Biology subjects

Mayer, N.

Publications and source records attributed to Mayer, N..

3 recordsLinked to original sources

bioRxiv2026

Urbanization and wealth alter arthropod biodiversity and pollination services in community gardens

1. As city populations expand globally, understanding how urbanization shapes ecosystem services is increasingly important. Urban agriculture plays a key role in food access, particularly in low-income areas with limited access to fresh produce. Arthropods play important roles in these systems through pollination, herbivory, pest control, and nutrient cycling. Urban development of natural areas often reduces biodiversity, including that of arthropods. Additionally, urban biodiversity frequently correlates positively with socioeconomic conditions, a pattern known as the luxury effect. 2. In this study, we examined how gradients in urbanization and socioeconomic context relate to local and landscape habitat quality, arthropod abundance, and pollination services across 21 community gardens in the Denver, CO Metro Area. To quantify ecosystem services, we employed a sentinel plant, Cucumis sativus (cucumber), and collected arthropods (insects, myriapods, arachnids, isopods), assigning them to functional groups based on their known feeding behavior. We evaluated direct and indirect pathways linking urban matrix characteristics to arthropod-mediated ecosystem services. 3. The abundance of all arthropod groups (including pollinators, herbivores, and natural enemies) declined steeply with increasing impervious surface. Neighborhood wealth was associated only with bee species richness and Shannon diversity and displayed a hump-shaped pattern that peaked at wealth levels 35-46% above the national average, then declined. Multivariate GLMs revealed that Western honeybees (Apis mellifera) were the only species driving differences in bee community composition, with their abundance positively related to neighborhood wealth. 4. We also observed pollen limitation in our cucumber plants, and as bee Shannon diversity increased, cucumber production increased. Environmental covariates alone showed no direct relationship with cucumber production, indicating that insect pollination mediated this effect. This work identifies the biophysical and social-ecological drivers of urban arthropod biodiversity and ecosystem services, revealing where crop production may be most vulnerable to decline in cities.

ecology↗

bioRxiv2026

Platelet Molecular Maturation Links Platelet Aging and the Platelet Storage Lesion

Human platelets change over their 7-10 day lifespan, yet the molecular mechanisms underlying platelet aging remain poorly defined. Using two independent RNA sequencing datasets of fluorescence-activated cell sorted young and old human platelets, we developed a unified transcriptomic model to characterize RNA metabolism across the platelet lifespan, which we termed platelet molecular maturation. This was applied to RNA sequencing data from room-temperature stored platelets (up to 7 days) and cold-stored platelets (7, 14, or 21 days). We identified highly concordant aging signatures, including 6,015 shared expressed genes and 2,008 shared differentially expressed genes (DEGs) with strongly correlated fold changes, demonstrating a conserved platelet aging program. Nucleotide-level analyses revealed preferential 3'-directed degradation among downregulated transcripts during endogenous platelet aging and room-temperature storage, supporting an organized RNA decay process that was correlated with platelet function changes. Room-temperature storage recapitulated platelet molecular maturation, showing concordance with aging-related gene expression changes and enrichment of downregulated gene sets. In contrast, cold-storage significantly attenuated platelet molecular maturation and 3'-directed degradation. A total of 669 genes were consistently differentially expressed between room-temperature and cold-stored platelets, while no DEGs were detected during cold-storage, indicating transcriptional stability. Platelet transcript stability in cold-storage correlated with preserved platelet hemostatic function. These findings establish platelet molecular maturation as a conserved, functionally relevant model linking endogenous platelet aging to platelet storage lesions and providing mechanistic insight into preserved platelet hemostatic function in cold-storage. This atlas of platelet RNA metabolism supports biomarker discovery and strategies to improve storage. KEY POINTSO_LIBy integrating multiple high-quality RNA sequencing datasets with novel analytic approaches tailored to the biology of anucleate platelets, we show that platelet aging is not a passive process of transcript decay, but follows a structured and reproducible molecular trajectory both endogenously and in storage, which we term platelet molecular maturation. C_LIO_LIStorage temperature emerged as a dominant modifier of this trajectory, with cold-storage markedly slowing RNA metabolic kinetics and preserving transcripts associated with younger, more hemostatically competent platelets. C_LIO_LITogether, these findings provide mechanistic insight into the platelet storage lesion and identify transcriptomic features that may serve as biomarkers or therapeutic targets to extend platelet shelf life. C_LI

genomics↗

bioRxiv2019

The microstructure of laminin-111 compensates for dystroglycan loss in functional differentiation of mammary epithelial cells

AbstractLaminin-111, an extracellular matrix (ECM) glycoprotein found in the basement membrane of mammary gland epithelia, is essential for lactation. In mammary epithelial cells, dystroglycan (Dg) is believed to be necessary for polymerization of laminin-111 into networks, thus we asked whether correct polymerization could compensate for Dg loss. Artificially polymerized laminin-111 and the laminin-glycoprotein mix Matrigel, both formed branching, spread networks with fractal dimensions from 1.7-1.8, whereas laminin-111 in media formed small aggregates without fractal properties (a fractal dimension of 2). In Dg knockout cells, either polymerized laminin-111 or Matrigel readily attached to the cell surface, whereas aggregated laminin-111 did not. In contrast, polymerized and aggregated laminin-111 bound similarly to Dg knock-ins. Both polymerized laminin-111 and Matrigel promoted cell rounding, clustering, formation of tight junctions, and expression of milk proteins, whereas aggregated Ln-1 did not attach to cells or promote functional differentiation. HighlightsO_LILaminin assembles into a fractal network when in presence of either the cell surface receptor dystroglycan or acidic glycoproteins or an acidic buffer. C_LIO_LIWhen this microstructure is recreated with an acidic treatment, laminin binds readily to dystroglycan null cells and induces functional differentiation of mammary epithelial cells. C_LI

bioengineering↗