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

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

Arkansas, Kentucky, Louisiana, Mississippi, Missou↗

Sea-level rise and coastal forests on the Gulf of Mexico

In this report, we review literature pertaining to the response of coastal forests on the Gulf of Mexico to sea-level rise. The report is divided into chapters that discuss effects of sea-level rise on non-mangrove forests, effects of sea-level rise on mangrove forests, and responses of Gulf coast trees to increased flooding and salinity. An assessment of the extent of coastal forest likely to be affected by sea-level rise in the near future is beyond the scope of this report. Chapter 1 discusses sea-level effects on non-mangrove forests of the Gulf of Mexico including descriptions of how coastlines and, therefore, coastal forests have changed through the Holo~ene, a discussion of how coastal geomorphology and hydrology may affect interactions of coastal forest with sea-level rise, and an evaluation of the role that hurricanes might play in coastal forest retreat. Literature on geological changes throughout the Holocene is not fully reviewed; sufficient information is given to place current rates of coastal forest retreat into historical perspective. Similarly, effects of hurricanes on coastal forests are not fully reviewed. Information that is pertinent to the role of hurricanes in coastal forest retreat and to the effects of hurricanes on the forest's interaction with sea level is presented. For more extensive reviews of hurricane effects on coastal forests of the Caribbean and the southeastern United States, the reader is referred to issues of BioScience (1994, Vol 44, no. 4), Biotropica (1991, "Special Issue: Ecosystem, Plant, and Animal Responses to Hurricanes in the Caribbean", Vol. 23, No. 4, Part A) and the Journal of Coastal Research (1991, "Impacts of Hurricane Hugo, Special Issue No. 8; and 1995, "Imprcts of Hurricane Andrew on the Coastal Zones of Florida and Louisiana: 22-26 August 1992", Special Issue No. 21). Selected pertinent information from Virginia, South and North Carolina has been included in this review, because much of our knowledge of coastal forest response to hurricanes, salinity and flooding comes from the Atlantic coast. These areas are floristically similar to the northern Gulf of Mexico. Species distribution of coastal forest trees and shrubs on the Gulf of Mexico are listed in Appendix 1. Extensive research has been conducted on the responses of individual tree species to increased salinity and flooding. Synthesis of this research, although very important for evaluating effects of sea-level rise and various hydrological modifications on coastal forest, is beyond the scope of this review. These studies are included as an annotated bibliography (Appendix 2). Selected field studies on tree responses to changes in hydrology and salinity (impoundments, drainage, etc.) are referenced in Appendix 3. A review of mangrove response to sea-level rise is included in Chapter 2. Mangrove forests are discussed in the context of Holocene changes in geomorphology. Predictions of the fate of mangroves in the face of future sea-level rise, as well as a review of factors that affect interactions between mangroves and sea-level rise are discussed. Selected references from outside the United States are included, because much of our knowledge of how mangroves react to sea-level rise comes from other tropical areas of the world. A discussion of hurricane effects on the mangroves of south Florida highlights gaps in our knowledge of how hurricanes affect responses of mangrove vegetation to sea-level rise there. Mangrove responses to temperature and elevated CO2 are briefly mentioned. These factors, as well as sea level, are expected to change in the future and may affect mangrove distribution.

Open-File Report↗

Drier forest composition associated with hydrologic change in the Apalachicola River floodplain, Florida

Forests of the Apalachicola River floodplain had shorter flood durations, were drier in composition, and had 17 percent fewer trees in 2004 than in 1976. The change to drier forest composition is expected to continue for at least 80 more years. Floodplain drying was caused by large declines in river levels resulting from erosion of the river channel after 1954 and from decreased flows in spring and summer months since the 1970s. Water-level declines have been greatest at low and medium flows, which are the most common flows (occurring about 80 percent of the time). Water levels have remained relatively unchanged during large floods which continue to occur about three times per decade. A study conducted by the U.S. Geological Survey compared temporal changes in hydrologic conditions, forest composition, forest characteristics, and individual species of trees, as well as estimated the potential for change in composition of floodplain forests in the nontidal reach of the Apalachicola River. The study was conducted with the cooperation of the Florida Department of Environmental Protection and the Northwest Florida Water Management District. Forest composition and field observations from studies conducted in 1976-1984 (termed “1976 data”) were used as baseline data for comparison with data from plots sampled in 2004-2006 (“2004 data”). Flood durations were shorter in all periods subsequent to 1923-1976. The periods of record used to calculate flood durations for forest data were subsets of the complete record available (1923-2004). At sampled plots in all forest types and reaches combined, flood durations changed an average of more than 70 percent toward the baseline flood duration of the next drier forest type. For all forest types, changes in flood durations toward the next drier type were greatest in the upper reach (95.9 percent) and least in the lower reach (42.0 percent). All forests are expected to be 38.2 percent drier in species composition by 2085, the year when the median age of surviving 2004 subcanopy trees will reach the median age (99 years) of the 2004 large canopy trees. The change will be greatest for forests in the upper reach (45.0 percent). Forest composition changes from pre-1954 to 2085 were calculated using Floodplain Indices from 1976 and 2004 tree-size classes and replicate plots. Species composition in high bottomland hardwood forests is expected to continue to change, and some low bottomland hardwood forests are expected to become high bottomland hardwood forests. Organisms associated with floodplain forests will be affected by the changes in tree species, which will alter the timing of leaf-out, fruiting, and leaf-drop, the types of fruit and debris produced, and soil chemistry. Swamps will contain more bottomland hardwood species, but will also have an overall loss of tree density. The density of trees in swamps significantly decreased by 37 percent from 1976 to 2004. Of the estimated 4.3 million (17 percent) fewer trees that existed in the nontidal floodplain in 2004 than in 1976, 3.3 million trees belonged to four swamp species: popash, Ogeechee tupelo, water tupelo, and bald cypress. Water tupelo, the most important tree in the nontidal floodplain in terms of basal area and density, has declined in number of trees by nearly 20 percent since 1976. Ogeechee tupelo, the species valuable to the tupelo honey industry, has declined in number of trees by at least 44 percent. Greater hydrologic variability in recent years may be the reason swamps have had a large decrease in tree density. Drier conditions are detrimental for the growth of swamp species, and periodic large floods kill invading bottomland hardwood trees. The loss of canopy density in swamps may result in the swamp floor being exposed to more light with an increase in the amount of ground cover present, which in turn, would reduce tree replacement. The microclimate of the swamp floor would become warmer due to the decrease in shade and inundation. Soils would become dehydrated more quickly in dry periods and debris would decompose more quickly. A loss of tree density in swamps would lead to a decrease in tree and leaf litter biomass, which would have additional effects on swamp organisms. The loss of litter would result in a loss of substrate for benthic organisms in the floodplain and, ultimately, in the downstream waters of the river and estuary.

Florida↗

Landscape level reforestation priorities for forest breeding landbirds in the Mississippi Alluvial Valley

Thousands of ha of cleared wetlands are being reforested annually in the Mississippi Alluvial Valley (MAV). Despite the expansive and long-term impacts of reforestation on the biological communities of the MAV, there is generally a lack of landscape level planning in its implementation. To address this deficiency we used raster-based digital data to assess the value of forest restoration to migratory landbirds for each ha within the MAV. Raster themes were developed that reflected distance from 3 existing forest cover parameters: (1) extant forest, (2) contiguous forest patches between 1,012 and 40,000 ha, and (3) forest cores with contiguous area <5,200 ha. Forest core habitat was any forest habitat >1 km from an agricultural, urban, or pastoral edge. Two additional raster themes were developed that combined information on the proportion of forest cover and average size of forest patches, respectively, within landscapes of 50,000, 100,000, 150,000, and 200,000 ha. Data from these 5 themes were amalgamated into a single raster using a weighting system that gave increased emphasis to existing forest cores, larger forest patches, and moderately forested landscapes while deemphasizing reforestation near small or isolated forest fragments and within largely agricultural landscapes. This amalgamated raster was then modified by the geographic location of historical forest cover and the current extent of public land ownership to assign a reforestation priority score to each ha in the MAV. However, because reforestation is not required on areas with extant forest cover and because restoration is unlikely on areas of open water and urban communities, these lands were not assigned a reforestation priority score. These spatially explicit reforestation priority scores were used to simulate reforestation of 368,000 ha (5%) of the highest priority lands in the MAV. Targeting restoration to these high priority areas resulted in a 54% increase in forest core - an area of forest core that exceeded the area of simulated reforestation. Bird Conservation Regions, developed within the framework of the Partners in Flight: Mississippi Alluvial Valley Bird Conservation Plan, encompassed a large proportion (circa 70%) of the area with highest priority for reforestation. Similarly, lands with high reforestation priority often were enrolled in the Wetland Reserve Program.

Book chapter↗

Assessing rates of forest change and fragmentation in Alabama, USA, using the vegetation change tracker model

Forest change is of great concern for land use decision makers and conservation communities. Quantitative and spatial forest change information is critical for addressing many pressing issues, including global climate change, carbon budgets, and sustainability. In this study, our analysis focuses on the differences in geospatial patterns and their changes between federal forests and nonfederal forests in Alabama over the time period 1987–2005, by interpreting 163 Landsat Thematic Mapper (TM) scenes using a vegetation change tracker (VCT) model. Our analysis revealed that for the most part of 1990 s and between 2000 and 2005, Alabama lost about 2% of its forest on an annual basis due to disturbances, but much of the losses were balanced by forest regeneration from previous disturbances. The disturbance maps revealed that federal forests were reasonably well protected, with the fragmentation remaining relatively stable over time. In contrast, nonfederal forests, which are predominant in area share (about 95%), were heavily disturbed, clearly demonstrating decreasing levels of fragmentation during the time period 1987–1993 giving way to a subsequent accelerating fragmentation during the time period 1994–2005. Additionally, the identification of the statistical relationships between forest fragmentation status and forest loss rate and forest net change rate in relation to land ownership implied the distinct differences in forest cutting rate and cutting patterns between federal forests and nonfederal forests. The forest spatial change information derived from the model has provided valuable insights regarding regional forest management practices and disturbance regimes, which are closely associated with regional economics and environmental concerns.

Forest Ecology and Management↗

Agricultural land-use change alters the structure and diversity of Amazon riparian forests

Riparian forests play key roles in protecting biodiversity and water resources , making them priorities for conservation in human-dominated landscapes, but fragmentation associated with expanding tropical croplands threatens their ecological integrity. We compared the structure of tropical riparian forests within intact and cropland catchments in a region of intensive soybean production in the southeastern Brazilian Amazon. We studied forest plots (varying from 120 to 210 m long) that bisected riparian zone forests and headwater streams in ten catchments. Four plots were within large areas of intact primary forest and six were in bands of protected riparian forest along streams within croplands as required by the Brazilian Forest Code. We found that riparian forests in croplands harbored fewer species of trees and seedlings/saplings, and had higher proportions of opportunistic, pioneer tree species. We also found greater variation in tree species composition, and higher internal dissimilarity in croplands compared with forests. The observed patterns in tree species composition were driven mainly by differences between riparian forest-cropland edges and those bordering intact upland forests. Forests nearest to streams in cropland and forested catchments were more similar to one another. Results suggest that wider buffers are needed at the edges of croplands to maintain riparian forest structure. The minimum 30-m riparian buffers now required by the Brazilian Forest Code may thus be insufficient to prevent long-term shifts in riparian forest species composition and structure.

Biological Conservation↗

Combining MODIS and Landsat imagery to estimate and map boreal forest cover loss

Estimation of forest cover change is important for boreal forests, one of the most extensive forested biomes, due to its unique role in global timber stock, carbon sequestration and deposition, and high vulnerability to the effects of global climate change. We used time-series data from the MODerate Resolution Imaging Spectroradiometer (MODIS) to produce annual forest cover loss hotspot maps. These maps were used to assign all blocks (18.5 by 18.5 km) partitioning the boreal biome into strata of high, medium and low likelihood of forest cover loss. A stratified random sample of 118 blocks was interpreted for forest cover and forest cover loss using high spatial resolution Landsat imagery from 2000 and 2005. Area of forest cover gross loss from 2000 to 2005 within the boreal biome is estimated to be 1.63% (standard error 0.10%) of the total biome area, and represents a 4.02% reduction in year 2000 forest cover. The proportion of identified forest cover loss relative to regional forest area is much higher in North America than in Eurasia (5.63% to 3.00%). Of the total forest cover loss identified, 58.9% is attributable to wildfires. The MODIS pan-boreal change hotspot estimates reveal significant increases in forest cover loss due to wildfires in 2002 and 2003, with 2003 being the peak year of loss within the 5-year study period. Overall, the precision of the aggregate forest cover loss estimates derived from the Landsat data and the value of the MODIS-derived map displaying the spatial and temporal patterns of forest loss demonstrate the efficacy of this protocol for operational, cost-effective, and timely biome-wide monitoring of gross forest cover loss.

Remote Sensing of Environment↗

Forest area and distribution in the Mississippi alluvial valley: Implications for breeding bird conservation

Knowing the current forest distribution and patch size characteristics is integral to the development of geographically defined, habitat-based conservation objectives for breeding birds. Towards this end, we classified 2.6 million ha of forest cover within the Mississippi Alluvial Valley using 1992 thematic mapper satellite imagery. Although historically this area, from southern Illinois to southern Louisiana, was dominated by forested wetlands, forest cover remains on less than 25% of the floodplain. Remaining forest cover is comprised of > 38,000 discrete forest patches > 2 ha. Mean patch area (64.1±5.2 ha; x̄ ±SE) was highly skewed towards small fragment size. Larger patches had a higher proportion of more hydric forest cover classes than did smaller patches which had a higher proportion of less hydric forest cover classes. Public lands accounted for 16% of remaining forested wetlands. Fewer than 100 forest patches exceeded our hypothesized habitat objective (4000 ha minimum contiguous forest area) intended to support self-sustaining populations of forest breeding birds. To increase the number of forest patches exceeding 4000 ha contiguous area, and thereby increase the likelihood of successful forest bird conservation, we recommend afforestation adjoining existing forest fragments ≥1012 ha and focused within designated Forest Bird Conservation Regions.

Journal of Biogeography↗

Nest survival of forest birds in the Mississippi Alluvial Valley

In the Mississippi Alluvial Valley, flood control has led to a drastic reduction in the area of forest habitat and altered the patchwork of forest cover types. Silvicultural management of the remaining fragmented forests has changed to reflect the altered hydrology of the forests, current economic conditions of the area, and demand for forest products. Because forest type and silvicultural management impact forest birds, differences in avian productivity within these forests directly impact bird conservation. To assist in conservation planning, we evaluated daily nest survival, nest predation rates, and brood parasitism rates of forest birds in relation to different forest cover types and silvicultural management strategies within this floodplain. Within bottomland hardwood forests, nest success of blue-gray gnatcatcher ( Polioptila caerulea , 13%), eastern towhee ( Pipilo erythrophthalmus , 28%), indigo bunting ( Passerina cyanea , 18%), northern cardinal ( Cardinalis cardinalis , 22%), and yellow-billed cuckoo ( Coccyzus americanus , 18%) did not differ from that within intensively managed cottonwood plantations. However, average daily survival of 542 open-cup nests of 19 bird species in bottomland hardwoods (0.9516 ± 0.0028, ∼27% nest success) was greater than that of 543 nests of 18 species in cottonwood plantations (0.9298 ± 0.0035, ∼15% nest success). Differences in daily nest survival rates likely resulted from a combination of differences in the predator community -- particularly fire ants ( Solenopsis invicta ) -- and a marked difference in species composition of birds breeding within these 2 forest types. At least 39% of nests in bottomland hardwood forests and 65% of nests in cottonwood plantations were depredated. Rates of parasitism by brown-headed cowbirds ( Molothrus ater ) were greater in managed cottonwoods (24%) than in bottomland hardwoods (9%). Nest success in planted cottonwood plantations for 18 species combined (∼14%), and for yellow-breasted chat ( Icteria virens , 7%), eastern towhee (14%), indigo bunting (14%), and northern cardinal (17%) did not differ from nest success in cottonwood plantations that were coppiced from root sprouts following pulpwood harvest. Within bottomland hardwood forests, uneven-aged group-selection timber harvest reduced the combined daily nest survival of all species from 0.958 to 0.938, which reduced nest success by about 14%. Specifically, timber harvest reduced nest success of species that nest in the forest midstory and canopy, such as Acadian flycatcher ( Empidonax virescens ), from 32% before harvest to 14% after harvest. Conversely, those species that nest primarily in the shrubby understory-such as northern cardinal-were not affected by timber harvest and maintained an overall nest success of about 33%. Thus, birds nesting in the understory of bottomland hardwood forests are not adversely impacted by selective timber harvest, but there is a short-term reduction in nest success for birds that nest in the canopy and midstory.

Louisiana, Mississippi↗

Nitrogen dynamics across silvicultural canopy gaps in young forests of western Oregon

Silvicultural canopy gaps are emerging as an alternative management tool to accelerate development of complex forest structure in young, even-aged forests of the Pacific Northwest. The effect of gap creation on available nitrogen (N) is of concern to managers because N is often a limiting nutrient in Pacific Northwest forests. We investigated patterns of N availability in the forest floor and upper mineral soil (0-10 cm) across 6-8-year-old silvicultural canopy gaps in three 50-70-year-old Douglas-fir forests spanning a wide range of soil N capital in the Coast Range and Cascade Mountains of western Oregon. We used extractable ammonium (NH 4 + ) and nitrate (NO 3 - ) pools, net N mineralization and nitrification rates, and NH 4 + and NO 3 - ion exchange resin (IER) concentrations to quantify N availability along north-south transects run through the centers of 0.4 and 0.1 ha gaps. In addition, we measured several factors known to influence N availability, including litterfall, moisture, temperature, and decomposition rates. In general, gap-forest differences in N availability were more pronounced in the mineral soil than in the forest floor. Mineral soil extractable NH 4 + and NO 3 - pools, net N mineralization and nitrification rates, and NH 4 + and NO 3 - IER concentrations were all significantly elevated in gaps relative to adjacent forest, and in several cases exhibited significantly greater spatial variability in gaps than forest. Nitrogen availability along the edges of gaps more often resembled levels in the adjacent forest than in gap centers. For the majority of response variables, there were no significant differences between northern and southern transect positions, nor between 0.4 and 0.1 ha gaps. Forest floor and mineral soil gravimetric percent moisture and temperature showed few differences along transects, while litterfall carbon (C) inputs and litterfall C:N ratios in gaps were significantly lower than in the adjacent forest. Reciprocal transfer incubations of mineral soil samples between gap and forest positions revealed that soil originating from gaps had greater net nitrification rates than forest samples, regardless of incubation environment. Overall, our results suggest that increased N availability in 6-8-year-old silvicultural gaps in young western Oregon forests may be due more to the quality and quantity of litterfall inputs resulting from early-seral species colonizing gaps than by changes in temperature and moisture conditions caused by gap creation.

Forest Ecology and Management↗

Conservation–Protection of forests for wildlife in the Mississippi Alluvial Valley

The nearly ubiquitous bottomland hardwood forests that historically dominated the Mississippi Alluvial Valley have been greatly reduced in area. In addition, changes in hydrology and forest management have altered the structure and composition of the remaining forests. To ameliorate the detrimental impact of these changes on wildlife, conservation plans have emphasized restoration to increase interior forest habitat, while presuming negligible loss of extant forest in this ecoregion. Without conservation-protection, however, existing forests are subject to conversion to other uses. We assessed the conservation-protection status of land within the Mississippi Alluvial Valley and found that only 10% of total area was protected. Even so, 28% of extant forest was in the current conservation estate. Based on forest patch area, location, and hydrologic influence, we prioritized the attributed need of forest patches for additional conservation-protection. For forest bird conservation, we found 4712 forest patches warranted consideration for conservation-protection but only 109 of these forest patches met our conservation threshold of >2000 ha of core-forest that was >250 m from an edge. Overall, 35% of the area of forest patches considered for conservation-protection was protected within the conservation estate. However, those forest patches identified as most in need of conservation-protection had <10% of their area protected within the current conservation estate.

Forests↗

Spatial scaling of core and dominant forest cover in the Upper Mississippi and Illinois River floodplains, USA

Different organisms respond to spatial structure in different terms and across different spatial scales. As a consequence, efforts to reverse habitat loss and fragmentation through strategic habitat restoration ought to account for the different habitat density and scale requirements of various taxonomic groups. Here, we estimated the local density of floodplain forest surrounding each of ~20 million 10-m forested pixels of the Upper Mississippi and Illinois River floodplains by using moving windows of multiple sizes (1–100 ha). We further identified forest pixels that met two local density thresholds: ‘core’ forest pixels were nested in a 100% (unfragmented) forested window and ‘dominant’ forest pixels were those nested in a >60% forested window. Finally, we fit two scaling functions to declines in the proportion of forest cover meeting these criteria with increasing window length for 107 management-relevant focal areas: a power function (i.e. self-similar, fractal-like scaling) and an exponential decay function (fractal dimension depends on scale). The exponential decay function consistently explained more variation in changes to the proportion of forest meeting both the ‘core’ and ‘dominant’ criteria with increasing window length than did the power function, suggesting that elevation, soil type, hydrology, and human land use constrain these forest types to a limited range of scales. To examine these scales, we transformed the decay constants to measures of the distance at which the probability of forest meeting the ‘core’ and ‘dominant’ criteria was cut in half ( S 1/2 , m). S 1/2 for core forest was typically between ~55 and ~95 m depending on location along the river, indicating that core forest cover is restricted to extremely fine scales. In contrast, half of all dominant forest cover was lost at scales that were typically between ~525 and 750 m, but S 1/2 was as long as 1,800 m. S 1/2 is a simple measure that (1) condenses information derived from multi-scale analyses, (2) allows for comparisons of the amount of forest habitat available to species with different habitat density and scale requirements, and (3) can be used as an index of the spatial continuity of habitat types that do not scale fractally.

Illinois, Iowa, Minnesota, Missouri, Wisconsin↗

Heterogeneous movement of insectivorous Amazonian birds through primary and secondary forest: A case study using multistate models with radiotelemetry data

Given rates of deforestation, disturbance, and secondary forest accumulation in tropical rainforests, there is a great need to quantify habitat use and movement among different habitats. This need is particularly pronounced for animals most sensitive to disturbance, such as insectivorous understory birds. Here we use multistate capture&ndash;recapture models with radiotelemetry data to determine the successional stage at which within-day movement probabilities of Amazonian birds in secondary forest are similar to those in primary forest. We radio-tracked three common understory insectivore species in primary and secondary forest at the Biological Dynamics of Forest Fragments project near Manaus, Brazil: two woodcreepers, Glyphorynchus spirurus ( n = 19) and Xiphorhynchus pardalotus ( n = 18), and the terrestrial antthrush Formicarius colma ( n = 19 ) . Forest age was a strong predictor of fidelity to a given habitat. All three species showed greater fidelity to primary forest than to 8&ndash;14-year-old secondary forest, indicating the latter&rsquo;s relatively poor quality. The two woodcreeper species used 12&ndash;18-year-old secondary forest in a manner comparable to continuous forest, but F . colma avoided moving even to 27&ndash;31-year-old secondary forest&mdash;the oldest at our site. Our results suggest that managers concerned with less sensitive species can assume that forest reserves connected by 12&ndash;18-year-old secondary forest corridors are effectively connected. On the other hand, >30 years are required after land abandonment before secondary forest serves as a primary forest-like conduit for movement by F . colma ; more sensitive terrestrial insectivores may take longer still.

Manaus↗

Comparing forest fragmentation and its drivers in China and the USA with Globcover v2.2

Forest loss and fragmentation are of major concern to the international community, in large part because they impact so many important environmental processes. The main objective of this study was to assess the differences in forest fragmentation patterns and drivers between China and the conterminous United States (USA). Using the latest 300-m resolution global land cover product, Globcover v2.2, a comparative analysis of forest fragmentation patterns and drivers was made. The fragmentation patterns were characterized by using a forest fragmentation model built on the sliding window analysis technique in association with landscape indices. Results showed that China’s forests were substantially more fragmented than those of the USA. This was evidenced by a large difference in the amount of interior forest area share, with China having 48% interior forest versus the 66% for the USA. China’s forest fragmentation was primarily attributed to anthropogenic disturbances, driven particularly by agricultural expansion from an increasing and large population, as well as poor forest management practices. In contrast, USA forests were principally fragmented by natural land cover types. However, USA urban sprawl contributed more to forest fragmentation than in China. This is closely tied to the USA’s economy, lifestyle and institutional processes. Fragmentation maps were generated from this study, which provide valuable insights and implications regarding habitat planning for rare and endangered species. Such maps enable development of strategic plans for sustainable forest management by identifying areas with high amounts of human-induced fragmentation, which improve risk assessments and enable better targeting for protection and remediation efforts. Because forest fragmentation is a long-term, complex process that is highly related to political, institutional, economic and philosophical arenas, both nations need to take effective and comprehensive measures to mitigate the negative effects of forest loss and fragmentation on the existing forest ecosystems.

Journal of Environmental Management↗

Assessment of forest fragmentation in southern New England using remote sensing and geographic information systems technology

Spatial patterns and rates of forest fragmentation were assessed using digital remote sensing data for a region in southern New England that included 157 townships in southern New Hampshire and northeastern Massachusetts. The study area has undergone marked population increases over the last several decades. Following classification of 1973 and 1988 Landsat Multispectral Scanner data into forest and nonforest classes, data were incorporated into a geographic information system. The natural logarithms of forest area to perimeter ratios, referred to as the forest continuity index, were used to assess patterns and trends of forest fragmentation across the region Forest continuity index values were extracted from each township for both data sets and compared with population data. Forest continuity index values were found to decrease with increasing population density until about 200 persons per square kilometer, after which the relationship stabilized. With slight population increases at low densities forest continuity index values declined sharply, implying abrupt increases in forest fragmentation. Results from the study indicated good negative correlations (r 2 values of 0.81 and 0.77) between the Multispectral Scanner-derived forest continuity index and natural logs of township population density. Socioeconomic indicators such as affluence and commuting patterns did not appear to correlate well with forest fragmentation estimates. Decreases in forest continuity index values occurred throughout much of the study region between 1973 and 1988, suggesting that forest fragmentation is occurring over large regions within the eastern United States. It is technologically feasible to assess patterns and rates of forest fragmentation across much larger areas than analyzed in this study; such analyses would provide useful overviews enabling objective assessment of the magnitude of forest fragmentation.

Massachusetts, New Hampshire↗

Mapping annual forest cover in sub-humid and semi-arid regions through analysis of landsat and PALSAR imagery

Accurately mapping the spatial distribution of forests in sub-humid to semi-arid regions over years is a challenging task and causes difficulty to forest management. Relatively large uncertainties still exist in the spatial distribution of forests and deforestation in the sub-humid and semi-arid regions. Numerous publications have used either optical or synthetic aperture radar (SAR) remote sensing imagery, but the resultant forest cover maps often have large errors. In this study, we proposed a pixel- and rule-based algorithm to identify and map annual forests from 2007 to 2010 in Oklahoma, USA, a transition region with various climate and landscapes, using the integration of the L-band ALOS PALSAR Fine Beam Dual Polarization (FBD) mosaic dataset and Landsat images. The overall accuracy and Kappa coefficient of the PALSAR/Landsat forest map were about 88.2% and 0.75 in 2010, with the user and producer accuracy about 93.4% and 75.7%, based on the 3,270 random ground plots collected in 2012 and 2013. Compared with the forest products from JAXA, NLCD, OKESM and OKFRA, the PALSAR/Landsat forest map showed great improvement. The area of the PALSAR/Landsat forest was about 40,149 km2 in 2010, which was close to the area from OKFRA (40,468 km2), but much larger than those from JAXA (32,403 km2) and NLCD (37,628 km2). We analyzed annual forest cover dynamics, and the results show extensive deforestation (2,761 km2, 6.9% of the total forest area in 2010) and reforestation (3,630 km2, 9.0%) in the southeast and central Oklahoma, and the total area of forests increased by 684 km2 from 2007 to 2010. This study clearly demonstrates the potential of data fusion between PALSAR and Landsat images for mapping annual forest cover dynamics in sub-humid to semi-arid regions, and the resultant forest maps would be helpful to forest management.

Oklahoma↗

Fire history across forest types in the southern Beartooth Mountains, Wyoming

Fire is a critical ecosystem process that has played a key role in shaping forests throughout the Beartooth Mountains in northwestern Wyoming. The highly variable topography of the area provides ideal conditions to compare fire regimes across contiguous forest types, yet pyro-dendrochronological research in this area is limited. We reconstructed fire frequency, tree age structure, and post-fire tree growth response in the Clarks Fork Ranger District of the Shoshone National Forest to infer variations in historical fire behavior and stand effects. We collected fire-scarred trees and plot-based tree ages on plots ranging 0.5-5 km 2 in size across two forest types separated by 2 km: a lower-elevation forest of mixed Douglas-fir and lodgepole pine and a higher elevation treeline forest dominated by whitebark pine. Fires occurred in the lower-elevation forest in 1664, 1706, 1785, 1804, 1846, and 1900 with a mean fire return interval of 47 years. The fires in 1804 and 1900 were also recorded in the higher elevation forest, with significant tree mortality at high elevation in the 1900 fire. Both forests were multi-aged with little evidence of tree cohorts in response to severe, stand-replacing events. On average, tree growth increased after fires, with mean ring widths after fire 39% wider in Douglas-fir and 40% wider in lodgepole pine than pre-fire averages, suggesting that some tree mortality likely occurred in association with lower-elevation forest fires. Burns were more frequent in the lower-elevation forest and were occasionally able to spread into the upper-elevation whitebark stand. Although we suspect the transition of fires from low-to high-elevation occurred during drier years, we did not find any relationship between fire years and available climatic reconstructions via superposed epoch analysis. Regeneration during the 20 th Century in the whitebark forest documents recovery of this forest after the 1900 moderate-severity fire event. Finally, especially in the lower-elevation Douglas-fir forest, the period since the last recorded fire (1900) appears to be longer than any fire-free period in the historical record, suggesting that fire exclusion may be creating changes in landscape and patch-scale stand structures, which will likely impact future fire behavior, especially the extent of crown-replacing fire, in these forests.

Wyoming↗

Forest bird populations at the Big Island National Wildlife Refuge Complex, Hawai'i

E ndemic Hawaiian forest birds have experienced dramatic population declines. The Big Island National Wildlife Refuge Complex (Refuge Complex) was established for the conservation of endangered forest birds and their habitats. Surveys have been conducted at two units of the Refuge Complex to monitor forest bird populations and their response to management actions. We analyzed survey data from 1987 to 2019 at the Hakalau Forest Unit (HFU) and from 1995 to 2019 at the Kona Forest Unit (KFU). We analyzed three strata at HFU: open-forest, closed-forest, and afforested-pasture, and two strata at KFU: upper (>1,524 m elevation) and lower (<1,524 m). In all years, ‘i‘iwi Vestiaria coccinea , ‘apapane Himatione sanguinea , and Hawai'i ‘amakihi Chlorodrepanis virens virens were the most abundant species at HFU. Three endangered forest bird species, Hawai'i ‘ākepa Loxops coccineus , ‘alawī Loxops mana (also known as Hawai'i creeper) and ‘akiapōlā‘au Hemignathus wilsoni , had much lower densities. The most abundant species at KFU was ‘apapane, followed by Hawai'i ‘amakihi at much lower densities. We found a continuation of several trends observed in previous analyses at HFU up to 2012, with most species’ trends upward in afforested-pasture stratum, stable in the open-forest stratum, and downward in the closed-forest stratum. However, more species were showing downward trends in all three strata during the most recent decade. Results were mixed at KFU, with most species’ trends downward in the upper stratum and upward in the lower stratum. Populations of endangered species were either locally extirpated at KFU or in numbers too low to reliably estimate population abundance. The Refuge Complex is important for conservation of forest birds on Hawai'i Island. Our results show that HFU supports the majority of three endangered forest bird species. Threats to forest birds at the Refuge Complex appear to be having a negative impact. These threats include habitat loss, disease, feral ungulates, and nonnative predators. Continuing and enhancing management actions, such as forest restoration and removal of invasive species, could help mitigate these impacts and allow the Refuge Complex to remain a key site for forest bird conservation in Hawai'i.

Hawaii↗