Search for: All records

Particulate phases transport trace metals (TM) and thereby exert a major control on TM distribution in the ocean. Particulate TMs can be classified by their origin as lithogenic (crustal material), biogenic (cellular), or authigenic (formed in situ), but distinguishing these fractions analytically in field samples is a challenge often addressed using operational definitions and assumptions. These different phases require accurate characterization because they have distinct roles in the biogeochemical iron cycle. Particles collected from the upper 2,000 m of the northwest subtropical Atlantic Ocean over four seasonal cruises throughout 2019 were digested with a chemical leach to operationally distinguish labile particulate material from refractory lithogenics. Direct measurements of cellular iron (Fe) were used to calculate the biogenic contribution to the labile Fe fraction, and any remaining labile material was defined as authigenic. Total particulate Fe (PFe) inventories varied <15% between seasons despite strong seasonality in dust inputs. Across seasons, the total PFe inventory (±1SD) was composed of 73 ± 13% lithogenic, 18 ± 7% authigenic, and 10 ± 8% biogenic Fe above the deep chlorophyll maximum (DCM), and 69 ± 8% lithogenic, 30 ± 8% authigenic, and 1.1 ± 0.5% biogenic Fe below the DCM. Data from three other ocean regions further reveal the importance of the authigenic fraction across broad productivity and Fe gradients, comprising ca. 20%–27% of total PFe.

Ocean ecosystem models predict that warming and increased surface ocean stratification will trigger a series of ecosystem events, reducing the biological export of particulate carbon to the ocean interior. We present a nearly three-decade time series from the open ocean that documents a biological response to ocean warming and nutrient reductions wherein particulate carbon export is maintained, counter to expectations. Carbon export is maintained through a combination of phytoplankton community change to favor cyanobacteria with high cellular carbon-to-phosphorus ratios and enhanced shallow phosphorus recycling leading to increased nutrient use efficiency. These results suggest that surface ocean ecosystems may be more responsive and adapt more rapidly to changes in the hydrographic system than is currently envisioned in earth ecosystem models, with positive consequences for ocean carbon uptake.

Climate warming likely drives ocean deoxygenation, but models still cannot fully explain observed declines in oxygen. One unconstrained parameter is the oxygen demand per carbon respired for complete remineralization of organic matter (i.e., the total respiration quotient,r_Σ‐O2:C). Here, we tested ifr_Σ‐O2:Cdeclined with depth by quantifying suspended concentrations of particulate organic carbon (POC), particulate organic nitrogen (PON), particulate organic phosphorus (POP), particulate chemical oxygen demand (PCOD), and total oxygen demand (Σ‐O₂ = PCOD + 2PON) down to a depth of 1,000 m in the Sargasso Sea. The respiration quotient (r_‐O2:C = PCOD:POC) and total respiration quotient (r_Σ‐O2:C = Σ‐O₂:POC) declined with depth in the euphotic zone, but increased vertically in the disphotic zone. C:N andr_Σ‐O2:Nchanged with depth, but surface values were similar to values at 1,000 m. C:P, N:P, andr_Σ‐O2:Pmostly decreased with depth. We hypothesize thatr_Σ‐O2:Cis linked to multiple environmental factors that change with depth, such as phytoplankton community structure and the preferential production/removal of biomolecules. Using a global model, we show that the global distribution of dissolved oxygen is equally sensitive tor_‐O2:Cvarying between surface biomes versus vertically during remineralization. Additionally, adjusting the model'sr_‐O2:Cwith depth to match our observations resulted in less dissolved oxygen throughout the upper ocean. Most of this loss occurred in the tropical Pacific thermocline, where oxygen models underestimate deoxygenation the most. This study aims to improve our understanding of biological oxygen demand as warming‐induced deoxygenation continues.