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The intensification of land use over past millennia has accelerated habitat loss and fragmentation. This is hypothesized to lead to reductions in population sizes and restrictions in gene flow, processes that amplify genetic drift with profound negative impacts on species and populations. However, empirical data on the population genetic impacts of habitat fragmentation remain limited, particularly for presumed abundant species such as insects. Reports of dramatic insect and arthropod declines are increasing, and their short generation times and limited dispersal capacities make them especially vulnerable to habitat fragmentation. To substantiate the hypothesis that habitat fragmentation negatively impacts genetic composition and demography, we combined historical agricultural land use data from Denmark with whole-genome resequencing of 25 populations of the collembolan Entomobrya nicoleti from natural grasslands. Abundance data indicate that agricultural expansion reduces habitat suitability and fragments populations. Demographic modelling shows that intensification of agricultural land use coincides with severe declines in effective population sizes. It is likely that these declines have yet to reach their full effect on current levels of genetic diversity because of the 'drift debt,' where the genetic diversity of recently declined populations will erode over future generations. Gene flow estimates revealed sharp recent declines that coincide with agricultural intensification. Our results underscore that even seemingly abundant species in fragmented landscapes can experience severe reductions in effective population size and gene flow. These demographic shifts predict future genetic erosion, highlighting the delayed yet inevitable consequences of habitat fragmentation for population persistence.
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http://dx.doi.org/10.1111/mec.17820 | DOI Listing |
J Mol Cell Cardiol
September 2025
Cardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA. Electronic address:
Selective therapeutic targeting of cardiomyocytes (CMs) and non-myocytes (NMs) within the heart is an active field of research. The success of those novel therapeutic strategies is linked to the ability to accurately assess uptake and gene delivery efficiencies in clinically relevant animal models. Nevertheless, quantification at the single cell level remains a significant challenge.
View Article and Find Full Text PDFArch Med Res
September 2025
Universidad Autónoma de Nuevo León, College of Medicine, Biochemistry and Molecular Medicine Department, Monterrey, Mexico; Universidad Autónoma de Nuevo León, Center for Research and Development in Health Sciences, Neurometabolism Unit, Monterrey, Mexico. Electronic address:
Background: Long-chain ceramides have been implicated in anxiety-like behavior and in priming microglial activation, suggesting a possible lipid-immune crosstalk in emotional regulation.
Methods: We systemically administered a mixture of C16:0, C18:0, C22:0, C24:0, and C24:1 ceramides to adult male and female mice. Anxiety-like behavior was assessed with behavioral tests.
Immunobiology
August 2025
Center for Cellular Engineering, Department of Transfusion Medicine and Center for Cellular Engineering, NIH Clinical Center, Bethesda, MD 20892, USA. Electronic address:
Background: Hematopoietic progenitor cells (HPCs) and mononuclear cells (MNCs) are critical components of cell-based therapies, including bone marrow transplantation and regenerative treatments. Evaluation of the characteristics of these products during collection, storage, and transport is essential for maintaining cell viability and functionality. In this study, we evaluated the functional and molecular stability of samples collected for the evaluation of fresh HPC and MNC products.
View Article and Find Full Text PDFJ Am Heart Assoc
September 2025
Background: Cardiac issues following radiotherapy are increasingly prevalent among patients with thoracic cancer and coronary disease. However, the mechanisms underlying radiotherapy-induced plaque instability and changes in plaque characteristics on imaging remain unclear. This study used single-cell RNA sequencing to identify key features of vulnerable plaques following radiotherapy.
View Article and Find Full Text PDFFunct Integr Genomics
September 2025
Department of Otolaryngology-Head and Neck Surgery, Maternal and Child Health Hospital of Hubei Province, NO.745 Wuluo Road, Hongshan District, Wuhan, 430070, Hubei Province, China.
Background: Head and neck squamous cell carcinoma (HNSCC) stands as a significant global health concern, marked by its substantial impact on both morbidity and mortality rates. Although previous studies have suggested that circular RNAs (circRNAs) may influence HNSCC progression, the underlying mechanisms remain largely unclear.
Methods: In this study, we first used quantitative real-time polymerase chain reaction (qRT-PCR) to measure the expression levels of circSHPRH in HNSCC tissues and cell lines.