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ABSTRACT Beachrock is a type of carbonate‐cemented rock that forms via rapid cementation in the intertidal zone. Beachrock is a valuable geological tool as an indicator of paleoshorelines and may protect shorelines from erosion. Previous studies present a range of hypotheses about the processes enabling rapid beachrock formation, which span purely physicochemical mechanisms to a significant role for microbially mediated carbonate precipitation. We designed a set of in situ field experiments to explore the rates and mechanisms of beachrock formation on Little Ambergris Cay (Turks and Caicos Islands). Our field site has evidence for rapid beachrock cementation, including the incorporation of 20th century anthropogenic detritus into beachrock. We deployed pouches of sterilized ooid sand in the upper intertidal zone and assessed the extent of cementation and biofilm development after durations of 4 days, 2.5 months, and 5 months. We observed incipient meniscus cements after only 4 days of incubation in the field, suggesting that physicochemical processes are important in driving initial cementation. After 2.5 months, we observed substantial biofilm colonization on our experimental substrates, with interwoven networks ofHalomicronemafilaments binding clusters of ooids to the nylon pouches. After 5 months, we observed incipient beachrock formation in the form of coherent aggregates of ooids up to 1 cm in diameter, bound together by both networks of microbial filaments and incipient cements. We interpret that the cyanobacteria‐dominated beachrock biofilm community on Little Ambergris Cay plays an important role in beachrock formation through the physical stabilization of sediment as cementation proceeds. Together, this combination of physicochemical and microbial mechanisms enables fresh rock to form in as little as 150 days. 

Abstract Lacustrine carbonates are a powerful archive of paleoenvironmental information but are susceptible to post‐depositional alteration. Microbial metabolisms can drive such alteration by changing carbonate saturationin situ, thereby driving dissolution or precipitation. The net impact these microbial processes have on the primary δ¹⁸O, δ¹³C, and Δ₄₇values of lacustrine carbonate is not fully known. We studied the evolution of microbial community structure and the porewater and sediment geochemistry in the upper ~30 cm of sediment from two shoreline sites at Green Lake, Fayetteville, NY over 2 years of seasonal sampling. We linked seasonal and depth‐based changes of porewater carbonate chemistry to microbial community composition, in situ carbon cycling (using δ¹³C values of carbonate, dissolved inorganic carbon (DIC), and organic matter), and dominant allochems and facies. We interpret that microbial processes are a dominant control on carbon cycling within the sediment, affecting porewater DIC, aqueous carbon chemistry, and carbonate carbon and clumped isotope geochemistry. Across all seasons and sites, microbial organic matter remineralization lowers the δ¹³C of the porewater DIC. Elevated carbonate saturation states in the sediment porewaters (Ω > 3) were attributed to microbes from groups capable of sulfate reduction, which were abundant in the sediment below 5 cm depth. The nearshore carbonate sediments at Green Lake are mainly composed of microbialite intraclasts/oncoids, charophytes, larger calcite crystals, and authigenic micrite—each with a different origin. Authigenic micrite is interpreted to have precipitated in situ from the supersaturated porewaters from microbial metabolism. The stable carbon isotope values (δ¹³C_carb) and clumped isotope values (Δ₄₇) of bulk carbonate sediments from the same depth horizons and site varied depending on both the sampling season and the specific location within a site, indicating localized (μm to mm) controls on carbon and clumped isotope values. Our results suggest that biological processes are a dominant control on carbon chemistry within the sedimentary subsurface of the shorelines of Green Lake, from actively forming microbialites to pore space organic matter remineralization and micrite authigenesis. A combination of biological activity, hydrologic balance, and allochem composition of the sediments set the stable carbon, oxygen, and clumped isotope signals preserved by the Green Lake carbonate sediments. 

Abstract The measured carbon isotopic compositions of carbonate sediments (δ¹³C_carb) on modern platforms are commonly¹³C‐enriched compared to predicted values for minerals forming in isotopic equilibrium with the dissolved inorganic carbon (DIC) of modern seawater. This offset undermines the assumption that δ¹³C_carbvalues of analogous facies in the rock record are an accurate archive of information about Earth's global carbon cycle. We present a new data set of the diurnal variation in carbonate chemistry and seawater δ¹³C_DICvalues on a modern carbonate platform. These data demonstrate that δ¹³C_carbvalues on modern platforms are broadly representative of seawater, but only after accounting for the recent decrease in the δ¹³C value of atmospheric CO₂and shallow seawater DIC due to anthropogenic carbon release, a phenomenon commonly referred to as the¹³C Suess effect. These findings highlight an important, yet overlooked, aspect of some modern carbonate systems, which must inform their use as ancient analogs.