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Reductions in groundwater withdrawals from Northern Tampa Bay well fields were initiated in mid-2002 to improve the hydrologic condition of wetlands in these areas by allowing surface and groundwater levels to recover to previously higher levels. Following these reductions, water levels at some long-term wetland monitoring sites have recovered, while others have not recovered as expected. To understand why water levels for some wetlands have not increased, nine wetlands with varying impacts from well field pumping were examined based on four factors known to influence the hydrologic condition of wetlands in west-central Florida. These factors are the level of the potentiometric surface of the Upper Floridan aquifer underlying the wetland, recent karst activity near and beneath the wetland, permeability of the underlying sediments, and the topographic position of the wetland in the landscape. The combination of two factors, the presence of recent karst activity below or near the wetlands and the depth to the potentiometric surface of the Upper Floridan aquifer below the wetlands, had the most influence on the hydrologic recovery of the study wetlands. The study wetlands are located in an area where numerous localized surface or buried depressions (karst features or sinkholes) are common throughout the mantled karst landscape, which increases the hydrologic connection between the wetlands and the underlying aquifers. Breaches or breaks in the underlying sediments or in the intermediate confining unit due to recent karst subsidence activity act as pathways for downward leakage. For the study wetlands, the leakage potential increased when the vertical separation between the potentiometric surface of the Upper Floridan aquifer and the wetland-bottom elevation (a surrogate for the wetland water level) increased. The increase in the potentiometric surface of the Upper Floridan aquifer below the wetland was the primary factor influencing the hydrologic recovery of the study wetlands, even in areas affected by karst subsidence. For one of the study wetlands influenced by karst subsidence (S-44 Cypress at Starkey well field), the potentiometric surface of the Upper Floridan aquifer increased to the level of the wetland-bottom elevation following the reductions in groundwater withdrawals. Despite the karst subsidence in the wetland, having the level of the potentiometric surface just below the wetland bottom limited the downward leakage potential and resulted in an increase in the flooded area and duration of the wetland hydroperiod. In contrast, two study wetlands affected by karst subsidence (W-12 Cypress and W-16 Marsh at Cypress Creek) remained mostly dry during the period of groundwater withdrawal reductions, even though the median elevation of the potentiometric surface of the Upper Floridan aquifer rose about 5 feet in this area of the well field. These wetlands are located in an area of the well field where large groundwater withdrawals are concentrated, and during the last 20 years (1989-2009) the wetlands were inundated only during periods of extreme rainfall. During these brief inundation periods, the wetland water levels receded after 1 to 2 months, much more rapidly than wetlands located in areas without karst subsidence or concentrated pumping, indicating the increased leakage between the wetlands and underlying aquifers. Because of this interconnection, water levels in these wetlands and others impacted by karst subsidence in this region will not recover if the potentiometric surface of the Upper Floridan aquifer remains at its current (2009) elevation (median distance of about 10 feet below the wetland-bottom elevation). Low permeability sediments and the absence of karst features underlying the wetlands had a positive influence on the wetland recovery following the reductions in groundwater withdrawals. In these settings, intact low permeability subsurface layers help maintain water within and beneath the wetland, and limit the downward leakage potential to the Upper Floridan aquifer. For wetlands in these settings, the increase in potentiometric surface of the Upper Floridan aquifer below the study wetland-bottom elevations resulted in an increase in the flooded area and the duration of the wetland hydroperiod. Although of less importance than the other three factors, a low-lying topographical position benefited the hydrologic condition of several of the study wetlands (S-68 Cypress and W-12 Cypress) both before and after the reductions in groundwater withdrawals. Compared to wetlands in a higher topographical position, those in a lower position had longer hydroperiods because of their greater ability to receive more runoff from higher elevation wetlands and to establish surface-water connections to other isolated wetlands and surface-water bodies through low-lying surface-water channels during wet conditions. In addition, wetlands in low-lying areas benefited from groundwater inflow when groundwater levels were higher than wetland water levels.
Comparing altered wetlands to natural wetlands in the same region improves the ability to interpret the gradual and cumulative effects of human development on freshwater wetlands. Hydrologic differences require explicit attention because they affect nearly all wetland functions and are an overriding influence on other comparisons involving wetland water quality and ecology. This study adopts several new approaches to quantify wetland hydrologic characteristics and then describes and compares the hydrology, water quality, and ecology of 10 isolated freshwater marsh and cypress wetlands in the mantled karst landscape of central Florida. Four of the wetlands are natural, and the other six have water levels indirectly lowered by ground-water withdrawals on municipally owned well fields. For several decades, the water levels in four of these altered wetlands have been raised by adding ground water in a mitigation process called augmentation. The two wetlands left unaugmented were impaired because their water levels were lowered. Multifaceted comparisons between the altered and natural wetlands are used to examine differences between marshes and cypress wetlands and to describe the effects of augmentation practices on the wetland ecosystems. In the karstic geologic setting, both natural and altered wetlands predominantly lost water to the surficial aquifer. Water leaking out of the wetlands created water-table mounds below the wetlands. The smallest mounds radiated only slightly beyond the vegetated area of the wetlands. The largest and steepest mounds occurred below two of the augmented wetlands. There, rapid leakage rates regenerated a largely absent surficial aquifer and mounds encompassed areas 7-8 times as large as the wetlands. Wetland leakage rates, estimated using a daily water-budget analysis applied over multiple years and normalized as inches per day, varied thirtyfold from the slowest leaking natural wetland to the fastest leaking augmented wetland. Leakage rates increased as the size of the flooded area decreased and as the downward head difference between the wetland and the underlying Upper Floridan aquifer increased. Allowing one of the augmented wetlands to dry up for about 2.5 months in the spring of 2004, and then refilling it, generated a net savings of augmentation water despite the amount of water required to recreate the water-table mound beneath the wetland. Runoff from the surrounding uplands was an important component of the water budget in all of the unaugmented wetlands and two of the augmented wetlands. At a minimum, runoff contributed from half (45 percent) to twice (182 percent) as much water as direct rainfall at individual wetlands. Wetland flooded areas, derived using wetland water levels and bathymetric data and presented as a percentage of total wetland area, were used to compare and contrast hydrologic conditions among the 10 wetlands. The percentages of the natural wetland areas that flooded during the study were comparable, despite differences in the sizes of the wetlands. The percent flooded area in each wetland was calculated daily over the study period and monthly for up to 16 years using historical water-level data. Historical flooding in the natural wetlands spanned a greater range in area and had more pronounced seasonality than historical flooding at either the impaired or augmented wetlands. Flooding in the impaired and natural wetlands was similar, however, during 2 years of the study with substantially reduced well-field pumping and above average rainfall. Comparisons indicated several hydrologic differences between the marsh and cypress wetlands in this study. The natural and impaired marshes leaked at about half the rate of the natural and impaired cypress wetlands, and the marshes collectively were underlain by geologic material with lower vertical leakance values than the cypress wetlands. The natural marshes had higher evaporation rates compared to cypress
The source of water is important to the ecological function of Missouri River flood-plain wetlands. There are four potential sources of water to flood-plain wetlands: direct flow from the river channel during high river stage, ground-water movement into the wetlands in response to river-stage changes and aquifer recharge, direct precipitation, and runoff from surrounding uplands. Concurrent measurements of river stage, rainfall, ground-water level, and wetland stage were compared for two Missouri River flood-plain wetlands located near Rocheport, Missouri, to characterize the spatial and temporal relations between river stage, rainfall, ground-water levels and wetland stage, determine the source of water to each wetland, and compare measured and estimated stage and ground-water levels at each site. The two sites chosen for this study were wetland NC-5, a non-connected, 50 feet deep scour constantly filled with water, formed during the flood of 1993, and wetland TC-1, a shallow, temporary wetland intermittently filled with water. Because these two wetlands bracket a range of wetland types of the Missouri River flood plain, the responses of other Missouri River wetlands to changes in river stage, rainfall, and runoff should be similar to the responses exhibited by wetlands NC-5 and TC-1. For wetlands deep enough to intersect the ground-water table in the alluvial aquifer, such as wetland NC-5, the ground-water response factor can estimate flood-plain wetland stage changes in response to known river-stage changes. Measured maximum stage and ground-water-level changes at NC-5 fall within the range of estimated changes using the ground-water response factor. Measured maximum ground-water-level changes at TC-1 are similar to, but consistently greater than the estimated values, and are most likely the result of alluvial deposits with higher than average hydraulic conductivity located between wetland TC-1 and the Missouri River. Similarity between ground-water level and stage hydrography at wetland NC-5 indicate that ground-water-level fluctuations caused by river-stage changes control the stage of wetland NC-5. A 2-day lag time exists between river-stage changes and ground water and stage changes at wetland NC-5. The lack of a measurable response of wetland NC-5 stage to rainfall indicate that rainfall is not a large source of water to wetland NC-5. Stage in wetland TC-1 only increased at high river stage in June and July 1999, and from runoff caused by local rainfall during the winter. The 2-day lag time between peak stages at wetland TC-1 and peak Missouri River stages compared to the 1-day lag time between Missouri River stage and ground-water peaks at wetland TC-1 indicates ground-water flow does not directly affect wetland stage at TC-1, but surface-water flow does affect wetland stage at TC-1 during high river stage. Comparing wetland TC-1 stage to potential water sources indicates the most likely explanation for the rise in stage at wetland TC-1 is surface runoff supplied via seepage through the levees and upward flow of ground water through alluvial deposits of higher hydraulic conductivity during high river stage. The rate of decrease in wetland TC-1 stage was limited by the rate at which ground-water level decreased. Stage response to rainfall at wetland TC-1 during the winter months and no response to greater rainfall amounts during spring and summer months indicate that evapotranspiration may limit the affect of rainfall on stage at wetland TC-1 during the growing season.
Freshwater wetlands are an integral part of central Florida, where thousands are distributed across the landscape. However, their relatively small size and vast numbers challenge efforts to characterize them collectively as a statewide water resource. Wetlands are a dominant landscape feature in Florida; in 1996, an estimated 11.4 million acres of wetlands occupied 29 percent of the area of the State. Wetlands represent a greater percentage of the land surface in Florida than in any other state in the conterminous United States. Statewide, 90 percent of the total wetland area is freshwater wetlands and 10 percent is coastal wetlands. About 55 percent of the freshwater wetlands in Florida are forested, 25 percent are marshes and emergent wetlands, 18 percent are scrub-shrub wetlands, and the remaining 2 percent are freshwater ponds. Freshwater wetlands are distributed differently in central Florida than in other parts of the State. In the panhandle and in northern Florida, there are fewer isolated wetlands than in the central and southern parts of the State, and few of those wetlands are affected by activities such as groundwater withdrawals. In southern Florida, the vast wetlands of the Everglades and the Big Cypress Swamp blanket the landscape and form contiguous shallow expanses of water, which often exhibit slow but continuous flow toward the southwestern coast. In contrast, the wetlands of central Florida are relatively small, numerous, mostly isolated, and widely distributed. In many places, wetlands are flanked by uplands, generating a mosaic of contrasting environments-unique wildlife habitat often adjacent to dense human development. As the population of central Florida increases, the number of residents living near wetlands also increases. Living in close proximity to wetlands provides many Floridians with an increased awareness of nature and an opportunity to examine the relationship between people and wetlands. Specifically, these residents can observe how wetlands are affected by human activities. Freshwater wetlands are unique and complex ecosystems defined by characteristic properties. Wetlands usually have standing water during at least part of the year, although water depths can vary from a few inches to as much as several feet from one wetland to another. The hydrologic behavior of wetlands is influenced by drainage basin characteristics, as well as by natural variations in climate. Wetlands in central Florida (especially forested wetlands) often have acidic waters that are darkly stained from organic substances released by decomposing leaves and other plant material. Wetlands are characterized by biogeochemical cycles in which vital elements such as carbon, nitrogen, phosphorus, and others are transformed as they move between wetland soils and sediments, the open water, and the atmosphere. Wetlands are populated with plants that can thrive under conditions of saturated soils and low dissolved-oxygen concentrations. The bottoms of many wetlands, especially marshes, are covered with decayed plant material that can accumulate over time to form brown peat or black muck soils. Wetlands are inhabited by animals that need standing water to complete some or all of their life cycles, and they also provide periodic food, water, and shelter for many other animals that spend most of their lives on dry land. The complex and interrelated components of wetlands directly affect one another and there are numerous feedback mechanisms.
The extent and duration of the flooded area were compared in two reference wetlands and nine wetlands in well fields in the northern Tampa Bay region, Florida, to determine whether reductions in well-field groundwater-withdrawal rates resulted in increases in wetland flooded area. Flooded area, expressed as a percentage of the total wetland area, was used to provide a quantitative and comparable line of evidence for describing the hydrologic conditions in isolated wetlands of different sizes and locations. Flooded-area frequencies were quantified for periods with different groundwater-withdrawal rates that bracket reductions in well-field groundwater withdrawals. Four-year pre-reduction and post-reduction periods were applied to wetlands in Cypress Creek and Cross Bar Ranch well fields, whereas 3-year periods were applied to wetlands in Starkey well field. The reduced groundwater-withdrawal rates in Cypress Creek and Cross Bar Ranch well fields were 30 and 24 percent less than their pre-reduction rates, respectively. The reduced groundwater-withdrawal rate in the Starkey well field was 64 percent less. Total rainfall amounts were similar (differed by 1 percent or less) in the respective pre- and post-reduction periods, which minimized the effect that rainfall variability had on the analysis. Flooded-area patterns at the reference wetlands, which were unaffected by groundwater withdrawals, were similar during pre- and post-reduction periods, indicating that short-term rainfall variability within those periods did not affect the longer-term patterns of flooded-area extent and duration. One well-field wetland (W-33) experienced an extent and duration of flooded area similar to that observed at the reference wetlands. About 61–100 percent of W-33 was flooded 41 percent of the time during the pre-reduction period and 45 percent of the time in the post-reduction period. The amount of time the wetland was dry decreased from 40 percent in the pre-reduction period to 26 percent in the post-reduction period. The median elevation of the potentiometric surface of the Upper Floridan aquifer increased beneath this wetland by about 4 feet after reductions in groundwater-withdrawal rates. Four well-field wetlands (W-17, W-56, Starkey N, and Starkey 108) had substantial increases in the extent and duration of the flooded area after reductions in groundwater-withdrawal rates. These four wetlands were dry for 25–45 percent less time during the post-reduction period, when the pre- and post-reduction periods were compared. Up to 20 percent of W-56 was flooded more than three times as long after reductions in groundwater-withdrawal rates. All parts of W-17 were flooded for as much as 10 percent of the time in the post-reduction period. Parts of Starkey N and Starkey 108 were flooded for more than twice as much time after reductions in groundwater-withdrawal rates. The median elevation of the potentiometric surface of the Upper Floridan aquifer was about 4–8 feet higher beneath W-17 and W-56 after reductions in groundwater-withdrawal rates, whereas the median elevation increased beneath Starkey N and Starkey 108 by about 4 feet after reductions in groundwater-withdrawal rates. Four other well-field wetlands (W-41, Q-1, Starkey D, and Starkey E) were mostly dry before reductions in groundwater-withdrawal rates and remained mostly dry after the reductions. W-41 was dry 23 percent less time in the post-reduction period, but most of the increase in flooded area was confined to less than 20 percent of the total wetland area. Q-1 was dry for only 12 percent less time in the post-reduction period. The median elevation of the potentiometric surface of the Upper Floridan aquifer increased beneath W-41 by about 5 feet and beneath Q-1 by about 2 feet after reductions in groundwater-withdrawal rates. The extent and duration of the flooded area was unchanged at Starkey D when the post-reduction period was compared to the pre-reduction period. At Starkey E the extent of the flooded area decreased slightly during the post-reduction period. Even though groundwater-withdrawal rates at Starkey well field decreased in the post-reduction period, the median elevation of the potentiometric surface of the Upper Floridan aquifer did not increase beneath Starkey D and Starkey E after reductions in groundwater-withdrawal rates from this well field. Factors such as the high permeability of sediments beneath the wetlands, subsidence, or sinkholes could contribute to continued downward leakage from these four wetlands and the lack of recovery of wetland water levels. Plant zonation in the two reference wetlands and the nine well-field wetlands was described using data collected by the Southwest Florida Water Management District and Tampa Bay Water, a regional utility, in their Wetland Assessment Procedure (WAP). A scoring system was used to describe the distribution of trees, woody shrubs, and groundcover in zones at three depths along a transect line through each wetland. The locations of the three zones were identified on contoured wetland bathymetry maps and were discussed in relation to areas of the wetland bottom that flooded for different periods of time during the study. Higher scores are characteristic of a greater extent and duration of wetland flooded area. WAP scores and weighted average scores for wetland vegetation were generally consistent with the results of the flooded area analysis. The WAP scores and weighted average scores were higher overall and did not decline with time at four wetlands in well fields (W-33, W-56, Starkey N, and Starkey 108) during the years following reductions in groundwater-withdrawal rates. These four wetlands also had increases in the extent and duration of the flooded area during the post-reduction period. Scores for trees were more consistent than scores for shrubs and groundcover. WAP scores remained relatively low or generally declined at five well-field wetlands (Q-1, W-17, W-41, Starkey D, and Starkey E) during the years following reductions in groundwater-withdrawal rates, and weighted average scores either declined over time or remained low. These five wetlands either did not have an increase in the extent and duration of the flooded area, or if there was an increase, it was small.
This 18-month field study addresses the seasonal and spatial patterns and processes controlling methylmercury (MeHg) production, bioaccumulation, and export from natural and agricultural wetlands of the Yolo Bypass Wildlife Area (YBWA). The data were collected in conjuntion with a Proposition 40 grant from the State Water Resources Control Board in support of the development of Best Management Practices (BMP's) for reducing MeHg loading from agricultural lands in the wetland-dominated Yolo Bypass to the Sacramento-San Joaquin River Delta. The four managemenr-based questions addressed in this study were: 1. Is there a different among agricultural and managfed wetland types in terms of Me Hg dynamic (production, degradation, bioaccumulation, or export)? 2. Does water residence time influence MeHg dynamics? 3. Does the application of sulfate-based fertilizer impact MeHg production rates? 4. Does the presence (or absence) of vegetation influence MeHg production rates? Measurements of MeHg concentrations in sediment, water, and biota (plants, invertebrates, and fish) were made to assess management-level patterns in five wetland types, which included three type of shallowly-flooded agricultural wetlands (white rice, wild rice, and fallow) and two types of managed wetlands (permanently and seasonally flooded). To strengthen our understanding of the processes underlying the seasonal and spatial patterns of MeHg cycling, additional exploratory factors were measured including ancillary sediment and water quality parameters, stable isotope fractionation (oxygen, sulfur, carbon, and nitrogen), photodemethylation rates, and daily-integrated hydrologic budgets. Samples and field data were collected from May 2007 to July 2008, and nearly all sample analyses were completed by September 2008 as per the Quality Assurance Program Plan (QAPP) requirements. Although wetland type was a major factor that drove the study design, within-field hydrology also proved to be an important factor controlling aqueous MeHg and total mercury (THg) concentrations and export. Overall, agricultural wetlands exhibited higher MeHg concentrations in overlying water, sediment, and biota than did managed seasonal and permanent wetlands. This appears to be partly due to higher rates of sediment in microbial production of MeHg on agricultural wetlands during the fall through spring period. Both sulfate- and iron-reducing bacteria have been implicated in the MeHg production process, and both were demonstrably active in all wetlands studied; however, sulfate-reducing bacteria were not stimulated by the addition of sulfate-based fertilizer to agricultural wetlands, suggesting that easily-degraded (labile) organic matter, rather than sulfate, was limiting their activity in these field types. The data suggest that agriculturally-managed soils promoted MeHg production through 1) enhanced microbial activity via higher temperatures and larger pools of labile carbon, and 2) enhanced pools of microbially available inorganic divalent mercury (Hg(II)) resulting from a decrease in reduced-sulfur, solid-phase minerals under oxic or only mildly reducing conditions. MeHg mass balances were assessed by comparing filed-specific MeHg loads for inlets vs. outlet flows. The overall mass balance for MeHg in surface water during the summer irrigation period (June - September 2007) indicated little to no net MeHg export from the six agricultural wetlands taken as a whole. Of the six agricultural wetlands, there was net overall MeHg export from two fields (one fallow and one white rice) during August, and from four of the six fields (one fallow, one white rice, and two wild rice) during September) Over the entire summer irrigation period, two of the fields (one fallow and one wild rive) showed net MeHg export, and the other four fields showed wither net import or no significant change. Rates of measured photomethylation and exchange between sediment and water pools suggest that both processes may be responsible for the lack of MeHg export. Despite significant differences during winter months between fields in surface water concentrations of MeHg, MeHg loads were not calculated in mid-winter because flood waters had overtopped field boundaries and field fidelity could not be established. During the summer 2007 irrigation season, surface water out-flows from agricultural wetlands were 9%-36% of inlet flows, and evaporation rates explained most of this water loss, with infiltration likely accounting for the remainder. Unfiltered aqueous MeHg concentrations increased from <1 ng L -1 in source waters to up to 10 ng L -1 in agricultural wetland drains during the summer irrigation period. Increases in solute concentration caused by evapoconcentration were estimated by determining concentration factors (outflow/inflow) for chloride (a conservative dissolved constituent) and by measuring oxygen isotope ratios ( 18 O/ 16 O, expressed as δ 18 O) in water. Increases in MeHg concentration from inflows-to-outflows exceeded those caused by evapoconcentration on several fields during the summer irrigation season. This was especially true when initial surface water MeHg concentrations were low, as seen in the southern block of fields receiving irrigation water directly from the Toe Drain. The northern block of fields received irrigation water from Greens Lake, which included Toe Drain water plus recirculated drain water from other agricultural fields within the Yolo Bypass and west of the Yolo Bypass; as such, the northern fields showed a smaller percentage increase in MeHg concentration because initial MeHg concentrations in surface water inflows were greater than in inputs to the southern fields. Mercury concentrations in fish were greater in agricultural wetlands white rice and wild rice) than in the two permanently flooded wetlands. Additionally, Hg concentrations in biota showed a general increase from inlets to outlets withing agricultural wetlands, but not within permanent wetlands. This was particular evident in white rice fields where caged western mosquitofish at the outlets had Hg concentrations that were more than 4 times higher than in caged fish held at the inlets. Similar spatial patterns in Hg bioaccumulation in agricultural and permanent wetlands were seen for wild populations of western mosquitofish and Mississippi silversides. In contrast to fish, invertebrates, such as water-boatman (Corixidae) and back swimmers (Notonectidae), had greater Hg concentrations in permanent wetlands than in tempoarirly flooded agricultural wetlands, Fish THg concentrations were weakly correlated with water MeHg,a and not correlated with sediment MeHg. In contrast, invertebrate MeHg concentrations were more strongly correlated with sediment MeHg than with water MeHg concentrations. These results illustrate the complexity of MeHg bioaccumulation through food webs and indicate the importance of simultaneously using multiple biosentinels when monitoring MeHg production and bioaccumulation. Despite high sediment production rates and water concentrations in agricultural wetlands, MeHg export was physically limited by hydrologic export for all wetlands studied. We suggest that load reduction is maximized by limiting water throughout, but that on-site biota exposure is maximized by this loner water residence time. While field-specific hydrologic loads could not be fully quantified during flood conditions in February 2008, we suggest that the primary period of MeHg export from Yolo Bypass Wildlife Area is during those winter flooding periods when overall microbial activity and MeHg production in agricultural soils is fueled by the decomposition of rice straw, and when hydrologic flowthrough is maximal. Local stakeholders participated in two workshops related to this study, demonstrating an interest in understanding factors controlling MeHg production, export, and bioaccumulation. The results of this field study show that permanently flooded, naturally vegetated wetlands are unlikely to a large source of MeHg production within the YBWA, in contrast with agriculturally-managed wetlands. MeHg loading to Toe Drain waters of the Yolo Bypass may be reduced by lowering rated of hydrologic export from agricultural wetlands during the growing season and especially during rice harvest, However, under these water-holding conditions, biota living within agricultural wetlands may thus be exposed to higher MeHg concentrations in surface water, As observed in this study, rapid bioacculumaltion over a 2-month period led to MeHg concentrations in invertebrates and fish more than 6 and 11 times higher, respectively, than proposed TMDL target values to protect wildlife (0.03 ppm ww). The results of this field study, together with the information from YBWA stakeholders, provide a more definitive understanding of how MeHg cycling and bioaccumulation respond to habitat differences and specific management practices. These results directly address 4 core components of CBDA's Mercury Strategy for the Bay-Delta Ecosystem (Wiener et al., 2003a): a) Quantification and evaluation of THg and MeHg sources, b) Quantification of effects of ecosystem restoration on MeHg exposure, c) Assessment of ecological risk, and d) Identification and testing of potential management approaches for reducing MeHg contamination. In addition, the quantitative results reported here assess the effect of current land use practices in the Yolo Bypass MeHg production, bioaccumulation and export, and provide process-based advice towards achieving current goals of the RWQCB-CVR's Sacramento -- San Joaquin Delta Estuary TMDL for Methyl & Total Mercury (Wood et al., 2010b). Further work is necessary to evaluate biotic exposure in the Yolo Bypass Wildlife Area at higher trophic levels (e.g. birds), to quantify winter hydrologic flux of MeHg to the larger Delta ecosystem, and to evaluate rice straw management options to limit labile carbon supplies to surface sediment during winter months. In summary, agricultural management of rice fields -- specifically the periodic flooding and production of easily degraded organic matter -- promotes the production of MeHg beyond rates seen in naturally vegetated wetlands, whether seasonally or permanently flooded., The exported load from MeHg from these agricultural wetlands may be controlled by limiting hydrologic export from fields to enhance on-site MeHg removal processes, but the tradeoff is that this impoundement increases Me Hg exposure to resident organisms.
Two internally drained karstic wetlands in central Florida-Boggy Marsh at the Hilochee Wildlife Management Area and a large unnamed wetland at the Lyonia Preserve-were studied during 2001-03 to gain a better understanding of the net-recharge function that these wetlands provide, the significance of exchanges with ground water with regard to wetland water budgets, and the variability in wetland hydrologic response to a range of climate conditions. These natural, relatively remote and unaltered wetlands were selected to provide a baseline of natural wetland hydrologic variability to which anthropogenic influences on wetland hydrology could be compared. Large departures from normal rainfall during the study were fortuitous, and allowed monitoring of hydrologic processes over a wide range of climate conditions. Wetland responses varied greatly as a result of climate conditions that ranged from moderate drought to extremely moist. Anthropogenic activities influenced water levels at both study sites; however, because these activities were brief relative to the duration of the study, sufficient data were collected during unimpacted periods to allow for the following conclusions to be made. Water budgets developed for Boggy Marsh and the Lyonia large wetland showed strong similarity between the flux terms of rainfall, evaporation, net change in storage, and the net ground-water exchange residual. Runoff was assumed to be negligible. Of the total annual flux at Boggy Marsh, rainfall accounted for 45 percent; evaporation accounted for 25 percent; net change in storage accounted for 25 percent; and the net residual accounted for 5 percent. At the Lyonia large wetland, rainfall accounted for 44 percent; evaporation accounted for 29 percent; net change in storage accounted for 21 percent; and the net residual accounted for 6 percent of the total annual flux. Wetland storage and ground-water exchange were important when compared to the total water budget at both wetlands. Even though rainfall was far above average during the study, wetland evaporation volumetrically exceeded rainfall. Ground-water inflow was effective in partially offsetting the negative residual between rainfall and evaporation, thus adding to wetland storage. Ground-water inflow was most common at both wetlands when rainfall continued for days or weeks, or during a week with more than about 2.5 inches of rainfall. Large decreases in wetland storage were associated with large negative fluxes of evaporation and ground-water exchange. The response of wetland water levels to rainfall showed a strong and similar relation at both study sites; however, the greater variability in the relation of wetland water-level change to rainfall at higher rainfall rates indicated that hydrologic processes other than rainfall became more important in the response of the wetland. Changes in wetland water levels seemed to be related more to vertical gradients than to lateral gradients. The largest wetland water-level rises were associated mostly with lower vertical gradients, when vertical head differences were below the 18-month average; however, at the Lyonia large wetland, extremely large lateral gradients toward the wetland during late June 2002 may have contributed to substantial gains in wetland water. During the remainder of the study, wetland water-level rises were associated mostly with decreasing vertical gradients and highly variable lateral gradients. Conversely, wetland water-level decreases were associated mostly with increasing vertical gradients and lateral gradients away from the wetland, particularly during the dry season. The potential for lateral ground-water exchange with the wetlands varied substantially more than that for vertical exchange. Potential for vertical losses of wetland water to ground water was highest during a dry period from December 2001 to June 2002, during the wet season of 2002, and for several months into the following dry season. Lateral he
Ground-water contaminant plumes that are flowing toward or currently discharging to wetland areas present unique remediation problems because of the hydrologic connections between ground water and surface water and the sensitive habitats in wetlands. Because wetlands typically have a large diversity of microorganisms and redox conditions that could enhance biodegradation, they are ideal environments for natural attenuation of organic contaminants, which is a treatment method that would leave the ecosystem largely undisturbed and be cost effective. During 1992-97, the U.S. Geological Survey investigated the natural attenuation of chlorinated volatile organic compounds (VOC's) in a contaminant plume that discharges from a sand aquifer to a freshwater tidal wetland along the West Branch Canal Creek at Aberdeen Proving Ground, Maryland. Characterization of the hydrogeology and geochemistry along flowpaths in the wetland area and determination of the occurrence and rates of biodegradation and sorption show that natural attenuation could be a feasible remediation method for the contaminant plume that extends along the West Branch Canal Creek. The aquifer, which received contaminants in the past from sources that were located upgradient of the current eastern boundary of the wetland, is about 40 to 45 feet thick in the study area. The overlying wetland sediments consist of two distinct layers that have a combined thickness of about 6 to 12 feet--an upper unit of peat and a lower unit of silty to sandy clay or clayey sand. Head distributions show strong vertical gradients, and flow directions are predominantly upward through the wetland sediments. Tidal fluctuations, however, cause some reversals in ground-water-flow directions and changes in discharge locations, which affect the distribution and transport of contaminants. The average linear velocity of ground water is estimated to be about 2 to 3 feet per year along vertical flow lines in the wetland area, and the total ground-water discharge along a 1-foot-wide strip of the wetland extending from the eastern wetland boundary to the creek is in the range of 0.13 to 0.25 feet squared per day. The major parent contaminants in the aquifer were trichloroethylene (TCE); 1,1,2,2-tetrachloroethane (PCA); carbon tetrachloride (CT); and chloroform (CF). The aquifer was typically aerobic, but ground water in the wetland sediments became increasingly anaerobic along the upward flow direction. Iron-reducing conditions were predominant in the lower wetland sediment unit composed of clayey sand and silt, and methanogenesis was predominant in an upper unit composed of peat. Total concentrations of VOC's and the relative proportions of parent compounds to anaerobic daughter products changed substantially as the contaminants were transported upward through these changing redox environments. Concentrations of the parent compounds TCE and PCA ranged from about 100 to 2,000 micrograms per liter in the aquifer beneath the wetland, whereas concentrations of daughter products were low or undetectable. In contrast, the parent compounds commonly were not detected in ground water in the wetland sediments, but the daughter compounds 1,2- dichloro-ethylene (12DCE), vinyl chloride (VC), 1,1,2-trichloroethane (112TCA), and 1,2-dichloroethane (12DCA) were observed. 12DCE and VC were the dominant daughter products in the wetland sediments, even where PCA was the primary parent contaminant discharging to the wetland. The presence of these daughter products in water in the wetland sediments indicates that TCE and PCA are degraded by reductive dechlorination reactions in the naturally anaerobic wetland sediments. Although production of daughter products was observed, total concentrations of the VOC's decreased upward through the 6- to 12-feet-thick wetland sediments and were less than 5 micrograms per liter near the surface. The daughter products are apparently further degraded by these anaerobic processes to non-chlorinated, non-toxic endproducts, or are removed by other attenuation processes such as aerobic degradation or volatilization. Several sets of anaerobic microcosms, some amended with TCE concentrations of 400 or 990 micrograms per liter (3.0 or 7.5 micromoles per liter) and one amended with PCA concentration of 480 micrograms per liter (2.9 micromoles per liter), were constructed in the laboratory using wetland sediment and ground water from the study area. These microcosm experiments confirmed field observations that 12DCE and VC are the dominant daughter products from anaerobic biodegradation of both TCE and PCA. Production of 112TCA and 12DCA also was observed in the PCA-amended microcosms, but concentrations were lower than those of 12DCE and VC. These results indicate that degradation of PCA occurs through both hydrogenolysis and dichloroelimination pathways under anaerobic conditions. Daughter products were not observed in sterile controls, except for relatively low concentrations of 12DCE in the PCA-amended controls, suggesting that the reactions were predominantly microbially mediated. Parent and daughter concentrations in the microcosms decreased to less than 5 micrograms per liter in less than 34 days under methanogenic conditions, thus showing extremely rapid biodegradation rates in these organic-rich wetland sediments. Maximum potential rate constants for biodegradation of TCE and PCA, which were calculated from the microcosm exper-iments assuming first-order degradation rates, ranged from 0.10 to 0.31 per day under methanogenic conditions, corresponding to half-lives of 2 to 7 days. The rate constant for TCE biodegradation under sulfate-reducing conditions was 0.045 West Branch, Aberdeen Proving Ground, Maryland 3 per day (half-life of 15 days), which is lower than under methanogenic conditions. These estimated rate constants for the wetland sediments are two to three orders of magnitude higher than those reported in the literature for TCE biodegradation in microcosms constructed with sandy aquifer sediments. Aerobic biodegradation rates for cis-12DCE, trans-12DCE, and VC were in the same range as those measured for TCE and PCA under anaerobic conditions in microcosm experiments. Thus, production of these daughter products by anaerobic biodegradation of TCE and PCA could be balanced by their consumption where oxygen is available in the wetland sediment, such as near roots and land surface. In the aerobic microcosm experiments, biodegradation of cis-12DCE, trans-12DCE, and VC occurred only if methane consumption occurred, indicating that methanotrophs were involved in the process. Aerobic biodegradation was fastest for vinyl chloride and slowest for TCE in the microcosm experiments. These results agree with other laboratory and field studies that have shown faster degradation by methane-utilizing cultures when the compounds are less halogenated. Equilibrium sorption isotherms were measured in 24-hour batch tests and used to estimate distribution coefficients ( K d 's) to describe the ratios of sorbed to aqueous concentrations of PCA and the daughter products cis-12DCE, trans-12DCE, and VC. The estimated K d's for PCA, cis-12DCE, trans-12DCE, and VC were about 2.3, 1.8, 2.4, and 1.3 liters per kilogram of sediment, respectively. Sorbed concentrations of PCA, cis-12DCE, and trans-12DCE in the wetland sediments, therefore, would be expected to be about twice the concentration measured in the water, whereas sorbed concentrations of VC would not be much greater than the aqueous concentrations. Coefficients of retardation, which were calculated using the K d 's and an advective flow velocity of about 2 feet per year, indicate that sorption alone would cause the movement of the contaminants in the wetland sediments to be 6 to 10 times slower than the advective ground-water flow. Biodegradation and sorption, therefore, are significant natural attenuation mechanisms for chlorinated hydrocarbons in these wetland sediments. The relatively thin layers of wetland sediments are critical in reducing contaminant concentrations and toxicity of the ground water before it discharges to the wetland surface and the creek, and natural attenuation in the wetland sediments could be an effective remediation method for the ground-water contaminants.
We examined the relationship between local- (wetland) and landscape-level factors and breeding bird abundances on 1,190 depressional wetlands in the Prairie Pothole Region of North and South Dakota during the breeding seasons in 1995–97. The surveyed wetlands were selected from five wetland classes (alkali, permanent, semipermanent, seasonal, or temporary), two wetland types (natural or restored), and two landowner groups (private or Federal). We recorded 133 species of birds in the surveyed wetlands during the 3 years. We analyzed the nine most common (or focal) species (that is, species that were present in 25 percent or more of the 1,190 wetlands): the Red-winged Blackbird ( Agelaius phoeniceus ), Blue-winged Teal ( Anas discors ), Mallard (Anas platyrhynchos ), American Coot ( Fulica americana ), Gadwall ( Anas strepera ), Common Yellowthroat ( Geothlypis trichas ), Yellow-headed Blackbird ( Xanthocephalus xanthocephalus ), Northern Shoveler ( Anas clypeata ), and Savannah Sparrow ( Passerculus sandwichensis ). Our results emphasize the ecological value of all wetland classes, natural and restored wetlands, and publicly and privately owned wetlands in this region, including wetlands that are generally smaller and shallower (that is, temporary and seasonal wetlands) and thus most vulnerable to drainage. Blue-winged Teal, Northern Shoveler, Gadwall, Common Yellowthroat, and Red-winged Blackbird had higher abundances on Federal than on private wetlands. Abundances differed among wetland classes for seven of the nine focal species: Blue-winged Teal, Northern Shoveler, Mallard, American Coot, Common Yellowthroat, Yellow-headed Blackbird, Red-winged Blackbird. American Coot had higher abundances on restored wetlands than on natural wetlands overall, and Gadwall and Common Yellowthroat had higher abundances on private restored wetlands than on private natural wetlands. The Common Yellowthroat was the only species that had higher abundances on restored private wetlands than on restored Federal wetlands. After adjusting for wetland size and the date and location of the surveys, our results demonstrated that incorporating wetland- and landscape-level factors in models can improve our ability to predict abundances of wetland birds in this region. The top model for eight of the nine focal species included wetland- and landscape-level factors, whereas the best model for Blue-winged Teal included only wetland-level attributes. Although local factors (for example, percent open water or emergent vegetation) in individual wetlands are important factors for some wetland breeding birds, it is important that natural resource managers consider landscape-level factors beyond the local factors in their conservation plans for wetland birds.
1. Wetlands are critical components of freshwater biodiversity and provide ecosystem services, but human activities have resulted in large-scale loss of these habitats across the globe. To offset this loss, mitigation wetlands are frequently constructed, but their ability to replicate the functions of natural wetlands remains uncertain. Further, monitoring of mitigation wetlands is limited and often focused exclusively on vegetation and physical characteristics. 2. Wetland fauna are assumed to be present if suitable habitat restoration is achieved, but this assumption is rarely tested. We used the macroinvertebrate community as a proxy for wetland function to compare created mitigation wetlands, natural wetlands impacted but not destroyed by road construction activity, and unimpacted reference wetlands along a highway corridor in the Greater Yellowstone Ecosystem. Unlike most other studies of invertebrate communities in created wetlands which have occurred in warm climates, our study area has a cold temperate climate with short growing seasons. 3. We estimated macroinvertebrate taxonomic richness and used linear models to test for effects of wetland design features (wetland age, isolation, depth, vegetation, size, and pH) on invertebrate richness. We also used non-metric multidimensional scaling to examine differences in community composition among wetland types and used indicator species analysis to determine which taxa were causing observed differences. 4. Taxonomic richness of macroinvertebrates was lower in created wetlands than impacted or reference wetlands, whereas richness was similar in impacted and reference wetlands. Wetland age was positively correlated with taxonomic richness. The amount of aquatic vegetation in wetlands had the greatest influence on taxonomic richness, so that recently created wetlands with little vegetation had the simplest invertebrate communities. Community composition of invertebrates in created wetlands also differed from community composition in reference and impacted wetlands. Most notably, created wetlands lacked some passive dispersers that were common in other wetland types, although we found no relationship between taxonomic richness and wetland isolation. 5. Overall, constructed wetlands had diminished and altered macroinvertebrate communities relative to reference and impacted wetlands, suggesting that longer times may be required for wetland mitigation projects in cold temperate climates to attain full functionality.
Wetland creation is a common practice to mitigate for the loss of natural wetlands. However, there is still uncertainty about how effectively created wetlands replace habitat provided by natural wetlands. This uncertainty is due in part because post-construction monitoring of biological communities, and vertebrates especially, is rare and typically short-term (<5 years). We estimated occupancy of 4 amphibian species in 8 created mitigation wetlands, 7 impacted wetlands, and 7 reference wetlands in the Greater Yellowstone Ecosystem in Wyoming, USA. Mitigation wetlands were created to replace wetland habitat that was lost during road construction and ranged in age from 1 to 10 years when sampled. Impacted wetlands were natural wetlands partially filled by road construction and were adjacent to a highway. We sampled for amphibian larvae during 6 summers from 2013 to 2020 and used multi-species occupancy models that estimated detection and occupancy of each of 4 amphibian species to determine how amphibian responses changed over time, especially in mitigation wetlands. Occupancy did not differ between impacted and reference wetlands for any of the 4 amphibian species. Western Toads ( Anaxyrus boreas ) were most common (although briefly) in created wetlands, and occupancy of Columbia Spotted Frogs ( Rana luteiventris ), Western Tiger Salamanders ( Ambystoma mavortium ), and Boreal Chorus Frogs ( Pseudacris maculata ) was lower in created wetlands than in impacted or reference wetlands. Individual wetland area was positively associated with occupancy for all 4 species and wetland vegetation cover was positively associated with Boreal Chorus Frog and Columbia Spotted Frog occupancy; these results emphasize the importance of design characteristics when planning mitigation wetlands. The link between wetland age and occupancy was complex and included threshold and quadratic relationships for three of the four species, but only Boreal Chorus Frog occupancy was still increasing slowly at the end of our study. Our results indicate created wetlands did not attain the suitability of impacted and natural wetlands for local amphibians, even several years after construction. The complex relationships between wetland age and species-specific occupancy illustrate the importance of long-term monitoring in describing population responses to the construction of wetlands as mitigation for wetland loss.