Net Dimethylsulfide Production Research Articles

Dimethyl sulfide cycling in the sea surface microlayer in the southwestern Pacific – Part 2: Processes and rates

Abstract. As the sea surface microlayer (SML) is the uppermost oceanic layer and differs in biogeochemical composition to the underlying subsurface water (SSW), it is important to determine whether processes in the SML modulate gas exchange, particularly for climate active gases. Enrichment of dimethyl sulfide (DMS) and its precursor dimethylsulfoniopropionate (DMSP) has been reported in the SML, but it remains unclear how this is maintained whilst DMS is lost to the atmosphere. To examine this, a comprehensive study of DMS source and sink processes, including production, consumption, and net response to irradiance, was carried out in deck-board incubations of SML water at five locations in different water masses in the southwestern Pacific east of New Zealand. Net consumption of DMSP and production of DMS in the light and dark occurred at all sites. The net response of DMS and DMSP to irradiance varied between stations but was always lower than conversion of DMSP to DMS in the dark. In addition, DMS photolytic turnover was slower than reported elsewhere, which was unexpected given the high light exposure in the SML incubations. Although no relationships were apparent between DMS process rates and biogeochemical variables, including chlorophyll a, bacteria, and phytoplankton groups, net bacterial DMSP consumption was correlated with DMSP and DMS concentrations and also dinoflagellate and Gymnodinium spp. biomass, supporting the findings of a companion study that dinoflagellates play an important role in DMS cycling in the SML. However, net DMS production rates and accumulation were low relative to regional air–sea DMS loss, indicating that DMS cycling within the SML is unlikely to influence regional DMS emissions.

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.

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.

Contrasting effects of acidification and warming on dimethylsulfide concentrations during a temperate estuarine fall bloom mesocosm experiment

Abstract. The effects of ocean acidification and warming on the concentrations of dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) were investigated during a mesocosm experiment in the Lower St. Lawrence Estuary (LSLE) in the fall of 2014. Twelve mesocosms covering a range of pHT (pH on the total hydrogen ion concentration scale) from 8.0 to 7.2, corresponding to a range of CO2 partial pressures (pCO2) from 440 to 2900 µatm, at two temperatures (in situ and +5 ∘C; 10 and 15 ∘C) were monitored during 13 days. All mesocosms were characterized by the rapid development of a diatom bloom dominated by Skeletonema costatum, followed by its decline upon the exhaustion of nitrate and silicic acid. Neither the acidification nor the warming resulted in a significant impact on the abundance of bacteria over the experiment. However, warming the water by 5 ∘C resulted in a significant increase in the average bacterial production (BP) in all 15 ∘C mesocosms as compared to 10 ∘C, with no detectable effect of pCO2 on BP. Variations in total DMSP (DMSPt = particulate + dissolved DMSP) concentrations tracked the development of the bloom, although the rise in DMSPt persisted for a few days after the peaks in chlorophyll a. Average concentrations of DMSPt were not affected by acidification or warming. Initially low concentrations of DMS (<1 nmol L−1) increased to reach peak values ranging from 30 to 130 nmol L−1 towards the end of the experiment. Increasing the pCO2 reduced the averaged DMS concentrations by 66 % and 69 % at 10 and 15 ∘C, respectively, over the duration of the experiment. On the other hand, a 5 ∘C warming increased DMS concentrations by an average of 240 % as compared to in situ temperature, resulting in a positive offset of the adverse pCO2 impact. Significant positive correlations found between bacterial production and concentrations of DMS throughout our experiment point towards temperature-associated enhancement of bacterial DMSP metabolism as a likely driver of the mitigating effect of warming on the negative impact of acidification on the net production of DMS in the LSLE and potentially the global ocean.

Processes That Contribute to Decreased Dimethyl Sulfide Production in Response to Ocean Acidification in Subtropical Waters

Long-term time series data show that ocean acidification is occurring in the subtropical oceans. As a component of an in situ mesocosm experiment carried out off Gran Canaria in the subtropical North Atlantic, we examined the influence of ocean acidification on the net production of dimethylsulfide (DMS). Over 23 days under oligotrophic conditions, time-integrated DMS concentrations showed an inverse relationship of −0.21 ± 0.02 nmol DMS nmol−1 H+ across the gradient of H+ concentration of 8.8–23.3 nmol l−1, equivalent to a range of pCO2 of 400–1,252 atm. Proportionally similar decreases in the concentrations of both dissolved and particulate dimethylsulfoniopropionate (DMSP) were observed in relation to increasing H+ concentration between the mesocosms. The reduced net production of DMSP with increased acidity appeared to result from a decrease in abundance of a DMSP-rich nanophytoplankton population. A 35S-DMSP tracer approach was used to determine rates of dissolved DMSP catabolism, including DMS production, across the mesocosm treatments. Over a phase of increasing DMS concentrations during the experiment, the specific rates of DMS production were significantly reduced at elevated H+ concentration. These rates were closely correlated to the rates of net DMS production indicating that transformation of dissolved DMSP to DMS by bacteria was a major component of DMS production. It was not possible to resolve whether catabolism of DMSP was directly influenced by H+ concentrations or was an indirect response in the bacterial community composition associated with reduced DMSP availability. There is a pressing need to understand how subtropical planktonic communities respond to the predicted gradual prolonged ocean acidification, as alterations in the emission of DMS from the vast subtropical oceans could influence atmospheric chemistry and potentially climate, over a large proportion of the Earth's surface.

Quantification of dimethyl sulfide (DMS) production in the sea anemone <i>Aiptasia</i> sp. to simulate the sea-to-air flux from coral reefs

Abstract. The production of dimethyl sulfide (DMS) is poorly quantified in tropical reef environments but forms an essential process that couples marine and terrestrial sulfur cycles and affects climate. Here we quantified net aqueous DMS production and the concentration of its cellular precursor dimethylsulfoniopropionate (DMSP) in the sea anemone Aiptasia sp., a model organism to study coral-related processes. Bleached anemones did not show net DMS production whereas symbiotic anemones produced DMS concentrations (mean ± standard error) of 160.7 ± 44.22 nmol g−1 dry weight (DW) after 48 h incubation. Symbiotic and bleached individuals showed DMSP concentrations of 32.7 ± 6.00 and 0.6 ± 0.19 µmol g−1 DW, respectively. We applied these findings to a Monte Carlo simulation to demonstrate that net aqueous DMS production accounts for only 20 % of gross aqueous DMS production. Monte Carlo-based estimations of sea-to-air fluxes of gaseous DMS showed that reefs may release 0.1 to 26.3 µmol DMS m−2 coral surface area (CSA) d−1 into the atmosphere with 40 % probability for rates between 0.5 and 1.5 µmol m−2 CSA d−1. These predictions were in agreement with directly quantified fluxes in previous studies. Conversion to a flux normalised to sea surface area (SSA) (range 0.1 to 17.4, with the highest probability for 0.3 to 1.0 µmol DMS m−2 SSA d−1) suggests that coral reefs emit gaseous DMS at lower rates than the average global oceanic DMS flux of 4.6 µmol m−2 SSA d−1 (19.6 Tg sulfur per year). The large difference between simulated gross and quantified net aqueous DMS production in corals suggests that the current and future potential for its production in tropical reefs is critically governed by DMS consumption processes. Hence, more research is required to assess the sensitivity of DMS-consumption pathways to ongoing environmental change in order to address the impact of predicted degradation of coral reefs on DMS production in tropical coastal ecosystems and its impact on future atmospheric DMS concentrations and climate.

Spectral irradiance dependence of sunlight effects on plankton dimethylsulfide production

We investigated the short‐term effects of variable solar irradiance and spectrum on the gross biological production of dimethylsulfide (DMS), a trace gas with potential climatic effects, in eight experiments performed at different times of the year in a northwest Mediterranean coastal site. Experimentally determined net community DMS production, DMS photolysis, and dark microbial DMS consumption rates were used to calculate gross community DMS production by budgeting. In addition, the composition of the bacterioplankton and phytoplankton communities in the initial samples, and the photoinhibition of bulk bacterial heterotrophic activity and phytoplankton photosynthetic efficiency were monitored. Our results show that: (1) gross DMS production is irradiance dependent, with a maximum short‐term stimulation factor of 2‐ to 6‐fold compared to dark incubations; (2) its spectral shape is variable but generally similar to that of phytoplankton photoinhibition or photodamage, with more effective stimulation at shorter ultraviolet wavelengths; and (3) stronger stimulation occurs when samples are overexposed with respect to their prior exposure. Remarkably, the photoresponse of gross DMS production was in most cases strong enough to (at least) compensate the photochemical DMS loss at the water subsurface. Such response would prevent DMS depletion in stratified and highly irradiated waters. Since the initial microbial communities were representative of meso‐ to oligotrophic conditions, our observations should apply to a wide variety of oceanic regimes.

Macroscale patterns of the biological cycling of dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) in the Northwest Atlantic

The influence of the seasonal development of microplankton communities on the cycling of dimethylsulfide (DMS) and its precursor dimethylsulfoniopropionate (DMSP) was investigated along a South–North gradient (36–59°N) in the Northwest (NW) Atlantic Ocean. Three surveys allowed the sampling of surface mixed layer (SML) waters at stations extending from the subtropical gyre to the Greenland Current during May, July and October 2003. Pools and transformation rates of DMSP and DMS were quantified and related to prevailing physical and biochemical conditions, phytoplankton abundance and taxonomic composition, as well as bacterioplankton abundance and leucine uptake. The South–North progression of the diatom bloom, a prominent feature in the NW Atlantic, did not influence the production of DMS whereas conditions in the N Atlantic Drift lead to a persistent bloom of DMSP-rich flagellate-dominated phytoplankton community and high net DMS production rates. Macroscale patterns of the observed variables were further explored using principal component analysis (PCA). The first axis of the PCA showed a strong association between the spatio-temporal distribution of DMSP and the abundance of several phytoplankton groups including dinoflagellates and prymnesiophytes, as well as with microbial-mediated DMSPd consumption and yields and rates of the conversion of DMSP into DMS. The second axis revealed a strong association between concentrations of DMS and SML depth and photosynthetically active radiation, a result supporting the prominent role of solar radiation as a driver of DMS dynamics.

Decreased marine dimethyl sulfide production under elevated CO2 levels in mesocosm and in vitro studies

Environmental contextAs atmospheric CO2 levels rise due to human activities, more of the gas dissolves in the oceans, increasing their acidity. The effect of these seawater changes on marine organisms is largely unknown. We examine the consequences of higher CO2 levels on the production by plankton of dimethyl sulfide, a climatically active gas. We find that higher CO2 levels leads to lower concentrations of dimethyl sulfide in the seawater, which has potentially important implications for the future climate. AbstractThe oceans have absorbed approximately half of the CO2 produced by human activities and it is inevitable that surface seawaters will become increasingly acidified. The effect of lower pH on marine organisms and ocean–atmosphere exchanges is largely unknown but organisms with CaCO3 structural components are likely to be particularly affected. Because calcifying phytoplankton are significant producers of dimethyl sulfide (DMS), it is vital to understand how lower seawater pH may affect DMS production and emission to the atmosphere. Here we show, by mesocosm (Raunefjorden, Norway, April–May 2003) and in vitro studies, that the net production of DMS and its cellular precursor dimethylsulfoniopropionate (DMSP) is approximately halved in microbial communities subjected to doubled CO2 levels. Our findings provide evidence that the amount of DMS entering the atmosphere could decrease in the future. Because atmospheric oxidation of DMS can lead to climate cooling by increasing cloud albedo, a consequence of reduced DMS emissions from a lower pH ocean would be an enhancement in global warming.

Influence of salinity on dimethyl sulfide and methanethiol formation in estuarine sediments and its side effect on nitrous oxide emissions

We investigated the regulatory effect of salinity on the production of dimethylsulfide (DMS) and methanethiol (MeSH) in estuarine sediments and the potential interactions with the nitrous oxide (N2O) reductase step of the denitrification pathway. This was achieved by monitoring DMS, MeSH and N2O accumulation in sediment slurries retrieved from a temperate estuary (Ave, NW Portugal). Treatments were performed with and without amendments of potential sulfur gas precursors, DMSP (0–50 μM) or methionine (0–500 μM) at different salinities (0, 15 and 30 ppt). Experimental increases of salinity inhibited DMS accumulation under both oxic and anoxic incubation conditions, and the pattern was observed whether DMSP or methionine was added or not, i.e. lower salinities stimulated DMS net production. In contrast, MeSH tended to accumulate to higher concentrations in higher salinity treatments (15 and 30 ppt). Our results also suggest that while salinity had a direct influence on N2O accumulation, it also may modulated N2O production through its regulatory effect on the formation of MeSH, a compound previously shown to inhibit N2O reduction activity. Overall, our results suggest that changes in salinity may have an important regulatory role in net production of DMS, MeSH and N2O and their potential emissions to the atmosphere.

Fate of dimethylsulfoniopropionate (DMSP) during the decline of the northwest Atlantic Ocean spring diatom bloom

A 7 d Lagrangian process study of the biogeochemical cycling of dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) was conducted within a decaying diatom bloom in the northwest Atlantic Ocean in spring 2003. Ambient profiles of DMSP and DMS were surveyed daily in the water column and were used to estimate in situ net transformation rates. Phytoplankton and bacterioplankton abundance were determined within the surface mixed layer (SML) as well as at the deep chlorophyll maximum (DCM), and sinking fluxes of particulate DMSP (DMSPp) below 75 to 100 m were assessed using free-drifting particle interceptor traps. Chlorophyll a (chl a) concentration and diatom abundance declined in the SML over the course of the study period, and the phytoplankton chl a biomass progressively settled above the nitracline forming the DCM. The decline of the diatom bloom coincided with the settling of DMSP p out of the SML and the formation of a DMSP-rich layer at the DCM. The low daily sinking loss rate of DMSPp at 75 m (< 2 % d -1 ) provided confirmation of the efficient retention of DMSP p at the DCM. The decaying bloom gave rise to an initial release of dissolved DMSP (DMSP d ) in the upper water column, which was rapidly consumed by the growing bacterial community. The rapid loss of DMSP d was accompanied by significant increases in net production of DMS in the SML and fluxes of DMS to the atmosphere. Despite this increase in DMS dynamics, overall in situ net production rates remained fairly low during the 7 d period (≤0.4 nmol DMS l -1 d -1 ), suggesting that demethylation by the developing bacterial community dominated DMSP d -consuming processes.

Dimethylsulfide production in Sargasso Sea eddies

Abstract Lagrangian time series of dimethylsulfide (DMS) concentrations from a cyclonic and an anticyclonic eddy in the Sargasso Sea were used in conjunction with measured DMS loss rates and a model of vertical mixing to estimate gross DMS production in the upper 60 m during summer 2004. Loss terms included biological consumption, photolysis, and ventilation to the atmosphere. The time- and depth (0–60 m)-averaged gross DMS production was estimated to be 0.73±0.09 nM d −1 in the cyclonic eddy and 0.90±0.15 nM d −1 in the anticyclonic eddy, with respective DMS replacement times of 5±1 and 6±1 d. The higher estimated rate of gross production and lower measured loss rate constants in the anticyclonic eddy were equally responsible for this eddy's 50% higher DMS inventory (0–60 m). When normalized to chlorophyll and total dimethylsulfoniopropionate (DMSP), estimated gross production in the anticyclonic eddy was about twice that in the cyclonic eddy, consistent with the greater fraction of phytoplankton that were DMSP producers in the anticyclonic eddy. Higher rates of gross production were estimated below the mixed layer, contributing to the subsurface DMS maximum found in both eddies. In both eddies, gas exchange, microbial consumption, and photolysis were roughly equal DMS loss terms in the surface mixed layer (0.2–0.4 nM d −1 ). Vertical mixing was a substantial source of DMS to the surface mixed layer in both eddies (0.2–0.3 nM d −1 ) owing to the relatively high DMS concentrations below the mixed layer. Estimated net biological DMS production rates (gross production minus microbial consumption) in the mixed layer were substantially lower (by almost a factor of 3) than those estimated in a previous study of the Sargasso Sea, which may explain the relatively low mixed-layer DMS concentrations found here during July 2004 (∼3 nM) compared to previous summers (∼4–6 nM).

DMSP and DMS dynamics during a mesoscale iron fertilization experiment in the Northeast Pacific–Part II: Biological cycling

Dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) biological cycling rates were determined during SERIES, a mesoscale iron-fertilization experiment conducted in the high-nutrient low-chlorophyll (HNLC) waters of the northeast subarctic Pacific. The iron fertilization resulted in the rapid development of a nanoplankton assemblage that persisted for 11 days before abruptly crashing. The nanoplankton bloom was followed by a diatom bloom, accompanied by an important increase in bacterial abundance and production. These iron-induced alterations of the plankton assemblage coincided with changes in the size and biological cycling of the DMSP and DMS pools. The initial nanoplankton bloom resulted in increases in particulate DMSP (DMSPp; 77–180 nmol L−1), dissolved DMSP (DMSPd; 1–24 nmol L−1), and biological gross (0.11–0.78 nmol L−1 h−1) and net (0.04–0.74 nmol L−1 h−1) DMS production rates. During the nanoplankton bloom, DMSPd consumption by bacteria exceeded their sulfur demand and the excess sulfur was probably released as DMS, consistent with the high gross DMS production rates observed during that period. The crash of the nanoplankton bloom was marked by the rapid decline of DMSPp, DMSPd, and gross DMS production to their initial values. Following the crash of the nanoplankton bloom, bacterial production and estimated sulfur demand reached transient maxima of 9.3 μg C L−1 d−1 and 14.2 nmol S L−1 d−1, respectively. During this period of high bacterial production, bacterial DMSPd consumption was also very high (6 nmol L−1 h−1), but none of the consumed DMSPd was converted into DMS and a net biological DMS consumption was measured. This transient period initiated a rapid decrease in DMS concentrations inside the iron-enriched patch, which persisted during the following diatom bloom due to low biological gross and net DMS production that prevented the replenishment of DMS. Our results show that the impact of Fe fertilization on DMS production in HNLC waters result from a complex interplay between the dynamics of the algal blooms and their influence on bacterial DMSP and DMS metabolism.

Modeling analysis of the effect of iron enrichment on dimethyl sulfide dynamics in the NE Pacific (SERIES experiment)

The large‐scale iron enrichment conducted in the NE Pacific during the Subarctic Ecosystem Response to Iron Enrichment Study (SERIES) triggered a phytoplankton bloom dominated successively by nanophytoplankton and large diatoms. During the first 14 days, surface dimethyl sulfide (DMS) levels increased both inside (up to 22 nmol L−1) and outside (up to 19 nmol L−1) the patch, with no consistent Fe effect. Later, DMS concentrations became sixfold lower inside the patch than outside. In this study, we used a DMS budget module embedded in a one‐dimensional ocean turbulence model to investigate the contribution of the interacting physical, photochemical, and biological processes to this particular DMS response. Temporal variations in biological net DMS production were reconstructed using an inverse modeling approach. Our results show that short‐term (days) variations in both the physical processes (i.e., turbulent mixing and ventilation) and the biological cycling of DMS are needed to explain the time evolution of DMS concentrations both outside and inside the Fe‐enriched patch. The biological net DMS production was generally high (up to 0.35 nmol L−1 h−1) and comparable outside and inside the patch during the first 10 days, corresponding to the observed accumulation of DMS inside and outside the patch. Later, it became negative (net DMS biological consumption) inside the patch, suggesting a change in dimethylsulfoniopropionate bacterial metabolism. This study stresses the importance of short‐term variations in biological processes and their sensitivity to the physical environment in shaping the DMS response to iron enrichment.

Vertically resolved cycling of dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) in the Northwest Atlantic in spring

In May 1998, profiles of ambient concentration and net changes of particulate dimethylsulfoniopropionate (DMSPp), dissolved dimethylsulfoniopropionate (DMSPd), and dimethylsulfide (DMS) were measured in three bio geographic provinces of the Northwest Atlantic: Northwest Atlantic Continental Shelf (Grand Banks), North Atlantic Drift, and North Atlantic Subtropical Gyre (Sargasso Sea). All stations/depths exhibited large losses of DMSPp(up to 18.0 nmol·L–1·day–1). DMSP and DMS cycling varied in relation to the type and development stage of the plankton assemblages. The postdiatom bloom conditions on the Grand Banks were associated with an efficient utilization of DMSP by microzooplankton and bacteria. Bacterial DMS production balanced the DMS bacterial consumption, resulting in little net DMS production (0.3 nmol·L–1·day–1). This contrasted with the North Atlantic Drift and Sargasso Sea stations where flagellates were thriving and most of the DMSPploss was recovered in the dissolved pool, indicating a less active microbial DMSP metabolism. DMSPdcleavage was high in these latter cases and exceeded DMS bacterial consumption, allowing a net production of DMS (up to 1.8 nmol·L–1·day–1). These results indicate that maximum DMS net production occurs in growing algal systems where the production of DMSPdresulting from microzooplankton grazing exceeds the bacterial requirement in carbon and sulfur.

Microbial production and consumption of dimethyl sulfide (DMS) in a sea grass (Zostera noltii)-dominated marine intertidal sediment ecosystem (Bassin d'Arcachon, France).

The relation between net dimethyl sulfide (DMS) production and changes in near surface (0-5 mm) oxygen concentrations in a sea grass (Zostera noltii Hornem)-covered intertidal sediment ecosystem was examined during a diel cycle. Sediment covered with Zostera was found to be more oxygenated than uncovered sediment during the period of photosynthesis. This phenomenon was probably caused by radial oxygen loss of the Zostera root-rhizome system. The population sizes of the three functional groups of microbes mainly responsible for the concentration of DMS, the dimethylsulfoniopropionate (DMSP)-demethylating, DMSP-cleaving and DMS-oxidizing bacteria, were quantified by most probable number (MPN) methodologies. Sediments with Zostera supported substantially higher populations of both aerobic (149x10(6) cm(-3) DMSP-utilizing and 0.4x10(6) cm(-3) DMS-oxidizing) and anaerobic (43x10(6) cm(-3) DMSP-utilizing and 0.4x10(6) cm(-3) DMS-oxidizing) microorganisms than sediments without Zostera (DMSP-utilizing aerobes and anaerobes both 2x10(6) cm(-3) and DMS-oxidizing aerobes and anaerobes both 0.2x10(6) cm(-3)). Experiments conducted with sediment cores and sediment slurries suggested that the net production of DMS in these sediments was significantly lower during oxic periods than during anoxic periods. Intact sediment cores with and without Zostera produced DMS when incubated under anoxic/dark conditions (97.0 and 53.6 nmol DMS m(-2) h(-1), respectively), while oxic/light-incubated cores did not produce detectable amounts of DMS. In addition, kinetic parameter values (V(max) and K(m)) for DMSP degradation in cell suspensions of isolated DMSP-demethylating and DMSP-cleaving bacteria were measured and compared to documented values for other strains. Both V(max) and K(m) values for DMSP-demethylating organisms were found to be relatively low (14.4-20.1 nmol DMSP mg protein(-1) min(-1) and 4.1-15.5 µM, respectively) while these parameter values varied widely in the group of the DMSP-cleaving organisms (6.7-1000 nmol DMSP mg protein(-1) min(-1) and 2-2000 µM, respectively). It was hypothesized that a diel rhythm in DMS emission occurred, with a relatively low net production during the day and a high net production during the night. Environmental changes which result in increased anoxic conditions in coastal sediments, such as an increase in eutrophication, may therefore result in increased atmospheric DMS emission rates.

Microbial production and consumption of dimethyl sulfide (DMS) in a sea grass ( Zostera noltii)-dominated marine intertidal sediment ecosystem (Bassin d’Arcachon, France)

The relation between net dimethyl sulfide (DMS) production and changes in near surface (0–5 mm) oxygen concentrations in a sea grass ( Zostera noltii Hornem)-covered intertidal sediment ecosystem was examined during a diel cycle. Sediment covered with Zostera was found to be more oxygenated than uncovered sediment during the period of photosynthesis. This phenomenon was probably caused by radial oxygen loss of the Zostera root-rhizome system. The population sizes of the three functional groups of microbes mainly responsible for the concentration of DMS, the dimethylsulfoniopropionate (DMSP)-demethylating, DMSP-cleaving and DMS-oxidizing bacteria, were quantified by most probable number (MPN) methodologies. Sediments with Zostera supported substantially higher populations of both aerobic (149×10 6 cm −3 DMSP-utilizing and 0.4×10 6 cm −3 DMS-oxidizing) and anaerobic (43×10 6 cm −3 DMSP-utilizing and 0.4×10 6 cm −3 DMS-oxidizing) microorganisms than sediments without Zostera (DMSP-utilizing aerobes and anaerobes both 2×10 6 cm −3 and DMS-oxidizing aerobes and anaerobes both 0.2×10 6 cm −3). Experiments conducted with sediment cores and sediment slurries suggested that the net production of DMS in these sediments was significantly lower during oxic periods than during anoxic periods. Intact sediment cores with and without Zostera produced DMS when incubated under anoxic/dark conditions (97.0 and 53.6 nmol DMS m −2 h −1, respectively), while oxic/light-incubated cores did not produce detectable amounts of DMS. In addition, kinetic parameter values ( V max and K m) for DMSP degradation in cell suspensions of isolated DMSP-demethylating and DMSP-cleaving bacteria were measured and compared to documented values for other strains. Both V max and K m values for DMSP-demethylating organisms were found to be relatively low (14.4–20.1 nmol DMSP mg protein −1 min −1 and 4.1–15.5 μM, respectively) while these parameter values varied widely in the group of the DMSP-cleaving organisms (6.7–1000 nmol DMSP mg protein −1 min −1 and 2–2000 μM, respectively). It was hypothesized that a diel rhythm in DMS emission occurred, with a relatively low net production during the day and a high net production during the night. Environmental changes which result in increased anoxic conditions in coastal sediments, such as an increase in eutrophication, may therefore result in increased atmospheric DMS emission rates.

Dynamics of dimethylsulfide production from dissolved dimethylsulfoniopropionate in the Labrador Sea

MEPS Marine Ecology Progress Series Contact the journal Facebook Twitter RSS Mailing List Subscribe to our mailing list via Mailchimp HomeLatest VolumeAbout the JournalEditorsTheme Sections MEPS 202:27-40 (2000) - doi:10.3354/meps202027 Dynamics of dimethylsulfide production from dissolved dimethylsulfoniopropionate in the Labrador Sea Sabine Schultes1,2, Maurice Levasseur1,*, Sonia Michaud1, Guy Cantin1, Gordon Wolfe1, Michel Gosselin2, Stephen de Mora2 1Institut Maurice-Lamontagne, Ministère des Pêches et des Océans, C.P. 1000, Mont-Joli, Québec G5H 3Z4, Canada 2Département d¹océanographie, Université du Québec à Rimouski, 310 Allée des Ursulines, Rimouski, Québec G5L 3A1, Canada *Corresponding author. E-mail: levasseurm@dfo-mpo.gc.ca ABSTRACT: The dynamics of the cleavage of dissolved dimethylsulfoniopropionate (DMSPd) to dimethylsulfide (DMS) were measured experimentally in the surface waters of the Labrador Sea in spring 1997. At in situ DMSPd concentrations, DMS production and consumption processes were generally in balance. Two stations in the central Labrador Sea displayed net DMS production of approximately 2 nmol l-1 h-1, DMSPd net consumption of 3.48 nmol l-1 h-1 and a net DMS production yield from DMSPd of 60% at near in situ DMSPd concentrations. Similar to general bacterial substrate utilization in cold waters, DMS production in the Labrador Sea seemed to be temperature and substrate limited. Following DMSPd additions, linear and non-linear net DMS production were observed. The non-linear response was characterized by a lag in DMS production and was associated with the cold, polar waters of the Labrador and West Greenland Currents. Net DMS production rates measured after DMSPd addition were proportional to the added amount of DMSPd. No saturation of the net DMS production rate was observed for concentrations up to 5000 nmol DMSPd l-1. First order rate constants determined for these DMS production kinetics suggest an average turnover time of DMSPd by cleavage to DMS of 3.8 d (2.7 to 5.2 d). At water temperatures of -1.3 to 8°C, potential net DMS production rates measured following DMSPd additions were comparable and even higher than those previously published for temperate and warm oceanic and coastal regions. The net DMS production potential varied by 1 order of magnitude (1.7 to 18.4 nmol DMS l-1 h-1) throughout the study area. Causal links established with path analysis indicate that this potential seemed to be controlled by water temperature and chlorophyll a concentrations. KEY WORDS: Dimethylsulfide (DMS) · Dimethylsulfoniopropionate (DMSP) · Production rates · Low temperature · Bacteria · Substrate utilization Full text in pdf format PreviousNextExport citation RSS - Facebook - Tweet - linkedIn Cited by Published in MEPS Vol. 202. Online publication date: August 28, 2000 Print ISSN: 0171-8630; Online ISSN: 1616-1599 Copyright © 2000 Inter-Research.

Dimethylsulfide (DMS) production by size-fractionated particles in the Labrador Sea

We measured the production of dimethylsulfide (DMS) by size-fractionated particles during a cruise in the Labrador Sea in May-June 1997. The experiments were conducted at 2 stations characterised by low levels of nitrate and high levels of phytoplankton biomass and particulate dirnethylsulfo~~~opropionate (DMSP,). Samples were size fractionated to assess the size distribution of DMSPp and the potential DMS production associated with the different size fractions. The potential for DMS production was estimated by incubating the filters in pre-filtered and boiled seawater amended with 500 nM of dissolved DMSP (DMSPd). At both stations, the highest DMSPp concentrations were measured in the 2 to 11 and >20 1-lm size fractions. Elevated potential net DMS production rates were also associated with these 2 size fractions, whch were responsible for 40 to 53% and 23 to 31 % of the cumulative production, respectively. Only 4 /, of the potential net DMS production was measured in the 0.7 to 2 I.lm fraction, which presumably contained many of the freeliving bacteria. The potential net DMS production rates of the different size fractions were linearly related (Spearman correlation coefficient = 0.86) to the concentratlons of DMSPp in the fractions. These results suggest that DMSP-cleaving activity was spatially associated with DMSP-producing algae or DMSP-rich detritus (e.g. faecal pellets, marine snow).

Microbial formation of dimethyl sulfide in anoxic sphagnum peat

Peat bogs dominated by Sphagnum spp. have relatively high areal rates of dimethyl sulfide (DMS) emission to the atmosphere. DMS was produced in anoxic slurries of Sphagnum peat with a linear time course and with an average rate of 40.4 (range, 22.0 to 68.6) nmol per liter of slurry (middot) day(sup-1) observed in nine batches of slurry. Methanethiol (MeSH) was produced at roughly similar rates over the typical 4- to 8-day incubations. DMS and MeSH production in these acidic (pH 4.2 to 4.6) peats were biological, as they were stopped completely by autoclaving and inhibited strongly by addition of antibiotics and 500 (mu)M chloroform. Endogenous DMS production may be due to the degradation of S-methyl-methionine, dimethyl sulfoxide, or methoxyaromatic compounds (e.g., syringic acid), each of which stimulated DMS formation when added at 5 to 10 (mu)M concentrations. However, on the basis of the high rates of thiol (MeSH and ethanethiol) methylation activity that we observed and the availability of endogenous MeSH, we suggest that methylation of MeSH is the major pathway leading to DMS formation in anaerobic peat. Solid-phase adsorption of MeSH plays a key role in its availability for biomethylation reactions. Additions of acetate (1.5 mM) or compounds which could cause acetate to accumulate (e.g., glucose, alanine, and 2-bromoethanesulfonate) suppressed DMS formation. It is likely that acetogenic bacteria are involved in DMS formation, but our data are insufficient to allow firm conclusions about the metabolic pathways or organisms involved. Our observations are the first which point to the methylation of MeSH as the major mechanism for endogenous DMS production in any environment. The rates of net DMS production observed are sufficient to explain the relatively high fluxes of DMS emitted to the atmosphere from Sphagnum sp.-dominated wetlands.