Forty-second breeding bird census: Climax maple-birch-beech forest
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No abstract available.
I calculated avian conservation scores, based on published quantitative assessment of bird presence (typically relative abundance) and regional Partners in Flight conservation concern score of each species. I related these avian conservation scores to severity of forest perturbation (i.e., % retention) and number of years since perturbation for forest stands within North America. I characterized avian response to perturbation by comparing avian conservation score on perturbed stands with that of paired unperturbed reference stands. Positive avian response to perturbation, representative of improved avian conservation status, was found when forest retention was >20% of coniferous forests or 25%–75% of hardwood forests. Positive avian response was greatest ~10 years after perturbation that retained 58% of conifer forests or 49% of hardwood forests. Increased avian conservation scores following perturbation may last for up to 23 years after perturbation but occur and diminish sooner with greater forest retention. Average annual avian response, over 23 years post-perturbation, was greatest when 30%–50% of hardwood stands were retained and when 50%–70% of conifer stands were retained.
Wintering birds were captured with mist nets at 12 pairs of forested sites in the New World tropics in 1984 and 1985 to compare populations in small isolated woodlands (generally 5-50 ha) with those in extensive forests (> 1,000 ha). Net-hours of effort were similar in large and small sites, as were total birds captured and banded, but species composition was very different. Members of the Todidae, Dendrocolaptidae, Formicariidae and Thraupinae were significantly more common in extensive forest than in small isolated tracts, indicating that these birds are especially vulnerable to effects of forest fragmentation. However, in winter many species of North American migrants, even species that are restricted to extensive forest during the breeding season, were just as common in small forest fragments as in extensive forest. A high percentage of the North American migrants banded in January 1984 (40 to 50 % for some species) were recaptured in 1985.
Background Dry mixed-conifer forests of the southwestern United States are experiencing rapid, anthropogenically driven fire regime change. Prior to the Euro-American settlement, most of these forests experienced frequent surface fires but are now vulnerable to uncharacteristically large, high-severity fires. Fire directly influences the structure and composition of these forests and, in turn, the wildlife that inhabit them. Changing fire regimes result in a certain decline of some species and uncertain consequences for others. The Mexican spotted owl ( Strix occidentalis lucida ) is a federally listed threatened species of particular note in southwestern mixed-conifer forests. High-severity fire is cited as the owl’s primary threat in the revised species recovery plan, but uncertainties surround the impacts of high-severity fire on the habitat of the threatened owl, particularly across a timeframe longer than a few years. Our objective was to explore the long-term (100-year) effects of fire severity on elements of forest structure vital for Mexican spotted owl nesting. We quantified structural attributes for nest/roost habitat across mixed-conifer forests that burned at varying severity levels and time periods in the last century. We then examined the drivers of structural attributes by detecting statistical differences between severity classes and time periods through permutational multivariate analysis of variance. Results High-severity fire has the strongest deleterious impact on elements of forest structure (total basal area, percent medium tree basal area, percent large tree basal area, large tree density, and canopy cover) vital to Mexican spotted owl nesting, and although the structural differences between severity classes diminish with time, it took ≥ 80–100 years to reach the structural conditions desired for Mexican spotted owl nesting after stand-replacing fires. The most important attribute measured, canopy cover, required 90–100 years after high-severity fires to reach levels most suitable for Mexican spotted owls in the Lincoln National Forest. Conclusions As fires increase in frequency, severity, and size compared to the last century, the Lincoln National Forest is projected to face an overall decrease in the structural conditions needed for Mexican spotted owl nesting habitat in this region. Short intervals between uncharacteristically high-severity fires in particular pose an imminent threat to nesting habitat.
Synthesis of results from several Arctic and boreal research programmes provides evidence for the strong role of high-latitude ecosystems in the climate system. Average surface air temperature has increased 0.3??C per decade during the twentieth century in the western North American Arctic and boreal forest zones. Precipitation has also increased, but changes in soil moisture are uncertain. Disturbance rates have increased in the boreal forest; for example, there has been a doubling of the area burned in North America in the past 20 years. The disturbance regime in tundra may not have changed. Tundra has a 3-6-fold higher winter albedo than boreal forest, but summer albedo and energy partitioning differ more strongly among ecosystems within either tundra or boreal forest than between these two biomes. This indicates a need to improve our understanding of vegetation dynamics within, as well as between, biomes. If regional surface warming were to continue, changes in albedo and energy absorption would likely act as a positive feedback to regional warming due to earlier melting of snow and, over the long term, the northward movement of treeline. Surface drying and a change in dominance from mosses to vascular plants would also enhance sensible heat flux and regional warming in tundra. In the boreal forest of western North America, deciduous forests have twice the albedo of conifer forests in both winter and summer, 50-80% higher evapotranspiration, and therefore only 30-50% of the sensible heat flux of conifers in summer. Therefore, a warming-induced increase in fire frequency that increased the proportion of deciduous forests in the landscape, would act as a negative feedback to regional warming. Changes in thermokarst and the aerial extent of wetlands, lakes, and ponds would alter high-latitude methane flux. There is currently a wide discrepancy among estimates of the size and direction of CO2 flux between high-latitude ecosystems and the atmosphere. These discrepancies relate more strongly to the approach and assumptions for extrapolation than to inconsistencies in the underlying data. Inverse modelling from atmospheric CO2 concentrations suggests that high latitudes are neutral or net sinks for atmospheric CO2, whereas field measurements suggest that high latitudes are neutral or a net CO2 source. Both approaches rely on assumptions that are difficult to verify. The most parsimonious explanation of the available data is that drying in tundra and disturbance in boreal forest enhance CO2 efflux. Nevertheless, many areas of both tundra and boreal forests remain net sinks due to regional variation in climate and local variation in topographically determined soil moisture. Improved understanding of the role of high-latitude ecosystems in the climate system requires a concerted research effort that focuses on geographical variation in the processes controlling land-atmosphere exchange, species composition, and ecosystem structure. Future studies must be conducted over a long enough time-period to detect and quantify ecosystem feedbacks.
Restoring forest ecosystems has become an increasingly high priority for land managers across the American West. Millions of hectares of forest are in need of drastic yet strategic reductions in density (e.g., basal area). Meeting the restoration and management goals requires quantifying metrics of vertical and horizontal forest structure, which has relied upon field‐based measurements, manned airborne or satellite remote sensing datasets. We used unmanned aerial vehicle (UAV ) image‐derived Structure‐from‐Motion (SfM) models and high‐resolution multispectral orthoimagery in this study to quantify vertical and horizontal forest structure at both the fine‐ (<4 ha) and mid‐scales (4–400 ha) across a forest density gradient. We then used these forest structure estimates to assess specific objectives of a forest restoration treatment. At the fine‐scale, we found that estimates of individual tree height and canopy diameter were most accurate in low‐density conditions, with accuracies degrading significantly in high‐density conditions. Mid‐scale estimates of canopy cover and forest density followed a similar pattern across the density gradient, demonstrating the effectiveness of UAV image‐derived estimates in low‐ to medium‐density conditions as well as the challenges associated with high‐density conditions. We found that post‐treatment conditions met a majority of the prescription objectives and demonstrate the UAV image application in quantifying changes from a mechanical thinning treatment. We provide a novel approach to forest restoration monitoring using UAV ‐derived data, one that considers varying density conditions and spatial scales. Future research should consider a more spatially extensive sampling design, including different restoration treatments, as well as experimenting with different combinations of equipment, flight parameters, and data processing workflows.
American black bears (Ursus americanus) are endemic to North America, having speciated from other ursids some 1.2 to 1.8 million years ago (Kurtn & Anderson 1994). During that time, black bears came to occupy nearly all of the forested areas of the North American continent. Historically, black bears were one of the most important mammals to indigenous peoples of North America by providing food, fat, hides, and tools (Raybourne 1987). Bears also played important roles in indigenous culture as symbols of strength, hard work, and love (see Rockwell 1991). In the 18th and 19th centuries in the U.S., Canada, and Mexico, European settlers with firearms reduced black bear numbers (Williams 1930), but the axe and plow had equally negative effects on bear populations as forests gave way to agriculture and livestock. Black bears also faced intense pressure from unregulated market hunting, poaching, and predator control programs. Black bears disappeared from large portions of their North American range, being relegated to swamps, thickets, rugged mountains, and other areas deemed too inaccessible, unsuitable, or undesirable to be occupied by humans (Pelton & van Manen 1994). In the early 20th century, Canadian and U.S. governments established national parks, forests, and refuges, and state and provincial legislatures created wildlife management agencies and enacted regulations to manage wildlife populations. By the late 20th century, the combination of public land infrastructure, habitat improvements, harvest regulations, law enforcement, and information-education programs resulted in significant increases in black bear numbers and range expansions in the U.S. and Canada (Pelton & van Manen 1994), aided in no small part by the remarkable adaptability of this animal (Pelton 2003; Scheick & McCown 2014). Today, the American black bear is one of the most iconic, abundant, and economically important bear species in the world. Unfortunately, black bear populations in Mexico have not recovered similarly to those in the U.S and Canada, and the status of the species there is uncertain.
Chestnut-dominated forests of the Caucasus Mountain area of Russia are very similar to former chestnut-dominated forests in eastern North America. The distribution, pathology, and reproductive status of European chestnut ( Castanea sativa ) in the Caucasus are described and compared to that of American chestnut ( C. dentata ). Chestnut forests are distributed continuously along the southern slope of the Caucasus mountains near the Black Sea, and are found in isolated populations on the north side of the Caucasus, at elevations ranging from 200 to 1300 meters. Chestnut blight was apparently introduced into the region after 1880 and continues to destroy chestnut forests today. Chestnut in the Caucasus is also infected by several other fungal and bacterial parasites and the joint infection of blight and bacteria may be especially dangerous for chestnut trees. Chestnut-dominated forests comprise only a few percent of total forest cover in the Caucasus Biosphere Preserve, and usually occur in mountain valleys or coves with deep brown soil. The age structure and reproductive status of chestnut in the Caucasus was investigated on six study plots in the Caucasus Biosphere Forest Preserve near the upper altitudinal limit of chestnut. Although chestnut is at least 70 percent of the overstory on these sites, there are very few trees less than 50 years old, and very few recent seedlings on any of the plots. Most large chestnut trees appear to have originated as basal spouts from previously established stems. Although chestnut seed production appears adequate, we suspect that competition with shrubs and other tree seedlings, and predation by herbivores and rodents, now prevent the establishment and survival of chestnut seedlings in the Biosphere Preserve.
North American Breeding Bird Survey data show that wood thrush (Hylocichla mustelina) populations in eastern U.S. forests have declined 1.8% per year during 1966-95. The declining quality of breeding forest tracts in North America is one possible cause for the apparent decline of some neotropical migratory birds, such as the wood thrush. In Georgia, however, wood thrush populations have declined during a period of increasing pine forest area and larger patch sizes. We hypothesized that forest management practices such as thinning and prescribed burning might create unsuitable habitat for wood thrushes. We conducted a four-year before/after, treatment/control experiment at the Piedmont National Wildlife Refuge in central Georgia to study to the effects of a treatment of thinning and prescribed burning on wood thrush demographic parameters. We simultaneously monitored wood thrush adults and juveniles with mark-recapture, radio-telemetry, nest searches, and plot-map surveys. Our analyses showed that wood thrushes were less likely to emigrate from the study compartments after the treatment, and wood thrushes exhibited some tendency to increase preference for hardwood habitats and decrease preference for pine habitats following the treatment. However, we observed no effects of treatment on nest success, adult survival, and adult and juvenile dispersal distances. We also found that female wood thrushes had lower survival rates than males during the breeding season, and we documented large-scale, within-year dispersal movements of adult (up to 17 km) and juvenile (up to 7 km) wood thrushes. We conclude that landscape level habitat quantity and quality must be considered during songbird management decisions. The documentation of sex- and age-specific wood thrush survival and movement rates was critical for construction of a set of population models. We used three stochastic models to learn more about wood thrush population dynamics and make predictions about population growth rates, reproductive success, and the effect of habitat changes on wood thrush populations. The simplest source/sink population model suggests that the Piedmont National Wildlife Refuge's wood thrush population is probably stable or increasing, and wood thrush populations in treated areas had higher growth rates than birds in untreated areas. We were able to use the individual-based model of wood thrush productivity to predict fecundity, a parameter that we could not measure directly in the field. Again, females on treated areas had higher fecundity than birds on untreated areas. Our spatially-based model predicted that wood thrush populations should respond positively to predicted changes in the age/size class structure of the Refuge's pine forests. Our model also showed that most wood thrushes leave the Refuge's forest compartments during the breeding season, and these dispersal movements are extremely important to understanding and managing wood thrush populations. The use of prescribed burning and retention shelterwood silviculture at the Piedmont National Wildlife Refuge does not appear to negatively affect the local wood thrush population. Continued use of the current management regime should result in adequate nesting, foraging, and escape habitats for wood thrushes. However, landscape-level habitat availability and quality, including lands outside the Refuge, must be considered when making management decisions that may affect wood thrushes.
Ungulate browsing in predator depleted North American landscapes is believed to be causing widespread tree recruitment failures. However, canopy disturbances and variations in ungulate densities are sources of heterogeneity that can buffer ecosystems against herbivory. Relatively little is known about the functional response (the rate of consumption in relation to food availability) of ungulates in eastern temperate forests, and therefore how “top down” control of vegetation may vary with disturbance type, intensity, and timing. This knowledge gap is relevant in the Northeastern United States today with the recent arrival of hemlock woolly adelgid (HWA; Adelges tsugae ) that is killing eastern hemlocks ( Tsuga canadensis ) and initiating salvage logging as a management response. We used an existing experiment in central New England begun in 2005, which simulated severe adelgid infestation and intensive logging of intact hemlock forest, to examine the functional response of combined moose ( Alces americanus ) and white-tailed deer ( Odocoileus virginianus ) foraging in two different time periods after disturbance (3 and 7 years). We predicted that browsing impacts would be linear or accelerating (Type I or Type III response) in year 3 when regenerating stem densities were relatively low and decelerating (Type II response) in year 7 when stem densities increased. We sampled and compared woody regeneration and browsing among logged and simulated insect attack treatments and two intact controls (hemlock and hardwood forest) in 2008 and again in 2012. We then used AIC model selection to compare the three major functional response models (Types I, II, and III) of ungulate browsing in relation to forage density. We also examined relative use of the different stand types by comparing pellet group density and remote camera images. In 2008, total and proportional browse consumption increased with stem density, and peaked in logged plots, revealing a Type I response. In 2012, stem densities were greatest in girdled plots, but proportional browse consumption was highest at intermediate stem densities in logged plots, exhibiting a Type III (rather than a Type II) functional response. Our results revealed shifting top–down control by herbivores at different stages of stand recovery after disturbance and in different understory conditions resulting from logging vs. simulated adelgid attack. If forest managers wish to promote tree regeneration in hemlock stands that is more resistant to ungulate browsers, leaving HWA-infested stands unmanaged may be a better option than preemptively logging them.