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Macroevolution of plasmids: a model for plasmid speciation.

A new evolutionary model for diversification in plasmid incompatibility groups (plasmid speciation) is suggested. The model is based on the formation of plasmid cointegrates from two compatible plasmids. The existence of plasmid cointegrates is well known, however, their potential key role in plasmid macroevolution has not yet been recognized. In a hypothesis presented here, one of the rep genes is supposed to be relaxed from selection in plasmid cointegrates and thus becomes free to accumulate mutations. These mutations can lead to a change in incompatibility specificity. Evidence supporting this hypothesis comes from the common occurrence of multi-replicon plasmids in nature as well as from experimental studies on plasmid cointegrate formation. A more speculative extension of this model hypothesizes an evolutionary scenario for origin of the eubacterial single-replicon genome and the eukaryotic multi-replicon genome, as well as the place of plasmids and viruses in this picture.

Bacteria↗

Chemical speciation of arsenic in the livers of higher trophic marine animals.

Concentrations of total arsenic and individual arsenic compounds were determined in livers of cetaceans (Dall's porpoise and short-finned pilot whale), pinnipeds (harp and ringed seals), sirenian (dugong), and sea turtles (green and loggerhead turtles) to characterize arsenic accumulation profiles in higher trophic marine animals. Hepatic arsenic concentrations in sea turtles were highest among the species examined. Chemical speciation of arsenic revealed that arsenobetaine was the major arsenic compound in almost all the species. In contrast, arsenobetaine was a minor constituent in dugong. Dimethylarsinic acid, methylarsonic acid, arsenocholine, tetramethylarsonium ion, arsenite, and an unidentified arsenic compound were also detected as minor constituents. However, the composition of arsenic compounds was different among these species. These results might reflect the differences in the metabolism of arsenic and/or the compositions of arsenic compounds in their preys. To our knowledge, this is the first report on the large variation in the composition of arsenic species in liver of marine mammals and sea turtles.

Animals↗

Isolation of dissolved organic matter (DOM) from surface waters using reverse osmosis and its impact on the reactivity of DOM to formation and speciation of disinfection by-products.

Dissolved organic matter (DOM) from three low-hardness surface waters was isolated and concentrated using a reverse osmosis (RO) membrane system. The efficacy of the RO isolation method and its impact on the subsequent reactivity between DOM and chlorine were examined. DOM mass balances (quantified as dissolved organic carbon) ranged from 96.1 to 102.1% for the three waters tested, and DOM mass recoveries of 93.9 to 98.2% indicated successful isolation, minimal fractionation. and negligible loss of organic matter. RO isolates were diluted using distilled and deionized water in the laboratory to reconstitute the source waters. Both source water (collected at the time of isolation) and reconstituted source water samples were chlorinated. Formation of several disinfection by-products (DBPs: e.g., THMs, HAA9, HANs, and HKs) were measured. For all waters tested, DBP formation of source and corresponding reconstituted source water agreed within 95% confidence intervals. Therefore, RO isolation had no impact on the DOM reactivity of the three low-hardness surface waters tested in this study. In addition, the degree of bromine substitution, as expressed by the bromine incorporation factor, was calculated. Comparison of bromine incorporation factors for source and reconstituted source waters further indicated that, as with the total DBP formations, bromine speciation and the relative occurrence of individual species in THMs and HAA9 did not change as a result of the isolation. Overall, in terms of DBP formation, RO isolation appears to maintain the integrity and reactivity of DOM.

Disinfection↗

Aluminum speciation in natural waters: measurement using Donnan membrane technique and modeling using NICA-Donnan.

The study of Al speciation is of interest for the assessment of soil and water quality. For the measurement of "free" aluminum (Al3+), a recently developed Donnan membrane technique was tested by measuring Al3+ in aluminum-fluoride solutions and gibbsite suspensions. It shows that the Donnan membrane technique can measure free Al3+ reliably up to 10(-9) M and the equilibration takes 3-4 days. Next, Al binding to humic acid (HA) purified from a forest soil was measured using either the Donnan membrane technique or gibbsite suspension. Results were compared with those predicted with the non-ideal consistent competitive adsorption (NICA)-Donnan model. The predictions using the generic parameters without fitting were in reasonable agreement with the measured data. Finally, the Donnan membrane technique was used to determine Al binding to dissolved organic matter (DOM) in the solutions of 24 soil samples at pH interval of 3-7. Measurements agree well with the predictions using the NICA-Donnan model assuming 30% of DOM is HA and 30% is fulvic acid. With this model, the effects of pH and DOM changes on the concentration of Al in 81 soil solutions were predicted reasonably without adjustment of model parameters. The comparison between the results of analysis and the modeling provides a mutual validation for the two methods.

Adsorption↗

Temporal variability of dissolved P speciation in a eutrophic reservoir--implications for predicating algal growth.

Weak-anion exchange chromatography was used to explore the temporal variability in the speciation of dissolved P in the surface layer of a eutrophic reservoir. Authentic free ortho-P ion was the most common form of P on three of the five sampling occasions-including during a bloom of the green algae Botryococcus braunii indicating that the bloom was not P limited. Conversely, the absence of authentic ortho-P during a bloom of the dinoflagellate Ceratium hirundinella suggested the bloom was either P limited or co-limited. These observations were confirmed by algal-growth bioassay experiments.

Chlorophyta↗

Speciation of heavy metals in marine sediments vs their bioaccumulation by mussels.

Total contents and speciation of selected heavy metals, including Al, Fe, Co, Ni, Pb, Zn, Cu, Cr, were measured in sediment samples and mussels Mya arenaria and Astarte borealis collected in the Horsund Fjord off Spitsbergen (Norwegian Sea) and the Bay of Gdansk (Baltic Sea). The investigation aimed at revealing differences in the accumulation pattern of heavy metals in mussels inhabiting sediments characterized by varying metal bioavailability. The contents of metals adsorbed to sediments and associated with iron and manganese hydroxides, which were obtained by sequential extraction, were utilized as a measure of metal bioavailability. The contents of Cd, Pb, Zn, Cu and Cr in mussels collected off Spitsbergen were generally lower than those in mussels from the Baltic Sea. In sediments collected off Spitsbergen the bioavailable fraction represented a small proportion (0-3.7% adsorbed metals and 0-11% associated with metals hydroxides) of total heavy metal contents. In sediments from the Baltic Sea the percentages of metals adsorbed and bound to hydroxides were 1-46% and 1-13%, respectively. The differences in bioavailable metal contents measured in sediments were utilized to explain the different contents of metals in mussels collected in the corresponding sites.

Adsorption↗

The effects of chemical remediation treatments on the extractability and speciation of cadmium and lead in contaminated soils.

Two rural soils contaminated by cadmium (Cd) and lead (Pb) were used to evaluate the effect of different chemical treatments on changes in speciation and extractability of Cd and Pb, and in phytoavailability to wheat. Triplicates of seven chemical treatments were tested to compare and evaluate the remediation techniques for contaminated soils using pot experiments. Treatments applied were calcium carbonate, a high quantity of phosphate salt, hog composts, iron oxide, manganese oxide, zeolite, and unamended control. Wheat (Triticum aestivum) was planted in the different amended soils for a further one month to evaluate the effectiveness of treatments on uptake of Cd and Pb by the wheat shoots. Results indicated that addition of calcium carbonate, manganese oxide, or zeolite reduces the extractability of Cd or Pb in both soils, and significantly reduce the uptake of Cd and Pb by wheat shoots. Changes in the extractability and metal sequential fractionations indicate that the exchangeable (or available) form of Cd and Pb in two soils can be transformed into unavailable forms after these amendments.

Biological Availability↗

Elemental gas phase atmospheric mercury as it interacts with the ambient aerosol and its subsequent speciation and deposition

A model describing the interaction of gas phase elemental atmospheric mercury, H(g)(o), with the ambient aerosol has been linked to hybrid single-particle Lagrangian integrated trajectory (HYSPLIT_4) a hybrid dispersion and deposition model. The integrated modelling system allows H(g)(o) emitted from an anthropogenic source in the presence(g) of the local aerosol to be followed and calculates the deposition fluxes to terrestrial and water receptors resulting from the interaction between the H(g)(o) and the aerosol. The model includes a source-based parameterized description of the ambient aerosol, a gas-phase diffusion and adsorption model for the interaction of H(g)(o) and the ambient particulate matter under conditions of low relative humidity, and an aqueous phase Hg chemistry model to allow for complete or partial deliquescence of the particles under conditions of high humidity. The model is, thus, able not only to calculate deposition fluxes, but also the speciation of the Hg compounds deposited; this is of great importance in the modelling of the atmospheric Hg cycle due to the difference in the properties of elemental and oxidized Hg.

Journal Article↗

Speciation of selenium in plant water extracts by ion exchange chromatography-hydride generation atomic absorption spectrometry.

Determination of selenium (Se) speciation in plants is important in studying the bioavailability and toxicity of Se in Se-contaminated soil/sediment. In this study, we used an anion exchange resin (Dowex 1-10X) to separate Se into non-amino acid organic Se, Se-amino acids, selenite (Se [IV]) and selenate (Se [VI]) in a plant (Stanleya pinnata) extract. The hydride generation atomic absorption spectrometry (HGAAS) was used to determine concentrations of these Se compounds in plant extracts. Results showed that Se compounds can be quantitatively separated by the resin column. Recovery of five spiked standard Se compounds (trimethylselenonium ion (TMSe+), dimethylselenoxide (DMSeO), selenomethionine (Semet), Se [IV] and Se [VII]) in the plant extract ranged from 92.9 to 103%. Water extractable Se accounted for 60.4-72.6% of the total Se in the plant. Among the soluble Se compounds in the plant extract, Se-amino acids were 73-85.5%, Se [VI] ranged from 7.5 to 19.5% and non-amino acid organic Se was less than 7%. Se [IV] in most samples was below the detection limit (1 microg/g). This study showed that considerable amounts of the accumulated Se [VI] in the plant was metabolized to Se-amino acids during growth of the plant.

Chromatography, Ion Exchange↗

Aluminium speciation in forest soil solution--modelling the contribution of low molecular weight organic acids.

The concentrations of Al bound to identified low molecular weight organic acids (LMWOAs), phosphate and humic compounds in soil solutions (O1, O2, E, B1 and B2 horizons) from Fennoscandinavian coniferous forest soils were calculated. Two models were evaluated: WHAM (Winderemere Humic Aqueous Model) and a model treating the natural organic acids as monoprotic. The WHAM model was calibrated to find an average charge balance of unity, and then used for Al speciation. This was achieved considering approximately 80% of the natural fulvic acid to be 'active'. For the monoprotic model, constants obtained from previous fitting of soil solution data were used and the model was calibrated using acid/base titrations. The modelling confirms that the low molecular weight acids are important complex formers, binding on average 11-42% (O), 19-20% (E), and 0-30% (B) of the total Al in solution depending on the model used. The monoprotic model yielded higher concentrations than WHAM. Both models predicted that the major part of Al in solution was organically complexed to humic substances and LMWOAs, which was consistent with analytical values of 'quickly reacting' Al (monomenc inorganic forms; 12-14% of Al(tot) on average in the E and B1 solutions). Both models could predict the magnitude of the analytical values (RMSD = 4-5 microM). On average the WHAM model showed a better fit for the E horizon solutions and the monoprotic model for the upper B horizon. The pH dependence of the low molecular weight fraction of Al was modelled in the pH range 3-5.5 for a 'typical' O1 and E solution assuming no other changes in soil solution composition. The extrapolation showed that the models had a different pH dependence. The concentration of Al bound to LMWOAs in WHAM decreased with higher pH while the opposite was seen for the monoprotic model. Also the influence of the concentration of total Al in solution was modelled. The models showed similar trends but for the 'typical' O1 horizon sample the monoprotic model yielded higher concentrations of Al bound to LMWOAs than WHAM.

Aluminum↗

Partitioning and speciation of chromium, copper, and arsenic in CCA-contaminated soils: influence of soil composition.

This study focused on the influence of soil composition and physicochemical characteristics on the retention and partitioning of Cu, Cr and As in nine chromated copper arsenate (CCA) artificially contaminated soils. A statistical mixture design was used to set up the number of soils and their respective composition. Sequential extraction and modified solvent extraction were used to assess Cu and Cr partitioning and As speciation [As(III) or As(V)]. It was found that peat had a strong influence on CEC (232 meq/100 g), on buffer capacity and on Cu and Cr retention, whereas kaolinite's contribution to the CEC was minor (38 meq/100 g). Average metal retention in mineral soils was low (58% for Cu and 23% for Cr) but increased dramatically in highly organic soils (96% for Cu and 78% for Cr). However, both organic and mineral soils demonstrated a very high sorption of added As (71-81%). Levels of Cu and Cr in a soluble or exchangeable form (F1) in highly organic soils were very low, whereas the levels strongly bound to organic matter were much higher. Conversely, in mineral soils, 47% of Cu and 18% of Cr were found in F1. As a result, Cr and Cu in moderately and highly organic contaminated soils were present in less mobile and less bioavailable forms, whereas in mineral soils, the labile fraction was higher. The modified method used for selective determination of mineral As species in CCA-contaminated soils was found to be quantitative and reliable. Results revealed that arsenic was principally in the pentavalent state. Nevertheless, in organic soils, arsenite was found in significant proportions (average value of 29% in highly organic soils). This indicates that some reduction of arsenate to arsenite occurred since the original species in CCA is As(V).

Arsenates↗

Mercury speciation and accumulation in Bangladesh freshwater and anadromous fish.

Total mercury concentration in the muscle of 417 fish of 12 common freshwater and four anadromous species from Bangladesh were low, varying from 2 to 430 ng/g fresh wt. Depending on Hg speciation, three types of accumulation mechanisms were defined. Type I covers the majority of species and describes a pattern widely accepted as 'normal', with increasing levels of organic (methyl) mercury with length (age), combined to a low and constant inorganic level. This accumulation pattern leads to a relative increase of the organic mercury fraction with age, eventually reaching 90-100% of organic mercury in full grown specimens. Type II is found in both planktivorous genera only and showed increasing levels of inorganic mercury combined to low and constant organic mercury levels, leading to a relative decrease in organic mercury fraction with age. This unexpected pattern was only reported in cases of some marine species where it seemed to be linked to demethylation mechanisms or regional influences on Hg levels. A third intermediate accumulation pattern with increasing concentrations of both the organic and the inorganic Hg fraction with age was found in one bottom dwelling species only. The implications of these observations for the accumulation mechanisms of mercury in fish are discussed.

Animals↗

Copper sorption by chitosan in the presence of citrate ions: influence of metal speciation on sorption mechanism and uptake capacities.

The presence of organic ligands in a solution containing metal ions modifies metal speciation, which in turn changes the sorption mechanism, optimum pH range and maximum sorption capacity. The present work investigates the sorption of copper by chitosan in the presence of citrate at different metal/ligand ratios. Copper uptake in acidic solution takes place through electrostatic attraction between the protonated amine groups of chitosan and anionic copper-citrate complexes (mainly Cu(OH)L2- but also a small fraction of CuL-). Sorption was negligible below pH 3 due to competition from dissociated anionic ligand and counter ions brought about by dissociation of the acid used for pH control. Actually, copper sorption begins to be significant when the fraction of anionic copper-complexes exceeds that of anionic copper-free ligand. So sorption capacity strongly increases up to pH 4.5-5.5. Above pH 5.5, the progressive decrease of amine protonation leads to a linear decrease in sorption capacity. An excess of ligand leads to an increase in the fraction of free dissociated (anionic) ligand that may compete for electrostatic attraction on protonated amine groups and therefore leads to a decrease in sorption capacities.

Chelating Agents↗

Effects of Si speciation on the in vitro bioactivity of glasses.

The surface reactivity of glasses belonging to the (mol%) 31SiO2-11P2O5-(58-x)CaO-xMgO series, with x ranging from 0 to 32, was studied in Kokubo's simulated body fluid (SBF). Scanning electron microscopy, inductively coupled plasma spectroscopy and Fourier transform infrared spectroscopy were used to characterise the glass surface and the SBF compositional changes. All glasses develop surface layers rich in silica and calcium phosphate. An increasing surface activity with increasing MgO/CaO ratio was observed. In a previous investigation using magic-angle spinning nuclear magnetic resonance it was found that there is an increasing abundance of Q0 species in the glass structure with increasing MgO content. The present work shows that, when immersed in SBF, Q0-rich glasses are easily leached to form a silica gel layer. It is concluded that MgO in the glass indirectly improves the early stages of mineralisation by favouring Q0 speciation. This mechanism plays an important role in glass bioactivity.

Glass↗

A flow system for the determination of metal speciation in soil by sequential extraction.

A flow extraction system with on-line and off-line flame atomic absorption spectrometric (FAAS) detection was developed to speed up, facilitate, and improve the accuracy of sequential extraction for metal speciation in solid materials. A flow extraction system with off-line detection was more advantageous than the on-line detection. In the proposed system, extraction was performed in a closed extraction chamber where extractants were flowing through sequentially. The extract from each extraction was collected in 4-10 fractions to obtain a total of approximately 180 ml for subsequent FAAS determination. The system is simple, easy to construct and operate. It has less risk of contamination and human error. A widely used three-step sequential extraction scheme was used to evaluate the novel system by analyzing Ca, Fe, Mn, Cu, and Zn in a certified reference material. The extraction time for three-step sequential extraction of soil sample was 4 h. The analytical results for Ca, Fe, Mn, Cu, and Zn of a soil certified reference material using the proposed system were compared with those of the conventional batch extraction.

Environmental Monitoring↗

Correlations between speciation of Cd, Cu, Pb And Zn in sediment and their concentrations in total soft tissue of green-lipped mussel Perna viridis from the west coast of Peninsular Malaysia.

Total concentrations and speciation of cadmium (Cd), copper (Cu), lead (Pb) and zinc (Zn) in surface sediment samples were correlated with the respective metal measured in the total soft tissue of the green-lipped mussel Perna viridis, collected from water off the west coast of Peninsular Malaysia. The aim of this study is to relate the possible differences in the accumulation patterns of the heavy metals in P. viridis to those in the surface sediment. The sequential extraction technique was employed to fractionate the sediment into 'freely leachable and exchangeable' (EFLE), 'acid-reducible,' 'oxidisable-organic' and 'resistant' fractions. The results showed that significant (P<.05) correlations were observed between Cd in P. viridis and Cd in the sediment (EFLE fraction and total Cd), Cu in P viridis and Cu in the sediment (EFLE and 'acid-reducible' fractions and total Cu) and Pb in P viridis and Pb in the sediment ('oxidisable-organic' fraction and total Pb). No significant correlation (P > .05) was found between Zn in P viridis and all the sediment geochemical fractions of Zn and total Zn in the sediment. This indicated that Zn was possibly regulated from the soft tissue of P. viridis. The present results supported the use of P viridis as a suitable biomonitoring agent for Cd, Cu and Pb.

Animals↗

Selection of a suitable mobile phase for the speciation of four arsenic compounds in drinking water samples using ion-exchange chromatography coupled to inductively coupled plasma mass spectrometry.

The performance of two mobile phase buffers, phosphate and TRIS, were compared for the speciation of four arsenic species: arsenate (As(V)), arsenite (As(III)), mono methylarsonic acid (MMA), and dimethyl arsinic acid (DMA) in drinking water, using ion-exchange chromatography inductivelycoupled plasma mass spectrometry (IEC-ICP-MS). The mobile phase containing TRIS acetate buffer ("TRIS") demonstrated superior perfomance in baseline separation of all four arsenic species and the internal standard. It is also applicable to high-throughput sample analysis as it minimized the frequency required to clean the sampling interface due to salt build-up when compared to the phosphate mobile phase. The method was evaluated for its precision, accuracy, linearity and detection limits. The method was successfully applied for the analysis of drinking water samples.

Arsenicals↗

Geochemical speciation of heavy metals in semiarid soils of the central Ebro Valley (Spain).

This study describes the chemical speciation of Fe, Mn, Zn and Cr in four selected soil types representative of the more abundant agricultural soils in the central Ebro river valley in Aragón. Gypsisols, Calcisols, Solonchaks and Solonetzs represent around 20% of the total soil surface in the region. A total of 12 selected sites have been sampled and five subsamples were taken in each site to create a composite sample. The four elements have been analysed by the sequential extraction procedure of Tessier et al. [Anal. Chem. 51 (1979) 844.] by emission atomic spectrometry of solid state (ICP OES). Very little amounts of Fe and Mn were retrieved from the exchangeable phase, the ready available for biogeochemistry cycles in the ecosystems. Therefore, low quantities of Fe and Mn can be taken up by plants in these alkaline soils. Cr was not detected in the bioavailable forms as well as Zn that was only present in negligible amounts in very few samples. The absence of mobile forms of Cr in all soils eliminates the toxic risk both in the trophic chain and from its migration downwards the soil profile. The largest contents of Fe, Zn and Cr were retrieved from the residual phase where metals are strongly bound to minerals, whereas Mn from the carbonate and oxide phases amounts 80% of its total content. Gypsisols and Calcisols have the lowest metal contents while the highest are found in Solonetzs and Solonchaks.

Biological Availability↗