Distribution of arsenic species in an open seagrass ecosystem: relationship to trophic groups, habitats and feeding zones

2012 ◽  
Vol 9 (1) ◽  
pp. 77 ◽  
Author(s):  
A. Price ◽  
W. Maher ◽  
J. Kirby ◽  
F. Krikowa ◽  
E. Duncan ◽  
...  
Keyword(s):  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Trophic Levels ◽  
Arsenic Content ◽  
Trophic Groups ◽  
Marine Systems ◽  
Seagrass Ecosystem ◽  
High Concentrations ◽  
Species Specific ◽  
Arsenic Source

Environmental contextAlthough arsenic occurs at high concentrations in many marine systems, the influencing factors are poorly understood. The arsenic content of sediments, detritus, suspended particles and organisms have been investigated from different trophic levels in an open seagrass ecosystem. Total arsenic concentrations and arsenic species were organism-specific and determined by a variety of factors including exposure, diet and the organism physiology. AbstractThe distribution and speciation of arsenic within an open marine seagrass ecosystem in Lake Macquarie, NSW, Australia is described. Twenty-six estuarine species were collected from five trophic groups (autotrophs, suspension-feeders, herbivores, detritivores and omnivores, and carnivores). Sediment, detritus, epibiota and micro-invertebrates were also collected and were classified as arsenic source samples. There were no significant differences in arsenic concentrations between trophic groups and between pelagic and benthic feeders. Benthic-dwelling species generally contained higher arsenic concentrations than pelagic-dwelling species. Sediments, seagrass blades and detritus contained mostly inorganic arsenic (50–90 %) and arsenoribosides (10–26 %), with some methylarsonate (9.4–14.6 %) and dimethyarsinate (7.9–9.7 %) in seagrass blades and detritus. Macroalgae contained mostly arsenoribosides (40–100 %). Epibiota and other animals contained predominately arsenobetaine (63–100 %) and varying amounts of dimethyarsinate (0–26 %), monomethyarsonate (0–14.6 %), inorganic arsenic (0–2 %), trimethylarsenic oxide (0–6.6 %), arsenocholine (0–12 %) and tetramethylarsonium ion (0–4.5 %). It was concluded that arsenic concentrations and species within the organisms of the Lake Macquarie ecosystem are species-specific and determined by a variety of factors including exposure, diet and the physiology of the organisms.

scholarly journals Total Arsenic Determination and Speciation in Infant Food Products by Ion Chromatography-Inductively Coupled Plasma-Mass Spectrometry

2004 ◽  
Vol 87 (1) ◽  
pp. 244-252 ◽  
Author(s):  
Nohora P Vela ◽  
Douglas T Heitkemper
Keyword(s):  
Inductively Coupled Plasma ◽  
Inorganic Arsenic ◽  
Dry Weight ◽  
Food Products ◽  
Arsenic Species ◽  
Arsenic Content ◽  
Infant Food ◽  
Sweet Potatoes ◽  
Green Beans ◽  
Inductively Coupled

Abstract Health risk associated with dietary arsenic intake may be different for infants and adults. Seafood is the main contributor to arsenic intake for adults while terrestrial-based food is the primary source for infants. Processed infant food products such as rice-based cereals, mixed rice/formula cereals, milk-based infant formula, applesauce and purée of peaches, pears, carrots, sweet potatoes, green beans, and squash were evaluated for total and speciated arsenic content. Arsenic concentrations found in rice-based cereals (63–320 ng/g dry weight) were similar to those reported for raw rice. Results for the analysis of powdered infant formula by inductively coupled plasma-mass spectrometry (ICP-MS) indicated a narrow and low arsenic concentration range (12 to 17 ng/g). Arsenic content in purée infant food products, including rice cereals, fruits, and vegetables, varies from <1 to 24 ng/g wet weight. Sample treatment with trifluoroacetic acid at 100°C were an efficient and mild method for extraction of arsenic species present in different food matrixes as compared to alternative methods that included sonication and accelerated solvent extraction. Extraction recoveries from 94 to 128% were obtained when the summation of species was compared to total arsenic. The ion chromatography (IC)-ICP-MS method selected for arsenic speciation allowed for the quantitative determination of inorganic arsenic [As(III) + As(V)], dimethylarsinic acid (DMA), and methylarsonic acid (MMA). Inorganic arsenic and DMA are the main species found in rice-based and mixed rice/formula cereals, although traces of MMA were also detected. Inorganic arsenic was present in freeze-dried sweet potatoes, carrots, green beans, and peaches. MMA and DMA were not detected in these samples. Arsenic species in squash, pears, and applesauce were not detected above the method detection limit [5 ng/g dry weight for As(III), MMA, and DMA and 10 ng/g dry weight for As(V)].

The degradation of arsenoribosides from Ecklonia radiata tissues decomposed in natural and microbially manipulated microcosms

2014 ◽  
Vol 11 (3) ◽  
pp. 289 ◽  
Author(s):  
Elliott G. Duncan ◽  
William A. Maher ◽  
Simon D. Foster ◽  
Frank Krikowa ◽  
Katarina M. Mikac
Keyword(s):  
Species Diversity ◽  
Degradation Products ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Microbial Composition ◽  
Ecklonia Radiata ◽  
Marine Systems ◽  
Degradation Step ◽  
Sand Sediments ◽  
Macro Algae

Environmental context Arsenoribosides are the major arsenic species in marine macro-algae, yet inorganic arsenic is the major arsenic species found in seawater. We investigated the degradation of arsenoribosides associated with Ecklonia radiata by the use of microcosms containing both natural and autoclaved seawater and sand. The decomposition and persistence of arsenic species was linked to the use of autoclaved seawater and sand, which suggests that arsenoriboside degradation is governed by the microbial composition of microenvironments within marine systems. Abstract We investigated the influence of microbial communities on the degradation of arsenoribosides from E. radiata tissues decomposing in sand and seawater-based microcosms. During the first 30 days, arsenic was released from decomposing E. radiata tissues into seawater and sand porewaters in all microcosms. In microcosms containing autoclaved seawater and autoclaved sand, arsenic was shown to persist in soluble forms at concentrations (9–18µg per microcosm) far higher than those present initially (~3µg per microcosm). Arsenoribosides were lost from decomposing E. radiata tissues in all microcosms with previously established arsenoriboside degradation products, such as thio-arsenic species, dimethylarsinoylethanol (DMAE), dimethylarsenate (DMA) and arsenate (AsV) observed in all microcosms. DMAE and DMA persisted in the seawater and sand porewaters of microcosms containing autoclaved seawater and autoclaved sand. This suggests that the degradation step from arsenoribosides → DMAE occurs on algal surfaces, whereas the step from DMAE → AsV occurs predominantly in the water-column or sand–sediments. This study also demonstrates that disruptions to microbial connectivity (defined as the ability of microbes to recolonise vacant habitats) result in alterations to arsenic cycling. Thus, the re-cycling of arsenoribosides released from marine macro-algae is driven by microbial complexity plus microbial connectivity rather than species diversity as such, as previously assumed.

Arsenic cycling in marine systems: degradation of arsenosugars to arsenate in decomposing algae, and preliminary evidence for the formation of recalcitrant arsenic

2011 ◽  
Vol 8 (1) ◽  
pp. 44 ◽  
Author(s):  
Jana Navratilova ◽  
Georg Raber ◽  
Steven J. Fisher ◽  
Kevin A. Francesconi
Keyword(s):  
Direct Contact ◽  
Marine Algae ◽  
Marine Alga ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Preliminary Evidence ◽  
Arsenic Compounds ◽  
Marine Systems ◽  
Inorganic Species ◽  
Unknown Structure

Environmental context Despite high levels of complex organoarsenic compounds in marine organisms, arsenic in seawater is present almost entirely as inorganic species. We examine the arsenic products from a marine alga allowed to decompose under simulated natural coastal conditions, and demonstrate a multi-step conversion of organic arsenicals to inorganic arsenic. The results support the hypothesis that the arsenic marine cycle begins and ends with inorganic arsenic. Abstract Time series laboratory experiments were performed to follow the degradation of arsenic compounds naturally present in marine algae. Samples of the brown alga Ecklonia radiata, which contains three major arsenosugars, were packed into 12 tubes open to air at one end only, and allowed to naturally decompose under moist conditions. During the subsequent 25 days, single tubes were removed at intervals of 1–4 days; their contents were cut into four sections (from open to closed end) and analysed for arsenic species by HPLC/ICPMS following an aqueous methanol extraction. In the sections without direct contact with air, the original arsenosugars were degraded primarily to arsenate via two major intermediates, dimethylarsinoylethanol (DMAE) and dimethylarsinate (DMA). The section with direct contact with air degraded more slowly and significant amounts of arsenosugars remained after 25 days. We also report preliminary data suggesting that the amount of non-extractable or recalcitrant arsenic (i.e. insoluble after sequential extractions with water/methanol, acetone, and hexane) increased with time. Furthermore, we show that treatment of the pellet with 0.1-M trifluoroacetic acid at 95°C solubilises a significant amount of this recalcitrant arsenic, and that the arsenic is present mainly as a cationic species of currently unknown structure.

Arsenic accumulation and speciation in freshwater fish living in arsenic-contaminated waters

2007 ◽  
Vol 4 (1) ◽  
pp. 11 ◽  
Author(s):  
Patcharin Jankong ◽  
Cherif Chalhoub ◽  
Norbert Kienzl ◽  
Walter Goessler ◽  
Kevin A. Francesconi ◽  
...  
Keyword(s):  
Freshwater Fish ◽  
Muscle Tissue ◽  
Fish Species ◽  
Reference Site ◽  
Arsenic Concentration ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Contaminated Sites ◽  
Arsenic Content ◽  
Human Populations

Environmental context. Inorganic arsenic, a well-known human carcinogen, represents a major worldwide environmental problem because contaminated water supplies have lead to widespread human exposure. This study investigates the arsenic content of freshwater fish from arsenic-contaminated and non-contaminated sites in Thailand, and reports high arsenic concentrations and significant amounts of inorganic arsenic in the edible muscle tissue. The data suggest that freshwater fish may represent a significant source of inorganic arsenic to some human populations. Abstract. Striped snakehead (Channa striata), carnivorous freshwater fish that serve as popular food in Thailand, were collected from a reference site (1.4 µg As L–1) and from two arsenic-contaminated ponds (Pond A, 550 µg As L–1; Pond B, 990 µg As L–1) in southern Thailand and analysed for arsenic by inductively coupled plasma mass spectrometry (ICPMS) and for arsenic species by HPLC-ICPMS performed on aqueous methanol extracts of muscle, liver and gill (n = 3 fish from each site). Mean total arsenic concentration in muscle tissue of C. striata collected from the reference site was 1.9 µg As g–1 (dry mass) while fish from the contaminated sites contained 13.1 µg As g–1 (Pond A) and 22.2 µg As g–1 (Pond B). Liver and gill tissues showed similar increasing arsenic concentrations on going from the reference site to Ponds A and B, with Pond B showing the highest levels. Speciation analysis on the three tissues showed that, although arsenate was the major extractable arsenical in reference fish (e.g. 0.73 µg As g–1 in muscle tissue), dimethylarsinate was by far the dominant arsenic species in fish from the two contaminated sites. Three non-carnivorous fish species (Danio regina, Rasbora heteromorpha and Puntius orphoides), collected from Pond B only, had lower arsenic concentrations (7.9–11.3 µg As g–1 in muscle tissue) than did C. striata, and contained appreciable amounts of trimethylarsine oxide together with two other major arsenicals, arsenate and dimethylarsinate, and smaller quantities of arsenite and methylarsonate. The study shows for the first time a clear effect of water arsenic concentrations on natural fish tissue arsenic concentrations, and is the first report of a freshwater fish species attaining arsenic concentrations comparable with those found in marine fish species. Furthermore, the high concentrations of toxic inorganic arsenic (predominantly arsenate) in the muscle tissue of the edible fish C. striata have human health implications and warrant wider investigations.

Arsenic distribution and species in two Zostera capricorni seagrass ecosystems, New South Wales, Australia

2011 ◽  
Vol 8 (1) ◽  
pp. 9 ◽  
Author(s):  
William A. Maher ◽  
Simon D. Foster ◽  
Anne M. Taylor ◽  
Frank Krikowa ◽  
Elliot G. Duncan ◽  
...  
Keyword(s):  
Food Web ◽  
Nitrogen Isotopes ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Trophic Levels ◽  
Marine Animals ◽  
South Wales ◽  
Arsenic Distribution ◽  
Seagrass Ecosystems ◽  
Zostera Capricorni

Environmental context Arsenic concentrations and species were determined in seagrass ecosystems where the food web was established using carbon and nitrogen isotopes. There was a clear increase in the proportion of arsenobetaine in tissues of higher trophic level organisms, which is attributed to an increasing arsenobetaine content of the diet and the more efficient assimilation and retention of arsenobetaine over other arsenic species. The results provide an explanation for the prominence of arsenobetaine in higher marine animals. Abstract Arsenic concentrations and species were compared in biota from two Zostera capricorni ecosystems. Mean arsenic concentrations were not significantly different for non‐vegetative sediment, rhizosphere sediment, Z. capricorni blades, roots, rhizomes, epiphytes, amphipods, polychaetes, molluscs, crustaceans and fish, but were significantly different in detritus. Sediments and plant tissues contained mostly inorganic arsenic and PO4–arsenoriboside. Detritus contained mostly PO4–arsenoriboside. Fish tissues contained predominately arsenobetaine. Other animals had lower proportions of arsenobetaine and variable quantities of minor arsenic species. Bioconcentration but not biomagnification of arsenic is occurring with no evidence of arsenic hyper accumulation. The proportion of arsenobetaine increases through the food web and is attributed to a shift from a mixed diet at lower trophic levels to animals containing mostly arsenobetaine at higher trophic levels and the more efficient retention of arsenobetaine, compared to other arsenic species.

Ecological factors affecting the accumulation and speciation of arsenic in twelve Australian coastal bivalve molluscs

2018 ◽  
Vol 15 (2) ◽  
pp. 46 ◽  
Author(s):  
William Maher ◽  
Joel Waring ◽  
Frank Krikowa ◽  
Elliott Duncan ◽  
Simon Foster
Keyword(s):  
Food Webs ◽  
De Novo ◽  
Ecological Factors ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Dry Mass ◽  
Water Soluble ◽  
Trophic Levels ◽  
Bivalve Molluscs ◽  
Deposit Feeders

Environmental contextKnowledge of the pathways by which arsenic is accumulated and transferred in marine ecosystems is scarce. Molluscs are important keystone organisms providing a link between primary producers (micro and macroalgae) and higher trophic levels such as fish. The present study examines the accumulation and species of arsenic in common bivalve molluscs from south-east Australia to understand the cycling of arsenic in marine food webs. AbstractThe present paper reports the whole-tissue total arsenic concentrations and water-soluble arsenic species in 12 common coastal Australian bivalve mollusc species. Mean arsenic concentrations ranged from 18 to 57 µg g−1 dry mass. Planktivores had significantly less arsenic (20–40 µg g−1; 22 ± 3 µg g−1) than did suspension and deposit feeders (36–57 µg g−1; 43 ± 7 µg g−1), with those associated with fine clay–silt sediments (49 ± 7 µg g−1) having significantly more arsenic than those associated with sand substrates (31 ± 11 µg g−1 ). Most planktivores and suspension feeders had similar arsenic species, with high proportions of arsenobetaine (AB) (64–92 %) and relatively low proportions of other arsenic species (0.55–15.8 %). Lower proportions of AB (13–57 %) and larger proportions of inorganic arsenic (6–7 %) were found in deposit feeders, reflecting increased exposure to inorganic arsenic in sediments. The study indicated that at lower trophic levels, organisms feed on algae and suspended matter containing a range of arsenic species including arsenosugars and AB. The implications for arsenic cycling are that as all bivalve molluscs accumulate AB and are a source of AB in benthic food webs. Because all bivalve molluscs also contained appreciable concentrations of arsenoriboses, precursors are present for the de novo synthesis of AB. As well, deposit feeders have higher proportions of inorganic arsenic that can be metabolised to different end products when ingested by higher trophic organisms

Arsenic metabolism in cyanobacteria

2016 ◽  
Vol 13 (4) ◽  
pp. 577 ◽  
Author(s):  
Shin-ichi Miyashita ◽  
Chisato Murota ◽  
Keisuke Kondo ◽  
Shoko Fujiwara ◽  
Mikio Tsuzuki
Keyword(s):  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Dimethylarsinic Acid ◽  
Arsenic Compound ◽  
Arsenic Compounds ◽  
Arsenic Metabolism ◽  
Methylarsonic Acid ◽  
Membrane Bound ◽  
Arsenic Transport ◽  
High Concentrations

Environmental context Cyanobacteria are ecologically important, photosynthetic organisms that are widely distributed throughout the environment. They play a central role in arsenic transformations in terms of both mineralisation and formation of organoarsenic species as the primary producers in aquatic ecosystems. In this review, arsenic resistance, transport and biotransformation in cyanobacteria are reviewed and compared with those in other organisms. Abstract Arsenic is a toxic element that is widely distributed in the lithosphere, hydrosphere and biosphere. Some species of cyanobacteria can grow in high concentrations of arsenate (pentavalent inorganic arsenic compound) (100mM) and in low-millimolar concentrations of arsenite (trivalent inorganic arsenic compound). Arsenate, which is a molecular analogue of phosphate, is taken up by cells through phosphate transporters, and inhibits oxidative phosphorylation and photophosphorylation. Arsenite, which enters the cell through a concentration gradient, shows higher toxicity than arsenate by binding to sulfhydryl groups and impairing the functions of many proteins. Detoxification mechanisms for arsenic in cyanobacterial cells include efflux of intracellular inorganic arsenic compounds, and biosynthesis of methylarsonic acid and dimethylarsinic acid through methylation of intracellular inorganic arsenic compounds. In some cyanobacteria, ars genes coding for an arsenate reductase (arsC), a membrane-bound protein involved in arsenic efflux (arsB) and an arsenite S-adenosylmethionine methyltransferase (arsM) have been found. Furthermore, cyanobacteria can produce more complex arsenic species such as arsenosugars. In this review, arsenic metabolism in cyanobacteria is reviewed, compared with that in other organisms. Knowledge gaps remain regarding both arsenic transport (e.g. uptake of methylated arsenicals and excretion of arsenate) and biotransformation (especially production of lipid-soluble arsenicals). Further studies in these areas are required, not only for a better understanding of the role of cyanobacteria in the circulation of arsenic in aquatic environments, but also for their application to arsenic bioremediation.

scholarly journals Variability in nitrogen-derived trophic levels of Arctic marine biota

Polar Biology ◽  
2020 ◽  
Author(s):  
Renske P. J. Hoondert ◽  
Nico W. van den Brink ◽  
Martine J. van den Heuvel-Greve ◽  
Ad M. J. Ragas ◽  
A. Jan Hendriks
Keyword(s):  
Stable Isotopes ◽  
Enrichment Factors ◽  
Trophic Levels ◽  
The Arctic ◽  
Marine Biota ◽  
Arctic Ecosystems ◽  
Arctic Species ◽  
Single Region ◽  
Benthic Food ◽  
Species Specific

AbstractStable isotopes are often used to provide an indication of the trophic level (TL) of species. TLs may be derived by using food-web-specific enrichment factors in combination with a representative baseline species. It is challenging to sample stable isotopes for all species, regions and seasons in Arctic ecosystems, e.g. because of practical constraints. Species-specific TLs derived from a single region may be used as a proxy for TLs for the Arctic as a whole. However, its suitability is hampered by incomplete knowledge on the variation in TLs. We quantified variation in TLs of Arctic species by collating data on stable isotopes across the Arctic, including corresponding fractionation factors and baseline species. These were used to generate TL distributions for species in both pelagic and benthic food webs for four Arctic areas, which were then used to determine intra-sample, intra-study, intra-region and inter-region variation in TLs. Considerable variation in TLs of species between areas was observed. This is likely due to differences in parameter choice in estimating TLs (e.g. choice of baseline species) and seasonal, temporal and spatial influences. TLs between regions were higher than the variance observed within regions, studies or samples. This implies that TLs derived within one region may not be suitable as a proxy for the Arctic as a whole. The TL distributions derived in this study may be useful in bioaccumulation and climate change studies, as these provide insight in the variability of trophic levels of Arctic species.

scholarly journals The sorption of inorganic arsenic on modified sepiolite: Effect of hydrated iron(III)-oxide

2014 ◽  
Vol 79 (7) ◽  
pp. 815-828 ◽  
Author(s):  
Nikola Ilic ◽  
Slavica Lazarevic ◽  
Vladana Rajakovic-Ognjanovic ◽  
Ljubinka Rajakovic ◽  
Djordje Janackovic ◽  
...  
Keyword(s):  
Sorption Capacity ◽  
Arsenic Removal ◽  
Ph Value ◽  
Inorganic Arsenic ◽  
Arsenic Species ◽  
Deionized Water ◽  
Order Kinetic ◽  
Initial Ph ◽  
Order Kinetic Model ◽  
Pseudo Second Order

The sorption of inorganic arsenic species, As(III) and As(V), from water by sepiolite modified with hydrated iron(III) oxide was investigated at 25 ?C through batch studies. The influence of the initial pH value, the initial As concentrations, the contact time and types of water on the sorption capacity was investigated. Two types of water were used, deionized and groundwater. The maximal sorption capacity for As(III) from deionized water was observed at initial and final pH value 7.0, while the bonding of As(V) was observed to be almost pH independent for pH value in the range from 2.0 to 7.0, and the significant decrease in the sorption capacity was observed at pH values above 7.0. The sorption capacity at initial pH 7.0 was about 10 mg g?1 for As(III) and 4.2 mg g?1 for As(V) in deionized water. The capacity in groundwater was decreased by 40 % for As(III) and by 20 % for As(V). The Langmuir model and pseudo-second order kinetic model revealed good agreement with the experimental results. The results show that Fe(III)-modified sepiolite exhibits significant affinity for arsenic removal and it has a potential for the application in water purification processes.

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