Current ecological and evolutionary research are increasingly moving from species- to trait-based approaches because traits provide a stronger link to organism’s function and fitness. Trait databases covering a large number of species are becoming available, but such data remains scarce for certain groups. Amphibians are among the most diverse vertebrate groups on Earth, and constitute an abundant component of major terrestrial and freshwater ecosystems. They are also facing rapid population declines worldwide, which is likely to affect trait composition in local communities, thereby impacting ecosystem processes and services. In this context, we introduce AmphiBIO, a comprehensive database of natural history traits for amphibians worldwide. The database releases information on 17 traits related to ecology, morphology and reproduction features of amphibians. We compiled data from more than 1,500 literature sources, and for more than 6,500 species of all orders (Anura, Caudata and Gymnophiona), 61 families and 531 genera. This database has the potential to allow unprecedented large-scale analyses in ecology, evolution, and conservation of amphibians.
|Design Type(s)||data integration objective • database creation objective • species comparison design|
|Measurement Type(s)||ecological traits|
|Technology Type(s)||data item extraction from journal article|
|Sample Characteristic(s)||Anura • Caudata • Gymnophiona|
Machine-accessible metadata file describing the reported data (ISA-Tab format)
Background & Summary
Organisms’ life forms and ecological strategies (simply referred to as ‘traits’) reflect the outcome of continuous evolutionary pressures by biotic and abiotic factors1,2. Traits strongly determine the species’ ability to persist in a variety of environments, including interactions with other species2–5. At evolutionary time scales, the expression of new traits may create opportunities for phylogenetic lineages to explore novel niches, escape from predation or competition, and hence promote speciation by adaptive radiation6–8. At the ecological scale, traits are especially relevant in the study of community assembly where species coexistence is determined by different processes that influence trait composition of the community (e.g., coexisting species share more or less similar traits than expected by chance)4,9,10. Furthermore, species traits are linked to ecosystem functions and services necessary for human well-being (e.g., burrowing behavior alters soil properties, body size is associated with animal nutrient transport capacity, and feeding habits control food web structure)11–14. However, recent biodiversity loss due to anthropogenic causes raise questions about the ability of ecosystems to continue providing these benefits15. Therefore, understanding the mechanisms influencing patterns in trait diversity (or functional diversity), including human disturbance, is increasingly needed in face of rapid global changes16,17.
The last decade experienced a surge in the availability of natural history trait (i.e., morphological, ecological and reproduction traits) databases with broad taxonomic coverage18–22 allowing unprecedented broad scale approaches in ecology and evolution23–26. Such data are still scarce for many amphibian species27–29. Amphibians are among the most diverse vertebrate groups on Earth, with more than 7,400 species and dozens of new species described every year30. They are abundant in many terrestrial and freshwater ecosystems, where they perform important ecosystem functions31,32. They are also the most threatened vertebrate group worldwide, with many species on the edge of extinction33,34. As such, it is urgent to improve our knowledge on amphibian traits in order to assess and predict their response to environmental changes and create conservation strategies that guarantee their survival.
In this context, we introduce AmphiBIO, an extensive database containing natural history traits for 6,775 amphibian species globally. AmphiBIO releases information on error-checked and referenced traits related to ecology, morphology and reproduction features of amphibians. Trait information was assembled from more than 1,500 literature sources, including peer-reviewed papers, existing life history databases, and other aggregated sources, in order to stimulate more comprehensive research in ecology, evolution, and conservation of amphibians. To enhance data quality, we implemented a protocol in which incorporated data were double-checked for potential errors. By making this data available to the scientific community we aim to advance the sharing of biological data and support a more integrative trait-based evolutionary and ecological science.
In order to select a comprehensive set of relevant traits, while being as efficient as possible on the balance between searching effort and data collection, we surveyed amphibian traits commonly reported in scientific literature and/or existent in smaller data sets. Based on this initial survey, we selected 17 traits related to amphibian ecology, morphology, and reproduction, as described in Table 1. These traits reflect a variety of ecological strategies, niches, and functional roles, also collected for other vertebrate groups, which opens possibilities of joint analyses with other databases (e.g., PanTHERIA18, EltonTraits20, and21).
We conducted a systematic search in the literature primarily from peer-reviewed scientific publications, accessed on-line through academic platforms such as Google Scholar, Web of Science and Zoological Record, although printed material was also consulted whenever available. Furthermore, we assembled data from books, field guides, specialized websites (e.g., amphibiaweb.org), and from gray literature (e.g., technical reports, government documents, monographs, theses and dissertations). We also incorporated data from eleven smaller pre-existing data sets available on-line or kindly provided by their authors (Table 2), and previous data compilations by the authors.
We followed Frost30 for taxonomy. Due to the increasing number of amphibian species discovered every year, we limited our taxonomic coverage on the list of species described until 2011 (6,775 species)30. We standardized taxonomic classification from the various literature sources, as well as resolved formatting inconsistencies or spelling errors, using the Amphibian Species of the World website (http://research.amnh.org/vz/herpetology/amphibia/). Future versions of AmphiBIO will include newly discovered species and taxonomic revisions following Amphibian Species of the World.
AmphiBIO can be downloaded from Figshare repository record (Data Citation 1) under a CC-BY license, which permits distribution of derivatives.
Details for the trait data are summarized in Table 1. In total, we extracted and aggregated the data from the 1,788 literature sources. The data provided here has 30% of data completeness, revealing the limited knowledge on life history traits for most amphibians31,35,36. Analyzing by Order, this corresponds to 29.5% of possible data for Anura, 35.4% for Caudata and 20% for Gymnophiona (Fig. 1). The lower average data completeness for Gymnophiona is probably related to fossorial and cryptic habits that make ecological data scarcer for this group35. In addition, missing information for Gymnophiona is in accordance with the vast percentage of data deficient species (e.g., on the IUCN redlist). However, data completeness varies largely among traits (Fig. 1). Specifically, traits representing overall habitat use, body size and coarse reproduction features (Reproductive_output_y and Breeding strategy) received the larger proportion of data completeness. In contrast, traits related to Diet, time of activity (Diel and Seasonality), body mass, age at maturity, size at maturity, longevity, litter size and offspring size, were more difficult to obtain, and missing information was more common.
For categorical traits, such as Habitat, Diet, Diel and Seasonality, we reported multiple trait categories if documented so in the literature (Table 1). For instance, a frog may be documented by one author as ground-dwelling, but may have been found perching on trees by other authors. In this case, we reported both terrestrial and arboreal behaviors for that species. We adopted a binary classification for categorical traits, where a 1 was assigned if a specific trait category was recorded in the literature for a given taxon, and a NA was assigned if a specific trait category has never been recorded in the literature for a given taxon. We advise caution when interpreting NA, considering that a given trait may not be definitely absent, but rather it has never been reported so in the literature, at least to our knowledge. By adopting this categorization scheme, we hope to accommodate the lack of sufficient ecological knowledge for the vast majority on amphibian species31,35,36. We do not use relative importance of trait categories as this information was absent in most literature searches; therefore we assume trait categories as equally important.
In Anura, we reported body size as snout to vent length (SVL). In Gymnophiona and Caudata, body size is reported as total length (TL). When TL was not reported for Caudata, but individual measurements for SVL and tail length were available, we reported TL as the sum of SVL and tail length. Given tail autotomy in several groups, some references report only SVL for Caudata. In these cases, we reported SVL and flagged this information in the field ‘OBS’. There is no standardization for the measurement of egg size in amphibians. Sometimes this measure is presented in the literature as ‘vitellus diameter’, which considers embryo dimensions. It can also be referred to as ‘total diameter’, when the thickness of external jelly capsules is also considered. As a rule, our data on egg size refer to vitellus diameter, except for the species of which there are only available data for total diameter. However, this later information is not present in the database. Further details for each trait data is given in Table 1. Moreover, any issue we considered important at the moment of data searching, such as discordances between current species name and the name in the literature record, was reported in the field ‘OBS’.
We implemented three procedures to detect inconsistency in data entry before publishing the first version of this database. Data identified as outliers by any of the adopted validation procedures were flagged, checked for validity based on multiple literature sources, and either corrected or purged whenever necessary from the database.
Firstly, we used Bonferroni’s test of Studentized residuals to identify outliers in continuous variables that were unusual with respected to allometric relationships with body size37. Because there may be vast differences in trait variation between different taxonomic levels, in order to maximize the detection of outliers that could be checked for validity we repeated this procedure considering allometric relationships within taxonomic levels (i.e., Order, Family and Genus). To have sufficient statistical power, we omitted clades composed by less than 6 species with data. Secondly, we used ANOVA with taxonomic level as the grouping variable to identify data values that were significant outliers from general trends (standardized residual >3)38. Similarly to Bonferroni’s test, we fitted separate one-way ANOVAs for each taxonomic level (i.e., Order, Family and Genus), and omitted clades composed by less than 6 species. Thirdly, we applied the Attribute Value Frequency (AVF) algorithm to detect outliers in categorical variables39. AVF score represents the infrequentness of an attribute value by calculating the number of times this value is found in the dataset39. In all cases, correction was applied whenever necessary.
A total of 11,614 cells from our database were flagged and validated. We found an error rate of ~0.01% and no other errors after another 100 random data sample. AmphiBIO will undoubtedly benefit from further quality control and curation. We aim to facilitate this process by sharing through this archive online (see Usage Notes).
The data release is available from Figshare repository record (Data Citation 1) in a compressed (.zip) folder containing four files as described below. Lack of information is indicated as NA.
(1) ASC file, Windows-1,252 encoding.
(2) ASC file, Windows-1,252 encoding.
(3) PDF file.
(4) PDF file.
Header information (Headers describe the information of each column):
(1) id, Order, Family, Genus, Species, Fos, Ter, Aqu, Arb, Leaves, Flowers, Seeds, Fruits, Arthro, Vert, Diu, Noc, Crepu, Wet_warm, Wet_cold, Dry_warm, Dry_cold, Body_mass_g, Age_at_maturity_min_y, Age_at_maturity_max_y, Body_size_mm, Size_at_maturity_min_mm, Size_at_maturity_max_mm, Longevity_max_y, Litter_size_min_n, Litter_size_max_n, Reproductive_output_y, Offspring_size_min_mm, Offspring_size_max_mm, Dir, Lar, Viv, OBS.
(2) id, Order, Family, Genus, Species, Reference.
(3) Does not apply.
(4) Does not apply.
How to cite this article: Oliveira, B. F. et al. AmphiBIO, a global database for amphibian ecological traits. Sci. Data. 4:170123 doi: 10.1038/sdata.2017.123 (2017).
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Petchey, O. L. & Gaston, K. J. Functional diversity: back to basics and looking forward. Ecol. Lett. 9, 741–758 (2006).
McGill, B. J., Enquist, B. J., Weiher, E. & Westoby, M. Rebuilding community ecology from functional traits. Trends Ecol. Evol. 21, 178–185 (2006).
Petchey, O. L. & Gaston, K. J. Extinction and the loss of functional diversity. Proc. Biol. Sci. 269, 1721–1727 (2002).
Ingram, T. & Shurin, J. B. Trait-based assembly and phylogenetic structure in northeast Pacific rockfish assemblages. Ecology 90, 2444–2453 (2009).
Swenson, N. G. & Weiser, M. D. Plant geography upon the basis of functional traits: an example from eastern North American trees. Ecology 91, 2234–2241 (2010).
Pyron, R. A. & Burbrink, F. T. Extinction, ecological opportunity, and the origins of global snake diversity. Evolution 66, 163–178 (2012).
Arbuckle, K. & Speed, M. P. Antipredator defenses predict diversification rates. Proc. Natl. Acad. Sci. 112, 13597–13602 (2015).
Shi, J. J. & Rabosky, D. L. Speciation dynamics during the global radiation of extant bats. Evolution (NY) 69, 1528–1545 (2015).
Webb, C. O., Ackerly, D. D., McPeek, M. A. & Donoghue, M. J. Phylogenies and Community Ecology. Annu. Rev. Ecol. Syst. 33, 475–505 (2002).
Cavender-Bares, J., Ackerly, D. D., Baum, D. A. & Bazzaz, F. A. Phylogenetic overdispersion in Floridian oak communities. Am. Nat. 163, 823–843 (2004).
Tilman, D., Lehman, C. L. & Thomson, K. T. Plant diversity and ecosystem productivity: theoretical considerations. Proc. Natl. Acad. Sci. USA 94, 1857–1861 (1997).
Díaz, S. et al. Incorporating plant functional diversity effects in ecosystem service assessments. Proc. Natl. Acad. Sci. USA 104, 20684–20689 (2007).
Flynn, D. F. B., Mirotchnick, N., Jain, M., Palmer, M. I. & Naeem, S. Functional and phylogenetic diversity as predictors of biodiversity-ecosystem-function relationships. Ecology 92, 1573–1581 (2011).
Soliveres, S. et al. Biodiversity at multiple trophic levels is needed for ecosystem multifunctionality. Nature 536, 456–459 (2016).
Díaz, S. et al. Functional traits, the phylogeny of function, and ecosystem service vulnerability. Ecol. Evol 3, 2958–2975 (2013).
Vitousek, P. M. Human Domination of Earth’s Ecosystems. Science (80-.) 277, 494–499 (1997).
Chapin, F. S. et al. Consequences of changing biodiversity. Nature 405, 234–242 (2000).
Jones, K. E. et al. PanTHERIA: a species-level database of life history, ecology, and geography of extant and recently extinct mammals. Ecology 90, 2648 (2009).
Kattge, J. et al. TRY—a global database of plant traits. Glob. Chang. Biol 17, 2905–2935 (2011).
Wilman, H. et al. EltonTraits 1.0: Species-level foraging attributes of the world’s birds and mammals. Ecology 95, 2027–2027 (2014).
Myhrvold, N. P. et al. An amniote life-history database to perform comparative analyses with birds, mammals, and reptiles. Ecology 96, 3109–0 (2015).
Madin, J. S. et al. The Coral Trait database, a curated database of trait information for coral species from the global oceans. Sci. Data 3, 160017 (2016).
Safi, K., Armour-Marshall, K., Baillie, J. E. M. & Isaac, N. J. B. Global Patterns of Evolutionary Distinct and Globally Endangered Amphibians and Mammals. PLoS ONE 8, e63582 (2013).
Valcu, M., Dale, J. & Kempenaers, B. rangeMapper: a platform for the study of macroecology of life-history traits. Glob. Ecol. Biogeogr 21, 945–951 (2012).
Boyer, A. G. & Jetz, W. Extinctions and the loss of ecological function in island bird communities. Glob. Ecol. Biogeogr 23, 679–688 (2014).
Oliveira, B. F. et al. Species and functional diversity accumulate differently in mammals. Glob. Ecol. Biogeogr 25, 1119–1130 (2016).
Michaels, C. J., Gini, B. F. & Preziosi, R. F. The importance of natural history and species-specific approaches in amphibian ex-situ conservation. Herpetol. J. 24, 135–145 (2014).
Trochet, A. et al. A database of life-history traits of European amphibians. BDJ 2, e4123 (2014).
Catenazzi, A. State of the World’s Amphibians. Annu. Rev. Environ. Resour. 40, 91–119 (2015).
Frost, D. R. Amphibian Species of the World: an Online Reference. Version 5.5 (31 January, 2011). American Museum of Natural History, New York, USA. Available at http://research.amnh.org/vz/herpetology/amphibia/ (2017).
Cortes, A. M., Ruiz-Agudelo, C. A., Valencia-Aguilar, A. & Ladle, R. J. Ecological functions of neotropical amphibians and reptiles: a review. Univ. Sci. 20, 229 (2014).
Wells, K. D. The ecology and behavior of amphibians (University of Chicago Press, 2007).
Stuart, S. N. et al. Status and trends of amphibian declines and extinctions worldwide. Science 306, 1783–1786 (2004).
Stuart, S. N. & Lynx, Edicions. Conservation International. IUCN--The World Conservation Union. Threatened amphibians of the world (Lynx Edicions, 2008).
Gower, D. J. & Wilkinson, M. Conservation Biology of Caecilian Amphibians. Conserv. Biol. 19, 45–55 (2005).
Wiens, J. J. Global patterns of diversification and species richness in amphibians. Am. Nat. 170, S86–106 (2007).
Cook, R. D. & Weisberg, S . Residuals and influence in regression (Chapman and Hall, 1982).
Zuur, A. F., Ieno, E. N. & Elphick, C. S. A protocol for data exploration to avoid common statistical problems. Methods Ecol. Evol 1, 3–14 (2010).
Koufakou, A., Ortiz, E. G., Georgiopoulos, M., Anagnostopoulos, G. C. & Reynolds, K. M . in 19th IEEE International Conference on Tools with Artificial Intelligence(ICTAI 2007) 210–217 (IEEE, 2007).
Byrne, P. G., Roberts, J. D. & Simmons, L. W. Sperm competition selects for increased testes mass in Australian frogs. J. Evol. Biol 15, 347–355 (2002).
Sodhi, N. S. et al. Measuring the meltdown: drivers of global amphibian extinction and decline. PLoS ONE 3, e1636 (2008).
Moen, D. S. & Wiens, J. J. Phylogenetic evidence for competitively driven divergence: body-size evolution in caribbean treefrogs (Hylidae: Osteopilus). Evolution (NY) 63, 195–214 (2009).
Guyer, C. & Boback, S. Auburn University, COSAM Collections: reptiles and Amphibians Project databases Available at http://www.auburn.edu/academic/science_math/cosam/collections/reptiles_amphibians/projects/vertbodysize.htm (2011).
Santos, J. C. Fast Molecular Evolution Associated with High Active Metabolic Rates in Poison Frogs. Mol. Biol. Evol. 29, 2001–2018 (2012).
Zhang, L. & Lu, X. Amphibians live longer at higher altitudes but not at higher latitudes. Biol. J. Linn. Soc. 106, 623–632 (2012).
Han, X. & Fu, J. Does life history shape sexual size dimorphism in anurans? A comparative analysis. BMC Evol. Biol. 13, 27 (2013).
Foden, W. B. et al. Identifying the World’s Most Climate Change Vulnerable Species: a Systematic Trait-Based Assessment of all Birds, Amphibians and Corals. PLoS ONE 8, e65427 (2013).
Nali, R. C., Zamudio, K. R., Haddad, C. F. B. & Prado, C. P. A. Size-Dependent Selective Mechanisms on Males and Females and the Evolution of Sexual Size Dimorphism in Frogs. Am. Nat. 184, 727–740 (2014).
Slavenko, A. & Meiri, S. Mean body sizes of amphibian species are poorly predicted by climate. J. Biogeogr. 42, 1246–1254 (2015).
Oliveira, B. F., São-Pedro, V. A., Santos-Barrera, G., Penone, C., & Costa, G. C. figshare https://doi.org/10.6084/m9.figshare.4644424 (2017)
BFO thank the financial support from Universidade Federal do Rio Grande do Norte, CAPES and Science without Borders. GCC was supported by CNPq grants 563352/2010-8, 302776/2012-5 and 201413/2014-0. GCC and VASP were supported by NSF Dimensions of biodiversity grants #DEB-1136586 and 1136588. GCC and CP were supported by CAPES/Science without Borders grant PVE 018/2012. GSB was supported by Universidad Nacional Autónoma de México. We thank two undergraduate students, Fernando de Carvalho Araújo and Paulo Fernandes, which helped gather data.
The authors declare no competing financial interests.
About this article
Cite this article
Oliveira, B., São-Pedro, V., Santos-Barrera, G. et al. AmphiBIO, a global database for amphibian ecological traits. Sci Data 4, 170123 (2017). https://doi.org/10.1038/sdata.2017.123
Proceedings of the Royal Society B: Biological Sciences (2020)
Global Ecology and Biogeography (2020)
International Journal for Parasitology (2020)
Heterogeneous relationships between rates of speciation and body size evolution across vertebrate clades
Nature Ecology & Evolution (2020)