Biology subjects

Garratt, M.

Publications and source records attributed to Garratt, M..

7 recordsLinked to original sources

bioRxiv2026

Annual ploughing turns wildflower plantings into ecological traps for ground-nesting wild bees

Wildflower plantings are an important conservation measure for supporting wild bee diversity. They aim to enhance floral resources for nutrition, but do not explicitly consider that bees also require suitable nesting and overwintering resources. Wildflower plantings may provide nesting habitat for ground-nesting bees, but the effects of soil management, e.g. ploughing, on ground-nesting bees are hardly known. To study how ploughing and age of wildflower plantings affect ground-nesting bees, we sampled bees on ploughed and unploughed wildflower plantings aged 0-4 years. We used emergence traps to sample bees directly after emergence from the ground, allowing inference on nest numbers. We found that ploughing and wildflower planting age negatively affected overwintering bee nest numbers. Nesting peaked in the year of wildflower planting establishment and declined thereafter, indicating lower habitat suitability at later successional stages. Annual ploughing caused the greatest reduction in nest numbers (-72 %), providing evidence for an ecological trap.

ecology↗

bioRxiv2026

Targeting Estrogen to the Brain via the Prodrug DHED does not Protect Against Metabolic Dysfunction in Obese, OVX mice.

Menopausal hormone therapy (MHT) is prescribed for climacteric symptoms including hot flushes and weight gain and contains estrogens such as 17 beta-estradiol (17{beta}E2). However, estrogen receptor activation by MHT may increase reproductive cancers and cardiovascular event risk in some people. As the protective metabolic effects of 17{beta}E2 are partly mediated through the arcuate nucleus of the hypothalamus, restricting 17{beta}E2 actions to the brain could serve as a safer mechanism of MHT. 10{beta},17{beta}-Dihydroxyestra-1,4-dien-3-one (DHED) is a prodrug of 17{beta}E2 which is enzymatically converted to the parent hormone exclusively within the brain. DHED has demonstrated positive benefit in rodent models of centrally-mediated maladies including hot flushes, depression and cognitive decline, without peripheral hormonal burden. Therefore, we hypothesized that DHED treatment in obese female mice would act within the hypothalamus to provide the same beneficial metabolic effects as 17{beta}E2. Female mice were ovariectomized, placed on a high fat diet and split into either control, DHED, or 17{beta}E2 treatment groups. Body weight, uterus weight and glucose tolerance were recorded along with gonadal hormone receptor expression in the brain. Delivery of DHED at a similar dose as 17{beta}E2 failed to improve metabolic parameters or recapitulate the hypothalamic responses induced by 17{beta}E2. Delivery of DHED at higher doses, which elicited estrogen-like actions within the brain, still failed to improve metabolic health. Our findings suggest that peripheral actions, in addition to hypothalamic targets, may be required to mediate 17{beta}E2s protective effects on metabolism and that brain-targeted MHT may be unsuitable for improving metabolic health during menopause.

physiology↗

bioRxiv2026

Threading the needle: Spatial constraints sharpen visual sensitivity in honeybees

Navigating dense clutter requires honeybees to execute rapid visuomotor comparisons to identify the best route. How they resolve perceptual inputs to make a passage choice from multiple options is an open question. We studied this in a free flying paradigm where bees were challenged to choose between a taller and shorter aperture with varying height difference. We monitored choice across four height difference ratios at three spatial scales. Bees chose the taller aperture in all tests, but the precision of these choices depended heavily on the absolute size of the gap. For each size scale of aperture pairs, psychometric modelling revealed that when making a choice bees generally evaluate the relative height difference, conforming to Webers law. However, bees choices were non-uniformly sensitive across aperture size scales. Bees had greater sensitivity at the smallest spatial scale, where the likelihood of collision danger is larger. This deviation in behaviour due to absolute aperture size suggests a dynamic risk-cost trade-off. Bees appear to prioritise costly, high-acuity inspections only when imposed by critical physical constraints of the environment, relaxing this vigilance at safer, larger scales to conserve energy.

animal behavior and cognition↗

bioRxiv2025

Reducing ploughing promotes ground-nesting flying insects

Many flying insects, such as bees, wasps, and hoverflies, live aboveground, but depend on soil for nesting, development, and overwintering. In agricultural landscapes, soil is managed for production and therefore frequently subjected to disturbances such as ploughing. The impacts of ploughing on flying insects that spend part of their life cycle belowground remain largely unknown. To investigate the effects of ploughing on ground-nesting flying insects, we conducted a two-year field experiment in flower strips subjected to different treatments, ranging from annual ploughing to four years without ploughing. Insects emerging from the soil were sampled using emergence traps, allowing a direct assessment of their response to ploughing at different frequencies. For each treatment, we measured insect biomass, abundance, and body size. We found that ploughing substantially reduced flying insect biomass. When sites were left unploughed, biomass increased rapidly, particularly during the first years of recovery. However, regardless of the time since the last disturbance, ploughing always reduced insect biomass to similarly low levels, driven primarily by declines in the abundance of large insects. Our findings highlight that even moderate reductions in ploughing frequency, for example, only every second year, can benefit ground-nesting flying insects and point to the potential for incorporating reduced ploughing frequencies into agricultural management and agri-environmental schemes.

ecology↗

bioRxiv2022

Lifespan Extension in Female Mice By Early, Transient Exposure to Adult Female Olfactory Cues

Several previous lines of research have suggested, indirectly, that mouse lifespan is particularly susceptible to endocrine or nutritional signals in the first few weeks of life, as tested by manipulations of litter size, growth hormone levels, or mutations with effects specifically on early-life growth rate. The pace of early development in mice can also be influenced by exposure of nursing and weanling mice to olfactory cues. In particular, odors of same-sex adult mice can in some circumstances delay maturation. We hypothesized that olfactory information might also have a sex-specific effect on lifespan, and we show here that lifespan of female mice can be increased significantly by odors from adult females administered transiently, i.e. from 3 days until 60 days of age. Female lifespan was not modified by male odors, nor was male lifespan susceptible to odors from adults of either sex. Conditional deletion of the G protein Go in the olfactory system, which leads to impaired accessory olfactory system function and blunted reproductive priming responses to male odors in females, did not modify the effect of female odors on female lifespan. Our data provide support for the idea that very young mice are susceptible to influences that can have long-lasting effects on disease resistance, and provide the first example of lifespan extension by olfactory cues in mice.

evolutionary biology↗

bioRxiv2020

Castration delays epigenetic aging and feminises DNA methylation at androgen-regulated loci

In mammals, females generally live longer than males. Nevertheless, the mechanisms underpinning sex-dependent longevity are currently unclear. Epigenetic clocks are powerful biological biomarkers capable of precisely estimating chronological age using only DNA methylation data. These clocks have been used to identify novel factors influencing the aging rate, but few studies have examined the performance of epigenetic clocks in divergent mammalian species. In this study, we developed the first epigenetic clock for domesticated sheep (Ovis aries), and using 185 CpG sites can predict chronological age with a median absolute error of 5.1 months from ear punch and blood samples. We have discovered that castrated male sheep have a decelerated aging rate compared to intact males, mediated at least in part by the removal of androgens. Furthermore, we identified several androgen-sensitive CpG dinucleotides that become progressively hypomethylated with age in intact males, but remain stable in castrated males and females. Many of these androgen sensitive demethylating sites are regulatory in nature and located in genes with known androgen-dependent regulation, such as MKLN1, LMO4 and FN1. Comparable sex-specific methylation differences in MKLN1 also exist in mouse muscle (p=0.003) but not blood, indicating that androgen dependent demethylation exists in multiple mammalian groups, in a tissue-specific manner. In characterising these sites, we identify biologically plausible mechanisms explaining how androgens drive male-accelerated aging.

developmental biology↗

bioRxiv2020

Sex hormones underlying 17a-Estradiol effects on neuroinflammation

17--estradiol (17aE2) treatment extends lifespan in male mice and can reduce neuroinflammatory responses in the hypothalamus of 12-month-old males. Although 17aE2 improves longevity in males, female mice are unaffected, suggesting a sexually dimorphic pattern of lifespan regulation. We tested whether the sex-specific effects of 17aE2 on neuroinflammatory responses are mediated by sex hormones and whether hypothalamic changes extend to other brain regions in old age. Manipulating sex hormone levels through gonadectomy, we show that sex-specific effects of 17aE2 on age-associated gliosis are brain region-specific and are partially dependent on gonadal hormone production. 17aE2 treatment started at 4 months of age protected 25-month-old males from hypothalamic inflammation. Castration prior to 17aE2 exposure reduced the effect of 17aE2 on hypothalamic astrogliosis. By contrast, sex-specific changes in microgliosis with 17aE2 were not significantly affected by castration in males. While 17aE2 treatment had no effect of hypothalamic astrocytes or microglia in intact females, ovariectomy significantly increased the occurrence of hypothalamic gliosis evaluated in 25-month-old females, which was partially reduced by 17aE2. In the hippocampus, both male and female gonadally-derived hormones influenced the severity of gliosis and the responsiveness to 17aE2 in a regiondependent manner. The male-specific effects of 17aE2 correlate with changes in hypothalamic ER expression, highlighting a receptor through which 17aE2 could act. The results of this study demonstrate that neuroinflammatory responses to 17aE2 are partially controlled by the presence of sex-specific gonads. Interactions between sex-steroids and neuroinflammation could, therefore, influence late-life health and disease onset, leading to sexual dimorphism in aging.

neuroscience↗