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Research about Central Appalachians

Source-linked reports with geographic coverage including Central Appalachians.

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Lead exposure of red-shouldered hawks during the breeding season in the central Appalachians, USA

Lead is toxic to humans and wildlife. Most studies of lead exposure of raptors focus on the winter, non-breeding season when they scavenge heavily. We evaluated blood lead concentrations (BLCs) of red-shouldered hawks (Buteo lineatus) during the non-scavenging season in the eastern United States. BLCs of 53 of 70 hawks were above the limit of detection ( x¯ = 9.25 µg/dL ± 19.81; ± SD). Adult hawks had higher BLCs ( x¯ = 12.86 µg/dL ± 24.72) than did nestlings ( x¯ = 3.25 µg/dL ± 2.62; p ≤ 0.001, χ2 = 13.2). There was no difference in BLCs of adult hawks among physiographic provinces but there were differences between urban and non-urban settings (p = 0.04, χ2 = 4.2). Soils and invertebrate hawk prey also had quantifiable lead concentrations. Our work shows that red-shouldered hawks are exposed to lead when not scavenging, and suggests pathways by which these birds may be exposed.

Central Appalachians

Early genetic outcomes of American black bear reintroductions in the Central Appalachians, USA

Habitat loss and overexploitation extirpated American black bears (Ursus americanus) from most of the Central Appalachians, USA, by the early twentieth century. To attempt to restore bears to the southwestern portion of this region, 2 reintroductions that used small founder groups (n = 27 and 55 bears), but different release methods (hard versus soft), were conducted during the 1990s. We collected hair samples from black bears in the reintroduced Big South Fork (BSF) and Kentucky–Virginia populations (KVP), their respective Great Smoky Mountains (GSM) and Shenandoah National Park (SNP) source populations, and a neighboring population in southern West Virginia (SWV) to investigate the early genetic outcomes of bear reintroduction. Despite having undergone genetic bottlenecks, genetic diversity remained similar between reintroduced populations and their sources ~15 years after the founder events (ranges: AR = 4.86–5.61; HO = 0.67–0.75; HE = 0.65–0.71). Effective population sizes of the reintroduced KVP and BSF (NE = 31 and 36, respectively) were substantially smaller than their respective SNP and GSM sources (NE = 119 and 156, respectively), supporting founder effects. Genetic structure analysis indicated that the hard released (i.e., no acclimation period) KVP founder group likely declined considerably, whereas the soft released BSF founder group remained mostly intact, suggesting superior effectiveness of soft releases. Asymmetrical gene flow via immigration from the SWV has resulted in the KVP recovering from the initial founder group reduction. Sustained isolation, small NE, and small population size of the BSF may warrant continued genetic monitoring to determine if gene flow from neighboring populations is established or NE declines. For future bear reintroductions, we suggest managers consider sourcing founders from populations with high genetic diversity and soft-releasing bears to locales that are, if possible, within the dispersal capability of extant populations to mitigate the potential consequences of founder effects and isolation.

Central Appalachians

Field trip guidebook for the post-meeting field trip: The Central Appalachians

The lower Paleozoic rocks to be examined on this trip through the central Appalachians represent an extreme range of depositional environments. The lithofacies we will examine range from pelagic radiolarian chert and interbedded mudstone that originated on the deep floor of the Iapetus Ocean, through mud cracked supratidal dolomitic laminites that formed during episodes of emergence of the long-lived Laurentian carbonate platform, to meandering fluvial conglomerate and interstratified overbank mudstone packages deposited in the latest stages of infilling of the Taconic foredeep. In many ways this field trip is about contrasts. The Upper Cambrian (Furongian) and Lower Ordovician deposits of the Sauk megasequence record deposition controlled primarily by eustatic sea level sea level fluctuations that influenced deposition along the passive, southern (Appalachian) margin of the paleocontinent of Laurentia. The only tectonic influence apparent in these passive margin deposits is the expected thickening of the carbonate stack toward the platform margin as compared to the thinner (and typically shallower) facies that formed farther in toward the paleoshoreline. Carbonates overwhelmingly dominate the passive margin succession. Clastic influx was minimal and consisted largely of eastward transport of clean cratonic sands across the platform from the adjacent inner detrital belt to the west during higher order (2nd and 3rd order) regressions. In contrast, Middle and Upper Ordovician deposits of the Tippecanoe megasequence record the strong influence of tectonics, specifically Iapetus closure. The first signal of this tectonic transformation was the arrival of arc-related ash beds that abound in the active margin carbonates. Subsequent intensification of Taconic orogenesis resulted in the foundering of the carbonate platform under the onslaught of fine siliciclastics arriving from offshore tectonic sources to the east, creating a deep marine flysch basin where graptolitic shale and sandstone turbidites accumulated. The foreland basin thus created would fill with progressively coarser and more shallow/proximal clastic facies through the Upper Ordovician, culminating in deposition of fluvial redbeds that cap the Taconic clastic wedge. Arguably the most controversial rocks within the Tippecanoe Sequence in this area are unusual, Lower Ordovician deep marine facies that are associated with the much younger flysch of the Martinsburg Formation in the Great Valley of eastern Pennsylvania. Long considered the erosional remnants of a Taconic-style thrust sheet, and referred to as the Hamburg Klippe, these deep marine deposits have recently been reinterpreted as olistostromal deposits that were introduced by gravity sliding into the flysch basin contemporaneous with Martinsburg deposition. Besides their constituent lithofacies, rocks of the Sauk and Tippecanoe megasequences also present a stark contrast in faunas. Cambrian and Lower Ordovician faunas predate the Great Ordovician Biodiversification Event (GOBE), a global event that saw unprecedented diversification within many major invertebrate groups (mollusks, corals, and bryozoans to name a few) that previously were only minor components of the marine fauna. Unfortunately, the much higher diversity of Middle and Upper Ordovician faunas wrought by the GOBE is somewhat muted in this region by the stresses introduced by conversion of the Appalachian shelf into a flysch basin. Another noteworthy difference between the Cambrian and Ordovician biota related to the paleogeographic setting of the rocks to be examined on this trip derives from their evolution in the shallow marine environments of Laurentia. Several shelf-wide extinctions decimated the shallow marine faunas of the Laurentian shelf through the late Cambrian producing stage-level biostratigraphic units known as biomeres. The biomere phenomenon is discussed in this guidebook and a few stops to examine Cambrian faunas and one biomere boundary extinction are included to provide contrast with stage boundary extinctions that occurred later, in the Ordovician, that lack the defining attributes of the biomere boundary extinctions. Again, it’s all about contrast.

Central Appalachians