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Hydrology and chemistry of selected prairie wetlands in the Cottonwood Lake area, Stutsman County, North Dakota, 1979-82

The relation of hydrologic setting and temporal variability in hydrology to nutrient content and geochemical characteristics of a group of prairie wetlands and adjacent ground water was studied during the period 1979-82. Although data were collected from many wetlands and wells at the study site, emphasis in this report primarily is on four wetlands two seasonal and two semipermanent and four wells contiguous to them along a hydrologic section. The seasonal wetlands, T8 and T3, contained water only for a few weeks to months after filling in spring and early summer; both were completely dry by August. The semipermanent wetlands, PI and P8, contained water throughout each year and were ice covered in winter. One wetland, T8, recharges ground water. Wetlands PI and P8 are in areas of ground-water discharge. None of the wetlands received water by channelized surface-water inlets. Only wetland P8 had a channelized surface-water outlet. Ground-water-level data showed that high points of the water table did not always occur beneath land-surface highs. Reversals of ground-water flow occurred occasionally between two of the wetlands, T3 and PI. Significant differences existed in the chemical composition of the wetlands based on their hydrologic setting. In general, the dominant cation and anion in the wetlands were potassium and bicarbonate in wetland T8, calcium and sulfate in wetland T3, magnesium and sulfate in wetland PI, and magnesium and bicarbonate in wetland P8. Significant seasonal differences existed in the water chemistry of the wetlands in ground-water discharge areas. Water in three of the wetlands, T3, Pi, and P8, was most dilute while they filled in spring after icemelt. Concentration increased during the open-water period, and two of the wetlands, PI and P8, became most concentrated under ice cover. Concentrations of total phosphorus and total nitrogen were greatest in wetlands in areas of ground-water recharge and least in wetlands in areas of ground-water discharge. Differences in the chemistry of water from wells in the adjacent ground water resulted primarily from the positions of the wells in the ground-water flow system. The chemical type of water from well 12, which was located in a ground-water recharge area, was calcium sodium bicarbonate. Water from well 4, located downgradient from wetland T8, and from well 16, located downgradient from wetland PI, typically was a calcium sulfate type. Water from well 13, located between wetlands T3 and PI in an area of changing ground-water flow directions, was a magnesium sulfate type. Data from this study show that an understanding of hydrologic conditions is important in the interpretation of the water chemistry of wetlands in the study area.

Professional Paper↗

Use of Wetland Habitats by Selected Nongame Water Birds in Maine

We examined the use of 87 palustrine and lacustrine wetlands by nongame water birds in central and eastern Maine using 3,527 h of observation (1,501 visits) made during April-August, 1977-85. Wetlands used by 15 species of water birds were distinguished from those not used, according to 20 habitat features. The species were the common loon (Gavia immer) , pied-billed grebe (Podilymbus podiceps), double-crested cormorant (Phalacrocorax auritus), American bittern (Botaurus lentiginosus), great blue heron (Ardea herodias), green-backed heron (Butorides striatus), osprey (Pandion haliaetus), bald eagle (Haliaeetus leucocephalus), northern harrier (Circus cyaneus), Virgima rail (Rallus limicola), sora (Porzana carolina), spotted sandpiper (Actitis macularia), common snipe (Gallinago gallinago), herring gull (Larus argentatus), and belted kingfisher (Ceryle alcyon). Predictive models of habitat use were developed for each species. Water birds were classified by similarity of habitats used, and species use was contrasted by wetland type. Smaller, isolated wetlands were used by fewer (P < 0.05) species than larger wetlands in complexes; many species had large area-requirements (pied-billed grebe, common loon, herring gull, double-crested cormorant, bald eagle) or preferred to use wetlands near other wetlands (common loon, herring gull, great blue heron, spotted sandpiper, osprey, bald eagle). Wetland area contributed more to overall variation in species richness on wetlands than wetland isolation, although on small wetlands (<3.6 ha) isolation was a better predictor of species richness than wetland area. Wetlands with intermediate amounts (33-66%) of emergent vegetation supported more species (P< 0.05) than closed (>66%) or open (<33%) wetlands. Low pH typified wetlands used by large-bodied piscivores (common loon, cormorant, osprey). Other water birds were associated with more densely vegetated, chemically buffered wetlands. Habitat features associated with wetland use by each waterbird species are reported, as are numerical responses of waterbird populations to wetland features and estimates of annual variation in habitat occupancy. Lacustrine wetlands supported a distinct, low diversity community of water birds, including most fish-eating species. Waterbird diversity at forested palustrine wetlands was intermediate between lacustrine communities and more species-rich assemblages at palustrine emergent and scrub-shrub wetlands. Regional variation in wetland characteristics and water bird use was associated with surficial geology, soils, and management practices. Management for nongame water birds in Maine should consider providing emergent and aquatic-bed vegetation with variable cover-to-water ratios, accommodating species-specific habitat needs, focusing on species of restricted distribution and low abundance, and maintaining wetland complexes. Bird use and habitat information from 87 wetlands and models of habitat selection for each species are provided in appendixes.

Fish and Wildlife Research↗

Nitrogen and phosphorus loading from drained wetlands adjacent to Upper Klamath and Agency lakes, Oregon

Upper Klamath Lake and the connecting Agency Lake constitute a large, shallow lake in south-central Oregon that the historical record indicates has likely been eutrophic since its discovery by non-Native Americans. In recent decades, however, the lake has had annual occurrences of near-monoculture blooms of the blue-green alga Aphanizomenon flos-aquae that are thought to be a result of accelerated eutrophication. In 1988, two sucker species endemic to the lake, the Lost River sucker ( Deltistes luxatus ) and the shortnose sucker ( Chasmistes brevirostris ), were listed as endangered by the U.S. Fish and Wildlife Service, and it has been proposed that their decline is due to the poor water quality associated with extremely long and productive algal blooms. It has also been proposed that the effluent drained from wetlands has contributed to accelerated eutrophication. Since the turn of century, most of the wetlands adjacent to Upper Klamath Lake have been drained for agriculture--cultivation of crops and grazing of cattle. Wetland areas were reclaimed from the lake by building dikes to isolate them from the lake, constructing a series of drainage ditches, and installing pumps to drain the water and maintain a lowered water table. A consequence of lowering the water table is the increased ability of air and oxygenated water to move through the subsurface and facilitate the rapid aerobic decomposition of the peat soils. Nutrients, nitrogen and phosphorus, are then liberated, leach into adjacent ditches, and are subsequently pumped to the lake or its tributaries. The rate of peat decomposition may be related to the time since drainage and the type of agricultural land use. On lands cultivated for crops, farming practices, such as disking and furrowing, could enhance the movement of air and oxygenated water, resulting in a rapid rate of decomposition. In contrast, on grazed lands, the compaction of soils by cattle probably inhibits the movement of air and oxygenated water and results in a slower rate of decomposition relative to drained wetlands used for the cultivation of crops. This report presents the results of a cooperative study between the U.S. Geological Survey and the Bureau of Reclamation whose overall objective was to determine the nutrient loading to Upper Klamath Lake from adjacent drained wetlands. Nutrient loading from drained wetlands was estimated using two independent techniques. The first method involved the measurement of the quantity and quality of water discharged by pumps draining the wetlands. The second method was used to estimate the initial (before drainage) and present-day nutrient mass of the organic soils within the drained wetlands and to calculate the change (or loss) in nutrient mass. In an effort to estimate the nutrient contributions from the water pumped off selected drained wetlands adjacent to Upper Klamath Lake, annual loads and yields of total nitrogen and total phosphorus were estimated from concentration data and the volume of water pumped during the water year. In general, there was little variation among sites or among years in the annual total nitrogen (median load of about 18 tons per year and median yield of about 8 pounds per acre per year) or the annual total phosphorus (median load of about 3 tons per year and median yield of about 2 pounds per acre per year) contributions. The sum of the annual loads of nitrogen and phosphorus calculated for each of the pumping stations in 1995 was 80 tons per year and 15 tons per year, respectively. In 1995, soil-coring activities were undertaken to ascertain the nature and extent of the organic soils in the drained and undrained wetlands. The present-day nutrient mass was calculated for each drained wetland using the nutrient content (concentration) and the present-day peat mass. The initial nutrient mass prior to drainage was estimated for each drained wetland by using the initial nutrient content (assumed to be equal to the nutrient content of the undrained wetlands) and the initial peat mass as determined using the amount of accumulated decomposition residue. The cumulative loss of nutrient mass since drainage was calculated as the change between initial and present-day nutrient mass for each drained area. The cumulative yield of total nitrogen and total phosphorus loss from the organic soils of individual wetlands since drainage ranged from 3,000 to 70,000 pounds per acre and from 0 to 1,300 pounds per acre, respectively. For all the drained wetlands sampled, the cumulative nitrogen and phosphorus loss since drainage totaled 250,000 tons and 4,300 tons, respectively. This represents about 30 percent and 22 percent of the mass of nitrogen and phosphorus, respectively, that initially existed in the organic soils. The loss of nutrients from the drained wetlands is considered to be a maximum estimate of the possible contribution of nutrients to Upper Klamath Lake from the peat soils of the drained wetlands sampled. However, not all the nutrients released by the soils are discharged to the lake. Nutrients lost from the peat soils of the drained wetlands may have been taken up by crops and harvested or consumed by grazing cattle. In addition, nitrogen can be lost to the atmosphere by denitrification and the volatilization of ammonia; phosphorus may be bound to adjacent soil layers by adsorption. The annual nutrient loss for the period 1994&ndash;95 was calculated using a first-order rate law to describe nutrient loss since drainage began. For individual drained wetlands, the yield of nitrogen and phosphorus lost from the organic soils for the period 1994&ndash;95 ranged from 27 to 540 pounds per acre per year and from 0 to 15 pounds per acre per year, respectively. The total mass of nitrogen and phosphorus loss during this period was 3,000 tons per year and 60 tons per year, respectively, for all drained wetlands that were sampled. The yield and mass of nutrient loss determined in this fashion reflect what might be expected on the basis of time-averaged or longterm contributions of nutrients to the lake and do not reflect the specific conditions existing during the period 1994&ndash;95. The results of this study could be useful in helping to prioritize which drained wetlands may provide the greatest benefits with regard to reducing nutrient loads to the lake if restoration or land-use modifications are instituted. Recent acquisition and planned restoration of drained wetland areas at the Wood River and Williamson River North properties may produce significant reduction in the quantity of nutrients released by the decomposition of peat soils of these areas. If the water table rises to predrainage levels, the peats soils may become inundated most of the year, resulting in the continued long-term storage of nutrients within the peat soils by reducing aerobic decomposition. The maximum benefit, in terms of decreasing potential nutrient loss due to peat decomposition, could be the reduction of total nitrogen and total phosphorus loss to about one-half that of the 1994&ndash;95 annual loss estimated for all the drained wetlands sampled for this study.

Oregon↗

Invertebrate egg banks of restored, natural, and drained wetlands in the Prairie Pothole Region of the United States

Analogous to ‘seed banks,’ ‘egg banks’ are important for seasonal succession and maintenance of invertebrate species diversity throughout wet and dry cycles in the prairie pothole region. Further, recruitment of invertebrates from relic egg banks in the sediments and dispersal of eggs into wetlands is believed to be important for reestablishment of invertebrates in recently restored wetlands. Alhough tens-ofthousands of wetlands have been restored in the prairie pothole region of the United States, studies have not been conducted to evaluate the recovery of invertebrate egg banks in restored wetlands. We used taxon richness and abundance as indicators of potential egg bank recovery and compared these parameters in restored wetlands to those of non-drained and drained wetlands with a history of cultivation and also to reference wetlands with no history of cultivation. We found few significant differences among wetland categories within three physiographic regions (Glaciated Plains, Missouri Coteau, and Prairie Coteau). Most statistical comparisons indicated that restored wetlands had invertebrate egg banks similar to reference, nondrained, and drained wetlands. The one exception was drained seasonal wetlands in the Glaciated Plains, which had significantly lower taxon richness and invertebrate abundance than the other wetland categories. Trends did suggest that invertebrate egg bank taxon richness and abundance are increasing in restored seasonal wetlands relative to their drained analogues, whereas a similar trend was not observed for restored semi-permanent wetlands. Although recovery was not related to years since restoration, comparisons of restored wetlands with reference wetlands suggest that recovery potential may be inversely related to the extent of wetland drainage and intensive agriculture that varies spatially in the prairie pothole region. Our research suggests that periodic drawdowns of semi-permanent restored wetlands may be needed to promote production and development of invertebrate egg banks. Inoculation of restored wetlands may also be needed in areas where extensive wetland drainage has resulted in fewer wetland habitats to provide sources of passively dispersed eggs to newly restored wetlands.

Iowa, Minnesota, Montana, North Dakota, South Dako↗

Pesticide concentrations in wetlands on the Lake Traverse Indian Reservation, South and North Dakota, July 2015

During July 2015, water samples were collected from 18 wetlands on the Lake Traverse Indian Reservation in northeastern South Dakota and southeastern North Dakota and analyzed for physical properties and 54 pesticides. This study by the U.S. Geological Survey in cooperation with the Sisseton-Wahpeton Oyate was designed to provide an update on pesticide concentrations of the same 18 wetlands that were sampled for a reconnaissance-level assessment during July 2006. The purpose of this report is to present the results of the assessment of pesticide concentrations in selected Lake Traverse Indian Reservation wetlands during July 2015 and provide a comparison of pesticide concentrations between 2006 and 2015. Of the 54 pesticides that were analyzed for in the samples collected during July 2015, 47 pesticides were not detected in any samples. Seven pesticides—2-chloro-4-isopropylamino-6-amino-s-triazine (CIAT); 2,4–D; acetachlor; atrazine; glyphosate; metolachlor; and prometon—were detected in the 2015 samples with estimated concentrations or concentrations greater than the laboratory reporting level, and most pesticides were detected at low concentrations in only a few samples. Samples from all wetlands contained at least one detected pesticide. The maximum number of pesticides detected in a wetland sample was six, and the median number of pesticides detected was three. The most commonly detected pesticides in the 2015 samples were atrazine and the atrazine degradate CIAT (also known as deethylatrazine), which were detected in 14 and 13 of the wetlands sampled, respectively. Glyphosate was detected in samples from 11 wetlands, and metolachlor was detected in samples from 10 wetlands. The other detected pesticides were 2,4–D (4 wetlands), acetochlor (3 wetlands), and prometon (1 wetland). The same pesticides that were detected in the 2006 samples were detected in the 2015 samples, with the exception of simazine, which was detected only in one sample in 2006. Atrazine and CIAT were the most commonly detected pesticides in both sampling years; however, atrazine and CIAT were detected in fewer wetlands in 2015 (14 and 13 wetlands, respectively) than in 2006 (17 wetlands for both pesticides). The pesticides 2,4–D and prometon also were detected in fewer wetlands in 2015 than 2006, and simazine was only detected in 2006. In contrast, acetochlor, glyphosate, and metolachlor were detected in samples from more wetlands in 2015 than in 2006. In samples from individual wetlands, the number of pesticides detected was similar between 2006 and 2015. At least one pesticide was detected in all wetlands in 2015, and all but one wetland had pesticide detections in 2006. Concentrations of pesticides detected in samples from wetlands were compared to selected water-quality (human-health and aquatic-life) benchmarks. None of the concentrations in either 2006 or 2015 were greater than water-quality benchmarks, with the exception of atrazine. All detections of atrazine in the 2006 and 2015 samples were greater than the acute benchmark of 0.001 microgram per liter (μg/L) for vascular plants. In addition, some concentrations of 2,4–D and atrazine were within an order of magnitude of a water-quality benchmark. The 2,4–D concentrations in the 2015 samples from three wetlands were within an order of magnitude of the U.S. Environmental Protection Agency’s Maximum Contaminant Level of 70 μg/L (that is, sample concentrations were greater than 7.0 μg/L). The maximum dissolved atrazine concentration of 0.185 μg/L in the 2015 samples along with the concentrations in 2006 samples from two wetlands were within an order of magnitude of the acute benchmark of less than 1 μg/L for nonvascular plants (that is, concentrations were greater than 0.1 μg/L).

North Dakota, South Dakota↗

Bathymetry and vegetation in isolated marsh and cypress wetlands in the northern Tampa Bay Area, 2000-2004

Wetland bathymetry and vegetation mapping are two commonly used lines of evidence for assessing the hydrologic and ecologic status of expansive coastal and riverine wetlands. For small isolated freshwater wetlands, however, bathymetric data coupled with vegetation assessments are generally scarce, despite the prevalence of isolated wetlands in many regions of the United States and the recognized importance of topography as a control on inundation patterns and vegetation distribution. In the northern Tampa Bay area of west-central Florida, bathymetry was mapped and vegetation was assessed in five marsh and five cypress wetlands. These 10 isolated wetlands were grouped into three categories based on the effects of ground-water withdrawals from regional municipal well fields: natural (no effect), impaired (drier than natural), and augmented (wetlands with artificially augmented water levels). Delineation of the wetland perimeter was a critical component for estimating wetland-surface area and stored water volume. The wetland perimeter was delineated by the presence of Serenoa repens (the 'palmetto fringe') at 9 of the 10 sites. At the 10th site, where the palmetto fringe was absent, hydric-soils indicators were used to delineate the perimeter. Bathymetric data were collected using one or more techniques, depending on the physical characteristics of each wetland. Wetland stage was measured hourly using continuous stage recorders. Wetland vegetation was assessed semiannually for 2 1/2 years in fixed plots located at three distinct elevations. Vegetation assessments were used to determine the community composition and the relative abundance of obligate, facultative wet, and facultative species at each elevation. Bathymetry maps were generated, and stage-area and stage-volume relations were developed for all 10 wetlands. Bathymetric data sets containing a high density of data points collected at frequent and regular spatial intervals provided the most useful stage-area and stage-volume relations. Bathymetric maps of several wetlands also were generated using a low density of data points collected along transect lines or contour lines. In a comparative analysis of the three mapping approaches, stage-area and stage-volume relations based on transect data alone underestimated (by 50-100 percent over certain ranges of stage) the wetland area and volume compared to results using a high density of data points. Adding data points collected along one elevation contour below the wetland perimeter to the transect data set greatly improved the agreement of the resulting stage-area and stage-volume relations to the high-density mapping approach. Stage-area relations and routinely monitored stage data were used to compare and contrast the average flooded area in a natural marsh and an impaired marsh over a 2-year period. Vegetation assessments used together with flooded-area information provided the potential for extrapolating vegetation results from points or transects to wetlands as a whole. A comparison of the frequency of flooding of different areas of the wetland and the species composition in vegetation plots at different elevations indicated the dependence of vegetation on inundation frequency. Because of the broad tolerances of many wetlands plants to a range of inundation conditions, however, vegetation assessments alone provided less definitive evidence of the hydrologic differences between the two sites, and hydrologic changes occurring during the 2 years, than the flooded-area frequencies. Combining flooded-area frequencies with vegetation assessments could provide a more versatile and insightful approach for determining the ecological status of wetlands than using vegetation and stage data alone. Flooded-area frequencies may further provide a useful approach for assessing the ecological status of wetlands where historical vegetation surveys and stage data are lacking. Comparing the contemporary flooded-area frequencies a

Scientific Investigations Report↗

Characterization of microtopography and its influence on vegetation patterns in created wetlands

Created wetlands are increasingly used to mitigate wetland loss. Thus, identifying wetland creation methods that enhance ecosystem development might increase the likelihood of mitigation success. Noting that the microtopographic variation found in natural wetland settings may not commonly be found in created wetlands, this study explores relationships between induced microtopography, hydrology, and plant species richness/diversity in non-tidal freshwater wetlands, comparing results from two created wetland complexes with those from a mature reference wetland complex in northern Virginia. Elevation, steel rod oxidation depth, and species cover were measured along replicate multiscale (0.5 m-, 1 m-, 2 m-, and 4 m-diameter) tangentially conjoined circular transects in each wetland. Microtopography was surveyed using a total station and results used to derive three roughness indices: tortuosity, limiting slope, and limiting elevation difference. Steel rod oxidation depth was used to estimate water table depth, with data collected four times during the growing season for each study site. Plant species cover was estimated visually in 0.2 m 2 plots surveyed at peak growth and used to assess species richness, diversity, and wetland prevalence index. Differences in each attribute were examined among disked and non-disked created wetlands and compared to a natural wetland as a reference. Disked and non-disked created wetlands differed in microtopography, both in terms of limiting elevation difference and tortuosity. However, both were within the range of microtopography encompassed by natural wetlands. Disked wetlands supported higher plant diversity and species richness than either natural or non-disked wetlands, as well as greater within-site species assemblage variability than non-disked wetlands. Irrespective of creation method, plant diversity in created wetlands was correlated with tortuosity and limiting elevation difference, similar to correlations observed for natural wetlands. Vegetation was more hydrophytic at disked sites than at non-disked sites, and of equivalent wetland indicator status to natural sites, even though all sites appeared comparable in terms of hydrology. Results suggest that disking may enhance vegetation community development, thus better supporting the goals of wetland mitigation.

Virginia↗

Strength in Numbers: Describing the Flooded Area of Isolated Wetlands

Thousands of isolated, freshwater wetlands are scattered across the karst1 landscape of central Florida. Most are small (less than 15 acres), shallow, marsh and cypress wetlands that flood and dry seasonally. Wetland health is threatened when wetland flooding patterns are altered either by human activities, such as land-use change and ground-water pumping, or by changes in climate. Yet the small sizes and vast numbers of isolated wetlands in Florida challenge our efforts to characterize them collectively as a statewide water resource. In the northern Tampa Bay area of west-central Florida alone, water levels are measured monthly in more than 400 wetlands by the Southwest Florida Water Management Distirct (SWFWMD). Many wetlands have over a decade of measurements. The usefulness of long-term monitoring of wetland water levels would greatly increase if it described not just the depth of water at a point in the wetland, but also the amount of the total wetland area that was flooded. Water levels can be used to estimate the flooded area of a wetland if the elevation contours of the wetland bottom are determined by bathymetric mapping. Despite the recognized importance of the flooded area to wetland vegetation, bathymetric maps are not available to describe the flooded areas of even a representative number of Florida's isolated wetlands. Information on the bathymetry of isolated wetlands is rare because it is labor intensive to collect the land-surface elevation data needed to create the maps. Five marshes and five cypress wetlands were studied by the U.S. Geological Survey (USGS) during 2000 to 2004 as part of a large interdisciplinary study of isolated wetlands in central Florida. The wetlands are located either in municipal well fields or on publicly owned lands (fig. 1). The 10 wetlands share similar geology and climate, but differ in their ground-water settings. All have historical water-level data and multiple vegetation surveys. A comprehensive report by Haag and others (2005) documents bathymetric mapping approaches, the frequency of flooding in different areas of the wetlands, and the relation between flooding and vegetation in these wetlands. This fact sheet describes bathymetric mapping approaches and partial results from two natural marshes (Hillsborough River State Park Marsh, and Green Swamp Marsh) and one impaired marsh (W-29 Marsh) that is located on a municipal well field and is affected by ground-water withdrawals. (fig. 1).

Fact Sheet↗

Impacts of water development on aquatic macroinvertebrates, amphibians, and plants in wetlands of a semi-arid landscape

We compared the macroinvertebrate and amphibian communities of 12 excavated and 12 natural wetlands in western North Dakota, USA, to assess the effects of artificially lengthened hydroperiods on the biotic communities of wetlands in this semi-arid region. Excavated wetlands were much deeper and captured greater volumes of water than natural wetlands. Most excavated wetlands maintained water throughout the study period (May to October 1999), whereas most of the natural wetlands were dry by June. Excavated wetlands were largely unvegetated or contained submergent and deep-marsh plant species. The natural wetlands had two well-defined vegetative zones populated by plant species typical of wet meadows and shallow marshes. Excavated wetlands had a richer aquatic macroinvertebrate community that included several predatory taxa not found in natural wetlands. Taxa adapted to the short hydroperiods of seasonal wetlands were largely absent from excavated wetlands. The amphibian community of natural and excavated wetlands included the boreal chorus frog ( Pseudacris maculata ), northern leopard frog ( Rana pipiens ), plains spadefoot ( Scaphiopus bombifrons ), Woodhouse's toad ( Bufo woodhousii woodhousii ), and tiger salamander ( Ambystoma tigrinum ). The plains spadefoot occurred only in natural wetlands while tiger salamanders occurred in all 12 excavated wetlands and only one natural wetland. Boreal chorus frogs and northern leopard frogs were present in both wetland types; however, they successfully reproduced only in wetlands lacking tiger salamanders. Artificially extending the hydroperiod of wetlands by excavation has greatly influenced the composition of native biotic communities adapted to the naturally short hydroperiods of wetlands in this semi-arid region. The compositional change of the biotic communities can be related to hydrological changes and biotic interactions, especially predation related to excavation.

Aquatic Ecosystem Health & Management↗

Dynamic use of wetlands by black ducks and mallards: Evidence against competitive exclusion

The decline of the American black duck ( Anas rubripes ) has been attributed to competition from mallards ( A. platyrhynchos ) that led to exclusive use of fertile wetlands by mallards. Data from annual breeding waterfowl surveys provide instantaneous, single observations of breeding pairs, which are used to estimate breeding population size and evaluate the condition of habitat. Data from these surveys have been used to document habitat use by black ducks and mallards. We used quiet-observation surveys from elevated platforms to study sympatric black ducks and mallards in northern Maine during the breeding season. Our objectives were to document occupancy of wetlands by breeding black ducks and mallards throughout the day during prenesting and early nesting periods to determine whether 1) wetlands were occupied by only a single species, 2) pairs of the same species occupied wetlands throughout the period, and 3) single observations of short duration adequately determine numbers and species using a wetland. We observed ducks at 5-minute intervals from elevated platforms on wetland margins to determine numbers and species of indicated pairs using each wetland over time. We visited 80% of the wetlands ≥2 times, with mean total time per wetland averaging 267 minutes. For each wetland we determined the most frequently observed grouping of black ducks and mallards from all combinations recorded during all intervals (e.g., 1 black duck [BO] pair during 9 intervals; 2 mallard [MA] pairs and 1 BO pair during 22 intervals; 0 pairs during 3 intervals). A single pair, a lone male, or no ducks were recorded during 34% of the 5-minute intervals. For wetlands with >2 hours of observations ( n =65 ), all but 2 were used by ≥2 different combinations of ducks. On most wetlands, the most frequent grouping was observed during <40% of the intervals. To simulate aerial surveys, we randomly selected 1 5-minute interval for each wetland. On average, the number of indicated pairs recorded during random 5-minute intervals was less than half of the total black duck pairs (2.0 vs. 4.4, P = 0.009 ), total mallard pairs (1.1 vs. 2.6, P= 0.0001), and pairs of both species combined (3.2 vs. 7.0, P= 0.0001) determined for each wetland based on total observations. On wetlands used by both species, random counts detected one or both species 49% of the time. Although 53 of the 65 wetlands observed ≥2 hours were used by both species, random visits detected both species on only 27 wetlands. Our data do not support assertions that the mallard has caused the decline of black ducks through interspecific competition for habitat, or that wetlands are occupied continuously by single pairs that aggressively exclude conspecifics. Our data indicated that single, short-duration visits with disturbance to wetlands are unreliable and inappropriate to document seasonal use of wetlands by breeding black ducks and mallards.

Maine↗

Estimating Water Storage Capacity of Existing and Potentially Restorable Wetland Depressions in a Subbasin of the Red River of the North

Executive Summary Concern over flooding along rivers in the Prairie Pothole Region has stimulated interest in developing spatially distributed hydrologic models to simulate the effects of wetland water storage on peak river flows. Such models require spatial data on the storage volume and interception area of existing and restorable wetlands in the watershed of interest. In most cases, information on these model inputs is lacking because resolution of existing topographic maps is inadequate to estimate volume and areas of existing and restorable wetlands. Consequently, most studies have relied on wetland area to volume or interception area relationships to estimate wetland basin storage characteristics by using available surface area data obtained as a product from remotely sensed data (e.g., National Wetlands Inventory). Though application of areal input data to estimate volume and interception areas is widely used, a drawback is that there is little information available to provide guidance regarding the application, limitations, and biases associated with such approaches. Another limitation of previous modeling efforts is that water stored by wetlands within a watershed is treated as a simple lump storage component that is filled prior to routing overflow to a pour point or gaging station. This approach does not account for dynamic wetland processes that influence water stored in prairie wetlands. Further, most models have not considered the influence of human-induced hydrologic changes, such as land use, that greatly influence quantity of surface water inputs and, ultimately, the rate that a wetland basin fills and spills. The goals of this study were to (1) develop and improve methodologies for estimating and spatially depicting wetland storage volumes and interceptions areas and (2) develop models and approaches for estimating/simulating the water storage capacity of potentially restorable and existing wetlands under various restoration, land use, and climatic scenarios. To address these goals, we developed models and approaches to spatially represent storage volumes and interception areas of existing and potentially restorable wetlands in the upper Mustinka subbasin within Grant County, Minn. We then developed and applied a model to simulate wetland water storage increases that would result from restoring 25 and 50 percent of the farmed and drained wetlands in the upper Mustinka subbasin. The model simulations were performed during the growing season (May-October) for relatively wet (1993; 0.79 m of precipitation) and dry (1987; 0.40 m of precipitation) years. Results from the simulations indicated that the 25 percent restoration scenario would increase water storage by 21-24 percent and that a 50 percent scenario would increase storage by 34-38 percent. Additionally, we estimated that wetlands in the subbasin have potential to store 11.57-20.98 percent of the total precipitation that fell over the entire subbasin area (52,758 ha). Our simulation results indicated that there is considerable potential to enhance water storage in the subbasin; however, evaluation and calibration of the model is necessary before simulation results can be applied to management and planning decisions. In this report we present guidance for the development and application of models (e.g., surface area-volume predictive models, hydrology simulation model) to simulate wetland water storage to provide a basis from which to understand and predict the effects of natural or human-induced hydrologic alterations. In developing these approaches, we tried to use simple and widely available input data to simulate wetland hydrology and predict wetland water storage for a specific precipitation event or a series of events. Further, the hydrology simulation model accounted for land use and soil type, which influence surface water inputs to wetlands. Although information presented in this report is specific to the Mustinka subbasin, the approaches

Open-File Report↗

Hydrogeologic characterization and assessment of bioremediation of chlorinated benzenes and benzene in wetland areas, Standard Chlorine of Delaware, Inc. Superfund Site, New Castle County, Delaware, 2009-12

Wetlands at the Standard Chlorine of Delaware, Inc. Superfund Site (SCD) in New Castle County, Delaware, are affected by contamination with chlorobenzenes and benzene from past waste storage and disposal, spills, leaks, and contaminated groundwater discharge. In cooperation with the U.S. Environmental Protection Agency, the U.S. Geological Survey began an investigation in June 2009 to characterize the hydrogeology and geochemistry in the wetlands and assess the feasibility of monitored natural attenuation and enhanced bioremediation as remedial strategies. Groundwater flow in the wetland study area is predominantly vertically upward in the wetland sediments and the underlying aquifer, and groundwater discharge accounts for a minimum of 47 percent of the total discharge for the subwatershed of tidal Red Lion Creek. Thus, groundwater transport of contaminants to surface water could be significant. The major contaminants detected in groundwater in the wetland study area included benzene, monochlorobenzene, and tri- and di-chlorobenzenes. Shallow wetland groundwater in the northwest part of the wetland study area was characterized by high concentrations of total chlorinated benzenes and benzene (maximum about 75,000 micrograms per liter [μg/L]), low pH, and high chloride. In the northeast part of the wetland study area, wetland groundwater had low to moderate concentrations of total chlorinated benzenes and benzene (generally not greater than 10,000 μg/L), moderate pH, and high sulfate concentrations. Concentrations in the groundwater in excess of 1 percent of the solubility of the individual chlorinated benzenes indicate that a contaminant source is present in the wetland sediments as dense nonaqueous phase liquids (DNAPLs). Consistently higher contaminant concentrations in the shallow wetland groundwater than deeper in the wetland sediments or the aquifer also indicate a continued source in the wetland sediments, which could include dissolution of DNAPLs and desorption from the sediments. When highly reducing, methanogenic, or sulfate-reducing conditions existed in the wetland groundwater, molar composition of the volatile organic compounds (VOCs) showed that chlorobenzene and benzene were predominant, indicating biodegradation of the chlorinated benzenes through reductive dechlorination pathways. Temporal changes in redox conditions between 2009 and 2011–12 have shifted the locations in the wetland study area where reductive dechlorination is evident. Microbial community analyses of sediment showed relatively high cell numbers and diversity of populations ( Dehalococcoides , Dehalobacter , Desulfitobacterium , and Geobacter ) that are known to contain species capable of reductive dechlorination, confirming groundwater geochemistry evidence of the occurrence of reductive dechlorination. Natural attenuation was not sufficient, however, to reduce total VOC concentrations along upward groundwater flowpaths in the wetland sediments, most likely due to the additional source of contaminants in the upper sediments. In situ microcosms that were unamended except for the addition of 13 C-labeled contaminants in some treatments, confirmed that the native microbial community was able to biodegrade the higher chlorinated benzenes through reductive dechlorination and that 1,2-dichlorobenzene, chlorobenzene, and benzene could be degraded to carbon dioxide through oxidation pathways. Microcosms that were bioaugmented with the anaerobic dechlorinating consortium WBC-2 and deployed in the wetland sediments showed reductive dechlorination of tri-, di-, and monochlorobenzene, and 13 C-chlorobenzene treatments showed complete degradation of chlorobenzene to carbon dioxide under anaerobic conditions. Experiments with a continuous flow, fixed-film bioreactor seeded with native microorganisms in groundwater from the wetland area showed both aerobic and anaerobic biodegradation of dichlorobenzenes, monochlorobenzene, and benzene, although monochlorobenzene and benzene degradation rates decreased under anaerobic conditions compared to aerobic conditions. In two bioreactors with established biofilms of WBC-2, percent removals of all chlorinated benzene compounds (medians of 86 to 94 percent) under anaerobic conditions were as high as those observed for the bioreactors seeded only with native microorganisms from the site groundwater, and benzene removal was greater in the WBC-2 bioaugmented bioreactors. The high percent removals in the WBC-2 bioreactors without the need for an acclimation period indicates that the same dechlorinators are involved in the chlorinated benzene degradation as those for the chlorinated ethanes and ethenes that the culture was developed to degrade. The ability of the WBC-2 culture to completely reduce the chlorinated benzenes and benzene, even in the presence of high sulfate and sulfide concentrations, is unique for known dechlorinating cultures. The availability of the established culture WBC-2, as well as the ability of the native wetland microbial community to degrade the site contaminants under anaerobic and aerobic conditions, provides flexibility in considering bioremediation options for the wetland areas at SCD.

Delaware↗

Nitrate fate and transport through current and former depressional wetlands in an agricultural landscape, Choptank Watershed, Maryland, United States

Understanding local groundwater hydrology and geochemistry is critical for evaluating the effectiveness of wetlands at mitigating agricultural impacts on surface waters. The effectiveness of depressional wetlands at mitigating nitrate (NO 3 ) transport from fertilized row crops, through groundwater, to local streams was examined in the watershed of the upper Choptank River, a tributary of Chesapeake Bay on the Atlantic Coastal Plain. Hydrologic, geochemical, and water quality data were collected from January of 2008 through December of 2009 from surface waters and networks of piezometers installed in and around current or former depressional wetlands of three major types along a gradient of anthropogenic alteration: (1) natural wetlands with native vegetation (i.e., forested); (2) prior-converted croplands, which are former wetlands located in cultivated fields; and (3) hydrologically restored wetlands, including one wetland restoration and one shallow water management area. These data were collected to estimate the orientation of groundwater flow paths and likely interactions of groundwater containing NO 3 from agricultural sources with reducing conditions associated with wetlands of different types. Natural wetlands were found to have longer periods of soil saturation and reducing conditions conducive to denitrification compared to the other wetland types studied. Because natural wetlands are typically located in groundwater recharge areas along watershed divides, nitrogen (N) from nearby agriculture was not intercepted. However, these wetlands likely improve water quality in adjacent streams via dilution. Soil and geochemical conditions conducive to denitrification were also present in restored wetlands and prior-converted croplands, and substantial losses of agricultural NO 3 were observed in groundwater flowing through these wetland sediments. However, delivery of NO 3 from agricultural areas through groundwater to these wetlands resulting in opportunities for denitrification were limited, particularly where reducing conditions did not extend throughout the entire thickness of the surficial aquifer allowing NO 3 to pass conservatively beneath a wetland along deeper groundwater flow paths. The complexity of N fate and transport associated with depressional wetlands complicates the understanding of their importance to water quality in adjacent streams. Although depressional wetlands often contribute low NO 3 water to local streams, their effectiveness as landscape sinks, for N from adjacent agriculture varies with natural conditions, such as the thickness of the aquifer and the extent of reducing conditions. Measurement of such natural geologic, hydrologic, and geochemical conditions are therefore fundamental to understanding N mitigation in individual wetlands.

Maryl↗

Spatiotemporal patterns of wetland occurrence in the prairie pothole region of eastern South Dakota

We evaluated changes in wetland abundance, size, and classification between average (19791986) and above-average (19951999) precipitation periods for two physiographic regions in eastern South Dakota. Temporal shifts in wetland numbers, area, and class varied by topographic location. In high wetland density areas (> 8 wetlands/100 ha), our data suggests that larger, semipermanent wetlands expanded and absorbed nearby wetland basins into their margins, resulting in a net "loss" or disappearance of temporary and seasonal wetlands in above-average water condition years. "Losses" described here are not deemed permanent as in cases of draining or filling, and wetlands may re-form when water conditions return to normal. Nevertheless, temporary disappearance of smaller more isolated wetlands may have implications for breeding waterfowl and other fauna. Percent change of semipermanent basin numbers was positively correlated with wetland density, whereas the opposite was true for seasonal wetlands. Loss of temporary wetlands was correlated with wetland aggregation within the sample area. However, in low wetland density areas, the number and size of seasonal and temporary wetlands generally increased following above-average precipitation. We suggest that wetlands' spatial arrangement be considered along with traditional wetland quantification techniques to better account for shifts in wetland habitat in dry versus wet years. ?? 2009 The Society of Wetland Scientists.

Wetlands↗

Ecosystem services: developing sustainable management paradigms based on wetland functions and processes

In the late nineteenth century and twentieth century, there was considerable interest and activity to develop the United States for agricultural, mining, and many other purposes to improve the quality of human life standards and prosperity. Most of the work to support this development was focused along disciplinary lines with little attention focused on ecosystem service trade-offs or synergisms, especially those that transcended boundaries of scientific disciplines and specific interest groups. Concurrently, human population size has increased substantially and its use of ecosystem services has increased more than five-fold over just the past century. Consequently, the contemporary landscape has been highly modified for human use, leaving behind a fragmented landscape where basic ecosystem functions and processes have been broadly altered. Over this period, climate change also interacted with other anthropogenic effects, resulting in modern environmental problems having a complexity that is without historical precedent. The challenge before the scientific community is to develop new science paradigms that integrate relevant scientific disciplines to properly frame and evaluate modern environmental problems in a systems-type approach to better inform the decision-making process. Wetland science is a relatively new discipline that grew out of the conservation movement of the early twentieth century. In the United States, most of the conservation attention in the earlier days was on wildlife, but a growing human awareness of the importance of the environment led to the passage of the National Environmental Policy Act in 1969. Concurrently, there was a broadening interest in conservation science, and the scientific study of wetlands gradually gained acceptance as a scientific discipline. Pioneering wetland scientists became formally organized when they formed The Society of Wetland Scientists in 1980 and established a publication outlet to share wetland research findings. In comparison to older and more traditional scientific disciplines, the wetland sciences may be better equipped to tackle today’s complex problems. Since its emergence as a scientific discipline, the study of wetlands has frequently required interdisciplinary and integrated approaches. This interdisciplinary/integrated approach is largely the result of the fact that wetlands cannot be studied in isolation of upland areas that contribute surface and subsurface water, solutes, sediments, and nutrients into wetland basins. However, challenges still remain in thoroughly integrating the wetland sciences with scientific disciplines involved in upland studies, especially those involved with agriculture, development, and other land-conversion activities that influence wetland hydrology, chemistry, and sedimentation. One way to facilitate this integration is to develop an understanding of how human activities affect wetland ecosystem services, especially the trade-offs and synergisms that occur when land-use changes are made. Used in this context, an understanding of the real costs of managing for a particular ecosystem service or groups of services can be determined and quantified in terms of reduced delivery of other services and in overall sustainability of the wetland and the landscapes that support them. In this chapter, we discuss some of the more salient aspects of a few common wetland types to give the reader some background on the diversity of functions that wetlands perform and the specific ecosystem services they provide to society. Wetlands are among the most complex ecosystems on the planet, and it is often difficult to communicate to a diverse public all of the positive services wetlands provide to mankind. Our goal is to help the reader develop an understanding that management options can be approached as societal choices where decisions can be made within a spatial and temporal context to identify trade-offs, synergies, and effects on long-term sustainability of wetland ecosystems. This will be especially relevant as we move into alternate climate futures where our portfolio of management options for mitigating damage to ecosystem function or detrimental cascading effects must be diverse and effective.

Book chapter↗

Quantifying hydrologic controls on local- and landscape-scale indicators of coastal wetland loss

Background and Aims Coastal wetlands have evolved to withstand stressful abiotic conditions through the maintenance of hydrologic feedbacks among vegetation production and flooding. However, disruption of these feedbacks can lead to ecosystem collapse, or a regime shift from vegetated wetland to open water. To prevent the loss of critical coastal wetland habitat, we must improve understanding of the abiotic-biotic linkages among flooding and wetland stability. The aim of this research was to identify characteristic landscape patterns and thresholds of wetland degradation that can be used to identify areas of vulnerability, reduce flooding threats, and improve habitat quality. Methods We measured local- and landscape-scale responses of coastal wetland vegetation to flooding stress in healthy and degrading coastal wetlands. We hypothesized that conversion of Spartina patens wetlands to open water could be defined by a distinct change in landscape configuration pattern, and that this change would occur at a discrete elevation threshold. Key Results Despite similarities in total land and water cover, we observed differences in the landscape configuration of vegetated and open water pixels in healthy and degrading wetlands. Healthy wetlands were more aggregated, and degrading wetlands were more fragmented. Generally, greater aggregation was associated with higher wetland elevation and better drainage, compared to fragmented wetlands, which had lower elevation and poor drainage. The relationship between vegetation cover and elevation was non-linear, and the conversion from vegetated wetland to open water occurred beyond an elevation threshold of hydrologic stress. Conclusions The elevation threshold defined a transition zone where healthy, aggregated, wetland converted to a degrading, fragmented, wetland beyond an elevation threshold of 0.09 m NAVD88 (0.27 m MSL), and complete conversion to open water occurred beyond 0.03 m NAVD88 (0.21 m MSL). This work illustrates that changes in landscape configuration can be used as an indicator of wetland loss, with specific elevation thresholds to inform restoration and conservation planning to maximize wetland stability in anticipation of flooding threats.

Louisiana, Texas↗

Using stable isotopes of water and strontium to investigate the hydrology of a natural and a constructed wetland

Wetlands cannot exist without water, but wetland hydrology is difficult to characterize. As a result, compensatory wetland mitigation often only assumes the proper hydrology has been created. In this study, water sources and mass transfer processes in a natural and constructed wetland complex were investigated using isotopes of water and strontium. Water isotope profiles in the saturated zone revealed that the natural wetland and one site in the constructed wetland were primarily fed by ground water; profiles in another constructed wetland site showed recent rain was the predominant source of water in the root zone. Water isotopes in the capillary fringe indicated that the residence time for rain is less in the natural wetland than in the constructed wetland, thus transpiration (an important water sink) was greater in the natural wetland. Strontium isotopes showed a systematic difference between the natural and constructed wetlands that we attribute to the presence or absence of peat. In the peat‐rich natural wetland, δ 87 Sr in the pore water increased along the flowline due to preferential weathering of minerals containing radiogenic Sr in response to elevated Fe concentrations in the water. In the constructed wetland, where peat thickness was thin and Fe concentrations in water were negligible, δ 87 Sr did not increase along the flowline. The source of the peat (on‐site or off‐site derived) applied in the constructed wetland controlled the δ 87 Sr at the top of the profile, but the effects were restricted by strong cation exchange in the underlying fluvial sediments. Based on the results of this study, neither constructed wetland site duplicated the water source and weathering environment of the adjoining natural wetland. Moreover, stable isotopes were shown to be effective tools for investigating wetlands and gaining insight not easily obtained using non‐isotopic techniques. These tools have potential widespread application to wetlands that have distinct isotopic endmember sources.

Ground Water↗

Wetland and water supply

The Geological Survey has received numerous inquiries about the effects of proposed changes in the wetland environment. The nature of the inquiries suggests a general confusion in the public mind as to wetland values and an increasing concern by the public with the need for facts as a basis for sound decisions when public action is required. Perhaps the largest gap in our knowledge is in regard to the role played by the wetland in the natural water scheme. Specialists in such fields as agriculture and conservation have studied the wetland in relation to its special uses and values for farming and as a habitat for fish and wildlife. However, except as studied incidentally by these specialists, the role of the wetland with respect to water has been largely neglected. This facet of the wetland problem is of direct concern to the Geological Survey. We commonly speak of water in terms of its place in the hydrologic environment---as, for example, surface water or ground water. These terms imply that water can be neatly pigeonholed. With respect to the wetland environment nothing can be further from the truth. In fact, one objective of this discussion is to demonstrate that for the wetland environment surface water, ground water, and soil water cannot be separated realistically, but are closely interrelated and must be studied together. It should be noted that this statement holds true for the hydrologic environment in general, and that the wetland environment is by no means unique in this respect. Our second and principal objective is to identify some of the problems that must be studied in order to clarify the role of the wetland in relation to water supply. We have chosen to approach these objectives by briefly describing one area for which we have some information, and by using this example to point out some of the problems that need study. First, however, let us define what we, as geohydrologists, mean by wetland and briefly consider wetland classifications. For our purpose wetlands are land areas that are covered with shallow water or subjected to intermittent flooding and subsequent slow drainage, and which generally are characterized by an accumulation of organic matter hereafter termed swamp deposits.' These wetlands may be classified in a number of different ways depending on the purpose of the classifier. For example, the Fish and Wildlife Service classifies wetlands into 20 different types based on water quality (fresh or salty), drainage, and vegetation. At the risk of some oversimplification we might consider 4 types of wetland from the standpoint of hydrology: (1) fresh-water swamps in which the swamp deposits are underlain by glacial till or bedrock; (2)fresh-water swamps in which the swamp deposits are underlain by marine or lacustrine clay and silt; (3) fresh-water swamps in which the swamp deposits are underlain by glacial outwash or alluvium consisting mostly of sand or sand and gravel; and (4) salt .marshes and salt meadows. The three fresh-water types of wetland are of interest with respect to water supply, and of these, the type in which swamp deposits are underlain by glacial outwash is of particular interest in New England. In the Ipswich River basin above the Geological Survey gaging station at South Middleton, Mass., is an area of 44 square miles which forms the headwaters section of the basin. The relief of the area is low. About half the area consists of hills mostly underlain by bedrock but mantled by a thin layer of glacial till. The other half consists Of lowlands---including swamps, low terraces and plains---underlain by glacial outwash, Swampland, used hereafter as a synonym for wetland, forms about a fourth of the area. Some of the swamps occupy depressions in the till blanket and are situated at somewhat higher levels than the lowlands. The largest swamps, however, border the Ipswich River and its tributaries. Here the swamp deposits, which consist of muck and peat mixed with s

Circular↗