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Abstract Gene flow can affect evolutionary inference when species are undersampled. Here, we evaluate the effects of gene flow and geographic sampling on demographic inference of 2 hummingbirds that hybridize, Allen’s hummingbird (Selasphorus sasin) and rufous hummingbird (Selasphorus rufus). Using whole-genome data and extensive geographic sampling, we find widespread connectivity, with introgression far beyond the Allen’s × rufous hybrid zone, although the Z chromosome resists introgression beyond the hybrid zone. We test alternative hypotheses of speciation history of Allen’s, rufous, and Calliope (S. calliope) hummingbird and find that rufous hummingbird is the sister taxon to Allen’s hummingbird, and Calliope hummingbird is the outgroup. A model treating the 2 subspecies of Allen’s hummingbird as a single panmictic population fit observed genetic data better than models treating the subspecies as distinct populations, in contrast to morphological and behavioral differences and analyses of spatial population structure. With additional sampling, our study builds upon recent studies that came to conflicting conclusions regarding the evolutionary histories of these 2 species. Our results stress the importance of thorough geographic sampling when assessing demographic history in the presence of gene flow. 

Synopsis Animal wings produce an acoustic signature in flight. Many owls are able to suppress this noise to fly quietly relative to other birds. Instead of silent flight, certain birds have conversely evolved to produce extra sound with their wings for communication. The papers in this symposium synthesize ongoing research in “animal aeroacoustics”: the study of how animal flight produces an acoustic signature, its biological context, and possible bio-inspired engineering applications. Three papers present research on flycatchers and doves, highlighting work that continues to uncover new physical mechanisms by which bird wings can make communication sounds. Quiet flight evolves in the context of a predator–prey interaction, either to help predators such as owls hear its prey better, or to prevent the prey from hearing the approaching predator. Two papers present work on hearing in owls and insect prey. Additional papers focus on the sounds produced by wings during flight, and on the fluid mechanics of force production by flapping wings. For instance, there is evidence that birds such as nightbirds, hawks, or falcons may also have quiet flight. Bat flight appears to be quieter than bird flight, for reasons that are not fully explored. Several research avenues remain open, including the role of flapping versus gliding flight or the physical acoustic mechanisms by which flight sounds are reduced. The convergent interest of the biology and engineering communities on quiet owl flight comes at a time of nascent developments in the energy and transportation sectors, where noise and its perception are formidable obstacles. 

Abstract The metallicity and gas density dependence of interstellar depletions, the dust-to-gas (D/G), and dust-to-metal (D/M) ratios have important implications for how accurately we can trace the chemical enrichment of the universe, either by using FIR dust emission as a tracer of the ISM or by using spectroscopy of damped Ly α systems to measure chemical abundances over a wide range of redshifts. We collect and compare large samples of depletion measurements in the Milky Way (MW), Large Magellanic Cloud (LMC) ( Z = 0.5 Z ⊙ ), and Small Magellanic Cloud (SMC) ( Z = 0.2 Z ⊙ ). The relations between the depletions of different elements do not strongly vary between the three galaxies, implying that abundance ratios should trace depletions accurately down to 20% solar metallicity. From the depletions, we derive D/G and D/M. The D/G increases with density, consistent with the more efficient accretion of gas-phase metals onto dust grains in the denser ISM. For log N (H) > 21 cm −2 , the depletion of metallicity tracers (S, Zn) exceeds −0.5 dex, even at 20% solar metallicity. The gas fraction of metals increases from the MW to the LMC (factor 3) and SMC (factor 6), compensating for the reduction in total heavy element abundances and resulting in those three galaxies having the same neutral gas-phase metallicities. The D/G derived from depletions are respective factors of 2 (LMC) and 5 (SMC) higher than the D/G derived from FIR, 21 cm, and CO emission, likely due to the combined uncertainties on the dust FIR opacity and on the depletion of carbon and oxygen. 

Abstract Allen’s (Selasphorus sasin) and Rufous (S. rufus) hummingbird have long been suspected to hybridize, and potentially form a hybrid zone where their ranges overlap in southern Oregon. Migratory Allen’s Hummingbird (S. s. sasin) breeds along a narrow strip of the California coast up to the Oregon border, while Rufous Hummingbird breeds from southern Oregon to Alaska. Analysis of behavioral and morphological data for 183 males and morphological data from 138 females showed that Allen’s and Rufous hummingbird form a hybrid zone in southern Oregon and northern California. Linear discriminant function analysis and cline analysis of 20 phenotypic characters for males and 9 phenotypic characters for females suggested the center of the coastal transect of this north–south hybrid zone spanned from Bandon, Oregon (Coos County), to Port Orford, Oregon (Curry County). The contact zone extended north into the breeding range of Rufous (into Florence, Lane County, Oregon) and south into the range of Allen’s (into Arcata, Humboldt County, California). Sporadic inland sampling suggested the hybrid zone extended at least 94 km inland from the coast. Behavioral data included courtship displays, which were composed of discrete, modular, behavioral elements. Sexual selection acted on these courtship displays, as behavioral clines related to courtship behaviors were more narrow than morphological clines. Some of the courtship behaviors analyzed included previously undescribed diagnostic behavioral characters for Allen’s and Rufous hummingbird. 

Abstract Allen's Hummingbird comprises two subspecies, one migratory (Selasphorus sasin sasin) and one nonmigratory (S. s. sedentarius). The nonmigratory subspecies, previously endemic to the California Channel Islands, apparently colonized the California mainland on the Palos Verdes Peninsula some time before 1970 and now breeds throughout coastal southern California. We sequenced and compared populations of mainland nonmigratory Allen's Hummingbird to Channel Island populations from Santa Catalina, San Clemente, and Santa Cruz Island. We found no evidence of founder effects on the mainland population. Values of nucleotide diversity on the mainland were higher than on the Channel Islands. There were low levels of divergence between the Channel Islands and the mainland, and Santa Cruz Island was the most genetically distinct. Ecological niche models showed that rainfall and temperature variables on the Channel Islands are similar in the Los Angeles basin and predicted continued expansion of nonmigratory Allen's Hummingbird north along the coast and inland. We also reviewed previous genetic studies of vertebrate species found on the Channel Islands and mainland and showed that broad conclusions regarding island–mainland patterns remain elusive. Challenges include the idiosyncratic nature of colonization itself as well as the lack of a comprehensive approach that incorporates similar markers and sampling strategies across taxa, which, within the context of a comparative study of island–mainland relationships, may lead to inconsistent results.