Methane in Lakes: Variability in Stable Carbon Isotopic Composition and the Potential Importance of Groundwater Input

Methane (CH4) is an important component of the carbon (C) cycling in lakes. CH4 production enables carbon in sediments to be either reintroduced to the food web via CH4 oxidation or emitted as a greenhouse gas making lakes one of the largest natural sources of atmospheric CH4. Large stable carbon isotopic fractionation during CH4 oxidation makes changes in 13C:12C ratio (δ13C) a powerful and widely used tool to determine the extent to which lake CH4 is oxidized, rather than emitted. This relies on correct δ13C values of original CH4 sources, the variability of which has rarely been investigated systematically in lakes. In this study, we measured δ13C in CH4 bubbles in littoral sediments and in CH4 dissolved in the anoxic hypolimnion of six boreal lakes with different characteristics. The results indicate that δ13C of CH4 sources is consistently higher (less 13C depletion) in littoral sediments than in deep waters across boreal and subarctic lakes. Variability in organic matter substrates across depths is a potential explanation. In one of the studied lakes available data from nearby soils showed correspondence between δ13C-CH4 in groundwater and deep lake water, and input from the catchment of CH4via groundwater exceeded atmospheric CH4 emissions tenfold over a period of 1 month. It indicates that lateral hydrological transport of CH4 can explain the observed δ13C-CH4 patterns and be important for lake CH4 cycling. Our results have important consequences for modelling and process assessments relative to lake CH4 using δ13C, including for CH4 oxidation, which is a key regulator of lake CH4 emissions.

A standardized database of Marine Isotope Stage 5e sea-level proxies in southern Africa (Angola, Namibia and South Africa)

Evidence for sea-level change during and around Marine Isotope Stage (MIS) 5e (ca. 125 ka) in southern Africa derives from a wide variety of geomorphic and sedimentological sea-level indicators, supported in the past 2 decades by absolute chronological control, particularly on littoral deposits, some of which have a quantifiable relationship to former sea level. In addition to these proxies, data provided by both terrestrial (dune sediments and archaeological remains) and marine (lagoonal and nearshore littoral sediments) limiting points provide broad constraints on sea level. Here, we review publications describing such data points. Using the framework of the World Atlas of Last Interglacial Shorelines, we insert in a standardized database (https://doi.org/10.5281/zenodo.4459297, Cooper and Green, 2020) all the elements available to assess former palaeo-relative sea level (palaeo-RSL) and the chronological constraints associated with them (including uncertainties). Overall, we reviewed 71 studies, from which we extracted 39 sea-level indicators and 26 limiting points. As far as age attribution is concerned, early analysis of molluscs and whole-rock beachrock samples using U series allowed dating of several sea-level indicators during the 1980s, but the more widespread application of optically stimulated luminescence (OSL) dating since 2004 has yielded many more (and more accurate) sea-level indicators from several sites. This has helped resolve the nature and timing of MIS 5e shorelines and has the potential to further elucidate the apparent presence of two or more sea-level peaks at several South African sites during this interval. The standardized sea-level database presented in this paper is the first of its kind for this region. Future research should be directed to improve the stratigraphic description of last interglacial shorelines and to obtain better dating, high-accuracy elevation measurements with better palaeo-RSL interpretation.

Changing sources and processes sustaining surface CO₂ and CH₄ fluxes along a tropical river to reservoir system

Freshwaters are important emitters of carbon dioxide (CO2) and methane (CH4), two potent greenhouse gases (GHGs). While aquatic surface GHG fluxes have been extensively measured, there is much less information about their underlying sources. In lakes and reservoirs, surface GHG can originate from horizontal riverine flow, the hypolimnion, littoral sediments, and water column metabolism. These sources are generally studied separately, leading to a fragmented assessment of their relative role in sustaining CO2 and CH4 surface fluxes. In this study, we quantified sources and sinks of CO2 and CH4 in the epilimnion along a hydrological continuum in a permanently stratified tropical reservoir (Borneo). Results showed that horizontal inputs are an important source of both CO2 and CH4 (>90 % of surface emissions) in the upstream reservoir branches. However, this contribution fades along the hydrological continuum, becoming negligible in the main basin of the reservoir, where CO2 and CH4 are uncoupled and driven by different processes. In the main basin, vertical CO2 inputs and sediment CH4 inputs contributed to on average 60 % and 23 % respectively to the surface fluxes of the corresponding gas. Water column metabolism exhibited wide amplitude and range for both gases, making it a highly variable component, but with a large potential to influence surface GHG budgets in either direction. Overall our results show that sources sustaining surface CO2 and CH4 fluxes vary spatially and between the two gases, with internal metabolism acting as a fluctuating but key modulator. However, this study also highlights challenges and knowledge gaps related to estimating ecosystem-scale CO2 and CH4 metabolism, which hinder aquatic GHG flux predictions.

Sources and processes sustaining surface CO₂ and CH₄ fluxes in a tropical reservoir: the importance of water column metabolism

Freshwaters are important emitters of carbon dioxide (CO2) and methane (CH4) to the atmosphere, two potent greenhouse gases (GHG). While aquatic surface GHG fluxes have been extensively measured, there is much less information about their underlying sources. In lakes and reservoirs, surface GHG can originate from horizontal riverine flow, the hypolimnion, littoral sediments, and water column metabolism. These processes are generally studied separately, leading to a fragmented assessment of their relative role in sustaining CO2 and CH4 surface fluxes. In this study, we quantified sources/sinks of CO2 and CH4 in the epilimnion along a hydrological continuum in a permanently stratified tropical reservoir (Borneo Island). Results showed that horizontal inputs are an important source of both CO2 and CH4 (18 to 100 % of surface emissions) in the upstream reservoir branches. However, this contribution fades along the hydrological continuum, becoming negligible in the main basin of the reservoir, where CO2 and CH4 are uncoupled and driven by different processes. In the main basin, vertical CO2 inputs and sediment CH4 inputs contributed to on average 60 and 23 % respectively to the surface fluxes of the corresponding gas. Water column metabolism exhibited wide amplitude and range for both gases, making it the most influential but uncertain component in the epilimnetic gas budgets. Overall our results show that while sources sustaining surface CO2 and CH4 fluxes vary spatially and between the two gases, internal water metabolism remains a dominant driver. However, this study also highlights challenges and knowledge gaps related to estimating ecosystem-scale CO2 and CH4 metabolism, which hinder aquatic GHG flux predictions.

A standardized database of MIS 5e sea-level proxies in southern Africa (Angola, Namibia and South Africa)

Evidence for sea-level change during and around Marine Isotopic Stage 5e (ca. 125 ka) in southern Africa derives from a wide variety of geomorphic and sedimentological sea-level indicators, supported in the past 2 decades by absolute chronological control. In addition to these proxies, data provided by both terrestrial (dune sediments and archaeological remains) and marine (lagoonal and nearshore littoral sediments) limiting points provide broad constraints on sea level. Here, we review publications describing these data points. Using the framework of the World Atlas of Last Interglacial Shorelines, we insert in a standardized database all the elements needed to assess former paleo relative sea level, and the chronological constraints associated with them (including uncertainties). Overall, we reviewed 69 studies, from which we extracted 35 sea-level indicators and 25 limiting points. As far as age attribution is concerned, early dating of molluscs and whole-rock beachrock samples using U-Series allowed ating of several sea-level indicators during the 1980s but the more widespread application of Optically Stimulated Luminescence dating since 2004 has yielded many more (and more accurate) dates from several sites. This has helped resolve the nature and timing of MIS5e shorelines and has the potential to further elucidate the apparent presence of two or more sea-level peaks at several South African sites during this interval. The standardized sea-level database presented in this paper is the first of its kind for this region. Future research should be directed to improve the stratigraphic description of LIG shorelines and to obtain better dating, high-accuracy elevation measurements with better palaeo-RSL interpretation.

Mercury trends and cycling in northern Wisconsin related to atmospheric and hydrologic processes

Atmospheric deposition is the principal source of mercury (Hg) to remote northern landscapes, but its fate depends on multiple factors and internal feedbacks. Here we document long-term trends and cycles of Hg in the air, precipitation, surface water, and fish of northern Wisconsin that span the past three decades, and we investigate relationships to atmospheric processes and other variables, especially the regional water cycle. Consistent with declining emission inventories, there was evidence of declining trends in these time series, but the time series for Hg in some lakes and most fish were dominated by a near-decadal oscillation that tracked the regional oscillation of water levels. Concentrations of important solutes (SO4, dissolved organic carbon) and the acid–base status of lake water also tracked water levels in ways that cannot be attributed to simple dilution or concentration. The explanatory mechanism is analogous to the “reservoir effect” wherein littoral sediments are periodically exposed and reflooded, altering the internal cycles of sulfur, carbon, and mercury. These climatically driven, near-decadal oscillations confound short or sparse time series and complicate relationships among Hg emissions, deposition, and bioaccumulation.