Abstract
The glycerol dialkyl glycerol tetraether (GDGT) lipids of archaea and bacteria have been extensively studied in both modern and ancient wetlands, but their specific biological sources and biogeochemical significance in such settings remain unclear. The stable carbon isotopic composition of GDGTs, and associated tetraether lipids such as butanetriol - DGTs (BDGTs), can help reveal aspects of the carbon metabolism of their source organism. Here we present an in-depth compound-specific analyses of archaeal (isoGDGTs and BDGT-0) and bacterial (brGDGTs) tetraether lipid δ13C values from the Florida Everglades wetland, supplemented by 16S rRNA gene profiling of the archaeal community. We interpret this alongside GDGT δ13C analyses from three additional freshwater wetland sediments, and two ancient wetland deposits (lignites) from the Miocene. Our data suggests that isoGDGT-0 δ13C values, which range from –22.5‰ to −36.5‰ across our wetland sites, could to some degree reflect the relative importance of the acetotrophic and CO2-reducing hydrogenotrophic methanogenic pathways, though definitively delineating between the two is challenging due to (a) potential incorporation of dissolved inorganic carbon (DIC) by CO2 reducers, and (b) the diluting effect of GDGTs derived from seemingly heterotrophic/fermentative Bathyarchaeia, the most abundant archaeal class in the Everglades. In the Everglades, which harbours abundant Methanomassiliicoccales, BDGT-0 is significantly more 13C-depleted than all other lipids, with a δ13C signature at certain depths (∼−40.0 to −45.0‰) that is consistent with an important source from these (likely) methylotrophic methanogens. This adds to a growing body of evidence on the underappreciated role of methylotrophic methanogenesis, largely driven by Methanomassiliicoccales, in the freshwater methane cycle. However, slightly more 13C-enriched values (∼−35.0‰) at certain depths in the same site provide evidence for additional, possibly heterotrophic sources under certain conditions, and BDGT-0 δ13C values in the Miocene lignite (≈ δ13C of TOC) are consistent with a solely heterotrophic source. Where available for measurement, δ13C values of isoGDGTs-1 to -3, averaging –32.7 ± 2.3‰, were significantly more 13C-depleted than isoGDGT-0, suggesting a different mixture of sources, likely including an autotrophic/mixotrophic component derived from archaea belonging to the Crenarchaeota, Nitrososphaeria (formerly Thaumarchaeota) and/or MBG-D/DHVEG-1. Finally, brGDGT δ13C values are generally consistent with their proposed bacterial heterotrophic origin and biosynthetic effects, averaging out at around 4‰ depleted relative to total organic carbon (TOC). Importantly, we find no significant variation between the δ13C values of different brGDGTs across our wetland types. This highlights that spatial and temporal changes in commonly applied brGDGT-based proxies likely do not co-occur with changes in the heterotrophic lifestyle of their producer(s), discounting a possible confounding factor in brGDGT palaeothermometry. Taken together, our results yield insights into wetland archaeal communities and the lipids they produce, and underline the applicability of tetraether δ13C analyses in probing aspects of microbial carbon cycling in modern and ancient wetland sediments.
| Original language | English |
|---|---|
| Pages (from-to) | 1-25 |
| Number of pages | 25 |
| Journal | Geochimica et Cosmochimica Acta |
| Volume | 320 |
| Early online date | 26 Dec 2021 |
| DOIs | |
| Publication status | Published - 18 Jan 2022 |
Bibliographical note
Funding Information:We thank Roger Summons and the Summons Lab at MIT for the use of the preparative-HPLC. We thank Vera A. Korasidis (Smithsonian Institution) and Malcolm Wallace (University of Melbourne) for access to the lignite samples, and we are grateful to Yolanda Foo, Fotis Sgouridis, Ioanna Petropoulou and Penny Timms (UoB) for laboratory support. For work completed at the University of Bristol, we thank the National Environmental Research Council (NERC; Reference: CC010) and National Environmental Isotope Facility (NEIF; www.isotopesuk.org ) for funding and maintenance of the GC-MS, HPLC-MS and GC-C-IRMS instruments used. We thank Xavier Comas at the Department of Geosciences, Florida Atlantic University, for his hospitality and assistance in accessing and sampling in the Florida Everglades. We also thank Mari Könönen for samples from Sebangau, Indonesia, and Sarah Finkelstein and Marissa Davies for samples from James Bay Lowlands. J. Blewett is supported by a NERC GW4 + Doctoral Training Partnership studentship from the Natural Environment Research Council (NE/ L002434/1) and is thankful for the support and additional funding from CASE partner, Elementar UK Ltd. B.D.A. Naafs acknowledges funding through a Royal Society Tata University Research Fellowship. A. Pearson and F. Elling acknowledge support from US NSF grant OCE-1843285. We thank the reviewers and editors for their thoughtful comments that greatly improved the manuscript.
Funding Information:
We thank Roger Summons and the Summons Lab at MIT for the use of the preparative-HPLC. We thank Vera A. Korasidis (Smithsonian Institution) and Malcolm Wallace (University of Melbourne) for access to the lignite samples, and we are grateful to Yolanda Foo, Fotis Sgouridis, Ioanna Petropoulou and Penny Timms (UoB) for laboratory support. For work completed at the University of Bristol, we thank the National Environmental Research Council (NERC; Reference: CC010) and National Environmental Isotope Facility (NEIF; www.isotopesuk.org) for funding and maintenance of the GC-MS, HPLC-MS and GC-C-IRMS instruments used. We thank Xavier Comas at the Department of Geosciences, Florida Atlantic University, for his hospitality and assistance in accessing and sampling in the Florida Everglades. We also thank Mari K?n?nen for samples from Sebangau, Indonesia, and Sarah Finkelstein and Marissa Davies for samples from James Bay Lowlands. J. Blewett is supported by a NERC GW4 + Doctoral Training Partnership studentship from the Natural Environment Research Council (NE/ L002434/1) and is thankful for the support and additional funding from CASE partner, Elementar UK Ltd. B.D.A. Naafs acknowledges funding through a Royal Society Tata University Research Fellowship. A. Pearson and F. Elling acknowledge support from US NSF grant OCE-1843285. We thank the reviewers and editors for their thoughtful comments that greatly improved the manuscript. We acknowledge the Indigenous peoples of all the lands studied in this paper. Given the focus of this study on the Everglades, it is particularly appropriate to acknowledge its rich indigenous history, including the lands of the Calusa, Taino, Tequesta, Mayaimi, Guacata, Jeaga, Miccosukee and Seminole. We recognise the context of colonial violence and removal of people from this land as well as the ongoing stewardship of the Miccosukee and Seminole Tribes. The 16S rRNA sequence datasets generated for this study can be found in the NCBI repository under the SRA BioProject ID PRJNA767362 (http://www.ncbi.nlm.nih.gov/bioproject/767362). All other data is available in the form of supplementary tables.
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