Colwell
Frederick S.
Colwell
Frederick S.
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ArticleAncient metabolisms of a thermophilic subseafloor bacterium(Frontiers Media, 2021-12-01) Smith, Amy R. ; Mueller, Ryan ; Fisk, Martin ; Colwell, Frederick S.The ancient origins of metabolism may be rooted deep in oceanic crust, and these early metabolisms may have persisted in the habitable thermal anoxic aquifer where conditions remain similar to those when they first appeared. The Wood–Ljungdahl pathway for acetogenesis is a key early biosynthetic pathway with the potential to influence ocean chemistry and productivity, but its contemporary role in oceanic crust is not well established. Here, we describe the genome of a novel acetogen from a thermal suboceanic aquifer olivine biofilm in the basaltic crust of the Juan de Fuca Ridge (JdFR) whose genome suggests it may utilize an ancient chemosynthetic lifestyle. This organism encodes the genes for the complete canonical Wood–Ljungdahl pathway, but is potentially unable to use sulfate and certain organic carbon sources such as lipids and carbohydrates to supplement its energy requirements, unlike other known acetogens. Instead, this organism may use peptides and amino acids for energy or as organic carbon sources. Additionally, genes involved in surface adhesion, the import of metallic cations found in Fe-bearing minerals, and use of molecular hydrogen, a product of serpentinization reactions between water and olivine, are prevalent within the genome. These adaptations are likely a reflection of local environmental micro-niches, where cells are adapted to life in biofilms using ancient chemosynthetic metabolisms dependent on H2 and iron minerals. Since this organism is phylogenetically distinct from a related acetogenic group of Clostridiales, we propose it as a new species, Candidatus Acetocimmeria pyornia.
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ArticleIdentification and removal of contaminant sequences from ribosomal gene databases : lessons from the Census of Deep Life(Frontiers Media, 2018-04-30) Sheik, Cody S. ; Kiel Reese, Brandi ; Twing, Katrina I. ; Sylvan, Jason B. ; Grim, Sharon L. ; Schrenk, Matthew O. ; Sogin, Mitchell L. ; Colwell, Frederick S.Earth’s subsurface environment is one of the largest, yet least studied, biomes on Earth, and many questions remain regarding what microorganisms are indigenous to the subsurface. Through the activity of the Census of Deep Life (CoDL) and the Deep Carbon Observatory, an open access 16S ribosomal RNA gene sequence database from diverse subsurface environments has been compiled. However, due to low quantities of biomass in the deep subsurface, the potential for incorporation of contaminants from reagents used during sample collection, processing, and/or sequencing is high. Thus, to understand the ecology of subsurface microorganisms (i.e., the distribution, richness, or survival), it is necessary to minimize, identify, and remove contaminant sequences that will skew the relative abundances of all taxa in the sample. In this meta-analysis, we identify putative contaminants associated with the CoDL dataset, recommend best practices for removing contaminants from samples, and propose a series of best practices for subsurface microbiology sampling. The most abundant putative contaminant genera observed, independent of evenness across samples, were Propionibacterium, Aquabacterium, Ralstonia, and Acinetobacter. While the top five most frequently observed genera were Pseudomonas, Propionibacterium, Acinetobacter, Ralstonia, and Sphingomonas. The majority of the most frequently observed genera (high evenness) were associated with reagent or potential human contamination. Additionally, in DNA extraction blanks, we observed potential archaeal contaminants, including methanogens, which have not been discussed in previous contamination studies. Such contaminants would directly affect the interpretation of subsurface molecular studies, as methanogenesis is an important subsurface biogeochemical process. Utilizing previously identified contaminant genera, we found that ∼27% of the total dataset were identified as contaminant sequences that likely originate from DNA extraction and DNA cleanup methods. Thus, controls must be taken at every step of the collection and processing procedure when working with low biomass environments such as, but not limited to, portions of Earth’s deep subsurface. Taken together, we stress that the CoDL dataset is an incredible resource for the broader research community interested in subsurface life, and steps to remove contamination derived sequences must be taken prior to using this dataset.
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ArticleAges and magnetic structures of the South China Sea constrained by deep tow magnetic surveys and IODP Expedition 349(John Wiley & Sons, 2014-12-27) Li, Chun-Feng ; Xu, Xing ; Lin, Jian ; Sun, Zhen ; Zhu, Jian ; Yao, Yongjian ; Zhao, Xixi ; Liu, Qingsong ; Kulhanek, Denise K. ; Wang, Jian ; Song, Taoran ; Zhao, Junfeng ; Qiu, Ning ; Guan, Yongxian ; Zhou, Zhiyuan ; Williams, Trevor ; Bao, Rui ; Briais, Anne ; Brown, Elizabeth A. ; Chen, Yifeng ; Clift, Peter D. ; Colwell, Frederick S. ; Dadd, Kelsie A. ; Ding, Weiwei ; Almeida, Ivan Hernandez ; Huang, Xiao-Long ; Hyun, Sangmin ; Jiang, Tao ; Koppers, Anthony A. P. ; Li, Qianyu ; Liu, Chuanlian ; Liu, Zhifei ; Nagai, Renata H. ; Peleo-Alampay, Alyssa ; Su, Xin ; Tejada, Maria Luisa G. ; Trinh, Hai Son ; Yeh, Yi-Ching ; Zhang, Chuanlun ; Zhang, Fan ; Zhang, Guo-LiangCombined analyses of deep tow magnetic anomalies and International Ocean Discovery Program Expedition 349 cores show that initial seafloor spreading started around 33 Ma in the northeastern South China Sea (SCS), but varied slightly by 1–2 Myr along the northern continent-ocean boundary (COB). A southward ridge jump of ∼20 km occurred around 23.6 Ma in the East Subbasin; this timing also slightly varied along the ridge and was coeval to the onset of seafloor spreading in the Southwest Subbasin, which propagated for about 400 km southwestward from ∼23.6 to ∼21.5 Ma. The terminal age of seafloor spreading is ∼15 Ma in the East Subbasin and ∼16 Ma in the Southwest Subbasin. The full spreading rate in the East Subbasin varied largely from ∼20 to ∼80 km/Myr, but mostly decreased with time except for the period between ∼26.0 Ma and the ridge jump (∼23.6 Ma), within which the rate was the fastest at ∼70 km/Myr on average. The spreading rates are not correlated, in most cases, to magnetic anomaly amplitudes that reflect basement magnetization contrasts. Shipboard magnetic measurements reveal at least one magnetic reversal in the top 100 m of basaltic layers, in addition to large vertical intensity variations. These complexities are caused by late-stage lava flows that are magnetized in a different polarity from the primary basaltic layer emplaced during the main phase of crustal accretion. Deep tow magnetic modeling also reveals this smearing in basement magnetizations by incorporating a contamination coefficient of 0.5, which partly alleviates the problem of assuming a magnetic blocking model of constant thickness and uniform magnetization. The primary contribution to magnetic anomalies of the SCS is not in the top 100 m of the igneous basement.
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ArticleMicrobial activity in the marine deep biosphere : progress and prospects(Frontiers Media, 2013-07-11) Orcutt, Beth N. ; LaRowe, Douglas E. ; Biddle, Jennifer F. ; Colwell, Frederick S. ; Glazer, Brian T. ; Kiel Reese, Brandi ; Kirkpatrick, John B. ; Lapham, Laura L. ; Mills, Heath J. ; Sylvan, Jason B. ; Wankel, Scott D. ; Wheat, C. GeoffreyThe vast marine deep biosphere consists of microbial habitats within sediment, pore waters, upper basaltic crust and the fluids that circulate throughout it. A wide range of temperature, pressure, pH, and electron donor and acceptor conditions exists—all of which can combine to affect carbon and nutrient cycling and result in gradients on spatial scales ranging from millimeters to kilometers. Diverse and mostly uncharacterized microorganisms live in these habitats, and potentially play a role in mediating global scale biogeochemical processes. Quantifying the rates at which microbial activity in the subsurface occurs is a challenging endeavor, yet developing an understanding of these rates is essential to determine the impact of subsurface life on Earth's global biogeochemical cycles, and for understanding how microorganisms in these “extreme” environments survive (or even thrive). Here, we synthesize recent advances and discoveries pertaining to microbial activity in the marine deep subsurface, and we highlight topics about which there is still little understanding and suggest potential paths forward to address them. This publication is the result of a workshop held in August 2012 by the NSF-funded Center for Dark Energy Biosphere Investigations (C-DEBI) “theme team” on microbial activity (www.darkenergybiosphere.org).
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ArticleSeismic stratigraphy of the central South China Sea basin and implications for neotectonics(John Wiley & Sons, 2015-03-16) Li, Chun-Feng ; Li, Jiabiao ; Ding, Weiwei ; Franke, Dieter ; Yao, Yongjian ; Shi, Hesheng ; Pang, Xiong ; Cao, Ying ; Lin, Jian ; Kulhanek, Denise K. ; Williams, Trevor ; Bao, Rui ; Briais, Anne ; Brown, Elizabeth A. ; Chen, Yifeng ; Clift, Peter D. ; Colwell, Frederick S. ; Dadd, Kelsie A. ; Hernandez-Almeida, Ivan ; Huang, Xiao-Long ; Hyun, Sangmin ; Jiang, Tao ; Koppers, Anthony A. P. ; Li, Qianyu ; Liu, Chuanlian ; Liu, Qingsong ; Liu, Zhifei ; Nagai, Renata H. ; Peleo-Alampay, Alyssa ; Su, Xin ; Sun, Zhen ; Tejada, Maria Luisa G. ; Trinh, Hai Son ; Yeh, Yi-Ching ; Zhang, Chuanlun ; Zhang, Fan ; Zhang, Guo-Liang ; Zhao, XixiCoring/logging data and physical property measurements from International Ocean Discovery Program Expedition 349 are integrated with, and correlated to, reflection seismic data to map seismic sequence boundaries and facies of the central basin and neighboring regions of the South China Sea. First-order sequence boundaries are interpreted, which are Oligocene/Miocene, middle Miocene/late Miocene, Miocene/Pliocene, and Pliocene/Pleistocene boundaries. A characteristic early Pleistocene strong reflector is also identified, which marks the top of extensive carbonate-rich deposition in the southern East and Southwest Subbasins. The fossil spreading ridge and the boundary between the East and Southwest Subbasins acted as major sedimentary barriers, across which seismic facies changes sharply and cannot be easily correlated. The sharp seismic facies change along the Miocene-Pliocene boundary indicates that a dramatic regional tectonostratigraphic event occurred at about 5 Ma, coeval with the onsets of uplift of Taiwan and accelerated subsidence and transgression in the northern margin. The depocenter or the area of the highest sedimentation rate switched from the northern East Subbasin during the Miocene to the Southwest Subbasin and the area close to the fossil ridge in the southern East Subbasin in the Pleistocene. The most active faulting and vertical uplifting now occur in the southern East Subbasin, caused most likely by the active and fastest subduction/obduction in the southern segment of the Manila Trench and the collision between the northeast Palawan and the Luzon arc. Timing of magmatic intrusions and seamounts constrained by seismic stratigraphy in the central basin varies and does not show temporal pulsing in their activities.