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Research about Waquoit Bay National Estuarine Research Reserve

Source-linked reports with geographic coverage including Waquoit Bay National Estuarine Research Reserve.

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Higher temperature sensitivity of ecosystem respiration in low marsh compared to high elevation marsh ecosystems

Salt marsh habitats contain some of the highest quantities of soil organic carbon (C) per unit area, but increasing anthropogenic stressors threaten their ability to maintain themselves as large C reservoirs in some regions. We quantify rates of C gas exchange (methane [CH 4 ] and carbon dioxide [CO 2 ]) monthly across a 16-month period from a low nitrogen “reference” salt marsh on Cape Cod in New England using static chambers. While the summer period is the most dynamic period of marsh C gas exchange, we observed substantial fluxes in the early summer through late fall, highlighting the importance of including shoulder seasons in studies of marsh C exchange. We estimate annual ecosystem respiration between 108 and 252 g C m −2 yr −1 , which varied based on temperature and elevation. This flux is lower than in other nearby marshes, which we attribute to the frequently inundated, microtidal nature of the site, resulting in the majority of respired CO 2 being exported via lateral, not vertical, fluxes from this marsh. We observed significantly higher temperature sensitivity from the low elevation of the marsh compared to the high marsh. Recent acceleration in the rate of sea level rise is leading to a well-documented expansion of low marsh into high marsh vegetation zones in this marsh system and others in the region. While rates of C burial are higher in the low marsh compared to the high marsh, the higher temperature sensitivity of respiration in the low marsh may diminish the longevity of marsh C stocks with climate warming.

Massachusetts

Mechanisms and magnitude of dissolved silica release from a New England salt marsh

Salt marshes are sites of silica (SiO 2 ) cycling and export to adjacent coastal systems, where silica availability can exert an important control over coastal marine primary productivity. Mineral weathering and biologic fixation concentrate silica in these systems; however, the relative contributions of geologic versus biogenic silica dissolution to this export are not known. We collected water samples from the tidal creek of a relatively undisturbed New England (USA) salt marsh over 13 tidal cycles in spring, summer, and fall 2014–2016 to determine patterns of dissolved silica (DSi) concentration in the water entering and leaving the marsh. DSi concentrations in the tidal creek peaked in the summer and were at a minimum in the fall. Additionally, we analyzed DSi concentrations and Ge/Si ratios in marsh porewater and groundwater samples as a tracer of DSi origin. Ge/Si ratios in the porewater, subterranean estuary, and fresh groundwater averaged 6.3 ± 0.31 µmol/mol, which is consistent with production via silicate weathering rather than biogenic silica dissolution. These results highlight a previously unstudied role marsh sediment plays in coastal biogeochemistry by supplying DSi to coastal ecosystems. This marsh exported 1170 mmol DSi m −2 year −1 , 85% of which originated from porewater exchange, with minor contributions from brackish groundwater discharge from the subterranean estuary. Examining these values in the context of the other known DSi inputs indicates that coastal marshes provide ~ 75% of the annual silica inputs into the adjacent estuary, Waquoit Bay.

Massachusetts

Revisiting 228Th as a tool for determining sedimentation and mass accumulation rates

The use of 228Th has seen limited application for determining sedimentation and mass accumulation rates in coastal and marine environments. Recent analytical advances have enabled rapid, precise measurements of particle-bound 228Th using a radium delayed coincidence counting system (RaDeCC). Herein we review the 228Th cycle in the marine environment and revisit the historical use of 228Th as a tracer for determining sediment vertical accretion and mass accumulation rates in light of new measurement techniques. Case studies comparing accumulation rates from 228Th and 210Pb are presented for a micro-tidal salt marsh and a marginal sea environment. 228Th and 210Pb have been previously measured in mangrove, deltaic, continental shelf and ocean basin environments, and a literature synthesis reveals that 228Th (measured via alpha or gamma spectrometry) derived accumulation rates are generally equal to or greater than estimates derived from 210Pb, reflecting different integration periods. Use of 228Th is well-suited for shallow (<15 cm) cores over decadal timescales. Application is limited to relatively homogenous sediment profiles with minor variations in grain size and minimal bioturbation. When appropriate conditions are met, complimentary use of 228Th and 210Pb can demonstrate that the upper layers of a core are undisturbed and can improve spatial coverage in mapping accumulation rates due to the higher sample throughput for sediment 228Th.

Massachusetts

Pore water exchange-driven inorganic carbon export from intertidal salt marshes

Respiration in intertidal salt marshes generates dissolved inorganic carbon (DIC) that is exported to the coastal ocean by tidal exchange with the marsh platform. Understanding the link between physical drivers of water exchange and chemical flux is a key to constraining coastal wetland contributions to regional carbon budgets. The spatial and temporal (seasonal, annual) variability of marsh pore water exchange and DIC export was assessed from a microtidal salt marsh (Sage Lot Pond, Massachusetts). Spatial variability was constrained from 224 Ra : 228 Th disequilibria across two hydrologic units within the marsh sediments. Disequilibrium between the more soluble 224 Ra and its sediment-bound parent 228 Th reveals significant pore water exchange in the upper 5 cm of the marsh surface (0–36 L m −2 d −1 ) that is most intense in low marsh elevation zones, driven by tidal overtopping. Surficial sediment DIC transport ranges from 0.0 to 0.7 g C m −2 d −1 . The sub-surface sediment horizon intersected by mean low tide was disproportionately impacted by tidal pumping (20–80 L m −2 d −1 ) and supplied a seasonal DIC flux of 1.7–5.4 g C m −2 d −1 . Export exceeded 10 g C m −2 d −1 for another marsh unit, demonstrating that fluxes can vary substantially across salt marshes under similar conditions within the same estuary. Seasonal and annual variability in marsh pore water exchange, constrained from tidal time-series of radium isotopes, was driven in part by variability in mean sea level. Rising sea levels will further inundate high marsh elevation zones, which may lead to greater DIC export.

Massachusetts

Carbon dioxide fluxes reflect plant zonation and belowground biomass in a coastal marsh

Coastal wetlands are major global carbon sinks; however, they are heterogeneous and dynamic ecosystems. To characterize spatial and temporal variability in a New England salt marsh, greenhouse gas (GHG) fluxes were compared among major plant‐defined zones during growing seasons. Carbon dioxide (CO 2 ) and methane (CH 4 ) fluxes were compared in two mensurative experiments during summer months (2012–2014) that included low marsh ( Spartina alterniflora ), high marsh ( Distichlis spicata and Juncus gerardii ‐dominated), invasive Phragmites australis zones, and unvegetated ponds. Day‐ and nighttime fluxes were also contrasted in the native marsh zones. N 2 O fluxes were measured in parallel with CO 2 and CH 4 fluxes, but were not found to be significant. To test the relationships of CO 2 and CH 4 fluxes with several native plant metrics, a multivariate nonlinear model was used. Invasive P. australis zones (−7 to −15 μmol CO 2 ·m −2 ·s −1 ) and S. alterniflora low marsh zones (up to −14 μmol CO 2 ·m −2 ·s −1 ) displayed highest average CO 2 uptake rates, while those in the native high marsh zone (less than −2 μmol CO 2 ·m −2 ·s −1 ) were much lower. Unvegetated ponds were typically small sources of CO 2 to the atmosphere (<0.5 μmol CO 2 ·m −2 ·s −1 ). Nighttime emissions of CO 2 averaged only 35% of daytime uptake in the low marsh zone, but they exceeded daytime CO 2 uptake by up to threefold in the native high marsh zone. Based on modeling, belowground biomass was the plant metric most strongly correlated with CO 2 fluxes in native marsh zones, while none of the plant variables correlated significantly with CH 4 fluxes. Methane fluxes did not vary between day and night and did not significantly offset CO 2 uptake in any vegetated marsh zones based on sustained global warming potential calculations. These findings suggest that attention to spatial zonation as well as expanded measurements and modeling of GHG emissions across greater temporal scales will help to improve accuracy of carbon accounting in coastal marshes.

Massachusetts