Taphonomy and origin of an accumulate of soft-bodied cephalopods in the Oxford Clay Formation (Jurassic, England)

An exceptionally well-preserved fauna from a new exposure in the Peterborough Member (Oxford Clay Formation) of southern England, equivalent to the famous and now inaccessible Lagerstätte at Christian Malford, Wiltshire, is described. It comes from a single bed and includes coleoid cephalopods with phosphatized soft tissues, and fully articulated fish. The level is unusual in that it lacks permanent benthos and is dominated by 'rain-out' from the upper water column. It was deposited on a sea floor that experienced prolonged periods of anoxia and which was overlain by a water column that was at least intermittently stratified. It is postulated that the coleoids formed large shoals that were killed en masse , together with other elements of the associated fauna, in one or more catastrophic mass mortality events that affected a significant area of the Peterborough Member sea. During the event(s), many of the coleoids preyed upon moribund fish and other coleoids, sometimes of the same species, before becoming overcome themselves. Crucially for the phosphatization of their soft tissues, the substrate surface was 'soupy' and allowed them to sink to a zone of rapid diagenesis where levels of dissolved phosphorus were greatly augmented by the large number of associated decaying carcasses.     

Pore Waters and the Transformation of Nutrients in Marine Subtidal Sands

The contents of ammonia, nitrites, nitrates, phosphates, and silicates were measured in pore waters of subtidal sands in Vostok Bay, the Sea of Japan. The exchange of nutrients between sand and pore waters was studied in the laboratory using a running-water system while percolating the ground with seawater. The composition of pore waters depended on the method and length of time spent sampling, and also on the distance from the ground surface. Statistical analysis did not reveal stable profiles of nutrient concentrations in sand. The velocities of the release and consumption of nutrients in the experiments were rather low and depended on temperature, length of time spent sampling, duration of measurements, and distance from the sand surface. Release and consumption were connected with absorption and desorption, and were not due solely to the biological process of mineralization of organic matter. Analysis of the data obtained is complicated by the canalization of the water flow in the sand and by the consolidation of the sediment during the measurements. The comparison of pore and near-bottom waters makes it possible to hypothesize that the mineralization of organic matter and the release of nutrients into the pore waters occur throughout the whole column of sediment. The mixing of the seawater and groundwater occurs as a result of advection processes, the most important of which is wave percolation.     

Spatio-temporal variability in benthic mineralization processes in the eastern English Channel

The effect of phytodetritus derived from Phaeocystis sp. bloom on benthic mineralization processes has been determined at four intertidal stations along the French coast of the eastern English Channel. Sites were chosen to offer a diversity of sediment types, from permeable sandy beach to estuarine mudflats. Sediment Oxygen Demand (SOD) as well as total fluxes of Dissolved Inorganic Nitrogen (DIN) at the sediment–water interface were determined by using whole core incubation technique and diffusive fluxes were predicted from interstitial water concentrations. In the absence of phytodetritus deposits, a marked gradient of granulometric characteristics and organic matter contents were observed, and resulted in more intensive mineralization processes in muddy sediments. Highly significant correlations (P < 0.05) were evidenced between SOD and porosity, bacterial biomass, Organic Carbon and Organic Nitrogen, evidencing the direct link between sediment texture, organic matter accumulation and microbial activity. The spring bloom led to a massive input of organic matter in surficial sediments and mineralization rates significantly increased while higher DIN release towards the water column was observed. A modification of the mineralization pathways was evidenced but clearly depended on the sediment type. With a global view, benthic mineralization processes in the intertidal zone provided significant a part of DIN inputs in the coastal zone while water column was depleted in nutrients.     

Measurements of Seasonal Rates and Annual Budgets of Organic Carbon Fluxes in an Antarctic Coastal Environment at Signy Island, South Orkney Islands, Suggest a Broad Balance between Production and Decomposition

We report here the first comprehensive seasonal study of benthic microbial activity in an Antarctic coastal environment. Measurements were made from December 1990 to February 1992 of oxygen uptake and sulfate reduction by inshore coastal sediments at Signy Island, South Orkney Islands, Antarctica. From these measurements the rate of benthic mineralization of organic matter was calculated. In addition, both the deposition rate of organic matter to the bottom sediment and the organic carbon content of the bottom sediment were measured during the same period. Organic matter input to the sediment was small under winter ice cover, and the benthic respiratory activity and the organic content of the surface sediment declined during this period as available organic matter was depleted. On an annual basis, about 32% of benthic organic matter mineralization was anoxic, but the proportion of anoxic compared with oxic mineralization increased during the winter as organic matter was increasingly buried by the amphipod infauna. Fresh organic input occurred as the sea ice melted and ice algae biomass sedimented onto the bottom, and input was sustained during the spring after ice breakup by continued primary production in the water column. The benthic respiratory rate and benthic organic matter content correspondingly increased towards the end of winter with the input of this fresh organic matter. The rates of oxygen uptake during the southern summer (80 to 90 mmol of O₂ m^-2 day^-1) were as high as those reported for other sediments at much higher environmental temperatures, and the annual mineralization of organic matter was equally high (12 mol of C m^-2 year^-1). Seasonal variations of benthic activity in this antarctic coastal sediment were regulated by the input and availability of organic matter and not by seasonal water temperature, which was relatively constant at between -1.8 and 0.5°C. We conclude that despite the low environmental temperature, organic matter degradation broadly balanced organic matter production, although there may be significant interrannual variations in the sources of the organic matter inputs.     

Biogenic nanosized iron oxides obtained from cultivation of iron bacteria from the genus <Emphasis Type="Italic">Leptothrix</Emphasis>

A detailed investigation of nanostructured iron oxides/(oxy)hydroxides gathered after cultivation of bacteria from the genus Leptothrix as iron (II) oxidizers is presented. A specific type of medium is selected for the cultivation of the bacteria. Results for sediment powder and bio-film on glass substrate samples from the same media are discussed. XRD, Raman spectroscopy, SEM, and TEM images and PPMS measurements are used to prove the exact composition of the biogenic products and to interpret the oxidation process. Analysis of the data collected shows that around 80 % of the iron (II) from the growth medium has been transformed into iron (III) in the form of different (oxy)hydroxides, with the rest found to be in a mixed 2,5 valence in magnetite. Our investigation shows that the bio-film sample has a phase content different from that of the powdered biomass and that lepidocrocite (γ-FeOOH) is the predominant and the initial biogenic phase in both samples. Magnetite nanoparticles are a secondary product in the bio-film, part of which possesses a defective quasi-maghemite surface layer. In the powdered biomass, the oxidation steps are not fully completed. The initial products are non-stoichiometric and due to the mixed ferric and ferrous ions present, they develop into: (i) lepidocrocite (γ-FeOOH) as a basic sediment, (ii) magnetite (Fe₃O₄) and (iii) goethite (α-FeOOH) in small quantities. The average size of all iron-bearing particles is found to be below 30 nm. The magnetic measurements performed show a superparamagnetic behavior of the material at room temperature.     

The influence of nitrate on the phosphorus flux to and from oxygen depleted lake sediments

Addition of nitrate to an oxygen depleted sediment leads to a stimulation of the mineralization process if a major part of the nitrate is dissimilatorily reduced. This may cause an increased release of phosphate from some sediments. Nitrate, however, maintains a high redox potential at the sediment surface and thus prevents a release of iron-bound phosphorus. These two counteracting effects of nitrate addition to sediment-water systems were demonstrated in laboratory experiments. A high supply of nitrate to a phosphorus-saturated sediment caused an increased release of phosphate and ammonium once the nitrate had been used up. However, from other sediments there was no or very little release of phosphate but an increased release of ammonium caused by high nitrate dissimilation, probably due to the very high capacity of these sediments to bind liberated phosphate or due to storage of phosphorus in an increased bacterial biomass. Phosphorus fractionation, before and after the experiments with the sediments, provided information on transfers to, from and within the sediments.     

Biogeochemical changes at the sediment–water interface during redox transitions in an acidic reservoir: exchange of protons,acidity and electron donors and acceptors

Redox transitions induced by seasonal changes in water column O₂ concentration can have important effects on solutes exchange across the sediment–water interface in systems polluted with acid mine drainage (AMD), thus influencing natural attenuation and bioremediation processes. The effect of such transitions was studied in a mesocosm experiment with water and sediment cores from an acidic reservoir (El Sancho, SW Spain). Rates of aerobic organic matter mineralization and oxidation of reduced inorganic compounds increased under oxic conditions (OX). Anaerobic process, like Fe(III) and sulfate reduction, also increased due to higher O₂ availability and penetration depth in the sediment, resulting in higher regeneration rates of their corresponding anaerobic e^? acceptors. The contribution of the different processes to oxygen uptake changed considerably over time. pH decreased due to the precipitation of schwertmannite and the release of H⁺ from the sediment, favouring the dissolution of Al-hydroxides and hydroxysulfates at the sediment surface. The increase in dissolved Al was the main contributor to water column acidity during OX. Changes in organic matter degradation rates and co-precipitation and dissolution of dissolved organic carbon and nitrogen with redox-sensitive Fe(III) compounds affected considerably C and N cycling at the sediment–water interface during redox transitions. The release of NO₂^? and NO₃^? during the hypoxic period could be attributed to ammonium oxidation coupled to ferric iron reduction (Feammox). Considering the multiple effects of redox transitions at the sediment–water interface is critical for the successful outcome of natural attenuation and bioremediation of AMD impacted aquatic environments.     

Organic matter mineralization in an organic-rich sediment: Experimental stimulation of sulfate reduction by fish food pellets

Abstract The combined effects of organic matter additions and temperature on short chain fatty acid (SCFA) turnover, sulfate reduction and nutrient accumulation were examined in an organic-rich fish farm sediment. Fish food pellets, which contribute significantly to the organic matter loss from fish farms, were added to surface sediment at three loadings (2.8; 14.0; 28.0 mg ww g⁻¹ ww sediment; equivalent to organic matter loadings measured during fish farming) and incubated for 30 days in anaerobic bags at 5°C and 15°C. SCFA accumulated to high levels (acetate up to 85 mM, propionate up to 17 mM, butyrate up to 25 mM) in sediments amended with food pellets, and sulfate reduction was stimulated up to 30 times relative to unamended sediments. Sulfate reducers appeared saturated with substrates (SCFA) even in the lowest additions. A low C/N ratio (0.4–1.8) of the major mineralization products (TCO₂ and NH₄⁺) indicated preferential nitrogen mineralization in amended sediment compared with the total particulate pool (C/N = 8.8–11.9) and added food pellets (C/N = 8.4).     

The impact of desiccation of a freshwater marsh (Garcines Nord,Camargue, France) on sediment-water-vegetation interactions

The impact of desiccation on a marsh sediment was studied both in the laboratory and in the field. Changes in the sediment chemistry of a homogenized sediment suspension during desiccation were studied in the laboratory. FeS was oxidized completely. A considerable mineralization of organic phosphate took place, from both the acid soluble organic phosphate fraction and from the residual organic phosphate fraction, but no significant mineralization of organic matter was observed. The o-P formed during the mineralization was recovered partly in the Fe(OOH) ≈P fraction and partly in the CaC₃≈P fraction. An upward flux was found. During spring and summer 1990 the water inlet to a shallow permanent freshwater marsh with a surface of about 1.5 hectares was blocked, in order to desiccate the marsh by evaporation. The sediments initially consisted of a black anoxic organic top layer and a less organic anoxic gray layer. During the desiccation of the sediment a brown oxic surface layer was formed from the black layer and an increase of pH and Eh occurred. Subsequent rainfall made the Eh increase further but caused a decrease in pH indicating an increase in bacterial activity. A progressive oxidation of FeS was observed. An increase in Tot-P in the surface layer and a decrease in the gray and the black layer of the sediment occurred, probably due to a capillary upward flux. A mineralization of organic matter was observed in the two deeper layers. In the upper brown layer this mineralization was less evident, probably because it has been masked by the capillary movement. A net C loss of 40% was calculated to have occurred in the layer 0–40 cm. In the deeper layers a decrease in Tot-N was observed, whereas no important increase occurred in the top layer. Over a sediment layer of 40 cm a N loss of 50% was calculated. C- and N losses occurred simultaneously, suggesting the importance of mineralization as a source of inorg-N for denitrification. The chemical and physical changes in the sediment during desiccation affected layers down to 40 cm. This means that not only the top layer of a sediment but also deeper layers are active in systems of which part of the sediment dries occasionally. Fractionation of the surface sediment phosphate showed an increase of Fe(OOH) ≈ P in the top layer due to the oxidation of FeS to Fe(OOH), enlarging the P-adsorption capacity of the sediment. A mineralization of about 50% of acid soluble organic phosphate occurred. After rainfall, a net increase in residual organic phosphate occured presumably due to an increase of bacterial activity. Drying may therefore be utilized as a tool, in wetland management, to eliminate organic nitrogen and carbon from the sediment. In rice culture, it may be used to make part of the organic nitrogen available to the rice.     

Development of radiographic and microscopic techniques for the characterization of bacterial transport in intact sediment cores from Oyster, Virginia.

The objective of this study was to ascertain the physical and mineralogical properties responsible for the retention of bacteria in subsurface sediments. The sediment core chosen for this study was a fine-grained, quartz-rich sand with minor amounts of Fe and Al hydroxides. A bacterial transport experiment was performed using an intact core collected from a recent excavation of the Butler's Bluff member of the Nassawadox formation in the borrow pit at Oyster, VA. and a 14C-labeled bacterial strain OYS2-A was selected for its relatively low adhesion. After the bacterial breakthrough was observed in the effluent, the intact core was dissected to determine the internal distribution of the injected bacteria retained in the sediment. The sediment was dried, epoxy fixed, and thin sectioned. The distribution of 14C activity in the thin sections was mapped using a phosphor screen and X-ray film. The remainder of the core was subsampled and the 14C activity of the subsamples was determined by liquid scintillation counting. The phosphor imaging technique was capable of directly imaging the distribution of radiolabeled bacteria in thin sections, because of its high sensitivity and linear response over a large activity range. The phosphor imaging signal intensity was utilized as a measure of bacterial concentration. The distribution of bacteria at the millimeter scale in the thin sections was compared to the grain size, porosity, and mineralogy as measured by scanning electron microscopy (SEM) and energy dispersive spectrum (EDS) analyses. No apparent correlation was observed between the retention or collision efficiency of bacteria in the sediment and the amount of Fe and Al hydroxides. This apparent lack of correlation can be qualitatively explained by combination of several factors including a nearly neutral surface charge of the bacterial strain, and texture of the Fe and Al hydroxides in the sediment. The combination of phosphor imaging with SEM-EDS proved to be a robust method for relating the physical and mineralogical microscopic properties of poorly indurated sediment to the distribution of adsorbed bacteria, allowing bacterial retention mechanisms to be unambiguously unraveled.     

Regeneration of inorganic phosphorus and nitrogen from decomposition of seston in a freshwater sediment

The mineralization of phosphorus and nitrogen from seston was studied in consolidated sediment from the shallow Lake Arreskov (July and November) and in suspensions without sediment (July). In the suspension experiment, phosphorus and nitrogen were mineralized in the same proportions as they occurred in the seston. During the 30 days suspension experiment, 47 and 43% of the particulate phosphorus and nitrogen, respectively, was mineralized with constant rates.Addition of seston to the sediment had an immediate enhancing effect on oxygen uptake, phosphate and ammonia release, whereas nitrate release decreased due to denitrification. The enhanced rates lasted for 2–5 weeks, while the decrease in nitrate release persisted throughout the experiment. The increase in oxygen uptake (equivalent to 21% of the seston carbon) was, however, only observed in the July experiment. The release of phosphorus and nitrogen from seston decomposing on the sediment surface differed from the suspension experiments. Thus, between 91 and 111% of the phosphorus in the seston was released during the experiments. Due to opposite directed effects on ammonium and nitrate release, the resulting net release of nitrogen was relatively low.A comparison of C/N/P ratios in seston, sediment and flux rates indicated that nitrogen was mineralized faster than phosphorus and carbon. Some of this nitrogen was lost through denitrification and therefore not measurable in the flux of inorganic nitrogen ions. This investigation also suggests that decomposition of newly settled organic matter in sediments have indirect effects on sediment-water exchanges (e.g. by changing of redox potentials and stimulation of denitrification) that modifies the release of mineralized phosphate and nitrogen from the sediment.     

Benthic fauna bio-irrigation effects on nutrient regeneration in fish farm sediments

Impacts of organic enrichment and a modified benthic fauna community (caused by fish farming) on benthic mineralization rates and nutrient cycling were studied in sediments at one Danish and one Cypriote fish farm. Sediment organic matter concentration and macrofauna community composition were manipulated in microcosms and changes in total benthic metabolism (oxygen consumption, TCO₂ production), anaerobic metabolism (sulfate reduction rates), nutrient fluxes and sediment parameters were followed for a period of 3 weeks. Mineralization rates were found to be highly correlated with irrigation velocities and largest fauna effects were found in the Danish sediments with the large and active irrigating climax species (Nereis diversicolor and Macoma balthica). Eastern Mediterranean climax species (Glycera rouxii and Naineris laevigata) also stimulated mineralization rates but to a smaller extent due to lower irrigation, whereas the opportunistic species (Capitella in Danish sediment and Hermodice carunculata in Cypriote sediment) showed less effect on mineralization. Ammonium and phosphate release increased with increasing irrigation velocities, but much less in Cyprus indicating higher nutrient retention at the ultra-oligotrophic location compared to eutrophic Danish site. Irrigation velocities, and thus mineralization rates, increased by organic matter loading, indicating larger fauna-induced oxidation in enriched environments. The result implies that a change in fauna structure in fish farm sediment towards smaller opportunistic polychaete species with lower irrigation will result in slower mineralization rates and potentially increase accumulation of organic waste products.     

Biogeochemical processes in the groundwater discharge zone of urban streams

The influence of biogeochemical processes on nitrogen and organic matter transformation and transport was investigated for two urban streams receiving groundwater discharge during the dry summer baseflow period. A multiple lines of evidence approach involving catchment-, and stream reach-scale investigations were undertaken to describe the factors that influence pore water biogeochemical processes. At the catchment-scale gaining stream reaches were identified from water table mapping and groundwater discharge estimated to be between 0.1 and 0.8 m³ m^?2 d^?1 from baseflow analysis. Sediment temperature profiles also suggested that the high groundwater discharge limited stream water infiltration into the sediments. At the stream reach-scale, dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) concentrations were higher in stream water than in groundwater. However, DOC and DON concentrations were greatest in sediment pore water. This suggests that biodegradation of sediment organic matter contributes dissolved organic matter (DOM) to the streams along with that delivered with groundwater flow. Pore water ammonium (NH₄ ⁺) was closely associated with areas of high pore water DOM concentrations and evidence of sulfate (SO₄ ^2?) reduction (low concentration and SO₄:Cl ratio). This indicates that anoxic DOM mineralization was occurring associated with SO₄ ^2? reduction. However the distribution of anoxic mineralization was limited to the center of the streambed, and was not constrained by the distribution of sediment organic matter which was higher along the banks. Lower sediment temperatures measured along the banks compared to the center suggests, at least qualitatively, that groundwater discharge is higher along the banks. Based on this evidence anoxic mineralization is influenced by groundwater residence time, and is only measurable along the center of the stream where groundwater flux rates are lower. This study therefore shows that the distribution of biogeochemical processes in stream sediments, such as anoxic mineralization, is strongly influenced by both the biogeochemical conditions and pore water residence time.     

Organic Matter Mineralization with Reduction of Ferric Iron in Anaerobic Sediments

The potential for ferric iron reduction with fermentable substrates, fermentation products, and complex organic matter as electron donors was investigated with sediments from freshwater and brackish water sites in the Potomac River Estuary. In enrichments with glucose and hematite, iron reduction was a minor pathway for electron flow, and fermentation products accumulated. The substitution of amorphous ferric oxyhydroxide for hematite in glucose enrichments increased iron reduction 50-fold because the fermentation products could also be metabolized with concomitant iron reduction. Acetate, hydrogen, propionate, butyrate, ethanol, methanol, and trimethylamine stimulated the reduction of amorphous ferric oxyhydroxide in enrichments inoculated with sediments but not in uninoculated or heat-killed controls. The addition of ferric iron inhibited methane production in sediments. The degree of inhibition of methane production by various forms of ferric iron was related to the effectiveness of these ferric compounds as electron acceptors for the metabolism of acetate. The addition of acetate or hydrogen relieved the inhibition of methane production by ferric iron. The decrease of electron equivalents proceeding to methane in sediments supplemented with amorphous ferric oxyhydroxides was compensated for by a corresponding increase of electron equivalents in ferrous iron. These results indicate that iron reduction can outcompete methanogenic food chains for sediment organic matter. Thus, when amorphous ferric oxyhydroxides are available in anaerobic sediments, the transfer of electrons from organic matter to ferric iron can be a major pathway for organic matter decomposition.     

Solute dynamics in a North Brazilian mangrove: the influence of sediment permeability and freshwater input

Although water in mangrove sediments influences nutrient cycling in both, mangrove forest and estuary, little information exists on seasonal and vertical distribution of dissolved organic and inorganic compounds in the sediment column. We studied the influence of sediment texture and chemistry, permeability (K), tides, and rainfall on dissolved organic carbon (DOC) and nitrogen (DON), dissolved inorganic phosphate (DIP) and salinity in creek and sediment waters of a mangrove in Pará, Brazil. Water samples were taken from boreholes and piezometers in the mangrove forest and from an adjacent tidal creek at neap and spring tides, during the dry and rainy season. Forest sediment was analysed for carbon (C), nitrogen (N), salinity and permeability. Clay, C and N decreased with depth. Sediment permeability (K) was lowest (<0.1 m day⁻¹) in the upper, clay-rich and crab-burrow-free mud layer. In the deeper, fine sand strata, K ranged from 0.7 to 1.8 m day⁻¹. Tidal range in the creek was 3.5 and 5.5 m for neap and spring tides, respectively. Salinity, DOC, DON and DIP in creek water were inversely related to tidal height. Piezometer data revealed significant water level changes in deeper, sandy sediment layer, which followed, time-lagged, the tidal fluctuations. In contrast, tide did not affect the water level in the upper sediment due to low permeability. Compared with creek water, sediment water was enriched in DOC, DON and DIP because of organic matter input and mineralization. In deeper layers, solute concentration was most likely affected by sorption processes (DOC and DIP) and reduction reactions (DIP). During the rainy season, DOC and DON in creek and sediment water were higher than in the dry season. DIP appeared invariant to seasonal changes. In the rainy season, salt flushing from surface sediments resulted in higher salinities at intermediate sediment depths, while in the deeper layers salinity was lower due to exchange with water from the tidal creek.     

Effect of temperature on submerged macrophyte litter decomposition within sediments from a large shallow and subtropical freshwater lake

In shallow aquatic systems, the majority of organic matter mineralization occurs in the sediments. Several factors including temperature control mineralization rates, however, the underlying causes of the effects are not well understood in subtropical lakes. In this study, we determined the influence of temperature on organic matter degradation by taking sediments from four sites in a subtropical large shallow freshwater lake, and monitoring organic matter composition and enzymes in microcosm experiments at five temperatures from 5 to 40°C. Following a three-month incubation, it was found that the mineralization of submerged plants in sediments was strongly influenced by temperature. Removal efficiency of total organic carbon in sediments ranged from 4.3 to 22.6% at 5°C, and reached 46.7–55.5% at 40°C. In addition, the removal efficiency of organic matter and the relative recalcitrant carbon decomposition depended on sediment type. For sediments in the site located in the lake center, recalcitrant and labile carbon decomposition had equivalent responses to the different temperatures. For sediments with dominance of submerged macrophytes, the humic acids were low even at high temperature. Thus, the annual deposition of plant litter in sediments favored organic carbon decomposition rather than humification.     

Reevaluation of coleoid cephalopod relationships based on modified arms in the Jurassic coleoid Mastigophora

Mastigophora brevipinnis Owen, 1856, is a 'fossil teuthid' presently considered to be a member of the coleoid cephalopod Suborder Loligosepiina Jeletzky, which in turn has been placed by various authors in or near the Vampyromorpha Grimpe. Recent morphological and biochemical analyses indicate that vampyromorphs are more closely related to the Octopoda than to the Decapodiformes. Fossils of Mastigophora from the Oxford Clay (Jurassic: Callovian) show soft-tissue preservation and evidence of arm crown specialization. Some of these fossils have up to eight short, thick arms with circular sucker-like structures and filiform distal extensions, plus what appear to be the bases of two thinner ventrolateral arms. The latter lack proximal suckers and curve medially to insert into the arm crown, similar to the tentacles that are the modified ventrolateral arms of living squids and cuttlefishes. This suggests that the thinner structures were decapod-like tentacles. If Mastigophora had tentacles homologous with those of modern decapods, then it was a decapod, because this synapomorphy defines the Decapodiformes. This indication of decapod affinities for Mastigophora brings into question the relationships of the other 'fossil teuthids'. The inferred relationship of the Loligosepiina, including Mastigophora , with the Vampyromorpha, based largely on similarities of gladius morphology with that of living Vampyroteuthis , may reflect shared plesiomorphic characters.     

The determination of ferric iron in plants by HPLC using the microbial iron chelator desferrioxamine E

Common methods for plant iron determination are based on atomic absorption spectroscopy, radioactive measurements or extraction with subsequent spectrophotometry. However, accuracy is often a problem due to background, contamination and interfering compounds. We here describe a novel method for the easy determination of ferric iron in plants by chelation with a highly effective microbial siderophore and separation by high performance liquid chromatography (HPLC). After addition of colourless desferrioxamine E (DFE) to plant fluids, the soluble iron is trapped as a brown-red ferrioxamine E (FoxE) complex which is subsequently separated by HPLC on a reversed phase column. The formed FoxE complex can be identified due to its ligand-to-metal charge transfer band at 435 nm. Alternatively, elution of both, DFE and FoxE can be followed as separate peaks at 220 nm wavelength with characteristic retention times. The extraordinarily high stability constant of DFE with ferric iron of K=10³² enables extraction of iron from a variety of ferrous and ferric iron compounds and allows quantitation after separation by HPLC without interference by coloured by-products. Thus, iron bound to protein, amino acids, citrate and other organic acid ligands and even insoluble ferric hydroxides and phosphates can be solubilized in the presence desferrioxamine E. The “Ferrioxamine E method” can be applied to all kinds of plant fluids (apoplasmic, xylem, phloem, intracellular) either at physiological pH or even at acid pH values. The FoxE complex is stable down to pH 1 allowing protein removal by perchloric acid treatment and HPLC separation in the presence of trifluoroacetic acid containing eluents. Published online December 2004     

The impact of Chironomus plumosus larvae on organic matter decay and nutrient (N, P) exchange in a shallow eutrophic lake sediment following a phytoplankton sedimentation

The importance of Chironomus plumosus larvae onbenthic metabolism and nutrient exchange across thesediment–water interface was evaluated in a shalloweutrophic lake (Lake Arreskov, Denmark) following aphytoplankton sedimentation. Chironomus plumosuslarvae were added to laboratory sediment microcosms,corresponding to a density of 2825 larvae m⁻².Non-inhabited microcosms served as controls. Asedimentation pulse of organic matter was simulated byadding fresh algal material (Chlamydomonasreinhardii) to sediment cores (36 g dryweight m⁻²). The mineralization was followed bymeasuring fluxes of O₂, CO₂, dissolvedinorganic nitrogen and phosphate. A rapid clearance ofalgae from the water column in faunated microcosmssuggested that chironomids may be of major importancein controlling phytoplankton concentrations in shalloweutrophic lakes. Chironomids increased the sedimentO₂ uptake ≈ 3 times more than what wouldbe expected from their own respiration, indicating astimulation of microbial activity and decomposition oforganic matter in the sediment. Addition of algaeenhanced the release of CO₂, NH⁺ ₄ ando-P. The excess inorganic C, N and P released inamended non-inhabited sediment after 36 dayscorresponded to 65, 31 and 58% of the C, N and P inthe added algae. In sediment inhabited by Chironomus plumosus the corresponding numbers were147, 45 and 73%, indicating that mineralization oforganic matter also from the indigenous sediment poolwas stimulated by chironomids. This revised version was published online in July 2006 with corrections to the Cover Date.     

Iron–sulphur–phosphorus Interactions: Implications for Sediment Buffering Capacity in a Mediterranean Eutrophic Lagoon (Sacca di Goro,Italy)

The interactions among sedimentary cycles of sulphur, iron and phosphorus were investigated in the eutrophic Sacca di Goro lagoon (Northern Adriatic coast, Italy) in order to assess the iron buffering capacity of the sediment. Three stations were chosen, which represented different primary producer communities, hydrodynamics and sediment characteristics. Station G was close to the outlet of the Po di Volano river, station 4 was in the central part of the lagoon under tidal influence and station 17, in the sheltered zone, was affected by macroalgal blooms. From January 1997 to January 1998, sediment cores were sampled approximately every 2 months. In parallel, temperature, salinity and dissolved oxygen were determined in the water column. Sedimentary profiles of Eh, pH, dissolved sulphide (DS), acid volatile sulphide (AVS), chromium reducible sulphur (CRS), iron and phosphorus pools were determined in the 0–10 cm sediment horizon. Bacterial sulphate reduction rates were measured only at station 17. Iron pools, AVS and CRS followed similar patterns at all the considered stations, with lower values in the 0–2 cm sediment horizon and peaks in the deepest sediment layer (5–10 cm horizon). Overall, the labile Fe accounted for an annual average of 115.6 ± 3.0 μmol cm⁻³, with peaks of labile ferric iron up to 40 μmol cm⁻³. The great iron availability and reactivity accounted for an efficient buffering capacity against sulphides, with the accumulation of AVS and CRS, specially at station G where the iron buffer was replenished by iron-rich freshwaters. At station 17, in spite of a great iron availability the buffering capacity was less efficient due to macroalgal blooms and accumulation of labile organic matter, whose decomposition stimulated bacterial sulfate reduction and the inherent sulphide production both in the pore-water (DS: 4.0 ± 3.7 mM) and in the deepest water column (DS: 85 μM). The iron and sulphur interactions had also implications for P cycling, since in summer the ferric iron reduction was accompanied by a significant increase of pore-water and exchangeable phosphates. The AVS to labile Fe and AVS to TRIS (AVS + CRS) ratios were used to assess the sediment capacity of precipitating and retaining sulphides. These ratios were then compared with the chemical buffer capacity, demonstrating their suitability as indicators of buffering capacity towards sulphides.