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Forest canopy gap dynamics: Quantifying forest gaps and understanding gap – level forest regeneration in Upper Mississippi River floodplain forests

In most forest systems, the dynamics of forest canopy gap development play an important role in the transition from relatively short-lived early successional tree species to longer-lived, late successional tree species. In resilient forest systems, tree seedlings establish within newly created canopy gaps and grow to close the gap within one or two decades of disturbance. However, evidence in portions of the Upper Mississippi River System indicates that floodplain forests do not appear to be following these same trajectories, with canopy gaps instead seeming to fail to recruit new tree seedlings and reverting to non-forested cover types. Because of the heavy dominance of short-lived tree species in current UMRS forests, there is concern that continued failure of canopy gaps to recruit back to forest could be an early indicator of long-term, widespread forest loss as gaps become larger and larger and begin to coalesce into large, non-forested areas. Little research to date has documented either the density and distribution of forest canopy gaps across the UMRS or the vegetative conditions within those gaps to provide an initial assessment of forest dynamics in those areas. The current study utilizes both remotely sensed data and field sampling to assess the conditions of forest canopy gaps within 6 navigation pools on the Upper Mississippi River and one pool on the Illinois River. In general, canopy gap distributions and characteristics are similar across the study, with most pools ranging from 3% to 5% of forest canopy in gaps. Gap sizes are also relatively uniform, with most pools averaging 0.09 to 0.14 ha per gap. The highest proportion of forest cover in canopy gaps at the pool level was driven by the total number of gaps and not gap size, indicating that canopy gap formation in this system is commonly due to individual tree or small clump mortality. Undesirable competing vegetation was dominant in most canopy gaps, with reed canarygrass and native forbs being most prevalent in upper pools and vines most problematic in the lower pools. In the upper pools, very little viable forest regeneration is occurring within canopy gaps. The viability of forest regeneration increases in middle and lower pools, though competing vegetation continues to be a problem. Overall, canopy gaps appear 3 most likely to recruit back to forest in lower pools, and chronic forest loss facilitated by regeneration failures seems most likely in upper pools. However, competing vegetation in lower pools may still interact with woody regeneration to limit effective reestablishment of forest canopy.

Illinois, Iowa, Minnesota, Missouri, Wisconsin↗

Forest bird populations at the Pu‘u Wa‘a Wa‘a Forest Bird Sanctuary and Pu‘u Wa‘a Wa‘a Forest Reserve, Hawai‘i

Endemic Hawaiian forest birds have exhibited dramatic population declines since human colonization of Hawai‘i. The Pu‘u Wa‘awa‘a Forest Bird Sanctuary and adjacent Pu‘u Wa‘awa‘a Forest Reserve on Hawai‘i Island were established in 2002 to conserve endemic forest birds and their habitats. Surveys have been conducted in this area to monitor forest bird populations and their response to management actions since 1979. We analyzed point-transect distance sampling survey data collected between 1990 and 2022 in the Pu‘u Wa‘awa‘a Forest Bird Sanctuary and forested portions of the adjacent forest reserve. There were 20 passerine or psittacine species detected of which 6 were native species and 14 were non-native species. In all years, Hawai‘i ‘amakihi (Chlorodrepanis virens virens), ‘apapane (Himatione sanguinea), and warbling white-eye (Zosterops japonicus) were the most abundant species, and in most years ‘i‘iwi (Drepanis coccinea) was the fourth most abundant species. ‘I‘iwi and Hawai‘i ‘amakihi had stable long-term (1990–2022) population trends, and trends for ‘apapane were inconclusive, while warbling white-eye had upward trends. In recent years (2016–2022), ‘apapane had downward trends, ‘i‘iwi and warbling white-eye had upward trends, and trends for ‘amakihi were inconclusive. Populations of Hawai‘i ‘elepaio (Chasiempis sandwichensis) and the endangered Hawai‘i ‘ākepa (Loxops coccineus) and ‘alawī (Loxops mana) were either locally extirpated or in numbers too low to reliably estimate population densities and trends. The Pu‘u Wa‘awa‘a Forest Bird Sanctuary and adjacent Pu‘u Wa‘awa‘a Forest Reserve are important for the conservation of forest birds on Hawai‘i Island as one of few areas of mesic to dry forests being specifically managed for forest bird conservation. Conservation efforts at the Pu‘u Wa‘awa‘a Forest Bird Sanctuary and Pu‘u Wa‘awa‘a Forest Reserve would benefit from continued annual surveys and regular monitoring, and timely analysis of survey data to track responses in forest bird populations to evaluate and adapt management actions.

Hawaii↗

Same streams in a different forest? Investigations of forest harvest legacies and future trajectories across 30 years of stream habitat monitoring on the Tongass National Forest, Alaska

The effects of timber harvest practices and climate change have altered forest ecosystems in southeast Alaska. However, quantification of patterns and trends in stream habitats associated with these forests is limited owing to a paucity of data available in remote watersheds. Here, we analyzed a 30-year dataset from southeast Alaska's Tongass National Forest to understand how these factors shape stream habitats. First, we examined differences between broad management classes (i.e., harvested and non-harvested) that have been used to guide stream channel restoration goals. Second, we assessed associations between intrinsic landscape characteristics, watershed management, and timber harvest legacies on aquatic habitat metrics. And third, we examined trends in stream habitat metrics over the duration of the dataset to anticipate future management challenges for these systems. Small effect sizes for some harvest-related predictors suggest that some stream habitat metrics, such as pool densities, are less responsive than others, and management practices such as protecting riparian buffers as well as post-harvest restoration may help conserve fish habitats. Large wood densities increased with time since harvest at sites harvested >50 years ago, indicating that multiple decades of post-harvest forest regrowth may contribute large wood to streams (possibly alder), but that it is not enough time for old-growth trees (e.g., spruce, Picea, or hemlock, Tsuga,), classified as key wood, to develop and be delivered to streams. The declining trend in key wood (i.e., the largest size class of wood) regardless of management history may reflect that pre-harvest legacy old-growth trees are declining along streams, with low replacement. The introduction of wood to maintain complex stream habitats may fill this gap until riparian stands again contribute structural key wood to streams. Trend analyses indicate an increasing spatial extent of undercut banks that may also be influenced by shifting hydrologic regimes under climate change.

Alaska↗

Status and trends of forest bird populations at Hakalau Forest National Wildlife Refuge, 1987–2024

Since 1985, the Hakalau Forest Unit of the Big Island National Wildlife Refuge Complex (hereafter, Hakalau) has protected the largest endemic forest bird diversity in the State of Hawaii. This includes three endangered and one threatened species and their habitats. Hakalau’s vast area (155 km2), mostly high elevation (>1500 m) montane forest, provides refuge from avian malaria (Plasmodium relictum) vectored by introduced southern house mosquitoes (Culex quinquefasciatus). However, increases in the seasonal temperatures optimal for disease carrying mosquitoes associated with climate change have coincided with recent downward trends of native species in the closed forest area of the refuge (1450–1750 m), where disease is most likely to occur. Therefore, to inform refuge management with the most updated information on these populations and their trends, we analyzed forest bird survey data collected using point transect distance sampling with new survey data from 2021–2024. We stratified our analysis across management units, including the open forest and pasture since 1987, and the closed forest since 1999, and across four elevation ranges (<1500, 1500–1700, 1700–1900, and >1900 m) since 1999. We used distance sampling to estimate species- and strata-specific abundances and applied log-linear regression to detect trends across the timeseries. We found a continuation of previous trends, wherein most native forest birds declined in the closed forest strata (mostly below 1700 m) and increased in the highest elevation and pasture strata. Patterns were highly species-specific for the three lower elevations and open forest strata. ‘Apapane (Himatione sanguinea) and warbling white-eye (Zosterops japonicus), the most abundant native and introduced bird species, respectively, increased in nearly all strata. ‘I‘iwi (Drepanis coccinea) and Hawai‘i ‘amakihi (Chlorodrepanis virens virens), also common, decreased in closed forest, were stable in open forest, and increased in pasture. Both species were generally stable or increasing across all elevation bands, except Hawaiʻi ʻamakihi decreased in the below 1500 m and the 1500–1700 m elevation bands. All three of the federally endangered forest bird species declined in closed forest. Hawai‘i ‘ākepa (Loxops coccineus) also declined in the open forest and 1700–1900 m band and was the only species to decline overall. ‘Akiapōlā‘au (Hemignathus wilsoni) declined in closed forest but increased overall. ‘Alawī (Loxops mana, also known as Hawai‘i creeper) also decreased in the closed forest, but was stable to increasing in most strata and remained stable overall. Hawaiʻi ʻelepaio (Chasiempis sandwichensis) declined in closed forest, was stable in open forest and most elevation strata, and increased in pasture. ʻŌmaʻo (Myadestes obscurus) was stable in open and closed forest and at middle elevations and increased in the pasture. Introduced red-billedleiothrix (Leiothrix lutea) declined in closed forest, was stable in the open forest and at most elevations, and increased in the pasture. Coinciding with these changes, seasonal conditions for vector occurrence have continued to lengthen in the lower elevation strata through 2024, while Hakalau’s outplanting efforts continued to increase forest cover in the pasture, suggesting that disease-free habitat may have decreased in the closed forest and increased in the pasture. The declines in the closed forest and mixture of trends in the open forest and middle elevations bands suggest emigration into the higher elevation strata from lower elevation strata, and that possible threats have suppressed forest birds even at elevations >1500 m.

Hawaii↗

Forest turnover rates follow global and regional patterns of productivity

Using a global database, we found that forest turnover rates (the average of tree mortality and recruitment rates) parallel broad-scale patterns of net primary productivity. First, forest turnover was higher in tropical than in temperate forests. Second, as recently demonstrated by others, Amazonian forest turnover was higher on fertile than infertile soils. Third, within temperate latitudes, turnover was highest in angiosperm forests, intermediate in mixed forests, and lowest in gymnosperm forests. Finally, within a single forest physiognomic type, turnover declined sharply with elevation (hence with temperature). These patterns of turnover in populations of trees are broadly similar to the patterns of turnover in populations of plant organs (leaves and roots) found in other studies. Our findings suggest a link between forest mass balance and the population dynamics of trees, and have implications for understanding and predicting the effects of environmental changes on forest structure and terrestrial carbon dynamics.

Ecology Letters↗

Variable effects of climate on forest growth in relation to climate extremes, disturbance, and forest dynamics

Changes in the frequency, duration, and severity of climate extremes are forecast to occur under global climate change. The impacts of climate extremes on forest productivity and health remain difficult to predict due to potential interactions with disturbance events and forest dynamics—changes in forest stand composition, density, size and age structure over time. Such interactions may lead to non-linear forest growth responses to climate involving thresholds and lag effects. Understanding how forest dynamics influence growth responses to climate is particularly important given stand structure and composition can be modified through management to increase forest resistance and resilience to climate change. To inform such adaptive management, we develop a hierarchical Bayesian state space model in which climate effects on tree growth are allowed to vary over time and in relation to past climate extremes, disturbance events, and forest dynamics. The model is an important step toward integrating disturbance and forest dynamics into predictions of forest growth responses to climate extremes. We apply the model to a dendrochronology data set from forest stands of varying composition, structure, and development stage in northeastern Minnesota that have experienced extreme climate years and forest tent caterpillar defoliation events. Mean forest growth was most sensitive to water balance variables representing climatic water deficit. Forest growth responses to water deficit were partitioned into responses driven by climatic threshold exceedances and interactions with insect defoliation. Forest growth was both resistant and resilient to climate extremes with the majority of forest growth responses occurring after multiple climatic threshold exceedances across seasons and years. Interactions between climate and disturbance were observed in a subset of years with insect defoliation increasing forest growth sensitivity to water availability. Forest growth was particularly sensitive to climate extremes during periods of high stem density following major regeneration events when average inter-tree competition was high. Results suggest the resistance and resilience of forest growth to climate extremes can be increased through management steps such as thinning to reduce competition during early stages of stand development and small-group selection harvests to maintain forest structures characteristic of older, mature stands.

Minnesota, Wisconsin↗

Patterns of floodplain forest mortality and recruitment along the Upper Mississippi and Illinois Rivers: Associations with forest fragmentation and flood inundation

Context Different rates of floodplain forest recruitment and mortality can reveal important changes in ecosystem processes that drive forest dynamics, resulting in net changes in forest cover, thereby influencing a wide range of river habitat and morphological characteristics. Objectives We evaluated characteristics of forest change areas in the Upper Mississippi River System. Methods An overlay technique was used to map patches of forest loss, gain, and persistence between 2010 and 2020 in relation to a series of explanatory variables. Results We quantified a net decline in forest cover ranging from 3.2 to 16.8% in the uppermost five study reaches, and a net increase in forest cover ranging from 0.5 to 4.6% in the southernmost three reaches. Patches of forest loss and persistence were similarly tall (> 15 m), dense (> 90% cover), silver maple ( Acer saccharinum ) dominated forests, whereas forest gain patches were short (< 15 m), less dense (< 66% cover) and more likely to be dominated by willow ( Salix) species. Both forest loss and gain patches were smaller than forest persistence patches and were typically found in areas with low neighborhood forest density (< 50% forested 10 ha neighborhood). Areas that experienced more than three flood events per growing season, more than 100 consecutive days of inundation during a single flood event, and more than 60 mean total days of inundation per growing season from 2011 to 2020 showed a net loss of forest cover in all study reaches. In contrast, net increases in forest cover were restricted to areas that experienced less than a single flood event per growing season, less than 40 consecutive days of inundation during a single flood event and less than 30 mean total days of inundation per growing season from 2011 to 2020. Conclusions Forest mortality along these river reaches is associated with forest fragmentation and an increasingly wetter hydrological regime.

Illinois, Iowa, Minnesota, Missouri, Wisconsin↗

Thermokarst rates intensify due to climate change and forest fragmentation in an Alaskan boreal forest lowland

Lowland boreal forest ecosystems in Alaska are dominated by wetlands comprised of a complex mosaic of fens, collapse-scar bogs, low shrub/scrub, and forests growing on elevated ice-rich permafrost soils. Thermokarst has affected the lowlands of the Tanana Flats in central Alaska for centuries, as thawing permafrost collapses forests that transition to wetlands. Located within the discontinuous permafrost zone, this region has significantly warmed over the past half-century, and much of these carbon-rich permafrost soils are now within ~0.5 &deg;C of thawing. Increased permafrost thaw in lowland boreal forests in response to warming may have consequences for the climate system. This study evaluates the trajectories and potential drivers of 60 years of forest change in a landscape subjected to permafrost thaw in unburned dominant forest types (paper birch and black spruce) associated with location on elevated permafrost plateau and across multiple time periods (1949, 1978, 1986, 1998, and 2009) using historical and contemporary aerial and satellite images for change detection. We developed (i) a deterministic statistical model to evaluate the potential climatic controls on forest change using gradient boosting and regression tree analysis, and (ii) a 30 &times; 30 m land cover map of the Tanana Flats to estimate the potential landscape-level losses of forest area due to thermokarst from 1949 to 2009. Over the 60-year period, we observed a nonlinear loss of birch forests and a relatively continuous gain of spruce forest associated with thermokarst and forest succession, while gradient boosting/regression tree models identify precipitation and forest fragmentation as the primary factors controlling birch and spruce forest change, respectively. Between 1950 and 2009, landscape-level analysis estimates a transition of ~15 km&sup2; or ~7% of birch forests to wetlands, where the greatest change followed warm periods. This work highlights that the vulnerability and resilience of lowland ice-rich permafrost ecosystems to climate changes depend on forest type.

Alaska↗

Thresholds in forest bird occurrence as a function of the amount of early-seral broadleaf forest at landscape scales

Recent declines in broadleaf-dominated, early-seral forest globally as a function of intensive forest management and/or fire suppression have raised concern about the viability of populations dependent on such forest types. However, quantitative information about the strength and direction of species associations with broadleaf cover at landscape scales are rare. Uncovering such habitat relationships is essential for understanding the demography of species and in developing sound conservation strategies. It is particularly important to detect points in habitat reduction where rates of population decline may accelerate or the likelihood of species occurrence drops rapidly (i.e., thresholds). Here, we use a large avian point-count data set ( N = 4375) from southwestern and northwestern Oregon along with segmented logistic regression to test for thresholds in forest bird occurrence as a function of broadleaf forest and early-seral broadleaf forest at local (150-m radius) and landscape (500&ndash;2000-m radius) scales. All 12 bird species examined showed positive responses to either broadleaf forest in general, and/or early-seral broadleaf forest. However, regional variation in species response to these conditions was high. We found considerable evidence for landscape thresholds in bird species occurrence as a function of broadleaf cover; threshold models received substantially greater support than linear models for eight of 12 species. Landscape thresholds in broadleaf forest ranged broadly from 1.35% to 24.55% mean canopy cover. Early-seral broadleaf thresholds tended to be much lower (0.22&ndash;1.87%). We found a strong negative relationship between the strength of species association with early-seral broadleaf forest and 42-year bird population trends; species most associated with this forest type have declined at the greatest rates. Taken together, these results provide the first support for the hypothesis that reductions in broadleaf-dominated early-seral forest due to succession and intensive forest management have led to population declines of constituent species in the Pacific northwestern United States. Forest management treatments that maintain or restore even small amounts of broadleaf vegetation could mitigate further declines.

Oregon↗

Forest evapotranspiration dynamics over a fragmented forest landscape under drought in southwestern Amazonia

Ongoing climate change and human conversion of forests to other land uses alter regional evapotranspiration dynamics and, consequently, impact associated hydrological systems in Amazonia. We studied the effects of drought and fragmentation on forest evapotranspiration using the surface energy balance-based model METRIC (Mapping Evapotranspiration at high Resolution with Internalized Calibration) for a fragmented forest landscape in Brazil's Amazonian state of Rondônia. Dry season (June-August) forest evapotranspiration estimates were produced for the 2009-2011 period that encompassed the 2010 drought event, one of the extreme droughts in the Amazon. METRIC evapotranspiration data were analyzed in relation to climate (monthly precipitation and cumulative water deficit) and forest fragmentation (edge distance from 100m to 1000m from forest edge and edge density). During the dry season of 2009, pre-drought, forest evapotranspiration did not fall below 110mm/month. However, the 2010 drought year showed a drastic decline in evapotranspiration by 32%, to 75mm/month, from July to August. In 2011, evapotranspiration rates were still depressed with August rates dropping as low as 85mm/month. Forest evapotranspiration dynamics were driven mainly by precipitation and corresponding water deficits in the drier years (2010 and 2011), although evapotranspiration deficits along the edges of forest fragments were locally significant, at the landscape scale. The forests near edges (to 100m) had progressively lower evapotranspiration levels than interior forests as dry seasons progressed and these differences were greatest in the 2010 drought year, reaching almost 5%. Our results suggest that during the driest months, fragmentation exacerbated both the rate and extent of evapotranspiration reductions over forest areas up to 100m from edges, equivalent to ~20% of the forested landscape in our study area.

Rondonia↗

Fuel reduction and woody debris dynamics with early season and late season prescribed fire in a Sierra Nevada mixed conifer forest

Fire exclusion has led to an unnatural accumulation and greater spatial continuity of organic material on the ground in many forests. This material serves both as potential fuel for forest fires and habitat for a large array of forest species. Managers must balance fuel reduction to reduce wildfire hazard with fuel retention targets to maintain other forest functions. This study reports fuel consumption and changes to coarse woody debris attributes with prescribed burns ignited under different fuel moisture conditions. Replicated early season burn, late season burn, and unburned control plots were established in old-growth mixed conifer forest in Sequoia National Park that had not experienced fire for more than 120 years. Early season burns were ignited during June 2002 when fuels were relatively moist, and late season burns were ignited during September/October 2001 when fuels were dry. Fuel loading and coarse woody debris abundance, cover, volume, and mass were evaluated prior to and after the burns. While both types of burns reduced fuel loading, early season burns consumed significantly less of the total dead and down organic matter than late season burns (67% versus 88%). This difference in fuel consumption between burning treatments was significant for most all woody fuel components evaluated, plus the litter and duff layers. Many logs were not entirely consumed – therefore the number of logs was not significantly changed by fire – but burning did reduce log length, cover, volume, and mass. Log cover, volume, and mass were reduced to a lesser extent by early season burns than late season burns, as a result of higher wood moisture levels. Early season burns also spread over less of the ground surface within the burn perimeter (73%) than late season burns (88%), and were significantly patchier. Organic material remaining after a fire can dam sediments and reduce erosion, while unburned patches may help mitigate the impact of fire on fire-sensitive species by creating refugia from which these species can recolonize burned areas. Early season burns may be an effective means of moderating potential ecosystem damage when treating heavy and/or continuous fuels resulting from long periods of fire exclusion, if burning during this season is not detrimental to other forest functions.

California↗

Effects of roads, topography, and land use on forest cover dynamics in the Brazilian Atlantic Forest

Roads and topography can determine patterns of land use and distribution of forest cover, particularly in tropical regions. We evaluated how road density, land use, and topography affected forest fragmentation, deforestation and forest regrowth in a Brazilian Atlantic Forest region near the city of São Paulo. We mapped roads and land use/land cover for three years (1962, 1981 and 2000) from historical aerial photographs, and summarized the distribution of roads, land use/land cover and topography within a grid of 94 non-overlapping 100 ha squares. We used generalized least squares regression models for data analysis. Our models showed that forest fragmentation and deforestation depended on topography, land use and road density, whereas forest regrowth depended primarily on land use. However, the relationships between these variables and forest dynamics changed in the two studied periods; land use and slope were the strongest predictors from 1962 to 1981, and past (1962) road density and land use were the strongest predictors for the following period (1981–2000). Roads had the strongest relationship with deforestation and forest fragmentation when the expansions of agriculture and buildings were limited to already deforested areas, and when there was a rapid expansion of development, under influence of São Paulo city. Furthermore, the past (1962) road network was more important than the recent road network (1981) when explaining forest dynamics between 1981 and 2000, suggesting a long-term effect of roads. Roads are permanent scars on the landscape and facilitate deforestation and forest fragmentation due to increased accessibility and land valorization, which control land-use and land-cover dynamics. Topography directly affected deforestation, agriculture and road expansion, mainly between 1962 and 1981. Forest are thus in peril where there are more roads, and long-term conservation strategies should consider ways to mitigate roads as permanent landscape features and drivers facilitators of deforestation and forest fragmentation.

São Paulo↗

Forest density intensifies the importance of snowpack to growth in water-limited pine forests

Warming climate and resulting declines in seasonal snowpack have been associated with drought stress and tree mortality in seasonally snow‐covered watersheds worldwide. Meanwhile, increasing forest density has further exacerbated drought stress due to intensified tree‐tree competition. Using a uniquely detailed dataset of population‐level forest growth (n=2495 sampled trees), we examined how inter‐annual variability in growth relates to snow volume across a range of forest densities (e.g., competitive environments) in sites spanning a broad aridity gradient across the United States. Forest growth was positively related to snowpack in water‐limited forests located at low latitude, and this relationship was intensified by forest density. However, forest growth was negatively related to snowpack in a higher latitude more energy‐limited forest, and this relationship did not interact with forest density. Future reductions in snowpack may have contrasting consequences, as growth may respond positively in energy‐limited forests and negatively in water‐limited forests; however, these declines may be mitigated by reducing stand density through forest thinning.

Ecological Applications↗

Occupancy dynamics in a tropical bird community: Unexpectedly high forest use by birds classified as non‐forest species

1. Worldwide loss of biodiversity necessitates a clear understanding of the factors driving population declines as well as informed predictions about which species and populations are at greatest risk. The biggest threat to the long-term persistence of populations is the reduction and changes in configuration of their natural habitat. 2. Inconsistencies have been noted in the responses of populations to the combined effects of habitat loss and fragmentation. These have been widely attributed to the effects of the matrix habitats in which remnant focal habitats are typically embedded. 3. We quantified the potential effects of the inter-patch matrix by estimating occupancy and colonization of forest and surrounding non-forest matrix (NF). We estimated species-specific parameters using a dynamic, multi-species hierarchical model on a bird community in southwestern Costa Rica. 4. Overall, we found higher probabilities of occupancy and colonization of forest relative to the NF across bird species, including those previously categorized as open habitat generalists not needing forest to persist. Forest dependency was a poor predictor of occupancy dynamics in our study region, largely predicting occupancy and colonization of only non-forest habitats. 5. Our results indicate that the protection of remnant forest habitats is key for the long-term persistence of all members of the bird community in this fragmented landscape, including species typically associated with open, non-forest habitats. 6. Synthesis and applications. We identified 39 bird species of conservation concern defined by having high estimates of forest occupancy, and low estimates of occupancy and colonization of non-forest. These species survive in forest but are unlikely to venture out into open, non-forested habitats, therefore, they are vulnerable to the effects of habitat loss and fragmentation. Our hierarchical community-level model can be used to estimate species-specific occupancy dynamics for focal and inter-patch matrix habitats to identify which species within a community are likely to be impacted most by habitat loss and fragmentation. This model can be applied to other taxa (i.e. amphibians, mammals and insects) to estimate species and community occurrence dynamics in response to current environmental conditions and to make predictions in response to future changes in habitat configurations.

Journal of Applied Ecology↗

Rapid assessment of U.S. forest and soil organic carbon storage and forest biomass carbon sequestration capacity

This report provides results of a rapid assessment of biological carbon stocks and forest biomass carbon sequestration capacity in the conterminous United States. Maps available from the U.S. Department of Agriculture are used to calculate estimates of current organic carbon storage in soils (73 petagrams of carbon, or PgC) and forest biomass (17 PgC). Of these totals, 3.5 PgC of soil organic carbon and 0.8 PgC of forest biomass carbon occur on lands managed by the U.S. Department of the Interior (DOI). Maps of potential vegetation are used to estimate hypothetical forest biomass carbon sequestration capacities that are 3–7 PgC higher than current forest biomass carbon storage in the conterminous United States. Most of the estimated hypothetical additional forest biomass carbon sequestration capacity is accrued in areas currently occupied by agriculture and development. Hypothetical forest biomass carbon sequestration capacities calculated for existing forests and woodlands are within ±1 PgC of estimated current forest biomass carbon storage. Hypothetical forest biomass sequestration capacities on lands managed by the DOI in the conterminous United States are 0–0.4 PgC higher than existing forest biomass carbon storage. Implications for forest and other land management practices are not considered in this report. Uncertainties in the values reported here are large and difficult to quantify, particularly for hypothetical carbon sequestration capacities. Nevertheless, this rapid assessment helps to frame policy and management discussion by providing estimates that can be compared to amounts necessary to reduce predicted future atmospheric carbon dioxide levels.

Open-File Report↗

Spatial extent of forested avalanche terrain impacted by wildfire across the Sawtooth National Forest

Forest structure is a major driver of mountain snowpacks and avalanche occurrence. Healthy forests can reduce the incidence of dangerous slab avalanches, slow avalanches when in motion, shorten their runout distances, and act as a safety buffer for backcountry users, infrastructure, and transportation corridors. Since 1984, wildfire area in the seasonal snow zone of the western United States has increased by 70% throughout the seasonal snow zone, creating significant changes to avalanche prone mountains and their connected communities. A major unknown is the impact a reduction of forested area due to forest fires will have on avalanche occurrence. We hypothesize increased potential for avalanching in forested areas impacted by wildfire. Reduced tree cover may make previously heavily forested terrain more susceptible to avalanching. Increases in the size of avalanche start zones, paths, and runouts due to forest fires may increase the destructive size of avalanches and create cascading ecological effects within the adjacent forested terrain. Forest fires may therefore increase the likelihood of avalanche release, resulting in further loss of tree cover and increased avalanche area as well as decreased protection for human infrastructure. In this study, we quantify avalanche area changes before and after the Ross Fork wildfire (2022) in Sawtooth National Forest, Idaho, USA. We utilized satellite imagery, a digital elevation model and historical fire spatial data to quantify and characterize avalanche area changes within the fire perimeter using the Auto-ATES workflow (Sykes et al., 2022). We found decreases in forest coverage that contributed to widespread increases in potential avalanche release areas, avalanche tracks, and potential runout zones throughout the study area as well as the creation of new potential avalanche release areas and a substantial decrease in non-avalanche connected terrain within the fire perimeter. These preliminary findings help inform avalanche and snow safety professionals as well as land managers working in wildfire-prone forested areas about potential post-wildfire changes in avalanche terrain.

Idaho↗

Assessment of forest geospatial patterns over the three giant forest areas of China

Geospatial patterns of forest fragmentation over the three traditional giant forested areas of China (Northeastern, southwestern and Southern China) were analyzed comparatively and reported based on a 250-m resolution land cover dataset. Specifically, the spatial patterns of forest fragmentation were characterized by combining geospatial metrics and forest fragmentation models. The driving forces resulting in the differences of the forest spatial patterns were also investigated. Results suggested that forests in southwest China had the highest severity of forest fragmentation, followed by south region and northeast region. The driving forces of forest fragmentation in China were primarily the giant population and improper exploitation of forests. In conclusion, the generated information in the study provided valuable insights and implications as to the fragmentation patterns and the conservation of biodiversity or genes, and the use of the chosen geospatial metrics and forest fragmentation models was quite useful for depicting forest fragmentation patterns. ?? 2008 Northeast Forestry University.

Journal of Forestry Research↗