Michael L. Morrison’s research while affiliated with Texas A&M University and other places

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Publications (309)


The number of red-listed animal species in each country relative to the number of dispersal studies. Dividing the number of threatened amphibian (A), reptile (B), avian (C), and mammal (D) species [26] by the number of dispersal studies reveals regions that are understudied relative to the number of threatened species. Across all vertebrate groups, countries in Asia, Africa, and South America appeared relatively understudied. Yellow colors represent a higher number of threatened species per study.
Log-transformed weighted dispersal estimates of anuran species (A) and urodele species (B) from telemetry and genetic studies. We display anuran and urodele species on the y-axis and log-transformed weighted dispersal on the x-axis. In anurans (i.e., frogs and toads), log-scale weighted dispersal estimates from telemetry studies (1.29 ± 0.50) and log-transformed weighted dispersal estimates from genetic studies (2.30 ± 0.38) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from telemetry studies was >95%. For urodeles (i.e., newts and salamanders), log-scale weighted dispersal estimates from telemetry studies (1.02 ± 0.17) and log-transformed weighted dispersal estimates from genetic studies (2.24 ± 0.43) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from telemetry studies was >95%.
Log-transformed weighted dispersal estimates of squamate species (A) and testudines (B) from demographic and genetic studies. We display squamates and testudines on the y-axis and log-transformed weighted dispersal on the x-axis. In squamates (i.e., snakes and lizards), log-scale weighted dispersal estimates from telemetry studies (1.40 ± 0.51) and log-transformed weighted dispersal estimates from genetic studies (2.03 ± 0.34) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from telemetry studies was >95%. For testudines (i.e., turtles and tortoises), log-scale weighted dispersal estimates from CMR studies (1.18 ± 0.25), telemetry studies (1.47 ± 0.60), and genetic studies (2.43 ± 0.37) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from telemetry and CMR studies was >95%. The posterior probability of the weighted dispersal from telemetry studies exceeding the weighted dispersal from CMR studies was 76%.
Log-transformed weighted dispersal estimates of Charadriiformes (A) and Passeriformes (B) from demographic and genetic studies. We display Charadriiformes and Passeriformes on the y-axis and log-transformed weighted dispersal on the x-axis. In Charadriiformes (e.g., shorebirds and seabirds), log-scale weighted dispersal estimates from CMR (0.60 ± 0.31), telemetry (1.14 ± 0.51), and genetic studies (2.32 ± 0.36) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from CMR and telemetry studies was >95%. Similarly, the posterior probability of the weighted dispersal from telemetry studies exceeding that from CMR studies was 95%. For passerines (e.g., sparrows and finches), log-scale weighted dispersal estimates from CMR studies (0.56 ± 0.32), telemetry studies (1.71 ± 0.74), and genetic studies (2.40 ± 0.42) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from telemetry and CMR studies was >95%. Similarly, the posterior probability of the weighted dispersal from telemetry studies exceeding that from CMR studies was >95%.
Log-transformed weighted dispersal estimates of Carnivora (A), Chiroptera (B), and primates (C) from demographic and genetic studies. We display carnivores, bats, and primates on the y-axis and log-transformed weighted dispersal on the x-axis. In carnivores (e.g., seals, bears, and wolves), log-scale weighted dispersal estimates from telemetry (1.36 ± 0.40) and genetic studies (2.77 ± 0.62) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from CMR and telemetry studies was >95%. For chiropterans (i.e., bats), log-scale weighted dispersal estimates from telemetry studies (1.01 ± 0.36) and genetic studies (2.75 ± 0.52) were compared using a univariate regression model. The posterior probability of the weighted dispersal from genetic studies exceeding the weighted dispersal from telemetry and CMR studies was >95%. For primates, (e.g., lemurs and monkeys), log-scale weighted dispersal estimates from CMR (1.74 ± 0.56), telemetry (1.46 ± 0.33), and genetic studies (2.31 ± 0.31) were compared using a univariate regression model. The posterior probability of the weighted dispersal exceeding that from telemetry and CMR studies was 99% and 85% respectively. The posterior probability of the weighted dispersal from CMR studies exceeding that from telemetry studies was 95%.
Comparing the Utility of Capture–Mark–Recapture, Telemetry, and Genetic Data in Assessing Population-Level Dispersal
  • Article
  • Full-text available

February 2025

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104 Reads

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Michael L. Morrison

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Gaps in dispersal data limit habitat protection efforts. We sought to characterize such gaps and compare the utility of dispersal data from demographic and genetic methods in making habitat protection decisions. Here, we used a search string to retrieve dispersal studies for amphibians, reptiles, birds, and mammals. We included studies based on a set of selection criteria. We used this sample of selected studies to assess for persistence of taxonomic and geographic biases. We extracted non-effective (i.e., demographic) and effective (i.e., genetic) dispersal rates. We weighted these dispersal rates by associated sample size and standard deviation to indicate the ability to capture population-level dispersal. We then tested for variation in weighted dispersal by study type using Bayesian mixed-effects models. Amphibians were the most under-represented taxonomic group in our sample. Dispersal studies were mostly retrieved from developed nations indicating the distribution of dispersal research reflected GDP rather than the number of threatened species. The magnitude of dispersal from genetic methods exceeded demographic methods in all vertebrate groups considered in our study. Further, genetic studies consistently sampled a larger number of individuals. Thus, genetic methods may be better suited to characterize population-level dispersal. However, demographic and genetic approaches enable examination of the dispersal process at varying spatial and temporal scales and a combination of these approaches can be used to address persistent gaps in dispersal and enable land-management decisions.

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Burrowing Owls Require Mutualist Species and Ample Interior Habitat Space

September 2024

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50 Reads

Mitigating habitat loss of western burrowing owls (Athene cunicularia hypugaea) often involves relocation from California ground squirrel (Otospermophilus beecheyi) burrows to offsite nest boxes. Naval Air Station Lemoore (NASL), Kings and Fresno counties, California, initiated this approach to displace a regionally important population from airfield grasslands. We examined monitoring data of burrowing owls and fossorial mammals at NASL to assess mitigation options. Occupied nests increased by 33 (61%), with 47 nest box installations in 1997–2001, peaked at 87 in 1999, then declined by 50 through 2013. Although ≥13 nest boxes were occupied in 2000, none were occupied in 2003–2013. Within a 43.1 ha isolated grassland monitored for 13 years, nest site reuse in ground squirrel burrows averaged only 17% between any 2 consecutive years. Compared to the average density across grassland study areas, ground squirrel burrow systems/ha numbered 43% higher within 60 m of occupied nests and non-breeding-season burrows. Vegetation clearing to restore kangaroo rat (Dipodomys n. nitratoides) habitat preceded a 7.4-fold increase in ground squirrel burrow systems and a 4-fold increase in occupied nests, but drought-induced extirpation of ground squirrels eliminated occupied nests from the 43.1 ha grassland study area. Ground cover near occupied nests averaged 58% of the mean vegetation height and 67% of the mean percentage of bare ground in the field. Both nest sites and non-breeding-season burrows occurred >60 m interior to field edges 1.4 times more than expected. Non-breeding-season burrows averaged 328 m from same-year nest sites, and only 7% of non-breeding-season burrows were also used as nest sites. Mitigating habitat loss should be made more effective by fostering natural burrow construction by fossorial mammals on patches of short-stature vegetation that is sufficiently expansive to support breeding colonies of ≥12 pairs averaging ≥60 m from the field’s edge and a separation between non-breeding-season burrows and nest burrows minimally equal to mean nearest-neighbor distances among nests.



Fig. 2 Visualization of genome assembly metrics. A) K-mer spectra generated from PacBio HiFi sequencing data using GenomeScope2.0. B) BlobToolKit Snail plot representing quality metrics for the primary Corynorhinus townsendii assembly (mCorTow1). The plot circle represents the full length of the assembly. The central red arc and corresponding line indicate the length of the longest scaffold. All other scaffold lengths are shown in dark gray ordered from largest to smallest moving clockwise with lengths indicated by the vertical axis located at 12 o'clock. The central light gray circle shows the cumulative scaffold count using log 10 scale. The dark and light orange arcs indicate the scaffold N50 and scaffold N90 values, respectively. The dark to light blue ratios around the outside of the circle represent the proportion of AT to GC content at 0.1% length intervals. C) The Omni-C contact map for genome assemblies Haplotype 1 and D) Haplotype 2. Contact maps translate the proximity of sequenced regions in 3D space to linear order of sequences. Scaffolds are separated by vertical and horizontal lines.
Reference genome of Townsend’s big-eared bat, Corynorhinus townsendii

December 2023

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48 Reads

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2 Citations

Journal of Heredity

Townsend's big-eared bat, Corynorhinus townsendii, is a cave- and mine-roosting species found largely in western North American. Considered a species of conservation concern throughout much of its range, protection efforts would greatly benefit from understanding patterns of population structure, genetic diversity, and local adaptation. To facilitate such research, we present the first de novo genome assembly of C. townsendii as part of the California Conservation Genomics Project (CCGP). Pacific Biosciences HiFi long reads and Omni-C chromatin-proximity sequencing technology were used to produce a de novo genome assembly, consistent with the standard CCGP reference genome protocol. This assembly comprises 391 scaffolds spanning 2.1 Gb, represented by a scaffold N50 of 174.6 Mb, a contig N50 of 23.4 Mb, and a BUSCO completeness score of 96.6%. This high-quality genome will be a key tool for informed conservation and management of this vulnerable species in California and across its range.


Map of recorded roosts of Corynorhinus townsendii in California from Harris et al. (2019) survey efforts. Image of C. townsendii provided by Devaughn Fraser.
Maps showing the present habitat suitability (probability of occurrence) for Corynorhinus townsendii in California based on known roost locations. (a) Model based on all roost occurrence records state‐wide, (b) model based on hibernacula only, (c) model based on maternity colonies only, and (d) model based on active‐season non‐maternity (transition) roosts only. The color ramp corresponds to predicted habitat suitability, where dark blue indicates low habitat suitability and yellow indicates high habitat suitability (scaled 0–100).
Map showing level III ecoregion‐specific habitat suitability for Corynorhinus townsendii in California based on known roost locations. The color ramp corresponds to predicted habitat suitability, where dark blue indicates low habitat suitability and yellow indicates high habitat suitability.
Climate‐related habitat suitability shifts in extent and location in Corynorhinus townsendii in California based on known roost locations. Colors indicate areas of contraction (red), expansion (blue), and areas that are currently suitable that will remain suitable in the future (yellow).
Climate‐related habitat suitability shifts for level III ecoregion‐specific models of Corynorhinus townsendii in California based on known roost locations. Colors indicate areas of contraction (red), expansion (blue), and areas that are currently suitable that will remain suitable in the future (yellow).
Predicting habitat suitability for Townsend's big‐eared bats across California in relation to climate change

December 2022

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199 Reads

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5 Citations

Effective management decisions depend on knowledge of species distribution and habitat use. Maps generated from species distribution models are important in predicting previously unknown occurrences of protected species. However, if populations are seasonally dynamic or locally adapted, failing to consider population level differences could lead to erroneous determinations of occurrence probability and ineffective management. The study goal was to model the distribution of a species of special concern, Townsend's big‐eared bats (Corynorhinus townsendii), in California. We incorporate seasonal and spatial differences to estimate the distribution under current and future climate conditions. We built species distribution models using all records from statewide roost surveys and by subsetting data to seasonal colonies, representing different phenological stages, and to Environmental Protection Agency Level III Ecoregions to understand how environmental needs vary based on these factors. We projected species' distribution for 2061–2080 in response to low and high emissions scenarios and calculated the expected range shifts. The estimated distribution differed between the combined (full dataset) and phenologically explicit models, while ecoregion‐specific models were largely congruent with the combined model. Across the majority of models, precipitation was the most important variable predicting the presence of C. townsendii roosts. Under future climate scenarios, distribution of C. townsendii is expected to contract throughout the state, however suitable areas will expand within some ecoregions. Comparison of phenologically explicit models with combined models indicates the combined models better predict the extent of the known range of C. townsendii in California. However, life‐history‐explicit models aid in understanding of different environmental needs and distribution of their major phenological stages. Differences between ecoregion‐specific and statewide predictions of habitat contractions highlight the need to consider regional variation when forecasting species' responses to climate change. These models can aid in directing seasonally explicit surveys and predicting regions most vulnerable under future climate conditions. The goal of our study was to model the current distribution of Townsend's big‐eared bats (Corynorhinus townsendii) and estimate range shifts under future climate conditions at different temporal and geographic scales. We built species distribution models in present and future conditions using all records from statewide roost surveys and by subsetting this data to seasonal colonies and to Environmental Protection Agency Level III ecoregions. As a whole, the range of C. townsendii is expected to decrease throughout California, but within some ecoregions suitable areas will increase, highlighting the need to consider intraspecific variation when building species distribution models.


Distance sampling survey effort to improve density estimates of northern bobwhite

June 2022

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47 Reads

Distance sampling from aerial platforms can provide researchers with precise and efficient density estimates for wildlife populations, particularly over large areas. The intensity of the distance sampling survey depends on the survey effort. Effort can be referred to as coverage, where transect spacing is determined by the observer's sightability distance of the object or animal. Managers and researchers in Texas often use helicopters to survey and collect data for northern bobwhite (Colinus virginianus) density estimates. For bobwhites, 100% coverage represents transect spacing of 200 m, assuming observers can cover out to 100 m on either side of the transects. Often surveys are conducted at 50% coverage or 400 m spacing to reduce cost. Still, the implications of lowering survey effort on the precision of density estimates are unknown, particularly in coverage prescriptions. We flew 2,641 km of line transects each December from 2014 to 2017 and detected 2,333 bobwhite coveys across 7,648 ha of rangeland on the San Antonio Viejo Ranch in Jim Hogg County, TX, USA. We conducted line‐transect distance sampling from a helicopter platform at 50 and 100% coverage and simulated results at coverage <50% using empirical data. Based on the results of simulated surveys at <100% coverage, surveying for bobwhites using helicopters with less than 50% coverage results in variable density estimates (wide 95% confidence intervals) and low precision (coefficient of variation >20%). Empirical surveys conducted at 50 and 100% coverage show little variation in density estimates between the 2 levels of coverage. However, when broken into substrata (areas less than ~1,000 ha), conducting surveys at 50% coverage resulted in <60 detections, which led to low precision in density estimates (coefficient of variation >20%). Our results are based on surveys conducted at the juncture of the Coastal Sand Sheet and Tamaulipan Thorn Scrub ecoregions in south Texas and need to be evaluated in other arid and semi‐arid rangeland systems. Survey design is an essential component of estimating wildlife populations via distance sampling. However, the number of transects flown is often based on logistics rather than survey precision. We evaluated the variance associated with estimates from varying levels of survey coverage while using line‐transect distance sampling for northern bobwhites in Texas.


Fig. 1. Sites on East Foundation lands where we recorded bat passes in 2015 (+), 2016 (×), and 2017 (○), including San Antonio Viejo (SAV), the Coloraditas Grazing Research and Demonstration Area pastures (CGRDA) on SAV, and El Sauz (ELS) in southern Texas, USA. Combined symbols represent sites that were surveyed in multiple years.
Fig. 2. Detection probability estimates through the sampling season for the 7 species of bats we detected on San Antonio Viejo and El Sauz in southern Texas, USA, during 2015, 2016, and 2017. A, Eastern red bat (Lasiurus borealis). B, Hoary bat (Lasiurus cinereus). C, Northern yellow bat (Lasiurus intermedius). D, Cave myotis (Myotis velifer). E, Evening bat (Nycticeius humeralis). F, Tricolored bat (Perimyotis subflavus). G, Mexican free-tailed bat (Tadarida brasiliensis). Dashed lines represent 95% confidence bands. We sampled from ordinal date 151 (31 May) to ordinal date 272 (29 September).
Fig. 3. Sample size calculations from our logistic regression model for the power to detect a 50% decline in occupancy over 25 years projected out to 100 survey sites for monitoring occupancy of bats in our study areas in southern Texas, USA, from data collected in 2015-2017. Individual curves represent various starting occupancy rates, and the horizontal lines represent the benchmark power values of 0.80 (gray) and 0.90 (black).
Monitoring Occupancy of Bats with Acoustic Data: Power and Sample Size Recommendations

March 2022

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478 Reads

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2 Citations

Western North American Naturalist

Bats are difficult to study due to their nocturnal, cryptic, and highly vagile nature. Ongoing advances in acoustic recording hardware and call classification software have made species detection and activity monitoring more feasible. Our objectives were to determine effort necessary to monitor bat assemblages using an occupancy framework and acoustic data, and to provide guidelines for researchers interested in developing similar monitoring programs. We collected data at two study areas in South Texas from June through September in 2015, 2016, and 2017. We used Pettersson D500X Mk II real-time full spectrum detectors and classified sound files using SonoBat bat call analysis software. We attempted to collect data during 2 visits to individual sites with up to 5 consecutive nights per visit each year. We estimated occupancy rates for each species in each study area using occupancy models in Program MARK and included terms to define trends in detection probability through the season. Over the 3 years of our study, we sampled 106 sites with 803 sampling nights and classified a total of 2880 sound files to 7 species. Datasets for 6 of the species supported models indicating detection probability varied throughout our sampling period. Our results generally indicate that sample sizes between 10 and 20 sites would be required to detect declines in occupancy of 50% over 25 years using 10 nights per site with a starting occupancy rate of 0.70. Detecting declines of 30% in 10 years may require > 75 sampling sites. Finally, our analysis shows that recognizing seasonal variation in detection probability, and then timing surveys accordingly, can greatly reduce sample size requirements.


Modeling the suitability of Texas karst regions for infection by Pseudogymnoascus destructans in bats

March 2022

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46 Reads

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3 Citations

Journal of Mammalogy

White-nose syndrome (WNS) is caused by the fungus Pseudogymnoascus destructans and has led to the deaths of millions of North American bats since it was first documented in New York in 2006. Since the first cases were recorded, WNS has spread rapidly across North America and is now confirmed or suspected in 40 US states and seven Canadian provinces. Often, the presence of P. destructans is detected in a cave or hibernaculum before signs of WNS manifest in the resident bat population, making presence of the fungus a more reliable assessment of potential epidemic spread than expansion of manifested WNS. An analysis of 43 cave internal climates across the state of Texas revealed a pattern of thermal suitability for P. destructans that correlated significantly with landscape (elevation, lithology) and external climate (mean surface temperature and precipitation). We generated a predictive model to assess the potential spread of P. destructans through Texas karst systems based on external features that correlate with suitable internal climates for fungal growth. Applications of this model to external climatic variables from 2019 showed seasonally varying patterns of suitability for fungal growth in select regions of Texas karst systems. Results from these surveys and models showed that internal climates of Texas caves are likely able to sustain the growth of P. destructans and could cause disease and resulting declines in Texas bats, and act as stepping-stones for the fungus, allowing it to travel southward into Mexican and Central American cave systems. The resulting work will inform researchers and natural resource managers of areas of significant concern to monitor for the spread of WNS.


Figure 1: Locations of captured albino Baiomys taylori from the San Antonio Viejo Ranch, Jim Hogg County, Texas, USA, 2021 (this study) and Stickel and Stickel (1949).
Figure 2: Habitat in which the albino B. taylori was captured on the San Antonio Viejo Ranch, Jim Hogg County, Texas, USA on three separate occasions (16 March 2021, 17 March 2021, and 2 April 2021).
Figure 3: Photographic evidence of an albino Baiomys taylori caught on the San Antonio Viejo Ranch, Jim Hogg County, Texas, USA on 16 March 2021, 17 March 2021, and 2 April 2021. A: Side view of a normal-pigmented B. taylori. B: Side view of albino B. taylori showing deep pink limbs and skin. C: Top view of albino B. taylori with red eyes visible. D. Front view from above of albino B. taylori.
First photographic record of albinism in Baiomys taylori (Rodentia: Cricetidae)

January 2022

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70 Reads

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2 Citations

Cases of albinism have been reported in less than 2% of living rodent species. Here, we report the first description of complete albinism in Baiomys taylori along with photographic evidence. This adult female was captured on three occasions as part of a long-term small mammal study on rangelands of extreme southern Texas. The individual was developing teats upon the third capture, an early sign of pregnancy. Despite selective pressures against albino phenotypes, this animal was able to survive to adulthood and potentially pass its albino alleles to offspring.


Citations (73)


... The phylogenetic position of C. mexicanus and C. leonpaniaguae within the genus Corynorhinus was examined using the newly assembled mitochondrial genomes plus the mitochondrial genomes of C. rafinesquii and C. townsendii available in the GenBank repository (#Genbank: NC_016872.1 and CM_0.47939.1, respectively [26,27]). We also include mitochondrial sequences of Plecotus auritus as an outgroup (#Genbank: NC_015484.1). ...

Reference:

Characterization of the mitochondrial genomes of the Mexican endemic bats Corynorhinus mexicanus and Corynorhinus leonpaniaguae (Chiroptera: Vespertilionidae)
Reference genome of Townsend’s big-eared bat, Corynorhinus townsendii

Journal of Heredity

... Although bats use a suite of natural structures for roosting, such as tree crevices, woodpecker cavities, and rock fields (Blomberg et al., 2021;Kalcounis-Rüppell et al., 2005;Tillon & Aulagnier, 2014), several bat species have a strong ecological association with humans because they often roost in anthropogenic structures (e.g., Voigt et al., 2016). These structures include, for example, buildings, bridges, culverts, tunnels, bat boxes, and mines (e.g., Detweiler & Bernard, 2023;Huang et al., 2022;Meierhofer et al., 2019;Mering & Chambers, 2014;Tobin & Chambers, 2017;Voigt et al., 2016). With the increasing rate of urbanization, bats are more likely to use these anthropogenic structures, underscoring the importance of comprehending the implications of this behavior on their fitness. ...

Structural and environmental predictors of presence and abundance of tri-colored bats in Texas culverts

... Disturbance of roosting sites is a significant threat to each species, and climate change may be exacerbating the challenges these species face. For example, a continued contraction of suitable habitat is expected over time due to climate change [82]. Because both species are roost-limited, and individuals are often observed foraging, and not at their roosts, we suggest management action for these species be based on prioritization of sampling areas where each species was observed and where threats were scored highest. ...

Predicting habitat suitability for Townsend's big‐eared bats across California in relation to climate change

... These structures, like buildings, were also associated with anthropogenic disturbance and pathogens. Human disturbance due to excursions or visitation of the mines (e.g., Harris et al., 2019) and active mining (Summers et al., 2023) were commonly identified in the literature, yet were not commonly quantified. Such activities can disrupt bats during the hibernation and maternity periods, which are characterized by high-energy expenditure and physiological stress (Kurta et al., 1989;Speakman & Thomas, 2003). ...

Assessment of the status of the Townsend’s big-eared bat in California

California Fish and Game

... P. destructans was first documented in North American in Albany, New York, U.S. in 2006 [17] and has since spread rapidly throughout the U.S. and Canada [17][18][19][20]. In 2018, the closest recorded outbreak of WNS was reported in San Antonio, Texas, U.S. [21,22]. The capacity of this fungus to thrive in climates across a wide range of temperatures (5-28 °C) [19,23,24] and its ease of dispersal via migratory species of bats and other hosts makes WNS a major threat to bat populations (see below). ...

Modeling the suitability of Texas karst regions for infection by Pseudogymnoascus destructans in bats
  • Citing Article
  • March 2022

Journal of Mammalogy

... As a result, while our study offers a snapshot of the types of habitats V. atricapilla are associated with, we have only limited ability to assess variability in V. atricapilla densities in response to changing habitat conditions following disturbance and for identifying thresholds for when vegetation structure and composition may become unsuitable as vegetation succession progresses. It is essential to understand V. atricapilla habitat selection in the context of vegetation succession, as this species is sympatric with other species of conservation concern, such as the globally Endangered Setophaga chrysoparia (Golden-cheeked Warbler), which occurs in higher densities in closed canopy juniper-oak woodlands that characterize later successional stages in the southeastern parts of the V. atricapilla distribution (Kroll 1980, Mueller et al. 2022.Viewing the vegetation communities that V. atricapilla rely on as complex systems with multiple stable states that depend on the frequency and time since disturbance is critical for effective conservation and for guiding the implementation of management (Long et al. 2021). ...

Demonstration of a multi‐species, multi‐response state‐and‐transition model approach for wildlife management

... Caves are key habitats for many bat species, which use them as resting and refuge places as well as breeding and parturition sites (Barros, Bernard & Ferreira, 2020;Kunz, 1982;Ormsbee, Kiser & Perlmeter, 2007;Meierhofer et al., 2022;Struebig et al., 2009). A single cave can host a high diversity of bat species. ...

Structural and environmental predictors of tricolored bat presence and abundance in Texas caves
  • Citing Article
  • December 2021

Journal of Mammalogy

... Birds are sociable [1], communicating with visual cues, sounds, and songs and engaging in behaviors such as cooperative breeding, flocking, and predator mobbing [2]. Birds can be found on all seven continents of the world, with the snow petrel breeding colonies in Antarctica stretching up to 440 km [3]. ...

Sociality and Antipredator Behavior
  • Citing Chapter
  • November 2021

... Given low Wildfires historically occurred at 13-25-yr intervals, but generally suppressed for the last 50-100 yr The last wildfire to affect the study area occurred in 1984 Portions of the survey area last burned using prescribed fire between 1999 and 2012 † Golden-cheeked warblers breed exclusively in central Texas (Ladd and Gass 2020). As such, we did not search for goldencheeked warblers at Wichita Mountains (but see Long et al. 2014). We did not detect black-capped vireos at Possum Kingdom prior to the current study but did detect a small number of black-capped vireos at Possum Kingdom in 2013 and 2014 (Long et al. 2015). ...

FIRST DOCUMENTED OBSERVATION OF THE FEDERALLY ENDANGERED GOLDEN-CHEEKED WARBLER (Setophaga chrysoparia) IN OKLAHOMA

... Unpublished data from JMH on past BLS surveys indicated that dipnets achieved higher community-wide detection probabilities than unbaited funnel or trashcan traps. These discrepancies highlight the importance of accounting for method-specific detection probabilities in population studies, particularly in systems with temporal method overlap and potential biases from predator presence, trap type, and baiting effects [144][145][146][147]. We also note that replicating pond types and hydroperiod conditions in this system was constrained by the ecological uniqueness and limited number of water-filled habitats available within the Tupelo-Cypress wetland during our survey period. ...

Variation in herpetofauna detection probabilities: implications for study design