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Large volumes of fluid flow through aged oceanic crust. Given the scale of this water flux, the exchange of organic and inorganic carbon that it mediates between the crust and deep ocean can be significant. However, off-axis carbon fluxes in older oceanic crust are still poorly constrained because access to low-temperature fluids from this environment is limited. At North Pond, a sedimented depression located on 8-million-year-old crust on the flank of the Mid-Atlantic Ridge, circulating crustal fluids are accessible through drilled borehole observatories. Here, fluids are cool (≤ 20°C), oxygenated and bear strong geochemical similarities to bottom seawater. In this study, we report concentrations and isotopic composition of dissolved organic and inorganic carbon from crustal fluids that were sampled six years after the installation of borehole observatories, which better represent the fluid geochemistry prior to drilling and perturbation. Radiocarbon-based signatures within carbon reservoirs support divergent shallow and deep fluid pathways within the crust. We also report a net loss of both dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC) from the fluid during isolation in the crust. The removal of DOC is isotopically selective and consistent with microbe-mediated DOC oxidation. The loss of DIC is consistent with carbonate precipitation, although geochemical signatures of DIC addition to the fluids from DOC oxidation and basalt weathering are also evident. Extrapolated to global fluxes, systems like North Pond could be responsible for a net loss of ~10^11 mol C/yr of DIC and ~10^11 mol C/yr of DOC during the circulation of fluids through oceanic crust at low temperatures. 

Abstract Climate change is affecting how energy and matter flow through ecosystems, thereby altering global carbon and nutrient cycles. Microorganisms play a fundamental role in carbon and nutrient cycling and are thus an integral link between ecosystems and climate. Here, we highlight a major black box hindering our ability to anticipate ecosystem climate responses: viral infections within complex microbial food webs. We show how understanding and predicting ecosystem responses to warming could be challenging—if not impossible—without accounting for the direct and indirect effects of viral infections on different microbes (bacteria, archaea, fungi, protists) that together perform diverse ecosystem functions. Importantly, understanding how rising temperatures associated with climate change influence viruses and virus-host dynamics is crucial to this task, yet is severely understudied. In this perspective, we (i) synthesize existing knowledge about virus-microbe-temperature interactions and (ii) identify important gaps to guide future investigations regarding how climate change might alter microbial food web effects on ecosystem functioning. To provide real-world context, we consider how these processes may operate in peatlands—globally significant carbon sinks that are threatened by climate change. We stress that understanding how warming affects biogeochemical cycles in any ecosystem hinges on disentangling complex interactions and temperature responses within microbial food webs.