Chemical and GC-MS characterization of marine dissolved lipids

The chloroform-extractable ‘lipid’ fraction of dissolved organic matter in seawater was analyzed by gravimetry, liquid chromatography, gas chromatography (GC), and gas chromatography—mass spectrometry (GC—MS). Gravimetric concentrations of dissolved lipids in the Gulf of Mexico were in the range of 60–160 μg 1^?1 in near-surface waters and 61–116 μg 1^?1 in near bottom waters and accounted for ～4% of the dissolved organic carbon. Over a 12-h sampling period and a 5-d sampling period extensive variability in dissolved lipid quantity and quality were observed. The major percentage of extractable weight was collected in the polar liquid chromatographic fraction (55–95%). Gas chromatographic concentrations of the aliphatic fractions were in the range of 0.014-0.187 μg 1^?1. Concentrations derived from gas chromatography were consistently lower than gravimetrically-derived concentrations. A number of compounds were tentatively identified by a combination of GC, GC—MS, and authentic standards. The major components of the analyzable dissolved lipids were n-alkanes (C₁₆C₃₂), pristane, phytane, methyl, ethyl and propyl esters of fatty acids. Minor components included olefins and cycloalkanes, aromatics, short-chained acids, and possibly a lactone and an alcohol. All concentrations and compounds were indicative of a fairly pristine environment. The n-alkane distribution appears to be the result of marine and terrestrial inputs superimposed on a chronic low-level background of oil pollution. It is suggested that the fatty acid esters and other fragment molecules are the résult of the degradation of humic substances. A number of potential indicators of source were isolated.     

Chemical and microbiological studies of sea-surface films in the Southern Gulf of California and off the West Coast of Baja California

Sea-surface films and the corresponding 10-cm subsurface waters were sampled on three cruises to the eutrophic and oligotrophic waters in the Gulf of California and off the west coast of Baja California. The following constituents and properties were measured: NH₄⁺, NO₂⁻, NO₃⁻, PO₄³⁻, SiO₃²⁻, urea, ATP and Chl-a; dissolved and particulate organic carbon and nitrogen; lipid, protein and carbohydrate; total viable and nitrifying bacteria; simulated in situ bacterial heterotrophy; microplankton and simulated in situ primary productivity; surface potential and film pressures; ultraviolet absorption; and film-formation rates using surface potential and chemical methods.Mean enrichment factors (film concentration/10-cm concentration) for the three cruises were: 1.1–2.4 for the soluble inorganic nutrients, dissolved organic carbon, nitrogen, urea, carbohydrate, and lipid; 1.3–2.0 for ATP, Chl-a, microplankton and bacteria; and 1.1–3.7 for particulate carbon and nitrogen and both dissolved and particulate protein. Particulate and dissolved carbon and nitrogen were the only constituents never depleted in the films relative to the subsurface waters. Systematic, significant correlations between the various chemical and biological parameters measured were few, reflecting the complexity of processes which form and maintain surface films.Protein, carbohydrate and lipid carbon accounted for 15–114% (mean = 50%) of the total particulate organic carbon and 14–42% (mean = 28%) of the total dissolved organic carbon in both the films and 10-cm waters. Lipid was not the major identified constituent of films, averaging 18% of the particulate organic carbon and 2.5% of the dissolved organic carbon. There was more protein relative to carbohydrate in film samples compared to 10-cm water; there was also more protein relative to carbohydrate in particulate compared to dissolved mater. Microplankton plus bacterial carbon averaged 16% of the particulate organic carbon in films and 19% in 10-cm waters.     

Phytoplankton driven distribution of dissolved and particulate lipids in a semi-enclosed temperate sea (Mediterranean): Spring to summer situation

The relationship between changes in lipid classes and phytoplankton composition and abundance in the northern Adriatic was studied during spring and summer 2008 at two stations with different nutrient levels, i.e. at the western mesotrophic and eastern oligotrophic areas. Changes in the phytoplankton community depended on temporal surface nutrient depletion and bottom accumulation; that is, microphytoplankton, mainly diatoms Pseudo-nitzschia sp., developed at nutrient richer surface layers of the mesotrophic area in spring and at deeper layers of the oligotrophic site in late summer. In other periods nanophytoplankton dominated. Dissolved organic carbon (DOC) and lipid content were comparable for the two stations, while particulate organic carbon (POC) was richer at the mesotrophic side. Total lipid concentrations varied in the range from 8.0 to 92.2 μg l⁻¹ and from 16.9 to 76.9 μg l⁻¹ in the dissolved and particulate fractions, respectively. DOC and POC contents were in the ranges from 0.77 to 1.58 mg l⁻¹ and from 0.06 to 0.56 mg l⁻¹, respectively. Lipid and organic carbon distribution did not follow phytoplankton progression, indicating decoupling between organic matter production and decomposition throughout the investigation period. The main sources of lipids were marine phytoplankton and bacteria. Low nutrient conditions caused increased biosynthesis of lipids. Also, increasing oligotrophy led to an increasing number of phytoplankton taxa. The synthesis and accumulation of glycolipids by the developed taxa were enhanced during nutrient exhaustion, contributing in late summer, on average, 20.2 and 22.0% at the mesotrophic and oligotrophic stations, respectively, in the particulate fraction. The distribution of bacterial lipids and lipid breakdown products implies that bacterial lipid degradation was significant in spring, while very probably lipid abiotic degradation took place during summer.     

Trace metals in the Göta river estuary

The concentrations of the trace metals Cd, Cu, Fe, Ni, Pb and Zn in the Göta River estuary have been investigated. The following metal fractions have been determined: acid-leachable, dissolved, labile and particulate.The estuary represents a salt wedge type estuary and is situated in a densely populated region of Sweden. The metal concentrations found for the dissolved fraction is in the range of what can be considered as background levels for freshwater. It is difficult to evaluate any estuarine processes other than conservative mixing for Cd, Cu, Ni and Zn. The dissolved levels in the freshwater end member are Cd, 9–25 ngl^?1; Cu, 1·1–1·4 μgl^?1; Fe, 20–75 μg l^?1: Ni, 0·7–0·9 μg l^?1: Pb 0·09–0·2 μg l^?1; and Zn, 6–7 μg l^?1:The results from the acid-leachable fraction show that at high suspended load the particles sediment in the river mouth. The trace metal levels in this fraction are subject to large variations.     

Factors influencing particulate lipid production in the East Atlantic Ocean

Extensive analyses of particulate lipids and lipid classes were conducted to gain insight into lipid production and related factors along the biogeochemical provinces of the Eastern Atlantic Ocean. Data are supported by particulate organic carbon (POC), chlorophyll a (Chl a), phaeopigments, Chl a concentrations and carbon content of eukaryotic micro-, nano- and picophytoplankton, including cell abundances for the latter two and for cyanobacteria and prokaryotic heterotrophs. We focused on the productive ocean surface (2 m depth and deep Chl a maximum (DCM)). Samples from the deep ocean provided information about the relative reactivity and preservation potential of particular lipid classes. Surface and DCM particulate lipid concentrations (3.5–29.4 μg L⁻¹) were higher than in samples from deep waters (3.2–9.3 μg L⁻¹) where an increased contribution to the POC pool was observed. The highest lipid concentrations were measured in high latitude temperate waters and in the North Atlantic Tropical Gyral Province (13–25°N). Factors responsible for the enhanced lipid synthesis in the eastern Atlantic appeared to be phytoplankton size (micro, nano, pico) and the low nutrient status with microphytoplankton having the most expressed influence in the surface and eukaryotic nano- and picophytoplankton in the DCM layer. Higher lipid to Chl a ratios suggest enhanced lipid biosynthesis in the nutrient poorer regions. The various lipid classes pointed to possible mechanisms of phytoplankton adaptation to the nutritional conditions. Thus, it is likely that adaptation comprises the replacement of membrane phospholipids by non-phosphorus containing glycolipids under low phosphorus conditions. The qualitative and quantitative lipid compositions revealed that phospholipids were the most degradable lipids, and their occurrence decreased with increasing depth. In contrast, wax esters, possibly originating from zooplankton, survived downward transport probably due to the fast sinking rate of particles (fecal pellets). The important contribution of glycolipids in deep waters reflected their relatively stable nature and degradation resistance. A lipid-based proxy for the lipid degradative state (Lipolysis Index) suggests that many lipid classes were quite resistant to degradation even in the deep ocean.     

The distribution of Mn,Fe, Zn,Cd and Cu in Baltic seawater; a study on the basis of one anchor station

A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl^?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl^?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn²⁺ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl^?1, indicating that the oxidation of Fe²⁺ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl^?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters.     

Development of lipids during a spring plankton bloom in the northern North Sea: II. Dissolved lipids and fatty acids

During the spring plankton bloom (1976) in the northern North Sea the fatty acid and lipid distribution of the chloroform extractable fraction of seawater was analyzed by gas chromatography and thin-layer chromatography. The fatty acids in the seawater made up about 3% of the total dissolved organic matter. Maximum concentrations during the first phytoplankton bloom were in the range of 5 μmol C dm^?3. Palmitic acid (30.4%) and oleic acid (21.4%) as well as myristic, stearic and palmitoleic acids were the main fatty acids. The concentrations of fatty acids were higher below the thermocline in the deeper layers of the water column. The oleic acid showed large fluctuations, especially below the thermocline and seemed to be bound in a polar fraction. Different lipid classes containing fatty acids were determined by thin-layer chromatography. An estimation showed that the free fatty acid fraction made up the main portion (47.9%), followed by the triacylglycerol fraction (22.8%) and a more polar fraction with 25.1%. The triacylglycerol fraction appears to be more stable than the other fraction in the water column.     

Degradation and dissolution of zooplanktonic organic matter and lipids in early diagenesis

A degradation experiment with zooplankton was carried out to investigate the diagenesis of zooplanktonic organic matter, lipids, and lipid classes. In addition, reactivities and the quantitative relation between bulk organic carbon and waxes (which are the biomarkers of zooplankton) were compared during the experiment to evaluate the possibility of estimating the contributions of zooplanktonic organic matter in organic carbon pools, such as settling particles and surface sediments, from the wax concentration. Lipids were found to be more labile than the bulk organic carbon. Major parts of the organic carbon and lipids which remained on day 120 were found in the particulate fraction, and the accumulations of stable organic carbon and lipids in the dissolved fraction were limited. Although the lipids were more labile than the bulk organic carbon in the early phase of the experiment, the degradation rate of lipids obviously decreased in the subsequent degradation period, demonstrating the presence of stable lipids in zooplankton. Whereas triglycerides readily decreased, phospholipids persisted, making a major contribution to particulate lipids throughout the experiment. Waxes and other structural lipids such as glycolipids were also stably preserved in particulate lipids, suggesting that stable lipids in particulate matter are composed of structural lipids and waxes during early diagenesis. The degradation rate of waxes showed values comparable to that of bulk organic carbon after 11 days of degradation, resulting in constant ratios of waxes/bulk organic carbon (0.8 ± 0.2%, n = 7) during the later incubation period (after 11 days). This result suggests that the ratio could prove useful in evaluating the zooplanktonic organic carbon in organic carbon pools such as surface sediments and settling particulates.     

Determination of volatile fatty acid turnover rates in organic-rich marine sediments

Volatile fatty acid (VFA) apparent turnover rates in organic-rich marine sediments were determined by measuring whole sediment VFA concentration and the corresponding first-order reaction rate constants. In order to measure VFA concentrations, bulk wet sediment samples were basified, freeze-dried, extracted with methanol, derivatized to form methyl esters of the VFAs, and analyzed by packed-column gas chromatography using hexanoic acid as an internal standard. The detection limits for acetate, propionate, iso-butyrate and butyrate were 1.0, 0.4, 0.2 and 0.2 μmol l^?1_s, respectively, for 600 ml samples. Rate constants for acetate and propionate were determined by anaerobically incubating samples at in-situ temperatures with tracer levels of ¹⁴C-labelled VFAs. Metabolized label was recovered as CO₂, CH₄, cellular material, water-soluble material, and VFA (ether-soluble) fractions. Apparent turnover rates measured during summer and winter in anoxic Cape Lookout Bight, North Carolina (U.S.A.) sediments were in the range of 19–330 μmol l^?1_s h^?1 for acetate and 0.7–7.0 μmol l^?1_s h^?1 for propionate.     

Wax esters and triacylglycerols in sinking particulate matter in the Peru upwelling area (15°S, 75°W)

The flux and composition of wax esters and triacylglycerols were measured in particulate matter collected by free-drifting sediment traps in the Peru upwelling area. The purpose was to assess diurnal variations in sources and vertical transport of these lipids. Traps were deployed for periods of 8–12 h during both day and night at the base of the euphotic zone (10–14m) and at about 50m. Although the flux of total particulate organic carbon varied 4×, the flux of wax esters varied by 84× and triacylglycerols by 30×. POC, wax esters, and triacylglycerols also showed different temporal patterns. The highest wax ester flux was measured in shallow traps at night and is attributed to increased inputs from zooplankton which feed near the surface at night. Triacylglycerol flux was high in both shallow and deep nocturnal traps, consistent with inputs of both phytoplankton and zooplankton lipids. The composition of these lipids was also quite variable and attests to the complex nature of the lipid sources.     

Nutrient (N,P and Si) and carbon partitioning in the stratified NW Mediterranean

The distribution of nutrients and carbon in the different pools present in the three functional layers (the upper, biogenic layer, the thermocline layer, and the deeper, biolythic layer) of the stratified NW Mediterranean Sea was examined. The stoichiometry between dissolved inorganic nutrients, which had low concentrations in the surface waters, indicated a deficiency in nitrogen, relative to phosphorus, and an excess nitrogen relative to phosphorus within the thermocline, as well as a general silicate deficiency relative to both N and P, even extending to the biolythic layer. The dissolved organic matter was highly depleted in N and, particularly, in P relative to C, with average DOC/DON ratios >60 and DOC/DOP ratios >1500 in all three layers. The particulate pool was also depleted in N and P relative to C, particularly in the biolythic layer. The concentration of biogenic silica was low relative to C, N and P, indicating that diatoms were unlikely to contribute a significant fraction of the seston biomass. Most (>80%) of the organic carbon was present as dissolved organic carbon. Total organic N and P comprised 50–80% of the N and P pool in the biogenic layer, and decreased with depth to represent 10–25% of these nutrient pools in the biolythic layer. The high total N:P ratios in all three depth layers (N/P ratio >20) indicated an overall phosphorus deficiency in the system. The high P depletion of the dissolved organic matter must derive from a very rapid recycling of the P-rich molecules within DOM, and the increasing C/N ratio of DOM with depth indicates that N is also recycled faster than C in the DOM. Because of the uniform depth distribution of the total dissolved nitrogen concentration, the increase in the percent inorganic N and the decline in the percent dissolved organic N with depth indicates that there must be biological transformations between these pools, with a dominance of DON production in surface waters and remineralisation in the underlying layers, from which dissolved inorganic nitrogen is supplied back to the biogenic layer. Downward fluxes of DON and DOC were estimated at 200–250 μmol N m⁻² d⁻¹ and 1.4–2.1 mmol C m⁻² d⁻¹, respectively, while there should be little or no export of P as dissolved organic matter. The downward DON flux exceeded the diffusive DIN supply of about 145 μmol N m⁻² d⁻¹ to the biogenic layer, suggesting that allochthonous N inputs must be important in the region.     

Particulate organic matter in the coastal and estuarine waters of Goa and its relationship with phytoplankton production

In the coastal and estuarine waters of Goa, particulate organic carbon (POC) varied from 0.52 to 2.51 mg l^?1 and from 0.28 to 5.24 mg l^?1 and particulate phosphorus (PP) varied from 0.71 to 5.18 μg l^?1 and from 0.78 to 20.34 μg l^?1, respectively. The mean values of chlorophyll and primary productivity were 1.94 mg m^?3 and 938.1 mg C m^?2 day^?1 in the coastal waters and 4.3 mg m^?3 and 636.5 mg C m^?1 day^?1 in the estuarine waters, respectively.$\text{POC}\text{chl}$ ratios were low in June and October even when POC values were quite high. The POC in surface waters was linearly correlated with the chlorophyll content. Also PP increased when chlorophyll and primary productivity remained high. The results suggest that the phytoplankton was sharply increasing and contributed to POC and PP content. The percentage of detritus calculated from the intercept values of chlorophyll on POC varied from 46 to 76% depending on season. Results indicate that the major portion of POC and PP during postmonsoon (October–January) is derived from phytoplankton production while the allochthonous matter predominate during monsoon (June–September).     

Incorporation of aged dissolved organic carbon (DOC) by oceanic particulate organic carbon (POC): An experimental approach using natural carbon isotopes

Incorporation of ¹⁴C-depleted (old) dissolved organic carbon (DOC) on/into particulate organic carbon (POC) has been suggested as a possible mechanism to explain the low Δ¹⁴C-POC values observed in the deep ocean [Druffel, E.R.M., Williams, P.M., 1990. Identification of a deep marine source of particulate organic carbon using bomb ¹⁴C. Nature, 347, 172–174.]. A shipboard incubation experiment was performed in the Sargasso Sea to test this hypothesis. Finely ground dried plankton was incubated in seawater samples from the deep Sargasso Sea, both with and without a biological poison (HgCl₂). Changes in parameters such as biochemical composition and carbon isotopic signatures of bulk POC and its organic compound classes were examined to study the roles of sorptive processes and biotic activity on POC character. Following a 13-day incubation, the relative abundance of the acid-insoluble organic fraction increased. Abundances of extractable lipids and total hydrolyzable amino acids decreased for both treatments, but by a greater extent in the non-poisoned treatment. The Δ¹⁴C values of POC recovered from the non-poisoned treatment were significantly lower than the value of the unaltered plankton material used for the incubation, indicating incorporation of ¹⁴C-depleted carbon, most likely DOC. The old carbon was present only in the lipid and acid-insoluble fractions. These results are consistent with previous findings of old carbon dominating the same organic fractions of sinking POC from the deep Northeast Pacific [Hwang, J., Druffel, E.R.M., 2003. Lipid-like material as the source of the uncharacterized organic carbon in the ocean? Science, 299, 881–884.]. However, the Δ¹⁴C values of POC recovered from the poisoned treatment did not change as much as those from the non-poisoned treatment suggesting that biological processes were involved in the incorporation of DOC on/into POC.     

Seamounts and organic matter—Is there an effect? The case of Sedlo and Seine seamounts,Part 2. Composition of suspended particulate organic matter

The suspended particulate organic matter (sPOM) around two isolated NE Atlantic seamounts, Seine (33°46′N 14°21′W; summit at ∼170 m) and Sedlo (40°19′N 26°40′W; summit at ∼780 m), was studied over a period of 2 years during four 2–4-week oceanographic surveys. Elemental (C and N), chlorophyll a and lipid biomarker concentrations and N stable isotopic values were variable close to the surface (40–90 m), although some chlorophyll a enrichment above the summits was discerned sporadically. Results from near-surface waters showed a generally “fresh”, mainly phytoplankton signature in sPOM with some seasonality, which was more pronounced around Sedlo. sPOM concentrations and composition changed with depth, apparently controlled by seasonality and proximity to the seamounts. A few metres above the Seine summit, the suspended particulate organic carbon (sPOC) concentrations and labile polyunsaturated fatty acids (% of lipids) were higher than elsewhere at similar depths (∼200 m) in summer 2004. In the same season at Sedlo, polyunsaturated fatty acids were also relatively more abundant (up to 43% of total lipids) around the topographic feature throughout the water column, indicating supply of more labile sPOM, perhaps by advection, downwelling or passive sinking of locally produced phytoplankton and/or in situ production. The high-quality sPOM that seems to be present around the seamounts could provide an important food source to the biological community.     

Amino acids in suspended particulate matter from oceanic and coastal waters of the Pacific

The concentration of 15 amino acids in hydrolyzed particulate matter from different regions and depths of the Pacific Ocean has been measured by gas—liquid chromatography. The relative composition was similar for all samples in the euphotic zone, where the particulate amino acid (PAA) concentration ranged from 370 to 2260 nmoles/1 in coastal waters and from 90 to 260 nmoles/1 in the open ocean. Total PAA concentration dropped rapidly with depth, levelling off at 10–40 nmoles/1 below 200 m. Glycine, serine, glutamic acid and aspartic acid were the most abundant PAA in deep equatorial water and in deep off-shore California water. The nitrogen content of PAA could often account for 100% of the total particulate organic nitrogen present, while PAA carbon contributed up to 50% of the total particulate organic carbon in euphotic waters and down to 20% in deep waters. The protein equivalent to the total PAA content of particulate matter in near-surface waters amounted to 11–32 μg/1 at oceanic stations and up to 270 μg/1 at coastal stations.     

Particulate protein measurement in oceanographic samples by dye binding

A modified version of the Coomassie Brilliant Blue dye binding protein assay has been developed for oceanographic samples and intercalibrated with the widely used Lowry assay. Particulate protein measurements were made at seven stations in the Gulf of Maine using the method. Measurements were made on cell-free homogenates. Protein concentration ranged from 2 to 212 μg l^?1 (0.02–0.68 μg at N l^?1) and averaged 58 μg l^?1. ETS activity, chlorophyll and particulate nitrogen were significantly correlated with protein concentrations.     

Potential source and diagenetic signatures of oceanic dissolved and particulate organic matter as distinguished by lipid biomarker distributions

Potential biogenic sources of ultrafiltered dissolved and suspended particulate organic matter (UDOM and POM, respectively) from the Sargasso Sea (SS) and North Central Pacific (NCP) Ocean were investigated using lipid biomarker compounds. Organic carbon (OC) concentrations were ~ 20–40 times greater in UDOM than POM and decreased with depth. However, total OC-normalized lipid concentrations were 2–3 orders of magnitude higher in POM than in UDOM. Particulate total lipids decreased 3–10-fold with depth, compared to 10–20% for dissolved total lipids. Total fatty acids (FA), the most abundant lipids, showed similar patterns as total lipids, comprising ~ 62–88% of the total lipids analyzed in UDOM and ~ 57–84% in POM.FA were dominated by straight-chain saturated compounds followed by monounsaturated, polyunsaturated, and branched FA. Polyunsaturated FA were enriched in POM vs. UDOM and in surface vs. deep waters for both UDOM and POM, likely reflecting the algal origins and greater reactivity of surface-derived materials. In both UDOM and POM, sterols of planktonic origin dominated, including cholest-5-en-3β-ol (C₂₇Δ⁵), 24-methylcholesta-5,24(28)E-dien-3β-ol (C₂₈Δ^5,24(28)) and 24-ethylcholest-5-3β-ol (C₂₉Δ⁵), with varying contributions from cholesta-5,22E-3β-ol (C₂₇Δ^5,22), 24-methylcholesta-5,22E-3β-ol (C₂₈Δ^5,22) and 24-ethylcholesta-5,22E-3β-ol (C₂₉Δ^5,22).Factor analysis of lipid biomarkers showed major differences between the UDOM and POM pools and for each pool as a function of depth, but not between the SS and NCP. While UDOM and POM biomarkers were both dominated by autochthonous sources, differences between the two pools suggest potential effects from some combination of source and diagenetic factors. The lipid biomarker data are further evaluated relative to previous studies of radiocarbon (¹⁴C) and elemental (C:N:P) characteristics of UDOM and POM in the SS and NCP.     

Particulate organic carbon export flux by 234Th/238U disequilibrium in the continental slope of the East China Sea

234Th is widely used to quantify the magnitude of upper ocean particulate organic carbon(POC)export in oceans.In the present work,the rates of particulate organic carbon export were measured based on the distribution patterns of234Th/238U disequilibrium in the water column within the continental slope of the East China Sea(ECS)during May 2011.The profiles of particulate and dissolved234Th activities at all three stations showed a relative deficit with respect to238U in the upper 100 m of the water column.The dissolved234Th scavenging rates and the particulate234Th removal rates and their residence times were calculated by a one-dimensional steady state model.The results showed that the dissolved234Th scavenging rates and the particulate234Th removal rates ranged from 12.4–61.4 dpm/(m3·d)andfrom3.8–21.8 dpm/(m3·d),respectively.The residence times of dissolved and particulate234Th were in the range of 3.4–158 d and 63.7–96.5 d,respectively.Combined with the measurement of POC/234Th ratios of suspended particles,POC export flux(calculated by carbon)from the euphotic zone was estimated in the study region,which ranged from 4.14–14.7 mmol/(m2·d),withanaverageof8.21mmol/(m2·d),occupying35%oftheprimeproductivity in the study area.The results of this study can provide new information for better understanding the carbon biogeochemical cycle within the continental slope of the ECS.     

Assessment of storage lipid accumulation patterns in eucalanoid copepods from the eastern tropical Pacific Ocean

Members of the copepod family Eucalanidae are widely distributed throughout the world׳s oceans and have been noted for their accumulation of storage lipids in high- and low-latitude environments. However, little is known about the lipid composition of eucalanoid copepods in low-latitude environments. The purpose of this study was to examine fatty acid and alcohol profiles in the storage lipids (wax esters and triacylglycerols) of Eucalanus inermis, Rhincalanus rostrifrons, R. nasutus, Pareucalanus attenuatus, and Subeucalanus subtenuis, collected primarily in the eastern tropical north Pacific near the Tehuantepec Bowl and Costa Rica Dome regions, noted for its oxygen minimum zone, during fall 2007 and winter 2008/2009. Adult copepods and particulate material were collected in the upper 50 m and from 200 to 300 m in the upper oxycline. Lipid profiles of particulate matter were generated to help ascertain information on ecological strategies of these species and on differential accumulation of dietary and modified fatty acids in the wax ester and triacylglycerol storage lipid components of these copepods in relation to their vertical distributions around the oxygen minimum zone. Additional data on phospholipid fatty acid and sterol/fatty alcohol fractions were also generated to obtain a comprehensive lipid data set for each sample. Rhincalanus spp. accumulated relatively large amounts of storage lipids (31–80% of dry mass (DM)), while E. inermis had moderate amounts (2–9% DM), and P. attenuatus and S. subtenuis had low quantities of storage lipid (0–1% DM). E. inermis and S. subtenuis primarily accumulated triacylglycerols (>90% of storage lipids), while P. attenuatus and Rhincalanus spp. primarily accumulated wax esters (>84% of storage lipids). Based on previously generated molecular phylogenies of the Eucalanidae family, these results appear to support genetic predisposition as a major factor explaining why a given species accumulates primarily triacylglycerols or wax esters, and also potentially dictating major fatty acid and alcohol accumulation patterns within the more highly modified wax ester fraction. Comparisons of fatty acid profiles between triacylglycerol and wax ester components in copepods with that in available prey suggested that copepod triacylglycerols were more reflective of dietary fatty acids, while wax esters contained a higher proportion of modified or de novo synthesized forms. Sterols and phospholipid fatty acids were similar between species, confirming high levels of regulation within these components. Similarities between triacylglycerol fatty acid profiles of E. inermis collected in surface waters and at >200 m depth indicate little to no feeding during their ontogenetic migration to deeper, low-oxygen waters.     

Chemistry of sediments in relation to trophic condition of eight Rotorua Lakes

Abstract

Chemical parameters (pH, Eh, carbon, Kjeldahl nitrogen, total phosphorus, 0.5M H₂SO₄‐extractable phosphorus, organic phosphorus, and water‐soluble phosphorus) were measured in the surface layers of sediments collected from various depths in Lakes Rotowhero, Okaro, Ngapouri, Rotokakahi, Okareka, Tikitapu, Okataina, and. Rotoma during October 1972. The sediments of the productive geothermal lake, Rotowhero, were markedly different from those of the cold‐water lakes: they had relatively low pH values, high carbon (mean 8.5%) and organic phosphorus (mean 4160 μg.g^?1) concentrations, and very high total phosphorus concentrations (mean 4770 μg.g^?1), probably as a result of enrichment by hot springs.

The mean concentrations in the sediments of the cold‐water lakes were carbon 3.2–7.9%, Kjeldahl nitrogen 3380–8310 μg.g^?1 and phosphorus 690–1780 μg.g^?1. These concentrations are within the ranges for New Zealand terrestrial topsoils, but the lake sediments appear enriched in phosphorus relative to local topsoils. Total carbon, nitrogen, and phosphorus concentrations of sediments tended to be highest in the eutrophic lakes (Okaro, Ngapouri) although the deep oligotrophic lakes (Okataina, Rotoma) had relatively high total phosphorus concentrations (means 1400, 1510 μg.g^?1). Overall, the carbon, nitrogen, and phosphorus concentrations of the sediments showed little relationship to the trophic state of the lake.

Organic phosphorus concentrations of the surface layers of sediments were similar in all the cold‐water lakes (mean 319 μg.g^?1). The proportion of the total phosphorus apparently ‘fixed’ in mineral material was minimal (0–1%) in sediments from the eutrophic and mesotrophic lakes, but in the oligotrophic lakes was similar to that in New Zealand topsoils (9–14%). Reducing conditions may cause solution of a high proportion of the ‘fixed’ phosphorus in the eutrophic lakes.

The water‐soluble phosphorus concentrations in the sediments of the five shallow cold‐water lakes (Okaro, Ngapouri, Rotokakahi, Okareka, Tikitapu) correlated positively with trophic state and with concentrations of dissolved phosphorus in the lake waters.

Carbon, nitrogen, and phosphorus concentrations in the sediments tended to vary with overlying water depth. This should be considered when comparisons are made between lakes.