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  1. Abstract

    Invasive species are a major threat to global biodiversity, yet also represent large‐scale unplanned ecological and evolutionary experiments to address fundamental questions in nature. Here we analyzed both native and invasive populations of predatory northern pike (Esox lucius) to characterize landscape genetic variation, determine the most likely origins of introduced populations, and investigate a presumably postglacial population from Southeast Alaska of unclear provenance. Using a set of 4329 SNPs from 351 individual Alaskan northern pike representing the most widespread geographic sampling to date, our results confirm low levels of genetic diversity in native populations (average 𝝅 of 3.18 × 10−4) and even less in invasive populations (average 𝝅 of 2.68 × 10−4) consistent with bottleneck effects. Our analyses indicate that invasive northern pike likely came from multiple introductions from different native Alaskan populations and subsequently dispersed from original introduction sites. At the broadest scale, invasive populations appear to have been founded from two distinct regions of Alaska, indicative of two independent introduction events. Genetic admixture resulting from introductions from multiple source populations may have mitigated the negative effects associated with genetic bottlenecks in this species with naturally low levels of genetic diversity. Genomic signatures strongly suggest an excess of rare, population‐specific alleles, pointing to a small number of founding individuals in both native and introduced populations consistent with a species' life history of limited dispersal and gene flow. Lastly, the results strongly suggest that a small isolated population of pike, located in Southeast Alaska, is native in origin rather than stemming from a contemporary introduction event. Although theory predicts that lack of genetic variation may limit colonization success of novel environments, we detected no evidence that a lack of standing variation limited the success of this genetically depauperate apex predator.

     
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  2. The Great Plains (GP) low-level jet (GPLLJ) contributes to GP warm season water resources (precipitation), wind resources, and severe weather outbreaks. Past research has shown that synoptic and local mesoscale physical mechanisms (Holton and Blackadar mechanisms) are required to explain GPLLJ variability. Although soil moisture–PBL interactions are central to local mechanistic theories, the diurnal effect of regional soil moisture anomalies on GPLLJ speed, northward penetration, and propensity for severe weather is not well known. In this study, two 31-member WRF-ARW stochastic kinetic energy backscatter scheme ensembles simulate a typical warm season GPLLJ case under CONUS-wide wet and dry soil moisture scenarios. In the GP (24°–48°N, 103°–90°W), ensemble mean differences in sensible heating and PBL height of 25–150 W m −2 and 100–700 m, respectively, at 2100 UTC (afternoon) culminate in GPLLJ 850-hPa wind speed differences of 1–4 m s −1 12 hours later (0900 UTC; early morning). Greater heat accumulation in the daytime PBL over dry soil impacts the east–west geopotential height gradient in the GP (synoptic conditions and Holton mechanism) resulting in a deeper thermal low in the northern GP, causing increases in the geostrophic wind. Enhanced daytime turbulent mixing over dry soil impacts the PBL structure (Blackadar mechanism), leading to increased ageostrophic wind. Overnight geostrophic and ageostrophic winds constructively interact, leading to a faster nocturnal GPLLJ over dry soil. Ensemble differences in CIN (~50–150 J kg −1 ) and CAPE (~500–1000 J kg −1 ) have implications for severe weather predictability. 
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  3. ABSTRACT For insects that depend on one or more bacterial endosymbionts for survival, it is critical that these bacteria are faithfully transmitted between insect generations. Cicadas harbor two essential bacterial endosymbionts, “ Candidatus Sulcia muelleri” and “ Candidatus Hodgkinia cicadicola.” In some cicada species, Hodgkinia has fragmented into multiple distinct but interdependent cellular and genomic lineages that can differ in abundance by more than two orders of magnitude. This complexity presents a potential problem for the host cicada, because low-abundance but essential Hodgkinia lineages risk being lost during the symbiont transmission bottleneck from mother to egg. Here we show that all cicada eggs seem to receive the full complement of Hodgkinia lineages, and that in cicadas with more complex Hodgkinia this outcome is achieved by increasing the number of Hodgkinia cells transmitted by up to 6-fold. We further show that cicada species with varying Hodgkinia complexity do not visibly alter their transmission mechanism at the resolution of cell biological structures. Together these data suggest that a major cicada adaptation to changes in endosymbiont complexity is an increase in the number of Hodgkinia cells transmitted to each egg. We hypothesize that the requirement to increase the symbiont titer is one of the costs associated with Hodgkinia fragmentation. IMPORTANCE Sap-feeding insects critically rely on one or more bacteria or fungi to provide essential nutrients that are not available at sufficient levels in their diets. These microbes are passed between insect generations when the mother places a small packet of microbes into each of her eggs before it is laid. We have previously described an unusual lineage fragmentation process in a nutritional endosymbiotic bacterium of cicadas called Hodgkinia . In some cicadas, a single Hodgkinia lineage has split into numerous related lineages, each performing a subset of original function and therefore each required for normal host function. Here we test how this splitting process affects symbiont transmission to eggs. We find that cicadas dramatically increase the titer of Hodgkinia cells passed to each egg in response to lineage fragmentation, and we hypothesize that this increase in bacterial cell count is one of the major costs associated with endosymbiont fragmentation. 
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  4. Abstract

    Low-level jets (LLJ) around the world critically support the food, water, and energy security in regions that they traverse. For the purposes of development planning and weather and climate prediction, it is important to improve understanding of how LLJs interact with the land surface and upper-atmospheric flow, and collectively, how LLJs have and may change over time. This study details the development and application of a new automated, dynamical objective classification of upper-atmospheric jet stream coupling based on a merging of the Bonner–Whiteman vertical wind shear classification and the finite-amplitude local wave activity diagnostic. The classification approach is transferable globally, but applied here only for the Great Plains (GP) LLJ (GPLLJ). The analysis spans the period from 1901 to 2010, enabled by the ECMWF climate-quality, coupled Earth reanalysis of the twentieth century. Overall, statistically significant declines in total GPLLJ event frequency over the twentieth century are detected across the entire GP corridor and attributed to declines in uncoupled GPLLJ frequency. Composites of lower- and upper-atmospheric flow are shown to capture major differences in the climatological, coupled GPLLJ, and uncoupled GPLLJ synoptic environments. Detailed analyses for southern, central, and northern GP subregions further highlight synoptic differences between weak and strong GPLLJs and provide quantification of correlations between total, coupled, and uncoupled GPLLJ frequencies and relevant atmospheric anomalies. Because uncoupled GPLLJs tend to be associated with decreased precipitation and low-level wind speed and enhanced U.S. ridge strength, this finding may suggest that support for drought over the twentieth century has waned.

     
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