Though a third of amphibian species worldwide are thought to be imperiled, existing assessments simply categorize extinction risk, providing little information on the rate of population losses. We conducted the first analysis of the rate of change in the probability that amphibians occupy ponds and other comparable habitat features across the United States. We found that overall occupancy by amphibians declined 3.7% annually from 2002 to 2011. Species that are Red-listed by the International Union for Conservation of Nature (IUCN) declined an average of 11.6% annually. All subsets of data examined had a declining trend including species in the IUCN Least Concern category. This analysis suggests that amphibian declines may be more widespread and severe than previously realized.
Citation: Adams MJ, Miller DAW, Muths E, Corn PS, Grant EHC, Bailey LL, et al. (2013) Trends in Amphibian Occupancy in the United States. PLoS ONE 8(5): e64347. doi:10.1371/journal.pone.0064347
Editor: Han Y. H. Chen, Lakehead University, Canada
Received: February 19, 2013; Accepted: April 12, 2013; Published: May 22, 2013
This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Funding: The authors have no funding or support to report.
Competing interests: The authors have declared that no competing interests exist.
Amphibians have received increasing attention since a crisis of declining populations was first recognized in the late 1980s –. In 2004, a comprehensive global assessment of amphibian status suggested that 32.5% of the world's species and 31.7% of the United States' species were declining . The current extinction rate for amphibians has been estimated to be 211 times the background rate . These numbers indicate that many species have conservation problems but they do not reveal the rate of population loss. Here, we use data from the U.S. Geological Survey's Amphibian Research and Monitoring Initiative (ARMI) to estimate the rate of change in the probability that amphibians occupy ponds and other comparable habitat features across the United States.
Documenting the rate of change in population parameters requires intensive studies that separate true changes in populations from changes in the probability of capture or detection when amphibians are present . Such studies are relatively rare and it is unusual to have sufficient trend data to assess patterns at a national scale. The occupancy estimates produced by ARMI are statistically unbiased because they use repeated surveys to account statistically for the probability of detecting a species that is present . Hence, our trend estimates based on these data are not influenced by changes in detection, though they rely on data points that each have associated error. Each occupancy estimate that we analyze applies to a species at a study area and each study area has a range of inference spanning tens to hundreds of sites. For heuristic purposes, the probability of site occupancy can be thought of as the expected proportion of sites occupied within the study area . These occupancy estimates span a broad range of habitats, geographic areas (Figure 1A), and species including International Union for Conservation of Nature (IUCN) categories ranging from Endangered to Least Concern (Figure 1B).
(A) Location of monitoring areas. (B) Distribution of species among IUCN categories. (C) Number of years monitored in each time series. (D) Mean annual estimates of probability of site occupancy and number of occupancy estimates (N).
Previous large analyses of amphibian time series relied on count data from individual populations –. We present the first broad assessment of amphibian trends to conform with a recommendation to document change in the number of populations rather than change in abundance .
We analyzed estimates of occupancy available at armi.usgs.gov. Each study within ARMI that generated these estimates used some form of repeated observation to detect amphibians –. An observation was usually a visual encounter survey but trapping and calling surveys were sometimes used for logistical reasons or to increase detection probability. Repeated observations were then used to estimate the proportion of sites where a species was present while accounting for imperfect detection . Because the probability of detecting a species that is present is estimated and accounted for in each occupancy estimate, methods need not be standardized across studies and any changes in detection probability over time will not bias trend estimates.
A site was a pond, watershed, plot, or for calling surveys, was the area within hearing distance of a point-survey location. A study area was the range of inference for a set of sites. Each study encompassed a variable number of sites that were monitored for the presence of target species. Multiple species of amphibian were monitored at many of the study areas. Each study generated annual estimates of occupancy using either a single-season occupancy estimator  or a multi-season dynamic occupancy model . In the latter case, a form of model was used that estimates occupancy each year without imposing trends. We analyzed all time-series with two or more consecutive annual occupancy estimates (Figure 1C).
For our analysis of these occupancy estimates, we used generalized-linear mixed models to estimate mean occupancy each year and mean trends in occupancy for each time series of occupancy estimates. We fit models using the lme4 package  in the R programming language . All models used a similar random effects structure with an among-time-series random effect to account for variation in mean occupancy (random intercept) and an among-time-series random effect for factors describing among year differences (random slope). Occupancy estimates were weighted by the inverse of their variance derived from their standard error. We replaced standard errors <0.04 with 0.04 so that no single occupancy estimate would be given disproportionate weight and to account for cases where standard errors were estimated poorly due to occupancy being close to 0 or 1.
To estimate mean occupancy each year, we treated year as a factor. To estimate mean trends over years, we treated year as a continuous covariate where year was standardized to have a mean of 0 for each time series. To compare trends among subsets of the data, we included a fixed effect for one of several grouping variables (IUCN category, taxon, geography, management agency). We allowed differences among groups in both the mean occupancy and the mean trend in occupancy across years. Models were run using a log-link function to estimate relative rates of change in occupancy over years. We report the annual rate of change which is eβ-1 where β is the instantaneous rate of change from the log-linear models. We used the delta method to obtain the SE for the annual rate of change. For comparison, we also ran models using an identity link to estimate absolute instantaneous changes in occupancy. We used likelihood-ratio tests (LRT) to evaluate the null hypothesis of no difference in trend among subsets of the data indicated by the grouping variables.
From 2002 to 2011, ARMI generated 612 estimates of the probability of site occupancy for 108 time series (range 2 to 9 years, Figure 1C), including 45 species and 3 species complexes at 34 study areas. Mean annual estimates of occupancy generally decreased (Figure 1D), changing at a rate of −3.7% (SE = 1.5) annually across all time series (N = 108). All subsets of data that we examined showed a declining trend (Figure 2). The time series for species categorized as Least Concern by the IUCN (N = 96) had a mean annual trend of −2.7% (SE = 1.6), while time series for species in the Endangered, Vulnerable, and Near Threatened categories (N = 12) had a mean annual trend of −11.6% (SE = 4.3). Although the number of imperiled species is highest in the western U.S. , , we did not find geographic differences in the rate of change in occupancy (LRT, , p = 0.906 for East vs. West; LRT, , p = 0.256 for North vs. South). We also did not find convincing differences between anurans and caudates (LRT, , p = 0.644) or on lands managed by different agencies (LRT, , p = 0.280). Conclusions did not differ when linear rather than log-linear models were fit (Table S1). We estimated trends for individual species using a separate model that treats species as a random effect (Table S2). However, data were sparse for most species and the strength of our analysis comes from examining mean trends across a large set of species and areas.
“Red-listed” includes species that the IUCN categorizes as Near Threatened, Vulnerable, or Endangered. The geographic regions of the United States are overlapping and are North or South of 39° latitude or East or West of −104° longitude. Major land managers include the U.S. Fish and Wildlife Service (USFWS) and the National Park Service (NPS). Plotted values are means and standard errors.
Statistically unbiased estimates of the rate of change in amphibian patch occupancy are necessary to understand the scale and severity of amphibian losses , . They are particularly useful for species considered to be of Least Concern whose trends may be more subtle than for species determined to be imperiled at some level by the IUCN. An average loss of 2.7% of occupied sites each year for the species of Least Concern monitored by ARMI is alarming given that these species are thought to be relatively unaffected by global amphibian declines. This finding suggests that the IUCN threat status has been underestimated for some of these species. This is not a criticism of the IUCN effort, but illustrates the added value of statistically robust monitoring data to inform managers and policy makers.
Sites sampled by ARMI were designed to be roughly equivalent to populations but the relationship between sites and populations is variable and not precisely known. We characterize our rate estimates as addressing change in the occupancy of habitat patches but in one study area the scale was small watersheds with an average of 8.6 ponds in each. Trends in occupancy should not be equated with trends in density . Occupancy studies necessarily include occupied and unoccupied patches. Therefore, trends in occupancy reflect a process involving both local extinctions at occupied patches and colonization of unoccupied patches .
Primary hypotheses to explain global amphibian declines are land use change, disease, global climate change, and interactions of these factors with each other or with other stressors like contaminants or habitat degradation . Anthropogenic habitat loss is rare at ARMI study areas. The fungal pathogen associated with chytridiomycosis is found throughout the US and is common in most ,  but not all  ARMI study areas where tested. Presence of the fungus resulted in reduced survival of adult amphibians in one study , but it is difficult to establish a direct link to declines in occupancy. Major die offs of amphibians were not observed in any of the studies analyzed here. The role of climate in changes in occupancy is difficult to evaluate for relatively short time series and we expect that patterns in occupancy caused by climate change will take years to become evident. The decade during which ARMI collected data experienced severe, but not unprecedented, drought . Because most of the amphibians monitored rely on the presence of water for reproduction and development, precipitation patterns are an obvious hypothesis to explain changes in occupancy . The relationship between occupancy trends and any potential driver is likely to vary across regions, habitats, and species necessitating careful specification of mechanisms prior to analysis of drivers.
Because the species and areas that ARMI monitors are not random, the declines we documented cannot be extrapolated directly to the rest of the U.S. or worldwide. This caveat also applies to all existing compilations of trends in amphibian abundance ,. However, it is useful to consider how our trend estimates may compare to the larger population of species and areas in the U.S, which in most cases have larger distributions than our monitoring areas (armi.usgs.gov/national_amphibian_atlas.php). The species and areas monitored by ARMI were generally selected to evaluate the status and trends of amphibians on federally-managed lands at the scale of management units . Such lands are sometimes perceived as better protected than private lands. In many cases, monitoring areas were selected to target a specific imperiled species but, by design, other local species were also monitored. Hence, our analysis includes a broad range of species that span most IUCN categories of endangerment (Figure 1B), but Least Concern species are overrepresented (86% compared to 63% nationally). Also, the first year of occupancy estimates was 2002, long after many severe declines are thought to have begun , –. These factors are evidence that our analysis may underestimate the actual rate of amphibian losses in the United States. However, we emphasize that the true direction and magnitude of sampling bias is unknown and the relatively short time period monitored may not be representative of longer trends. We also note that our estimates of trends are based on estimates of occupancy that each have associated error (see armi.usgs.gov for SEs). Nonetheless, the trends we found represent the only broad assessment of population losses for amphibians in the U.S.
There is more than one way to estimate trends in occupancy estimates. We used log-linear models to estimate occupancy in a given year as a proportion of the previous year's occupancy. A change from 0.5 to 0.25 and a change from 0.1 to 0.05 both represent a 50% decline though the latter might involve a change in the occupancy status of a small number of sites relative to the former. As a result, similar absolute changes in occupancy influence estimates of trend more for areas where occupancy is low than for areas where occupancy is high. An alternative approach is to use linear models that estimate absolute changes in occupancy. Both methods are valid, but their sensitivity to extreme occupancy estimates and the interpretation of their estimates differ. For example, both methods suggest declines in all subsets of data examined (Table S1), but the distribution of trend estimates produced by log-linear models has a greater number of extreme negative estimates (Figure 3).
We provide a synthesis of a monitoring program that is unique in its national scope and use of statistically unbiased occupancy estimates. Our trend estimates are consistent with other analyses showing that amphibians are declining , , , and go further by suggesting that species for which there has been little conservation concern or assessment focus (e.g., common species) may also be declining. While there was some variation across the U.S., the trend was consistently negative. Furthermore, declines are occurring on lands managed by federal agencies with the greatest observed rate of decline on National Park Service lands where management policy prescribes protection of natural ecosystem processes. Overall, the trends we documented suggest that amphibian declines may be more widespread and severe than previously thought.
Comparison of instantaneous trend estimates derived from linear and log-linear models of change in amphibian occupancy at ARMI monitoring areas, 2002–2011.
Trends in the probability of site occupancy by species for ARMI monitoring areas, 2002–2011. The estimated trend effects are annual proportional changes in occupancy and are conditional on a random effect for a variable coding species that was included in the statistical model. Caution should be taken in interpreting results for individual species as data are generally sparse. The strength of our study comes from making inferences across a broad set of species and areas.
Much of the ARMI data were collected in collaboration with one or more natural resource management agencies including the U.S. Fish and Wildlife Service, Bureau of Land Management, National Park Service, U.S. Forest Service, U.S. Department of Defense, or other entities. We thank L. Ball, R. Bury, K. Dodd, D. James, R. Kearney, J. Nichols, and C. Schwalbe for their role in the formation and direction of ARMI. We thank hundreds of people involved in collecting and maintaining ARMI data. In particular, A. Brand, B. Glorioso, B. Hossack, P. Kleeman, S. Mattfeldt, C. Pearl, M. Roth, W. Barichivich, D. Holmes, C. Rochester, C. Brown, A. Backlin, C. Brehme, S. Hathaway, E. Gallegos made major contributions. This manuscript benefited from suggestions by C. Eagle-Smith, J. Erickson, and W. Palen. This paper is contribution number 443 of the U. S. Geological Survey's Amphibian Research and Monitoring Initiative (ARMI). Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government.
Conceived and designed the experiments: MJA DAWM EM PSC EHCG LLB GMF RNF WJS HW SCW. Analyzed the data: MJA DAWM EHCG. Wrote the paper: MJA DAWM. Commented on the manuscript: EM PSC EHCG LLB GMF RNF WJS HW SCW.
- 1. Wake DB (1991) Declining amphibian populations. Science 253: 860. doi: 10.1126/science.253.5022.860
- 2. Wake DB, Vrendenburg VT (2008) Are we in the midst of the sixth mass extinction? A view from the world of amphibians. Proceedings of the National Academy of Sciences (USA) 105: 11466–11473. doi: 10.1073/pnas.0801921105
- 3. Wake DB (2012) Facing extinction in real time. Science 335: 1052–1053. doi: 10.1126/science.1218364
- 4. Stuart SN, Chanson JS, Cox NA, Young BE, Rodrigues ASL, et al. (2004) Status and trends of amphibian declines and extinctions worldwide. Science 306: 1783–1786. doi: 10.1126/science.1103538
- 5. McCallum ML (2007) Amphibian decline or extinction? Current declines dwarf background extinction rate. Journal of Herpetology 41: 483–491. doi: 10.1670/0022-1511(2007)41[483:adoecd]2.0.co;2
- 6. Schmidt BR (2003) Count data, detection probabilities, and the demography, dynamics, distribution, and decline of amphibians. Comptes Rendus Biologies 326: 119–124. doi: 10.1016/s1631-0691(03)00048-9
- 7. MacKenzie DI, Nichols JD, Royle JA, Pollock KH, Bailey LL, et al.. (2006) Occupancy estimation and modeling. Boston, MA, USA: Academic Press. 324 p.
- 8. Green DM (2003) The ecology of extinction: population fluctuation and decline in amphibians. Biological Conservation 111: 331–343. doi: 10.1016/s0006-3207(02)00302-6
- 9. Houlahan JE, Findlay CS, Schmidt BR, Meyer AH, Kuzmin SL (2000) Quantitative evidence for global amphibian population declines. Nature 404: 752–755. doi: 10.1038/35087661
- 10. Alford RA, Dixon PM, Pechmann JHK (2001) Global amphibian population declines. Nature 412: 499–500. doi: 10.1038/35087658
- 11. Green DM (1997) Perspective on amphibian declines: defining the problem and searching for answers. In: Green DM, editor. Amphibians in decline: Canadian studies of a global problem. Herpetological Conservation 1: Society for the Study of Amphibians and Reptiles, St. Louis, MO. pp. 291–308.
- 12. Adams MJ, Pearl CA, Galvan S, McCreary B (2011) Non-native species impacts on pond occupancy by an anuran. Journal of Wildlife Management 75: 30–35. doi: 10.1002/jwmg.29
- 13. Miller DAW, Brehme CS, Hines JE, Nichols JD, Fisher RN (2012) Joint estimation of habitat dynamics and species interactions: disturbance reduces co-occurrence of non-native predators with an endangered toad. Journal of Animal Ecology doi: 10.1111/j.1365-2656.2012.02001.x
- 14. Gould WR, Patla DA, Daley R, Corn PS, Hossack BR, et al. (2012) Estimating occupancy in large landscapes: evaluation of amphibian monitoring in the Greater Yellowstone Ecosystem. Wetlands 32: 379–389. doi: 10.1007/s13157-012-0273-0
- 15. Walls SC, Waddle H, Dorazio RM (2011) Estimating occupancy dynamics in an anuran assemblage from Louisiana, USA. Journal of Wildlife Management 75: 751–761. doi: 10.1002/jwmg.97
- 16. Walls SC, Barichivish WJ, Brown ME, Scott DE, Hossack BR (2013) Influence of drought on salamander occupancy of isolated wetlands on the southeastern coastal plain of the United States. Wetlands 33: 345–354. doi: 10.1007/s13157-013-0391-3
- 17. MacKenzie DI, Nichols JD, Lachman GB, Droege S, Royle JA, et al. (2002) Estimating site occupancy rates when detection probabilities are less than one. Ecology 83: 2248–2255. doi: 10.2307/3072056
- 18. MacKenzie DI, Nichols JD, Hines JE, Knutson MG, Franklin AB (2003) Estimating site occupancy, colonization, and local extinction when a species is detected imperfectly. Ecology 84: 2200–2207. doi: 10.1890/02-3090
- 19. Bates D, Maechler M (2010) lme4: Linear mixed-effects models using S4 classes. R package version 0.999375-37.
- 20. R Development Core Team (2008) R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0.
- 21. Bradford DF (2005) Factors implicated in amphibian population declines in the United States. In: Lannoo M, editor. Amphibian declines: the conservation status of United States species. Berkeley, California, USA: University of California. pp. 915–925.
- 22. Thompson WL, White GC, Gowan C (1998) Monitoring Vertebrate Populations. New York, New York, USA: Academic Press. 365 p.
- 23. Collins JP, Crump ML (2009) Extinction in our times: global amphibian declines. New York, NY, USA: Oxford University Press. 273 p.
- 24. Adams MJ, Chelgren ND, Reinitz D, Cole RA, Rachowicz LJ, et al. (2010) Using occupancy models to understand the distribution of an amphibian pathogen, Batrachochytrium dendrobatidis. Ecological Applications 20: 289–302. doi: 10.1890/08-2319.1
- 25. Muths E, Pilliod DS, Livo LJ (2008) Distribution and environmental limitations of an amphibian pathogen in the Rocky Mountains, USA. Biological Conservation 141: 1484–1492. doi: 10.1016/j.biocon.2008.09.012
- 26. Hossack BR, Adams MJ, Grant EHC, Pearl CA, Bettaso JB, et al. (2010) Low prevalence of chytrid fungus (Batrchochytrium dendrobatidis) in amphibians of U. S. headwater streams. Journal of Herpetology 44: 253–260. doi: 10.1670/09-058.1
- 27. Pilliod DS, Muths E, Scherer RD, Bartelt PE, Corn PS, et al. (2010) Effects of amphibian chytrid fungus on individual survival probability in wild boreal toads. Conservation Biology 24: 1259–1267. doi: 10.1111/j.1523-1739.2010.01506.x
- 28. Cook ER, Seager R, Heim RR Jr, Vose RS, Herweiger C, et al. (2010) Megadroughts in North America: placing IPCC projections of hydroclimatic change in a long-term palaeoclimate context. Journal of Quaternary Science 25: 48–61. doi: 10.1002/jqs.1303
- 29. Corn PS, Muths E, Adams MJ, Dodd CK (2005) The United States Geological Survey's Amphibian Research and Monitoring Initiative. Alytes 22: 65–71.
- 30. Corn PS, Stolzenburg W, Bury RB (1989) Acid precipitation studies in Colorado and Wyoming: interim report of surveys of montane amphibians and water chemistry. Fort Collins, Colorado, USA: U.S. Fish and Wildlife Service Biological Report 80(40.26). 56 p.
- 31. Fellers GM, Drost CA (1993) Disappearance of the Cascades frog (Rana cascadae) at the southern end of its range, California, USA. Biol Conserv 65: 177–181. doi: 10.1016/0006-3207(93)90447-9
- 32. Fisher RN, Shaffer HB (1996) The decline of amphibians in California's great central valley. Conserv Biol 10: 1387–1397. doi: 10.1046/j.1523-1739.1996.10051387.x