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1. Integrated carbon, sulfur, and nitrogen isotope chemostratigraphy of the Ediacaran Lantian Formation in South China: Spatial gradient, ocean redox oscillation, and fossil distribution

   https://doi.org/10.1111/gbi.12226  

   Wang, W. ; Guan, C. ; Zhou, C. ; Peng, Y. ; Pratt, L. M. ; Chen, X. ; Chen, L. ; Chen, Z. ; Yuan, X. ; Xiao, S. ( January 2017 , Geobiology)

   The Ediacaran Doushantuo Formation in South China is a prime target for geobiological investigation because it offers opportunities to integrate chemostratigraphic and paleobiological data. Previous studies were mostly focused on successions in shallow‐water shelf facies, but data from deep‐water successions are needed to fully understand basinal redox structures. Here, we report δ¹³C_carb, δ¹³C_org, δ³⁴S_pyr, δ³⁴S_CAS, and δ¹⁵N_seddata from a drill core of the fossiliferous Lantian Formation, which is a deep‐water equivalent of the Doushantuo Formation. Our data confirm a large (>10‰) spatial gradient in δ¹³C_carbin the lower Doushantuo/Lantian formations, but this gradient is probably due to the greater sensitivity of carbonate‐poor deep‐water sediments to isotopic mixing with¹³C‐depleted carbonate cements. A pronounced negative δ¹³C_carbexcursion (EN3) in the upper Doushantuo/Lantian formations, however, is spatially consistent and may be an equivalent of the Shuram excursion. δ³⁴S_pyris more negative in deeper‐water facies than in shallow‐water facies, particularly in the lower Doushantuo/Lantian formations, and this spatial pattern is interpreted as evidence for ocean redox stratification: Pyrite precipitated in euxinic deep waters has lower δ³⁴S_pyrthan that formed within shallow‐water sediments. The Lantian Formation was probably deposited in oscillating oxic and euxinic conditions. Euxinic black shales have higherTOCandTNcontents, but lower δ³⁴S_pyrand δ¹⁵N_sedvalues. In euxinic environments, pyrite was predominantly formed in the water column and organic nitrogen was predominantly derived from nitrogen fixation orNH₄⁺assimilation because of quantitative denitrification, resulting in lower δ³⁴S_pyrand δ¹⁵N_sedvalues. Benthic macroalgae and putative animals occur exclusively in euxinic black shales. If preserved in situ, these organisms must have lived in brief oxic episodes punctuating largely euxinic intervals, only to be decimated and preserved when the local environment switched back to euxinia again. Thus, taphonomy and ecology were the primary factors controlling the stratigraphic distribution of macrofossils in the Lantian Formation.

    

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2. Uncovering the spatial heterogeneity of Ediacaran carbon cycling

   https://doi.org/10.1111/gbi.12222  

   Li, C. ; Hardisty, D. S. ; Luo, G. ; Huang, J. ; Algeo, T. J. ; Cheng, M. ; Shi, W. ; An, Z. ; Tong, J. ; Xie, S. ; et al ( December 2016 , Geobiology)

   Records of the Ediacaran carbon cycle (635–541 million years ago) include the Shuram excursion (SE), the largest negative carbonate carbon isotope excursion in Earth history (down to −12‰). The nature of this excursion remains enigmatic given the difficulties of interpreting a perceived extreme global decrease in the δ¹³C of seawater dissolved inorganic carbon. Here, we present carbonate and organic carbon isotope (δ¹³C_carband δ¹³C_org) records from the Ediacaran Doushantuo Formation along a proximal‐to‐distal transect across the Yangtze Platform of South China as a test of the spatial variation of theSE. Contrary to expectations, our results show that the magnitude and morphology of this excursion and its relationship with coexisting δ¹³C_orgare highly heterogeneous across the platform. Integrated geochemical, mineralogical, petrographic, and stratigraphic evidence indicates that theSEis a primary marine signature. Data compilations demonstrate that theSEwas also accompanied globally by parallel negative shifts of δ³⁴S of carbonate‐associated sulfate (CAS) and increased⁸⁷Sr/⁸⁶Sr ratio and coastalCASconcentration, suggesting elevated continental weathering and coastal marine sulfate concentration during theSE. In light of these observations, we propose a heterogeneous oxidation model to explain the high spatial heterogeneity of theSEand coexisting δ¹³C_orgrecords of the Doushantuo, with likely relevance to theSEin other regions. In this model, we infer continued marine redox stratification through theSEbut with increased availability of oxidants (e.g., O₂and sulfate) limited to marginal near‐surface marine environments. Oxidation of limited spatiotemporal extent provides a mechanism to drive heterogeneous oxidation of subsurface reduced carbon mostly in shelf areas. Regardless of the mechanism driving theSE, future models must consider the evidence for spatial heterogeneity in δ¹³C presented in this study.

    

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3. Florida mangrove saltmarsh reference surface soils

   https://doi.org/10.6073/pasta/0e08cbe07c84488cb7b9dd16669946d0  

   Lewis, David Bruce ( January 2021 , Environmental Data Initiative)

   Site description. This data package consists of data obtained from sampling surface soil (the 0-7.6 cm depth profile) in black mangrove (Avicennia germinans) dominated forest and black needlerush (Juncus roemerianus) saltmarsh along the Gulf of Mexico coastline in peninsular west-central Florida, USA. This location has a subtropical climate with mean daily temperatures ranging from 15.4 °C in January to 27.8 °C in August, and annual precipitation of 1336 mm. Precipitation falls as rain primarily between June and September. Tides are semi-diurnal, with 0.57 m median amplitudes during the year preceding sampling (U.S. NOAA National Ocean Service, Clearwater Beach, Florida, station 8726724). Sea-level rise is 4.0 ± 0.6 mm per year (1973-2020 trend, mean ± 95 % confidence interval, NOAA NOS Clearwater Beach station). The A. germinans mangrove zone is either adjacent to water or fringed on the seaward side by a narrow band of red mangrove (Rhizophora mangle). A near-monoculture of J. roemerianus is often adjacent to and immediately landward of the A. germinans zone. The transition from the mangrove to the J. roemerianus zone is variable in our study area. An abrupt edge between closed-canopy mangrove and J. roemerianus monoculture may extend for up to several hundred meters in some locations, while other stretches of ecotone present a gradual transition where smaller, widely spaced trees are interspersed into the herbaceous marsh. Juncus roemerianus then extends landward to a high marsh patchwork of succulent halophytes (including Salicornia bigellovi, Sesuvium sp., and Batis maritima), scattered dwarf mangrove, and salt pans, followed in turn by upland vegetation that includes Pinus sp. and Serenoa repens. Field design and sample collection. We established three study sites spaced at approximately 5 km intervals along the western coastline of the central Florida peninsula. The sites consisted of the Salt Springs (28.3298°, -82.7274°), Energy Marine Center (28.2903°, -82.7278°), and Green Key (28.2530°, -82.7496°) sites on the Gulf of Mexico coastline in Pasco County, Florida, USA. At each site, we established three plot pairs, each consisting of one saltmarsh plot and one mangrove plot. Plots were 50 m^2 in size. Plots pairs within a site were separated by 230-1070 m, and the mangrove and saltmarsh plots composing a pair were 70-170 m apart. All plot pairs consisted of directly adjacent patches of mangrove forest and J. roemerianus saltmarsh, with the mangrove forests exhibiting a closed canopy and a tree architecture (height 4-6 m, crown width 1.5-3 m). Mangrove plots were located at approximately the midpoint between the seaward edge (water-mangrove interface) and landward edge (mangrove-marsh interface) of the mangrove zone. Saltmarsh plots were located 20-25 m away from any mangrove trees and into the J. roemerianus zone (i.e., landward from the mangrove-marsh interface). Plot pairs were coarsely similar in geomorphic setting, as all were located on the Gulf of Mexico coastline, rather than within major sheltering formations like Tampa Bay, and all plot pairs fit the tide-dominated domain of the Woodroffe classification (Woodroffe, 2002, "Coasts: Form, Process and Evolution", Cambridge University Press), given their conspicuous semi-diurnal tides. There was nevertheless some geomorphic variation, as some plot pairs were directly open to the Gulf of Mexico while others sat behind keys and spits or along small tidal creeks. Our use of a plot-pair approach is intended to control for this geomorphic variation. Plot center elevations (cm above mean sea level, NAVD 88) were estimated by overlaying the plot locations determined with a global positioning system (Garmin GPS 60, Olathe, KS, USA) on a LiDAR-derived bare-earth digital elevation model (Dewberry, Inc., 2019). The digital elevation model had a vertical accuracy of ± 10 cm (95 % CI) and a horizontal accuracy of ± 116 cm (95 % CI). Soil samples were collected via coring at low tide in June 2011. From each plot, we collected a composite soil sample consisting of three discrete 5.1 cm diameter soil cores taken at equidistant points to 7.6 cm depth. Cores were taken by tapping a sleeve into the soil until its top was flush with the soil surface, sliding a hand under the core, and lifting it up. Cores were then capped and transferred on ice to our laboratory at the University of South Florida (Tampa, Florida, USA), where they were combined in plastic zipper bags, and homogenized by hand into plot-level composite samples on the day they were collected. A damp soil subsample was immediately taken from each composite sample to initiate 1 y incubations for determination of active C and N (see below). The remainder of each composite sample was then placed in a drying oven (60 °C) for 1 week with frequent mixing of the soil to prevent aggregation and liberate water. Organic wetland soils are sometimes dried at 70 °C, however high drying temperatures can volatilize non-water liquids and oxidize and decompose organic matter, so 50 °C is also a common drying temperature for organic soils (Gardner 1986, "Methods of Soil Analysis: Part 1", Soil Science Society of America); we accordingly chose 60 °C as a compromise between sufficient water removal and avoidance of non-water mass loss. Bulk density was determined as soil dry mass per core volume (adding back the dry mass equivalent of the damp subsample removed prior to drying). Dried subsamples were obtained for determination of soil organic matter (SOM), mineral texture composition, and extractable and total carbon (C) and nitrogen (N) within the following week. Sample analyses. A dried subsample was apportioned from each composite sample to determine SOM as mass loss on ignition at 550 °C for 4 h. After organic matter was removed from soil via ignition, mineral particle size composition was determined using a combination of wet sieving and density separation in 49 mM (3 %) sodium hexametaphosphate ((NaPO_3)_6) following procedures in Kettler et al. (2001, Soil Science Society of America Journal 65, 849-852). The percentage of dry soil mass composed of silt and clay particles (hereafter, fines) was calculated as the mass lost from dispersed mineral soil after sieving (0.053 mm mesh sieve). Fines could have been slightly underestimated if any clay particles were burned off during the preceding ignition of soil. An additional subsample was taken from each composite sample to determine extractable N and organic C concentrations via 0.5 M potassium sulfate (K_2SO_4) extractions. We combined soil and extractant (ratio of 1 g dry soil:5 mL extractant) in plastic bottles, reciprocally shook the slurry for 1 h at 120 rpm, and then gravity filtered it through Fisher G6 (1.6 μm pore size) glass fiber filters, followed by colorimetric detection of nitrite (NO_2^-) + nitrate (NO_3^-) and ammonium (NH_4^+) in the filtrate (Hood Nowotny et al., 2010,Soil Science Society of America Journal 74, 1018-1027) using a microplate spectrophotometer (Biotek Epoch, Winooski, VT, USA). Filtrate was also analyzed for dissolved organic C (referred to hereafter as extractable organic C) and total dissolved N via combustion and oxidation followed by detection of the evolved CO_2 and N oxide gases on a Formacs HT TOC/TN analyzer (Skalar, Breda, The Netherlands). Extractable organic N was then computed as total dissolved N in filtrate minus extractable mineral N (itself the sum of extractable NH_4-N and NO_2-N + NO_3-N). We determined soil total C and N from dried, milled subsamples subjected to elemental analysis (ECS 4010, Costech, Inc., Valencia, CA, USA) at the University of South Florida Stable Isotope Laboratory. Median concentration of inorganic C in unvegetated surface soil at our sites is 0.5 % of soil mass (Anderson, 2019, Univ. of South Florida M.S. thesis via methods in Wang et al., 2011, Environmental Monitoring and Assessment 174, 241-257). Inorganic C concentrations are likely even lower in our samples from under vegetation, where organic matter would dilute the contribution of inorganic C to soil mass. Nevertheless, the presence of a small inorganic C pool in our soils may be counted in the total C values we report. Extractable organic C is necessarily of organic C origin given the method (sparging with HCl) used in detection. Active C and N represent the fractions of organic C and N that are mineralizable by soil microorganisms under aerobic conditions in long-term soil incubations. To quantify active C and N, 60 g of field-moist soil were apportioned from each composite sample, placed in a filtration apparatus, and incubated in the dark at 25 °C and field capacity moisture for 365 d (as in Lewis et al., 2014, Ecosphere 5, art59). Moisture levels were maintained by frequently weighing incubated soil and wetting them up to target mass. Daily CO_2 flux was quantified on 29 occasions at 0.5-3 week intervals during the incubation period (with shorter intervals earlier in the incubation), and these per day flux rates were integrated over the 365 d period to compute an estimate of active C. Observations of per day flux were made by sealing samples overnight in airtight chambers fitted with septa and quantifying headspace CO_2 accumulation by injecting headspace samples (obtained through the septa via needle and syringe) into an infrared gas analyzer (PP Systems EGM 4, Amesbury, MA, USA). To estimate active N, each incubated sample was leached with a C and N free, 35 psu solution containing micronutrients (Nadelhoffer, 1990, Soil Science Society of America Journal 54, 411-415) on 19 occasions at increasing 1-6 week intervals during the 365 d incubation, and then extracted in 0.5 M K_2SO_4 at the end of the incubation in order to remove any residual mineral N. Active N was then quantified as the total mass of mineral N leached and extracted. Mineral N in leached and extracted solutions was detected as NH_4-N and NO_2-N + NO_3-N via colorimetry as above. This incubation technique precludes new C and N inputs and persistently leaches mineral N, forcing microorganisms to meet demand by mineralizing existing pools, and thereby directly assays the potential activity of soil organic C and N pools present at the time of soil sampling. Because this analysis commences with disrupting soil physical structure, it is biased toward higher estimates of active fractions. Calculations. Non-mobile C and N fractions were computed as total C and N concentrations minus the extractable and active fractions of each element. This data package reports surface-soil constituents (moisture, fines, SOM, and C and N pools and fractions) in both gravimetric units (mass constituent / mass soil) and areal units (mass constituent / soil surface area integrated through 7.6 cm soil depth, the depth of sampling). Areal concentrations were computed as X × D × 7.6, where X is the gravimetric concentration of a soil constituent, D is soil bulk density (g dry soil / cm^3), and 7.6 is the sampling depth in cm. 

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4. Evidence of a Continuous Continental Permian-Triassic Boundary Section in western Equatorial Pangea, Palo Duro Basin, Northwest Texas, U.S.A.

   https://doi.org/10.3389/feart.2021.747777  

   Tabor, Neil J. ; Geissman, John ; Renne, Paul R. ; Mundil, Roland ; Mitchell, William S. ; Myers, Timothy S. ; Jackson, Jacob ; Looy, Cindy V. ; Kirchholtes, Renske P. ( May 2022 , Frontiers in Earth Science)

   The Whitehorse Group and Quartermaster Formation are extensive red-bed terrestrial sequences representing the final episode of sedimentation in the Palo Duro Basin in north-central Texas, U.S.A. Regionally, these strata record the culmination of a long-term regression sequence beginning in the middle to late Permian. The Whitehorse Group includes beds of abundant laminated to massive red quartz siltstone to fine sandstone and rare dolomite, laminated to massive gypsum, and claystones, as well as diagenetic gypsum. The Quartermaster Formation exhibits a change from nearly equal amounts of thin planar and lenticular fine sandstone and laminated to massive mudstone in its lower half to overlying strata with coarser-grained, cross-bedded sandstones indicative of meandering channels up to 7 m deep and rare overbank mudstones. Paleosols are absent in the Upper Whitehorse Group and only poorly developed in the Quartermaster Formation. Volcanic ash-fall deposits (tuffs) present in uppermost Whitehorse Group and lower Quartermaster Formation strata permit correlation among five stratigraphic sections distributed over ∼150 km and provide geochronologic age information for these rocks. Both the Whitehorse Group and Quartermaster Formation have traditionally been assigned to the late Permian Ochoan (Changhsingian) stage, and workers assumed that the Permian-Triassic boundary is characterized by a regionally significant unconformity. Chemostratigraphic or biostratigraphic evidence for this age assignment, however, have been lacking to date. Single zircon U-Pb CA-TIMS analyses from at least two distinct volcanic ash fall layers in the lower Quartermaster Formation, which were identified and collected from five different localities across the Palo Duro Basin, yield interpreted depositional ages ranging from 252.19 ± 0.30 to 251.74 ± 0.28 Ma. Single zircon U-Pb CA-TIMS analyses of detrital zircons from sandstones located only a few meters beneath the top of the Quartermaster Formation yield a range of dates from Mesoproterozoic (1418 Ma) to Middle Triassic (244.5 Ma; Anisian), the latter of which is interpreted as a maximum depositional age, which is no older than Anisian, thus indicating the Permian-Triassic boundary to lie somewhere within the lower Quartermaster Formation/upper Whitehorse Group succession. Stable carbon isotope data from 180 samples of early-burial dolomicrite cements preserve a chemostratigraphic signal that is similar among sections, with a large ∼−8‰ negative isotope excursion ∼20 m beneath the Whitehorse Group-Quartermaster Formation boundary. This large negative carbon isotope excursion is interpreted to be the same excursion associated with the end-Permian extinction and this is in concert with the new high precision radioisotopic age data presented and the fact that the excursion lies within a normal polarity stratigraphic magnetozone. Dolomite cement δ 13 C values remain less negative (between about −5 and −8 permil) into the lower part of the Quartermaster Formation before becoming more positive toward the top of the section. This long interval of negative δ 13 C values in the Quartermaster Formation is interpreted to represent the earliest Triassic (Induan) inception of biotic and ecosystem “recovery.” Oxygen isotope values of dolomicrite cements show a progressive trend toward more positive values through the boundary interval, suggesting substantially warmer conditions around the end-Permian extinction event and a trend toward cooler conditions after the earliest Triassic. Our observations on these strata show that the paleoenvironment and paleoclimate across the Permian-Triassic boundary in western, sub-equatorial Pangea was characterized by depositional systems that were not conducive to plant preservation. 

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5. Cryptic terrestrial fungus-like fossils of the early Ediacaran Period

   https://doi.org/10.1038/s41467-021-20975-1  

   Gan, Tian ; Luo, Taiyi ; Pang, Ke ; Zhou, Chuanming ; Zhou, Guanghong ; Wan, Bin ; Li, Gang ; Yi, Qiru ; Czaja, Andrew D. ; Xiao, Shuhai ( December 2021 , Nature Communications)

   null (Ed.)

   Abstract The colonization of land by fungi had a significant impact on the terrestrial ecosystem and biogeochemical cycles on Earth surface systems. Although fungi may have diverged ~1500–900 million years ago (Ma) or even as early as 2400 Ma, it is uncertain when fungi first colonized the land. Here we report pyritized fungus-like microfossils preserved in the basal Ediacaran Doushantuo Formation (~635 Ma) in South China. These micro-organisms colonized and were preserved in cryptic karstic cavities formed via meteoric water dissolution related to deglacial isostatic rebound after the terminal Cryogenian snowball Earth event. They are interpreted as eukaryotes and probable fungi, thus providing direct fossil evidence for the colonization of land by fungi and offering a key constraint on fungal terrestrialization. 

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