3 research outputs found
Sudden flamingo deaths in Kenyan rift valley lakes.
The East African Rift Valley Lakes Bogoria and Nakuru sometimes host around 75% of the world population of lesser flamingos Phoeniconaias minor. In this area, mysterious flamingo die-offs have occupied researchers for four decades. Recently, cyanobacterial toxins came into the fore as a possible explanation for mass mortalities because the main food source of lesser flamingos is the cyanobacterium Arthrospira fusiformis. We took weekly samples from July 2008 to November 2009 from Lakes Nakuru and Bogoria and analyzed them by high performance liquid chromatography for microcystins. Monthly, samples were cross-checked using protein phosphatase inhibition assays with lower detection limits and additionally screened for polar toxins. During our study period, three flamingo die-offs occurred at L. Bogoria and we were able to analyze tissues of 20 carcasses collected at the shoreline. No cyanotoxins were detected either in plankton samples or in flamingo tissues. Accordingly, other reasons such as food composition or bird diseases played a key role in the observed flamingo die-offs
A detailed time series assessment of the diet of Lesser Flamingos: further explanation for their itinerant behaviour
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Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation
Although genome-wide association studies have identified over 100 risk loci that explain ∼33% of familial risk for prostate cancer (PrCa), their functional effects on risk remain largely unknown. Here we use genotype data from 59,089 men of European and African American ancestries combined with cell-type-specific epigenetic data to build a genomic atlas of single-nucleotide polymorphism (SNP) heritability in PrCa. We find significant differences in heritability between variants in prostate-relevant epigenetic marks defined in normal versus tumour tissue as well as between tissue and cell lines. The majority of SNP heritability lies in regions marked by H3k27 acetylation in prostate adenoc7arcinoma cell line (LNCaP) or by DNaseI hypersensitive sites in cancer cell lines. We find a high degree of similarity between European and African American ancestries suggesting a similar genetic architecture from common variation underlying PrCa risk. Our findings showcase the power of integrating functional annotation with genetic data to understand the genetic basis of PrCa