{"title":"Featured Cover","authors":"Kuan Cheng, Han Li, Xiu Yuan, Yunlu Yin, Dandan Chen, Ying Wang, Xiaomin Li, Guojun Chen, Fangbai Li, Chao Peng, Yundang Wu, Tongxu Liu","doi":"10.1111/gbi.12531","DOIUrl":"https://doi.org/10.1111/gbi.12531","url":null,"abstract":"<p>Cover Caption: The cover image is based on the Research Article <i>Hematite-promoted nitrate-reducing Fe(II) oxidation by Acidovorax sp. strain BoFeN1: Roles of mineral catalysis and cell encrustation</i> by Kuan Cheng et al., https://doi.org/10.1111/gbi.12510\u0000 \u0000 <figure>\u0000 <div><picture>\u0000 <source></source></picture><p></p>\u0000 </div>\u0000 </figure>\u0000 </p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"20 6","pages":"i"},"PeriodicalIF":3.7,"publicationDate":"2022-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbi.12531","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5705789","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
GeobiologyPub Date : 2022-10-11DOI: 10.1111/gbi.12528
Katarína Holcová, Filip Scheiner
{"title":"An experimental study on post-mortem dissolution and overgrowth processes affecting coccolith assemblages: A rapid and complex process","authors":"Katarína Holcová, Filip Scheiner","doi":"10.1111/gbi.12528","DOIUrl":"https://doi.org/10.1111/gbi.12528","url":null,"abstract":"<p>Coccolith dissolution together with post-mortem morphological features are immensely important phenomena that can affect assemblage compositions, complicate taxonomic identification as well as provide valuable palaeoenvironmental insights. This study summarizes the effects of pH oscillations on post-mortem coccolith morphologies and the abundances and compositions of calcareous nannoplankton assemblages in three distinct types of material—(i) Cretaceous chalk, (ii) Miocene marls, and (iii) late Holocene calcareous ooze. Two independent experimental runs within a semi-enclosed system setting were realized to observe assemblage alterations. One experiment was realized with the presence of bacteria and, in contrast, the second one inhibited their potential effect on the studied system. The pH was gradually decreased within the range of 8.3–6.4 using a reaction of CO<sub>2</sub> with H<sub>2</sub>O forming weak carbonic acid (H<sub>2</sub>CO<sub>3</sub>), thereby affecting [<math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>CO</mi>\u0000 <mn>3</mn>\u0000 <mrow>\u0000 <mn>2</mn>\u0000 <mo>−</mo>\u0000 </mrow>\u0000 </msubsup>\u0000 </mrow>\u0000 </semantics></math>]. Further, a subsequent overgrowth study was carried out during spontaneous degassing accompanied by a gradual pH rise. The experiment revealed that the process and intensity of coccolith corrosion and subsequent overgrowth build-ups are influenced by a plethora of different factors such as (i) pH and associated seawater chemistry, (ii) mineral composition of the sediment, (iii) the presence of coccoliths within a protective substrate (faecal pellets, pores, pits), and (iv) the presence/absence of bacteria. Nannoplankton assemblages with corroded coccoliths or with coccoliths with overgrowth build-ups showed that the observed relative abundances of taxa experienced alteration from the original compositions. Additionally, extreme pH oscillations may result in enhanced morphological changes that make coccoliths unidentifiable structures, and might even evoke the absence of coccoliths in the fossil record.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"21 2","pages":"193-209"},"PeriodicalIF":3.7,"publicationDate":"2022-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5810260","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
GeobiologyPub Date : 2022-10-02DOI: 10.1111/gbi.12529
Scott R. Beeler, Fernando J. Gomez, Alexander S. Bradley
{"title":"Geospatial insights into the controls of microbialite formation at Laguna Negra, Argentina","authors":"Scott R. Beeler, Fernando J. Gomez, Alexander S. Bradley","doi":"10.1111/gbi.12529","DOIUrl":"https://doi.org/10.1111/gbi.12529","url":null,"abstract":"<p>Microbialites provide a record of the interaction of microorganisms with their environment constituting a record of microbial life and environments through geologic time. Our capacity to interpret this record is limited by an incomplete understanding of the microbial, geochemical, and physical processes that influence microbialite formation and morphogenesis. The modern system Laguna Negra in Catamarca Province, Argentina contains microbialites in a zone of carbonate precipitation associated with physico-chemical gradients and variable microbial community structure, making it an ideal location to study how these processes interact to drive microbialite formation. In this study, we investigated the geospatial relationships between carbonate morphology, geochemistry, and microbial community at the macro- (decimeter) to mega- (meter) scale by combining high-resolution imagery with field observations. We mapped the distribution of carbonate morphologies and allochtonously-derived volcaniclasts and correlated these with sedimentary matrices and geochemical parameters. Our work shows that the macroscale distribution of different carbonate morphologies spatially correlates with microbial mat distributions—a result consistent with previous microscale observations. Specifically, microbialitic carbonate morphologies more commonly occur associated with microbial mats while abiotically derived carbonate morphologies were less commonly associated with microbial mats. Spatial variability in the size and abundance of mineralized structures was also observed, however, the processes controlling this variability remains unclear and likely represent a combination of microbial, geochemical, and physical processes. Likewise, the processes controlling the spatial distribution of microbial mats at Laguna Negra are also unresolved. Our results suggest that in addition to the physical drivers observed in other modern environments, variability in the spatial distribution of microbialites and other carbonate morphologies at the macro- to megascale can be controlled by microbial processes. Overall, this study provides insight into the interpretation of microbialite occurrence and distributions in the geologic record and highlights the utility of geospatial statistics to probe the controls of microbialite formation in other environments.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"21 2","pages":"229-243"},"PeriodicalIF":3.7,"publicationDate":"2022-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"6063293","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
GeobiologyPub Date : 2022-09-27DOI: 10.1111/gbi.12524
Sam C. Spinks, Erik A. Sperling, Robert L. Thorne, Felicity LaFountain, Alistair J. R. White, Joseph Armstrong, Martijn Woltering, Ian M. Tyler
{"title":"Mesoproterozoic surface oxygenation accompanied major sedimentary manganese deposition at 1.4 and 1.1 Ga","authors":"Sam C. Spinks, Erik A. Sperling, Robert L. Thorne, Felicity LaFountain, Alistair J. R. White, Joseph Armstrong, Martijn Woltering, Ian M. Tyler","doi":"10.1111/gbi.12524","DOIUrl":"https://doi.org/10.1111/gbi.12524","url":null,"abstract":"<p>Manganese (Mn) oxidation in marine environments requires oxygen (O<sub>2</sub>) or other reactive oxygen species in the water column, and widespread Mn oxide deposition in ancient sedimentary rocks has long been used as a proxy for oxidation. The oxygenation of Earth's atmosphere and oceans across the Archean-Proterozoic boundary are associated with massive Mn deposits, whereas the interval from 1.8–1.0 Ga is generally believed to be a time of low atmospheric oxygen with an apparent hiatus in sedimentary Mn deposition. Here, we report geochemical and mineralogical analyses from 1.1 Ga manganiferous marine-shelf siltstones from the Bangemall Supergroup, Western Australia, which underlie recently discovered economically significant manganese deposits. Layers bearing Mn carbonate microspheres, comparable with major global Mn deposits, reveal that intense periods of sedimentary Mn deposition occurred in the late Mesoproterozoic. Iron geochemical data suggest anoxic-ferruginous seafloor conditions at the onset of Mn deposition, followed by oxic conditions in the water column as Mn deposition persisted and eventually ceased. These data imply there was spatially widespread surface oxygenation ~1.1 Ga with sufficiently oxic conditions in shelf environments to oxidize marine Mn(II). Comparable large stratiform Mn carbonate deposits also occur in ~1.4 Ga marine siltstones hosted in underlying sedimentary units. These deposits are greater or at least commensurate in scale (tonnage) to those that followed the major oxygenation transitions from the Neoproterozoic. Such a period of sedimentary manganogenesis is inconsistent with a model of persistently low O<sub>2</sub> throughout the entirety of the Mesoproterozoic and provides robust evidence for dynamic redox changes in the mid to late Mesoproterozoic.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"21 1","pages":"28-43"},"PeriodicalIF":3.7,"publicationDate":"2022-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbi.12524","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5856305","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Oxygen and carbon isotope variations in Chamelea gallina shells: Environmental influences and vital effects","authors":"Arianna Mancuso, Ruth Yam, Fiorella Prada, Marco Stagioni, Stefano Goffredo, Aldo Shemesh","doi":"10.1111/gbi.12526","DOIUrl":"https://doi.org/10.1111/gbi.12526","url":null,"abstract":"<p>Stable isotopes in mollusc shells, together with variable growth rates and other geochemical properties, can register different environmental clues, including seawater temperature, salinity and primary productivity. However, the strict biological control over the construction of biominerals exerted by many calcifying organisms can constrain the use of these organisms for paleoenvironmental reconstructions. Biologically controlled calcification is responsible for the so called vital effects that cause a departure from isotopic equilibrium during shell formation, resulting in lower shell oxygen and carbon compared to the equilibrium value. We investigated shell oxygen and carbon isotopic composition of the bivalve <i>Chamelea gallina</i> in six sites along with a latitudinal gradient on the Adriatic Sea (NE Mediterranean Sea). Seawater δ<sup>18</sup>O and δ<sup>13</sup>C<sub>DIC</sub> varied from North to South, reflecting variations in seawater temperature, salinity, and chlorophyll concentration among sites. Shell δ<sup>18</sup>O and δ<sup>13</sup>C differed among sites and exhibited a wide range of values along with the ~400 km latitudinal gradient, away from isotopic equilibrium for both isotopes. These results hampered the utilization of this bivalve as a proxy for environmental reconstructions, in spite of <i>C. gallina</i> showing promise as a warm temperature proxy. Rigorous calibration studies with a precise insight of environment and shell growth are crucial prior to considering this bivalve as a reliable paleoclimatic archive.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"21 1","pages":"119-132"},"PeriodicalIF":3.7,"publicationDate":"2022-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbi.12526","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5871427","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
GeobiologyPub Date : 2022-09-23DOI: 10.1111/gbi.12525
Toby A. Halamka, Jonathan H. Raberg, Jamie M. McFarlin, Adam D. Younkin, Christopher Mulligan, Xiao-Lei Liu, Sebastian H. Kopf
{"title":"Production of diverse brGDGTs by Acidobacterium Solibacter usitatus in response to temperature, pH, and O2 provides a culturing perspective on brGDGT proxies and biosynthesis","authors":"Toby A. Halamka, Jonathan H. Raberg, Jamie M. McFarlin, Adam D. Younkin, Christopher Mulligan, Xiao-Lei Liu, Sebastian H. Kopf","doi":"10.1111/gbi.12525","DOIUrl":"https://doi.org/10.1111/gbi.12525","url":null,"abstract":"<p>Branched glycerol dialkyl glycerol tetraethers (brGDGTs) are bacterial membrane lipids that are frequently employed as paleoenvironmental proxies because of the strong empirical correlations between their relative abundances and environmental temperature and pH. Despite the ubiquity of brGDGTs in modern and paleoenvironments, the source organisms of these enigmatic compounds have remained elusive, requiring paleoenvironmental applications to rely solely on observed environmental correlations. Previous laboratory and environmental studies have suggested that the globally abundant bacterial phylum of the Acidobacteria may be an important brGDGT producer in nature. Here, we report on experiments with a cultured Acidobacterium, <i>Solibacter usitatus</i>, that makes a large portion of its cellular membrane (24 ± 9% across all experiments) out of a structurally diverse set of tetraethers including the common brGDGTs Ia, IIa, IIIa, Ib, and IIb. <i>Solibacter usitatus</i> was grown across a range of conditions including temperatures from 15 to 30°C, pH from 5.0 to 6.5, and O<sub>2</sub> from 1% to 21%, and demonstrated pronounced shifts in the degree of brGDGT methylation across these growth conditions. The temperature response in culture was in close agreement with trends observed in published environmental datasets, supporting a physiological basis for the empirical relationship between brGDGT methylation number and temperature. However, brGDGT methylation at lower temperatures (15 and 20°C) was modulated by culture pH with higher pH systematically increasing the degree of methylation. In contrast, pH had little effect on brGDGT cyclization, supporting the hypothesis that changes in bacterial community composition may underlie the link between cyclization number and pH observed in environmental samples. Oxygen concentration likewise affected brGDGT methylation highlighting the potential for this environmental parameter to impact paleotemperature reconstruction. Low O<sub>2</sub> culture conditions further resulted in the production of uncommon brGDGT isomers that could be indicators of O<sub>2</sub> limitation. Finally, the production of brGTGTs (trialkyl tetraethers) in addition to the previously discovered iso-C15-based mono- and diethers in <i>S. usitatus</i> suggests a potential biosynthetic pathway for brGDGTs that uses homologs of the archaeal tetraether synthase (Tes) enzyme for tetraether synthesis from diethers.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"21 1","pages":"102-118"},"PeriodicalIF":3.7,"publicationDate":"2022-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbi.12525","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"6012816","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
GeobiologyPub Date : 2022-09-10DOI: 10.1111/gbi.12523
Christine Nims, Jena E. Johnson
{"title":"Exploring the secondary mineral products generated by microbial iron respiration in Archean ocean simulations","authors":"Christine Nims, Jena E. Johnson","doi":"10.1111/gbi.12523","DOIUrl":"https://doi.org/10.1111/gbi.12523","url":null,"abstract":"<p>Marine chemical sedimentary deposits known as Banded Iron Formations (BIFs) archive Archean ocean chemistry and, potentially, signs of ancient microbial life. BIFs contain a diversity of iron- and silica-rich minerals in disequilibrium, and thus many interpretations of these phases suggest they formed secondarily during early diagenetic processes. One such hypothesis posits that the early diagenetic microbial respiration of primary iron(III) oxides in BIFs resulted in the formation of other iron phases, including the iron-rich silicates, carbonates, and magnetite common in BIF assemblages. Here, we simulated this proposed pathway in laboratory incubations combining a model dissimilatory iron-reducing (DIR) bacterium, <i>Shewanella putrefaciens</i> CN32, and the ferric oxyhydroxide mineral ferrihydrite under conditions mimicking the predicted Archean seawater geochemistry. We assessed the impact of dissolved silica, calcium, and magnesium on the bioreduced precipitates. After harvesting the solid products from these experiments, we analyzed the reduced mineral phases using Raman spectroscopy, electron microscopy, powder x-ray diffraction, and spectrophotometric techniques to identify mineral precipitates and track the bulk distributions of Fe(II) and Fe(III). These techniques detected a diverse range of calcium carbonate morphologies and polymorphism in incubations with calcium, as well as secondary ferric oxide phases like goethite in silica-free experiments. We also identified aggregates of curling, iron- and silica-rich amorphous precipitates in all incubations amended with silica. Although ferric oxides persist even in our electron acceptor-limited incubations, our observations indicate that microbial iron reduction of ferrihydrite is a viable pathway for the formation of early iron silicate phases. This finding allows us to draw parallels between our experimental proto-silicates and the recently characterized iron silicate nanoinclusions in BIF chert deposits, suggesting that early iron silicates could possibly be signatures of iron-reducing metabolisms on early Earth.</p>","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"20 6","pages":"743-763"},"PeriodicalIF":3.7,"publicationDate":"2022-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbi.12523","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"6182599","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
GeobiologyPub Date : 2022-09-08DOI: 10.1111/gbi.12522
Ileana Pérez-Rodríguez, Stefan M. Sievert, Marilyn L. Fogel, Dionysis I. Foustoukos
{"title":"Physiological and metabolic responses of chemolithoautotrophic \u0000 \u0000 \u0000 \u0000 NO\u0000 3\u0000 −\u0000 \u0000 \u0000 reducers to high hydrostatic pressure","authors":"Ileana Pérez-Rodríguez, Stefan M. Sievert, Marilyn L. Fogel, Dionysis I. Foustoukos","doi":"10.1111/gbi.12522","DOIUrl":"https://doi.org/10.1111/gbi.12522","url":null,"abstract":"<p>We investigated the impact of pressure on thermophilic, chemolithoautotrophic <math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>NO</mi>\u0000 <mn>3</mn>\u0000 <mo>−</mo>\u0000 </msubsup>\u0000 </mrow>\u0000 </semantics></math> reducing bacteria of the phyla <i>Campylobacterota</i> and <i>Aquificota</i> isolated from deep-sea hydrothermal vents. Batch incubations at 5 and 20 MPa resulted in decreased <math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>NO</mi>\u0000 <mn>3</mn>\u0000 <mo>−</mo>\u0000 </msubsup>\u0000 </mrow>\u0000 </semantics></math> consumption, lower cell concentrations, and overall slower growth in <i>Caminibacter mediatlanticus</i> (<i>Campylobacterota</i>) and <i>Thermovibrio ammonificans</i> (<i>Aquificota</i>), relative to batch incubations near standard pressure (0.2 MPa) conditions. Nitrogen isotope fractionation effects from chemolithoautotrophic <math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>NO</mi>\u0000 <mn>3</mn>\u0000 <mo>−</mo>\u0000 </msubsup>\u0000 </mrow>\u0000 </semantics></math> reduction by both microorganisms were, on the contrary, maintained under all pressure conditions. Comparable chemolithoautotrophic <math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>NO</mi>\u0000 <mn>3</mn>\u0000 <mo>−</mo>\u0000 </msubsup>\u0000 </mrow>\u0000 </semantics></math> reducing activities between previously reported natural hydrothermal vent fluid microbial communities dominated by <i>Campylobacterota</i> at 25 MPa and <i>Campylobacterota</i> laboratory isolates at 0.2 MPa, suggest robust similarities in cell-specific <math>\u0000 <semantics>\u0000 <mrow>\u0000 <msubsup>\u0000 <mi>NO</mi>\u0000 <mn>3</mn>\u0000 <mo>−</mo>\u0000 </msubsup>\u0000 </mrow>\u0000 </semantics></math> reduction rates and doubling times between microbial populations and communities growing maximally under similar temperature conditions. Physiological and metabolic comparisons of our results with other studies of pressure effects on anaerobic chemolithoautotrophic processes (i.e., microbial S<sup>0</sup>-oxidation coupled to Fe(III) reduction and hydrogenotrophic methanogenesis) suggest that anaerobic chemolithoautotrophs relying on oxidation–reduction (redox) reactions that yield higher Gibbs energies experience larger shifts in cell-specific respiration rates and doubling times at increased pressures. Overall, our results advance understanding of the role of pressure, its relationship with temperature and r","PeriodicalId":173,"journal":{"name":"Geobiology","volume":"20 6","pages":"857-869"},"PeriodicalIF":3.7,"publicationDate":"2022-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"5768156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}