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Gardner, A. S.

Publications and source records attributed to Gardner, A. S..

2 recordsLinked to original sources

How air temperature and solar radiation impact life history traits in a wild insect

Ectotherms are essential components of all ecosystems and rely on external heat to regulate their body temperature. For most terrestrial ectotherms the primary sources of heat are ambient temperature and solar radiation. Many insects can use movement to respond to changes in temperature and solar radiation in order to manage their body temperature and optimise life history traits. However, we lack the understanding of the relative importance of temperature and shade that we need to predict how the combined effects of changes in air temperature and cloud cover will impact terrestrial insect populations. We reared developing nymphs of the field cricket (Gryllus campestris) at high and low air temperature sites with partially shaded and unshaded treatments at each site. Given the broad altitudinal range of this species, we tested the possibility of local adaptation to these climate variables by rearing nymphs from high and low altitude genetic lineages in all treatment combinations. We found that development time was strongly affected by air temperature, but not by a substantial increase in shade. This suggests that developing crickets can compensate for an increase in shade, presumably because in unshaded conditions they forgo some opportunities to gain energy from the sun. We found that mass at adulthood was affected by an interaction between availability of sun (shading treatment) and air temperature. This indicates that changes in cloud cover will impact insects differently in warmer and cooler areas. We found no evidence for local adaptation in these traits. Our findings underscore the need to consider both ambient temperature and solar radiation in predicting the impacts of climate change on insect populations, as shifts in temperature and cloud cover may have complex and region-specific effects on these vital ecosystem components.

evolutionary biology↗

Newly repopulated spinal cord microglia exhibit a unique transcriptome and coincide with sex-independent pain resolution

Microglia contribute to the initiation of pain, however, a translationally viable approach addressing how or when to modulate these cells remains elusive. We used a targeted, inducible, genetic microglial depletion strategy at both acute and acute-to-chronic transition phases in the clinically-relevant tibial fracture/casting pain model to determine the contribution of microglia to the initiation and maintenance of pain. We observed complete resolution of pain after transient microglial depletion at the acute-to-chronic phase, which coincided with the timeframe of full repopulation of microglia. These repopulated microglia were morphologically distinct from control microglia, signifying they may exhibit a unique transcriptome. RNA sequencing of repopulated spinal cord microglia identified genes of interest using weighted gene co-expression network analysis (WGCNA). We intersected these genes with a newly-generated single nuclei microglial dataset from human spinal cord dorsal horn and identified human-relevant genes that may ultimately promote pain resolution after injury. This work presents a novel approach to gene discovery in pain and provides comprehensive datasets for the development of future microglial-targeted therapeutics.

neuroscience↗