Historic and present-day forest conditions: Implications for bottomland hardwood forest restoration
No abstract available
Louisiana↗
SEARCH · Geology Reports
Results for “Forests”
Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Forest ecosystem reorganization underway in the Southwestern US: A preview of widespread forest changes in the Anthropocene
No abstract available.
Proceedings↗
How are native forest birds doing at the Pu`u Wa`awa`a Forest Bird Sanctuary?
No abstract available.
Hawaii↗
Forest ecosystem re-organization underway in the southwestern US: A preview of widespread forest changes in the anthropocene?
No abstract available.
Book chapter↗
Population status of the mountain yellow-legged frog (Rana muscosa) in the Angeles National Forest. Final report prepared for the United States Department of Agriculture, Angeles National Forest, Arcadia, California, through Interagency Agreement (5-01-69-019)
No abstract available at this time
Report↗
Hydrology, vegetation, and soils of riverine and tidal floodplain forests of the lower Suwannee River, Florida, and potential impacts of flow reductions
A study relating hydrologic conditions, soils, and vegetation of floodplain forests to river flow was conducted in the lower Suwannee River, Florida, from 1996 to 2000. The study was done by the U.S. Geological Survey in cooperation with the Suwannee River Water Management District to help determine the minimum flows and levels required for wetlands protection. The study area included forests within the 10-year floodplain of the Suwannee River from its confluence with the Santa Fe River to the tree line (lower limit of forests) near the Gulf of Mexico, and covered 18,600 hectares (ha) of forests, 75 percent of which were wetlands and 25 percent uplands. The floodplain was divided into three reaches, riverine, upper tidal, and lower tidal, based on changes in hydrology, vegetation, and soils with proximity to the coast. The Suwannee River is the second largest river in Florida in terms of average discharge. Median flow at the confluence of the Suwannee and Santa Fe Rivers is approximately 181 cubic meters per second (m3/s) or 6,480 cubic feet per second (ft3/s) (1933-99). At the upper end of the riverine reach, river stages are unaffected by tides and have a typical annual range of 4.1 meters (m). Tides affect river stages at low and medium flows in the upper tidal reach, and at all flows in the lower tidal reach. Median tidal range at the mouth of the Suwannee River is about 1 m. Salinity of river water in the lower tidal reach increases with decreasing flow and proximity to the Gulf of Mexico. Vertically averaged salinity in the river near the tree line is typically about 5 parts per thousand at medium flow. Land-surface elevation and topographic relief in the floodplain decrease with proximity to the coast. Elevations range from 4.1 to 7.3 m above sea level at the most upstream riverine transect and from 0.3 to 1.3 m above sea level on lower tidal transects. Surface soils in the riverine reach are predominantly mineral and dry soon after floods recede except in swamps. Surface soils in upper and lower tidal reaches are predominantly organic, saturated mucks. In the downstream part of the lower tidal reach, conductivities of surface soils are high enough (greater than 4 milli-mhos per centimeter) to exclude many tree species that are intolerant of salinity. Species richness of canopy and subcanopy plants in wetland forests in the lower Suwannee River is high compared to other river floodplains in North America. A total of 77 tree, shrub, and woody vine species were identified in the canopy and subcanopy of floodplain wetland forests (n = 8,376). Fourteen specific forest types were mapped using digitized aerial photographs, defined from vegetative sampling, and described in terms of plant species composition. For discussion purposes, some specific wetland types were combined, resulting in three general wetland forest types for each reach. Riverine high bottomland hardwoods have higher canopy species richness than all other forest types (40-42 species), with Quercus virginiana the most important canopy tree by basal area. The canopy composition of riverine low bottomland hardwoods is dominated by five species with Quercus laurifolia the most important by basal area. Riverine swamps occur in the lowest and wettest areas with Taxodium distichum the most important canopy species by basal area. Upper tidal bottomland hardwoods are differentiated from riverine forests by the presence of Sabal palmetto in the canopy. Upper tidal mixed forests and swamps are differentiated from riverine forests, in part, by the presence of Fraxinus profunda in the canopy. Nyssa aquatica, the most important canopy species by basal area in upper tidal swamps, is absent from most forests in the lower tidal reach where its distribution is probably restricted by salinity. Hydric hammocks, a wetland type that is rare outside of Florida, are found in the lower tidal reach and are flooded every 1-2 years by either storm surge or river floods. Lower tidal mixed forests and swamps have continuously saturated muck soils and are differentiated from upper tidal forests, in part, by the presence of Magnolia virginiana in the canopy. Lower tidal swamps have the highest density of canopy trees (about 1,200 trees per hectare) of all floodplain forest types, with Nyssa biflora the most important canopy species by basal area. Water use in the Suwannee River basin in Florida and Georgia is expected to increase over time because of anticipated growth and development in the region and adjacent areas. If increased water consumption reduced river flow, river stage would decrease and salinity would increase, resulting in a variety of impacts on forest composition, wetland biogeochemical processes, and fish and wildlife habitat. Forest composition in the floodplain is primarily determined by duration of inundation and saturation, depth and frequency of floods, and salinity. Long-term flow reductions would result in shallower flood depths, allowing drier and more tidal species to invade wetland forests of the riverine and upper tidal reaches. If flows were reduced 2.8-56 m3/s (100-2,000 ft3/s), an estimated 52-1,140 ha, respectively, would change to a drier forest type, and 36-788 ha, respectively, would change to a more tidal forest type. The greatest impacts would occur in swamps, where important swamp species such as Taxodium distichum and Nyssa aquatica could have increased competition not only from drier or more tidal species, but also from opportunistic bottomland hardwoods or invasive exotic species. Reduced flows could also result in a conversion of some wetland forests to uplands, increasing vulnerability to human disturbance, and decreasing tree basal area, species richness, and diversity of wildlife habitat. Salt-intolerant species would move upstream if flow reductions increased salinity in the lower tidal reach. If flows were reduced 2.8-56 m3/s (100-2,000 ft3/s), the area of forests along the tree line that would convert to marshes is estimated to be 72-618 ha, respectively. Loss of forests at the tree line would result in a loss of complex vertical structural diversity and woody micro-habitats that are used by many animals. These changes are already occurring due to sea level rise, but changes would occur more quickly if salinities increased as a result of flow reductions. The amount of inundated and saturated area in the floodplain forest of the riverine reach would decrease if flows were reduced. The greatest impacts would result from flow reductions that occurred at low flows, when inundated and saturated areas in the floodplain are limited. Drier conditions would result in oxidation of organic matter in swamp soils, which would reduce the soil's water-holding capacity and ability to retain water during droughts. Drier soils would increase vulnerability of the floodplain to fire and could also reduce the ability of riverine forests to remove nitrates and other pollutants from river water. Loss of inundated areas resulting from flow reductions at low flow would eliminate aquatic habitats that are critical to the survival of floodplain fishes and aquatic invertebrates, and are important to many other animals that use the floodplain. If flow reductions occurred during high flows, main channel fishes could decrease in diversity and abundance because they are seasonally dependent on flooded forests for food, shelter, and reproduction. In addition, aquatic organisms in the river and estuary could be adversely affected because they depend on particulate organic detritus and other floodplain exports as food sources.
Florida↗
Drying of floodplain forests associated with water-level decline in the Apalachicola River, Florida: Interim results, 2006
Floodplain forests of the Apalachicola River, Florida, are drier in composition today (2006) than they were before 1954, and drying is expected to continue for at least the next 50 years. Drier forest composition is probably caused by water-level declines that occurred as a result of physical changes in the main channel after 1954 and decreased flows in spring and summer months since the 1970s. Forest plots sampled from 2004 to 2006 were compared to forests sampled in the late 1970s (1976-79) using a Floodplain Index (FI) based on species dominance weighted by the Floodplain Species Category, a value that represents the tolerance of tree species to inundation and saturation in the floodplain and consequently, the typical historic floodplain habitat for that species. Two types of analyses were used to determine forest changes over time: replicate plot analysis comparing present (2004-06) canopy composition to late 1970s canopy composition at the same locations, and analyses comparing the composition of size classes of trees on plots in late 1970s and in present forests. An example of a size class analysis would be a comparison of the composition of the entire canopy (all trees greater than 7.5 cm (centimeter) diameter at breast height (dbh)) to the composition of the large canopy tree size class (greater than or equal to 25 cm dbh) at one location. The entire canopy, which has a mixture of both young and old trees, is probably indicative of more recent hydrologic conditions than the large canopy, which is assumed to have fewer young trees. Change in forest composition from the pre-1954 period to approximately 2050 was estimated by combining results from three analyses. The composition of pre-1954 forests was represented by the large canopy size class sampled in the late 1970s. The average FI for canopy trees was 3.0 percent drier than the average FI for the large canopy tree size class, indicating that the late 1970s forests were 3.0 percent drier than pre-1954 forests. The change from the late 1970s to the present was based on replicate plot analysis. The composition of 71 replicate plots sampled from 2004 to 2006 averaged 4.4 percent drier than forests sampled in the late 1970s. The potential composition of future forests (2050 or later) was estimated from the composition of the present subcanopy tree size class (less than 7.5 cm and greater than or equal to 2.5 cm dbh), which contains the greatest percentage of young trees and is indicative of recent hydrologic conditions. Subcanopy trees are the driest size class in present forests, with FIs averaging 31.0 percent drier than FIs for all canopy trees. Based on results from all three sets of data, present floodplain forests average 7.4 percent drier in composition than pre-1954 forests and have the potential to become at least 31.0 percent drier in the future. An overall total change in floodplain forests to an average composition 38.4 percent drier than pre-1954 forests is expected within approximately 50 years. The greatest effects of water-level decline have occurred in tupelo-cypress swamps where forest composition has become at least 8.8 percent drier in 2004-06 than in pre-1954 years. This change indicates that a net loss of swamps has already occurred in the Apalachicola River floodplain, and further losses are expected to continue over the next 50 years. Drying of floodplain forests will result in some low bottomland hardwood forests changing in composition to high bottomland hardwood forests. The composition of high bottomland hardwoods will also change, although periodic flooding is still occurring and will continue to limit most of the floodplain to bottomland hardwood species that are adapted to at least short periods of inundation and saturation.
Florida↗
A spatially explicit decision support model for restoration of forest bird habitat
The historical area of bottomland hardwood forest in the Mississippi Alluvial Valley has been reduced by >75%. Agricultural production was the primary motivator for deforestation; hence, clearing deliberately targeted higher and drier sites. Remaining forests are highly fragmented and hydrologically altered, with larger forest fragments subject to greater inundation, which has negatively affected many forest bird populations. We developed a spatially explicit decision support model, based on a Partners in Flight plan for forest bird conservation, that prioritizes forest restoration to reduce forest fragmentation and increase the area of forest core (interior forest >1 km from 'hostile' edge). Our primary objective was to increase the number of forest patches that harbor >2000 ha of forest core, but we also sought to increase the number and area of forest cores >5000 ha. Concurrently, we targeted restoration within local (320 km2) landscapes to achieve >60% forest cover. Finally, we emphasized restoration of higher-elevation bottomland hardwood forests in areas where restoration would not increase forest fragmentation. Reforestation of 10% of restorable land in the Mississippi Alluvial Valley (approximately 880,000 ha) targeted at priorities established by this decision support model resulted in approximately 824,000 ha of new forest core. This is more than 32 times the amount of core forest added through reforestation of randomly located fields (approximately 25,000 ha). The total area of forest core (1.6 million ha) that resulted from targeted restoration exceeded habitat objectives identified in the Partners in Flight Bird Conservation Plan and approached the area of forest core present in the 1950s.
Conservation Biology↗
Evaluating legacy effects of hyperabundant white-tailed deer (Odocoileus virginianus) in forested stands of Harriman and Bear Mountain State Parks, New York
Executive Summary White-tailed deer (Odocoileus virginianus) are among the most impactful herbivores in the eastern United States. Legacy forest effects, those accrued from intense herbivory over time, manifest as low seedling regeneration, high cover of plant species that are infrequently browsed by deer, presence or expansion of nonnative or invasive plant species, few herbaceous species, and diminished capacity for recovery. Interfering vegetation (that is, species that increase in cover and density due to avoidance by deer, such as American beech sprouts, Pennsylvania sedge, and hay-scented fern) increase competition for light and hinder recruitment of trees into the forest canopy. The lower Hudson Valley in New York has been heavily browsed by white-tailed deer since the early 20th century. The region has some of the lowest tree regeneration rates in New York State as a result of deer browsing and subsequent increases in interfering vegetation. The U.S. Geological Survey and the State University of New York College of Environmental Science and Forestry studied sites where deer hunting is permitted (case sites) and nearby sites where hunting is currently prohibited (control sites) to assess and identify forest structure and composition differences. Instead of using deer exclosures, which are time-consuming and expensive to install and maintain, we used a case-control study because such studies are well-suited to effects with long latency and rare outcomes. Case-control studies seek to describe the relation between an outcome of interest (in this study, forest understory recovery from chronic herbivory) and forest condition. We inferred recovery by comparing these characteristics on adjacent sites in the lower Hudson Valley with similar forest communities and land uses but different deer population management histories. Case plots were on lands where deer management has taken place annually for several decades. Control plots were on lands where deer populations have not been consistently managed to lowered abundance. We accounted for differences in forest recovery not attributable to deer by first matching case and control plots along several important environmental gradients (slope, aspect, elevation, moisture, canopy openness). By controlling for these gradients, we looked for associations between measured forest conditions and deer herbivory reduction through population management. We surveyed more than 200 plots in upland forest types across case and control sites where we assessed forest condition by estimating density (number per unit area) and composition and cover (percent) of important vegetation constituents in ground, shrub, subcanopy, and canopy layers of the forest. We recorded 37 tree species, 22 shrub species, 57 herbaceous species, and 19 species of grasses and sedges in our plot surveys, including a number of nonnative and invasive plants. We also estimated the ages of a number of common canopy trees by counting rings from cores extracted from individual stems. Effects of more than 100 years of chronic deer browsing manifested in low herbaceous ground cover and little to no tree recruitment (saplings) on lands without deer management. In contrast, sustained deer management resulted in forests with conditions that indicated substantial recovery from chronic herbivory in the ground, shrub, and subcanopy layers. Sites with ongoing deer management exhibited greater ground cover of tree seedlings and herbs and less ground cover of interfering vegetation and nonnative species. The well-developed sub-canopy layer of small trees, saplings, and tall shrubs on sites with deer management indicates a high potential for sapling recruitment to the canopy of the future forest. Of the 25 subcanopy trees sampled on control sites, most were more than 100 years old, indicating little to no regeneration in areas sampled for more than 100 years. The forest canopy, a relic of land uses of bygone days, requires a source of young trees to replace itself as older trees die. Without an abundant layer of young trees in the subcanopy, a forest cannot be sustained over time. Reduction in deer herbivory promotes forest recovery and could benefit Harriman and Bear Mountain State Parks (the control sites for the study), but removal of interfering vegetation may be necessary to mitigate legacy effects where they currently hinder ground layer recovery. To successfully promote a more desirable forest condition that includes elimination of nonnative plant species, promotion of tree recruitment into the forest canopy, and development of diverse and abundant herbaceous cover in ground layer vegetation, future management decisions could include information on herbivory reduction and management of interfering vegetation where necessary.
New York↗
Forest Types in the Lower Suwannee River Floodplain, Florida?-A Report and Interactive Map
A map of forest types in the lower Suwannee River floodplain, Florida, was created during a study conducted from 1996 to 2000 by the U.S. Geological Survey in cooperation with the Suwannee River Water Management District. The map is presented with this report on a compact disc with interactive viewing software. The forest map can be used by scientists for ecological studies in the floodplain based on land cover types and by landowners and management personnel making land use decisions. The study area is the 10-year floodplain of the lower Suwannee River from its confluence with the Santa Fe River to the lower limit of forests near the Gulf of Mexico. The floodplain is divided into three reaches: riverine (non-tidal), upper tidal, and lower tidal, due to changes in hydrology, vegetation, and soils with proximity to the coast. The 10-year floodplain covers about 21,170 hectares; nearly 88 percent of this area (18,580 hectares) is mapped as 14 major forest types. Approximately 29 percent (5,319 hectares) of these forests have been altered by agriculture or development. About 75 percent of the area of major forest types (13,994 hectares) is wetland forests and about 25 percent (4,586 hectares) is upland forests. Tidal wetland forests (8,955 hectares) cover a much greater area than riverine wetland forests (5,039 hectares). Oak/pine upland forests are present in the riverine and upper tidal reaches of the floodplain on elevations that are inundated only briefly during the highest floods. High bottomland hardwoods are present on the higher levees, ridges, and flats of the riverine reach where soils are usually sandy. Low bottomland hardwood forests are present in the riverine reach on swamp margins and low levees and flats that are flooded continuously for several weeks or longer every 1 to 3 years. Riverine swamps are present in the lowest and wettest areas of the non-tidal floodplain that are either inundated or saturated most of the time. Upper tidal bottomland hardwood forests are present on sandy soils on high flats and in transitional areas between upland forests and swamps. Upper tidal mixed forests are found on low levees or between swamps and higher forest types. Upper tidal swamps are present at elevations below median monthly high stage and usually have surface soils that are permanently saturated mucks. Lower tidal hammocks are found on higher elevations that do not receive regular tidal inundation but have a high water table and are briefly inundated by storm surges several times a decade. Lower tidal mixed forests include swamps with numerous small hummocks or less common larger hummocks. Lower tidal swamps are found on deep muck soils that are below the elevation of the median daily or monthly high stage. Seven additional land cover types (2,590 hectares) are mapped. Water in the main channel of the lower Suwannee River (1,767 hectares) was mapped separately from open water in the floodplain (239 hectares). Other land cover types are: seepage slopes (70 hectares), isolated forested wetlands (19 hectares), marshes upstream of the tree line (505 hectares), beds of emergent aquatic vegetation (21 hectares), and floodplain glades (46 hectares)
Water-Resources Investigations Report↗
Rapid peat development beneath created, maturing mangrove forests: Ecosystem changes across a 25-year chronosequence
Mangrove forests are among the world’s most productive and carbon‐rich ecosystems. Despite growing understanding of factors controlling mangrove forest soil carbon stocks, there is a need to advance understanding of the speed of peat development beneath maturing mangrove forests— especially in created and restored mangrove forests that are intended to compensate for ecosystem functions lost during mangrove forest conversion to other land uses. To better quantify the rate of soil organic matter development beneath created, maturing mangrove forests, we measured ecosystem changes across a 25‐year chronosequence. We compared ecosystem properties in created, maturing mangrove forests to adjacent natural mangrove forests. We also quantified site‐specific changes that occurred between 2010 and 2016. Soil organic matter accumulated rapidly beneath maturing mangrove forests as sandy soils transitioned to organic‐rich soils (peat). Within 25 years, a 20‐cm deep peat layer developed. The time required for created mangrove forests to reach equivalency with natural mangrove forests was estimated as: (1) < 15 years for herbaceous and juvenile vegetation; (2) ~55 years for adult trees; (3) ~25 years for the upper soil layer (0‐10 cm); and (4) ~45‐80 years for the lower soil layer (10‐30 cm). For soil elevation change, the created mangrove forests were equivalent to or surpassed natural mangrove forests within the first five years. A comparison to chronosequence studies from other ecosystems indicates that the rate of soil organic matter accumulation beneath maturing mangrove forests may be among the fastest globally. In most peatland ecosystems, soil organic matter formation occurs slowly (centuries, millennia); however, these results show that mangrove peat formation can occur within decades. Peat development, primarily due to sub‐surface root accumulation, enables mangrove forests to sequester carbon, adjust their elevation relative to sea level, and adapt to changing conditions at the dynamic land‐ocean interface. In the face of climate change and rising sea levels, coastal managers are increasingly concerned with the longevity and functionality of coastal restoration efforts. Our results advance understanding of the pace of ecosystem development in created, maturing mangrove forests, which can improve predictions of mangrove forest responses to global change and ecosystem restoration.
Florida↗
Temporal change in fragmentation of continental US forests
Changes in forest ecosystem function and condition arise from changes in forest fragmentation. Previous studies estimated forest fragmentation for the continental United States (US). In this study, new temporal land-cover data from the National Land Cover Database (NLCD) were used to estimate changes in forest fragmentation at multiple scales for the continental US. Early and late dates for the land-cover change data were ca. 1992 and ca. 2001. Forest density was used as a multi-scale index of fragmentation by measuring the proportion of forest in neighborhoods ranging in size from 2.25 to 5314.41 ha. The multi-scale forest density maps were classified using thresholds of 40% (patch), 60% (dominant), and 90% (interior) to analyze temporal change of fragmentation. The loss of dominant and interior forest showed distinct scale effects, whereas loss of patch forest was much less scale-dependent. Dominant forest loss doubled from the smallest to the largest spatial scale, while interior forest loss increased by approximately 80% from the smallest to the second largest spatial scale, then decreased somewhat. At the largest spatial scale, losses of dominant and interior forest were 5 and 10%, respectively, of their ca. 1992 amounts. In contrast, patch forest loss increased by only 25% from the smallest to largest spatial scale. These results indicate that continental US forests were sensitive to forest loss because of their already fragmented state. Forest loss would have had to occur in an unlikely spatial pattern in order to avoid the proportionately greater impact on dominant and interior forest at larger spatial scales.
Landscape Ecology↗
Kelp forest ecosystems: Biodiversity, stability, resilience and future
Kelp forests are phyletically diverse, structurally complex and highly productive components of coldwater rocky marine coastlines. This paper reviews the conditions in which kelp forests develop globally and where, why and at what rate they become deforested. The ecology and long archaeological history of kelp forests are examined through case studies from southern California, the Aleutian Islands and the western North Atlantic, well-studied locations that represent the widest possible range in kelp forest biodiversity. Global distribution of kelp forests is physiologically constrained by light at high latitudes and by nutrients, warm temperatures and other macrophytes at low latitudes. Within mid-latitude belts (roughly 40–60° latitude in both hemispheres) well-developed kelp forests are most threatened by herbivory, usually from sea urchins. Overfishing and extirpation of highly valued vertebrate apex predators often triggered herbivore population increases, leading to widespread kelp deforestation. Such deforestations have the most profound and lasting impacts on species-depauperate systems, such as those in Alaska and the western North Atlantic. Globally urchin-induced deforestation has been increasing over the past 2–3 decades. Continued fishing down of coastal food webs has resulted in shifting harvesting targets from apex predators to their invertebrate prey, including kelp-grazing herbivores. The recent global expansion of sea urchin harvesting has led to the widespread extirpation of this herbivore, and kelp forests have returned in some locations but, for the first time, these forests are devoid of vertebrate apex predators. In the western North Atlantic, large predatory crabs have recently filled this void and they have become the new apex predator in this system. Similar shifts from fish- to crab-dominance may have occurred in coastal zones of the United Kingdom and Japan, where large predatory finfish were extirpated long ago. Three North American case studies of kelp forests were examined to determine their long history with humans and project the status of future kelp forests to the year 2025. Fishing impacts on kelp forest systems have been both profound and much longer in duration than previously thought. Archaeological data suggest that coastal peoples exploited kelp forest organisms for thousands of years, occasionally resulting in localized losses of apex predators, outbreaks of sea urchin populations and probably small-scale deforestation. Over the past two centuries, commercial exploitation for export led to the extirpation of sea urchin predators, such as the sea otter in the North Pacific and predatory fishes like the cod in the North Atlantic. The large-scale removal of predators for export markets increased sea urchin abundances and promoted the decline of kelp forests over vast areas. Despite southern California having one of the longest known associations with coastal kelp forests, widespread deforestation is rare. It is possible that functional redundancies among predators and herbivores make this most diverse system most stable. Such biodiverse kelp forests may also resist invasion from non-native species. In the species-depauperate western North Atlantic, introduced algal competitors carpet the benthos and threaten future kelp dominance. There, other non-native herbivores and predators have become established and dominant components of this system. Climate changes have had measurable impacts on kelp forest ecosystems and efforts to control the emission of greenhouse gasses should be a global priority. However, overfishing appears to be the greatest manageable threat to kelp forest ecosystems over the 2025 time horizon. Management should focus on minimizing fishing impacts and restoring populations of functionally important species in these systems.
Environmental Conservation↗
Riparian buffers provide refugia during secondary forest succession
Aim Secondary forests regenerating from human disturbance are increasingly becoming a predominant forest type in many regions, and they play a significant role in forest community dynamics. Understanding the factors that underlie the variation in species responses during secondary succession is important for understanding community assembly and biodiversity monitoring and management. Because species vary in ecology and behaviour, responses to ecosystem change should vary among species. Here, we show that habitat type (riparian, upland), phylogeny, and species traits mediate anuran and lizard probability of occurrence and species richness in pasture and secondary forest. Location Sarapiquí and Osa Peninsula, Costa Rica. Methods We used phylogenetic occupancy models to estimate assemblage-level and species-specific responses to forest succession in 30 chronosequence sites that include pasture, secondary forest regenerating from pasture, and mature forest sites. Results For the majority of species, we found increasing probability of occurrence in upland habitats as forest regenerated from pasture to secondary forest and similar probability of occurrence in riparian habitats across pasture, secondary forest, and mature forest sites. Species' responses to forest stage were phylogenetically correlated, and the trend was especially strong for anuran response to pasture sites. Anurans with lentic larval habitat had a positive occupancy response to pasture upland habitat, and anurans with lotic larval habitat had a variable response to different forest stages compared to mature forest. Main Conclusions Our study, which focuses on sites that are minimally isolated from mature forest reference sites, indicated that anuran and lizard occupancy rapidly recovered to a level similar to mature forest in a relatively short time span (approximately 20 years). Riparian habitats are key ecosystem features in our system and provide refugia for organisms in early successional stages. Maintenance of vegetation along streams shows that we can mitigate forest conversion by maintaining riparian buffers.
Osa Peninsula, Sarapiquí↗