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Research about Great Smoky Mountains National Park

Source-linked reports with geographic coverage including Great Smoky Mountains National Park.

At least 19 recordsLinked to original sources

Development of genomic markers for monitoring and research on plethodontid salamanders

Despite the importance of plethodontid salamanders and their vulnerability to ongoing environmental change, they are inherently difficult to monitor due to their cryptic nature. Recent advances in genomics have created new opportunities for monitoring of populations and their responses to environmental perturbations. In this study, we developed a new target capture-based genomic panel for the purposes of genetic monitoring in plethodontid salamanders. We demonstrate its utility in several distantly related species and present an example application in two representative species with co-occurring distributions but different ecological attributes and expected patterns of population structure: Plethodon jordani and Desmognathus wrighti . Although the number of successfully assembled loci declined with phylogenetic distance from the original reference species ( Desmognathus spp), we obtained high-quality data from thousands of loci from species in all four genera tested ( Desmognathus , Plethodon , Eurycea , and Gyrinophilus ), which span the deepest split in Plethodontidae. Landscape genetic analyses detected weak but statistically significant geographic structure in P. jordani , and much stronger geographic structure in D. wrighti , as expected based on the lower population density and likely lower dispersal ability of D. wrighti . Our target capture panel is broadly applicable across salamanders in Plethodontidae and has the potential to provide data for a wide range of phylogenetic, biogeographic, and population genetics research questions.

North Carolina, Tennessee

Genetic structure of restored Brook Trout populations in the Southern Appalachian Mountains indicates successful reintroductions

Wildlife reintroduction is an important conservation tool for threatened species, yet identifying appropriate source populations poses a challenge. In particular, the possibility of outbreeding depression is cited as a constraint limiting the range of candidate source populations for translocation. When multiple source lineages are mixed during reintroduction, genetic monitoring is necessary to evaluate whether sources contribute equally to subsequent generations and whether they are interbreeding as expected. Moreover, statistical analysis of genetic data should account for complex life histories that might affect the timescale of admixture and genetic drift. Here, we use samples collected over a 23-year period and a stochastic age-structured model to analyze the genetic mixing process in reintroduced Brook Trout ( Salvelinus fontinalis ) populations in the Southern Appalachians. Each restored population was seeded with two to three source populations. Previous research inferred reproductive isolation between source populations leading to a proposal of splitting the species into multiple taxa. In contrast, we found patterns of ancestry that were consistent with random mating and no advantage for one source lineage over any other. Brook Trout from different source streams are mixing as expected in the restoration sites. This result does not support the hypothesis that Brook Trout in the Southern Appalachian Mountains includes several distinct species. Mixing different sources from the same watershed seems to be an effective way to increase genetic diversity of reintroduced populations while minimizing risk to source populations.

North Carolina, Tennessee

No long-term effect of black bear removal on elk calf recruitment in the southern Appalachians

In 2001 and 2002, 52 elk ( Cervus canadensis ; 21 males, 31 females), originally obtained from Elk Island National Park, Alberta, Canada, were transported and released into Cataloochee Valley in the northeastern portion of Great Smoky Mountains National Park (GRSM, Park), North Carolina, USA. The annual population growth rate ( λ ) was negative (0.996, 95% CI = 0.945–1.047) and predation by black bears ( Ursus americanus ) on elk calves was identified as an important determinant of population growth. From 2006 to 2008, 49 bears from the primary elk calving area (i.e., Cataloochee Valley) were trapped and translocated about 70 km to the southwestern portion of the Park just prior to elk calving. Per capita recruitment (i.e., the number of calves produced per adult female that survive to 1 year of age) increased from 0.306 prior to bear translocation (2001–2005) to 0.544 during years when bears were translocated (2006–2008) and λ increased to 1.118 (95% CI = 1.096–1.140). Our objective was to determine whether per capita calf recruitment rates after bear removal (2009–2019) at Cataloochee were similar to the higher rates estimated during bear removal (i.e., long-term response) or if they returned to rates before bear removal (i.e., short-term response), and how those rates compared with recruitment from portions of our study area where bears were not relocated. We documented 419 potential elk calving events and monitored 129 yearling and adult elk from 2001 to 2019. Known-fate models based on radio-telemetry and observational data supported calf recruitment returning to pre-2006 levels at Cataloochee (short-term response); recruitment of Cataloochee elk before and after bear relocation was lower (0.184) than during bear relocation (0.492). Recruitment rates of elk outside the removal area during the bear relocation period (0.478) were similar to before and after rates (0.420). In the Cataloochee Valley, cause-specific annual calf mortality rates due to predation by bears were 0.319 before, 0.120 during, and 0.306 after bear relocation. In contrast, the cause-specific annual mortality rate of calves in areas where bears were not relocated was 0.033 after the bear relocation period, with no bear predation on calves before or during bear relocation. The mean annual population growth rate for all monitored elk was 1.062 (95% CI = 0.979–1.140) after bear relocation based on the recruitment and survival data. Even though the effects of bear removal were temporary, the relocations were effective in achieving a short-term increase in elk recruitment, which was important for the reintroduction program given that the elk population was small and vulnerable to extirpation.

North Carolina

A multi-level modeling approach to guide management of female feral hogs in Great Smoky Mountains National Park

We trapped, anesthetized, and fit 16 female feral swine ( Sus scrofa ) with Global Positioning System (GPS) collars in Great Smoky Mountains National Park (GRSM) to develop predictive summer and winter models for more effective population control efforts. Given the highly diverse habitat and topography in GRSM and the spatial extent of our dataset, we employed Step Selection Function (SSF) to evaluate resource selection at the 3 rd -order level and Resource Selection Function (RSF) models at the 2 nd -order level for both summer and winter seasons. The summer SSF and RSF models suggested relatively similar levels of selection, whereas the winter models differed by method. We created a straightforward consensus model to better visualize the agreement and constraints of each set of models. In summer, feral swine used lower slopes regardless of elevation, especially those closer to human-dominated spaces such as along paved and gravel roadways. In winter, feral swine maintained preference for lower slopes but preferred oak-dominated forest areas and selection for human development was less than in summer. Wildlife managers can use these models to better focus feral swine surveillance and management in GRSM. Managers can identify areas of high use by season and plan control activities that are both accessible and highly efficient. The combination and consensus framework presented here can be applied to other systems where species’ habitat selection may result in incongruous results across different levels of selection or seasons of interest.

Tennessee

Tooth wear and the apparent consumption of human foods among American black bears (Ursus americanus) in Great Smoky Mountains National Park, USA

Stable isotope analyses of hair have been used to estimate the consumption of human foods by American black bears ( Ursus americanus ). Consumption of human foods influences body mass and reproductive success of bears. However, the underlying factors that cause some bears to become conflict bears and resort to consuming human foods as a portion of their diet are not fully understood. We collected hair samples for stable isotope analysis from 51 black bears in Great Smoky Mountains National Park, Tennessee, USA in 2006. We used δ 13 C values of hairs to determine if the bears were consuming C 3 -based (natural foods) or C 4 -based (human foods) diets, and δ 15 N values, which increase with more meat in the diet, as a further indication of the consumption of human foods. Male bears with the heaviest tooth wear had a combination of higher δ 15 N and δ 13 C values, suggesting that they consume human foods to a greater extent than do other black bears. Based on our results, we hypothesize that tooth wear, and thus dental health, may play a role in the consumption of human foods by larger, male bears.

Tennessee

Development of a ddPCR assay for the detection of the Smoky Madtom (Noturus baileyi) from eDNA in stream water samples

The Smoky Madtom Noturus baileyi is a federally endangered species, whose native distribution includes lower Abrams Creek in Great Smoky Mountains National Park (GRSM) and Citico Creek in nearby Cherokee National Forest. Due to challenges for bio-monitoring posed by its nocturnality and cryptic life history, an environmental DNA (eDNA)-based approach for detection would be useful to complement existing electrofishing and seining efforts to better understand the distribution of this species. We developed a probe-based droplet digital PCR (ddPCR) assay to detect Smoky Madtoms from non-invasively collected water samples. The assay was specific to N. baileyi and did not amplify concentrated genomic DNA of 16 co-occurring or regional fish species, including the yellowfin madtom N. flavipinnis and stonecat N. flavus . The assay limit of detection (LOD) was determined to be 4.18 copies (95% CI: 3.95, 4.41). Several 2 L water samples collected from throughout various streams in GRSM in 2016 and 2017 were tested for the presence of N. baileyi using the ddPCR assay. N. baileyi was detected at two different sites in 2016 and 2017 within Abrams Creek previously known to contain N. baileyi , but no novel detections in other sampled streams were observed. This assay should prove useful for continued surveys of N. baileyi in GRSM.

Great Smoky Mountains National Park

Fuels and vegetation changes in southwestern, unburned portions of Great Smoky Mountains National Park, USA, 2003-2019

Overstory basal area, ericaceous shrub cover ( Kalmia latifolia L. and Rhododendron maximum L.), and fuels (i.e., woody fuel loads and depths and O Horizon thickness) were assessed within Great Smoky Mountains National Park, USA, in 2003 − 2004. Due to recent wildfire activity within the southern Appalachian Mountain region (including Great Smoky Mountains National Park), the potential spread and expansion of ericaceous shrubs, and the impacts of the hemlock woolly adelgid ( Adelges tsugae Annand) on eastern hemlock ( Tsuga canadensis (L.) Carrière), these same ecosystem components were again assessed in 2019. Elevation and moisture regime (xeric, intermediate, and mesic) were included in this assessment as potential influential factors. An evaluation of repeated measurements from 40 plots suggested that O Horizon thickness did not change significantly over the 16-year period, but increased as elevation increased, and moisture regime (xeric O Horizon thickness > mesic O Horizon thickness) was a significant, related factor. The sum of 1-, 10-, and 100-h fuel loads (fuels less < 7.6 cm diameter) increased, whereas woody fuel depth decreased over the 16-year period. No significant changes in 1000-h fuel loads (> 7.6 cm diameter), total woody fuel loads, ericaceous shrub cover, total basal area, or live T. canadensis basal area were observed. Live T. canadensis basal area decreased with increasing elevation. Dead, standing T. canadensis basal area increased from 2003–2019, and that increase was most pronounced as elevation increased on xeric and intermediate sites. Overall, we found that: 1. hypothesized increases in total woody fuel loads and ericaceous shrub cover were not present; and 2. elevation and moisture regime were most related to observed changes in vegetation and fuel condition.

North Carolina, Tennessee

Black bear movement and food conditioning in an exurban landscape

Conflicts between humans and wildlife have become increasingly important challenges for resource managers along the urban‐wildland interface. Food conditioning (i.e., reliance by an animal on anthropogenic foods) of American black bears (Ursus americanus ) is related to conflict behavior (i.e., being bold or aggressive toward humans, consuming human food or garbage, causing property damage) and often occurs in communities adjacent to Great Smoky Mountains National Park (GRSM or Park), USA. The goal of our study was to evaluate black bear space use in GRSM and in exurban areas on surrounding private lands and to identify factors associated with food conditioning and conflict behavior. We radio‐collared 53 bears (29 males, 24 females) from 2015 to 2017 to compare space use characteristics and used carbon isotopic signatures (δ13C) from bear hair to assess food conditioning. We then performed an integrated step selection function (iSSF) analysis to characterize and compare movement and resource use as related to food conditioning. Based on the stable isotope analyses, 24 bears were classified as food conditioned (FC; 16 males and 8 females) and 37 were not food conditioned (NFC; 14 males and 23 females). Annual 95% kernel density estimate (KDE) home ranges and 50% KDE core area estimates of female and male bears did not differ by level of food conditioning (i.e., mean δ13C), but 95% and 50% home ranges of FC females were smaller than NFC females when data from 2015, a year of food scarcity and abnormally large home ranges, were excluded. The mean proportion of exurban development (e.g., roads, buildings, openings) within 95% KDE and 50% KDE home ranges of females increased with mean δ13C (i.e., greater food conditioning). The iSSF models indicated that FC bears were more likely to use forest openings associated with higher levels of development than NFC bears. We used those models to demonstrate how landscape modifications can reduce bear use of exurban areas, particularly for NFC bears. Our stable isotope, movement, and resource use data indicate that conflict behaviors displayed by many bears within GRSM were learned in areas outside Park boundaries. © 2020 The Wildlife Society.

Tennessee, North Carolina

Relationships between indicators of acid-base chemistry and fish assemblages in streams of the Great Smoky Mountains National Park

The acidity of many streams in the Great Smoky Mountains National Park (GRSM) has increased significantly since pre-industrial (∼1850) times due to the effects of highly acidic atmospheric deposition in poorly buffered watersheds. Extensive stream-monitoring programs since 1993 have shown that fish and macroinvertebrate assemblages have been adversely affected in many streams across the GRSM. Matching chemistry and fishery information collected from 389 surveys performed at 52 stream sites over a 22-year period were assessed using logistic regression analysis to help inform the U.S. Environmental Protection Agency’s assessment of the environmental impacts of emissions of oxides of nitrogen (NO x ) and sulfur (SO x ). Numerous logistic equations and associated curves were derived that defined the relations between acid neutralizing capacity (ANC) or pH and different levels of community richness, density, and biomass; and density and biomass of brook trout, rainbow trout, and small prey (minnow) populations in streams of the GRSM. The equations and curves describe the status of fish assemblages in the GRSM under contemporary emission levels and deposition loads of nitrogen (N) and sulfur (S) and provide a means to estimate how newly proposed (and various alternative) target deposition loads, which strongly influence stream ANC, might affect key ecological indicators. Several examples using ANC, community richness, and brook trout density are presented to illustrate the steps needed to predict how future changes in stream chemistry (resulting from different target deposition loads of N and S) will affect the probabilities of observing specific levels of selected biological indicators in GRSM streams. The implications of this study to the regulation of NO x and SO x emissions, water quality, and fisheries management in streams of the GRSM are discussed, but also qualified by the fact that specific examples provided need to be further explored before recommendations concerning their use as ecological indicators could be proposed.

North Carolina, Tennessee

Effects of sampling conditions on DNA-based estimates of American black bear abundance

DNA-based capture-mark-recapture techniques are commonly used to estimate American black bear ( Ursus americanus ) population abundance (N). Although the technique is well established, many questions remain regarding study design. In particular, relationships among N, capture probability of heterogeneity mixtures A and B (p A and p B , respectively, or p , collectively), the proportion of each mixture (&pi;), number of capture occasions (k), and probability of obtaining reliable estimates of N are not fully understood. We investigated these relationships using 1) an empirical dataset of DNA samples for which true N was unknown and 2) simulated datasets with known properties that represented a broader array of sampling conditions. For the empirical data analysis, we used the full closed population with heterogeneity data type in Program MARK to estimate N for a black bear population in Great Smoky Mountains National Park, Tennessee. We systematically reduced the number of those samples used in the analysis to evaluate the effect that changes in capture probabilities may have on parameter estimates. Model-averaged N for females and males were 161 (95% CI&thinsp;=&thinsp;114&ndash;272) and 100 (95% CI&thinsp;=&thinsp;74&ndash;167), respectively (pooled N&thinsp;=&thinsp;261, 95% CI&thinsp;=&thinsp;192&ndash;419), and the average weekly p was 0.09 for females and 0.12 for males. When we reduced the number of samples of the empirical data, support for heterogeneity models decreased. For the simulation analysis, we generated capture data with individual heterogeneity covering a range of sampling conditions commonly encountered in DNA-based capture-mark-recapture studies and examined the relationships between those conditions and accuracy (i.e., probability of obtaining an estimated N that is within 20% of true N), coverage (i.e., probability that 95% confidence interval includes true N), and precision (i.e., probability of obtaining a coefficient of variation &le;20%) of estimates using logistic regression. The capture probability for the larger of 2 mixture proportions of the population (i.e., p A or p B , depending on the value of &pi;) was most important for predicting accuracy and precision, whereas capture probabilities of both mixture proportions (p A and p B ) were important to explain variation in coverage. Based on sampling conditions similar to parameter estimates from the empirical dataset (p A &thinsp;=&thinsp;0.30, p B &thinsp;=&thinsp;0.05, N&thinsp;=&thinsp;250, &pi;&thinsp;=&thinsp;0.15, and k&thinsp;=&thinsp;10), predicted accuracy and precision were low (60% and 53%, respectively), whereas coverage was high (94%). Increasing p B , the capture probability for the predominate but most difficult to capture proportion of the population, was most effective to improve accuracy under those conditions. However, manipulation of other parameters may be more effective under different conditions. In general, the probabilities of obtaining accurate and precise estimates were best when p &ge;&thinsp;0.2. Our regression models can be used by managers to evaluate specific sampling scenarios and guide development of sampling frameworks or to assess reliability of DNA-based capture-mark-recapture studies.

Tennessee

Geologic map of the Great Smoky Mountains National Park region, Tennessee and North Carolina

The geology of the Great Smoky Mountains National Park region of Tennessee and North Carolina was studied from 1993 to 2003 as part of a cooperative investigation by the U.S. Geological Survey with the National Park Service (NPS). This work resulted in a 1:100,000-scale geologic map derived from mapping that was conducted at scales of 1:24,000 and 1:62,500. The geologic data are intended to support cooperative investigations with the NPS, the development of a new soil map by the Natural Resources Conservation Service, and the All Taxa Biodiversity Inventory. In response to a request by the NPS, we mapped previously unstudied areas, revised the geology where problems existed, and developed a map database for use in interdisciplinary research, land management, and interpretive programs for park visitors.

North Carolina, Tennessee

Demographics of an experimentally released population of elk in Great Smoky Mountains National Park

We assessed the potential for reestablishing elk ( Cervus elaphus ) in Great Smoky Mountains National Park (GSMNP), USA, by estimating vital rates of experimentally released animals from 2001 to 2006. Annual survival rates for calves ranged from 0.333 to 1.0 and averaged 0.592. Annual survival for subadult and adult elk (i.e., &ge;1 yr of age) ranged from 0.690 to 0.933, depending on age and sex. We used those and other vital rates to model projected population growth and viability using a stochastic individual-based model. The annual growth rate (&lambda;) of the modeled population over a 25-year period averaged 0.996 and declined from 1.059 the first year to 0.990 at year 25. The modeled population failed to attain a positive 25-year mean growth rate in 46.0% of the projections. Poor calf recruitment was an important determinant of low population growth. Predation by black bears ( Ursus americanus ) was the dominant calf mortality factor. Most of the variance of growth projections was due to demographic variation resulting from the small population size ( n = 61). Management actions such as predator control may help increase calf recruitment, but our projections suggest that the GSMNP elk population may be at risk for some time because of high demographic variation.

Great Smoky Mountains National Park

Diverse elevational diversity gradients in Great Smoky Mountains National Park, U.S.A.: Chapter 10

Why does the number of species vary geographically? The earliest naturalists puzzled over this question, as do many biogeographers and macroecologists today. Over the last 200-plus years, the most striking geographic pattern in species richness – the decline in species richness with increasing latitude – has received the most attention. Thanks to many recent theoretical developments, coupled with global-scale databases and satellite technology, the number of candidate mechanisms that shape the latitudinal diversity gradient has been whittled down to a manageable number.

Great Smoky Mountains National Park

Comparison of breeding bird and vegetation communities in primary and secondary forests of Great Smoky Mountains National Park

We compared breeding bird communities and vegetation characteristics at paired point locations in primary (undisturbed) and mature secondary forest (70-100 years old) sites in Great Smoky Mountains National Park, USA to understand how sites logged prior to creation of the park compare to undisturbed sites following 70 years of protection from human disturbance. We found that bird and vegetation communities are currently similar, but retain some differences in species composition. Rank abundance curves for primary and secondary forest bird communities showed very similar patterns of species dominance. Species composition was also similar on the two sites which shared 24 of the 25 most frequently recorded species. Nonetheless, comparisons of density estimates derived from distance sampling showed three bird species were more abundant on primary forest sites and that one bird species was significantly more abundant on secondary forest sites. Notably, comparisons based on raw counts (unadjusted for potential differences in detectability) produced somewhat different results. Analyses of vegetation samples for the paired sites also showed relative similarity, but with some differences between primary and secondary forests. Primary forest sites had more large trees (trees greater than 50 cm diameter at breast height) and late successional species. Primary forest sites had a denser tall shrub layer while secondary forest sites had a denser canopy layer. Nonetheless, tree species richness, basal area of live trees and number of standing snags did not differ between primary and secondary forest sites. Results indicate that breeding bird communities on sites within the park that were logged commercially 70 years ago are currently quite similar to bird communities on sites with no history of human disturbance. Similarities between the bird communities on previously disturbed and undisturbed sites in Great Smoky Mountains National Park may exceed those on more fragmented landscapes because large patches of primary forest, adjacent to commercially logged sites, remained in the park when it was established in 1935. These patches of primary forest may have served as source areas for commercially logged sites.

North Carolina, Tennessee

The crane flies (Diptera: Tipuloidea) of Great Smoky Mountains National Park

The list of crane flies (Diptera: Ptychopteridae, Tipuloidea, Trichoceridae) known from Great Smoky Mountains National Park is updated. Sampling in association with the All Taxa Biodiversity Inventory of Great Smoky Mountains National Park resulted in the addition of 107 new Park records, bringing the current list to 250 species. This species assemblage is much richer than those of surrounding areas, although similar in composition. Total richness is estimated to be between 450 and 500 species for Great Smoky Mountains National Park.

North Carolina, Tennesse

Bait stations, hard mast, and black bear population growth in Great Smoky Mountains National Park

Bait-station surveys are used by wildlife managers as an index to American black bear ( Ursus americanus ) population abundance, but the relationship is not well established. Hard mast surveys are similarly used to assess annual black bear food availability which may affect mortality and natality rates. We used data collected in Great Smoky Mountains National Park (GSMNP) from 1989 to 2003 to determine whether changes in the bait-station index (&Delta;BSI) were associated with estimated rates of bear population growth (&lambda;) and whether hard mast production was related to bear visitation to baits. We also evaluated whether hard mast production from previous years was related to &lambda;. Estimates of &lambda; were based on analysis of capture-recapture data with the Pradel temporal symmetry estimator. Using the Akaike's Information Criterion (AIC), our analysis revealed no direct relationship between &Delta;BSI and &lambda;. A simulation analysis indicated that our data were adequate to detect a relationship had one existed. Model fit was marginally improved when we added total oak mast production of the previous year as an interaction term suggesting that the BSI was confounded with environmental variables. Consequently the utility of the bait-station survey as a population monitoring technique is questionable at the spatial and temporal scales we studied. Mast survey data, however, were valuable covariates of &lambda;. Population growth for a given year was negatively related to oak mast production 4 and 5 years prior. That finding supported our hypothesis that mast failures can trigger reproductive synchrony, which may not be evident from the trapped sample until years later.

North Carolina, Tennessee

Generalized geologic map of bedrock lithologies and surficial deposits in the Great Smoky Mountains National Park region, Tennessee and North Carolina

The geology of the Great Smoky Mountain National Park (GSMNP) region of Tennessee and North Carolina was studied from 1993 to 2003 as part of a cooperative investigation with the National Park Service (NPS). This work has been compiled as a 1:100,000-scale map derived from mapping done at 1:24,000 and 1:62,500 scale. The geologic data are intended to support cooperative investigations with NPS, the development of a new soil map by the Natural Resources Conservation Service, and the All Taxa Biodiversity Inventory ( http://www.discoverlifeinamerica.org/ ). At the request of NPS, we mapped areas previously not visited, revised the geology where stratigraphic and structural problems existed, and developed a map database for use in interdisciplinary research, land management, and interpretive programs for park visitors.

North Carolina, Tennessee