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At least 577 records · Page 32Linked to original sources

Phosphorus and nitrogen legacy in a restoration wetland, upper Klamath lake, Oregon

The effects of sediment, ground-water, and surface-water processes on the timing, quantity, and mechanisms of N and P fluxes were investigated in the Wood River Wetland 57 years after agricultural practices ceased and seasonal and permanent wetland hydrologies were restored. Nutrient concentrations in standing water largely reflected ground water in winter, the largest annual water source in the closed-basin wetland. High concentrations of total P (22 mg L -1 ) and total N (30 mg L -1 ) accumulated in summer when water temperature, air temperature, and evapotranspiration were highest. High positive benthic fluxes of soluble reactive P and ammonium (NH 4 -N) were measured in two sections of the study area in June and August, averaging 46 and 24 mg m -2 d -1 , respectively. Nonetheless, a wetland mass balance simultaneously indicated a net loss of P and N by assimilation, denitrification (1.110.1 mg N m -2 h -1 ), or solute repartitioning. High nutrient concentrations pose a risk for water quality management. Shifts in the timing and magnitude of water inflows and outflows may improve biogeochemical function and water quality by optimizing seed germination and aquatic plant distribution, which would be especially important if the Wood River Wetland was reconnected with hyper-eutrophic Agency Lake. ?? 2009, The Society of Wetland Scientists.

Wetlands↗

The role of pH in structuring communities of Maine wetland macrophytes and chironomid larvae (Diptera)

Aquatic vascular plants, or macrophytes, are an important habitat component for many wetland organisms, and larvae of chironomid midges are ubiquitous components of wetland fauna. Many chironomids are primary consumers of algae and detritus and form an essential energetic link between allochthonous and autochthonous primary production and higher trophic levels, while others are predators and feed on smaller invertebrates. Live macrophytes serve mostly as habitat, whereas plant detritus serves as both habitat and as a food source. Assemblages of macrophytes and chrinomid larvae were surveyed in ten Maine wetlands, five with low pH (<5.0) and five with high pH (>5.5), and explained in terms of physical and chemical habitat variables. Macrophyte richness was significantly greater, and richness of chironomid larvae was lower, in low pH wetlands. There was no difference in chironomid abundance related to pH. However, community structure was related to pH, suggesting that competitive dominance of a few taxa was responsible for lower richness in low pH wetlands, whereas competition was weaker in high pH wetlands, making coexistence of more chironomid taxa possible. An examination of individual chironomid taxa by stepwise multiple regression showed that distribution of most taxa was controlled by water chemistry variables and macrophyte habit (i.e., floating, submergent).

Maine↗

Carbon budget of tidal wetlands, estuaries, and shelf waters of eastern North America

Carbon cycling in the coastal zone affects global carbon budgets and is critical for understanding the urgent issues of hypoxia, acidification, and tidal wetland loss. However, there are no regional carbon budgets spanning the three main ecosystems in coastal waters: tidal wetlands, estuaries, and shelf waters. Here we construct such a budget for eastern North America using historical data, empirical models, remote sensing algorithms, and process‐based models. Considering the net fluxes of total carbon at the domain boundaries, 59 ± 12% (± 2 standard errors) of the carbon entering is from rivers and 41 ± 12% is from the atmosphere, while 80 ± 9% of the carbon leaving is exported to the open ocean and 20 ± 9% is buried. Net lateral carbon transfers between the three main ecosystem types are comparable to fluxes at the domain boundaries. Each ecosystem type contributes substantially to exchange with the atmosphere, with CO 2 uptake split evenly between tidal wetlands and shelf waters, and estuarine CO 2 outgassing offsetting half of the uptake. Similarly, burial is about equal in tidal wetlands and shelf waters, while estuaries play a smaller but still substantial role. The importance of tidal wetlands and estuaries in the overall budget is remarkable given that they, respectively, make up only 2.4 and 8.9% of the study domain area. This study shows that coastal carbon budgets should explicitly include tidal wetlands, estuaries, shelf waters, and the linkages between them; ignoring any of them may produce a biased picture of coastal carbon cycling.

Global Biogeochemical Cycles↗

The role of environmental driving factors in historical and projected carbon dynamics of wetland ecosystems in Alaska

Wetlands are critical terrestrial ecosystems in Alaska, covering ~177,000 km 2 , an area greater than all the wetlands in the remainder of the United States. To assess the relative influence of changing climate, atmospheric carbon dioxide (CO 2 ) concentration, and fire regime on carbon balance in wetland ecosystems of Alaska, a modeling framework that incorporates a fire disturbance model and two biogeochemical models was used. Spatially explicit simulations were conducted at 1‐km resolution for the historical period (1950–2009) and future projection period (2010–2099). Simulations estimated that wetland ecosystems of Alaska lost 175 Tg carbon (C) in the historical period. Ecosystem C storage in 2009 was 5,556 Tg, with 89% of the C stored in soils. The estimated loss of C as CO 2 and biogenic methane (CH 4 ) emissions resulted in wetlands of Alaska increasing the greenhouse gas forcing of climate warming. Simulations for the projection period were conducted for six climate change scenarios constructed from two climate models forced under three CO 2 emission scenarios. Ecosystem C storage averaged among climate scenarios increased 3.94 Tg C/yr by 2099, with variability among the simulations ranging from 2.02 to 4.42 Tg C/yr. These increases were driven primarily by increases in net primary production (NPP) that were greater than losses from increased decomposition and fire. The NPP increase was driven by CO 2 fertilization (~5% per 100 parts per million by volume increase) and by increases in air temperature (~1% per °C increase). Increases in air temperature were estimated to be the primary cause for a projected 47.7% mean increase in biogenic CH 4 emissions among the simulations (~15% per °C increase). Ecosystem CO 2 sequestration offset the increase in CH 4 emissions during the 21st century to decrease the greenhouse gas forcing of climate warming. However, beyond 2100, we expect that this forcing will ultimately increase as wetland ecosystems transition from being a sink to a source of atmospheric CO 2 because of (1) decreasing sensitivity of NPP to increasing atmospheric CO 2 , (2) increasing availability of soil C for decomposition as permafrost thaws, and (3) continued positive sensitivity of biogenic CH 4 emissions to increases in soil temperature.

Alaska↗

Application of lidar to assess the habitat selection of an endangered small mammal in an estuarine wetland environment

Light detection and ranging (lidar) has emerged as a valuable tool for examining the fine-scale characteristics of vegetation. However, lidar is rarely used to examine coastal wetland vegetation or the habitat selection of small mammals. Extensive anthropogenic modification has threatened the endemic species in the estuarine wetlands of the California coast, such as the endangered salt marsh harvest mouse ( Reithrodontomys raviventris ; SMHM). A better understanding of SMHM habitat selection could help managers better protect this species. We assessed the ability of airborne topographic lidar imagery in measuring the vegetation structure of SMHM habitats in a coastal wetland with a narrow range of vegetation heights. We also aimed to better understand the role of vegetation structure in habitat selection at different spatial scales. Habitat selection was modeled from data compiled from 15 small mammal trapping grids collected in the highly urbanized San Francisco Estuary in California, USA. Analyses were conducted at three spatial scales: microhabitat (25 m 2 ), mesohabitat (2025 m 2 ), and macrohabitat (~10,000 m 2 ). A suite of structural covariates was derived from raw lidar data to examine vegetation complexity. We found that adding structural covariates to conventional habitat selection variables significantly improved our models. At the microhabitat scale in managed wetlands, SMHM preferred areas with denser and shorter vegetation and selected for proximity to levees and taller vegetation in tidal wetlands. At the mesohabitat scale, SMHM were associated with a lower percentage of bare ground and with pickleweed ( Salicornia pacifica ) presence. All covariates were insignificant at the macrohabitat scale. Our results suggest that SMHM preferentially selected microhabitats with access to tidal refugia and mesohabitats with consistent food sources. Our findings showed that lidar can contribute to improving our understanding of habitat selection of wildlife in coastal wetlands and help to guide future conservation of an endangered species.

Ecology and Evolution↗

Evidence for 20th century climate warming and wetland drying in the North American Prairie Pothole Region

The Prairie Pothole Region (PPR) of North America is a globally important resource that provides abundant and valuable ecosystem goods and services in the form of biodiversity, groundwater recharge, water purification, flood attenuation, and water and forage for agriculture. Numerous studies have found these wetlands, which number in the millions, to be highly sensitive to climate variability. Here, we compare wetland conditions between two 30-year periods (1946–1975; 1976–2005) using a hindcast simulation approach to determine if recent climate warming in the region has already resulted in changes in wetland condition. Simulations using the WETLANDSCAPE model show that 20th century climate change may have been sufficient to have a significant impact on wetland cover cycling. Modeled wetlands in the PPR's western Canadian prairies show the most dramatic effects: a recent trend toward shorter hydroperiods and less dynamic vegetation cycles, which already may have reduced the productivity of hundreds of wetland-dependent species.

Prairie Pothole Region↗

Simulating the effects of climate variability on waterbodies and wetland-dependent birds in the Prairie Pothole Region

Understanding how bird populations respond to changes in waterbody availability in the climatically variable Prairie Pothole Region (PPR) of North America hinges on being able to couple hydrological and climate modeling to represent potential future landscapes. Model experiments run with the Pothole Complex Hydrologic Model using downscaled climate data (variables relating to precipitation, temperature, and potential evapotranspiration at 1/8° spatial resolution under four general circulation climate models and two gas emissions scenarios) were used to forecast the abundances of six focal wetland‐dependent bird species in the Missouri Coteau portion of the PPR, providing ensemble scenarios at a spatial scale relevant to resource management. Although the projected number of May ponds (waterbodies present during bird breeding season) fluctuated through time with some decadal periodicity (and with the number present in a given year reflecting abundance over the previous three years), the ensemble model average indicated an increase in the average number of waterbodies present by the turn of the next century. Overall, the model experiments conservatively projected an 11.75% increase in the number of waterbodies present by 2090–2099 compared to a baseline period from 1967 to 2005 in the PPR. Wetland‐dependent bird occurrence and abundance were significantly associated with temporal patterns and decadal periodicity in waterbody dynamics. Because of the strong associations between wetland‐dependent bird occurrence and abundance and the number of prairie potholes, projected waterbody increases are forecasted to result in an 11.97% overall increase in occurrence and 8.63% increase in abundance of the six focal species by the end of the 21st century; these results contrast with forecasted drought‐associated declines in waterbodies and birds in the PPR. This integrated hydrological–climatological approach offers a means of assessing how wetland‐dependent bird populations may respond to changes in wetland habitat availability due to a changing climate. Our results provide information that can help managers decide how to mitigate the effects of climate shifts on the distribution of wetland habitat and biota.

North Dakota↗

Climate-driven changes in wetland hydroperiods predict losses in habitat suitability for amphibian breeding

Environmental regimes are shifting with accelerating climate change, disrupting interactions between species and ecosystems shaped by the climate of the pre-industrial era. Species assemblages that depend on a dynamic network of ephemeral and permanent habitats may be especially sensitive to changing climate, whereby shifting environmental regimes may limit species persistence in landscapes in ways not captured by species physiology or coarse habitat metrics alone. Here we forecasted the loss of montane and subalpine wetlands as breeding habitat for three amphibian species in the US Pacific Northwest, Ambystoma gracile , Ambystoma macrodactylum , and Rana cascadae . We combined historical and recent surveys to build occupancy models of current breeding habitat use. We combined these results with existing hydrological models to predict the loss of suitable breeding habitats by the 2080s due to increased wetland drying. We found that species-specific occupancy of wetlands used for reproduction was predicted by both abiotic (e.g., elevation, wetland area) and biotic (e.g., emergent vegetation) site-level characteristics. Among wetlands currently used for reproduction, we estimated that between 12% and 23% could become unsuitable for the aquatic phase of each species by the 2080s, with watershed-scale losses ranging from 0% to 80%. This suggests that wetland habitat loss could limit the persistence of these species in the Pacific Northwest, though impacts are expected to vary across landscapes. More broadly, we demonstrate a novel approach to quantifying species climate change vulnerability that can be used to identify areas of both risk and resilience in changing landscapes and help to prioritize the application of practical conservation solutions in areas of greatest need.

Washington↗

Integrating geographically isolated wetlands into land management decisions

Wetlands across the globe provide extensive ecosystem services. However, many wetlands – especially those surrounded by uplands, often referred to as geographically isolated wetlands (GIWs) – remain poorly protected. Protection and restoration of wetlands frequently requires information on their hydrologic connectivity to other surface waters, and their cumulative watershed‐scale effects. The integration of measurements and models can supply this information. However, the types of measurements and models that should be integrated are dependent on management questions and information compatibility. We summarize the importance of GIWs in watersheds and discuss what wetland connectivity means in both science and management contexts. We then describe the latest tools available to quantify GIW connectivity and explore crucial next steps to enhancing and integrating such tools. These advancements will ensure that appropriate tools are used in GIW decision making and maintaining the important ecosystem services that these wetlands support.

Frontiers in Ecology and the Environment↗

Drainage investment and wetland loss: an analysis of the national resources inventory data

The United States Soil Conservation Service (SCS) conducts a survey for the purpose of establishing an agricultural land use database. This survey is called the National Resources Inventory (NRI) database. The complex NRI land classification system, in conjunction with the quantitative information gathered by the survey, has numerous applications. The current paper uses the wetland area data gathered by the NRI in 1982 and 1987 to examine empirically the factors that generate wetland loss in the United States. The cross-section regression models listed here use the quantity of wetlands, the stock of drainage capital, the realty value of farmland and drainage costs to explain most of the cross-state variation in wetland loss rates. Wetlands preservation efforts by federal agencies assume that pecuniary economic factors play a decisive role in wetland drainage. The empirical models tested in the present paper validate this assumption.

Journal of Environmental Management↗

Assessing and measuring wetland hydrology

Virtually all ecological processes that occur in wetlands are influenced by the water that flows to, from, and within these wetlands. This chapter provides the “how-to” information for quantifying the various source and loss terms associated with wetland hydrology. The chapter is organized from a water-budget perspective, with sections associated with each of the water-budget components that are common in most wetland settings. Methods for quantifying the water contained within the wetland are presented first, followed by discussion of each separate component. Measurement accuracy and sources of error are discussed for each of the methods presented, and a separate section discusses the cumulative error associated with determining a water budget for a wetland. Exercises and field activities will provide hands-on experience that will facilitate greater understanding of these processes.

Book chapter↗

Effects of climate on numbers of northern prairie wetlands

The amount of water held in individual wetland basins depends not only on local climate patterns but also on groundwater flow regime, soil permeability, and basin size. Most wetland basins in the northern prairies hold water in some years and are dry in others. To assess the potential effect of climate change on the number of wetland basins holding water in a given year, one must first determine how much of the variability in number of wet basins is accounted for by climatic variables. I used multiple linear regression to examine the relationship between climate variables and percentage of wet basins throughout the Prairie Pothole Region of Canada and the United States. The region was divided into three areas: parkland, Canadian grassland, and United States grassland (i.e., North Dakota and South Dakota). The models - which included variables for spring and fall temperature, yearly precipitation, the previous year's count of wet basins, and for grassland areas, the previous fall precipitation - accounted for 63 to 65% of the variation in the number of wet basins. I then explored the sensitivities of the models to changes in temperature and precipitation, as might be associated with increased greenhouse gas concentrations. Parkland wetlands are shown to be much more vulnerable to increased temperatures than are wetlands in either Canadian or United States grasslands. Sensitivity to increased precipitation did not vary geographically. These results have implications for waterfowl and other wildlife populations that depend on availability of wetlands in the parklands for breeding or during periods of drought in the southern grasslands.

Climatic Change↗

Recent land cover history and nutrient retention in riparian wetlands

Wetland ecosystems are profoundly affected by altered nutrient and sediment loads received from anthropogenic activity in their surrounding watersheds. Our objective was to compare a gradient of agricultural and urban land cover history during the period from 1949 to 1997, with plant and soil nutrient concentrations in, and sediment deposition to, riparian wetlands in a rapidly urbanizing landscape. We observed that recent agricultural land cover was associated with increases in Nitrogen (N) and Phosphorus (P) concentrations in a native wetland plant species. Conversely, recent urban land cover appeared to alter receiving wetland environmental conditions by increasing the relative availability of P versus N, as reflected in an invasive, but not a native, plant species. In addition, increases in surface soil Fe content suggests recent inputs of terrestrial sediments associated specifically with increasing urban land cover. The observed correlation between urban land cover and riparian wetland plant tissue and surface soil nutrient concentrations and sediment deposition, suggest that urbanization specifically enhances the suitability of riparian wetland habitats for the invasive species Japanese stiltgrass [Microstegium vimenium (Trinius) A. Camus]. ?? 2009 Springer Science+Business Media, LLC.

Environmental Management↗

Estimated ultraviolet radiation doses in wetlands in six national parks

Ultraviolet-B radiation (UV-B, 280&ndash;320-nm wavelengths) doses were estimated for 1024 wetlands in six national parks: Acadia (Acadia), Glacier (Glacier), Great Smoky Mountains (Smoky), Olympic (Olympic), Rocky Mountain (Rocky), and Sequoia/Kings Canyon (Sequoia). Estimates were made using ground-based UV-B data (Brewer spectrophotometers), solar radiation models, GIS tools, field characterization of vegetative features, and quantification of DOC concentration and spectral absorbance. UV-B dose estimates were made for the summer solstice, at a depth of 1 cm in each wetland. The mean dose across all wetlands and parks was 19.3 W-h m &minus;2 (range of 3.4&ndash;32.1 W-h m &minus;2 ). The mean dose was lowest in Acadia (13.7 W-h m &minus;2 ) and highest in Rocky (24.4 W-h m &minus;2 ). Doses were significantly different among all parks. These wetland doses correspond to UV-B flux of 125.0 &mu;W cm &minus;2 (range 21.4&ndash;194.7 &mu;W cm &minus;2 ) based on a day length, averaged among all parks, of 15.5 h. Dissolved organic carbon (DOC), a key determinant of water-column UV-B flux, ranged from 0.6 (analytical detection limit) to 36.7 mg C L &minus;1 over all wetlands and parks, and reduced potential maximal UV-B doses at 1-cm depth by 1%&ndash;87 %. DOC concentration, as well as its effect on dose, was lowest in Sequoia and highest in Acadia (DOC was equivalent in Acadia, Glacier, and Rocky). Landscape reduction of potential maximal UV-B doses ranged from zero to 77% and was lowest in Sequoia. These regional differences in UV-B wetland dose illustrate the importance of considering all aspects of exposure in evaluating the potential impact of UV-B on aquatic organisms.

Acadia National Park, Glacier National Park, Great↗

Emerging dragonfly diversity at small Rhode Island (U.S.A.) wetlands along an urbanization gradient

Natal habitat use by dragonflies was assessed on an urban to rural land-use gradient at a set of 21 wetlands, during two emergence seasons (2004, 2005). The wetlands were characterized for urbanization level by using the first factor from a principal components analysis combining chloride concentration in the wetland and percent forest in the surrounding buffer zone. Measurements of species diversity and its components (species richness and evenness) were analyzed and compared along the urbanization gradient, as were distributions of individual species. Dragonfly diversity, species richness, and evenness did not change along the urbanization gradient, so urban wetlands served as natal habitat for numerous dragonfly species. However, several individual species displayed strong relationships to the degree of urbanization, and most were more commonly found at urban sites and at sites with fish. In contrast, relatively rare species were generally found at the rural end of the gradient. These results suggest that urban wetlands can play important roles as dragonfly habitat and in dragonfly conservation efforts, but that conservation of rural wetlands is also important for some dragonfly species.

Urban Ecosystems↗

Restoring coastal wetlands that were ditched for mosquito control: a preliminary assessment of hydro-leveling as a restoration technique

The wetlands surrounding Tampa Bay, Florida were extensively ditched for mosquito control in the 1950s. Spoil from ditch construction was placed adjacent to the wetlands ditches creating mound-like features (spoil-mounds). These mounds represent a loss of 14% of the wetland area in Tampa Bay. Spoil mounds interfere with tidal flow and are locations for non-native plants to colonize (e.g., Schinus terebinthifolius ). Removal of the spoil mounds to eliminate exotic plants, restore native vegetation, and re-establish natural hydrology is a restoration priority for environmental managers. Hydro-leveling, a new technique, was tested in a mangrove forest restoration project in 2004. Hydro-leveling uses a high pressure stream of water to wash sediment from the spoil mound into the adjacent wetland and ditch. To assess the effectiveness of this technique, we conducted vegetation surveys in areas that were hydro-leveled and in non-hydro-leveled areas 3 years post-project. Adult Schinus were reduced but not eliminated from hydro-leveled mounds. Schinus seedlings however were absent from hydro-leveled sites. Colonization by native species was sparse. Mangrove seedlings were essentially absent (≈2 m −2 ) from the centers of hydro-leveled mounds and were in low density on their edges (17 m −2 ) in comparison to surrounding mangrove forests (105 m −2 ). Hydro-leveling resulted in mortality of mangroves adjacent to the mounds being leveled. This was probably caused by burial of pneumatophores during the hydro-leveling process. For hydro-leveling to be a useful and successful restoration technique several requirements must be met. Spoil mounds must be lowered to the level of the surrounding wetlands. Spoil must be distributed further into the adjacent wetland to prevent burial of nearby native vegetation. Finally, native species may need to be planted on hydro-leveled areas to speed up the re-vegetation process.

Journal of Coastal Conservation↗

How plants influence resilience of salt marsh and mangrove wetlands to sea-level rise

This review evaluates the importance of plants and associated biological processes in determining the vulnerability of coastal wetlands to sea-level rise. Coastal wetlands occur across a broad sedimentary continuum from minerogenic to biogenic, providing an opportunity to examine the relative importance of biological processes in wetland resilience to sea-level rise. We explore how plants influence sediment accretion, elevation capital (vertical position in the tidal frame), and compaction or erosion of deposited material. We focus on salt marsh and mangrove wetlands, which occupy a similar physiographic niche and display similar physical and biological controls on resilience to sea-level rise. In both habitats, plants stabilize emergent mudflats and help sustain the wetland position in the tidal frame relative to ocean height through both surface and subsurface process controls on soil elevation. Plants influence soil elevations by modifying (1) mineral sediment deposition and retention, (2) organic matter contributions to soil volume, and (3) resistance to compaction and erosion. Recognition of the importance of plants in coastal wetland resilience to sea-level rise is key to accurate predictions about the future fate of salt marshes and mangrove forests and for development of effective management and restoration plans.

Estuaries and Coasts↗

Current advances in coastal wetland elevation dynamics: Introduction to the special issue

The thematic issue entitled, “Current Advances in Coastal Wetland Elevation Dynamics,” draws on topics from two special sessions at the CERF 2021 conference plus additional recent research describing scientific insights gained from the Surface Elevation Table–Marker Horizon (SET–MH) method and its application across the globe to quantify and understand subsurface process influences on wetland elevation change and wetland responses to sea-level rise. The findings group articles within each of five thematic topics. (1) A 30-year retrospective on the scientific insights gained on surface and shallow subsurface process dynamics. (2) Investigations of the subsurface soil process influences on wetland elevation. (3) How the scientific community applies the SET–MH method to quantify and understand wetland responses to RSLR and other environmental drivers such as altered hydrology and sediment supply. (4) How SET–MH data are used in long-term monitoring networks at different geographic scales. (5) Pairing the SET-MH method with (a) survey techniques to increase lateral coverage of wetland elevation trends and (b) geodetic measurements to increase vertical coverage of vertical land motion.

Estuaries and Coasts↗