Rensch's Rule describes a pattern of interspecific allometry in which sexual size dimorphism (SSD) increases with size among closely related species (i.e., among a group of related species, the largest ones tend to show more male-biased SSD). Sexual selection is often invoked to explain Rensch's Rule, as larger male body size is assumed to be favoured by sexual selection for increased fighting performance in contests for mating opportunities. Often, however, the correlation between size and performance is not well described. We studied a sexually selected performance trait, bite force in Anolis lizards, to determine whether patterns of SSD are linked to size-associated patterns of performance dimorphism at the macroevolutionary level, as expected under the sexual selection hypothesis for Rensch's Rule. Additionally, we tested whether allometric patterns of performance dimorphism differ between mainland and island species, as the latter have likely evolved under a stronger sexual selection regime. We found that SSD overwhelmingly explains the relationship between performance dimorphism and size in anoles, as expected under a sexual selection model for Rensch's Rule. However, residual performance dimorphism was higher in island than in mainland species, suggesting that these groups differ in performance dimorphism for reasons unrelated to size. Head size dimorphism was associated with residual performance dimorphism, but did not fully explain the difference in performance dimorphism between island and mainland species. Together, these findings highlight the need to interpret Rensch's Rule patterns of body size evolution cautiously, as allometric patterns of performance dimorphism and size dimorphism might not be equivalent.
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http://dx.doi.org/10.1093/jeb/voae148 | DOI Listing |
Alzheimers Dement
December 2024
Georgia Institute of Technology, Atlanta, GA, USA.
Background: Chronic stress promotes life-long risk for neuropsychiatric decline by increasing neuroinflammation and disrupting synaptic health and plasticity. Our lab and others have recently demonstrated that non-invasive gamma sensory stimulation (flicker) modulates immune signaling, restores microglial function, and improves cognitive performance in mouse models of Alzheimer's disease (AD). However, no research to date has studied the effects of flicker in the context of stress.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA.
Background: Several studies have indicated sex-specific genetic risk for Alzheimer's disease (AD), but these were centered on non-Hispanic White individuals of European ancestry. We sought to identify sex-specific genetic variants for AD in non-Hispanic and Hispanic subjects of admixed African ancestry.
Method: Participants were ages 60+, of African ancestry (≥25%), and diagnosed as cases or controls.
Alzheimers Dement
December 2024
Stanford University, Stanford, CA, USA.
Background: The X-chromosome remains largely unexplored in Alzheimer's disease (AD). We performed the first, stratified X-wide association study (XWAS) of AD to chart the role of X-chromosome genetic variation in AD sexual dimorphism and heterogeneity of APOE*4-related AD risk.
Method: The study overview is shown in Figure 1A.
Theranostics
January 2025
Department of Radiation Oncology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Local immunomodulation with nanoparticles (NPs) and focused ultrasound (FUS) is recognized for triggering anti-tumor immunity. However, the impact of these tumor immunomodulations on sex-specific microbiome diversity at distant sites and their correlation with therapeutic effectiveness remains unknown. Here, we conducted local intratumoral therapy using immunogenic cell death-enhancing Calreticulin-Nanoparticles (CRT-NPs) and FUS in male and female mice.
View Article and Find Full Text PDFSci Total Environ
December 2024
Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, 81 Meishan Road, Hefei 230032, China; MOE Key Laboratory of Population Health Across Life Cycle, 81 Meishan Road, Hefei 230032, Anhui, China. Electronic address:
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