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At least 883 records · Page 49Linked to original sources

Elk response to the La Mesa fire and current status in the Jemez Mountains

Faunal remains in local archeological sites and historic information suggest that elk populations in the Jemez Mountains were low from ca. 1200 A.D. through ca. 1900 A.D., when they were extirpated from this region. Elk were reintroduced to the Jemez country in 1948 and 1964- 1965, and their population apparently grew exponentially, reaching 1000 animals in the 1970's and about 7000 by 1991. Elk populations in Bandelier National Monument and adjoining areas increased rapidly after the 1977 La Mesa Fire. Winter use by elk in the La Mesa Fire area, centered on Bandelier, grew from about 100 animals in .1978 to around 1500 elk by 1992. The dramatic increase in the Bandelier elk herd (an annual growth rate of 21.3% and a 3.6 year population doubling time) was due in part to the creation of about 6000 hectares of grassy winter range in and around the park by the La Mesa Fire. Some of this local population increase reflects concentration of elk into this favorable wintering habitat from surrounding portions of the Jemez Mountains. Existing data are inadequate to determine whether elk populations are still growing rapidly in the Jemez Mountains. While annual aerial surveys since 1990 in Bandelier reveal no clear population trend, a variety of observations demonstrate increasing elk use of lower elevation areas. Negative resource impacts from today's high elk populations are beginning to be widely noted across the Jemez Mountains, especially in high-use portions of the Bandelier National Monument area. Affected resources range from plant communities to soils and even archeological sites. Given the large uncertainties associated with the current data on elk populations, care should be taken to avoid further population increases until the resource impacts of this new phenomenon (large numbers of elk) can be identified, desirable population levels identified (based to a significant degree upon ecological information and resource carrying capacities, as well as social considerations), and appropriate cooperative management strategies implemented.

General Technical Report↗

Net primary productivity of subalpine meadows in Yosemite National Park in relation to climate variability

Subalpine meadows are some of the most ecologically important components of mountain landscapes, and primary productivity is important to the maintenance of meadow functions. Understanding how changes in primary productivity are associated with variability in moisture and temperature will become increasingly important with current and anticipated changes in climate. Our objective was to describe patterns and variability in aboveground live vascular plant biomass in relation to climatic factors. We harvested aboveground biomass at peak growth from four 64-m 2 plots each in xeric, mesic, and hydric meadows annually from 1994 to 2000. Data from nearby weather stations provided independent variables of spring snow water content, snow-free date, and thawing degree days for a cumulative index of available energy. We assembled these climatic variables into a set of mixed effects analysis of covariance models to evaluate their relationships with annual aboveground net primary productivity (ANPP), and we used an information theoretic approach to compare the quality of fit among candidate models. ANPP in the xeric meadow was negatively related to snow water content and thawing degree days and in the mesic meadow was negatively related to snow water content. Relationships between ANPP and these 2 covariates in the hydric meadow were not significant. Increasing snow water content may limit ANPP in these meadows if anaerobic conditions delay microbial activity and nutrient availability. Increased thawing degree days may limit ANPP in xeric meadows by prematurely depleting soil moisture. Large within-year variation of ANPP in the hydric meadow limited sensitivity to the climatic variables. These relationships suggest that, under projected warmer and drier conditions, ANPP will increase in mesic meadows but remain unchanged in xeric meadows because declines associated with increased temperatures would offset the increases from decreased snow water content.

Western North American Naturalist↗

Valuation of rangeland ecosystem services

Economic valuation lends itself well to the anthropocentric orientation of ecosystem services. An economic perspective on ecosystems portrays them as natural assets providing a flow of goods and services valuable to individuals and society collectively. A few examples include the purification of drinking water, reduced risk from flooding and other extreme events, pollination of agricultural crops, climate regulation, and recreation opportunities from plant and animal habitat maintenance, among many others. Once these goods and services are identified and quantified, they can be monetized to complete the valuation process. The monetization of ecosystem goods and services (in the form of dollars) provides a common metric that allows for cross-comparison of attributes and evaluation of differing ecological scenarios. Complicating the monetization process is the fact that most of these goods and services are public and non-market in nature; meaning they are non-rival and non-exclusive and are typically not sold in a traditional market setting where monetary values are revealed. Instead, one must employ non-market valuation techniques, with primary valuation methods typically being very time and resource consuming, intimidating to non-economists, and often impractical. For these reasons, benefit transfer methods have gained popularity. This methodology harnesses the primary collection results of existing studies to make inferences about the economic values of non-market goods and services at an alternative policy site (in place and/or in time). For instance, if a primary valuation study on oak reestablishment on rangelands in southern California yielded a value of $30 per-acre associated with water regulation, this result can be transferred, with some adjustments, to say something about the value of an acre of oaks on rangelands in northern portions of the state. The economic valuation of rangeland ecosystem services has many roles. Economic values may be used as input into analyzing the costs and benefits associated with policies being proposed, or possibly already implemented. For example, with monetized values acting as a common metric, one could compare the 'benefits' of converting a rangeland ecosystem for commercial development (perhaps estimated at the market value of the developed land) with the foregone ecosystem service values (in addition to any land income lost) resulting from that land conversion. Similarly, ecosystem service values can be used to determine the level of return on an investment. rhis is a primary objective for private land conservation organizations who typically have very limited resources. Ecosystem service valuation can also have a role in damage assessments from incidents that require compensation such as oil spills. Additionally, valuation can be very informative when investigating regulatory programs that trade ecological assets such as wetland mitigation programs. Typically these programs are based simply on an 'acre for acre' criterion, and do not take into consideration varying welfare values associated with that ecosystem. Lastly, and most fundamental, ecosystem service valuation serves as a recognition tool for people of all backgrounds. Identifying and valuing ecosystem goods and services on rangelands brings to light the value these natural assets have to human welfare that often remain hidden do to their public and non-market attributes. This type of recognition is vital to the preservation of rangeland ecosystems in the future and the many ecological benefits they provide.

Conference Paper↗

Assessment and management of dead-wood habitat

The Bureau of Land Management (BLM) is in the process of revising its resource management plans for six districts in western and southern Oregon as the result of the settlement of a lawsuit brought by the American Forest Resource Council. A range of management alternatives is being considered and evaluated including at least one that will minimize reserves on O&C lands. In order to develop the bases for evaluating management alternatives, the agency needs to derive a reasonable range of objectives for key issues and resources. Dead-wood habitat for wildlife has been identified as a key resource for which decision-making tools and techniques need to be refined and clarified. Under the Northwest Forest Plan, reserves were to play an important role in providing habitat for species associated with dead wood (U.S. Department of Agriculture Forest Service and U.S. Department of the Interior Bureau of Land Management, 1994). Thus, the BLM needs to: 1) address the question of how dead wood will be provided if reserves are not included as a management strategy in the revised Resource Management Plan, and 2) be able to evaluate the effects of alternative land management approaches. Dead wood has become an increasingly important conservation issue in managed forests, as awareness of its function in providing wildlife habitat and in basic ecological processes has dramatically increased over the last several decades (Laudenslayer et al., 2002). A major concern of forest managers is providing dead wood habitat for terrestrial wildlife. Wildlife in Pacific Northwest forests have evolved with disturbances that create large amounts of dead wood; so, it is not surprising that many species are closely associated with standing (snags) or down, dead wood. In general, the occurrence or abundance of one-quarter to one-third of forest-dwelling vertebrate wildlife species, is strongly associated with availability of suitable dead-wood habitat (Bunnell et al., 1999; Rose et al., 2001). In Oregon and Washington, approximately 150 species of wildlife are reported to use dead wood in forests (O’Neil et al., 2001). Forty-seven sensitive and special-status species are associated with dead wood (Appendix A). These are key species for management consideration because concern over small or declining populations is often related to loss of suitable dead-wood habitat (Marshall et al., 1996). Primary excavators (woodpeckers) also are often the focus of dead-wood management, because they perform keystone functions in forest ecosystems by creating cavities for secondary cavity-nesters (Martin and Eadie, 1999; Aubry and Raley, 2002). A diverse guild of secondary cavity-users (including swallows, bluebirds, several species of ducks and owls, ash-throated flycatcher, flying squirrel, bats, and many other species) is unable to excavate dead wood, and therefore relies on cavities created by woodpeckers for nesting sites. Suitable nest cavities are essential for reproduction, and their availability limits population size (Newton, 1994). Thus, populations of secondary cavity-nesters are tightly linked to the habitat requirements of primary excavators. Although managers often focus on decaying wood as habitat for wildlife, the integral role dead wood plays in ecological processes is an equally important consideration for management. Rose et al. (2001) provide a thorough review of the ecological functions of dead wood in Pacific Northwest forests, briefly summarized here. Decaying wood functions in: soil development and productivity, nutrient cycling, nitrogen fixation, and carbon storage. From ridge tops, to headwater streams, to estuaries and coastal marine ecosystems, decaying wood is fundamental to diverse terrestrial and aquatic food webs. Wildlife species that use dead wood for cover or feeding are linked to these ecosystem processes through a broad array of functional roles, including facilitation of decay and trophic interactions with other organisms (Marcot, 2002; Marcot, 2003). For example, by puncturing bark and fragmenting sapwood, woodpeckers create sites favorable for wood-decaying organisms (Farris et al., 2004), which in turn create habitat for other species and facilitate nutrient cycling. Small mammals that use down wood for cover function in the dispersal of plant seeds and fungal spores (Carey et al., 1999). Resident cavitynesting birds may regulate insect populations by preying on overwintering arthropods (Jackson, 1979; Kroll and Fleet, 1979). These examples illustrate how dead wood not only directly provides habitat for a large number of wildlife species, but also forms the foundation of functional webs that critically influence forest ecosystems (Marcot, 2002; Marcot, 2003). The important and far-reaching implications of management of decaying wood highlight the need for conservation of dead-wood resources in managed forests. Consideration of the key ecological functions of species associated with dead wood can help guide management of dead wood in a framework consistent with the paradigm of ecosystem management (Marcot and Vander Heyden, 2001; Marcot, 2002.) As more information is revealed about the ecological and habitat values of decaying wood, concern has increased over a reduction in the current amounts of dead wood relative to historic levels (Ohmann and Waddell, 2002). Past management practices have tended to severely reduce amounts of dead wood throughout all stages of forest development (Hansen et al., 1991). The large amounts of legacy wood that characterize young post-disturbance forests are not realized in managed stands, because most of the wood volume is removed at harvest for economic and safety reasons. Mid-rotation thinning is used to “salvage” some mortality that might otherwise occur due to suppression, so fewer snags are recruited in mid-seral stages. Harvest rotations of 80 years or less truncate tree size in managed stands, and thus limit the production of large-diameter wood. As a consequence of these practices, dead wood has been reduced by as much as 90% after two rotations of managed Douglas-fir (Rose et al., 2001). Large legacy deadwood is becoming a scarce, critical habitat that will take decades to centuries to replace. Furthermore, management continues to have important direct and indirect effects on the amount and distribution of dead wood in forests. Current guidelines for managing dead wood may be inadequate to maintain habitat for all associated species because they largely focus on a single use of dead wood (nesting habitat) by a small suite of species (cavity-nesting birds), and may under represent the sizes and amounts of dead wood used by many wildlife species (Rose et al., 2001, Wilhere, 2003).

Open-File Report↗

Soil magnetic susceptibility: A quantitative proxy of soil drainage for use in ecological restoration

Flooded, saturated, or poorly drained soils are commonly anaerobic, leading to microbially induced magnetite/maghemite dissolution and decreased soil magnetic susceptibility (MS). Thus, MS is considerably higher in well-drained soils (MS typically 40-80 ?? 10-5 standard international [SI]) compared to poorly drained soils (MS typically 10-25 ?? 10-5 SI) in Illinois, other soil-forming factors being equal. Following calibration to standard soil probings, MS values can be used to rapidly and precisely delineate hydric from nonhydric soils in areas with relatively uniform parent material. Furthermore, soil MS has a moderate to strong association with individual tree species' distribution across soil moisture regimes, correlating inversely with independently reported rankings of a tree species' flood tolerance. Soil MS mapping can thus provide a simple, rapid, and quantitative means for precisely guiding reforestation with respect to plant species' adaptations to soil drainage classes. For instance, in native woodlands of east-central Illinois, Quercus alba , Prunus serotina, and Liriodendron tulipifera predominantly occur in moderately well-drained soils (MS 40-60 ?? 10-5 SI), whereas Acer saccharinum, Carya laciniosa, and Fraxinus pennsylvanica predominantly occur in poorly drained soils (MS <20 ?? 10-5 SI). Using a similar method, an MS contour map was used to guide restoration of mesic, wet mesic, and wet prairie species to pre-settlement distributions at Meadowbrook Park (Urbana, IL, U.S.A.). Through use of soil MS maps calibrated to soil drainage class and native vegetation occurrence, restoration efforts can be conducted more successfully and species distributions more accurately reconstructed at the microecosystem level. ?? 2008 Society for Ecological Restoration International.

Restoration Ecology↗

Effects of energy development on wetland plants and macroinvertebrate communities in Prairie Pothole Region wetlands

Energy production in the Williston Basin, USA, results in the coproduction of highly saline, sodium chloride-dominated water (brine). The Prairie Pothole Region (PPR) overlies the northeastern portion of the Williston Basin. Although PPR wetlands span a range of salinity, the dominant salt is sodium sulfate, and salinities are much lower than brine. Introduction of brine to wetlands can result in pronounced water-quality changes; however, the ecological effects of such contamination are poorly understood. We examined the effects of brine contamination on primary productivity, emergent macrophyte tissue chemistry, and invertebrate communities from 10 wetlands in the PPR. Based on a recognized Contamination Index (CI) used to identify brine contamination in the PPR, water-quality samples indicated that six wetlands were uncontaminated while four were contaminated. Across this gradient, we observed a significant decrease in above-ground biomass and a significant increase in tissue chloride concentrations of hardstem bulrush ( Schoenoplectus acutus ) with increased CI values. Additionally, a significant decrease in macroinvertebrate taxonomic richness with increased CI values was observed. These findings provide needed insight on the biological effects of brine contamination on PPR wetlands.

Journal of Freshwater Ecology↗

Historical range and variation (HRV)

Fire-prone landscapes are experiencing rapid and potentially persistent changes as the result of complex and potentially novel interactions of anthropogenic climate changes, shifting fire regimes, exotic plant, insect, and pathogen invasions, and industrial, agricultural, and urban development. Are these landscapes fully departed from historical conditions? Should they be managed as novel environments or as landscapes in transition? Historical range and variation is a benchmark representation of the conditions that describe fully functional, healthy ecosystems or landscapes. The HRV can provide an ecological reference against which contemporary and future conditions can be evaluated to determine status, trend, and magnitude of departure. This text describes the concepts of HRV, methods for developing HRV data sets, and application of HRV for fire management. We discuss the limitations of HRV, and its use under future climates that are no longer representative of historical conditions.

Book chapter↗

The influence of floral resources and microclimate on pollinator visitation in an agro-ecosystem

As agriculture expands to meet the needs of a growing global population, natural ecosystems are threatened by deforestation and habitat fragmentation. Tropical agroforestry systems offer a sustainable alternative to traditional agriculture by providing food for production while also supporting biodiversity and ecosystem services. Previous studies have shown that these systems may even improve crop pollination, but the mechanisms of how these improvements occur are still poorly understood. Using coffee as a focal crop, we explored how microclimatic conditions affected nectar traits (sugar and caffeine concentration) important for pollinator visitation. We also studied how microclimate, floral traits, floral availability at the coffee plant level, availability of floral resources provided by other plant species in the agroecosystem (neighborhood floral availability), and the presence of other bees affected the amount of time bees spent foraging on coffee flowers and the proportion of coffee pollen carried on their bodies. We explored these factors using the two dominant coffee species farmed on Puerto Rico, Coffea canephora and C. arabica , under sun and shade management. We found that high nectar sugar concentration and temperature were important predictors of short floral visits (<15 seconds), while increased number of bees and open coffee flowers were important predictors of longer floral visits (16-180 seconds). High nectar caffeine concentration was an important predictor of longer visits on C. arabica flowers while the opposite was observed for C. canephora flowers. For both species, high coffee floral availability was the main predicting factor for the proportion of coffee pollen on the bees bodies. Surprisingly, neither neighborhood floral availability nor the type of coffee plantation (agroforest/shade or sun) were important predictors of bee visitation. These results suggest non-coffee flowering plants in coffee plantations were neither competitors nor facilitators of coffee plantes for pollinators. Additionally, most of the bees surveyed were carrying 80% pollen from one species ( C. arabica or C. canephora ), likely resulting in little heterospecific pollen deposition between Coffea and non-Coffea flowers. Shade trees in coffee plantations do not detract from pollinator visitation to coffee flowers, suggesting that the provision of multiple ecological and wildlife conservation benefits by shade trees is not in conflict with a growers ability to maximize the benefits of insect pollination on fruit production.

Adjuntas Lares,Las Marias, Maricao, Puerto Rico Ut↗

Trajectories and tipping points of piñon–juniper woodlands after fire and thinning

Piñon–juniper (PJ) woodlands are a dominant community type across the Intermountain West, comprising over a million acres and experiencing critical effects from increasing wildfire. Large PJ mortality and regeneration failure after catastrophic wildfire have elevated concerns about the long-term viability of PJ woodlands. Thinning is increasingly used to safeguard forests from fire and in an attempt to increase climate resilience. We have only a limited understanding of how fire and thinning will affect the structure and function of PJ ecosystems. Here, we examined vegetation structure, microclimate conditions, and PJ regeneration dynamics following ~20 years post-fire and thinning treatments. We found that burned areas had undergone a state shift that did not show signs of returning to their previous state. This shift was characterized by (1) distinct plant community composition dominated by grasses; (2) a lack of PJ recruitment; (3) a decrease in the sizes of interspaces in between plants; (4) lower abundance of late successional biological soil crusts; (5) lower mean and minimum daily soil moisture values; (6) lower minimum daily vapor pressure deficit; and (7) higher photosynthetically active radiation. Thinning created distinct plant communities and served as an intermediate between intact and burned communities. More intensive thinning decreased PJ recruitment and late successional biocrust cover. Our results indicate that fire has the potential to create drier and more stressful microsite conditions, and that, in the absence of active management following fire, there may be shifts to persistent ecological states dominated by grasses. Additionally, more intensive thinning had a larger impact on community structure and recruitment than less intensive thinning, suggesting that careful consideration of goals could help avoid unintended consequences. While our results indicate the vulnerability of PJ ecosystems to fire, they also highlight management actions that could be adapted to create conditions that promote PJ re-establishment.

Colorado↗

Metabarcoding of fecal samples to determine herbivore diets: A case study of the endangered Pacific pocket mouse

Understanding the diet of an endangered species illuminates the animal’s ecology, habitat requirements, and conservation needs. However, direct observation of diet can be difficult, particularly for small, nocturnal animals such as the Pacific pocket mouse (Heteromyidae: Perognathus longimembris pacificus ). Very little is known of the dietary habits of this federally endangered rodent, hindering management and restoration efforts. We used a metabarcoding approach to identify source plants in fecal samples (N = 52) from the three remaining populations known. The internal transcribed spacers (ITS) of the nuclear ribosomal loci were sequenced following the Illumina MiSeq amplicon strategy and processed reads were mapped to reference databases. We evaluated a range of threshold mapping criteria and found the best-performing setting generally recovered two distinct mock communities in proportions similar to expectation. We tested our method on captive animals fed a known diet and recovered almost all plant sources, but found substantial heterogeneity among fecal pellets collected from the same individual at the same time. Observed richness did not increase with pooling of pellets from the same individual. In field-collected samples, we identified 4–14 plant genera in individual samples and 74 genera overall, but over 50 percent of reads mapped to just six species in five genera. We simulated the effects of sequencing error, variable read length, and chimera formation to infer taxon-specific rates of misassignment for the local flora, which were generally low with some exceptions. Richness at the species and genus levels did not reach a clear asymptote, suggesting that diet breadth remained underestimated in the current pool of samples. Large numbers of scat samples are therefore needed to make inferences about diet and resource selection in future studies of the Pacific pocket mouse. We conclude that our minimally invasive method is promising for determining herbivore diets given a library of sequences from local plants.

California↗

Grass buffers for playas in agricultural landscapes: A literature synthesis

We summarize current knowledge about grass buffers for protecting small, isolated wetlands in agricultural contexts, including information relevant to protecting playas from runoff containing sediments, nutrients, pesticides, and other contaminants, and information on how buffers may affect densities and productivity of grassland birds. Land-uses surrounding the approximately 60,000 playas within the Playa Lakes Region (PLR), including intensive agriculture, feedlots, and oil extraction, can contribute to severe degradation of playas. Farming and grazing can lead to significant sedimentation in nearby playas, eliminating their ability to hold water, support the region&rsquo;s biodiversity, or adequately recharge aquifers. Contaminants further degrade habitats and threaten the water quality of underlying aquifers, including the Ogallala Aquifer. Grass buffers hold promise as a management tool to reduce the amount of sediments and contaminants from agricultural runoff that enters playas. Effective buffer width is determined by acceptable sediment-reduction levels, potential water flow and velocity, landscape and soil variables, buffer species, and vegetation structure. Various models have been developed to predict buffer effectiveness; however, most of these models, including those provided by the Natural Resource Conservation Service (NRCS), remain unvalidated. The majority of buffer-effectiveness literature is based on simulated conditions in experimental trays or plots; no published studies of buffer design or effectiveness specifically address playas. Nonetheless, some general patterns have emerged regarding buffer design/effectiveness. Buffers 10&ndash;60 m wide are generally considered adequate for trapping most sediments, although in some cases buffers need to be >200 m. The U.S. Fish and Wildlife Service Partners for Wildlife Program in the Southern High Plains recommend a buffer width of ~33 m planted with a diverse mix of native shortgrasses and mixed grasses as a starting point. Most dissolved contaminants, however, are removed from runoff only when they infiltrate the soil, where microbes or other processes can break down or sequester contaminants. Promoting runoff infiltration requires wider buffers with denser stem densities than those required for filtering sediments, which may result in hydrological changes in playas. Ultimately, the balance between runoff and infiltration determines whether or not water eventually reaches a given basin. Long-term buffer effectiveness requires regular maintenance, including excavation to remove overburdens of sediments, repairing vegetation damage, and removing over-mature vegetation or invasions of noxious weeds. Buffers may not be enough to protect playas; best management practices (BMPs; e.g., conservation tillage, contour tilling, and mulching herbicides into soil after application) that diminish soil erosion and contaminant runoff also may be necessary. Nutrient loads in runoff can be minimized by balancing nutrient input with nutrient requirements for livestock and crops. Pesticide application practices also require careful evaluation. Mowing or grazing rather than use of herbicides offer alternatives for suppressing invasive or undesirable plant species in buffers. Future research should entail multiple-scale approaches at regional, wetland-complex, and individual watershed scales. Information needs include direct measures of buffer effectiveness in &lsquo;real-world&rsquo; systems, refinement and field tests of buffer-effectiveness models, how buffers may affect floral and faunal communities of playas, and basic ecological information on playa function and playa wildlife ecology. Understanding how wildlife communities respond to patch size and habitat fragmentation is crucial for addressing questions regarding habitat quality of grass buffers in playa systems.

Open-File Report↗

Structure and vulnerability of Pacific Northwest tidal wetlands – A summary of wetland climate change research by the Western Ecology Division, U.S. EPA

Climate change poses a serious threat to the tidal wetlands of the Pacific Northwest (PNW) region of the U.S. In response to this threat, scientists at the Western Ecology Division of the U.S. EPA at and the Western Fisheries Research Center of the U.S. Geological Survey, along with other partners, initiated a series of studies on the structure and vulnerability of tidal wetlands to climate change. One research thrust was to evaluate community structure of PNW marshes, experimentally assess the vulnerability of marsh plants to inundation and salinity stress (as would happen with sea level rise), and evaluate the utility of the National Wetland Inventory (NWI) classification system. Another research thrust was to develop tools that provide insights into possible impacts of climate change. This effort included enhancing the Sea Level Affecting Marshes Model (SLAMM) to predict the effects of sea level rise on submerged aquatic vegetation (Zostera marina) distributions, evaluating changes in river flow into coastal estuaries in response to precipitation changes, and synthesizing Pacific Coast estuary, watershed, and climate data in a downloadable tool. Because the research resulting from these efforts was published in multiple venues, we summarized them in this document. We anticipate that future research efforts by the U.S. EPA will continue with a focus on climate change impacts on a regional scale.

California, Oregon, Washington↗

Population structure and inbreeding vary with successional stage in created Spartina alterniflora marshes

Recruitment patterns in clonal plant populations are predicted to vary with seed dispersal capability and disturbance regime, such that species with small, widely dispersed seeds will become increasingly dominated by vegetative recruitment on disturbed areas following early colonization. Subsequent mortality due to competitive or stochastic effects is then predicted to cause a gradual decline in both clonal diversity and the ability of surviving clones to avoid geitonogamous mating and possible inbreeding depression. We tested predictions of these hypotheses by comparing four adjacent populations of the salt marsh plant, Spartina alterniflora, ranging in age from 2 to ∼50 yr, by measuring fine‐scale genetic structure at the level of both ramets and genets, and the rate of inbreeding. For this purpose, we sampled maternal tissue and seeds from discrete patches in the field and then genotyped both maternal and seedling tissue (germinated in a growth chamber) using standard molecular protocols. As predicted, we observed an increase in clonal diversity (measured as the complement of the Simpson Index corrected for finite sample sizes, 1 − D ) up to a maximum of 0.71 within 3‐m 2 patches at 16 yr, declining to 0.55 by ∼50 yr. Local recruitment of seedlings was evident as genetic structure occurring at the level of patches, as measured by the fixation index, θ, which was inversely correlated with diversity ( R 2 > 0.90 at all patch scales). Outcrossing rates were positively associated with clonal diversity, with the highest level (89%) at an intermediate level of 1 − D. The greatest selfing (32%) occurred in young (2‐yr‐old) patches with low diversity. Biparental inbreeding was minimal in all populations, never exceeding 1%. Inbreeding depression was inferred to be severe, as evidenced by near‐zero adult inbreeding coefficients. These results suggest a possible fitness trade‐off between clonal growth and the opportunity for outcrossing. We recommend that restoration plantings of clonal species with limited sexual recruitment capabilities should be designed to ensure adequate clonal diversity for the avoidance of inbreeding and the ability to adapt to subsequent environmental disturbances.

Louisiana↗

Contamination of the freshwater ecosystem by pesticides

A large part of our disquieting present-day pesticide problem is intimately tied to the freshwater ecosystem. Economic poisons are used in so many types of terrain to control so many kinds of organisms that almost all lakes and streams are likely to be contaminated. In addition to accidental contamination many pesticides are deliberately applied directly to fresh waters for suppression of aquatic animals or plants. The problem is intensified because of the extreme susceptibility of freshwater organisms. The complexity of freshwater environments and their variety makes it difficult to comprehend the total effect of pesticides.

Journal of Applied Ecology↗

Beyond barriers: Fish assemblage recovery following dam removal on the Cuyahoga River, a Lake Erie tributary

Dam removals are increasing globally, yet ecological outcomes vary widely because biological recovery depends on post-removal connectivity and access to source populations. We evaluated how multiple dam removals and remaining fragmentation influenced fish assemblage recovery in the Cuyahoga River (OH, United States), a historically polluted Great Lakes tributary now undergoing extensive remediation and restoration. Using fish assemblage data collected from 1984 to 2024 across reaches downstream, within, and upstream of the Gorge Plant Dam (GPD), an 18-m barrier slated for removal, we quantified spatial and temporal change with ordination, trajectory, and distance-based redundancy analyses. Downstream assemblages showed a clear shift through time and gained 15 newly detected taxa after the 2020 Brecksville Dam removal increased longitudinal connectivity to Lake Erie by 39 river kilometers, more than doubling free-flowing habitat below GPD. In contrast, assemblages upstream of GPD exhibited limited change and patterns consistent with redistribution of resident species rather than colonization-driven turnover. Across the full time series, site position relative to GPD and the rate of dam removal were the strongest predictors of assemblage variation, with habitat gradients (e.g. depth, velocity, turbidity, and canopy cover) further differentiating reaches. Together, these results show that connectivity and barrier position shape assemblage recovery following dam removal. Most newly detected taxa downstream were native, though three were nonnative, indicating trade-offs between recolonization and nonnative spread.

Ohio↗

Effects of climate change on ecological disturbance in the northern Rockies

Disturbances alter ecosystem, community, or population structure and change elements of the biological and/or physical environment. Climate changes can alter the timing, magnitude, frequency, and duration of disturbance events, as well as the interactions of disturbances on a landscape, and climate change may already be affecting disturbance events and regimes. Interactions among disturbance regimes, such as the cooccurrence in space and time of bark beetle outbreaks and wildfires, can result in highly visible, rapidly occurring, and persistent changes in landscape composition and structure. Understanding how altered disturbance patterns and multiple disturbance interactions might result in novel and emergent landscape behaviors is critical for addressing climate change impacts and for designing land management strategies that are appropriate for future climates This chapter describes the ecology of important disturbance regimes in the Northern Rockies region, and potential shifts in these regimes as a consequence of observed and projected climate change. We summarize five disturbance types present in the Northern Rockies that are sensitive to a changing climate--wildfires, bark beetles, white pine blister rust (Cronartium ribicola), other forest diseases, and nonnative plant invasions—and provide information that can help managers anticipate how, when, where, and why climate changes may alter the characteristics of disturbance regimes.

Rocky Mountains↗

Evidence for nutrient enrichment of high-elevation lakes in the Sierra Nevada, California

Long-term measurements (1983-2001) of nutrients and seston in Emerald Lake (Sierra Nevada, California) have revealed ecologically significant patterns. Nitrate, both during spring runoff and during growing seasons, declined from 1983 through 1995. Declining snowmelt nitrate was caused primarily by changes in snow regime induced by the 1987-1992 drought: years with shallow, early melting snowpacks had lower snowmelt nitrate concentrations owing to less labile N production in catchment soils and longer plant growing seasons. However, nitrate declines during growing seasons carried through the wetter years of 1993-2000 and are likely the result of increased P loading to the lake and the release of phytoplankton from P limitation. Contemporaneous with these changes was an increase in algal biomass and a shift from P limitation toward more frequent N limitation of phytoplankton abundance. Particulate carbon concentrations in the late 1990s were two- to threefold greater than in the early 1980s. These trends were reflected in a larger set of Sierra Nevada lakes sampled as part of synoptic surveys (n = 28). Between 1985 and 1999, nitrate decreased and total P increased in >70% of the lakes sampled. Our data suggest that lakes throughout the Sierra Nevada are experiencing measurable eutrophication in response to the atmospheric deposition of nutrients.

Limnology and Oceanography↗

Quantifying the extent of river fragmentation by hydropower dams in the Sarapiquí River Basin, Costa Rica

Costa Rica has recently experienced a rapid proliferation of dams for hydropower on rivers draining its northern Caribbean slope. In the Sarapiquí River Basin, eight hydropower plants were built between 1990 and 1999 and more projects are either under construction or proposed. The majority of these dams are small (<15 m tall) and operate as water diversion projects. While the potential environmental effects of individual projects are evaluated prior to dam construction, there is a need for consideration of the basin-scale ecological consequences of hydropower development. This study was a first attempt to quantify the extent of river fragmentation by dams in the Sarapiquí River Basin. Using simple spatial analyses, the length of river upstream from dams and the length of de-watered reaches downstream from dams was measured. Results indicated that there are currently 306.8 km of river (9.4% of the network) upstream from eight existing dams in the Sarapiquí River Basin and 30.6 km of rivers (0.9% of the network) with significantly reduced flow downstream from dams. Rivers upstream from dams primarily drain two life zones: Premontane Rain Forest (107.9 km) and Lower Montane Rain Forest (168.2 km). Simple spatial analyses can be used as a predictive or planning tool for considering the effects of future dams in a basin-scale context. In the Sarapiquí River Basin, we recommend that future dam projects be constructed on already dammed rivers to minimize additional river fragmentation and to protect remaining riverine connectivity.

Aquatic Conservation: Marine and Freshwater Ecosys↗