Senckenbergische Naturforschende Gesellschaft
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Although global- and catchment-scale hydrological models are often shown to accurately simulate long-term runoff time-series, far less is known about their suitability for capturing hydrological extremes, such as droughts. Here we evaluated simulations of hydrological droughts from nine catchment scale hydrological models (CHMs) and eight global scale hydrological models (GHMs) for eight large catchments: Upper Amazon, Lena, Upper Mississippi, Upper Niger, Rhine, Tagus, Upper Yangtze and Upper Yellow. The simulations were conducted within the framework of phase 2a of the Inter-Sectoral Impact Model Intercomparison Project (ISIMIP2a). We evaluated the ability of the CHMs, GHMs and their respective ensemble means (Ens-CHM and Ens-GHM) to simulate observed hydrological droughts of at least one month duration, over 31 years (1971–2001). Hydrological drought events were identified from runoff-deficits and the Standardised Runoff Index (SRI). In all catchments, the CHMs performed relatively better than the GHMs, for simulating monthly runoff-deficits. The number of drought events identified under different drought categories (i.e. SRI values of -1 to -1.49, -1.5 to -1.99, and ≤-2) varied significantly between models. All the models, as well as the two ensemble means, have limited abilities to accurately simulate drought events in all eight catchments, in terms of their occurrence and magnitude. Overall, there are opportunities to improve both CHMs and GHMs for better characterisation of hydrological droughts.
Driven by globalization, urbanization and climate change, the distribution range of invasive vector species has expanded to previously colder ecoregions. To reduce health-threatening impacts on humans, insect vectors are extensively studied. Population genomics can reveal the genomic basis of adaptation and help to identify emerging trends of vector expansion. By applying whole genome analyses and genotype-environment associations to populations of the main dengue vector Aedes aegypti, sampled along an altitudinal gradient in Nepal (200–1300 m), we identify putatively adaptive traits and describe the species' genomic footprint of climate adaptation to colder ecoregions. We found two differentiated clusters with significantly different allele frequencies in genes associated to climate adaptation between the highland population (1300 m) and all other lowland populations (≤800 m). We revealed nonsynonymous mutations in 13 of the candidate genes associated to either altitude, precipitation or cold tolerance and identified an isolation-by-environment differentiation pattern. Other than the expected gradual differentiation along the altitudinal gradient, our results reveal a distinct genomic differentiation of the highland population. Local high-altitude adaptation could be one explanation of the population's phenotypic cold tolerance. Carrying alleles relevant for survival under colder climate increases the likelihood of this highland population to a worldwide expansion into other colder ecoregions.
Background: Driven by globalization, urbanization and climate change, the distribution range of invasive vector species has expanded to previously colder ecoregions. To reduce health-threatening impacts on humans, insect vectors are extensively studied. Population genomics can reveal the genomic basis of adaptation and help to identify emerging trends of vector expansion.
Results: By applying whole genome analyses and genotype-environment associations to populations of the main dengue vector Ae. aegypti, sampled along an altitudinal temperature gradient in Nepal (200- 1300m), we identify adaptive traits and describe the species’ genomic footprint of climate adaptation to colder ecoregions. We found two clusters of differentiation with significantly different allele frequencies in genes associated to climate adaptation between the highland population (1300m) and all other lowland populations (≤ 800 m). We revealed non-synonymous mutations in 13 of the candidate genes associated to either altitude, precipitation or cold tolerance and identified an isolation-by-environment differentiation pattern.
Conclusion: Other than the expected gradual differentiation along the altitudinal gradient, our results reveal a distinct genomic differentiation of the highland population. This finding either indicates a differential invasion history to Nepal or local high-altitude adaptation explaining the population’s phenotypic cold tolerance. In any case, this highland population can be assumed to carry pre-adapted alleles relevant for the species’ invasion into colder ecoregions worldwide that way expanding their climate niche.