Cryptic species are a challenge for systematics, but their elucidation also may leave critical information gaps about the distribution, conservation status, and behavior of affected species. We use the leopard frogs of the eastern U.S. as a case study of this issue. We refined the known range of the recently described Rana kauffeldi, the Atlantic Coast Leopard Frog, relative to the region’s two other leopard frog species, conducted assessments of conservation status, and improved methods for separating the three species using morphological field characters. We conducted over 2,000 call and visual surveys and took photographs of and tissue samples from hundreds of frogs. Genetic analysis supported a three-species taxonomy and provided determinations for 220 individual photographed frogs. Rana kauffeldi was confirmed in eight U.S. states, from North Carolina to southern Connecticut, hewing closely to the Atlantic Coastal Plain. It can be reliably differentiated in life from R. pipiens, and from R. sphenocephala 90% of the time, based on such characters as the femoral reticulum patterning, dorsal spot size and number, and presence of a snout spot. However, the only diagnostic character separating R. kauffeldi from R. sphenocephala remains the breeding call described in 2014. Based on our field study, museum specimens, and prior survey data, we suggest that R. kauffeldi has declined substantially in the northern part of its range, but is more secure in the core of its range. We also report, for the first time, apparent extirpations of R. pipiens from the southeastern portion of its range, previously overlooked because of confusion with R. kauffeldi. We conclude with a generalized ecological research agenda for cryptic species. For R. kauffeldi, needs include descriptions of earlier life stages, studies of niche partitioning with sympatric congeners and the potential for hybridization, and identification of conservation actions to prevent further declines.
Citation: Schlesinger MD, Feinberg JA, Nazdrowicz NH, Kleopfer J, Beane JC, Bunnell JF, et al. (2018) Follow-up ecological studies for cryptic species discoveries: Decrypting the leopard frogs of the eastern U.S. PLoS ONE 13(11): e0205805. https://doi.org/10.1371/journal.pone.0205805
Editor: Jake Kerby, University of South Dakota, UNITED STATES
Received: December 20, 2017; Accepted: October 2, 2018; Published: November 9, 2018
Copyright: © 2018 Schlesinger et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: Data on leopard frog calling surveys, visual surveys, and other localities, as well as characteristics derived from photographs of live frogs, are archived at Zenodo: DOI 10.5281/zenodo.1464256. Location data in decimal degrees have been rounded to the tenths place, and in some cases removed entirely, to ensure the protection of at-risk species. Sources and details of environmental layer data used to generate the distribution model, which are not owned by the authors, may be requested from Tim Howard, New York Natural Heritage Program (email@example.com).
Funding: This study was funded by the Northeast Association of Fish and Wildlife Agencies as Regional Conservation Needs grant 2013-03, administered by the Wildlife Management Institute, with matching funds and in-kind from the authors' institutions. J. Feinberg, J. Burger, and E. Kiviat were also supported by grants from the Hudson River Foundation, and B. Shaffer and S. Wenner by the NSF (DEB 1239961). The funders provided support in the form of salaries for authors [MDS, JAF, NHN, JB, EK, SMW, HBS], but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section. EK and DPQ are affiliated with Hudsonia, Ltd. and CTHerpConsultant, LLC, respectively. The commercial affiliations of these two authors did not play any role in the study.
Competing interests: EK and DPQ are affiliated with Hudsonia, Ltd. and CTHerpConsultant, LLC, respectively. The commercial affiliations of these two authors did not play any role in the study. There are no patents or products in development to declare. This does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.
Conservation biologists agree that a clear understanding of a region’s species is essential for biodiversity conservation [1–3]. Knowledge of the status, distribution, and delimitation of individual species within a region is vital for management, as species have distinct habitat needs, ecologies, and behaviors that often require specific policies and management considerations [4–7]. Biological inventories combined with detailed natural history observation are important tools for this, not just to enumerate a region’s species, but also—in some cases—for revealing evidence of new species. Among new species discoveries, cryptic species, defined as species incorrectly grouped under a single taxonomic name, are particularly relevant in areas that are seemingly well understood . In most cases, cryptic species represent two or more species that are morphologically similar and easily confused with one another, but are phylogenetically distinct. For frogs as well as some other vocalizing taxa (e.g., insects, birds), otherwise cryptic species can often be differentiated by their audial signature, and bioacoustic analysis is an important tool for recognizing new or overlooked species . Investigations have uncovered cryptic species in a variety of settings, including surprising locations and among presumably well-known taxa [8,10–12].
The resolution of cryptic species can have ramifications that extend far beyond systematics. When the dust settles and the taxonomy is sorted out, many fundamental questions remain about the ecology, evolution, and conservation of most cryptic species complexes, including 1) What is the distribution of each species? 2) How reliably can the species be distinguished from one another in the field? 3) What bearing does the discovery of one have on our knowledge of the other(s)? 4) Can we reconstruct the historical distributions of each species from museum specimens alone? 5) What is the conservation status of each species? 6) Do cryptic species occur allopatrically or sympatrically with their congener(s)? If they are sympatric, is there niche partitioning, competition, or hybridization associated with range overlap? 7) Do the species have different ecological roles, including their potential role in ecosystem services? 8) For closely related species, what evolutionary mechanism led to speciation? and 9) Do the answers to these questions alter our interpretation of the scientific literature on the revised species complex? Our view is that the systematic clarification of a cryptic species complex is only a first step that must be followed by further investigation. Otherwise, species-specific management and conservation actions will almost certainly be misapplied, potentially to the risk of one or more species.
Several recent studies have followed cryptic species discoveries to attempt to answer some of the questions above, with informational needs varying by the nature of the different species complexes being explored. The recent split of trilling chorus frogs (Pseudacris spp.) and identification of a new species [13,14], for example, prompted local status assessments based on the newly identified species limits and demonstrated sharp declines in one of the contained species [15,16]. Confirmation of cryptic diversity in cavefish  was followed by conservation status assessments that showed many lineages to be of conservation concern . And Trillo et al.  followed the elucidation of cryptic diversity in Amazonian frogs  with a study of behavioral isolating mechanisms.
In this paper, we use the leopard frog species complex, with particular focus on the coastal northeastern United States, to illustrate the need for ecological research following a cryptic species discovery. In doing so, we present the first range-wide study of the newly described Atlantic Coast Leopard Frog (Rana [Lithobates] kauffeldi) along with new information on its two well-known regional congeners, the northern (R. pipiens) and southern (R. sphenocephala) leopard frogs. In the spirit of taxonomic stability, we retain the genus Rana for these frogs, following other recent publications on these species [21,22] that have rejected Lithobates based on currently available data.
Although the existence of three distinct northeastern leopard frogs has been well demonstrated through recent molecular and bioacoustical research [21,23], the natural history of these species has remained uncertain since the discovery of R. kauffeldi. This recent uncertainty is pre-dated by a long history of earlier confusion: despite the fact that some herpetologists had suggested that there might be undocumented leopard frog species in the northeastern U.S. [24–26], all of the region’s leopard frogs were considered R. pipiens for a substantial part of the previous century. Eventually that single-species framework gave way to a two-species taxonomy in the eastern US (adding R. utricularia, later renamed R. sphenocephala) following Pace . Decades later, Newman et al.  documented a distinct genetic lineage in leopard frogs from northern New Jersey, southern New York, and central Connecticut, and Feinberg et al.  formally described this new species as R. kauffeldi, reporting a broader range (Connecticut to North Carolina) documenting for the first time differences in the primary mating call, morphology, and color pattern compared to either R. pipiens, mainly to the north, and R. sphenocephala, whose more southerly range appeared to overlap partially with that of R. kauffeldi.
The preliminary range map in Feinberg et al.  was based on several lines of evidence: genetics from the New York City metropolitan area, museum specimens whose locality and physical appearance could be reliably associated with each species, and bioacoustical sampling from as far south as North Carolina. Those authors used data from three sites with co-located bioacoustics and genetic information to support their conclusion that the distinct mating call they documented was from a genetically distinct species. In addition, Feinberg et al.  built on previous observations of leopard frog patterning and morphology [24,25,27,28] to propose a set of characteristics for reliable distinction among the three species. Feinberg et al.  concluded that additional research was needed to ensure that the patterns reported based on their few samples were reliable range-wide, and so could be used to resolve areas of distributional uncertainty across the entire putative range of R. kauffeldi and to confirm characters that could be used to reliably distinguish animals in the field without genetics or bioacoustics.
In this paper, we provide a particularly complete example of the follow-up research that is necessary when the taxonomy is sorted out for a cryptic species complex, using the leopard frogs of the eastern U.S. as a case study. We refined the range of R. kauffeldi relative to the two other recognized leopard frog species in the region so that managers and researchers in the ten states represented by our authorship team were better informed about which species were present in their state, and mapped new, ecologically informed ranges for all three taxa. Updated knowledge of the three species’ distributions then informed our updated assessments of conservation status, which were especially important in areas where leopard frogs (sensu lato) are already of concern. Finally, we used confirmatory genetic data to improve methods for separating the three species using acoustical and morphological field characters that should facilitate future inventory, monitoring, status assessments, and conservation actions.
Field work conducted in 2014 and 2015 consisted of call and visual surveys to identify populations of each species, followed by sampling frog tissue for genetic analysis. We supplemented this work with examination of museum specimens and compilations of older survey data and a few more recent observations. Our study area was the entire potential range of R. kauffeldi as mapped by Feinberg et al. , encompassing the northeastern portion of the Atlantic Coastal Plain plus southern New England. Sampling occurred in the following U.S. states: Connecticut (CT), Delaware (DE), Maryland (DE), Massachusetts (MA), New Jersey (NJ), New York (NY), North Carolina (NC), Pennsylvania (PA), Rhode Island (RI), and Virginia (VA).
Permits for frog handling and tissue collection were issued by the following agencies: New York State Department of Environmental Conservation, Pennsylvania Fish and Boat Commission, Massachusetts Division of Fisheries and Wildlife, North Carolina Wildlife Resources Commission, Connecticut Department of Energy and Environmental Protection, Delaware Division of Fish and Wildlife, and Maryland Department of Natural Resources. In the other states special collection permission was unnecessary per state regulations or the authority granted state biologists. In states where leopard frogs had legal protection, our permits specifically referenced our permission to work on protected species.
Most calling surveys were conducted from roads or other public access points, and tissue collections were made from roads and from occupied habitats. Special permissions needed for site access were granted by the following agencies and organizations: U.S. Fish and Wildlife Service, The Nature Conservancy, New York State Office of Parks, Resources, and Historic Preservation, Orange County Land Trust (NY), Connecticut Department of Energy & Environmental Protection, Delaware Department of Conservation and Natural Resources, Bucks County (PA) Department of Parks and Recreation, New Jersey Division of Parks and Forestry, New Jersey Division of Fish and Wildlife, New Jersey Audubon Society, and New Jersey Conservation Foundation. For locations on private land, permission was granted by individual landowners prior to sampling.
Call and visual surveys
To locate populations of leopard frogs and identify sites for subsequent sampling, we conducted call surveys in a variety of wetland habitats throughout the study area. Dates of surveys ranged from late February to late March in southern latitudes and from late April to early June in northern latitudes in 2014 and 2015. Because many survey partners had existing frog monitoring programs, and volunteers comprised a portion of the workforce, we allowed for considerable flexibility in survey methodology. At a minimum, observers recorded the GPS coordinates of sampling locations, time spent listening, and species detected. Sampling locations were selected by observers based on habitat suitability, access, and safety considerations. Large wetlands could have multiple sampling locations. Observers were asked to spend a minimum of 3 minutes (though some spent fewer) at each sampling location and to record the survey duration. If survey duration was not recorded, we assumed that it was 3 minutes. Surveys began no earlier than one half-hour after sunset and ended by 1:00 a.m. Surveys were not conducted when temperatures were below 4 degrees Celsius or in heavy rain or high wind. Observers made audio recordings of calls of suspected leopard frogs and the acoustically similar (to R. kauffeldi) Wood Frog (R. sylvatica) for subsequent confirmation from members of the team most familiar with the species.
From spring through fall in 2014 and 2015, we visited sites where we had confirmed the presence of leopard frogs bioacoustically to capture frogs for photographic and genetic analyses. We also visited sites of unknown occupancy and suspected historical occupancy for visual surveys to determine presence. If we encountered leopard frogs, we captured and photographed them following standardized digital imaging protocols (below), clipped the last digit of one toe as a tissue samples, stored the sample in 95% ethanol and shipped them to the University of California, Los Angeles (UCLA) for genetic analysis. We followed the State University of New York College of Environmental Science and Forestry’s Institutional Animal Care and Use Committee protocol #140102, developed specifically for this project, for the temporary care and handling of captured frogs.
To aid in the identification of potentially reliable field characters, we photographed captured frogs from several specific angles (Fig 1) to clearly show the dorsal and ventral surfaces, snout profile, femoral reticulum, tympanum (right and left), and hind foot toe webbing, and matched each image with its corresponding tissue sample. This allowed us to explore many possible diagnostic features, including some of those referenced by Feinberg et al.  as well as earlier studies by Porter  and Moore .
Example of photographs of a captured leopard frog taken from prescribed angles (clockwise from lower left): right side, left side, dorsal, ventral, femoral reticulum, hind foot; and photo measurements (lower right) of head width (A), head length (B), snout width (C), and snout length (D).
We used our photographic data set to test the validity of these characters across the suspected range of R. kauffeldi. A single observer (ELW) with no explicit knowledge of character states suspected to differentiate these species evaluated photos of each genotyped frog to assess 1) number of dorsal spots from snout to vent occurring between the dorsolateral folds (conjoined spots were counted as two spots); 2) snout spot (large, small, or absent); 3) snout shape (blunt, pointed, or intermediate); 4) reticulum coloration (predominantly dark, predominantly light, or intermediate); 5) reticulum pattern (mostly large, connected blotches; or mostly small, unconnected dots); 6) left and right tympanum spot pattern (sharp dot, sharp blotch, or present but indistinct); 7) left and right tympanum spot color (white/cream, green, or brown/bronze); and 8) webbing on the first toe of the left and right hind food (curves all the way to the tip or stops about halfway to the tip). For all characters evaluated qualitatively, the observer had exemplar photographs to guide in interpretation (S1 Appendix).
We also used our dorsal photographs of genetically confirmed R. kauffeldi and R. sphenocephala to quantify snout shape and reticulum coloration, since these characters had been suggested previously to help distinguish these two species [21,29]. For snout shape, we imported each photo into ArcGIS 10.3  and drew lines in four locations (Fig 1): A) along the posterior edge of the eyes, perpendicular to the spine of the frog, connecting the visible edges of the head (“head width”); B) perpendicular from the tip of the snout to line (A) (“head length”); C) along the anterior edge of the eyes but otherwise as in (A) (“snout width”); D) from the tip of the snout to line (C) (“snout length”). We recorded the length of each line in arbitrary map units, and calculated three ratios: head length to head width (B/A), snout length to snout width (D/C), and snout width to head length (C/B). We characterized a subset of reticula using image processing software (S2 Appendix).
Genomic DNA extraction and PCR amplification were performed at UCLA following the methods in Newman et al. . We amplified the nuclear genes neurotrophin-3 (NTF3, 599 bp), tyrosinase (Tyr 557–585 bp), Rag-1 (647–683 bp), seven-in-absentia (SIA, 362–393 bp), and chemokine receptor 4 (CXCR4, 550 bp). PCR products were bidirectionally sequenced at Beckman Coulter Genomics (Danvers, MA, USA). Contigs were assembled and trimmed in Geneious version 6.1.6 . Consensus sequences for each locus were aligned with sequences from Newman et al.  using ClustalW in Geneious and manually adjusted.
To determine how all of the samples grouped into genetic population clusters, we used Structure version 2.3.2 [32,33] with an allelic data set (12–15% missing data) derived from our sequence data. We inferred haplotypes for each locus with a Bayesian algorithm using Phase version 2.1.1 [34,35]. Each allele was represented by a single haplotype. Phase input files were formatted from NEXUS files using a Perl script (RC Thomson, unpublished).
Following the same parameters as Newman et al. , we used Structure to determine the number of genetically distinct clusters (K) in our complete data set. We used the admixture model  and assumed correlation of allele frequencies among clusters and no other a priori population information. We ran 20 iterations of K values from 1 to 10, each with 100,000 generations plus a burn-in of 100,000 generations. We chose the appropriate K value by obtaining likelihood scores using the Evanno method . We then assigned species identifications based on their genetic makeup: frogs were designated as “pure” if they had a 90% or greater match with a single species, while those with a species match between 10% and 90% were designated as “admixed.” We confirmed the robustness of genetic assignment of individuals to PHASE parameter choice and that these results were further validated with likelihood-based phylogenetic methods (S3 Appendix).
Observation data and museum records
To supplement our field work and inform our reconstructions of the historical and current ranges of each species, we gathered observational and survey data from a variety of sources, including those outside the project team in cases where call recordings were available to confirm species identification. To determine the historical ranges of the three leopard frogs, we examined 2,522 museum specimens from the following institutions: American Museum of Natural History, Carnegie-Mellon Museum of Natural History, Cornell University Museum of Vertebrates, Harvard Museum of Comparative Zoology, National Museum of Canada, North Carolina Museum of Natural Sciences, Southern Connecticut State University, Smithsonian National Museum of Natural History, Texas Cooperative Museum, University of Connecticut, and Yale Peabody Museum of Natural History. Based on identification characters from Feinberg et al.  and our own findings, we determined probable species identifications that we used to inform maps of historical ranges. In a small percentage of cases (1–2% of specimens examined) where color patterns had faded or the typical characters used to determine species were unclear, we either made our best informed identification or did not assign a species; these few specimens did not substantially affect our historical distribution assessments. Most or all of these historical specimens had been preserved in formalin, making molecular examination challenging .
Call surveys and genetics.
To test whether the unique call described in Feinberg et al.  was associated with frogs genetically identified as R. kauffeldi, we examined the results of call surveys in the vicinity of locations of genetic samples for the three species. It was not feasible to match calls to genetics at the individual level because of difficulties with collecting tissue from specific, elusive callers in often impenetrable coastal marshes. Instead, we matched calls to genetics at the population level by comparing the genetic identity of sampled frogs (“pure” individuals only) to the results of nearby call surveys (within 100 m and 300 m of each genetically sampled frog).
Morphological and color characters.
We report simple summary statistics and frequencies of different character states for each species. To test for differences among species for particularly important or challenging characters, we used one-way ANOVAs in R version 3.0.2 . In case no single character was diagnostic in distinguishing among species, we used multivariate methods to explore the value of combinations of characters in identifying the species. We used the randomForest package  in R version 3.0.2  to run a random forests classification analysis  on the 16 characters obtained from photos with the genotyped species identification as the dependent variable. Only “pure” individuals were included. Missing values, resulting from photos of certain angles not being submitted or inconclusive images, were treated by running two separate analyses: one in which we imputed them using the function rf.impute and another in which we omitted cases with missing values for some characters. For each analysis, we built 1,000 trees and determined variable importance as the mean decrease in model accuracy without each variable following Strobl et al. .
Species distribution mapping and modeling.
Our final maps of species occurrence are based upon genotyped frogs from this study and Newman et al. , call surveys from this study and Feinberg et al. , incidental documentation of calling frogs by the authors, and other recorded calls or confirmed visual identifications (mainly from 2005–2013, but as far back as the 1990s and some from 2016 and 2017). We developed current range maps for each of the three northeastern leopard frog species using these presence points in combination with previous range maps [21,42] and watershed boundaries. We then used these maps to develop historical range maps (for R. kauffeldi and R. pipiens only) by incorporating museum specimens for which we felt confident in our species determination.
We built a “presence-only” species distribution model for R. kauffeldi following methods in Howard and Schlesinger . In brief, we attributed 169 presence points and 10,000 background points with 81 environmental layers representing climate, geology, topography, and land cover using 30-m grid cells (T. Howard, NY Natural Heritage Program, unpublished). Background points were restricted to a 171,704-km2 modeling area that encompassed the area of known presence, matching 8-digit Hydrological Unit Code boundaries . We used the randomForest package  in R version 3.0.2  to run a classification analysis  to distinguish areas of predicted presence of suitable habitat from areas of predicted lack of suitable habitat. We used the “out-of-bag” estimate of the error rate  and the confusion matrix as measures of the model’s accuracy, determined variable importance following Strobl et al. , and used the results of the analysis to predict the probability of suitable habitat for the modeling area.
Determining conservation status
To help prioritize conservation and management actions, we suggested conservation status ranks for R. kauffeldi for its entire range and for each state in which it was documented. We used the NatureServe and Natural Heritage Program methodology [45,46], to determine conservation status by evaluating a suite of factors representing rarity, threats, and trends to arrive at a G-rank (“global” rank, for the entire range; Table 1) or S-rank (for a state or other subnational jurisdiction). We focused on three rarity factors that we felt our data could best inform—range extent (area encompassed by the outer boundary of presence points), area of occupancy (number of 4-km2 grid cells occupied), and number of occurrences (estimated by counting a detection as a separate occurrence if separated by 5 km of suitable habitat or 1 km of unsuitable habitat; ). For each of these categories, the methodology uses wide value ranges and provides the opportunity to select multiple scores to encapsulate uncertainty.
From http://www.natureserve.org/conservation-tools/conservation-status-assessment. At the subnational level, S-ranks are used.
Our data were less well suited to addressing threat and trend factors, largely due to the lack of species-specific information on threats. Thus, we used the optional factor intrinsic vulnerability, a surrogate for threats representing susceptibility to impacts from human activities based on life history. Amphibians are highly sensitive to disease  and aquatic pollutants [49,50], and R. kauffeldi’s proximity to the coast makes it vulnerable to habitat degradation and loss from coastal storms and rising sea levels [21,51]. Rana kauffeldi and R. sphenocephala were both found to be susceptible to several amphibian diseases (including chytridiomycosis, ranavirus, and a perkinsus-like organism) when reared in outdoor pens on Long Island, in wetlands where leopard frog complex members are now extinct (JAF, unpublished data). On the other hand, R. kauffeldi is known from wetlands near heavy industry , suggesting it may be relatively insensitive to environmental toxins if suitable freshwater habitat exists. Some of these industrial wetlands in southern NY and northern NJ are threatened by development. We characterized intrinsic vulnerability as the combination rating “High or Moderate” for all jurisdictions to reflect the balance between these susceptibilities and apparent tolerances.
Information on trends was mostly lacking given the recent discovery of this species and the difficulty of identifying older museum specimens with certainty. We calculated a G-rank for the overall range and S-ranks for each state in two ways: using NatureServe’s element rank calculator  and based on our interpretation of the data.
We conducted call surveys at 1,004 point locations throughout the northeastern U.S. (Fig 2). Most points were surveyed once, with some surveyed multiple times, for a total of 2,159 surveys. Survey durations ranged from 1 to 110 minutes (mean = 5.76 minutes) and totaled approximately 207 hours. Surveys were conducted between 21 February 2014 and 15 June 2015. Additional call survey data dating back to 2006 were included as available.
Shaded relief map from https://nationalmap.gov/.
Calls from R. kauffeldi were documented as early as 10 March 2014 in MD and 14 March 2015 in DE. Outside the formal window of our field work, calls were documented on 3 February 2016 in NC, 21 February 2017 in VA, and 8 March 2016 in NY. The last call dates for R. kauffeldi in the two project years were 23 April 2014 in PA and 15 April 2015 in NJ. Calls have been heard sporadically in late April and May in NY (JAF, unpublished data), and 12 June 2006 (with the identification confirmed later) in NJ’s Meadowlands .
We collected tissue samples from 254 individual frogs for genetic analysis from throughout the putative range of R. kauffeldi and beyond to include samples of all three species across the region. Of these samples, 251 were successfully extracted, amplified, and sequenced. Three samples had DNA concentrations that were too low for successful PCR amplification and were removed from the analysis. Aligned sequence lengths for nuclear loci were similar to those for a broader set of leopard frog samples for the same loci : 527 bp (CXCR4), 530 bp (NTF3), 648 bp (Rag-1), 388 bp (SIA), and 549 bp (TYR). There were between 31 and 49 variable sites per locus. Individuals that received greater than three null haplotypes were removed from the analysis. In total, 243 of the original 251samples plus 50 individuals determined to be pure R. kauffeldi, R. pipiens, or R. sphenocephala by Newman et al.  went into the final analysis, for a total of 293 frogs. The results of Structure analyses from both the 80% and 90% probability Phase data sets were quantitatively similar (S3 Appendix); given that the 80% Phase probability set was slightly larger, we use it in the remaining analyses.
Bayesian cluster analysis in Structure resolved three clusters (lnL = 4314.60, DK = 130.93). Individuals with a cluster probability greater than 90% were assigned to that cluster, and individuals with a cluster assignment between 10% and 90% were designated as admixed. We assigned species identification to each cluster using the individuals from Newman et al.  as reference samples. A total of 262 individuals fell into one of the three clusters unambiguously, including 111 R. kauffeldi, 79 R. sphenocephala, and 72 R. pipiens (Fig 2). The remaining 32 individuals were considered potential hybrids that we identified by the dominant species based on admixture proportions.
The concatenated maximum likelihood phylogeny identified three major, but poorly supported, clades representing R. kauffeldi, R. pipiens, and R. sphenocephala. There were also a few individuals that could not be attributed to any of these three clades and were generally identified as admixed in the Structure analysis.
We identified and omitted from further analysis four samples that appeared, upon genotyping, to have identification or locality errors. Two samples from one site in central CT appeared to have their labels switched: one was visually R. pipiens but was genotyped as R. kauffeldi, while the other was visually R. kauffeldi but was genotyped as R. pipiens. Both species are known to occur at this site based on other individuals, and together with another site in central CT are the only known sympatric sites for these two species. Two additional samples are identified with question marks in Fig 2. One frog from the southern tip of the Delmarva Peninsula (Northampton Co., VA) appeared visually to be R. sphenocephala but was genotyped as R. kauffeldi. Only calls of R. sphenocephala have been documented in the area and appropriate habitat for R. kauffeldi does not appear to exist at that locality. An additional frog in western NJ near the Delaware River (Gloucester Co.) was genotyped as R. sphenocephala, but no other R. sphenocephala are known from that mesic area of the state. No photographs were associated with this sample, but another frog from the site appears visually to be R. kauffeldi. Leopard frogs from along the Delaware River (Delaware Co., PA) show field characters of both species, so we cannot rule out either species just across the river in NJ. All the above cases of confusion may be highly admixed frogs, and further investigation of these potential hybrid zones is certainly needed.
We confirmed Rana kauffeldi in eight eastern U.S. states: CT, NY, NJ, PA, DE, MD, VA, and NC. We did not detect R. kauffeldi in MA or RI, where only R. pipiens was detected. The two locations farthest from one another in CT and NC are 746 km apart, close to the 780 km estimated by Feinberg et al. . The range of R. kauffeldi that we estimate (Fig 3) covers just over 46,500 km2 from 208 m elevation in northern NJ to sea level in multiple locations. No R. kauffeldi were detected south of the 17°C isocline (i.e., annual average temperature greater than 17°C). Confirmed extremes of the range of R. kauffeldi were as follows (in WGS84): northernmost—Middlesex County, CT (lat 41.63, long -72.62); southernmost—Washington County, NC (lat 35.79, long -76.41); easternmost—Middlesex County, CT (lat 41.60, long -72.61); and westernmost—Sussex County, VA (lat 36.98, long -77.27). A frog collected in 1989 farther south in Hyde, NC (USNM 292558) appears to be R. kauffeldi, but we lack bioacoustic and genetic confirmation at that location.
Historical ranges for R. kauffeldi and R. pipiens are based on examination of museum specimens and recent detections. Question marks denote locations where museum specimens appear to be R. kauffeldi but no bioacoustic or genetic evidence is available, or where genetic determinations were questionable.
The species does not occur far from coastally influenced habitats. The maximum distance the species was documented from the ocean, bays, and estuaries was 40 km near the border of NJ and NY. Eighty-nine percent of R. kauffeldi locations were within 20 km, 77% were within 10 km, and just under 50% were within 1 km of coastal waters.
In portions of its range, R. kauffeldi overlaps with its close congeners. Rana pipiens and R. kauffeldi were documented to be syntopic at the two aforementioned sites in CT, and the ranges of R. sphenocephala and R. kauffeldi overlap broadly from central NJ south to NC, including several instances of syntopy. In central NJ, DE, and MD, they appear to be less frequently sympatric than in VA and NC.
Our survey data also support the view promoted by Feinberg et al.  that R. kauffeldi has disappeared from a large part of its historical range in southern NY and CT (Fig 3), including much of the Hudson Valley and all of Long Island. We could not verify recent reports of leopard frogs from these areas despite considerable survey effort.
We report apparent extirpations of R. pipiens from the southern portion of its known range from PA east through northwestern NJ, southeastern NY, southern CT, southern RI, and coastal MA. We confirmed multiple museum specimens as R. pipiens from these regions, but our surveys and those of the Pennsylvania Amphibian and Reptile Survey , including many historical locations for R. pipiens, have not yielded leopard frogs of any species at those locations (Fig 2), with the exception of a single population near Providence, RI, discovered in 2017. The southernmost location at which we documented extant R. pipiens in the northeastern U.S. was in Middlesex County, CT (lat 41.49, long -72.69). Locations in lower latitudes have been reported by others in central PA  and farther west.
Prior range maps of R. sphenocephala (e.g., [42,55]) included southern NY and northern NJ. As suggested by Feinberg et al. , we confirmed that these areas are occupied, or were formerly occupied, by R. kauffeldi or R. pipiens, not R. sphenocephala. One possible exception is the xeric Pine Barrens of Long Island (NY), where leopard frogs were once common, but few museum specimens exist from this habitat to verify species composition. The northernmost extant locality for R. sphenocephala in our surveys (and apparently anywhere in its entire range) is in Middlesex County, NJ (lat 40.42, long -74.35).
Match of calls to genetics
We found a near-perfect match of population-level calling with genetics of individual frogs. At 16 sites for R. kauffeldi, 18 sites for R. sphenocephala, and 3 sites for R. pipiens, genetically pure frogs of each species were confirmed where calling by that species was documented within 100 m; the only mismatch was one location (Sussex Co., DE) where R. kauffeldi was documented calling but the genetic identification of an individual from that location was R. sphenocephala. The same concordance between calls and genetics held for situations where calling frogs were documented within 300 m of genetic samples (23 sites for R. kauffeldi, 21 for R. sphenocephala, and 11 for R. pipiens); the only potential exceptions were three genetically R. kauffeldi sites that had both R. kauffeldi and R. sphenocephala calling, and the above-noted genetically R. sphenocephala site with R. kauffeldi calls.
Morphological and color characters
We examined 912 photographs of 220 leopard frogs with genetic identities as follows: 80 pure R. kauffeldi, 16 admixed R. kauffeldi, 45 pure R. pipiens, 5 admixed R. pipiens, 64 pure R. sphenocephala, and 10 admixed R. sphenocephala. Not all 220 frogs had suitable photographs of all characters, so sample sizes for each character varied slightly. The comparisons below were based on examination of pure individuals only.
Rana kauffeldi had fewer dorsal spots on average than both R. pipiens and R. sphenocephala in a one-way ANOVA (F174,2 = 15.08, P < 0.0001, with Tukey HSD post-hoc tests), although there was considerable overlap among species (S4 Appendix; Fig 4). Rana sphenocephala and R. pipiens had similar numbers of spots.
Open circles are statistical outliers.
Rana kauffeldi was readily distinguished from R. pipiens by smaller body spots (85% of R. kauffeldi had spots smaller than the eye vs. 36% for R. pipiens), the frequent absence of a snout spot (85% absent vs. 29%), reticula characterized as predominantly dark (97% vs. 0%), and overall duller coloration (S4 Appendix; Fig 5).
Typical patterns in femoral reticula (top row) and dorsal spotting (bottom row) in three species of leopard frogs in the northeastern U.S.
Rana kauffeldi and R. sphenocephala were more challenging to differentiate, as no single character reliably distinguished the two species. Nearly all R. kauffeldi reticula appeared predominantly dark with small, unconnected dots of light pigment, while most R. sphenocephala reticula appeared predominantly light with large, connected blotches of dark pigment (S4 Appendix; Fig 5). The overall coloration of R. kauffeldi was typically duller than that of R. sphenocephala. Rana kauffeldi had sharp tympanum spots less frequently (58% of frogs) than R. sphenocephala (91%), and the snout of R. kauffeldi was more frequently characterized as “blunt” (62% of frogs) than that of R. sphenocephala (13%). The three head measurement ratios were not significantly different between the two species in a one-way ANOVA, although the ratio of snout width to head length was nearly so (F121,1 = 3.899, 0.05 < P < 0.10). The extent of toe webbing and the color of reticulum spots and blotches did not consistently differentiate the three species.
Characters used in combination provided accurate identification in most cases. Random forest analysis using 144 individuals with missing values imputed correctly classified R. kauffeldi and R. sphenocephala in over 90% of cases (out-of-bag estimate of error rate = 9.72%). The most important field characters in distinguishing between species were reticulum color, reticulum pattern, and snout shape. When the analysis was run with cases with missing values omitted (leaving n = 33 individuals), the error rate was similar (9.09%), although the order of important variables shifted somewhat, with ratio of snout width to head length, reticulum color, reticulum pattern, and ratio of head length to head width being most important.
Sample sizes of admixed individuals were insufficient for statistical analyses, but examination of the raw numbers (S4 Appendix) did not show the intermediacy of characteristics that would be expected to result from hybridization.
Habitat association and distribution model
Our surveys found that the basic habitat description in Feinberg et al.  holds. South of the glacial maximum, R. kauffeldi is a habitat specialist restricted to large coastal and riparian wetlands. In the southern portion of its range, it occurs primarily in riparian cypress-gum swamps. Along the Delaware River and Bay, it occupies large freshwater impoundments, tidal guts, and tidal freshwater marshes often dominated by introduced Common Reed (Phragmites australis) marshes that may be subject to salinity intrusions. In the northern, recently glaciated portion of its range, R. kauffeldi typically occupies large freshwater wetlands with open canopies that otherwise are indistinguishable from similar wetlands where it was not detected. Where R. sphenocephala is sympatric with R. kauffeldi, R. sphenocephala is a generalist, being found in nearly any semi-permanent (isolated) or permanent wetlands, created or natural, including tire ruts, fish hatchery ponds, waterfowl impoundments, and cypress-gum swamps. It also appears to be less restricted to xeric habitats in the southern portion of its range than in more northerly locations (e.g., New Jersey).
Our distribution model shows that suitable habitat for R. kauffeldi is concentrated along the coast and in riparian corridors (Fig 6). The model overall was very accurate, with an out-of-bag error estimate of 1.11%, although absences were predicted with greater accuracy (99%) than presences (34%). The factors most closely associated with the presence of R. kauffeldi were low elevation, high impervious surface and more wetlands in the surrounding landscape, and short distances to calcareous bedrock, saltwater or freshwater emergent wetlands, freshwater forested wetlands, and lakes and rivers.
Conservation status of Rana kauffeldi
Because we recognized that a two-year survey, even when supplemented with pre-survey data, could not reveal all locations of R. kauffeldi, we embraced the uncertainty allowed by the NatureServe approach. For example, when our counts of number of grid cells or number of occurrences fell near the boundaries of ranking categories, we selected both categories. We identified a considerable decline in NY and CT based on our surveys and Feinberg et al. , but the evidence for statewide decline in other states within the range was weaker, so we did not use trends factors for those states. We estimated a slight range-wide decline based on our surveys (Table 2).
Range extent is defined by the smallest polygon that encapsulates known occurrences. Area of occupancy is the area within the range in which the species actually occurs. Number of occurrences is intended to reflect number of populations, based on taxon-specific distances within which animals are assumed to be interacting. Long-term trend was estimated based on historical literature or museum specimens. Values given for these rank factors are the ranges encompassed by NatureServe’s categories. Calculated rank was generated by NatureServe’s element rank calculator , while Expert rank was assigned by biologists familiar with the species in that state.
The ranks generated by the rank calculator tended toward greater concern than those based on our expert opinion (compare the last two columns in Table 2), but we report both to be transparent about our process. In the core of R. kauffeldi’s range (NJ, DE, VA, and perhaps MD), we believe it to be secure, with many apparently large populations in protected wetlands. At the northern edge of its range (including eastern PA, southern CT, southern NY, and extreme northeastern NJ), R. kauffeldi is exceedingly rare and appears to have declined substantially. In NY, for example, the species once occurred across 11 counties and likely more than 100 populations; today it is known from only three counties and fewer than 10 populations. Declines in NY’s leopard frogs have been suspected for decades . While the species is common along the Delaware River, only a sliver of its range falls within PA, hence its suggested S1 status in that state. At the southern edge of our survey limits—and possibly the actual southern range limit for R. kauffeldi—in NC, it may be rare too, but this area needs additional field surveys to confirm the species’ status and actual southern limit. Throughout its range a rank of G3G4 (Vulnerable to Apparently Secure) seems appropriate.
Decrypting Rana kauffeldi
Our multi-year, 10-state investigation demonstrated conclusively that R. kauffeldi is a habitat specialist with a small range centered in the most densely populated region of the United States, and one of the most heavily populated mega-regions on earth . In several northern states, it is extremely rare, while in the southern portion of its range it is still broadly distributed and can be common. We have a much better idea of its distribution than we did just a few years ago, but some unexplained gaps remain. Fortunately, for those interested in surveying for this frog, methods for its identification in the field are also now better understood. The unique breeding call identified by Feinberg et al.  was reliably associated in our study with frogs genetically determined to be R. kauffeldi. Separation in the hand from R. pipiens based on morphology and color patterns is very reliable, while separation from R. sphenocephala is correct as much as 90% of the time.
Distribution and biogeography.
In the core of its mid-Atlantic range south of the Pleistocene glacial maximum, R. kauffeldi is a species exclusively of the Coastal Plain (Fig 7), and the degree to which its apparent western range margin matches that of the Coastal Plain is striking. The Coastal Plain physiographic region of the U.S. covers the Gulf and Atlantic coasts from southern Texas east to Florida and north to Long Island, NY . The region is characterized by low elevation, minimal topography, and unconsolidated sediments  and has recently been recognized as a global biodiversity hotspot . Within this physiographic region, several ecoregions—areas with similar geology, soils, climate, and vegetation —have been identified, of which the Mid-Atlantic Coastal Plain (MACP), Chesapeake Bay Lowlands (CBY), and North Atlantic Coast (NAC) are occupied in part by R. kauffeldi. The MACP has been described as “a factory for the generation of new and novel species” because of its dynamism and juxtaposition of natural communities .
Last glacial maximum is from Ray and Adams .
But since the last glacial maximum occurred only 20,000 years ago, R. kauffeldi has clearly moved out of its core region post-glacial retreat, (re)colonizing some previously glaciated regions along major river valleys to the north and east, and now occurs in the Piedmont, New England, and Valley and Ridge physiographic provinces. These ecoregions are characterized by greater topographic variation and a greater diversity of habitat types and soils than the core of the species range, perhaps reflecting the competitive or predator release that can characterize the opening of newly available habitat.
Apparent gaps in the range in areas with at least some suitable habitat—the northwestern shore of the Delmarva Peninsula and the western shore of the Chesapeake Bay from Baltimore, MD to mid-coastal VA—may be clarified with further sampling and continued examination of museum specimens and historical recordings. Examination of USNM museum specimens from the western shore of the Chesapeake Bay yielded little evidence of R. kauffeldi across that region apart from two specimens from Calvert County, MD that more closely resemble R. kauffeldi than they do R. sphenocephala. We note, however, that the distribution model identified little suitable habitat in the MD-to-VA gap. Our range map is based on confirmed observations, with the expectation that new observations may add to the known range. Our distribution model represents suitable habitat at a finer scale, with coastal impoundments and river valleys standing out and a clear signature of having sampled in part along roads in both the map and the variable importance rankings. The low success rate of the model in predicting presence may reflect local extirpations from still-suitable habitat. Future distribution modeling could use likely absence points instead of random background points, which may allow for more accurate predictions of presence points. The combined use of modeling, interpretation of aerial imagery, and field survey may also help fill these gaps over time.
Field identification and genetics.
While our study did not identify a definable single morphological or color character for distinguishing R. kauffeldi from R. sphenocephala, we did find that a combination of the femoral reticulum, tympanum spots, size and number of dorsal spots, snout shape, and overall coloration provided the correct identification more than nine out of ten times. For now, the primary mating call described by Feinberg et al.  remains the only truly diagnostic feature in the field, and our results strongly suggest that the three species (as defined genetically) are reliably distinguishable based on calls.
Characterizing the darkness of the femoral reticulum is critical to identifying R. kauffeldi correctly, especially in areas of sympatry with R. sphenocephala. Rana kauffeldi always had a reticulum with light spotting on a dark background, although reticula of R. sphenocephala could have either pattern. Our analysis using ImageJ (S2 Appendix) showed that reticular darkness averaged around 70% for R. kauffeldi and 55% for R. sphenocephala, showing that despite the categories used in our analysis, both frogs’ reticula can be more appropriately characterized as “mostly dark.” In most cases, characterizing the reticulum as “mostly dark” or “as much light as dark” will be sufficient. Because this feature is typically hidden when frogs are at rest, identification from photographs of sitting frogs will remain challenging.
Further challenging the correct field identification of non-calling frogs is potential hybridization, particularly between R. kauffeldi and R. sphenocephala. Over 10% of the frogs we DNA tested showed apparent admixture based on our small sample of genetic loci. Hybridization has been studied extensively in leopard frogs and documented in the wild for a number of species pairs [64–66]. The small number of genes we had to work with did not allow for detailed genetic analyses beyond simple typing, and may also explain some odd admixtures of R. kauffeldi with R. pipiens in the north and R. sphenocephala in the south. Further research using next-generation sequencing, either with RADseq  or target capture , would be a logical and important next step in characterizing admixture dynamics of these occasionally syntopic species.
Finally, it is worth noting that the confusion that has plagued leopard frog species delineation in the northeastern U.S. for decades  is similar to that in other parts of the range of this taxonomically challenging species complex. For example, starting in the 1970s, the single “Rana pipiens” species recognized in Mexico began to be split, based in large part on genetic and call data; approximately 20 species are currently recognized [69,70]. Genetic and call data have similarly shown that the southwestern US contains six members of the leopard species complex, rather than a single entity. Like the US treefrogs Hyla versicolor and H. chrysoscelis [55,71] and some species of Pseudacris , members of the leopard frog complex, including R. kauffeldi, appear to be species that cannot always be reliably distinguished without vocalizations. While this may render these taxa challenging for the field biologist, it also emphasizes the importance of follow-up research to document geographic and ecological ranges, regions of species overlap, and conservation needs of these frogs across their ranges.
Conservation, management, and information needs.
Often when cryptic species are first discovered, little is known about their distribution or conservation status (e.g., [72–74]). As more thorough studies accumulate, and particularly as their ranges and habitat preferences are determined, these taxa are often determined to have very limited distributions and to be of conservation concern (e.g., [75–77]). Often this is because they have small populations, which likely hindered their discovery in the first place. The identification of cryptic species as a special case of new species discovery likewise can yield species of concern, for the simple reason that when a species’ range is subdivided, both resulting ranges and population sizes are by definition reduced [8,13]. For example, several species of genetically distinct leopard frogs in the American Southwest R. pipiens “complex” [78–80] are now known to be of conservation concern [48,81]. In the southeastern U.S., Pauly et al.  determined that a single Threatened salamander species, Ambystoma “cingulatum,” was in fact two species, one of which (A. bishopi) was quickly upgraded to Endangered by the U.S. Fish and Wildlife Service . And slender salamanders formerly grouped together as Batrachoseps attenuatus may in fact comprise 39 species , many of which are globally rare.
In the current situation, R. kauffeldi overlaps with, and at the northern edge of its range, supplants R. sphenocephala. It has a far smaller range than R. sphenocephala, and while it is locally common and likely secure for the moment at the core of its range, it is vulnerable in places. Along with its small range, R. kauffeldi’s largely coastal distribution is a major reason for conservation concern . Most populations of R. kauffeldi exist within a highly developed urban and suburban matrix, and the frog’s need for large wetlands (as opposed to R. sphenocephala, which can occupy small ponds) may render it vulnerable to habitat fragmentation with wetland patches separated by inhospitable dispersal habitat. For species such as leopard frogs that spend considerable time in the uplands, the landscape surrounding the aquatic breeding habitat may also be crucial to long-term persistence [85–87]. Based on typical migration distances reported in the literature on other amphibian species , a terrestrial buffer around breeding habitat of several hundred meters is likely necessary to ensure suitable upland habitat, although in at least one highly urban setting the species appears to survive with little surrounding upland greenspace . Studies specific to R. kauffeldi are needed, including studies to determine genetic connectivity among populations to ensure that the isolated nature of some populations has not led to inbreeding depression . Fragmentation has additional, more immediate direct effects on mobile individuals in the form of road mortality. Highways and other major roads bisect leopard frog habitat throughout the Northeast, and frogs are often killed when crossing them. In fact, many of our samples were obtained from road-killed frogs. High-volume or multi-lane roads may serve as permanent, impenetrable barriers to dispersal, which, along with road mortality, can have considerable impacts on anuran richness and abundance [89,90].
Another conservation consideration is that a small geographic range is associated with greater risk of extinction across taxa and in amphibians specifically [91–94]. Rana kauffeldi appears to have the smallest range of any ranid frog on the East Coast, as posited by Feinberg et al. . Of the ranids that range from the mid-Atlantic south to Florida and in some cases west along the Gulf Coast (e.g., R. virgatipes, R. grylio, R. capito), only the extreme endemics R. sevosa  and R. okaloosae  are as restricted as R. kauffeldi. Apart from the pine barrens treefrog (Hyla andersoni) and New Jersey chorus frog (Pseudacris kalmi), no eastern US anuran north of Florida has as small a range as R. kauffeldi. A small range may make a species more susceptible to stochastic events, and for frogs, may exacerbate the impact of fungal pathogens like Batrachochytrium dendrobatidis (Bd; ). Bd has recently been documented in R. kauffeldi (JAF, unpublished data) as it has in R. pipiens and R. sphenocephala [96,97], and many other ranids .
Another point of concern for R. kauffeldi is the coastal proximity of many populations. Coastal populations of wetland organisms may be threatened by rising sea levels and increasing frequency and intensity of coastal storms, both of which may increase with climate change [99–101]. While the presence of R. kauffeldi was not strongly tied to climate parameters in our distribution model, the model was not designed to forecast distributional shifts with changing climate or its collateral effects like sea-level rise and storms. Storms may cause saltwater overwash into freshwater habitats, and ongoing research (Feinberg et al., unpubl. data) is addressing the tolerance of R. kauffeldi to brackish conditions and persistence in coastal sites after major storm events. In Delaware, large calling choruses of R. kauffeldi disappeared from freshwater impoundments along the Delaware Bay following storms that altered the coastline creating inlets that allowed for inflow of saltwater (J. White, pers. comm.). More inland (typically large-river riparian) populations of R. kauffeldi may be less vulnerable to these changing coastal conditions, but also possibly less adapted to storm-related flooding.
We recommend additional field inventory, especially during the late winter and early spring calling season when frogs are most easily identified, to clear up remaining uncertainties in the broad-scale distribution of Rana kauffeldi. Our understanding of the frog’s distribution at the edges of its range is least well understood, both because range edges are often difficult to characterize and because of the urban landscape of the northern edge. In New York and Connecticut, populations are highly disjunct, in part a function of the heavily developed landscape now dividing surviving populations. In between these populations, there are scattered reports of leopard frogs that are undocumented by recordings or photographs, but our field work did not confirm many of these reports. At the apparent southern edge of the range in North Carolina, the distribution of R. kauffeldi is just beginning to be understood, and it is not yet clear whether the frog is rare or common in the region and whether the southern range margin is set by physiography, climate, interspecific interactions, or other factors, or extends farther south than our efforts demonstrated. Many states have gaps in local distributional information which, along with an understanding of population vulnerability in habitat patches of different sizes and degrees of urbanization, are a critical need for better understanding the conservation status of R. kauffeldi.
Finally, we call attention to apparent extirpations of both R. kauffeldi from coastal regions of the Northeast and R. pipiens, from an extensive area near the southern edge of its former range. Rana pipiens can no longer be found in many locations in PA, NJ, NY, CT, RI, and MA where it once occurred based on museum specimens and historical literature. The recent (April 2017) discovery of a population near Providence, RI (CR, unpublished data) is one bright spot, but this considerable decline certainly warrants greater recognition and concern within the amphibian conservation community. Many extirpations of this species have been documented from western North America  and local declines have been noted in the Northeast  but widespread extirpation in this region has not previously been reported. Whether extirpations are a result of habitat loss, range shifting with a warming climate, introduced populations failing to sustain themselves, or some other factor is a topic for further research. The apparent northeastern retreat of R. pipiens echoes the recent finding that another ranid, the Wood Frog, R. sylvatica, is also retreating northward .
Ecological research agenda for cryptic species and conclusion
Cryptic species remain a fascinating, and rising challenge to systematics, ecology, and conservation, but one that is increasingly met with new research technologies. Much has been written about the problem of identifying cryptic species [8,10,18] and the implications for assessments of species diversity within taxa and globally [104–107]. Less attention has been paid to the follow-up studies necessary to answer basic questions about ecological, behavioral, and morphological differences among species in a cryptic complex. Here we present a framework for answering these important questions in phylogenetics, biogeography, ecology and behavior, morphology, conservation, and implications for scientific literature that should be a standard part of our ecological research agenda following cryptic species discovery (Table 3). This framework differs from one that might reasonably be applied to any newly discovered species in that it focuses on teasing out differences between two or more cryptic species within a complex.
As with any newly described species, there is still much to learn about R. kauffeldi’s ecology and natural history. Descriptions of R. kauffeldi egg masses and tadpoles are lacking , and the ability to distinguish species based especially on tadpoles would be a boon to detailed natural history, ecological, and demographic studies. For example, adaptations of the various life stages to particular environmental conditions and stressors may help explain the geographic and ecological distributions of the species. Given the highly urban setting of many populations, the susceptibility to environmental contaminants of the various life stages , and potential impacts of noise on anuran communication , are of great interest. Research into possible competitive interactions may shed light on any niche separation given the overlap with R. sphenocephala and R. pipiens and the suggestion of hybridization in both the genetic and morphological data, and help explain observed declines. Finally, additional taxonomic research using a combination of genetics, morphology, and bioacoustics may yet reveal more cryptic diversity within the North American leopard frog complex.
S1 Appendix. Exemplar photographs of characters used in analysis of leopard frog morphology and patterning.
S2 Appendix. Reticulum characterization with ImageJ.
S3 Appendix. Additional genetic methods and results.
S4 Appendix. Morphological and color characters from photographic analysis of 220 leopard frogs (Rana spp.) in the eastern U.S.
Frogs were identified using genetics and designated as “pure” if they had a 90% or greater match with a single species; individuals with a species match between 10% and 90% were designated as admixed. Sample sizes for each character are given because not every frog had photographs suitable for examination of that character.
This study, covering 10 US states, could not have been accomplished without a large network of professional and citizen biologists, plus a great deal of administrative help. For contributing field observation data and conducting surveys, we thank Sarah Acosta, Robert Andrle, Susan Andrle, Scott Angus, Patrick Burritt, Brian Bastarache, Dan Becker, Cliff Bernzweig, Randy Best, Amy Bloomfield, Mike Bottini, Al Breisch, Darnell Brister, Jennifer Brooks, Charlie Brown, Virginia Brown, Jenn Carlino, Andrea Chaloux, Chris Chapin, Charles Clarkson, Susanne Colten-Carey, JoAnn Corn, Marlin Corn, Jeff Corser, Brian Curry, Adrienne DenTex, Damon DePaolo, Kimberly DePaolo, Calum Devaney, Emily Dombroski, Sam Droege, Kaitlyn Friedman, Cait Field, Dave Fitzpatrick, Suzie Fowle, Nicole Gerard, Tony Gola, Chris Graham, Tim Green, Hank Gruner, Molly Hale, Jeff Hall, Vanessa Hartmann, Shaun Hicks, Stephanie Jennings, Meghan Jackson, Joe Janssen, Lori Johnson, Steve Johnson, Lindsay Keener-Eck, Judy Kelley-Moberg, Michael Klemens, Rory Larson, Darren Loomis, Kim Laidig, Kyle Loucks, Niklas Lowe, Rebecca French-Mesch, Annie McIntyre, Kristen Meistrell, Brian Munford, Beth Nicholls, Colin Osborn, Joe Pane, Ellen Pehek, Kelly Perkins, Andrea Petrullo, Bill Pitts, Eli Pitts, Justin Proctor, Richard Rego, Chris Rezendes, Sarah Riley, Richard Ring, Marc Rivadeneyra, Barrie Robbins-Pianka, Sarah Johnson, James Shelton, Nate Silver, Iain Sorrell, Renee St. Amand, Steven Straiton, Kelly Triece, Tom Tyning, Jim Utter, Rene Wendell, Jay Westerveld, Jim White, and Olivia Zukas. Steve Gotte, Toby Hibbitts, Susan Hochgraf, David Kizirian, Roy McDiarmid, James Poindexter, Jose Rosado, Laura Smyk, Ken Tighe, and Gregory Watkins-Colwell facilitated access to museum specimens or provided photographs. Tim Howard, Amy Conley, and other colleagues at the New York, Pennsylvania, Virginia, and Florida Natural Heritage programs compiled environmental data and scripts for species distribution modeling. For administrative support, we thank D.J. Evans, Fiona McKinney, Chris Urban, and the Research Foundation for SUNY. Hank Gruner, Michael Klemens, and an anonymous reviewer provided helpful feedback on a draft manuscript.
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