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A model to predict breeding-season productivity for multibrooded songbirds

Breeding-season productivity (the per capita number of offspring surviving to the end of the breeding season) is seldom estimated for multibrooded songbirds because of cost and logistical constraints. However, this parameter is critical for predictions of population growth rates and comparisons of seasonal productivity across geographic or temporal scales. We constructed a dynamic, stochastic, individual-based model of breeding-season productivity using demographic data from Wood Thrushes ( Hylocichla mustelina ) in central Georgia from 1993 to 1996. The model predicts breeding-season productivity as a function of adult survival, juvenile survival, nesting success, season length, renesting interval, and juvenile-care intervals. The model predicted that seasonal fecundity (number of fledglings produced) was 3.04, but only 2.04 juveniles per female survived to the end of the breeding season. Sensitivity analyses showed that differences in renesting interval, nesting success, fledglings per successful nest, and adult and juvenile survival caused variation in breeding-season productivity. Contrary to commonly held notions, season length and fledgling-care interval length did not cause variation in breeding-season productivity. This modeling exercise emphasizes the need for demographic data for songbird species, and we encourage biologists to use similar models to evaluate productivity in songbird populations.

The Auk

Forest area to support landbird population goals for the Mississippi Alluvial Valley

Historically, the Mississippi Alluvial Valley (MAV) (Partners in Flight Bird Conservation Region #26) was predominantly bottomland hardwood forest, but natural vegetation has been cleared from about 80 percent of this ecoregion and converted primarily to agriculture. Because most bird species that are of conservation concern in this region are dependent on forested wetlands, bottomland hardwood forest is the habitat of greatest conservation concern in the MAV. Past conservation planning for forest-dwelling birds in this region has focused on habitat objectives with presumptions regarding bird population goals being met through habitat provision. To better define population objectives, we estimated current populations of silvicolous birds on the basis of detections during 10 years of North American Breeding Bird Surveys (BBS). For each species, we used their estimated population and historical (1966–2015) change in their relative abundance, as assessed from BBS data, to establish regional population goals. We used the variance associated with historical BBS trends to estimate the minimum forest area required to sustain greater than or equal to (≥) 25 breeding pairs, which we combined with predicted probability of occupancy to identify sustainable forested habitat. For 54 species, we used published empirical density estimates, as affected by forest management, to estimate the proportion of the population objective that could be provisioned within sustainable forest patches. The area of presumed population-sustaining habitat, under existing forest management, was sufficient to support the species’ population objective for 23 species. We estimated that the target populations of seven additional species (Black-and-white Warbler, Brown Thrasher, Cerulean Warbler, Eastern Towhee, Indigo Bunting, Wood Thrush, and Yellow-breasted Chat) could be supported by current forest area through widespread changes in forest management. Target populations of seven other species (American Robin, Barred Owl, Boat-tailed Grackle, Chipping Sparrow, Eastern Phoebe, Mississippi Kite, and Red-headed Woodpecker) were accommodated within the MAV when populations in both forest and nonforest habitats are considered. For the remaining 20 species, we estimated the population increase needed to achieve their population goals. For these species, we estimated the additional area of forest restoration required to achieve their population goal within sustainable forest patches or, alternatively, the additional area of occupied habitat required to support their population goal within both forest and nonforest habitat. An additional 700,000 hectares of sustainable forest habitat may be enough to attain the forest-dependent population goals for most bird species within the MAV.

Arkansas, Kentucky, Louisiana, Mississippi, Missou

Breeding birds of the upper Mississippi River floodplain forest: One community in a changing forest, 1994 to 1997

Floodplain forest on the upper Mississippi River (UMR), a unique habitat in the Midwest that is important for many bird species, has been reduced and is undergoing continued reduction and changes in structure and species diversity because of river engineering and invasive species. Hydrological changes are causing tree diversity to decline favoring Acer saccharinum (silver maple) and Fraxinus pennsylvanica (green ash). Invasive Phalaris arundinacea (reed canary grass, Phalaris ) threatens tree regeneration, and recent Agrilus planipennis (emerald ash borer) arrival threatens to decimate the important ash component of the forest canopy. During the 1990s, virtually no information was available about breeding songbird species and abundances on the UMR floodplain forest from along many river miles and a broad range of forest situations (for example, mainland, island, edge, interior). From 1994 to 1997, we surveyed breeding birds and sampled vegetation at 391 random points on UMR floodplain forest along a latitudinal gradient from Red Wing, Minnesota, to Clinton, Iowa, to characterize bird assemblages and associations with gradients in forest structure at survey points (local scale) and land cover composition within a 200-meter radius of survey points (landscape scale). Eighty-six bird species were detected during the study, but 28 species comprised 90 percent of all detections. Species that are typically associated with woodland edge or are tolerant of fragmentation were the most common: Setophaga ruticilla (American Redstart), Troglodytes aedon (House Wren), Turdus migratorius (American Robin), Quiscalus quiscula (Common Grackle), and Vireo gilvus (Warbling Vireo). Species typically associated with large forest patches— Setophaga cerulea (Cerulean Warbler), Hylocichla mustelina (Wood Thrush), and Dryocopus pileatus (Pileated Woodpecker)—were rare. Principal components analyses consistently described local habitat gradients related to canopy cover and Phalaris presence and described landscape gradients related to forest area and areas of open land cover types. However, nonmetric multidimensional scaling revealed no pattern in bird assemblages. Canonical correspondence analyses with local habitat variables for each year revealed that bird assemblages were affected by canopy cover, the presence of Phalaris , and the number of tree species. Four bird species were consistently associated with Phalaris presence or negatively with canopy cover, and no species were associated with the number of tree species variable. Although landscape variables were significantly related to the bird assemblage in canonical correspondence analyses, no bird species were consistently related to any landscape variable. These results indicate that there is one assemblage of forest birds on the UMR composed mainly of edge-tolerant species. Species associated with lower canopy cover and Phalaris presence may be favored to increase in abundance as canopy cover opens as trees die and Phalaris becomes more prevalent.

Illinois, Iowa, Minnesota, Wisconsin

Point counts of landbirds in bottomland hardwood forests of the Mississippi Alluvial Valley: How long and how many?

To quantify efficacy of point count sampling in bottomland hardwood forests, we examined the influence of point count duration on corresponding estimates of number of individuals and species recorded. To accomplish this we conducted a totalof 82 point counts 7 May-16 May 1992distributed among three habitats (Wet, Mesic, Dry) in each of three regions within the lower Mississippi Alluvial Valley (MAV). Each point count consisted of recording the number of individual birds (all species) seen or heard during the initial three minutes and per each minute thereafter for a period totaling ten minutes. In addition, we included 384 point counts recorded during an 8-week period in each of 3 years (1985-1987) among 56 randomly-selected forest patches within the bottomlands of western Tennessee. Each point count consisted of recording the number of individuals (excluding migrating species) during each of four, 5 minute intervals for a period totaling 20 minutes. To estimate minimum sample size, we determined sampling variation at each level (region, habitat, and locality) with the 82 point counts from the lower (MAV) and applied the procedures of Neter and Wasserman (1974:493; Applied linear statistical models). Neither the cumulative number of individuals nor number of species per sampling interval attained an asymptote after 10 or 20 minutes of sampling. For western Tennessee bottomlands, total individual and species counts relative to point count duration were similar among years and comparable to the pattern observed throughout the lower MAV. Across the MAV, we recorded a total of 1,62 1 birds distributed among 52 species with the majority (8721/1621) representing 8 species. More birds were recorded within 25-50 m than in either of the other distance categories. There was significant variation in numbers of individuals and species among point counts. For both, significant differences between region and patch (nested within region) occurred; neither habitat nor interaction between habitat and region was significant. For = 0.05 and L3 = 0.10, minimum sample size estimates (per factor level) varied by orders of magnitude depending upon the observed or specified range of desired detectable difference. For observed regional variation, 20 and 40 point counts were required to accommodate variability in total birds (MSE = 9.28) and species (MSE = 3.79), respectively; 25 percent of the mean could be achieved with 5 counts per factor level. Corresponding sample sizes required to detect differences of rarer species (e.g., Wood Thrush) were 500; for common species (e.g., Northern Cardinal) this same level of precision could be achieved with 100 counts.

Book chapter

Sample size and allocation of effort in point count sampling of birds in bottomland hardwood forests

To examine sample size requirements and optimum allocation of effort in point count sampling of bottomland hardwood forests, we computed minimum sample sizes from variation recorded during 82 point counts (May 7-May 16, 1992) from three localities containing three habitat types across three regions of the Mississippi Alluvial Valley (MAV). Also, we estimated the effect of increasing the number of points or visits by comparing results of 150 four-minute point counts obtained from each of four stands on Delta Experimental Forest (DEF) during May 8-May 21, 1991 and May 30-June 12, 1992. For each stand, we obtained bootstrap estimates of mean cumulative number of species each year from all possible combinations of six points and six visits. ANOVA was used to model cumulative species as a function of number of points visited, number of visits to each point, and interaction of points and visits. There was significant variation in numbers of birds and species between regions and localities (nested within region); neither habitat, nor the interaction between region and habitat, was significant. For a = 0.05 and a = 0.10, minimum sample size estimates (per factor level) varied by orders of magnitude depending upon the observed or specified range of desired detectable difference. For observed regional variation, 20 and 40 point counts were required to accommodate variability in total individuals (MSE = 9.28) and species (MSE = 3.79), respectively, whereas ? 25 percent of the mean could be achieved with five counts per factor level. Sample size sufficient to detect actual differences of Wood Thrush (Hylocichla mustelina) was >200, whereas the Prothonotary Warbler (Protonotaria citrea) required <10 counts. Differences in mean cumulative species were detected among number of points visited and among number of visits to a point. In the lower MAV, mean cumulative species increased with each added point through five points and with each additional visit through four visits. Although no interaction was detected between number of points and number of visits, when paired reciprocals were compared, more points invariably yielded a significantly greater cumulative number of species than more visits to a point. Still, 36 point counts per stand during each of two breeding seasons detected only 52 percent of the known available species pool in DEF.

Book chapter

Early avian research at the Savannah River Site, South Carolina: historical highlights and possibilities for the future

Avian biology and collection of baseline population data was a major part of the first decade (1951-1961) of field research at the Savannah River Site (SRS). Baseline inventories involving organisms and land-use types were part of the mission in the early contracts between the Atomic Energy Commission (now the Department of Energy) and the University of Georgia prior to the establishment of the Savannah River Ecology Laboratory (SREL) as a National Environmental Research Park Laboratory. About 27% of the SREL publications during this first decade dealt with birds. Since that time, research on the SRS landscape has expanded and broadened with less than 10% of the publications dealing with birds. SRS changed also from an agriculturally dominated area with ca. 40% open areas (fields, crops, pastures) to a timber-managed area with ca. 80% forests, 12% open areas, and 2% open water impoundments. Baseline breeding bird populations of the SRS in the 1950s were typical for the region with avian species richness and density increasing with the age and succession of the vegetation (0-26 species and densities of 0-741 pairs/km2 for the habitats surveyed). During the first decade at the SRS, the resident game bird population of Northern Bobwhites (Colinus virginianus) increased and the Mourning Dove (Zenaida rnacroura) population, a migratory upland game bird, remained stable. Current avian research efforts, as well as new opportunities to reexamine the breeding bird populations and the landscape of SRS, will provide a better understanding of the potential causes of declines of neotropical migratory birds, declines of resident and migratory game birds, and how habitat influences invasions and extinctions of breeding birds in the region. Emphasis for future research and monitoring should be on neotropical migratory bird populations in decline (Yellow-billed Cuckoo, Coccyzus americanus; Eastern Wood-Pewee, Contopus virens; Wood Thrush, Hylocichla mustelina; Prairie Warbler, Dendroica discolor; and Painted Bunting, Passerina ciris), resident species in decline (e.g., Loggerhead Shrike, Lanius ludovicianus), certain species groups (e.g., waterfowl and wading birds), important habitat, and recent invasions and extinctions of breeding species. Old growth forested wetlands should be monitored because of the large number of neotropical migratory birds that depend on this habitat in the southeastern United States. A variety of survey techniques will be needed to determine population trends: line transects, call or song playbacks, roadside point surveys (call counts for game birds), aerial surveys, and presence or absence of species within stratified areas of SRS. The SRS provides opportunity for avian research at the landscape level with the potential to solve problems important to the survival of many bird populations as well as to increase our knowledge on how to manage and conserve our avian natural resources for the future.

Book chapter

Bottomland hardwood establishment and avian colonization of reforested sites in the Mississippi Alluvial Valley

Reforestation of bottomland hardwood sites in the Mississippi Alluvial Valley has markedly increased in recent years, primarily due to financial incentive programs such as the Wetland Reserve Program, Partners for Wildlife Program, and state and private conservation programs. An avian conservation plan for the Mississippi Alluvial Valley proposes returning a substantial area of cropland to forested wetlands. Understanding how birds colonize reforested sites is important to assess the effectiveness of avian conservation. We evaluated establishment of woody species and assessed bird colonization on 89 reforested sites. These reforested sites were primarily planted with heavy-seeded oaks (Quercus spp.) and pecans (Carya illinoensis). Natural invasion of light-seeded species was expected to diversify these forests for wildlife and sustainable timber harvest. Planted tree species averaged 397 + 36 stems/ha-1, whereas naturally invading trees averaged 1675 + 241 stems/ha. However, naturally invading trees were shorter than planted trees and most natural invasion occurred <100 m from an existing forested edge. Even so, planted trees were relatively slow to develop vertical structure, especially when compared with tree species planted and managed for pulpwood production. Slow development of vertical structure resulted in grassland bird species, particularly dickcissel (Spiza americana) and red-winged blackbird (Agelaius phoeniceus), being the dominant avian colonizers for the first 7 years post-planting. High priority bird species (as defined by Partners in Flight), such as prothonotary warbler (Protonotaria citrea) and wood thrush (Hylocichla mustelina), were not frequently detected until stands were 15 years old. Canonical correspondence analysis revealed tree height had the greatest influence on the bird communities colonizing reforested sites. Because colonization by forest birds is dependent on tree height, we recommend inclusion of at least one fast-growing tree species (e.g., cottonwood [Populus deltoides], or sycamore [Platanus occidentalis]) in the planting stock to encourage rapid avian colonization.

Book chapter

Open season, 1947

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Wood Thrush