Dimethylsulfide Production Research Articles

Factors controlling the competition between <i>Phaeocystis</i> and diatoms in the Southern Ocean and implications for carbon export fluxes

Abstract. The high-latitude Southern Ocean phytoplankton community is shaped by the competition between Phaeocystis and silicifying diatoms, with the relative abundance of these two groups controlling primary and export production, the production of dimethylsulfide, the ratio of silicic acid and nitrate available in the water column, and the structure of the food web. Here, we investigate this competition using a regional physical–biogeochemical–ecological model (ROMS-BEC) configured at eddy-permitting resolution for the Southern Ocean south of 35∘ S. We improved ROMS-BEC by adding an explicit parameterization of Phaeocystis colonies so that the model, together with the previous addition of an explicit coccolithophore type, now includes all biogeochemically relevant Southern Ocean phytoplankton types. We find that Phaeocystis contribute 46±21 % (1σ in space) and 40±20 % to annual net primary production (NPP) and particulate organic carbon (POC) export south of 60∘ S, respectively, making them an important contributor to high-latitude carbon cycling. In our simulation, the relative importance of Phaeocystis and diatoms is mainly controlled by spatiotemporal variability in temperature and iron availability. In addition, in more coastal areas, such as the Ross Sea, the higher light sensitivity of Phaeocystis at low irradiances promotes the succession from Phaeocystis to diatoms. Differences in the biomass loss rates, such as aggregation or grazing by zooplankton, need to be considered to explain the simulated seasonal biomass evolution and carbon export fluxes.

Production, distribution and flux of dimethyl sulfide in the East China Sea and its contribution to atmospheric sulfate aerosols

Environmental context Dimethyl sulfide is an important biogenic gas, released from ocean to atmosphere, which contributes to aerosol formation and can therefore affect global climate. Studies on dimethyl sulfide in both seawater and atmosphere have linked the atmospheric chemistry of dimethyl sulfide with its circulation in the marine environment. This study showed that these biogenic emissions contribute to the sulfur cycle and particulate production, deepening our understanding of their role in the East China Sea. Abstract Dimethyl sulfide (DMS) is identified as an essential biogenic sulfur compound in the ocean. Its oxidation products are thought to be important contributors to cloud condensation nuclei, thereby influencing the earth’s radiative balance and climate. The concentrations of DMS and its precursor, dimethylsulfoniopropionate (DMSP) were measured in seawater and sediment pore water in the East China Sea (ECS) during summer. In addition, dissolved DMSP (DMSPd) degradation rates, DMS production and consumption rates, and sea-to-air flux of DMS were determined, and the biogenic contribution to atmospheric non-sea-salt sulfate (nss-SO42−) was evaluated in PM2.5 and PM10 aerosols over the study area. The spatial distributions of DMS and DMSP were closely related to that of chlorophyll-a and decreased from the inshore to the offshore. The concentration of DMSPd in sediment pore water was significantly higher than that in bottom water, which indicated that sediment is a net source of DMSPd for bottom water. The biological incubation experiments showed that ~36.0 % of decomposed DMSPd was degraded into DMS, while 78.7 % of produced DMS was consumed by bacteria within the surface water. The sea-to-air flux of DMS varied from 1.30 to 31.84 μmol m−2 day−1, with an average of 7.45 ± 6.30 μmol m−2 day−1. Biogenic contributions of the ECS to total nss-SO42− were estimated to be 13.0 % ± 9.9 % in PM2.5 and 13.5 % ± 5.1 % in PM10 samples respectively, which indicated that marine DMS release cannot be neglected in the ECS during summer.

Potential roles of dimethysulfoxide in regional sulfur cycling and phytoplankton physiological ecology in the NE Subarctic Pacific

AbstractWe measured the concentration and turnover rates of dimethylsulfoxide (DMSO) across the northeast Subarctic Pacific (NESAP) to better understand the role of this compound in regional sulfur cycling and phytoplankton physiological ecology. Using ship‐track observations and Lagrangian drifter surveys, we examined the spatial and temporal components of DMS and DMSO variability, comparing rates of DMSO reduction with simultaneous measurements of dimethylsulfide (DMS) oxidation and dimethylsulfoniopropionate (DMSP) cleavage. Our results show high concentrations and rapid turnover of DMSO across much of our NESAP survey region. DMS and DMSO concentrations ranged from < 1 nM to maxima of 26 nM and 183 nM, respectively, and exhibited a nonlinear positive relationship. Rate constants for DMSO reduction to DMS ranged from < 1 to 6.5 d−1 and were correlated to bacterial production and phytoplankton taxonomic composition. DMSO reduction rates exceeded dissolved DMSP cleavage at nearly all stations, and exceeded DMS oxidation rates at four stations where DMSO reduction and DMS oxidation were measured simultaneously. At these stations, net DMS production from DMSO ranged from 0.50 to 7.18 nM d−1. During our Lagrangian survey, DMSO concentrations decreased during periods of peak mid‐day irradiance. A strong correlation between DMSO concentrations, non‐photochemical quenching and photochemical efficiency of photosystem II (Fv/Fm) suggest a potential role for DMSO in photo‐protection, supporting previous suggestions of an anti‐oxidant function for this molecule. Our findings highlight the potential contribution of DMSO to net DMS production in the NESAP, and suggest a role for this compound in phytoplankton physiological ecology.

Spatial distribution and potential sources of methanesulfonic acid in High Asia glaciers

As a receptor of atmospheric deposition, glaciers are considered an ideal archive in the study of climate change and geochemical cycles. The deposition of methanesulfonic acid (MSA) in the glaciers provides good opportunities to study the biogeochemical cycle of sulfur in the cryosphere. In the present work, snow samples were collected from six High Asia glaciers along a north-to-south transect to determine the spatial distribution of MSA and elucidate its potential sources. The median MSA concentration in the Urumqi Glacier No.1 of Tien Shan was 138.8 ng mL−1, which was distinctly higher than those observed in the Tibetan Plateau (TP) glaciers and polar regions. The levels of MSA in the interior TP glaciers were higher than those observed in the margins of northeastern and southeastern TP. Good correlations between MSA and K+ (r = 0.86, n = 30, α = 0.01), Mg2+ (r = 0.86), and NH4+ (r = 0.73) were observed in continental glaciers. Principal component analysis indicated that MSA may have terrigenous material inputs. At Yulong Snow Mountain, MSA was correlated with Na+ (r = 0.76, n = 8, α = 0.1), a sea-salt tracer ion, suggesting that MSA may be derived from marine environments. According to dimethyl sulfide (DMS) production and NH3 emissions in High Asia, we deduced that the high concentrations of MSA in continental glaciers are possibly related to the sources of hypersaline soil environments and animal husbandry in nomadic areas. This work is useful for further studies on regional sulfur cycling and the impacts of human activities on climate change.

Effects of microplastics exposure on ingestion, fecundity, development, and dimethylsulfide production in Tigriopus japonicus (Harpacticoida, copepod)

The effects of microplastics pollution on the marine ecosystem have aroused attention. Copepod grazing stimulates dimethylsulfide (DMS) release from dimethylsulfoniopropionate (DMSP) in phytoplankton, but the effect of microplastics exposure on DMS and DMSP production during copepod feeding has not yet been revealed. Here, we investigated the effects of polyethylene (PE) and polyamide-nylon 6 (PA 6) microplastics on ecotoxicity and DMS/DMSP production in the copepod Tigriopus japonicus. The microplastics had detrimental effects on feeding, egestion, reproduction, survival, and DMS and DMSP production in T. japonicus and presented significant dose-response relationships. The 24 h-EC50 for ingestion rates (IRs) of female T. japonicus exposed to PE and PA 6 were 57.6 and 58.9 mg L−1, respectively. In comparison, the body size of the copepods was not significantly affected by the microplastics during one generation of culture. Ingesting fluorescently labeled microplastics confirmed that microplastics were ingested by T. japonicus and adhered to the organs of the body surface. T. japonicus grazing promoted DMS release originating from degradation of DMSP in algal cells. Grazing-activated DMS production decreased because of reduced IR in the presence of microplastics. These results provide new insight into the biogeochemical cycle of sulfur during feeding in copepods exposed to microplastics.

Distribution of Dimethylsulfoniopropionate Degradation Genes Reflects Strong Water Current Dependencies in the Sanriku Coastal Region in Japan: From Mesocosm to Field Study

Dimethyl sulfide (DMS) is an important component of the global sulfur cycle as it is the most abundant sulfur compound that is emitted via the ocean surface to the atmosphere. Dimethylsulfoniopropionate (DMSP), the precursor of DMS, is mainly produced by phytoplankton and is degraded by marine bacteria. To reveal the role of bacteria in the regulation of DMSP degradation and DMS production, mesocosm and field studies were performed in the Sanriku Coast on the Pacific Ocean in northeast Japan. The responsible bacteria for the transformation of DMSP to DMS and the assimilation of DMSP were monitored, and the genes encoding DMSP lyase (dddD and dddP) and DMSP demethylase (dmdA) were analyzed. The mesocosm study showed that the dmdA subclade D was the dominant DMSP degradation gene in the free-living (FL) and particle-associated (PA) fractions. The dddD gene was found in higher abundance than the dddP gene in all the tested samples. Most importantly, DMS concentration was positively correlated with the abundance of the dddD gene. These results indicated that bacteria possessing dmdA and dddD genes were the major contributors to the DMSP degradation and DMS production, respectively. The genes dmdA subclade D and dddP were abundant in the Tsugaru Warm (TW) Current, while the dmdA subclade C/2 and dddD genes were dominant in the Oyashio (OY) Current. Functional gene network analysis also showed that the DMSP degradation genes were divided into OY and TW Current-related modules, and genes sharing similar functions were clustered in the same module. Our data suggest that environmental fluctuations resulted in habitat filtering and niche partitioning of bacteria possessing DMSP degradation genes. Overall, our findings provide novel insights into the distribution and abundance of DMSP degradation genes in a coastal region with different water current systems.

Atmospheric dimethyl sulfide and its significant influence on the sea-to-air flux calculation over the Southern Ocean

Our understanding about the atmospheric dimethyl sulfide (DMS) and its influence to sea-to-air flux calculation in the Southern Ocean is still limited due to insufficient investigations. Herein, high-resolution shipboard underway simultaneous surface seawater and atmospheric DMS measurements were conducted in the Southern Ocean from February 23 to March 31, 2018. A larger variation of DMS levels was found in atmosphere compared with that in seawater. Remarkably, a large-scale area with high seawater and atmospheric DMS concentrations up to 27.9 nM and 3.92 ppbv, respectively, was investigated outside of Ross Sea sector. Atmospheric DMS levels were strongly impacted by wind speed and air mass convection. The relationship between atmospheric DMS and air mass exposure to oceanic chlorophyll varied greatly depending on the area of investigation. Some other regions with high DMS production capacity were examined as well beside those along the cruise tracks based on the results of positive correlations with high slopes and back trajectories. Moreover, significant uncertainty of sea-to-air DMS flux over the Southern Ocean could be caused by follows: (1) the selecting of different gas transfer coefficients; (2) the negative flux values calculated under high atmospheric DMS levels together with low seawater DMS concentrations; and (3) the greatly overestimated flux, approximately 47.1–76.9%, without considering the atmospheric DMS. This study highlights the urgent demand of high-resolution observations of atmospheric DMS over the Southern Ocean to estimate DMS emission with high accuracy.

Identification of a functional dddD-Rh for dimethyl sulfide production in the Antarctic Rhodococcus sp. NJ-530.

Dimethylsulfoniopropionate (DMSP) is widespread in the oceans, and its biological metabolite, dimethyl sulfide (DMS), plays an important role in the atmosphere. The Antarctic region has become a hotspot in DMS studies due to the high spatial and temporal variability in DMS(P) concentration, but the level of bacterial DMS production remains unclear. In this study, a bacterium isolated from Antarctic floating ice, Rhodococcus sp. NJ-530, was found to metabolize DMSP into DMS, and the rate of DMS production was measured as 3.96 pmol·mg protein-1 ·h-1 . Rhodococcus sp. NJ-530 had a DddD-Rh enzyme containing two CaiB domains, which belonged to the CoA-transferase III superfamily. However, the DddD-Rh had a molecular weight of 73.21 kDa, which was very different from previously characterized DddD enzymes in sequence and evolution. In vitro assays showed that DddD-Rh was functional in the presence of acetyl-CoA. This was the first functional DddD from Gram-positive Actinobacteria. Moreover, a quantitative real-time polymerase chain reaction revealed that high temperature facilitated the expression of dddD-Rh, and changes of salinity had little effect on it. This study adds new evidence to the bacterial DMS production in the Southern Ocean and provides a basis for investigating the metabolic mechanism of DMSP in extreme environments.

Acrylic acid and related dimethylated sulfur compounds in the Bohai and Yellow seas during summer and winter

Abstract. Spatiotemporal distributions of dissolved acrylic acid (AAd) and related biogenic sulfur compounds including dimethylsulfide (DMS) and dissolved and total dimethylsulfoniopropionate (DMSPd and DMSPt) were investigated in the Bohai Sea (BS) and Yellow Sea (YS) during summer and winter. AAd and DMS production from DMSPd degradation and AAd degradation were analyzed. Significant seasonal variations in AAd and DMS(P) were observed. AAd exhibited similar distributions during summer and winter; i.e., relatively high values of AAd occurred in the BS and the northern YS, and the concentrations decreased from inshore to offshore areas in the southern YS. Due to strong biological production from DMSP and abundant terrestrial inputs from rivers in summer, the AAd concentrations in the surface seawater during summer (30.01 nmol L−1) were significantly higher than those during winter (14.98 nmol L−1). The average concentration sequence along the transects during summer (AAd > DMSPt > DMS > DMSPd) showed that particulate DMSP (DMSPp) acted as a DMS producer and that terrestrial sources of AAd were present; in contrast, the sequence in winter was AAd > DMSPt > DMSPd > DMS. High values of AAd and DMS(P) were mostly observed in the upper layers, with occasional high values at the bottom. High AAd concentrations in the porewater, which could be transported to the bottom water, might result from the cleavage of intracellular DMSP and reduce bacterial metabolism in sediments. In addition, the production and degradation rates of biogenic sulfur compounds were significantly higher in summer than in winter, and the removal of AAd was primarily attributed to microbial consumption. Other sources of AAd existed aside from the production from DMSPd.

Variation in phytoplankton community and its implication to dimethylsulphide production at a coastal station off Goa, India

Seasonal hypoxia/suboxia (at times anoxia) towards the end of Southwest monsoon (SWM; June to September) at the coastal time series site off Goa, West coast of India was found to influence the dynamics of phytoplankton biomass, community structure and production of climatically active gas, dimethylsulphide (DMS). In this diatom dominated study region, high DMS production in the subsurface waters during late SWM might possible be attributed to the stress experienced by micro- and macro-algae from the prevailing low oxygen subsurface waters through different pathways specifically believed to be via methylation pathway (see Schafer et al., 2010). Based on laboratory experiments, we hypothesize presence of floating seaweeds mostly Sargassum species washed from the shore to the study site to contribute sizably to DMS production in the water column as they sink and degrade during the senescence phase. However, we are yet to address its loss/emission processes across the oxic-hypoxic boundary of seasonal (and permanent) oxygen minimum zone of the northern Indian Ocean, which is important from the viewpoint of global climate change.

Metagenomic Insights Into the Cycling of Dimethylsulfoniopropionate and Related Molecules in the Eastern China Marginal Seas.

The microbial cycling of dimethylsulfoniopropionate (DMSP) and its gaseous catabolites dimethylsulfide (DMS) and methanethiol (MeSH) are important processes in the global sulfur cycle, marine microbial food webs, signaling pathways, atmospheric chemistry, and potentially climate regulation. Many functional genes have been identified and used to study the genetic potential of microbes to produce and catabolize these organosulfur compounds in different marine environments. Here, we sampled seawater, marine sediment and hydrothermal sediment, and polymetallic sulfide in the eastern Chinese marginal seas and analyzed their microbial communities for the genetic potential to cycle DMSP, DMS, and MeSH using metagenomics. DMSP was abundant in all sediment samples, but was fivefold less prominent in those from hydrothermal samples. Indeed, Yellow Sea (YS) sediment samples had DMSP concentrations two orders of magnitude higher than in surface water samples. Bacterial genetic potential to synthesize DMSP (mainly in Rhodobacteraceae bacteria) was far higher than for phytoplankton in all samples, but particularly in the sediment where no algal DMSP synthesis genes were detected. Thus, we propose bacteria as important DMSP producers in these marine sediments. DMSP catabolic pathways mediated by the DMSP lyase DddP (prominent in Pseudomonas and Mesorhizobium bacteria) and DMSP demethylase DmdA enzymes (prominent in Rhodobacteraceae bacteria) and MddA-mediated MeSH S-methylation were very abundant in Bohai Sea and Yellow Sea sediments (BYSS) samples. In contrast, the genetic potential for DMSP degradation was very low in the hydrothermal sediment samples—dddP was the only catabolic gene detected and in only one sample. However, the potential for DMS production from MeSH (mddA) and DMS oxidation (dmoA and ddhA) was relatively abundant. This metagenomics study does not provide conclusive evidence for DMSP cycling; however, it does highlight the potential importance of bacteria in the synthesis and catabolism of DMSP and related compounds in diverse sediment environments.

Combined effects of elevated temperature and pCO2 on the production of DMSP and DMS in the culture of Amphidinium carterae

Ocean acidification and global warming might affect the production of dimethylsulfoniopropionate (DMSP), dimethylsulfide (DMS), and dissolved acrylic acid (AAd) by marine phytoplankton. Monoculture incubation experiments were conducted with the dinoflagellate Amphidinium carterae to investigate the effects of elevated CO2 concentration and temperature on growth and productions of DMSP, DMS, and AAd. Two pCO2 levels were set as 400 and 1000 μatm, and two temperatures were set as 20 and 23 °C. The growth of A. carterae remained unaffected by an increase of CO2 to 1000 μatm and a rise of temperature of 3 °C. Moreover, the elevated CO2 concentration and temperature had no significant effects on the concentrations and cell-normalized concentrations of DMSP, DMS, and AAd. No additive or synergistic effects of elevated CO2 concentration and temperature on A. carterae were observed, indicating that A. carterae was insensitive to elevated CO2 and temperature in short time incubation.

Distribution Characteristics of Dimethylated Sulfur Compounds and Turnover of Dimethylsulfide in the Northern South China Sea During Summer

AbstractSpatial distributions of dimethylsulfide (DMS), dimethylsulfoniopropionate (DMSP), and dimethyl sulfoxide (DMSO) in the northern South China Sea were determined in the summer of 2015. The mean concentrations of DMS, particulate DMSP (DMSPp), dissolved DMSP (DMSPd), dissolved DMSO (DMSOd), and particulate DMSO (DMSOp) in the surface seawater were 2.8 ± 1.0, 6.8 ± 1.5, 14.0 ± 3.1, 12.2 ± 3.2, and 9.2 ± 2.6 nmol L−1, respectively. The contributions of three principal removal pathways of DMS were investigated. The average biological production and consumption rates of DMS in the surface seawater were 6.15 ± 1.12 and 4.63 ± 1.32 nmol L−1 day−1. Deck incubation experiments showed that the photooxidation rates of DMS for different radiation bands followed the order: KUVB > KUVA > Kvisible light. The DMS photooxidation rates were higher in the coastal waters than in the open ocean, which might be associated with the higher concentrations of dissolved organic matter of terrigenous input. The sea‐to‐air fluxes of DMS ranged from 1.6 to 50.3 μmol m−2 day−1 with an average value of 15.6 ± 11.6 μmol m−2 day−1. Based on the respective turnover times of DMS, the contributions of biological consumption, photooxidation, and sea‐to‐air exchange to the sink of DMS were 32.6 ± 11.0%, 23.2 ± 8.9%, and 44.1 ± 19.2%, respectively, suggesting that the three removal pathways were all critical to the migration and transformation of DMS in the surface seawater during summer.

Factors controlling the competition between Phaeocystis and diatoms in the Southern Ocean

Abstract. The high-latitude Southern Ocean phytoplankton community is shaped by the competition between Phaeocystis and silicifying diatoms, with the relative abundance of these two groups controlling primary and export production, the production of dimethylsulfide, the ratio of silicic acid and nitrate available in the water column, and the structure of the food web. Here, we investigate this competition using a regional physical-biogeochemical-ecological model (ROMS-BEC) configured at eddy-permitting resolution for the Southern Ocean south of 35° S. We extended ROMS-BEC by an explicit parameterization of Phaeocystis colonies, so that the model, together with the previous addition of an explicit coccolithophore type, now includes all biogeochemically relevant Southern Ocean phytoplankton types. We find that Phaeocystis contribute 46 % and 40 % to annual NPP and POC export south of 60° S, respectively, making them an important contributor to high-latitude carbon cycling. In our simulation, the relative importance of Phaeocystis and diatoms is mainly controlled by the temporal variability in temperature and iron availability. The higher light sensitivity of Phaeocystis at low irradiances promotes the succession from Phaeocystis to diatoms in more coastal areas, such as the Ross Sea. Still, differences in the biomass loss rates, such as aggregation or grazing by zooplankton, need to be considered to explain the simulated seasonal biomass evolution.

A meta-analysis of microcosm experiments shows that dimethyl sulfide (DMS) production in polar waters is insensitive to ocean acidification

Abstract. Emissions of dimethylsulfide (DMS) from the polar oceans play a key role in atmospheric processes and climate. Therefore, it is important to increase our understanding of how DMS production in these regions may respond to climate change. The polar oceans are particularly vulnerable to ocean acidification (OA). However, our understanding of the polar DMS response is limited to two studies conducted in Arctic waters, where in both cases DMS concentrations decreased with increasing acidity. Here, we report on our findings from seven summertime shipboard microcosm experiments undertaken in a variety of locations in the Arctic Ocean and Southern Ocean. These experiments reveal no significant effects of short-term OA on the net production of DMS by planktonic communities. This is in contrast to similar experiments from temperate north-western European shelf waters where surface ocean communities responded to OA with significant increases in dissolved DMS concentrations. A meta-analysis of the findings from both temperate and polar waters (n=18 experiments) reveals clear regional differences in the DMS response to OA. Based on our findings, we hypothesize that the differences in DMS response between temperate and polar waters reflect the natural variability in carbonate chemistry to which the respective communities of each region may already be adapted. If so, future temperate oceans could be more sensitive to OA, resulting in an increase in DMS emissions to the atmosphere, whilst perhaps surprisingly DMS emissions from the polar oceans may remain relatively unchanged. By demonstrating that DMS emissions from geographically distinct regions may vary in their response to OA, our results may facilitate a better understanding of Earth's future climate. Our study suggests that the way in which processes that generate DMS respond to OA may be regionally distinct, and this should be taken into account in predicting future DMS emissions and their influence on Earth's climate.

Unprecedented DMSP Concentrations in a Massive Dinoflagellate Bloom in Monterey Bay, CA

AbstractThe organic sulfur compound dimethylsulfoniopropionate (DMSP) is synthesized by numerous species of marine phytoplankton, and its volatile degradation products are a major source of biogenic sulfur to the atmosphere. A massive bloom of the dinoflagellate Akashiwo sanguinea occurred in Monterey Bay, CA, USA, in the fall of 2016 and led to exceptionally high seawater DMSP concentrations that peaked at 4,240 nM. Bacterial consumption rates showed that only a small fraction of the DMSP standing stock flowed through the dissolved DMSP pool per day, contributing to the high DMSP concentrations and creating conditions conducive to production of dimethylsulfide (DMS). Conservative calculations of DMS yield from this persistent A. sanguinea bloom suggest substantial regional‐scale inputs of DMS‐sulfur to the atmosphere. Other recently reported major coastal blooms of A. sanguinea, along with indications that this species may benefit from climate change conditions, reveal a mechanism that could alter oceanic contributions to atmospheric sulfur pools.

Dynamics of dimethylsulphide and associated compounds in the coastal waters of Goa, west coast of India

Abstract Concentrations of total dimethylsulphoniopropionate (DMSPt), Dimethylsulphide (DMS) and total dimethylsulphoxide (DMSOt) were measured at a coastal time series site, west coast of India, from September 2009 to December 2013. While, DMSPt varied between 0.35 and 252 nM (avg. 24 ± 32.3 nM), DMS varied from 0.5 to 442 nM (avg. 22.5 ± 48.3 nM). The annual phytoplankton regime and succession was observed to play a key role in DMSP and DMS production. DMSPt, DMS and DMSOt showed high temporal variability with maximum concentrations observed during the southwest monsoon (SWM; June to September). While the least DMSP and DMS (

Role of Calanus sinicus (Copepoda, Calanoida) on Dimethylsulfide and Dimethylsulfoniopropionate Production in Jiaozhou Bay

AbstractThe role of copepod Calanus sinicus on the production of dimethylsulfide (DMS)/dimethylsulfoniopropionate (DMSP) in Jiaozhou Bay was evaluated in field measurements and laboratory experiments. Samples at 10 sites in the bay were collected monthly from June 2010 to May 2011 (except for March 2011), and zooplankton species composition was analyzed. Effects of C. sinicus grazing on DMS/DMSP production at different conditions (i.e., algal diets, food concentrations, and salinities) were assessed in the laboratory. Data from the field experiment showed that C. sinicus was the dominant copepod in Jiaozhou Bay (up to 123 individuals/m3 in May 2011) and preferred to graze on diatom. DMS and DMSP concentrations depend on not only phytoplankton abundance but also phytoplankton species and bacterial abundance. In the laboratory experiment, compared with Gymnodinium sp. or Emiliania huxleyi, C. sinicus feeding on Isochrysis galbana and Chaetoceros curvisetus exhibited increased DMS concentration, whereas high salinity inhibited DMS production. Copepod ingested 0.5%–35% of DMSP in filtered phytoplankton, and copepod DMSP ingestion turnover rate in Jiaozhou Bay was up to 29 pmol L−1 d−1. Although the microbial DMSP consumption rate was 10–2,620‐fold of copepod turnover rate, copepod grazing was still one of the important routes in DMSP loss processes through food chain. This study indicated that DMSP was transferred from phytoplankton to copepod body, fecal pellet, and seawater through copepod grazing. Our results provided important information to understand the biogeochemical cycle of DMSP in Jiaozhou Bay.

Distribution, Occurrence, and Fate of Biogenic Dimethylated Sulfur Compounds in the Yellow Sea and Bohai Sea During Spring

AbstractThe spatial distributions of biogenic dimethylated sulfur compounds (BDSCs), including dimethylsulfide (DMS), dimethylsulfoniopropionate (DMSP), and dimethylsulfoxide, were determined in the Yellow Sea and Bohai Sea during a survey in April–May 2014 and the occurrence and fate of BDSCs in the surface seawater were investigated. The concentrations of DMS and DMSP were significantly correlated with the stocks of chlorophyll a and a decreasing trend was observed from the inshore to the offshore areas. In situ incubation experiments indicated that more than half of the degraded dissolved DMSP (DMSPd) was transformed into DMS. Irradiation experiments showed that the photooxidation of DMS under ultraviolet B, ultraviolet A, and visible light accounted for 23.9%, 71.8%, and 4.3% of the total photooxidation of DMS, respectively. The sea‐to‐air fluxes of DMS ranged from 0.24 to 34.11 μmol m−2 day−1 with a mean of 8.84 μmol m−2 day−1. A comparison of the DMS production rate and main removal rates indicated that bioproduction cannot completely maintain the removal of DMS and might not be the only but the primary source of DMS in the surface seawater. Additionally, the average turnover times of microbial consumption, photooxidation, and sea‐to‐air exchange of DMS were 1.53, 1.16, and 4.28 day and the contributions of the three removal pathways were 40.0%, 41.2%, and 18.8% respectively; this indicated that microbial consumption and photooxidation played dominant roles in controlling the removal of DMS from the surface seawater.

Sea Ice and Water Mass Influence Dimethylsulfide Concentrations in the Central Arctic Ocean

Dimethylsulfide (DMS) is a biogenic trace gas with importance to aerosol formation. DMS is produced by microbial degradation of dimethylsulfoniopropionate (DMSP), an abundant metabolite in marine microalgae. We analyzed DMS and DMSP concentrations in surface water in the central Arctic Ocean during two expeditions north of 79°N in 2011 and 2015. We identified three regions, which were characterized by different DMS and DMSP concentrations, dependent on the regional water masses and the relative movement of sea ice and water to each other. In addition, correlations between DMS and DMSP and correlation of the two sulfur compounds to autotrophic biomass (as chlorophyll a) differed in the regions. In the area of the nutrient rich Atlantic water inflow and short contact of this water with sea ice, DMS is present in high concentrations and correlates to DMSP as well as chlorophyll a. At two stations, particularly high DMS concentrations were found in conjunction with under-ice phytoplankton biomass peaks. In contrast, in mixed Atlantic and Pacific water with strong polar influence, where long-term contact between sea ice and water causes persistent stratification, only little DMS is found. Further, the correlations to DMSP and chlorophyll a are lost and the ratio of DMS to DMSP is about one order of magnitude lower, pointing towards consumption of DMSP without the production of DMS. We conclude that the duration of sea ice influence and source of the surface water do not only lead to differences in phytoplankton productivity, resulting in different DMSP concentrations, but also influence microbial recycling of DMSP to DMS or other compounds. DMS production, as possible source for aerosols, is thus presumably lower in the strongly sea ice influenced central Arctic areas than what could be expected from DMSP concentration or biomass.