Abstract:Protected-area systems should conserve intraspecific genetic diversity. Because genetic data require resources to obtain, several approaches have been proposed for generating plans for protected-area systems (prioritizations) when genetic data are not available. Yet such surrogate-based approaches remain poorly tested. We evaluated the effectiveness of potential surrogate-based approaches based on microsatellite genetic data collected across the Iberian Peninsula for 7 amphibian and 3 reptilian species. Long-t… Show more
“…Given that high-resolution genetic data for all taxa will not be available soon, we propose to use proxies of genetic differentiation as a spatially explicit surrogate of the potential genetic differentiation within the distribution of a given taxon, which can represent different populations across landscapes. Studies that considered genetic variation for spatial analysis of systematic conservation planning are extremely rare 40 , 41 . In the context of CWR conservation, Parra-Quijano et al 42 , 43 introduced an ecogeographic land characterization that assumes that adaptive genetic features vary according to environmental variation.…”
Section: Resultsmentioning
confidence: 99%
“…The passive accumulation of genomic divergence among populations can also lead to speciation, by processes other than natural selection alone 46 . Although isolation by distance is a common pattern, distance alone tends to not be a good surrogate for representing broad-scale genetic diversity, because it has the potential to miss genetically distinct groups of populations 41 . Therefore, population structure should be accounted for when targeting to represent, conserve and monitor genetic variation 9 .…”
Crop wild relatives (CWR) intra- and interspecific diversity is essential for crop breeding and food security. However, intraspecific genetic diversity, which is central given the idiosyncratic threats to species in landscapes, is usually not considered in planning frameworks. Here, we introduce an approach to develop proxies of genetic differentiation to identify conservation areas, applying systematic conservation planning tools that produce hierarchical prioritizations of the landscape. It accounts for: (i) evolutionary processes, including historical and environmental drivers of genetic diversity, and (ii) threat processes, considering taxa-specific tolerance to human-modified habitats, and their extinction risk status. Our analyses can be used as inputs for developing national action plans for the conservation and use of CWR. Our results also inform public policy to mitigate threat processes to CWR (like crops living modified organisms or agriculture subsidies), and could advise future research (e.g. for potential germplasm collecting). Although we focus on Mesoamerican CWR within Mexico, our methodology offers opportunities to effectively guide conservation and monitoring strategies to safeguard the evolutionary resilience of any taxa, including in regions of complex evolutionary histories and mosaic landscapes.
“…Given that high-resolution genetic data for all taxa will not be available soon, we propose to use proxies of genetic differentiation as a spatially explicit surrogate of the potential genetic differentiation within the distribution of a given taxon, which can represent different populations across landscapes. Studies that considered genetic variation for spatial analysis of systematic conservation planning are extremely rare 40 , 41 . In the context of CWR conservation, Parra-Quijano et al 42 , 43 introduced an ecogeographic land characterization that assumes that adaptive genetic features vary according to environmental variation.…”
Section: Resultsmentioning
confidence: 99%
“…The passive accumulation of genomic divergence among populations can also lead to speciation, by processes other than natural selection alone 46 . Although isolation by distance is a common pattern, distance alone tends to not be a good surrogate for representing broad-scale genetic diversity, because it has the potential to miss genetically distinct groups of populations 41 . Therefore, population structure should be accounted for when targeting to represent, conserve and monitor genetic variation 9 .…”
Crop wild relatives (CWR) intra- and interspecific diversity is essential for crop breeding and food security. However, intraspecific genetic diversity, which is central given the idiosyncratic threats to species in landscapes, is usually not considered in planning frameworks. Here, we introduce an approach to develop proxies of genetic differentiation to identify conservation areas, applying systematic conservation planning tools that produce hierarchical prioritizations of the landscape. It accounts for: (i) evolutionary processes, including historical and environmental drivers of genetic diversity, and (ii) threat processes, considering taxa-specific tolerance to human-modified habitats, and their extinction risk status. Our analyses can be used as inputs for developing national action plans for the conservation and use of CWR. Our results also inform public policy to mitigate threat processes to CWR (like crops living modified organisms or agriculture subsidies), and could advise future research (e.g. for potential germplasm collecting). Although we focus on Mesoamerican CWR within Mexico, our methodology offers opportunities to effectively guide conservation and monitoring strategies to safeguard the evolutionary resilience of any taxa, including in regions of complex evolutionary histories and mosaic landscapes.
“…Further, with a PacBio reference genome underway and overseas efforts to sequence the American lobster ( Homarus americanus ) genome, we anticipate future opportunities to explore signatures of local adaptation that incorporate transcriptomic, phenotypic, and experimental data. In the interim, the “holistic” nature of ordination analyses provide a useful starting point for understanding local adaptation in kōura (Capblancq et al, 2018; Steane et al, 2014) that can be combined with place‐based knowledge to inform management, for example, by identifying populations with distinct adaptive variation (e.g., Figure 7; Barbosa et al, 2018) and by prioritizing source populations for translocation that share similar historical water flow regimes to recipient sites (Hanson et al, 2020).…”
Relationships with place provide critical context for characterizing biocultural diversity. Yet, genetic and genomic studies are rarely informed by Indigenous or local knowledge, processes, and practices, including the movement of culturally significant species. Here, we show how place-based knowledge can better reveal the biocultural complexities of genetic or genomic data derived from culturally significant species.As a case study, we focus on culturally significant southern freshwater kōura (crayfish) in Aotearoa me Te Waipounamu (New Zealand, herein Aotearoa NZ). Our results, based on genotyping-by-sequencing markers, reveal strong population genetic structure along with signatures of population admixture in 19 genetically depauperate populations across the east coast of Te Waipounamu. Environment association and differentiation analyses for local adaptation also indicate a role for hydroclimatic variables-including temperature, precipitation, and water flow regimes-in shaping local adaptation in kōura. Through trusted partnerships between community and researchers, weaving genomic markers with place-based knowledge has both provided
“…In particular, individually based, spatially explicit eco‐evolutionary models make use of data from a range disciplines that traditionally worked in isolation, and broaden the scope of their application to conservation (Armansin, Stow, Cantor et al., 2020; Schumaker and Brookes, 2018). These developments are timely given the limited resources available for conservation (Frankham et al., 2010; Robinson et al., 2020) and the poor performance of surrogates of genetic diversity (Hanson, Veríssimo, Velo‐Antón et al., 2020).…”
Genetic bottlenecks can reduce effective population sizes (Ne), increase the rate at which genetic variation is lost via drift, increase the frequency of deleterious mutations and thereby accentuate inbreeding risk and lower evolutionary potential. Here, we tested for the presence of a genetic bottleneck in the endangered Australian sea lion (Neophoca cinerea), estimated Ne and predicted future losses of genetic variation under a range of scenarios. We used 2238 genome‐wide neutral single‐nucleotide polymorphisms (SNPs) from 72 individuals sampled from colonies off the southern (SA) and western (WA) coastline of Australia. Coalescent analyses using approximate Bayesian computation (ABC) methods indicated that both the SA and WA populations have experienced a historical genetic bottleneck. Using LD‐based methods, we estimated contemporary Ne to be 160 (CI = 146–178) and 424 (CI = 397–458) for the WA and SA populations respectively. Modelled future population declines suggested that disease epidemics prompted the highest increases in inbreeding relative to fishery‐related mortalities and other modelled threats. Small effective sizes and relatively low genetic variation leave this species vulnerable, and these risks may be compounded if current population declines are not reversed.
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