Characterizing the current population structure of potentially invasive species provides a critical context for identifying source populations and for understanding why invasions are successful. Non-native populations inevitably lose genetic diversity during initial colonization events, but subsequent admixture among independently introduced lineages may increase both genetic variation and adaptive potential. Here we characterize the population structure of the gypsy moth (Lymantria dispar Linnaeus), one of the world's most destructive forest pests. Native to Eurasia and recently introduced to North America, the current distribution of gypsy moth includes forests throughout the temperate region of the northern hemisphere. Analyses of microsatellite loci and mitochondrial DNA sequences for 1738 individuals identified four genetic clusters within L. dispar. Three of these clusters correspond to the three named subspecies; North American populations represent a distinct fourth cluster, presumably a consequence of the population bottleneck and allele frequency change that accompanied introduction. We find no evidence that admixture has been an important catalyst of the successful invasion and range expansion in North America. However, we do find evidence of ongoing hybridization between subspecies and increased genetic variation in gypsy moth populations from Eastern Asia, populations that now pose a threat of further human-mediated introductions. Finally, we show that current patterns of variation can be explained in terms of climate and habitat changes during the Pleistocene, a time when temperate forests expanded and contracted. Deeply diverged matrilines in Europe imply that gypsy moths have been there for a long time and are not recent arrivals from Asia.

The anaerobic decomposition of particulate organic tnatter (POM) was examined in the anoxic pelagic sediments of hypereutrophic Wintergreen Lake. Degradation of sedimented POM occurred rapidly as shown by increased production and release of ammonia, hydrogen sulphide, volatile fatty acids and methane from the sediments 2-3 weeks after large inputs of organic matter. Maximum concentrations of most metabolites were found at the sediment-water interface, indicating that the initial anaerobic degradation of freshly deposited POM occurred at this site. The absence of the inorganic electron acceptors, nitrate and sulphate, suggested that fermentation and methanogenesis were the major anaerobic processes involved in the dissimilation of organic matter in these sediments during stratified periods. The amount of carbon input converted to methane in the sediments was determined from May to early November 1976 and 1977. Carbon output as methane was measured by quantifying methane lost from the sediments by ebullition and by estimating soluble methane lost to the water column by diffusion. Total methane release during summer stratification accounted for 34% of the particulate organic carbon input to the sediments in 1976 and 44^/^ in 1977. Methane release was directly related to the rate of sedimentation of POM. However, methane production was temporarily inhibited following high rates of sedimentation in 1976, suggesting that the rate of organic loading may be an important factor controlling anaerobic decomposition in these sediments.

Global trade facilitates the inadvertent movement of insect pests and subsequent establishment of populations outside their native ranges. Despite phytosanitary measures, nonnative insects arrive at United States (U.S.) ports of entry as larvae in solid wood packaging material (SWPM). Identification of wood-boring larval insects is important for pest risk analysis and management, but is difficult beyond family level due to highly conserved morphology. Therefore, we integrated DNA barcoding and rearing of larvae to identify wood-boring insects in SWPM. From 2012 to 2015, we obtained larvae of 338 longhorned beetles (Cerambycidae) and 38 metallic wood boring beetles (Buprestidae) intercepted in SWPM associated with imported products at six U.S. ports. We identified 265 specimens to species or genus using DNA barcodes. Ninety-three larvae were reared to adults and identified morphologically. No conflict was found between the two approaches, which together identified 275 cerambycids (23 genera) and 16 buprestids (4 genera). Our integrated approach confirmed novel DNA barcodes for seven species (10 specimens) of woodborers not in public databases. This study demonstrates the utility of DNA barcoding as a tool for regulatory agencies. We provide important documentation of potential beetle pests that may cross country borders through the SWPM pathway.

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