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Wyoming Basin Rapid Ecoregional Assessment

The Wyoming Basin Rapid Ecoregional Assessment was conducted in partnership with the Bureau of Land Management (BLM). The overall goals of the BLM Rapid Ecoregional Assessments (REAs) are to identify important ecosystems and wildlife habitats at broad spatial scales; identify where these resources are at risk from Change Agents, including development, wildfire, invasive species, disease and climate change; quantify cumulative effects of anthropogenic stressors; and assess current levels of risk to ecological resources across a range of spatial scales and jurisdictional boundaries by assessing all lands within an ecoregion. There are several components of the REAs. Management Questions, developed by the BLM and stakeholders for the ecoregion, identify the regionally significant information needed for addressing land-management responsibilities. Conservation Elements represent regionally significant species and ecological communities that are of management concern. Change Agents that currently affect or are likely to affect the condition of species and communities in the future are identified and assessed. REAs also identify areas that have high conservation potential that are referred to as “large intact areas.” At the ecoregion level, the ecological value of large intact areas is based on the assumption that because these areas have not been greatly altered by human activities (such as development), they are more likely to contain a variety of plant and animal communities and to be resilient and resistant to changes resulting from natural disturbances such as fire, insect outbreaks, and disease. The Wyoming Basin Ecoregion encompasses approximately 133,656 square kilometers (51,604.87 square miles), including portions of Wyoming, Colorado, Utah, Idaho, and Montana. The Wyoming Basin has some of the highest quality wildlife habitats remaining in the Intermountain West. The wide variety of habitats includes intermountain basins dominated by sagebrush shrublands interspersed with deciduous and conifer woodlands and montane or subalpine forests at higher elevations. The Wyoming Basin also supports ranching and agricultural operations that are important to the region’s economy and vital to conserving habitats for wildlife. The region also contains abundant energy resources, including large natural gas reserves and areas of high wind-energy potential. Combined with increased residential and industrial development, fast-paced energy development is resulting in notable land-use changes, including habitat loss and fragmentation. In the Wyoming Basin REA, we evaluated the following seven communities as Conservation Elements: streams and rivers, wetlands, riparian forests and shrublands, sagebrush steppe, desert shrublands, foothill shrublands and woodlands, and mountain forests and alpine zones. We evaluated a total of 14 species and species assemblages as Conservation Elements: aspen forests and woodlands, five-needle pine forests and woodlands, juniper woodlands, cutthroat trout, three-species fish assemblage, northern leatherside chub, sauger, spadefoot assemblage, greater sage-grouse, golden eagle, ferruginous hawk, sagebrush-obligate birds, pygmy rabbit, and mule deer. We evaluated Management Questions (Core and Integrated) for each species and community for the Wyoming Basin REA. Core Management Questions address primary management issues, including (1) where is the Conservation Element, and what are its key ecological attributes (characteristics of species and communities that may affect their long-term persistence or viability); (2) what and where are the Change Agents; and (3) how do the Change Agents affect the key ecological attributes? Integrated Management Questions synthesize the Core Management Questions as follows: (1) where are the areas with high landscape-level ecological values; (2) where are the areas with high landscape-level risks; and (3) where are the potential areas for conservation, restoration, and development? The associated maps and key findings for each Management Question are summarized for each Conservation Element in individual chapters. Additional chapters on landscape intactness and an REA synthesis are included.

Colorado, Idaho, Montana, Utah, Wyoming

Patterns in diurnal airspace use by migratory landbirds along an ecological barrier

Migratory bird populations and survival are affected by conditions experienced during migration. While many studies and conservation and management efforts focus on terrestrial stoppage and staging areas, the aerial environment through which migrants move also is subjected to anthropogenic impacts with potential consequences to migratory movement and survival. During autumn migration, the northern coastline of Lake Superior acts as an ecological barrier for many landbirds migrating out of the boreal forests of North America. From 24 observation points, we assessed the diurnal movements of birds throughout autumn migration, 2008-2010, within a 210 km by 10 km coastal region along the northern coast of Lake Superior. Several raptor species showed patterns in airspace associated with topographic features such as proximity to the coastline and presence of ridgelines. Funneling movement, commonly used to describe the concentration of raptors along a migratory diversion line that either prevents or enhances migration progress, occurred only for Bald and Golden Eagles. This suggests a "leaky" migration funnel for most migratory raptors (e.g., migrating birds exiting the purported migration corridor). Passerines migrating during the late season showed more spatial and temporal structure in airspace distribution than raptors, including funneling and an association with airspace near the coast. We conclude that a) the diurnal use of airspace by many migratory landbirds is patterned in space and time, b) autumn count sites situated along ecological barriers substantially underestimate the number of raptors due to 'leakage' out of these concentration areas, and c) the magnitude and structure of diurnal passerine movements in airspace have been overlooked. The heavy and structured use of airspace by migratory landbirds, especially the airspace associated with anthropogenic development (e.g., buildings, towers, turbines) necessitates a shift in focus to airspace management and conservation attention for these animals.

Minnesota

Palila restoration research, 1996−2012

The Palila Restoration Project was initiated in 1996 by the U.S. Geological Survey to assist government agencies mitigate the effects of realigning Saddle Road (Highway 200) through Palila Critical Habitat (U.S. Fish and Wildlife Service 1998, Federal Highway Administration 1999). Ecological research on the palila (Loxioides bailleui), an endangered Hawaiian forest bird, carried out by the U.S. Geological Survey (formerly organized as the Research Division of U.S. Fish and Wildlife Service) since 1987 and research conducted by the Palila Restoration Project provided the scientific bases for developing a recovery strategy (U.S. Fish and Wildlife Service 2006) and its adaptive implementation. The main objectives of the Palila Restoration Project were to develop techniques for reintroducing the palila to a portion of its former range, investigate the biological threats to the palila and its habitat, and synthesize the existing body of ecological knowledge concerning the palila. Five broad study themes formed the research framework: 1. Population reintroduction and restoration 2. Demography and breeding ecology 3. Habitat use and food ecology 4. Vegetation ecology 5. Predator ecology and management An element that was not included in the research program of the project was the ecology and management of introduced ungulates, which has historically constituted the single greatest threat to Palila Critical Habitat (Banko et al. 2009). The absence of ungulate studies should not be interpreted to mean that we believe ungulates no longer damage palila habitat. Other research has already established that removing alien browsers and grazers from Mauna Kea is essential for the recovery of the subalpine forest on which palila now depend (Scowcroft and Giffin 1983; Scowcroft and Sakai 1983; Scowcroft and Conrad 1988, 1992; Hess et al. 1999). Moreover, the Federal District Court of Hawai‘i has ordered the state of Hawai‘i to remove browsing ungulates from Palila Critical Habitat (Banko et al. 2009, Hess and Banko 2011). This final report summarizes results of Palila Restoration Project research from December 1996 to December 2012. Even though some results contained in this report have been published in scientific journals and other technical reports (Appendix I), they are included here to provide a comprehensive chronicle of all project activities.

Hawaii

Mapping the vulnerability of giant sequoias after extreme drought in California using remote sensing

Between 2012 and 2016, California suffered one of the most severe droughts on record. During this period Sequoiadendron giganteum (giant sequoias) in the Sequoia and Kings Canyon National Parks (SEKI), California, USA experienced canopy water content (CWC) loss, unprecedented foliage senescence, and, in a few cases, death. We present an assessment of the vulnerability of giant sequoia populations to droughts that is currently lacking and needed for management. We used a temporal trend of remotely sensed CWC obtained between 2015 and 2017, and recently georeferenced giant sequoia crowns to quantify the vulnerability of 7,408 individuals in 10 groves in the northern portion of SEKI. CWC is sensitive to changes in liquid water in tree canopies; therefore, it is a useful metric for quantifying the response of sequoia trees to drought. Temporal trends indicated that 9% of giant sequoias had a significant decline or consistently low CWC, suggesting these trees were likely operating at low photosynthetic capacity and potentially at high risk to drought stress. We also found that 20% of the giant sequoias had an increase or consistently high level of CWC, indicating these trees were at low risk to drought stress. These vulnerability categories were used in a random forest model with a combination of topographic, fire-related, and climate variables to generate high-resolution vulnerability risk maps. These maps show that higher risk is associated with lower elevation and higher climate water deficit. We also found that sequoias at higher elevations but located near meadows had higher vulnerability risk. These results and the vulnerability maps can identify vulnerable sequoias that may be difficult to save or locations of refugia to be protected, and thus may aid forest managers in preparation for future droughts.

California

Studies to assess natural resource recovery and evaluate monitoring methods for restored bottomland hardwood forests

The Natural Resource Damage Assessment and Restoration process assesses natural resource injury due to oil or chemical spills and calculates the damages to compensate the public for those injuries. Ecological restoration provides a means for recovering resources injured or lost due to contamination from oil or chemical spills by restoring the injured site after remediation, or acquiring or reconstructing equivalent resources off site to replace those lost due to the spill. In the case of restored forests, once restoration is implemented, monitoring of forest ecology helps keep recovery on track, with the maturation of forest vegetation, recovered soil conditions, and development of microbial, fungal, and faunal communities, necessary for ecologically functioning forests. This series of papers focuses on applying methods for monitoring restoration progress in forest vegetation and soils, and amphibian, avian, and mammalian communities, assessing strengths and weaknesses of different methods, and evaluating levels of effort needed to obtain accurate indications of forest ecological condition.

Integrated Environmental Assessment and Management

Interactions among invasive plants: Lessons from Hawai‘i

Most ecosystems have multiple-plant invaders rather than single-plant invaders, yet ecological studies and management actions focus largely on single invader species. There is a need for general principles regarding invader interactions across varying environmental conditions, so that secondary invasions can be anticipated and managers can allocate resources toward pretreatment or postremoval actions. By reviewing removal experiments conducted in three Hawaiian ecosystems (a dry tropical forest, a seasonally dry mesic forest, and a lowland wet forest), we evaluate the roles environmental harshness, priority effects, productivity potential, and species interactions have in influencing secondary invasions, defined here as invasions that are influenced either positively (facilitation) or negatively (inhibition/priority effects) by existing invaders. We generate a conceptual model with a surprise index to describe whether long-term plant invader composition and dominance is predictable or stochastic after a system perturbation such as a removal experiment. Under extremely low resource availability, the surprise index is low, whereas under intermediate-level resource environments, invader dominance is more stochastic and the surprise index is high. At high resource levels, the surprise index is intermediate: Invaders are likely abundant in the environment but their response to a perturbation is more predictable than at intermediate resource levels. We suggest further testing across environmental gradients to determine key variables that dictate the predictability of postremoval invader composition.

Hawai'i

Environmental predictors of shrubby cinquefoil ( Dasiphora fruticosa ) habitat and quality as host for Maine’s endangered Clayton’s copper butterfly ( Lycaena dorcas claytoni )

Population size of habitat-specialized butterflies is limited in part by host plant distribution and abundance. Effective conservation for host-specialist species requires knowledge of host-plant habitat conditions and relationships with the specialist species. Clayton’s copper butterfly ( Lycaena dorcas claytoni ) is a Maine state-endangered species that relies exclusively on shrubby cinquefoil ( Dasiphora fruticosa ) as its host. Dasiphora fruticosa occurs in 28 wetlands in Maine, ten of which are occupied by L. d. claytoni. Little is known about environmental conditions that support large, persistent stands of D. fruticosa in Maine. We evaluated the environment (hydrology, pore water and peat nutrients) associated with D. fruticosa distribution, age, and condition in Maine wetlands supporting robust stands of D. fruticosa to compare with L. d. claytoni occurrence. Although dominant water source in D. fruticosa —containing wetlands included both groundwater discharge and surface-flow, D. fruticosa coverage was greater in wetlands with consistent growing season water levels that dropped into or below the root zone by late season, and its distributions within wetlands reflected pore water hydrogen ion and conductivity gradients. Flooding magnitude and duration were greatest during the L.d. claytoni larval feeding period, whereas, mean depth to water table and upwelling increased and were most variable following the L. d. claytoni egg-laying period that precedes D. fruticosa senescence. Oldest sampled shrubs were 37 years, and older shrubs were larger and slower-growing. Encounter rates of L. d. claytoni were greater in wetlands with larger D. fruticosa plants of intermediate age and greater bloom density. Wetland management that combines conditions associated with D. fruticosa abundance (e.g., non-forested, seasonally consistent water levels with high conductivity) and L. d. claytoni occurrence (e.g., drawdown below the root zone following egg-laying, abundant blooms on intermediate-aged D. fruticosa, nearby D. fruticosa -containing wetlands) will aid L. d. claytoni conservation.

Wetlands Ecology and Management

Carbon storage, timber production, and biodiversity: comparing ecosystem services with multi-criteria decision analysis

Increasingly, land managers seek ways to manage forests for multiple ecosystem services and functions, yet considerable challenges exist in comparing disparate services and balancing trade-offs among them. We applied multi-criteria decision analysis (MCDA) and forest simulation models to simultaneously consider three objectives: (1) storing carbon, (2) producing timber and wood products, and (3) sustaining biodiversity. We used the Forest Vegetation Simulator (FVS) applied to 42 northern hardwood sites to simulate forest development over 100 years and to estimate carbon storage and timber production. We estimated biodiversity implications with occupancy models for 51 terrestrial bird species that were linked to FVS outputs. We simulated four alternative management prescriptions that spanned a range of harvesting intensities and forest structure retention. We found that silvicultural approaches emphasizing less frequent harvesting and greater structural retention could be expected to achieve the greatest net carbon storage but also produce less timber. More intensive prescriptions would enhance biodiversity because positive responses of early successional species exceeded negative responses of late successional species within the heavily forested study area. The combinations of weights assigned to objectives had a large influence on which prescriptions were scored as optimal. Overall, we found that a diversity of silvicultural approaches is likely to be preferable to any single approach, emphasizing the need for landscape-scale management to provide a full range of ecosystem goods and services. Our analytical framework that combined MCDA with forest simulation modeling was a powerful tool in understanding trade-offs among management objectives and how they can be simultaneously accommodated.

Ecological Applications

Competitive interactions and resource partitioning between northern spotted owls and barred owls in western Oregon

The federally threatened northern spotted owl ( Strix occidentalis caurina ) is the focus of intensive conservation efforts that have led to much forested land being reserved as habitat for the owl and associated wildlife species throughout the Pacific Northwest of the United States. Recently, however, a relatively new threat to spotted owls has emerged in the form of an invasive competitor: the congeneric barred owl ( S. varia ). As barred owls have rapidly expanded their populations into the entire range of the northern spotted owl, mounting evidence indicates that they are displacing, hybridizing with, and even killing spotted owls. The range expansion by barred owls into western North America has made an already complex conservation issue even more contentious, and a lack of information on the ecological relationships between the 2 species has hampered recovery efforts for northern spotted owls. We investigated spatial relationships, habitat use, diets, survival, and reproduction of sympatric spotted owls and barred owls in western Oregon, USA, during 2007–2009. Our overall objective was to determine the potential for and possible consequences of competition for space, habitat, and food between these previously allopatric owl species. Our study included 29 spotted owls and 28 barred owls that were radio-marked in 36 neighboring territories and monitored over a 24-month period. Based on repeated surveys of both species, the number of territories occupied by pairs of barred owls in the 745-km 2 study area (82) greatly outnumbered those occupied by pairs of spotted owls (15). Estimates of mean size of home ranges and core-use areas of spotted owls (1,843 ha and 305 ha, respectively) were 2–4 times larger than those of barred owls (581 ha and 188 ha, respectively). Individual spotted and barred owls in adjacent territories often had overlapping home ranges, but interspecific space sharing was largely restricted to broader foraging areas in the home range with minimal spatial overlap among core-use areas. We used an information-theoretic approach to rank discrete-choice models representing alternative hypotheses about the influence of forest conditions, topography, and interspecific interactions on species-specific patterns of nighttime resource selection. Spotted owls spent a disproportionate amount of time foraging on steep slopes in ravines dominated by old (>120 yr) conifer trees. Barred owls used available forest types more evenly than spotted owls, and were most strongly associated with patches of large hardwood and conifer trees that occupied relatively flat areas along streams. Spotted and barred owls differed in the relative use of old conifer forest (greater for spotted owls) and slope conditions (steeper slopes for spotted owls), but we found no evidence that the 2 species differed in their use of young, mature, and riparian-hardwood forest types. Mean overlap in proportional use of different forest types between individual spotted owls and barred owls in adjacent territories was 81% (range = 30–99%). The best model of habitat use for spotted owls indicated that the relative probability of a location being used was substantially reduced if the location was within or in close proximity to a core-use area of a barred owl. We used pellet analysis and measures of food-niche overlap to determine the potential for dietary competition between spatially associated pairs of spotted owls and barred owls. We identified 1,223 prey items from 15 territories occupied by spotted owls and 4,299 prey items from 24 territories occupied by barred owls. Diets of both species were dominated by nocturnal mammals, but diets of barred owls included many terrestrial, aquatic, and diurnal prey species that were rare or absent in diets of spotted owls. Northern flying squirrels ( Glaucomys sabrinus ), woodrats ( Neotoma fuscipes , N. cinerea ), and lagomorphs ( Lepus americanus , Sylvilagus bachmani ) were primary prey for both owl species, accounting for 81% and 49% of total dietary biomass for spotted owls and barred owls, respectively. Mean dietary overlap between pairs of spotted and barred owls in adjacent territories was moderate (42%; range = 28–70%). Barred owls displayed demographic superiority over spotted owls; annual survival probability of spotted owls from known-fate analyses (0.81, SE = 0.05) was lower than that of barred owls (0.92, SE = 0.04), and pairs of barred owls produced an average of 4.4 times more young than pairs of spotted owls over a 3-year period. We found a strong, positive relationship between seasonal (6-month) survival probabilities of both species and the proportion of old (>120 yr) conifer forest within individual home ranges, which suggested that availability of old forest was a potential limiting factor in the competitive relationship between these 2 species. The annual number of young produced by spotted owls increased linearly with increasing distance from a territory center of a pair of barred owls, and all spotted owls that attempted to nest within 1.5 km of a nest used by barred owls failed to successfully produce young. We identified strong associations between the presence of barred owls and the behavior and fitness potential of spotted owls, as shown by changes in movements, habitat use, and reproductive output of spotted owls exposed to different levels of spatial overlap with territorial barred owls. When viewed collectively, our results support the hypothesis that interference competition with barred owls for territorial space can constrain the availability of critical resources required for successful recruitment and reproduction of spotted owls. Availability of old forests and associated prey species appeared to be the most strongly limiting factors in the competitive relationship between these species, indicating that further loss of these conditions can lead to increases in competitive pressure. Our findings have broad implications for the conservation of spotted owls, as they suggest that spatial heterogeneity in vital rates may not arise solely because of differences among territories in the quality or abundance of forest habitat, but also because of the spatial distribution of a newly established competitor. Experimental removal of barred owls could be used to test this hypothesis and determine whether localized control of barred owl numbers is an ecologically practical and socio-politically acceptable management tool to consider in conservation strategies for spotted owls.

Oregon

Resource manager information needs regarding hydrologic regime shifts for the North Pacific Landscape Conservation

Landscape Conservation Cooperatives (LCCs) are a network of 22 public-private partnerships, defined by ecoregion, that share and provide science to ensure the sustainability of land, water, wildlife, and cultural resources in North America. LCCs were established by the U.S. Department of the Interior (DOI) in recognition of the fact that response to climate change must be coordinated on a landscape-level basis because important resources, ecosystem processes, and resource management challenges extend beyond most of the boundaries considered in current natural resource management. The North Pacific LCC (NPLCC) covers the range of the Pacific coastal temperate rainforest, including an area of 528,360 km 2 spanning 22 degrees of latitude from the Kenai Peninsula, Alaska, to Bodega Bay, California. The coverage area includes parts of four States, two Canadian provinces, and more than 100 Tribes and First Nation language groups. It extends from alpine areas at the crest of coastal mountains across subalpine, montane, and lowland forests to the nearshore marine environment. This wide range of latitudes and elevation zones; terrestrial, freshwater, and marine habitats; and complex jurisdictional boundaries hosts a diversity of natural resources and their corresponding management issues are equally diverse. As evidenced by the Science and Traditional Ecological Knowledge (S-TEK) Strategy guiding principles, identifying and responding to the needs of resource managers is key to the success of the NPLCC. To help achieve this goal of the NPLCC, the U.S. Geological Survey (USGS) has organized several workshops with resource managers and resource scientists to identify management information needs relevant to the priority topics identified in the S-TEK Strategy. Here, we detail the results from a first workshop to address the effects of changes in hydrologic regime on rivers, streams, and riparian corridors. The workshop focused on a subset of the full NPLCC geography and was structured to answer the following questions: What are the valued resources and services that may be affected by hydrologic regime changes in the region? What are the management goals for those resources? How is climate change anticipated to affect valued resources and goals? What adaptation strategies may managers use in response to anticipated changes in resources due to climate-related hydrologic change? What information is needed to inform and use management responses?

Open-File Report

Sea otters in the northern Pacific Ocean

About 250 years ago sea otters ( Enhydra lutris ) were distributed continuously from central Baja California, north and west along the Pacific Rim to Machatka Peninsula in Russia, and south along the Kuril Island to northern Japan (Kenyon 1969; Fig. 1a). Several hundred thousand sea otters may have occurred in the north Pacific region when commercial hunting began in the 18th century (Riedman and Estes 1990). At least two attributes of the sea otter have influenced humans, likely for as long as they have resided together along the coast of the north Pacific Ocean. First, sea otters rely on a dense fur, among the finest in the world, for insulation in the cold waters of the Pacific Ocean. The demand for sea otter fur led to their near extinction in the 19th century. The fur harvest, begun about 1740 and halted by international treaty in 1911, left surviving colonies, each likely numbering less than a few hundred animals, in California, south-central Alaska, and the Aleutian, Medney, and Kuril Islands (Fig. 1a). These individuals provided the nucleus for the recovery of the species. Today more than 100,000 sea otters occur throughout about 75% of their original range (fig. 1b). Immigration has resulted in near-complete occupation of the Aleutian and Kuril archipelagos and the Alaska peninsula. Successful translocations have resulted in viable populations in southeast Alaska, Washington, and British Columbia. Large amounts of unoccupied habitat remain along the coasts of Russia, Canada, the United States, and Mexico. The second potential source of conflict between sea otters and humans is that sea otters prey on and often limit some benthic invertebrate populations. Because some of these invertebrates are aso used by humans (Estes and VanBlaricom 1985), human perceptions about the effects of sea otter foraging on invertebrates sometimes differ. By limiting populations of herbivorous invertebrates ( e.g. , sea urchins [Echinoidea]) otters help maintain the integrity of kelp forest communities. At the same time, sea otter predation on other marine invertebrates can lead to direct competition with humans for resources. These interactions add complex dimensions to the conservation and management of sea otters, in large part because of wide-ranging social, ecological, and economic consequences of sea otter foraging. Long-term data on abundance and distribution are available for relatively few sea otter populations. Here we summarize such data from three populations: Being Island, Russia; Prince William Sound, Alaska; and Olympic Peninsula, Washington. The Bering Island population resulted from natural emigration and represents complete recovery. Prince William Sounds represents near recovery of a remnant population, whereas the Washington population was established via translocations from Alaska and is just beginning to recover. We will compare growth rates and current status among these populations. Because of its unique status and growth characteristics, the California sea otter is not treated in this article.

Book chapter

Valleys of fire: Historical fire regimes of forest-grassland ecotones across the montane landscape of the Valles Caldera National Preserve, New Mexico, USA

Context Montane grasslands and forest-grassland ecotones are unique and dynamic components of many landscapes, but the processes that regulate their dynamics are difficult to observe over ecologically relevant time spans. Objectives We aimed to demonstrate the efficacy of using grassland-forest ecotone trees to reconstruct spatial and temporal properties of the historical fire regime in a complex landscape of montane forests and adjacent grasslands. Methods We sampled and crossdated fire-scarred trees along ecotones and compared variations in historical fire occurrence within and among nine adjoining valle basins in a 10,158 ha landscape. We analyzed fire year extensiveness, climate regulation, and the occurrence of consecutive fire years. Results The resulting tree-ring record covers 1240–2005 AD, with 296 trees recording 125 replicated fire years during the analysis period 1601–1902 AD . Mean fire intervals for all events recorded on two or more trees ranged from 4.7 to 13.6 years in individual valles , and a mean of 2.4 ± 1.7 (SD) years at the landscape scale. Between 1660 and 1902, extensive fires occurring in six or more valles occurred 15 times, on average at ~ 17-year intervals; 29 moderately widespread fires (3–5 valles ) occurred during this period, at 8.7 year intervals on average. Widespread events occurred in years with a significantly lower Palmer Drought Severity Index (PDSI) preceded by years of significantly positive PDSI, indicating conditions favorable for fine fuel production. Spatial reconstruction of fire extent revealed multiple occurrences of consecutive-year fires burning non-overlapping areas, associated with persistent low PDSI anomalies preceded by positive conditions in antecedent years. Conclusions A landscape spatiotemporal approach to reconstructing fire regimes of montane forest-grassland complexes provides a valuable baseline for guiding prescribed and natural fire management at large spatial scales.

New Mexico

Tidal freshwater forested wetlands: Future research needs and an overview of restoration: Chapter 17

Studies of tidal freshwater forested wetlands are few in contrast to the diversity of conditions and information needs that exist for this ecosystem type. Basic information is lacking on the physiological ecology of major wetland tree species under natural settings, the structure and dynamics of pure and mixed species communities, soil-plant interactions, biogeochemistry, hydrology, soils, wildlife habitat, primary biotic and abiotic functions, and the response of these systems to natural and human-caused disruptions. Existing information is often not in a form that can be applied to ecosystem problems, especially those related to management, restoration, or creation of tidal swamps. Accordingly, there is a critical need for research on fundamental biotic and abiotic processes and functions in tidal forested wetland landscapes on a local and regional scale. In this chapter, we detail those research needs, and we highlight some restoration ideas for tidal freshwater forested wetlands with the hope that much additional research will follow.

Book chapter

Postfire management in forested public lands of the western USA

Forest ecosystems in the western United States evolved over many millennia in response to disturbances such as wildfires. Land use and management practices have altered these ecosystems, however, including fire regimes in some areas. Forest ecosystems are especially vulnerable to postfire management practices because such practices may influence forest dynamics and aquatic systems for decades to centuries. Thus, there is an increasing need to evaluate the effect of postfire treatments from the perspective of ecosystem recovery. We examined, via the published literature and our collective experience, the ecological effects of some common postfire treatments. Based on this examination, promising postfire restoration measures include retention of large trees, rehabilitation of firelines and roads, and, in some cases, planting of native species. The following practices are generally inconsistent with efforts to restore ecosystem functions after fire: seeding exotic species, livestock grazing, placement of physical structures in and near stream channels, ground-based postfire logging, removal of large trees, and road construction. Practices that adversely affect soil integrity, persistence or recovery of native species, riparian functions, or water quality generally impede ecological recovery after fire. Although research provides a basis for evaluating the efficacy of postfire treatments, there is a continuing need to increase our understanding of the effects of such treatments within the context of societal and ecological goals for forested public lands of the western United States.

Western United States

Watering the forest for the trees: An emerging priority for managing water in forest landscapes

Widespread threats to forests resulting from drought stress are prompting a re-evaluation of priorities for water management on forest lands. In contrast to the widely held view that forest management should emphasize providing water for downstream uses, we argue that maintaining forest health in the context of a changing climate may require focusing on the forests themselves and on strategies to reduce their vulnerability to increasing water stress. Management strategies would need to be tailored to specific landscapes but could include thinning, planting and selecting for drought-tolerant species, irrigating, and making more water available to plants for transpiration. Hydrologic modeling reveals that specific management actions could reduce tree mortality due to drought stress. Adopting water conservation for vegetation as a priority for managing water on forested lands would represent a fundamental change in perspective and potentially involve trade-offs with other downstream uses of water.

Frontiers in Ecology and the Environment

Site-scale disturbance best predicts moss, vascular plant, and amphibian indices in Ohio wetlands

Loss of wetland habitats and their associated biological communities is a major environmental concern. Quality assessment indices (QAIs) and indices of biological integrity (IBIs) are useful for assessing the responses of taxa to wetland habitat quality and land use in the surrounding landscape. We synthesized the results of our previous predictive modeling studies of five IBIs and QAIs for communities of mosses, vascular plants, and amphibians in forested and emergent wetlands in Ohio (USA). Overall, the single best predictor of these indices was a metric that estimated site-scale (i.e., within the wetland boundaries) substrate and habitat development, alteration, and disturbance. The second most important predictor was a metric that assessed site-scale wetland plant community types and quality, degree of interspersion, and microtopography. Landscape-scale variables better predicted moss and amphibian indices than either vascular plant index. Our results indicate that applying management practices that reduce the effects of site-scale anthropogenic disturbances and increase habitat complexity, such as creating forested buffers surrounding wetlands, increasing wetland contiguity, and creating hummocks and tussocks may simultaneously enhance amphibian, vascular plant, and moss communities in forested and emergent wetlands. Such a focused strategy may enable management agencies to more effectively apportion resources for wetland restoration and construction projects.

Ecological Restoration

Influence of landscape characteristics on retention of expandable radiocollars on young ungulates

One tool used for wildlife management is the deployment of radiocollars to gain knowledge of animal populations. Understanding the influence of individual factors (e.g., species, collar characteristics) and landscape characteristics (e.g., forested cover, shrubs, and fencing) on retention of expandable radiocollars for ungulates is important for obtaining empirical data on factors influencing ecology of young-of-the-year ungulates. During 2001–2009, we captured and radiocollared 198 white-tailed deer (Odocoileus virginianus) fawns, 142 pronghorn (Antilocapra americana) fawns, and 73 mule deer (O. hemionus) fawns in South Dakota, Minnesota, and California, USA. We documented 72 (36.4%), 8 (5.6%), and 7 (9.6%) premature (2, SE = 0.1, n = 75) compared with areas where fawns shed collars (x = 3.24 km/km 2 , SE = 0.1, n = 56) prior to 270 days. Researchers of fawns should consider that radiocollars can be shed prematurely when estimating desired sample size to yield a suitable strength of inference about some natural process of interest.

California;Minnesota;South Dakota