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Fawcett, K.

Publications and source records attributed to Fawcett, K..

2 recordsLinked to original sources

Terrain ruggedness and human activities influence the distribution of Grauer's gorillas and eastern chimpanzees in the Tayna Nature Reserve, Democratic Republic of Congo

The Albertine Rift Hotspot in east-central Africa is one of the most biodiverse regions in the world. It hosts a number of conservation-priority species, including Critically Endangered Grauers gorillas and Endangered eastern chimpanzees. Yet, prolonged insecurity in the region has made wildlife monitoring and conservation challenging. This is particularly true of the northeastern limits of the range of Grauers gorillas, where wide stretches of unprotected forest could harbor behaviorally and genetically unique peripheral populations of great apes and other species. Here, we developed a rapid wildlife survey method to map population distributions and monitor the impact of various human activities in the Tayna Nature Reserve in eastern Democratic Republic of Congo. Despite a lack of surveys since the early 2000s, we find that Grauers gorillas and eastern chimpanzees, as well as a number of smaller-bodied species, have persisted in Tayna. Observations of gorilla and chimpanzee signs were highly heterogeneous. They were less dense near human settlements and artisanal mines and peaked in areas with rugged terrain. The association with rugged terrain may be a result of historical anthropogenic pressure, behavioral avoidance of human activities, and/or ecological preference. Maintaining connectivity between patches of suitable great ape habitat will be critical for long-term great ape conservation in the Albertine Rift region. Our findings also demonstrate the utility of priority species monitoring driven by local communities for conservation initiatives.

ecology↗

SNPs associated with HHIP expression have differential effects on lung function in males and females

Adult lung function is highly heritable and 279 genetic loci were recently reported as associated with spirometry-based measures of lung function. Though lung development and function differ between males and females throughout life, there has been no genome-wide study to identify genetic variants with differential effects on lung function in males and females. Here, we present the first genome-wide genotype-by-sex interaction study on four lung function traits in 303,612 participants from the UK Biobank. We detected five SNPs showing genome-wide significant (P<5 x 10-8) interactions with sex on lung function, as well as 21 suggestively significant interactions (P<1 x 10-6). The strongest sex interaction signal came from rs7697189 at 4:145436894 on forced expiratory volume in 1 second (FEV1) (P = 3.15 x 10-15), and was replicated (P = 0.016) in 75,696 individuals in the SpiroMeta consortium. Sex-stratified analyses demonstrated that the minor (C) allele of rs7697189 increased lung function to a greater extent in males than females (untransformed FEV1 {beta} = 0.028 [SE 0.0022] litres in males vs {beta} = 0.009 [SE 0.0014] litres in females), and this effect was not accounted for by differential effects on height, smoking or age at puberty. This SNP resides upstream of the gene encoding hedgehog-interacting protein (HHIP) and has previously been reported for association with lung function and HHIP expression in lung tissue. In our analyses, while HHIP expression in lung tissue was significantly different between the sexes with females having higher expression (most significant probeset P=6.90 x 10-6) after adjusting for age and smoking, rs7697189 did not demonstrate sex differential effects on expression. Establishing the mechanism by which HHIP SNPs have different effects on lung function in males and females will be important for our understanding of lung health and diseases, such as chronic obstructive pulmonary disease (COPD), in both sexes.

genetics↗