Three-spined stickleback armour predicted by body size, minimum winter temperature and pH

Similar phenotypes evolve under equivalent environmental conditions through parallel evolution. Because they have repeatedly invaded and adapted to new freshwater environments, the three-spined stickleback (Gasterosteus aculeatus) offers a powerful system for understanding the agents of selection in nature that drive parallel evolution. Here we examine the ecological and environmental variables responsible for morphological variation in three-spined stickleback populations across its European range. We collected fish from 85 populations, encompassing much of the European latitudinal range of the species and including lowland rivers and lakes, coastal lagoons, and moorland ponds. We measured biotic and environmental variables at all sites along with morphological traits for 2,358 individuals. Using an information theory approach, we identified body size, minimum average winter temperature and pH as primary predictors of stickleback armour evolution, challenging current hypotheses for stickleback morphological diversification and demonstrating the fundamental role played by body size and scaling in mediating responses to selection. Stickleback lateral plate phenotype represents a potentially powerful tool for monitoring change in climate variables across the northern temperate region

Species abundance distributions: moving beyond single prediction theories to integration within an ecological framework

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75247/1/j.1461-0248.2007.01094.x.pd

Do precocial mammals develop at a faster rate? A comparison of rates of skull development in Sigmodon fulviventer and Mus musculus domesticus

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/72993/1/j.1420-9101.2003.00568.x.pd

Comprehensive analysis of epigenetic clocks reveals associations between disproportionate biological ageing and hippocampal volume

The concept of age acceleration, the difference between biological age and chronological age, is of growing interest, particularly with respect to age-related disorders, such as Alzheimer’s Disease (AD). Whilst studies have reported associations with AD risk and related phenotypes, there remains a lack of consensus on these associations. Here we aimed to comprehensively investigate the relationship between five recognised measures of age acceleration, based on DNA methylation patterns (DNAm age), and cross-sectional and longitudinal cognition and AD-related neuroimaging phenotypes (volumetric MRI and Amyloid-β PET) in the Australian Imaging, Biomarkers and Lifestyle (AIBL) and the Alzheimer’s Disease Neuroimaging Initiative (ADNI). Significant associations were observed between age acceleration using the Hannum epigenetic clock and cross-sectional hippocampal volume in AIBL and replicated in ADNI. In AIBL, several other findings were observed cross-sectionally, including a significant association between hippocampal volume and the Hannum and Phenoage epigenetic clocks. Further, significant associations were also observed between hippocampal volume and the Zhang and Phenoage epigenetic clocks within Amyloid-β positive individuals. However, these were not validated within the ADNI cohort. No associations between age acceleration and other Alzheimer’s disease-related phenotypes, including measures of cognition or brain Amyloid-β burden, were observed, and there was no association with longitudinal change in any phenotype. This study presents a link between age acceleration, as determined using DNA methylation, and hippocampal volume that was statistically significant across two highly characterised cohorts. The results presented in this study contribute to a growing literature that supports the role of epigenetic modifications in ageing and AD-related phenotypes

Use of SMS texts for facilitating access to online alcohol interventions: a feasibility study

A41 Use of SMS texts for facilitating access to online alcohol interventions: a feasibility study In: Addiction Science & Clinical Practice 2017, 12(Suppl 1): A4