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Small-scale reef fisheries are important commercial and subsistence activities that support the livelihoods of millions of people in tropical regions. Tropical marine fisheries typically target a diversity of species caught with a matching diversity of fishing gears and practices. Here, we explored how multiple fishing gears select for distinct functional traits of fish assemblages inside a large multiple use marine environmental protected area off northeastern Brazil. In 1833 landing interviews with local fishers, we identified 101 species, which were categorized according to six traits: body size, schooling behavior, mobility, position in the water column, diet and period of activity. Our research is the first to explore the broad patterns of gear selectivity with regards to fish functional traits for different habitat types. While gears used in reef habitats were highly selective of sedentary and benthic species that form schools with few individuals, gears used in coastal lagoons were selective of highly mobile pelagic species that form large schools. We found a low competitive interaction between different gear types, meaning there was a low overlap in trait selectivity between fishing gears. We also found direct associations between gears and fish functional traits: hooks and line targeted species that exhibit limited mobility capabilities, making these species more vulnerable to local levels of fishing effort. In contrast, nets and fish corrals targeted mobile species that exhibited a greater diversity of functional traits. Some of our results contrasted with the current literature on the topic, with differences highlighting the need for more research to clarify global patterns of trait selectivity by gear type. Our results have implications for fisheries management in northeastern Brazil: gear bans and effort caps are commonly used management measures that can foster fisheries sustainability by minimizing impacts to fish assemblage functions. [ABSTRACT FROM AUTHOR]

After the recent discovery that common genetic variation in 8q24 influences inherited risk of prostate cancer, we genotyped 2,973 SNPs in up to 7,518 men with and without prostate cancer from five populations. We identified seven risk variants, five of them previously undescribed, spanning 430 kb and each independently predicting risk for prostate cancer (P = 7.9 × 10−19 for the strongest association, and P < 1.5 × 10−4 for five of the variants, after controlling for each of the others). The variants define common genotypes that span a more than fivefold range of susceptibility to cancer in some populations. None of the prostate cancer risk variants aligns to a known gene or alters the coding sequence of an encoded protein. [ABSTRACT FROM AUTHOR]

Multiple sclerosis is a common disease with proven heritability, but, despite large-scale attempts, no underlying risk genes have been identified. Traditional linkage scans have so far identified only one risk haplotype for multiple sclerosis (at HLA on chromosome 6), which explains only a fraction of the increased risk to siblings. Association scans such as admixture mapping have much more power, in principle, to find the weak factors that must explain most of the disease risk. We describe here the first high-powered admixture scan, focusing on 605 African American cases and 1,043 African American controls, and report a locus on chromosome 1 that is significantly associated with multiple sclerosis. [ABSTRACT FROM AUTHOR]

Population stratification refers to differences in allele frequencies between cases and controls due to systematic differences in ancestry rather than association of genes with disease. It has been proposed that false positive associations due to stratification can be controlled by genotyping a few dozen unlinked genetic markers. To assess stratification empirically, we analyzed data from 11 case-control and case-cohort association studies. We did not detect statistically significant evidence for stratification but did observe that assessments based on a few dozen markers lack power to rule out moderate levels of stratification that could cause false positive associations in studies designed to detect modest genetic risk factors. After increasing the number of markers and samples in a case-cohort study (the design most immune to stratification), we found that stratification was in fact present. Our results suggest that modest amounts of stratification can exist even in well designed studies. [ABSTRACT FROM AUTHOR]

The ability to detect recent natural selection in the human population would have profound implications for the study of human history and for medicine. Here, we introduce a framework for detecting the genetic imprint of recent positive selection by analysing long-range haplotypes in human populations. We first identify haplotypes ata locus of interest (core haplotypes). We then assess the age of each core haplotype by the decay of its association to alleles at various distances from the locus, as measured by extended haplotype homozygosity (EHH). Core haplotypes that have unusually high EHH and a high population frequency indicate the presence of a mutation that rose to prominence in the human gene pool faster than expected under neutral evolution. We applied this approach to investigate selection at two genes carrying common variants implicated in resistance to malaria: G6PD[SUP 1] and CD40 ligand[SUP 2]. At both loci, the core haplotypes carrying the proposed protective mutation stand out and show significant evidence of selection. More generally, the method could be used to scan the entire genome for evidence of recent positive selection. [ABSTRACT FROM AUTHOR]

Figure #3 was missing the sample size boxes within each plot, whereas figure#4 was missing the axis labels. Correction to: Coral Reefs (2021) 40:1915-1929 https://doi.org/10.1007/s00338-021-02192-w Author discovered last two figures that were uploaded during proofing have minor inconsistencies. [Extracted from the article]