Eurostopodus mystacalis
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA959058 | ENA |
REPOSITORIES: ENA
Similar Datasets
Project description:Eurostopodus mystacalis albogularis Genome sequencing and assembly
| PRJNA485162 | ENA
Project description:Because of their strong dependence on the environment, the spatial distribution of pond-breeding amphibians can be greatly influenced by anthropogenic habitat alteration. In some agricultural landscapes in Brazil, the anuran Pseudopaludicola mystacalis appears to be highly influenced by land use. Because adult males and tadpoles of this species are usually found in marshy areas with cattle hoof prints, we hypothesized that P. mystacalis preferentially occupies aquatic habitats with marshy areas that are trampled by cattle. To test our hypothesis, we assessed whether the occurrence of P. mystacalis is associated with the presence of cattle and trampled marshy areas, and which environmental features best explain the spatial distribution and abundance of P. mystacalis. To do so, we sampled 38 aquatic habitats in an area intensely used for livestock in southeastern Brazil. We found that the presence of cattle and trampled marshy areas in aquatic habitats are positively associated to P. mystacalis occurrence. Additionally, the abundance of calling males is better predicted by variables of landscape and local habitat structure. Specifically, the size of trampled marshy areas and the proportion of herbaceous vegetation within the aquatic habitat are positively associated with abundance, while distance to nearest aquatic habitat are negatively associated with abundance of calling males. All three of these variables can be directly or indirectly linked to the presence of cattle or grazing management. Therefore, this work shows evidence that Pseudopaludicola mystacalis is positively influenced by grazing management with cattle, and draws attention to other unknown potential consequences of different land use to fresh water diversity.
| S-EPMC5033334 | biostudies-literature
Project description:modENCODE_submission_5986 This submission comes from a modENCODE project of Jason Lieb. For full list of modENCODE projects, see http://www.genome.gov/26524648 Project Goal: The focus of our analysis will be elements that specify nucleosome positioning and occupancy, control domains of gene expression, induce repression of the X chromosome, guide mitotic segregation and genome duplication, govern homolog pairing and recombination during meiosis, and organize chromosome positioning within the nucleus. Our 126 strategically selected targets include RNA polymerase II isoforms, dosage-compensation proteins, centromere components, homolog-pairing facilitators, recombination markers, and nuclear-envelope constituents. We will integrate information generated with existing knowledge on the biology of the targets and perform ChIP-seq analysis on mutant and RNAi extracts lacking selected target proteins. For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODEDataReleasePolicyFinal2008.pdf EXPERIMENT TYPE: CHIP-seq. BIOLOGICAL SOURCE: Strain: N2; Developmental Stage: L3 Larva; Genotype: wild type; Sex: mixed Male and Hermaphrodite population; EXPERIMENTAL FACTORS: Developmental Stage L3 Larva; temp (temperature) 20 degree celsius; Strain N2; Antibody NURF-1 SDQ3525 (target is NURF-1)
2013-08-28 | E-GEOD-50296 | biostudies-arrayexpress