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At least 73 records · Page 4Linked to original sources

Mineral resource potential and geology of the Routt National Forest and the Middle Park Ranger District of the Arapaho National Forest, Colorado, with a section on salable minerals

The assessment of the mineral resource potential of the Routt National Forest and the Middle Park Ranger District of the Arapaho National Forest, Colorado, was conducted so that the mineral resources of the forest can be considered along with other resources in land use planning. This report discusses the potential for as yet undiscovered mineral and energy resources within the forest. Mineral resource information is given in terms of mineral deposit types and their geologic settings, and mineral deposit types are defined by geologic characteristics of known deposits that may occur within or near the forest. All available information regarding mineral deposits or occurrences and energy resources, as of June 1994, was assembled to assess the mineral and energy potential. Geologic maps were compiled and mineral and energy potential maps were also created for deposit types within the forest.

Colorado↗

A Comparison of Forest Survey Data with Forest Dynamics Simulators FORCLIM and ZELIG along Climatic Gradients in the Pacific Northwest

Two forest dynamics simulators are compared along climatic gradients in the Pacific Northwest. The ZELIG and FORCLIM models are tested against forest survey data from western Oregon. Their ability to generate accurate patterns of forest basal area and species composition is evaluated for series of sites with contrasting climate. Projections from both models approximate the basal area and composition patterns for three sites along the elevation gradient at H.J. Andrews Experimental Forest in the western Cascade Range. The ZELIG model is somewhat more accurate than FORCLIM at the two low-elevation sites. Attempts to project forest composition along broader climatic gradients reveal limitations of ZELIG, however. For example, ZELIG is less accurate than FORCLIM at projecting the average composition of a west Cascades ecoregion selected for intensive analysis. Also, along a gradient consisting of several sites on an east to west transect at 44.1oN latitude, both the FORCLIM model and the actual data show strong changes in composition and total basal area, but the ZELIG model shows a limited response. ZELIG does not simulate the declines in forest basal area and the diminished dominance of mesic coniferous species east of the Cascade crest. We conclude that ZELIG is suitable for analyses of certain sites for which it has been calibrated. FORCLIM can be applied in analyses involving a range of climatic conditions without requiring calibration for specific sites.

Scientific Investigations Report↗

Evaluating snow depth measurements from ground-penetrating radar and airborne lidar in boreal forest and tundra environments during the NASA SnowEx 2023 campaign

Snow is a vital component of high-latitude terrestrial systems, but environmental factors (e.g., permafrost) and complex vegetation challenge the accurate measurement of key snowpack properties. We evaluated local-scale ground-penetrating radar (GPR) and large-scale airborne lidar retrievals of snow depth collected during the NASA SnowEx 2023 campaign in tundra and boreal forest environments in Alaska along 44 short (3–12 m) transects. Compared to in situ observations, we identified modest biases for GPR snow depths (bias <0.03 m in tundra, +0.06 m in boreal forests) and larger biases for lidar snow depths in the boreal forests (–0.16 m). At the Upper Kuparuk-Toolik tundra site, lidar snow depths exhibited a small bias (–0.02 m), whereas the bias was much larger at the Arctic Coastal Plain tundra site (+0.19 m). For most sites, biases were primarily related to sub-snow vegetation, tussocks, and seasonally dynamic ground. However, we identified vertical alignment issues with the Arctic Coastal Plain lidar snow depth dataset that likely contributed to the higher bias. The complex ground surface and sub-snow vegetation in these environments present a challenge to established snow depth measurement methods, which needs to be considered when evaluating novel remote sensing approaches.

Alaska↗

Avian research on U.S. Forest Service Experimental Forests and Ranges: Emergent themes, opportunities, and challenges

Since 1908, U.S. Forest Service Experimental Forests and Ranges have been dedicated to long-term interdisciplinary research on a variety of ecological and management questions. They encompass a wide diversity of life zones and ecoregions, and provide access to research infrastructure, opportunities for controlled manipulations, and integration with other types of long-term data. These features have facilitated important advances in a number of areas of avian research, including furthering our understanding of population dynamics, the effects of forest management on birds, avian responses to disturbances such as fire and hurricanes, and other aspects of avian ecology and conservation. However, despite these contributions, this invaluable resource has been underutilized by ornithologists. Most of the Experimental Forests and Ranges have had no ornithological work done on them. We encourage the ornithological community, especially graduate students and new faculty, to take advantage of this largely untapped potential for long-term work, linkage with long-term data sets, multiple disciplines, and active forest management.

Forest Ecology and Management↗

Differences in ecosystem carbon distribution and nutrient cycling linked to forest tree species composition in a mid-successional boreal forest

In the boreal forest of Alaska, increased fire severity associated with climate change is expanding deciduous forest cover in areas previously dominated by black spruce ( Picea mariana ). Needle-leaf conifer and broad-leaf deciduous species are commonly associated with differences in tree growth, carbon (C) and nutrient cycling, and C accumulation in soils. Although this suggests that changes in tree species composition in Alaska could impact C and nutrient pools and fluxes, few studies have measured these linkages. We quantified C, nitrogen, phosphorus, and base cation pools and fluxes in three stands of black spruce and Alaska paper birch ( Betula neoalaskana ) that established following a single fire event in 1958. Paper birch consistently displayed characteristics of more rapid C and nutrient cycling, including greater aboveground net primary productivity, higher live foliage and litter nutrient concentrations, and larger ammonium and nitrate pools in the soil organic layer (SOL). Ecosystem C stocks (aboveground + SOL + 0–10 cm mineral soil) were similar for the two species; however, in black spruce, 78% of measured C was found in soil pools, primarily in the SOL, whereas aboveground biomass dominated ecosystem C pools in birch forest. Radiocarbon analysis indicated that approximately one-quarter of the black spruce SOL C accumulated prior to the 1958 fire, whereas no pre-fire C was observed in birch soils. Our findings suggest that tree species exert a strong influence over C and nutrient cycling in boreal forest and forest compositional shifts may have long-term implications for ecosystem C and nutrient dynamics.

Ecosystems↗

Twentieth-century shifts in forest structure in California: Denser forests, smaller trees, and increased dominance of oaks

We document changes in forest structure between historical(1930s) and contemporary (2000s) surveys of California vegetation through comparisons of tree abundance and size across the state and within several ecoregions. Across California, tree density in forested regions increased by 30% between the two time periods, whereas forest biomass in the same regions declined, as indicated by a 19% reduction in basal area. These changes reflect a demographic shift in forest structure: larger trees (>61 cm diameter at breast height) have declined, whereas smaller trees ( < 30 cm) have increased. Large tree declines were found in all surveyed regions of California, whereas small tree increases were found in every region except the south and central coast. Large tree declines were more severe in areas experiencing greater increases in climaticwater deficit since the 1930s, based on a hydrologicmodel of water balance for historical climates through the 20th century. Forest composition in California in the last century has also shifted toward increased dominance by oaks relative to pines, a pattern consistent with warming and increased water stress, and also with paleohistoric shifts in vegetation in California over the last 150,000 y.

California↗

Interannual variation of carbon fluxes from three contrasting evergreen forests: The role of forest dynamics and climate

Interannual variation of carbon fluxes can be attributed to a number of biotic and abiotic controls that operate at different spatial and temporal scales. Type and frequency of disturbance, forest dynamics, and climate regimes are important sources of variability. Assessing the variability of carbon fluxes from these specific sources can enhance the interpretation of past and current observations. Being able to separate the variability caused by forest dynamics from that induced by climate will also give us the ability to determine if the current observed carbon fluxes are within an expected range or whether the ecosystem is undergoing unexpected change. Sources of interannual variation in ecosystem carbon fluxes from three evergreen ecosystems, a tropical, a temperate coniferous, and a boreal forest, were explored using the simulation model STANDCARB. We identified key processes that introduced variation in annual fluxes, but their relative importance differed among the ecosystems studied. In the tropical site, intrinsic forest dynamics contributed ?? 30% of the total variation in annual carbon fluxes. In the temperate and boreal sites, where many forest processes occur over longer temporal scales than those at the tropical site, climate controlled more of the variation among annual fluxes. These results suggest that climate-related variability affects the rates of carbon exchange differently among sites. Simulations in which temperature, precipitation, and radiation varied from year to year (based on historical records of climate variation) had less net carbon stores than simulations in which these variables were held constant (based on historical records of monthly average climate), a result caused by the functional relationship between temperature and respiration. This suggests that, under a more variable temperature regime, large respiratory pulses may become more frequent and high enough to cause a reduction in ecosystem carbon stores. Our results also show that the variation of annual carbon fluxes poses an important challenge in our ability to determine whether an ecosystem is a source, a sink, or is neutral in regard to CO 2 at longer timescales. In simulations where climate change negatively affected ecosystem carbon stores, there was a 20% chance of committing Type II error, even with 20 years of sequential data. ?? 2009 by the Ecological Society of America.

Ecology↗

Growth of coast redwood and Douglas-fir following thinning in second-growth forests at Redwood National Park and Headwaters Forest Reserve

Managers of second-growth forests at Redwood National Park and the Bureau of Land Management’s Headwaters Forest Reserve encourage the development of late seral forest characteristics using mechanical thinning, where competing vegetation is removed to promote growth of residual trees. Yet the ability to quantify and reliably predict outcomes of treatments such as these is hindered by the long time scales at which forests respond to thinning. Here we present analyses of tree growth at Redwood National Park (RNP) and Headwaters Forest Reserve (HDWT) from sites that have had > 5 years to respond to thinning treatments. Compared to untreated stands, thinned stands had lower stem density (trees ha -1 ) and basal area (m 2 ha -1 ), primarily due to removal of Douglas-fir ( Pseudotsuga menziesii (Mirb.) Franco). Individual tree growth (basal area increment, BAI, m 2 yr -1 ) was related to tree size (basal area, m 2 ) and treatment history, with the highest growth rates observed in large trees. Both redwood ( Sequoia sempervirens (D. Don) Endl.) and Douglas-fir appeared to have a small, but detectable, positive growth response to thinning treatments. Early results suggest a large degree of variation among sites, with possible systematic differences in growth responses between RNP and HDWT. Future work will focus on identifying site-level differences (site quality, local competition, slope, aspect, stand age, distance from the ocean) to improve our understanding of the growth response.

Redwood National Park and Headwaters Forest Reserv↗

Consequences of increasing bioenergy demand on wood and forests: An application of the Global Forest Products Model

The Global Forest Products Model (GFPM) was applied to project the consequences for the global forest sector of doubling the rate of growth of bioenergy demand relative to a base scenario, other drivers being maintained constant. The results showed that this would lead to the convergence of the price of fuelwood and industrial roundwood, raising the price of industrial roundwood by nearly 30% in 2030. The price of sawnwood and panels would be 15% higher. The price of paper would be 3% higher. Concurrently, the demand for all manufactured wood products would be lower in all countries, but the production would rise in countries with competitive advantage. The global value added in wood processing industries would be 1% lower in 2030. The forest stock would be 2% lower for the world and 4% lower for Asia. These effects varied substantially by country. ?? 2011 Department of Forest Economics, SLU Ume??, Sweden.

Journal of Forest Economics↗

Mapping site index and volume increment from forest inventory, Landsat, and ecological variables in Tahoe National Forest, California, USA

High-resolution site index (SI) and mean annual increment (MAI) maps are desired for local forest management. We integrated field inventory, Landsat, and ecological variables to produce 30 m SI and MAI maps for the Tahoe National Forest (TNF) where different tree species coexist. We converted species-specific SI using adjustment factors. Then, the SI map was produced by ( i ) intensifying plots to expand the training sets to more climatic, topographic, soil, and forest reflective classes, ( ii ) using results from a stepwise regression to enable a weighted imputation that minimized the effects of outlier plots within classes, and ( iii ) local interpolation and strata median filling to assign values to pixels without direct imputations. The SI (reference age is 50 years) map had an R 2 of 0.7637, a root-mean-square error (RMSE) of 3.60, and a mean absolute error (MAE) of 3.07 m. The MAI map was similarly produced with an R 2 of 0.6882, an RMSE of 1.73, and a MAE of 1.20 m 3 ·ha −1 ·year −1 . Spatial patterns and trends of SI and MAI were analyzed to be related to elevation, aspect, slope, soil productivity, and forest type. The 30 m SI and MAI maps can be used to support decisions on fire, plantation, biodiversity, and carbon.

Canadian Journal of Forest Research↗

Tree-ring evidence of forest management moderating drought responses: Implications for dry, coniferous forests in the southwestern United States

Drought, coupled with rising temperatures, is an emerging threat to many forest types across the globe. At least to a degree, we expect management actions that reduce competition (e.g., thinning, prescribed fire, or both) to improve growth of residual trees during drought. The influences of management actions and drought on individual tree growth may be measured with high precision using tree-rings. Here, we summarize tree-ring-based assessments of the effectiveness of thinning and prescribed fire as drought adaptation tools, with special consideration for how these findings might apply to dry coniferous forests in the southwestern United States. The existing literature suggests that thinning treatments generally improve individual tree growth responses to drought, though the literature specific to southwestern coniferous forests is sparse. Assessments from studies beyond the southwestern United States indicate treatment effectiveness varies by thinning intensity, timing of the drought relative to treatments, and individualistic species responses. Several large-scale studies appear to conflict on specifics of how site aridity influences sensitivity to drought following thinning. Prescribed fire effects in the absence of thinning has received much less attention in terms of subsequent drought response. There are limitations for using tree-ring data to estimate drought responses (e.g., difficulties scaling up observations to stand- and landscape-levels). However, tree-rings describe an important dimension of drought effects for individual trees, and when coupled with additional information, such as stable isotopes, aid our understanding of key physiological mechanisms that underlie forest drought response.

Arizona, California, New Mexico, Nevada, Utah↗

Understanding the role of fog in forest hydrology: Stable isotopes as tools for determining input and partitioning of cloud water in montane forests

Understanding the hydrology of tropical montane cloud forests (TMCF) has become essential as deforestation of mountain areas proceeds at an increased rate worldwide. Passive and active cloud‐water collectors, throughfall and stemflow collectors, visibility or droplet size measurements, and micrometeorological sensors are typically used to measure the fog water inputs to ecosystems. In addition, stable isotopes may be used as a natural tracer for fog and rain. Previous studies have shown that the isotopic signature of fog tends to be more enriched in the heavier isotopes 2 H and 18 O than that of rain, due to differences in condensation temperature and history. Differences between fog and rain isotopes are largest when rain is from synoptic‐scale storms, and fog or orographic cloud water is generated locally. Smaller isotopic differences have been observed between rain and fog on mountains with orographic clouds, but only a few studies have been conducted. Quantifying fog deposition using isotope methods is more difficult in forests receiving mixed precipitation, because of limitations in the ability of sampling equipment to separate fog from rain, and because fog and rain may, under some conditions, have similar isotopic composition. This article describes the various types of fog most relevant to montane cloud forests and the importance of fog water deposition in the hydrologic budget. A brief overview of isotope hydrology provides the background needed to understand isotope applications in cloud forests. A summary of previous work explains isotopic differences between rain and fog in different environments, and how monitoring the isotopic signature of surface water, soil water and tree xylem water can yield estimates of the contribution of fog water to streamflow, groundwater recharge and transpiration. Next, instrumentation to measure fog and rain, and methods to determine isotopic concentrations in plant and soil water are discussed. The article concludes with the identification of some of the more pressing research questions in this field and offers various suggestions for future research.

Hydrological Processes↗

Examining forest structure with terrestrial lidar: Suggestions and novel techniques based on comparisons between scanners and forest treatments

Terrestrial laser scanners (TLSs) provide a tool to assess and monitor forest structure across forest landscapes. We present TLS methods, suggestions, and mapped guidelines for planning TLS acquisitions at varying scales and forest densities. We examined rates of point‐density decline with distance from two TLS that acquire data at relatively high and low point density and found that the rates were nearly identical between scanners ( p value <0.01), suggesting that our findings are applicable to a range of TLS types. Using unique, TLS‐adapted processing methods, we determined the relative accuracy of TLS‐derived plot‐scale estimates of tree height, diameter‐at‐breast‐height, height‐to‐canopy, tree counts, as well as treatment‐scale tree density and patch metrics, using both high point density and low point density TLS among thinned and nonthinned forest treatments. The high‐density TLS consistently provides more accurate estimates of plot‐level metrics ( R 2 = 0.46 to 0.87) than the low‐density TLS (R 2 = −0.14 to 0.53). At treatment scales, tree density estimates are similar among scanners ( R 2 = 0.95 vs. 0.71), as are canopy cover and patch metrics. We develop and present the normalized density‐distance index (NDDI), which can account for up to 59% of the variance in estimate error and can be used to guide TLS‐data acquisition plans. This index indicates whether a given location has generally higher point density (higher NDDI) relative to the distance from the scanner and can be used as a proxy for uncertainty. Using NDDI as a guide for fair comparison between scanners, both plot‐ and treatment‐scale estimates improved.

Earth and Space Science↗

Different fire-climate relationships on forested and non-forested landscapes in the Sierra Nevada ecoregion

In the California Sierra Nevada region, increased fire activity over the last 50 years has only occurred in the higher-elevation forests on US Forest Service (USFS) lands, and is not characteristic of the lower-elevation grasslands, woodlands and shrublands on state responsibility lands (Cal Fire). Increased fire activity on USFS lands was correlated with warmer and drier springs. Although this is consistent with recent global warming, we found an equally strong relationship between fire activity and climate in the first half of the 20th century. At lower elevations, warmer and drier conditions were not strongly tied to fire activity over the last 90 years, although prior-year precipitation was significant. It is hypothesised that the fire&ndash;climate relationship in forests is determined by climatic effects on spring and summer fuel moisture, with hotter and drier springs leading to a longer fire season and more extensive burning. In contrast, future fire activity in the foothills may be more dependent on rainfall patterns and their effect on the herbaceous fuel load. We predict spring and summer warming will have a significant impact on future fire regimes, primarily in higher-elevation forests. Lower elevation ecosystems are likely to be affected as much by global changes that directly involve land-use patterns as by climate change.

California↗

A multivariate model of plant species richness in forested systems: Old-growth montane forests with a long history of fire

Recently, efforts to develop multivariate models of plant species richness have been extended to include systems where trees play important roles as overstory elements mediating the influences of environment and disturbance on understory richness. We used structural equation modeling to examine the relationship of understory vascular plant species richness to understory abundance, forest structure, topographic slope, and surface fire history in lower montane forests on the North Rim of Grand Canyon National Park, USA based on data from eighty-two 0.1 ha plots. The questions of primary interest in this analysis were: (1) to what degree are influences of trees on understory richness mediated by effects on understory abundance? (2) To what degree are influences of fire history on richness mediated by effects on trees and/or understory abundance? (3) Can the influences of fire history on this system be related simply to time-since-fire or are there unique influences associated with long-term fire frequency? The results we obtained are consistent with the following inferences. First, it appears that pine trees had a strong inhibitory effect on the abundance of understory plants, which in turn led to lower understory species richness. Second, richness declined over time since the last fire. This pattern appears to result from several processes, including (1) a post-fire stimulation of germination, (2) a decline in understory abundance, and (3) an increase over time in pine abundance (which indirectly leads to reduced richness). Finally, once time-since-fire was statistically controlled, it was seen that areas with higher fire frequency have lower richness than expected, which appears to result from negative effects on understory abundance, possibly by depletions of soil nutrients from repeated surface fire. Overall, it appears that at large temporal and spatial scales, surface fire plays an important and complex role in structuring understory plant communities in old-growth montane forests. These results show how multivariate models of herbaceous richness can be expanded to apply to forested systems. Copyright ?? Oikos 2006.

Oikos↗

Fine-scale heterogeneity drives forest use by spring migrant landbirds across a broad, contiguous forest matrix

Much of our understanding of en route landbird habitat use comes from research performed at local scales, ignoring effects at larger spatial scales. We used a multiscale approach to investigate stopover habitat use by landbirds using transect surveys in 68 forested sites in southwestern Michigan, USA, during the springs of 2002 and 2003. We modeled relationships of bird density and arthropod abundance with broad-scale spatiotemporal factors (year, day of year, geographic location) and local landscape (forest composition and structure, presence of open water) as well as site-scale factors (bird density and arthropod abundance, which exchanged roles as predictor and response variables). We found migrant densities to be most influenced by fine-scale factors, such as the abundance of other avian taxa and substrate arthropods, followed by broader-scale factors, such as forest structure and location, within the local and broader surrounding landscape. We found that migrant habitat associations either did not directly match or were weakly associated with the availability of riparian or lacustrine water habitats at a local scale, even though our results suggested that birds using these habitat cues would have encountered more arthropods. Rather than finding indirect measures of food abundance—such as distance to a water source or forest cover at the landscape scale—important, our models best explained bird density by a direct relationship with site-scale food resources. Thus, the scale at which migrants demonstrate habitat selection appears to be influenced by proximate mechanisms such as high-quality habitat availability and the presence of large ecological features within the landscape. Not only do factors operating at multiple scales influence how birds use habitats, but scale also influences how we interpret research findings, in turn influencing conservation decisions.

Michigan↗

Arthropod prey of Wilson's Warblers in the understory of Douglas-fir forests

Availability of food resources is an important factor in avian habitat selection. Food resources for terrestrial birds often are closely related to vegetation structure and composition. Identification of plant species important in supporting food resources may facilitate vegetation management to achieve objectives for providing bird habitat. We used fecal analysis to describe the diet of adult Wilson's Warblers ( Wilsonia pusilla ) that foraged in the understory of Douglas-fir ( Pseudotsuga menziesii ) forests in western Oregon during the breeding season. We sampled arthropods at the same sites where diet data were collected, and compared abundance and biomass of prey among seven common shrub species. Wilson's Warblers ate more caterpillars (Lepidoptera larvae), flies (Diptera), beetles (Coleoptera), and Homoptera than expected based on availability. Deciduous shrubs supported higher abundances of arthropod taxa and size classes used as prey by Wilson's Warblers than did evergreen shrubs. The development and maintenance of deciduous understory vegetation in conifer forests of the Pacific Northwest may be fundamental for conservation of food webs that support breeding Wilson's Warblers and other shrub-associated, insectivorous songbirds.

Oregon↗

Forest conditions in the Absaroka division of the Yellowstone Forest Reserve, Montana and the Livingston and Big Timber quadrangles

The tract of land here designated the Absaroka division of the Yellowstone Forest Reserve was originally the Absaroka Forest Reserve. By proclamation of January 29, 1903, this reserve was merged with the Teton and the Yellowstone forest reserves, the whole taking the name of the Yellowstone Forest Reserve. The western, northern, and eastern boundaries, as then established and as applicable to the Absaroka division, are as follows: "Beginning at the point where the range line between ranges nine (9) and ten (10) east, principal meridian, Montana, intersects the northern boundary of the Yellowstone National Park; thence northerly along said surveyed and unsurveyed range line, allowing for the proper offset on the first (1st) standard parallel south, to the southwest corner of section eighteen (18), township four (4) south, range ten (10) east; thence easterly to the southeast corner of said section; thence northerly to the northeast corner of section six (6); said township: thence easterly to the southeast corner of section thirty-two (32), township three (3) south, range ten (10) east; thence northerly to the northeast corner of section five (5), said township; thence easterly along the township line to the northeast corner of township three (3) south, range eleven (11) east; thence southerly to the southeast corner of said township; thence easterly along the surveyed and unsurveyed township line to the point for the south- west corner of township three (3) south, range fourteen (14) east; thence northerly along the surveyed and unsurveyed range line to the northwest corner of township two (2) south, range fourteen (14) east; thence easterly to the northeast corner of said township; thence southerly to the point for the southeast corner of said township; thence easterly to the point for the northeast corner of township three (3) south, range fifteen (15) east; thence southerly to the point for the southeast corner of said township; thence easterly along the surveyed and unsurveyed township line to the northwest corner of township four (4) south, range eighteen (18) east; thence southerly along the range line to its intersection with the first (1st) standard parallel south; thence easterly along said parallel to the northeast corner of township six (6) south, range eighteen (18) east; thence southerly along the surveyed and unsurveyed range line to the southwest corner of township seven (7) south, range nineteen (19) east; thence easterly to the northwest comer of township eight (8) south, range twenty (20) east; thence southerly to the southwest corner of said township; thence easterly to the southeast corner of said township; thence southerly along the range line to its intersection with the boundary line between the States of Montana and Wyoming." The southern boundary of the area discussed is west from the point where the eastern boundary of the reserve intersects the Montana- Wyoming line to the southeast corner of township 9 north, range 14 east; thence along the northern boundary line of the Yellowstone National Park to the point where said boundary line of the park intersects the range line between ranges 9 and 10 east, principal meridian. The total area, as above delineated, includes 1,334,400 acres.

Montana↗