our model projections suggest that future anthropogenic warming further diminishes tropical pelagic diversity to a level not seen in millions of years.


Subject(s)
Biodiversity , Climate Change , Plankton/physiology , Animals , Fossils , Geologic Sediments , Tropical Climate
6.
Environ Toxicol Chem ; 39(2): 492-499, 2020 02.
Article in English | MEDLINE | ID: mdl-31692086

ABSTRACT

Tributyltin is an organotin chemical that has been commonly used in ship antifouling paints. Despite the global total prohibition of tributyltin-based paint in 2008, tributyltin continues to be found at toxic levels in areas of high maritime traffic such as ports and harbors. A remediation program was conducted at a New Zealand port to reduce tributyltin and copper concentrations to acceptable values. The present study assessed the efficacy of the program using a combination of chemical analyses and copepod bioassays. Sediment and water samples were collected at 3 locations along a spatial gradient within the port, and concentrations of various organotin compounds and trace metal levels were measured pre- and postremediation. The toxicity of sediment and elutriate samples was estimated by benthic and pelagic copepod bioassays. Although acute toxicity in sediment samples was reduced following remediation, reproductive success was still affected for the benthic copepod. This approach combining chemical analysis and bioassays is promising for assessing the efficacy of remediation processes at contaminated marine sites. Environ Toxicol Chem 2020;39:492-499. © 2019 SETAC.


Subject(s)
Copepoda/drug effects , Copper/analysis , Environmental Monitoring/methods , Environmental Restoration and Remediation , Trialkyltin Compounds/analysis , Water Pollutants, Chemical/analysis , Animals , Biological Assay , Copper/toxicity , Geologic Sediments/chemistry , New Zealand , Paint/analysis , Seawater/chemistry , Ships , Trialkyltin Compounds/toxicity , Water Pollutants, Chemical/toxicity
7.
Science ; 365(6451): 332-333, 2019 07 26.
Article in English | MEDLINE | ID: mdl-31346058
8.
Sci Rep ; 9(1): 9303, 2019 06 26.
Article in English | MEDLINE | ID: mdl-31243329

ABSTRACT

Global scale analyses have recently revealed that the latitudinal gradient in marine species richness is bimodal, peaking at low-mid latitudes but with a dip at the equator; and that marine species richness decreases with depth in many taxa. However, these overall and independently studied patterns may conceal regional differences that help support or qualify the causes in these gradients. Here, we analysed both latitudinal and depth gradients of species richness in the NW Pacific and its adjacent Arctic Ocean. We analysed 324,916 distribution records of 17,414 species from 0 to 10,900 m depth, latitude 0 to 90°N, and longitude 100 to 180°N. Species richness per c. 50 000 km2 hexagonal cells was calculated as alpha (local average), gamma (regional total) and ES50 (estimated species for 50 records) per latitudinal band and depth interval. We found that average ES50 and gamma species richness decreased per 5° latitudinal bands and 100 m depth intervals. However, average ES50 per hexagon showed that the highest species richness peaked around depth 2,000 m where the highest total number of species recorded. Most (83%) species occurred in shallow depths (0 to 500 m). The area around Bohol Island in the Philippines had the highest alpha species richness (more than 8,000 species per 50,000 km2). Both alpha and gamma diversity trends increased from the equator to latitude 10°N, then further decreased, but reached another peak at higher latitudes. The latitudes 60-70°N had the lowest gamma and alpha diversity where there is almost no ocean in our study area. Model selection on Generalized Additive Models (GAMs) showed that the combined effects of all environmental predictors produced the best model driving species richness in both shallow and deep sea. The results thus support recent hypotheses that biodiversity, while highest in the tropics and coastal depths, is decreasing at the equator and decreases with depth below ~2000 m. While we do find the declines of species richness with latitude and depth that reflect temperature gradients, local scale richness proved poorly correlated with many environmental variables. This demonstrates that while regional scale patterns in species richness may be related to temperature, that local scale richness depends on a greater variety of variables.

10.
Ecotoxicol Environ Saf ; 174: 611-617, 2019 Jun 15.
Article in English | MEDLINE | ID: mdl-30875554

ABSTRACT

Well validated and reliable biological assays using local and native species are required to characterise the impacts of pollution on ecosystem health. We identified a native estuarine pelagic copepod species suitable for assessing the ecotoxicological impact of anthropogenic contaminants. Gladioferens pectinatus fulfilled the necessary-selection criteria of: wide distribution and abundance across New Zealand estuaries, ease of maintenance in the laboratory, short life cycle, sensitivity to toxicants with different modes of action, and providing reproducibility of biological response to toxicants. Measured endpoints were survival and larval development rate for the nauplii, and survival, realized offspring and total potential offspring for adults. LC50 values for the survival of G. pectinatus exposed to copper, phenanthrene and chlorpyrifos were 170 (143-193), 181.3 (131.3-231.3) and 4.3 (3.8-4.9) µg/L, respectively. The most sensitive chronic endpoint identified for G. pectinatus was the larval development rate, with EC50 values of 49.8 (45-55.3), 31.3 (24.8-44.7) and 1.97 (1.6-2.31) µg/L for copper, phenanthrene and chlorpyrifos, respectively. The acute and chronic responses obtained for G. pectinatus against the three reference toxicants are comparable with those reported for other copepod species and confirm its sensitivity and suitability to assess the toxicity of New Zealand estuarine samples.


Subject(s)
Biological Assay/methods , Copepoda/drug effects , Toxicity Tests, Acute/methods , Toxicity Tests, Chronic/methods , Water Pollutants, Chemical/toxicity , Animals , Chlorpyrifos/toxicity , Copepoda/growth & development , Copper/toxicity , Larva/drug effects , Lethal Dose 50 , New Zealand , Phenanthrenes/toxicity , Reproducibility of Results
11.
Nat Ecol Evol ; 3(4): 539-551, 2019 04.
Article in English | MEDLINE | ID: mdl-30858594

ABSTRACT

Species distributions and abundances are undergoing rapid changes worldwide. This highlights the significance of reliable, integrated information for guiding and assessing actions and policies aimed at managing and sustaining the many functions and benefits of species. Here we synthesize the types of data and approaches that are required to achieve such an integration and conceptualize 'essential biodiversity variables' (EBVs) for a unified global capture of species populations in space and time. The inherent heterogeneity and sparseness of raw biodiversity data are overcome by the use of models and remotely sensed covariates to inform predictions that are contiguous in space and time and global in extent. We define the species population EBVs as a space-time-species-gram (cube) that simultaneously addresses the distribution or abundance of multiple species, with its resolution adjusted to represent available evidence and acceptable levels of uncertainty. This essential information enables the monitoring of single or aggregate spatial or taxonomic units at scales relevant to research and decision-making. When combined with ancillary environmental or species data, this fundamental species population information directly underpins a range of biodiversity and ecosystem function indicators. The unified concept we present links disparate data to downstream uses and informs a vision for species population monitoring in which data collection is closely integrated with models and infrastructure to support effective biodiversity assessment.


Subject(s)
Biodiversity , Animals , Models, Theoretical
12.
Biodivers Data J ; (7): e31375, 2019.
Article in English | MEDLINE | ID: mdl-30740024

ABSTRACT

BACKGROUND: Using this dataset, we examined the global geographical distributions of Solenidae species in relation to their endemicity, species richness and latitudinal ranges and then predicted their distributions under future climate change using species distribution modelling techniques (Saeedi et al. 2016a, Saeedi et al. 2016b). We found that the global latitudinal species richness in Solenidae is bi-modal, dipping at the equator most likely derived by high sea surface temperature (Saeedi et al. 2016b). We also found that most of the Solenidae species will shift their distribution ranges polewards due to global warming (Saeedi et al. 2016a). We also provided a comprehensive review of the taxon to test whether the latitudinal gradient in species richness was uni-modal with a peak in the tropics or northern hemisphere or asymmetric and bimodal as proposed previously (Chaudhary et al. 2016). NEW INFORMATION: This paper presents an integrated global geographic distribution dataset for 77 Solenidae taxa, including 3,034 geographic distribution records. This dataset was compiled after a careful data-collection and cleaning procedure over four years. Data were collected using field sampling, literature and from open-access databases. Then all the records went through quality control procedures such as validating the taxonomy of the species by examining and re-identifying the specimens in museum collections and using taxonomic and geographic data quality control tools in the World Register of Marine Species (WoRMS) and the r-OBIS package (Provoost and Bosch 2017). This dataset can thus be further used for taxonomical and biogeographical studies of Solenidae.

13.
14.
Nat Commun ; 9(1): 5085, 2018 11 30.
Article in English | MEDLINE | ID: mdl-30504796

ABSTRACT

Recently, we classified the oceans into 30 biogeographic realms based on species' endemicity. Castro-Insua et al. criticize the choices of dissimilarity coefficients and clustering approaches used in our paper, and reanalyse the data using alternative techniques. Here, we explain how the approaches used in our original paper yield results in line with existing biogeographical knowledge and are robust to alternative methods of analysis. We also repeat the analysis using several similarity coefficients and clustering algorithms, and a neural network theory method. Although each combination of methods produces outputs differing in detail, the overall pattern of realms is similar. The coarse nature of the present boundaries of the realms reflects the limited field data but may be improved with additional data and mapping to environmental variables.


Subject(s)
Cluster Analysis , Neural Networks, Computer , Algorithms
15.
Trends Ecol Evol ; 33(11): 803-805, 2018 11.
Article in English | MEDLINE | ID: mdl-30213659

ABSTRACT

The World Register of Marine Species (WoRMS) is a sustainable model of international collaboration around a centralised database that provides expert validated biodiversity data freely online. This model could be replicated for the over 1.2 million terrestrial and freshwater species to improve quality control and data management in biology and ecology globally.


Subject(s)
Aquatic Organisms/classification , Biodiversity , Databases, Factual , Informatics , Registries , Terminology as Topic
17.
Thomson, Scott A; Pyle, Richard L; Ahyong, Shane T; Alonso-Zarazaga, Miguel; Ammirati, Joe; Araya, Juan Francisco; Ascher, John S; Audisio, Tracy Lynn; Azevedo-Santos, Valter M; Bailly, Nicolas; Baker, William J; Balke, Michael; Barclay, Maxwell V. L; Barrett, Russell L; Benine, Ricardo C; Bickerstaff, James R. M; Bouchard, Patrice; Bour, Roger; Bourgoin, Thierry; Boyko, Christopher B; Breure, Abraham S. H; Brothers, Denis J; Byng, James W; Campbell, David; Ceriaco, Luis M. P; Cernak, Istvan; Cerretti, Pierfilippo; Chang, Chih-Han; Cho, Soowon; Copus, Joshua M; Costello, Mark J; Cseh, Andras; Csuzdi, Csaba; Culham, Alastair; D'Elia, Guillermo; d'Acoz, Cedric d'Udekem; Daneliya, Mikhail E; Dekker, Rene; Dickinson, Edward C; Dickinson, Timothy A; van Dijk, Peter Paul; Dijkstra, Klaas-Douwe B; Dima, Balint; Dmitriev, Dmitry A; Duistermaat, Leni; Dumbacher, John P; Eiserhardt, Wolf L; Ekrem, Torbjorn; Evenhuis, Neal L; Faille, Arnaud; Fernandez-Trianam, Jose L; Fiesler, Emile; Fishbein, Mark; Fordham, Barry G; Freitas, Andre V. L; Friol, Natalia R; Fritz, Uwe; Froslev, Tobias; Funk, Vicki A; Gaimari, Stephen D; Garbino, Guilherme S. T; Garraffoni, Andre R. S; Geml, Jozsef; Gill, Anthony C; Gray, Alan; Grazziotin, Felipe Gobbi; Greenslade, Penelope; Gutierrez, Eliecer E; Harvey, Mark S; Hazevoet, Cornelis J; He, Kai; He, Xiaolan; Helfer, Stephan; Helgen, Kristofer M; van Heteren, Anneke H; Garcia, Francisco Hita; Holstein, Norbert; Horvath, Margit K; Hovenkamp, Peter H; Hwang, Wei Song; Hyvonen, Jaakko; Islam, Melissa B; Iverson, John B; Ivie, Michael A; Jaafar, Zeehan; Jackson, Morgan D; Jayat, J. Pablo; Johnson, Norman F; Kaiser, Hinrich; Klitgard, Bente B; Knapp, Daniel G; Kojima, Jun-ichi; Koljalg, Urmas; Kontschan, Jeno; Krell, Frank-Thorsten; Krisai-Greilhuberm, Irmgard; Kullander, Sven; Latelle, Leonardo; Lattke, John E; Lencioni, Valeria; Lewis, Gwilym P; Lhano, Marcos G; Lujan, Nathan K; Luksenburg, Jolanda A; Mariaux, Jean; Marinho-Filho, Jader; Marshall, Christopher J; Mate, Jason F; McDonough, Molly M; Michel, Ellinor; Miranda, Vitor F. O; Mitroiulm, Mircea-Dan; Molinari, Jesus; Monks, Scott; Moore, Abigail J; Moratelli, Ricardo; Muranyi, David; Nakano, Takafumi; Nikolaeva, Svetlana; Noyes, John; Ohl, Michael; Oleas, Nora H; Orrell, Thomas; Pall-Gergele, Barna; Pape, Thomas; Papp, Viktor; Parenti, Lynne R; Patterson, David; Pavlinov, Igor Ya; Pine, Ronald H; Poczai, Peter; Prado, Jefferson; Prathapan, Divakaran; Rabeler, Richard K; Randall, John E; Rheindt, Frank E; Rhodin, Anders G. J; Rodriguez, Sara M; Rogers, D. Christopher; Roque, Fabio de O; Rowe, Kevin C; Ruedas, Luis A; Salazar-Bravo, Jorge; Salvador, Rodrigo B; Sangster, George; Sarmiento, Carlos E; Schigel, Dmitry S; Schmidt, Stefan; Schueler, Frederick W; Segers, Hendrik; Snow, Neil; Souza-Dias, Pedro G. B; Stals, Riaan; Stenroos, Soili; Stone, R. Douglas; Sturm, Charles F; Stys, Pavel; Teta, Pablo; Thomas, Daniel C; Timm, Robert M; Tindall, Brian J; Todd, Jonathan A; Triebel, Dagmar; Valdecasas, Antonio G; Vizzini, Alfredo; Vorontsova, Maria S; de Vos, Jurriaan M; Wagner, Philipp; Watling, Les; Weakley, Alan; Welter-Schultes, Francisco; Whitmore, Daniel; Wilding, Nicholas; Will, Kipling; Williams, Jason; Wilson, Karen; Winston, Judith E; Wuster, Wolfgang; Yanega, Douglas; Yeates, David K; Zaher, Hussam; Zhang, Guanyang; Zhang, Zhi-Qiang; Zhou, Hong-Zhang.
PLoS. Biol. ; 16(3): e2005075, 2018.
Article in English | Sec. Est. Saúde SP, SESSP-IBPROD, Sec. Est. Saúde SP | ID: but-ib15045
18.
Nat Commun ; 8(1): 1057, 2017 10 20.
Article in English | MEDLINE | ID: mdl-29051522

ABSTRACT

Marine biogeographic realms have been inferred from small groups of species in particular environments (e.g., coastal, pelagic), without a global map of realms based on statistical analysis of species across all higher taxa. Here we analyze the distribution of 65,000 species of marine animals and plants, and distinguish 30 distinct marine realms, a similar proportion per area as found for land. On average, 42% of species are unique to the realms. We reveal 18 continental-shelf and 12 offshore deep-sea realms, reflecting the wider ranges of species in the pelagic and deep-sea compared to coastal areas. The most widespread species are pelagic microscopic plankton and megafauna. Analysis of pelagic species recognizes five realms within which other realms are nested. These maps integrate the biogeography of coastal and deep-sea, pelagic and benthic environments, and show how land-barriers, salinity, depth, and environmental heterogeneity relate to the evolution of biota. The realms have applications for marine reserves, biodiversity assessments, and as an evolution relevant context for climate change studies.


Subject(s)
Aquatic Organisms , Animals , Oceans and Seas , Phylogeography
19.
Sci Adv ; 3(10): e1700419, 2017 10.
Article in English | MEDLINE | ID: mdl-29057321

ABSTRACT

Among the most enduring ecological challenges is an integrated theory explaining the latitudinal biodiversity gradient, including discrepancies observed at different spatial scales. Analysis of Reef Life Survey data for 4127 marine species at 2406 coral and rocky sites worldwide confirms that the total ecoregion richness peaks in low latitudes, near +15°N and -15°S. However, although richness at survey sites is maximal near the equator for vertebrates, it peaks at high latitudes for large mobile invertebrates. Site richness for different groups is dependent on abundance, which is in turn correlated with temperature for fishes and nutrients for macroinvertebrates. We suggest that temperature-mediated fish predation and herbivory have constrained mobile macroinvertebrate diversity at the site scale across the tropics. Conversely, at the ecoregion scale, richness responds positively to coral reef area, highlighting potentially huge global biodiversity losses with coral decline. Improved conservation outcomes require management frameworks, informed by hierarchical monitoring, that cover differing site- and regional-scale processes across diverse taxa, including attention to invertebrate species, which appear disproportionately threatened by warming seas.


Subject(s)
Aquatic Organisms , Biodiversity , Animals , Conservation of Natural Resources , Ecosystem , Environment , Geography , Models, Theoretical , Oceans and Seas , Population Density , Population Dynamics
20.
Curr Biol ; 27(13): 2051, 2017 07 10.
Article in English | MEDLINE | ID: mdl-28697353
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