Dark carbon fixation in stream carbon cyclingShow others and affiliations
2023 (English)In: Limnology and Oceanography, ISSN 0024-3590, E-ISSN 1939-5590Article in journal (Refereed) Epub ahead of print
Abstract [en]
Headwater streams are often characterized by turbulence, organic matter inputs from terrestrial systems, net heterotrophy, and the microbial loop supplying carbon and energy for consumers. However, ecological models overlook dark carbon fixation (DCF), the light-independent inorganic carbon uptake, mainly based on chemosynthesis, using energy yields from redox reactions. The quantification of microbial biomass production, including DCF, heterotrophic production (HP), gross primary production (GPP), and ecosystem respiration (ER) in lotic aquatic systems, has long yet to be addressed. Here, we investigate HP and DCF in water, sediment, and litter in addition to GPP and ER from streams in pristine rainforests in three distinct sub-basins of the Amazon River, assessing the variety of turbid, black, and clear waters. We observed mean (min-max) values of microbial biomass production of about 0.1 (0.02-1.2), 3.2 (0.8-14.1), and 0.1 (0.02-0.5) mg C m-2 h-1 in water, sediment, and litter samples, in which DCF : HP showed mean (min-max) values of 0.5 (0.2-2), 0.02 (0.001-0.07), and 0.2 (0.001-0.5). Hence, measurements yielded DCF of similar magnitude as HP in water and litter but significantly lower in sediment, indicating that DCF supplied more carbon to planktonic and litter microbes than in top sediments of streams. Literature comparisons show similar DCF and GPP, both being lower than ER in streams. Finally, we found stream DCF higher than in lentic systems, suggesting that flow and turbulence may accelerate chemosynthesis.
Place, publisher, year, edition, pages
WILEY , 2023.
National Category
Oceanography, Hydrology and Water Resources
Identifiers
URN: urn:nbn:se:liu:diva-198483DOI: 10.1002/lno.12430ISI: 001076678300001OAI: oai:DiVA.org:liu-198483DiVA, id: diva2:1805123
Note
Funding Agencies|The research was supported by grants to FM-S (CNPq 152325/2020-4, CAPES 001, CAPES/STINT Brazil-Sweden 2012/2085). AE-P acknowledges funding from the Swedish Research Council Formas (grant no. 2021-02429) and several grants from Brazilian Foundations CAPES [CNPq 152325/2020-4, CAPES/STINT Brazil-Sweden 2012/2085]; Swedish Research Council Formas [2021-02429]; Brazilian Foundations CAPES; FAPERJ (Cientista do Nosso Estado); CNPq (Universal and Ciencias sem Fronteiras) [2012-00048]; Swedish Research Council VR; European Research Council ERC [725546 METLAKE]; Formas [2018-01794]; CNPq [203366/2019-0, 314995/2020-0]; FAPERJ [E-26/201.118/2022, E-26/210.441/2021]
2023-10-162023-10-162024-03-14