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Cecil R. Schwalbe

Publications and source records attributed to Cecil R. Schwalbe.

9 recordsLinked to original sources

Modeling habitat connectivity to inform reintroductions: a case study with the Chiricahua Leopard Frog

Managing species with intensive tools such as reintroduction may focus on single sites or entire landscapes. For vagile species, long-term persistence will require colonization and establishment in neighboring habitats. Therefore, both suitable colonization sites and suitable dispersal corridors between sites are required. Assessment of landscapes for both requirements can contribute to ranking and selection of reintroduction areas, thereby improving management success. Following eradication of invasive American Bullfrogs ( Lithobates catesbeianus ) from most of Buenos Aires National Wildlife Refuge (BANWR; Arizona, United States), larval Chiricahua Leopard Frogs ( Lithobates chiricahuensis ) from a private pond were reintroduced into three stock ponds. Populations became established at all three reintroduction sites followed by colonization of neighboring ponds in subsequent years. Our aim was to better understand colonization patterns by the federally threatened L. chiricahuensis which could help inform other reintroduction efforts. We assessed the influence of four landscape features on colonization. Using surveys from 2007 and information about the landscape, we developed a habitat connectivity model, based on electrical circuit theory, that identified potential dispersal corridors after explicitly accounting for imperfect detection of frogs. Landscape features provided little insight into why some sites were colonized and others were not, results that are likely because of the uniformity of the BANWR landscape. While corridor modeling may be effective in more-complex landscapes, our results suggest focusing on local habitat will be more useful at BANWR. We also illustrate that existing data, even when limited in spatial or temporal resolution, can provide information useful in formulating management actions.

Journal of Herpetology

Spatial occupancy models for predicting metapopulation dynamics and viability following reintroduction

The reintroduction of a species into its historic range is a critical component of conservation programmes designed to restore extirpated metapopulations. However, many reintroduction efforts fail, and the lack of rigorous monitoring programmes and statistical models have prevented a general understanding of the factors affecting metapopulation viability following reintroduction. Spatially explicit metapopulation theory provides the basis for understanding the dynamics of fragmented populations linked by dispersal, but the theory has rarely been used to guide reintroduction programmes because most spatial metapopulation models require presence&ndash;absence data from every site in the network, and they do not allow for observation error such as imperfect detection. We develop a spatial occupancy model that relaxes these restrictive assumptions and allows for inference about metapopulation extinction risk and connectivity. We demonstrate the utility of the model using six years of data on the Chiricahua leopard frog Lithobates chiricahuensis , a threatened desert-breeding amphibian that was reintroduced to a network of sites in Arizona USA in 2003. Our results indicate that the model can generate precise predictions of extinction risk and produce connectivity maps that can guide conservation efforts following reintroduction. In the case of L. chiricahuensis , many sites were functionally isolated, and 82% of sites were characterized by intermittent water availability and high local extinction probabilities (0&middot;84, 95% CI: 0&middot;64&ndash;0&middot;99). However, under the current hydrological conditions and spatial arrangement of sites, the risk of metapopulation extinction is estimated to be <3% over a 50-year time horizon. Low metapopulation extinction risk appears to result from the high dispersal capability of the species, the high density of sites in the region and the existence of predator-free permanent wetlands with low local extinction probabilities. Should management be required, extinction risk can be reduced by either increasing the hydroperiod of existing sites or by creating new sites to increase connectivity. Synthesis and applications . This work demonstrates how spatio-temporal statistical models based on ecological theory can be applied to forecast the outcomes of conservation actions such as reintroduction. Our spatial occupancy model should be particularly useful when management agencies lack the funds to collect intensive individual-level data.

Arizona, New Mexico

Projecting climate effects on birds and reptiles of the Southwestern United States

We modeled the current and future breeding ranges of seven bird and five reptile species in the Southwestern United States with sets of landscape, biotic (plant), and climatic global circulation model (GCM) variables. For modeling purposes, we used PRISM data to characterize the climate of the Western United States between 1980 and 2009 (baseline for birds) and between 1940 and 2009 (baseline for reptiles). In contrast, we used a pre-selected set of GCMs that are known to be good predictors of southwestern climate (five individual and one ensemble GCM), for the A1B emission scenario, to characterize future climatic conditions in three time periods (2010–39; 2040–69; and, 2070–99). Our modeling approach relied on conceptual models for each target species to inform selection of candidate explanatory variables and to interpret the ecological meaning of developed probabilistic distribution models. We employed logistic regression and maximum entropy modeling techniques to create a set of probabilistic models for each target species. We considered climatic, landscape, and plant variables when developing and testing our probabilistic models. Climatic variables included the maximum and minimum mean monthly and seasonal temperature and precipitation for three time periods. Landscape features included terrain ruggedness and insolation. We also considered plant species distributions as candidate explanatory variables where prior ecological knowledge implicated a strong association between a plant and animal species. Projected changes in range varied widely among species, from major losses to major gains. Breeding bird ranges exhibited greater expansions and contractions than did reptile species. We project range losses for Williamson’s sapsucker and pygmy nuthatch of a magnitude that could move these two species close to extinction within the next century. Although both species currently have a relatively limited distribution, they can be locally common, and neither are presently considered candidates for prospective endangerment. We project range losses of over 40 percent, from its current extent of occurrence, for the plateau striped whiptail, Arizona black rattlesnake, and common lesser earless lizard. Currently, these reptile species are thought to be common or at least locally abundant throughout their ranges. The total contribution of plants in each distribution model was very small, but models that contained at least one plant always outperformed models with only physical variables (climatic or landscape). The magnitude of change in projected range increased further into the future, especially when a plant was in the model. Among bird species, those that had the strongest association with a landscape feature during the breeding season, such as terrain ruggedness and insolation, exhibited the smallest contractions in projected breeding range in the future. In contrast, bird species that had weak associations with landscape features, but strong climatic associations, suffered the greatest breeding range contractions. Thus, landscape effects appeared to buffer some of the negative effects of climate change for some species. Among bird species, magnitude of change in projected breeding range was positively related to the annual average temperature of their baseline distribution, thus species with the warmest breeding ranges exhibited the greatest changes in future breeding ranges. This pattern was not evident for reptiles, but might exist if additional species were included in the model. Our results provide managers with a series of projected range maps that will enable scientists, concerned citizens, and wildlife managers to identify what the potential effects of climate change will be on bird and reptile distributions in the Western United States. We hope that our results can be used in proactive ways to mitigate some of the potential effects of climate change on selected species.

Colorado Plateau;Sonoran Desert

Prevalence of the amphibian chytrid fungus (Batrachochytrium dendrobatidis) at Buenos Aires National Wildlife Refuge, Arizona, USA

Information on disease presence can be of use to natural resource managers, especially in areas supporting threatened and endangered species that occur coincidentally with species that are suspected vectors for disease. Ad hoc reports may be of limited utility (Muths et al. 2009), but a general sense of pathogen presence (or absence) can inform management directed at T&E species, especially in regions where disease is suspected to have caused population declines (Bradley et al. 2002). The Chiricahua Leopard Frog (Lithobates chiricahuensis), a species susceptible to infection by the amphibian chytrid fungus (Batrachochytrium dendrobatidis, Bd) (Bradley et al. 2002), and the non-native, invasive American Bullfrog (L. catesbeianus), a suspected vector for chytridiomycosis (Schloegel et al. 2012, Gervasi et al. 2013), both occur at Buenos Aires National Wildlife Refuge (BANWR) and surrounding lands in southern Arizona. Efforts to eradicate the bullfrog from BANWR began in 1997 (Suhre, 2010). Eradication from the southern portion of BANWR was successful by 2008 but the bullfrog remains present at the Arivaca Cienega and in areas immediately adjacent to the refuge (Fig. 1). Curtailing the re-invasion of the bullfrog into BANWR will require vigilance as to ensure the health of Chiricahua Leopard Frog populations.

Arizona

Southwestern desert resources

The southwestern deserts stretch from southeastern California to west Texas and then south to central Mexico. The landscape of this region is known as basin and range topography featuring to "sky islands" of forest rising from the desert lowlands which creates a uniquely diverse ecology. The region is further complicated by an international border, where governments have caused difficulties for many animal populations. This book puts a spotlight on individual research projects which are specific examples of work being done in the area and when they are all brought together, to shed a general light of understanding the biological and cultural resources of this vast region so that those same resources can be managed as effectively and efficiently as possible. The intent is to show that collaborative efforts among federal, state agency, university, and private sector researchers working with land managers, provides better science and better management than when scientists and land managers work independently.

Book

Challenges to natural resource monitoring in a small border park: terrestrial mammals at Coronado National Memorial, Cochise County, Arizona

Long-term monitoring in national parks is essential to meet National Park Service and other important public goals. Terrestrial mammals are often proposed for monitoring because large mammals are of interest to visitors and small mammals are important as prey. However, traditional monitoring strategies for mammals are often too expensive and complex to sustain for long periods, particularly in small parks. To evaluate potential strategies for long-term monitoring in small parks, we conducted an intensive one-year inventory of terrestrial mammals at Coronado National Memorial, located in Arizona on the U.S.-Mexico international border, then continued less-intensive monitoring at the site for 7 additional years. During 1996-2003 we confirmed 44 species of terrestrial mammals. Most species (40) were detected in the intensive first year of the study, but we continued to detect new species in later years. Mark-recapture data on small mammals indicated large inter-annual fluctuations in population size, but no significant trend over the 7-year period. Issues associated with the international border affected monitoring efforts and increased sampling costs. Our study confirms that sustained annual monitoring of mammals is probably not feasible in small park units like Coronado. However, comparisons of our data with past studies provide insight into important changes in the mammal community since the 1970s, including an increase in abundance and diversity of grassland rodents. Our results suggest that intensive inventories every 10-20 years may be a valuable and cost-effective approach for detecting long-term trends in terrestrial mammal communities in small natural areas.

Arizona

Divergence among barking frogs ( Eleutherodactylus augusti ) in the southwestern United States

Barking frogs ( Eleutherodactylus augusti ) are distributed from southern Mexico along the Sierra Madre Occidental into Arizona and the Sierra Madre Oriental into Texas and New Mexico. Barking frogs in Arizona and most of Texas live in rocky areas in oak woodland, while those in New Mexico and far western Texas live in rodent burrows in desertscrub. Barking frogs in each of the three states have distinct coloration and differ in sexually dimorphic characters, female vocalization, and skin toxicity. We analyzed advertisement call variation and conducted a phylogenetic analysis using mitochondrial DNA sequences (ND2 and tRNA regions) for barking frogs from these three states. Advertisement calls of frogs from Arizona were significantly longer in duration, higher in frequency, and had longer duration pulses than those of frogs from either New Mexico or Texas; frogs from these latter two sites were indistinguishable in these call variables. Phylogenetic analysis showed deep divisions among barking frogs from the three states. Differences in call structure, coloration, and mitochondrial DNA sequences strongly suggest that barking frogs in Arizona are reproductively isolated from those in New Mexico and Texas. Our results indicate that either northern populations are connected via gene flow through southern Mexico (i.e., they are subspecies as currently recognized), or represent independent lineages as originally described (i.e., western barking frogs, E. cactorum in AZ, and the eastern barking frogs, E. latrans in NM, TX).

Arizona, New Mexico, Texas

Bullfrogs: Introduced predators in southwestern wetlands

In the American Southwest, much of the native fish fauna is facing extinction (Minckley and Deacon 1991); frogs in California (Fellers and Drost 1993) and frogs and garter snakes in Arizona (Schwalbe and Rosen 1988) are also in critical decline. Habitat destruction and introduced predators appear to be primary causes of native frog declines (Jennings and Hayes 1994), and habitat modification often yields ponds and lakes especially suitable for introduced species. Introduced bullfrogs ( Rana catesbeiana ) have been blamed for amphibian declines in much of western North America (e.g., Hayes and Jennings 1986; Leonard et al. 1993; Vial and Saylor 1993). Extensive cannibalism by bullfrogs renders them especially potent predators at the population level. The tadpoles require only perennial water and grazeable plant material; hence, transforming young can sustain a dense adult bullfrog population even if alternate prey are depleted. This may increase the probability that native species may be extirpated by bullfrog predation. Introduced predatory fishes are apparently an important cause of frog declines (Hayes and Jennings 1986). They have been strongly implicated in one important case of decline of native ranid frog (family Ranidae, the "true" frogs; Bradford 1989). Some introduced crayfish may also be devastating in some areas (Jennings and Hayes 1994). In our study region, however, neither introduced fishes nor crayfish are dominant. We present results that sustain a "bullfrog hypothesis" for some native ranid declines, and we present our study as an example of how evidence accumulates to support such a hypothesis. In 1985 we began documenting historical localities for wetland herpetofaunas (reptiles and amphibians), based on museum records and personal interviews, then revisited these and additional areas to determine current species' status. Results of this process, plus circumstantial evidence, suggested that the bullfrog was a primary cause for declines of leopard frogs and garter snakes in southern Arizona (Schwalbe and Rosen 1988). In 1986-89 and 1992-93 we conducted removal censuses of bullfrogs at San Bernardino National Wildlife Refuge (SBNWR), Cochise County, Arizona. We simultaneously monitored native Chiricahua leopard frogs ( R. chiricahuensis ) and Mexican garter snakes ( Thamnophis eques ) at the sites of bullfrog removal. A control site, with no bullfrog removal, was established in comparable habitat at Buenos Aires National Wildlife Refuge (BANWR), Pima County, Arizona.

Book chapter