This data release comprises a dataset that contains sample collection information and microsatellite genotypes, and another dataset that contains single nucleotide polymorphism (SNP) genotypes with sample collection information for populations of white-tailed ptarmigan across the species' range. There is also an additional file (accession numbers.xlsx) linking samples to accession numbers in Genbank. This data was collected in order to address the following: The delineation of intraspecific units that are evolutionarily and demographically distinct is an important step in the development of species-specific management plans. Neutral genetic variation has served as the primary data source for delineating units for conservation, but with recent advances in genomic technology, we now have an unprecedented ability to utilize information about neutral and adaptive variation across the entire genome. Here, we use traditional genetic markers (microsatellites) and a newer reduced-representation genomic approach (single nucleotide polymorphisms) to delineate distinct groups of white-tailed ptarmigan (Lagopus leucura), an alpine-obligate species that is distributed in naturally fragmented habitats from Alaska to New Mexico.

Dataset containing information for white-tailed deer samples from Ohio, Pennsylvania, Maryland, Virginia and New York, genotyped for 11 microsatellites markers. Marker OvirQ should not be used as it presents alleles inconsistent with reported pattern, with some alleles separated by only 1 base pair and inconsistent between runs. Projected coordinates representing sampling location are in a user-defined CRS, similar to USA Contiguous Albers Equal Area Conic: "+proj=aea +lat_1=29.3 +lat_2=45.3 +lat_0=23 +lon_0=-96 +x_0=0 +y_0=0 +ellps=GRS80 +towgs84=0,0,0,0,0,0,0 +units=m +no_defs".

Dataset containing information for white-tailed deer samples from Ohio, Pennsylvania, Maryland, Virginia and New York, genotyped for 11 microsatellites markers. Marker OvirQ should not be used as it presents alleles inconsistent with reported pattern, with some alleles separated by only 1 base pair and inconsistent between runs. Projected coordinates representing sampling location are in a user-defined CRS, similar to USA Contiguous Albers Equal Area Conic: "+proj=aea +lat_1=29.3 +lat_2=45.3 +lat_0=23 +lon_0=-96 +x_0=0 +y_0=0 +ellps=GRS80 +towgs84=0,0,0,0,0,0,0 +units=m +no_defs".

This data set provides sample data and NCBI accession information for genomic sequencing of ptarmigan and grouse from Alaska.

This data set provides sample data and NCBI accession information for genomic sequencing of ptarmigan and grouse from Alaska.

This data set contains sampling information, allele sizes of 11 microsatellite loci, and Genbank accession numbers of ddRAD seq results for scoters (Melanitta sp.). Microsatellite data is provided for three North American species of scoter (black scoter, M. americana n = 61; white-winged scoter, M. deglandi, n = 208; surf scoter, M. perspicillata, n = 145) and their European congeners (common scoter, M. nigra, n = 19; velvet scoter, M. fusca, n = 20). Individuals with ddRAD results include 27 black scoters, 4 common scoters, 32 surf scoters, 28 white-winged scoters, and 4 velvet scoters.

This data set contains sampling information, allele sizes of 11 microsatellite loci, and Genbank accession numbers of ddRAD seq results for scoters (Melanitta sp.). Microsatellite data is provided for three North American species of scoter (black scoter, M. americana n = 61; white-winged scoter, M. deglandi, n = 208 ; surf scoter, M. perspicillata, n = 145) and their European congeners (common scoter, M. nigra, n = 19; velvet scoter, M. fusca, n = 20 ). Individuals with ddRAD results include 27 black scoters, 4 common scoters, 32 surf scoters, 28 white-winged scoters, and 4 velvet scoters.

These data were compiled to provide land-management relevant information on the native and nonnative subspecies (subsp.) of Phragmites australis (subsp. americanus and subsp. australis, respectively) in Glen Canyon National Recreation Area (NRA), Grand Canyon National Park (NP), Arches National Park, and Bill Williams National Wildlife Refuge. Specifically, the goals of this work were to determine the extent and distribution of Phragmites australis subspecies in the Glen and Grand Canyon regions, evaluate if P.a. subsp. americanus can be reliably distinguished from P.a. subsp. australis using morphological characters in this region, and determine if P.a. subsp. americanus exhibits genetic structure in the study area. The objectives of our study were to determine how prevalent the nonnative Phragmites is in the study area and support native plant material development for restoration activities in Glen Canyon NRA and Grand Canyon NP. These data represent real-time PCR cycle threshold values (Ct scores) for two target regions, nuclear microsatellite data for seven loci, and morphological data. These data were collected for 84 sites including five nonnative Phragmites locations and 79 native Phragmites locations. Tissue samples were mostly collected along the Colorado River between Glen Canyon Dam and Lake Mead, around Lake Powell, and in tributaries to the Colorado River from 2021 through 2024. Tissue samples and herbarium collections were collected from one to fifteen ramets across each stand, where multiple samples from one stand were spread across its full area. Reference samples for both the native and nonnative Phragmites, Phragmites australis subsp. berlandieri, and a hybrid of P.a. australis and P.a. americanus were acquired and included in analyses. Samples were dried and total genomic DNA was extracted using Qiagen DNeasy Plant MiniKits. Real-time polymerase chain reactions (PCR) with two target regions, AMER and AMAU, were used to identify nonnative Phragmites individuals (Lindsay et al, 2023). We then amplified 7 microsatellite loci (Saltonstall, 2003; Meyerson and others, 2010) using PCR and analyzed the fragments on an ABI 3730XL Genetic Analyzer with GeneScan LIZ500 internal size standard. Although P. australis is polyploid, these loci all had no more than two alleles, so were treated as diploid data. We then collected field and lab data on morphological characters for the stands we genetically tested, following previously described diagnostic characters (Swearington and Saltonstall, 2012; McTavish et al, 2023) These data can be used to evaluate if a stand of Phragmites is nonnative, native, or a hybrid of the two. It can also be used to determine genetic diversity and structure across the sampled stands. Finally, they can be used to assess morphological variability in native Phragmites stands across the region.

Collection data for rabbit tissues sequenced for metagenomic evaluation of selected tissues.

This data set provides sample information, microsatellite genotype, and NCBI accession numbers for mitochondrial DNA sequences of peregrine falcons (Falco peregrinus) from North America and Russia.