Experimental studies on dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) production by four marine microalgae

The production of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) by marine microalgae was investigated to elucidate more on the role of marine phytoplankton in ocean-atmosphere interactions in the global biogeochemical sulfur cycle.Axenic laboratory cultures of four marine microalgae–Isochrysis galbana 8701,Pavlova viridis,Platymonas sp.and Chlorella were tested for DMSP production and conversion into DMS.Among these four microalgae,Isochrysis galbana 8701 and Pavlova viridis are two species of Haptophyta,while Chlorella and Platymonas sp.belong to Chlorophyta.The results demonstrate that the four algae can produce various amounts of DMS(P),and their DMS(P) production was species specific.With similar cell size,more DMS was released by Haptophyta than that by Chlorophyta.DMS and dissolved DMSP (DMSPd) concentrations in algal cultures varied significantly during their life cycles.The highest release of DMS appeared in the senescent period for all the four algae.Variations in DMSP concentrations were in strong compliance with variations in algal cell densities during the growing period.A highly significant correlation was observed between the DMS and DMSPd concentrations in algal cultures,and there was a time lag for the variation trend of the DMS concentrations as compared with that of the DMSPd.The consistency of variation patterns of DMS and DMSPd implies that the DMSPd produced by phytoplankton cells has a marked effect on the production of DMS.In the present study,the authors’ results specify the significant contribution of the marine phytoplankton to DMS(P) production and the importance of biological control of DMS concentrations in oceanic water.     

Biogeochemistry of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) in the surface microlayer and subsurface water of the western North Atlantic during spring

Sixteen surface microlayer samples and corresponding subsurface water samples were collected in the western North Atlantic during April–May 2003 to study the distribution and cycling of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) and the factors influencing them. In the surface microlayer, high concentrations of DMS appeared mostly in the samples containing high levels of chlorophyll a, and a significant correlation was found between DMS and chlorophyll a concentrations. In addition, microlayer DMS concentrations were correlated with microlayer DMSPd (dissolved) concentrations. DMSPd was found to be enriched in the microlayer with an average enrichment factor (EF) of 5.19. However, no microlayer enrichment of DMS was found for most samples collected. Interestingly, the DMS production rates in the microlayer were much higher than those in the subsurface water. Enhanced DMS production in the microlayer was likely due to the higher concentrations of DMSPd in the microlayer. A consistent pattern was observed in this study in which the concentrations of DMS, DMSPd, DMSPp (particulate) and chlorophyll a in the microlayer were closely related to their corresponding subsurface water concentrations, suggesting that these constituents in the microlayer were directly dependent on the transport from the bulk liquid below. Enhanced DMS production in the microlayer further reinforces the conclusion that the surface microlayer has greater biological activity relative to the underlying water.     

Dimethylsulfide production in Sargasso Sea eddies

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).     

New and important roles for DMSP in marine microbial communities

The algal osmolyte dimethylsulfoniopropionate (DMSP) is recognised as the major precursor of marine dimethylsulfide (DMS), a volatile sulfur compound that affects atmospheric chemistry and global climate. Recent studies, using ³⁵S-DMSP tracer techniques, suggest that DMSP may play additional very important roles in the microbial ecology and biogeochemistry of the surface ocean. DMSP may serve as an intracellular osmolyte in bacteria that take up phytoplankton-derived DMSP from seawater. In addition, DMSP appears to support from 1 to 13% of the bacterial carbon demand in surface waters, making it one of the most significant single substrates for bacterioplankton so far identified. Furthermore, the sulfur from DMSP is efficiently incorporated into bacterial proteins (mostly into methionine) and DMSP appears to be a major source of sulfur for marine bacterioplankton. Assimilatory metabolism of DMSP is via methanethiol (MeSH) that is produced by a demethylation/demethiolation pathway which dominates DMSP degradation in situ. Based on the linkage between assimilatory metabolism of DMSP and bacterial growth, we offer a hypothesis whereby DMSP availability to bacteria controls the production of DMS by the competing DMSP lyase pathway. Also linked with the assimilatory metabolism of DMSP is the production of excess MeSH which, if not assimilated into protein, reacts to form dissolved non-volatile compounds. These include sulfate and DOM–metal–MeSH complexes, both of which represent major short-term end-products of DMSP degradation. Because production rates of MeSH in seawater are high (3–90 nM d⁻¹), reaction of MeSH with trace metals could affect metal availability and chemistry in seawater. Overall, results of recent studies provide evidence that DMSP plays important roles in the carbon, sulfur and perhaps metal and DOM cycles in marine microbial communities. These findings, coupled with the fact that the small fraction of DMSP converted to DMS may influence atmospheric chemistry and climate dynamics, draws attention to DMSP as a molecule of central importance to marine biogeochemical and ecological processes.     

DMSP and DMS dynamics and microzooplankton grazing in the Labrador Sea: application of the dilution technique

We adapted the dilution technique to study microzooplankton grazing of algal dimethylsulfoniopropionate (DMSP) vs. Chl a, and to estimate the impact of microzooplankton grazing on dimethyl sulfide (DMS) production in the Labrador Sea. Phytoplankton numbers were dominated by autotrophic nanoflagellates in the Labrador basin, but diatoms and colonial Phaeocystis pouchetii contributed significantly to phytomass at several high chlorophyll stations and on the Newfoundland and Greenland shelfs. Throughout the region, growth of algal Chl a and DMSP was generally high (0.2–1 d⁻¹), but grazing rates were lower and more variable, characteristic of the early spring bloom period. Production and consumption of Chl a vs. DMSP followed no clear pattern, and sometimes diverged greatly, likely because of their differing distributions among algal prey taxa and size class. In several experiments where Phaeocystis was abundant, we observed DMS production proportional to grazing rate, and we found clear evidence of DMS production by this haptophyte following physical stress such as sparging or filtration. It is possible that grazing-activated DMSP cleavage by Phaeocystis contributes to grazer deterrence: protozoa and copepods apparently avoided healthy colonies (as judged by relative growth and grazing rates of Chl a and DMSP), and grazing of Phaeocystis was significant only at one station where cells were in poor condition. Although we hoped to examine selective grazing on or against DMSP-containing algal prey, the dilution technique cannot differentiate selective ingestion and varying digestion rates of Chl a and DMSP. We also found that the dilution method alone was poorly suited for assessing the impact of grazing on dissolved sulfur pools, because of rapid microbial consumption and the artifactual release of DMSP and DMS during filtration. Measuring and understanding the many processes affecting organosulfur cycling by the microbial food web in natural populations remain a technical challenge that will likely require a combination of techniques to address.     

Biological control of short-term variations in the concentration of DMSP and DMS during a Phaeocystis spring bloom

In the spring of 1995, short-term variations in the concentration of particulate and dissolved dimethylsulfoniopropionate (DMSP) and dimethylsulfide (DMS) were monitored in the western Wadden Sea, a shallow coastal region in open connection with the North Sea. Significant correlations were found between abundance of Phaeocystis globosa and particulate DMSP; concentrations increased rapidly from 100 to 1650 nM in the middle of April. Highest DMS concentrations were found during the initial phase of the exponential growth of the bloom. DMS production and loss rates of DMSP and DMS were estimated experimentally during various phases of the bloom. DMS production and consumption were roughly in balance, with production only slightly exceeding consumption at the start of the bloom. Rates of production and consumption were highest during the exponential growth phase of Phaeocystis and declined in the course of the bloom (from 300–375 to less than 5 nmol dm⁻³ d⁻¹). Demethylation of DMSP increased during the bloom (from 11 to 1300 nmol dm⁻³ d⁻¹); it accounted for up to 100% of the DMSP loss at the end of the bloom. The shift from DMSP cleavage to demethylation in the course of a Phaeocystis bloom implies that DMS concentrations are not necessarily highest at the peak or towards the end of blooms.     

Significance of vertical flux as a sink for surface water DMSP and as a source for the sediment surface in coastal zones of northern Europe

In April 1997 and 1998 the significance of sedimentation as a sink for epipelagic dimethylsulphoniopropionate (DMSP) production and as a source for marine sediments was reassessed using a newly designed sediment trap. The behaviour of the traps in immersion was monitored continuously and the collection efficiency was evaluated with ²³⁴Th measurements. Net DMS(P) fluxes were corrected for some physical and biological losses during the whole sedimentation process providing reliable estimates of gross DMSP fluxes. It is shown that daily losses by sedimentation account for between 0.1% and 16% of seawater particulate DMSP (DMSPp) standing stocks, and between 3% and 75% of daily DMSPp production. In the Malangen fjord we observed temporal increases of DMSP production and standing stocks which resulted also in increases of DMSP vertical fluxes and DMS(P) concentrations at the sediment surface. This result illustrates how tight the coupling can be between pelagos and benthos, and confirms that DMS(P) concentration in the sediment was a reliable diagnostic indicator of vertical export from overlying waters in Malangen fjord. In Ullsfjord, however, DMS(P) concentrations in the sediment were poorly indicators of Phaeocystis pouchetii export during the early stage of growth of a bloom. The high load of DMS(P) in Balsfjord's sediments could neither be attributed to local vertical sedimentation nor to short-term lateral advection of fresh DMSP-containing phytoplanktonic material, and provides indication that this tracer sometimes also can be misleading. The highest loads of DMS(P) in sediments and the fastest rates of sedimentation occurred in the Southern Bight of the North Sea.     

海水温度对衰亡期浒苔释放生源硫影响的模拟研究

为研究浒苔释放生源硫的特征，本文对采集于黄海绿潮中期和末期的浒苔进行了实验室模拟培养，探讨了不同温度对衰亡期浒苔释放生源硫化物的影响。实验结果表明，在10~25℃温度范围内，温度升高能够加速浒苔的衰亡。二甲基硫（DMS）的平均释放速率范围为2.79~150.70 nmol/（L·g·d），二甲基硫基丙酸内盐（DMSP）的平均释放速率范围为2.16~113.26 nmol/（L·g·d）。温度升高能够使DMS和DMSP的释放速率加快，释放量增加，DMS最大平均释放速率在25℃条件下比10℃条件下升高了约60%，培养液中DMS浓度升高了2~3倍。采集于绿潮末期的浒苔培养液中的DMS和DMSP和采集于绿潮中期的浒苔相比，浓度有所增加，采集于浒苔绿潮末期浒苔培养液中DMS的最高平均浓度为418.41 nmol/L，约为中期的4倍；DMSP的最高平均浓度为316.14 nmol/L，是中期的3倍。浒苔绿潮的爆发会对水体中的硫体系循环产生影响，进而影响该海域生态环境。     

A model of dimethylsulfide dynamics for the subtropical North Atlantic

Dimethylsulfide (DMS) is a volatile sulfur compound produced by the marine biota. The flux of DMS to the atmosphere may act on climate via aerosol formation. It is therefore important to improve our understanding of the processes that regulate sea surface DMS concentrations for eventual inclusion into climate models. In order to simulate the dynamics of DMS concentrations in the mixed layer, a model of DMS production was developed and calibrated against a 1 year time-series of DMS and DMSP (dissolved and particulate) data collected in the Sargasso Sea at Hydrostation ‘S’. The model reproduces the observed divergence between the seasonal cycles of particulate DMSP, the DMS precursor produced by algae, and DMS produced through the microbial loop from the cleavage of dissolved DMSP. DMSP_p (particulate) reaches its maximum in the spring whereas DMSP_d (dissolved) and DMS reach maximum concentrations in summer. Several parameters had to vary seasonally and with depth in order to reproduce the data, pointing out the importance of physiological and structural changes in the plankton food web. These parameters include the intracellular S(DMSp):N ratio, the C:Chl ratio and the sinking rates of phytoplankton and detritus. For the Sargasso Sea, variations in the solar zenithal angle, which co-vary with the seasonal variations in the depth of the mixed layer, proved to be a convenient signal to drive the seasonal variation in the structure and dynamics of the plankton. Variations of the temperature and photosynthetically active radiation also help to reproduce the short-term variability of the annual S cycle. Results from a sensitivity analysis show that variations in DMSP_p are dependent mostly on parameters controlling phytoplankton biomass, whereas DMS is dependent mostly on variables controlling phytoplankton productivity.     

Plankton origin of particulate dimethylsulfoniopropionate in a Mediterranean oligotrophic coastal and shallow ecosystem

We report here dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) levels as a function of plankton communities and abiotic factors over a 12-month cycle in the Mediterranean oligotrophic coastal and shallow ecosystem of Niel Bay (N.W. Mediterranean Sea, France). Total particulate DMSP (DMSP_p) and DMS concentrations were highly seasonal, peaking during a spring (April) bloom at 8.9 nM and 73.9 nM, respectively. Significant positive correlations were found between total DMSP_p concentration and the abundance or biomass of the dinoflagellate Prorocentrum compressum (Spearman's rank correlation test: r = 0.704; p = 0.011). Similarly, DMS concentrations peaked during the development of blooms of P. compressum and Gymnodinium sp. There seemed to be a positive relationship between the chlorophyll a to pheopigment ratio and DMS concentrations, suggesting that DMS was released during phytoplankton growth. High DMS levels recorded in the shallow Niel Bay may also result from the activity of benthic macroalgae, and/or macrophytes such as Posidonia spp., or the resuspension of sulfur species accumulating in sediments. The fractionation of particulate DMSP into three size classes (>90 μm, 5–90 μm and 0.2–5 μm) revealed that 5–90 μm DMSP-containing particles made the greatest contribution to the total DMSP_p pool (annual mean contribution = 62%), with a maximal contribution in April (96%). This size class consisted mainly of dinoflagellates (annual mean contribution = 68%), with P. compressum and Gymnodinium sp. the predominant species, together accounting for up to 44% of the phytoplankton present. The positive correlation between DMSP concentration in the 5–90 μm size class and the abundance of P. compressum (Spearman's rank correlation test: r = 0.648; p = 0.023) suggests that this phytoplankton species would be the major DMSP producer in Niel Bay. The DMSP collected in the >90 μm fraction was principally associated with zooplankton organisms, dominated by copepods (nauplii and copepodites). DMSP_>90, not due to a specific zooplankton production, resulted from the phytoplankton cells ingested during grazing. The concomitant peaks of DMS concentration and zooplankton abundance suggest that zooplankton may play a role in releasing DMSP and/or DMS through sloppy feeding.     

Biogeochemical Variation in Dimethylsulfide, Phytoplankton Pigments and Heterotrophic Bacterial Production in the Subarctic North Pacific during Summer

Dimethylsulfide (DMS), chlorophyll a (Chl-a), accessory pigments (fucoxanthin, peridinin and 19-hexanoyloxyfucoxanthin), and bacterial production (BP) were measured in the surface layer (0–100 m) of the subarctic North Pacific, including the Bering Sea, during summer (14 July–5 September, 1997). In surface sewater, the concentrations of DMS and Chl-a varied widely from 1.3 to 13.2 nM (5.1 ± 3.0 nM, mean ± S.D., n = 48) and from 0.1 to 2.4 µg L^–1 (0.6 ± 0.6 µg L^–1, n = 24), respectively. In the subarctic North Pacific, DMS to Chl-a ratios (DMS/Chl-a) were higher on the eastern side than the western side (p < 0.0001). Below the euphotic zone, DMS/Chl-a ratios were law and the correlation between DMS and Chl-a was relatively strong (r ² = 0.700, n = 27, p < 0.0001). In the euphotic zone, DMS/Chl-a ratios were higher and the correlation between DMS and Chl-a was weak (r ² = 0.128, n = 50, p = 0.01). The wide variation in DMS/Chl-a ratios would be at least partially explained by the geographic variation in the taxonomic composition of phytoplankton, because of the negative correlation between DMS/Chl-a and fucoxanthin-to-Chl-a ratios (Fuc/Chl-a) (r ² = 0.476, n = 26, p = 0.0001). Furthermore, there was a positive correlation between DMS and BP (r ² = 0.380, n = 19, p = 0.005). This suggests that BP did not represent DMS and dimethylsulfoniopropionate (DMSP) removal by bacterial consumption but rather DMSP degradation to DMS by bacterial enzyme.     

Dimethylsulphide and dimethylsulphoniopropionate in Antarctic sea ice and their release during sea ice melting

This study presents concentrations of dimethylsulphide (DMS) and its precursor compound dimethylsulphoniopropionate (DMSP) in a variety of sea ice and seawater habitats in the Antarctic Sea Ice Zone (ASIZ) during spring and summer. Sixty-two sea ice cores of pack and fast ice were collected from twenty-seven sites across an area of the eastern ASIZ (64°E to 110°E; and the Antarctic coastline north to 62°S). Concentrations of DMS in 81 sections of sea ice ranged from < 0.3 to 75 nM, with an average of 12 nM. DMSP in 60 whole sea ice cores ranged from 25 to 796 nM and showed a negative relationship with ice thickness (y = 125x^− 0.8). Extremely high DMSP concentrations were found in 2 cores of rafted sea ice (2910 and 1110 nM). The relationship of DMSP with ice thickness (excluding rafted ice) suggests that the release of large amounts of DMSP during sea ice melting may occur in discrete areas defined by ice thickness distribution, and may produce ‘hot spots’ of elevated seawater DMS concentration of the order of 100 nM. During early summer across a 500 km transect through melting pack ice, elevated DMS concentrations (range 21–37 nM, mean 31 nM, n = 15) were found in surface seawater. This band of elevated DMS concentration appeared to have been associated with the release of sea ice DMS and DMSP rather than in situ production by an ice edge algal bloom, as chlorophyll a concentrations were relatively low (0.09–0.42 μg l^− 1). During fast ice melting in the area of Davis station, Prydz Bay, sea ice DMSP was released mostly as extracellular DMSP, since intracellular DMSP was negligible in both hyposaline brine (5 ppt) and in a melt water lens (4–5 ppt), while extracellular DMSP concentrations were as high as 149 and 54 nM, respectively in these habitats. DMS in a melt water lens was relatively high at 11 nM. During the ice-free summer in the coastal Davis area, DMS concentrations in surface seawater were highest immediately following breakout of the fast ice cover in late December (range 5–14 nM), and then remained at relatively low concentrations through to late February (< 0.3–6 nM). These measurements support the view that the melting of Antarctic sea ice produces elevated seawater DMS due to release of sea ice DMS and DMSP.     

Seasonal variations of dimethylsulfide (DMS) and dimethylsulfoniopropionate (DMSP) in the sea-surface microlayer and subsurface water of Jiaozhou Bay and its adjacent area

The distributions of DMS and its precursor dimethylsulfoniopropionate, in both dissolved (DMSP_d) and particulate fractions (DMSP_p) were determined in the seasurface microlayer and corresponding subsurface water of the Jiaozhou Bay, China and its adjacent area in May and August 2006. The concentrations of all these components showed a clear seasonal variation, with higher concentrations occurring in summer. This can be mainly attributed to the higher phytoplankton biomass observed in summer. Simultaneously, the enrichment extents of DMSP_d and DMSP_p in the microlayer also exhibited seasonal changes, with higher values in spring and lower ones in summer. Higher water temperature and stronger radiant intensity in summer can enhance their solubility and photochemical reaction in the microlayer water, reducing their enrichment factors (the ratio of concentration in the microlayer to that in the corresponding subsurface water). A statistically significant relationship was found between the microlayer and subsurface water concentrations of DMS, DMSP and chlorophyll a, demonstrating that the biogenic materials in the microlayer come primarily from the underlying water. Moreover, our data show that the concentrations of DMSP_p and DMS were significantly correlated with the levels of chlorophyll a, indicating that phytoplankton biomass might play an important role in controlling the distributions of biogenic sulfurs in the study area. The ratios of DMS/chlorophyll a and DMSP_p/chlorophyll a varied little from spring to summer, suggesting that there was no obvious change in the proportion of DMSP producers in the phytoplankton community. The mean sea-to-air flux of DMS from the study area was estimated to be 5.70 μmol/(m²·d), which highlights the effects of human impacts on DMS emission.     

Spatial variations of DMS, DMSP and phytoplankton in the Bay of Bengal during the summer monsoon 2001

Data on the distribution of dimethylsulphide (DMS) and dimethylsulphoniopropionate (DMSP) in relation to phytoplankton abundance in different oceanic environments is important to understand the biogeochemistry of DMS, which plays an important role in the radiation balance of the earth. During the summer monsoon of 2001 measurements were made for DMS and DMSPt (total DMSP) together with related biological parameters in the Bay of Bengal. Both DMS and DMSPt were restricted to the upper 40 m of the water column. Diatoms accounted for more than 95% of the phytoplankton and were the major contributors to the DMS and DMSPt pool. The mean concentration of DMS in the upper 40 m was observed to be around 1.8+/-1.9 nM in the study area, while DMSPt concentrations varied between 0.7 nM and 40.2 nM with a mean of 10.4+/-8.2 nM. The observed lower DMSPt in the northern Bay in spite of higher mean primary productivity, chlorophyll a and phytoplankton cell counts seemed to result from grazing. Though salinity divides the Bay into different biogeochemical provinces there is no relation between salinity and DMS or DMSPt. On the other hand DMS was linearly related to chlorophyll a:phaeopigments ratio. The results suggest the need for deeper insight into the role of diatoms in the biogeochemical cycling of DMS.     

西太平洋雅浦海沟区海水中CH4和DMSP的垂直变化特征

本研究首次探究了西太平洋雅浦海沟北段从表层到超深渊海水中甲烷（CH₄）及二甲基硫（DMS）的前体物质二甲基巯基丙酸内盐（DMSP）的浓度变化情况。结果表明:雅浦海沟海水甲烷浓度变化范围为1.49~3.87 nmol/L。其上层海水甲烷平均浓度最高，有明显的次表层极大现象。雅浦海沟氧最小层海水的甲烷平均浓度最低；在500~1 000 m中层水中甲烷浓度有一定程度的增大，1 000 m以下至底层甲烷浓度继续升高。研究海区溶解态DMSP（DMSPd）和总DMSP（DMSPt）平均浓度的垂直变化随深度呈先增大后减小趋势，颗粒态DMSP（DMSPp）的平均浓度随深度呈波动式变化，在中层达到最大。雅浦海沟CH₄和DMSP浓度垂直变化受浮游生物、微生物、光照、温度、压力、大洋环流等的复杂影响。在真光层海水中，CH₄浓度与DMSPd、DMSPp和DMSPt浓度表现为负相关关系，在200 m至底层海水中，CH₄浓度与DMSPd、DMSPp和DMSPt浓度表现为正相关关系，显示光照条件是造成雅浦海沟不同深度海水CH₄和DMSP浓度相关性差异的关键因素。     

塔玛亚历山大藻生成二甲基硫和二甲基硫丙酸的实验研究

主要研究在封闭培养条件下塔玛亚历山大藻（Alexandrium tamarense)生长周期内藻体细胞的二甲基硫丙酸（DMSP（）含量以及释放至水体的二甲基硫（DMS）含量，结果表明：（1）塔玛亚历山大藻藻体细胞DMSP含量变化与该藻细胞数量动态变化趋势相一致，在生长周期的第7天最高值；（2）藻体细胞的DMSP含量以及释放至水体的DMS含量均与藻体细胞数量有显著相关；（3）单位细胞DMSP生成量的变化与DMS释放量变化呈现相反的趋势，在DMS释放量最高时，单位细胞DMSP生成量最低。     

Determinations of dimethylsulphoniopropionate (DMSP) lyase activity using headspace analysis of dimethylsulphide (DMS)

The osmolyte dimethylsulphoniopropionate (DMSP) can be enzymatically cleaved to dimethylsulphide (DMS), acrylate and a proton. The enzyme involved in this reaction is dimethylpropiothetin dethiomethylase (DMSP lyase; enzyme classification number 4.4.1.3.). Although the importance of this reaction for the global sulphur cycle, the influence of DMS on atmospheric acidity and the possible effect on climate regulation have been widely recognised, our knowledge of DMSP lyases is limited to just a few studies. Activity measurements of DMSP lyases offer an important step towards a better understanding of the conditions under which DMS is produced. In the available published data somewhat similar methods have been used before, but a critical examination of the method limitations has not been reported. To encourage further research on this enzyme, we suggest and detail two protocols for measurements of DMSP lyase activity: An in vitro assay for crude cell extracts or purified enzyme and an in vivo method for whole cells, which we recently started to use. After addition of DMSP, samples incubated in a gas tight vial may produce DMS from enzymatic cleavage under suitable conditions, and a DMS production rate can be estimated from time-series measurements of DMS in the headspace of the vial. Headspace analysis of DMS is a useful and rapid technique to estimate and compare DMSP lyase activities from different sources. The relative rates of DMS production in the liquid and of the gas transfer between liquid and headspace, determine the rate of DMS production measured via headspace analysis. If DMS production in the liquid is higher than the rate of transfer, headspace measurements will not reflect the actual amount of DMS produced in the liquid. In this case, extracts have to be diluted to a level that ensures linearity between dilution factor and reduction of enzyme activity. Additionally, incubation volumes and vials should be selected to provide a high surface-to-volume ratio to ensure maximum flux of DMS from the aqueous phase into the headspace. The methods can be adapted to further investigate species- and strain-specific activities, biogeographical distribution, cellular location and biochemical properties of various DMSP lyases.     

Biogeochemistry of Dimethylsulfoniopropionate (DMSP) in the Surface Microlayer and Subsurface Seawater of Funka Bay,Japan

Twenty-eight sea surface microlayer samples, along with subsurface bulk water samples were collected in Funka Bay, Japan during October 2000–March 2001 and analyzed for dimethylsulfoniopropionate, dissolved (DMSP_d) and particulate (DMSP_p), and chlorophyll a. The aim of the study was to examine the extent of enrichment of DMSP in the microlayer and its relationship to chlorophyll a, as well as the production rate of dimethylsulfide (DMS) from DMSP and the factors that influence this. The enrichment factor (EF) of DMSP_d in the surface microlayer ranged from 0.81 to 4.6 with a mean of 1.85. In contrast, EF of DMSP_p in the microlayer varied widely from 0.85–10.5 with an average of 3.21. Chlorophyll a also appeared to be enriched in the microlayer relative to the subsurface water. This may be seen as an important cause of the observed enrichment of DMSP in the microlayer. The concentrations of DMSP_p in the surface microlayer showed a strong temporal variation, basically following the change in chlorophyll a levels. Moreover, the microlayer concentrations of DMSP_p were, on average, 3-fold higher than the microlayer concentrations of DMSP_d and there was a significant correlation between them. Additionally, there was a great variability in the ratios of DMSP_p to chlorophyll a over the study period, reflecting seasonal variation in the proportion of DMSP producers in the total phytoplankton assemblage. It is interesting that the production rate of DMS was enhanced in the microlayer and this rate was closely correlated with the microlayer DMSP_d concentration. Microlayer enrichment of chlorophyll a and higher DMS production rate in the microlayer provide favorable evidence supporting the view that the sea surface microlayer has a greater biological activity than the underlying water.     

Biological and physical controls on dissolved dimethylsulfide over the north-eastern continental shelf of New Zealand

Data presented in this paper are part of an extensive investigation of the physics of cross-shelf water mass exchange in the north-east of New Zealand and its effect on biological processes. Levels of dissolved dimethylsulfide (DMS) were quantified in relation to physical processes and phytoplankton biomass. Measurements were made at three main sites over the north-east continental shelf of New Zealand's North Island during a current-driven upwelling event in late spring 1996 (October) and an oceanic surface water intrusion event in summer 1997 (January). DMS concentrations in the euphotic zone ranged between 0.4 and 12.9 nmol dm⁻³. Integrated water column DMS concentrations ranged from 33 to 173 μmol m⁻² in late spring during the higher biomass (15–62 Chl-a mg m⁻²) month of October, and from 25 to 38 μmol m⁻² in summer during the generally lower biomass (16–42 Chl-a mg m⁻²) month of January. We observed high levels of DMS in the surface waters at an Inner Shelf site in association with a Noctiluca scintillans bloom which is likely to have enhanced lysis of DMSP-producing algal cells during phagotrophy. Integrated DMS concentrations increased three-fold at a Mid Shelf site over a period of a week in conjunction with a doubling of algal biomass. A high correlation (r²=0.911, significant <0.001) of integrated DMS and chlorophyll-a concentrations for compiled data from all stations indicated that chlorophyll-a biomass may be a reasonable predictor of DMS in this region, even under highly variable hydrographic conditions. Integrated bacterial production was inversely correlated to DMS production, indicating active bacterial consumption of DMS and/or its precursor.     

Occurrence and turnover of DMSP and DMS in deep waters of the Ross Sea,Antarctica

High concentrations of the phytoplankton metabolite dimethylsulfoniopropionate (DMSP) and its degradation product dimethylsulfide (DMS) are associated with blooms of Phaeocystis antarctica in the Ross Sea, Antarctica. Episodic and rapid vertical export of Phaeocystis biomass to deep water has been reported for the Ross Sea, therefore we examined the distribution and microbial consumption rates of DMSP and DMS throughout the sub-euphotic water column. Total DMSP (dissolved+particulate; DMSPt) was present at 0.5–22 nM at depths between 70 and 690 m during both the early bloom (November) and the late bloom (January). Sub-euphotic peaks of DMSP were sometimes associated with mid-water temperature maxima, and elevated DMSP below 70 m was found mainly in water masses characterized as Modified Circumpolar Deep Water or Antarctic Shelf Water. Overall, 50–94% of the integrated water-column DMSPt was found below the euphotic zone. At one station during the early bloom, local maxima of DMSPt (14 nM) and DMS (20 nM) were observed between 113 and 240 m and these maxima corresponded with high chlorophyll a concentrations, P. antarctica cell numbers, and Fv/Fm (the quantum yield of photosystem II). During the late bloom, a sub-euphotic maximum of DMSPt (15.8 nM) at 250 m cooccurred with peaks of chlorophyll a concentration, DMSP lyase activity, bacterial production and dissolved DMSP consumption rates. DMSP turnover contributed ～12% of the bacterial carbon demand between 200 and 400 m. DMS concentrations peaked at 286 m but the maximum concentration (0.42 nM) was far lower than observed during the early bloom, probably because of relatively rapid biological consumption of DMS (1–3 turnovers per day) which, in turn, contributed to elevated dissolved dimethylsulfoxide (DMSO) concentrations. Relatively stable DMSPt distributions at some sites suggest that rapid sinking of Phaeocystis biomass is probably not the major mechanism responsible for mesopelagic DMSP accumulations. Rather, subduction of near-surface water masses, lateral advective transport or trapping of slowly sinking P. antarctica biomass in intermediate water masses are more likely mechanisms. We found that a culture of P. antarctica maintained cellular integrity during 34 days of darkness, therefore the presence of intact cells (and DMSP) at depth can be explained even under a slow sinking/advection scenario. Whatever the mechanism, the large pools of DMSP and DMS below the euphotic zone suggest that export exerts a control on potential DMS emission from the surface waters of the Ross Sea.