Published whole tissue arsenic concentrations in polychaete species tissues range from 1.5-2739 µg arsenic/g dry mass. Higher mean total arsenic concentrations are found in deposit-feeding polychaetes relative to non-deposit-feeding polychaete species collected from the same locations. However, mean arsenic concentrations at some of the locations are skewed by the high arsenic concentrations of Tharyx marioni. There appears to be no direct correlation between sediment arsenic concentrations and polychaete arsenic concentrations. Arsenic bioaccumulation by polychaetes appears to be more controlled by the physiology of the polychaetes rather than exposure to arsenic via ingested material or the prevailing physiochemical conditions. Arsenic concentrations in polychaete tissues can vary greatly.Most polychaete species contain the majority of their arsenic as arsenobetaine (57-98%), with trace concentrations of inorganic arsenic (<1%) and other simple methylated species (<7.5%). However, this is not always the case, with unusually high proportions of arsenite (57%), arsenate (23%) and dimethylarsinic acid (83-87%) in some polychaete species. Arsenobetaine is probably accumulated by polychaetes via organic food sources within the sediment. The presence of relatively high proportions of phosphate arsenoriboside (up to 12%) in some opportunistic omnivorous Nereididae polychaete species may be due to ingestion of macroalgae, benthic diatoms and/or phytoplankton.Consideration of the ecology of individual polychaete species in terms of their habitat type, food preferences, physiology and exposure to arsenic species is needed for the assessment of arsenic uptake pathways and bioaccumulation of arsenic. Future research should collect a range of polychaete species from a wide variety of uncontaminated marine habitats to determine the influence of these ecological factors on total arsenic concentrations and species proportions.
Environmental Context. In well-oxygenated water and sediments, nearly all arsenic is present as arsenate (AsO43−). As arsenate is a phosphate (PO43−) analogue, organisms living in arsenate-rich environments must acquire the nutrient phosphorus yet avoid arsenic toxicity. Organisms take in and transform arsenic compounds by many means. Three major modes of arsenic biotransformation have been found to occur in the environment—redox transformation between arsenate and arsenite (AsO2−), the reduction and methylation of arsenic, and the biosynthesis of organoarsenic compounds such as arsenobetaine. These biotransformations lead to biogeochemical cycling of arsenic compounds and bioconcentration of arsenic in aquatic organisms and thence into the food web. Abstract. The paper reports the whole-tissue total arsenic concentrations and water-soluble arsenic species in eight common coastal Australian polychaete species. Laboratory experiments showed the period of depuration did not significantly alter the whole-tissue total arsenic concentrations in the two estuarine polychaete species tested. Significant differences were found between the whole-tissue total arsenic concentrations of the eight polychaete species (mean arsenic concentrations ranged from 18 to 101 µg g−1 dry mass). Total arsenic concentrations in polychaete species, grouped on the basis of a combination of their feeding guild and habitat type, were also significantly different with a significant interaction between these factors indicating that both factors simultaneously influence arsenic concentration in polychaetes. A large number of polychaete species contained similar arsenic species with high proportions of arsenobetaine (AB; 57–88%) and relatively low proportions of As3+, As5+, methyarsonic acid, dimethylarsinic acid, arsenocholine, trimethylarsoniopropionate, and tetramethylarsonium ion (not detected to 12%). All polychaete species contained arsenoribosides (5–30%). This study identified two Australian polychaete species with particularly unusual whole-tissue water-soluble arsenic species proportions: Australonuphis parateres contained a very high proportion of trimethylarsoniopropionate (~33%), while Notomastus estuarius had a very low proportion of arsenobetaine (9%) and high proportions of As3+ (~30%), As5+ (~8%), arsenoribosides (30%), and an unknown anionic arsenic species (~4%). Most polychaetes accumulate arsenobetaine, except deposit feeders inhabiting estuarine mud habitats. Thus most polychaetes, which are prey for higher organisms, are a source of arsenobetaine in benthic food webs. Deposit feeders inhabiting estuarine muddy substrates contain appreciable quantities of inorganic arsenic and arsenoribosides that may be metabolized to different end products in higher organisms.
Whole tissue trace metal concentrations of ten metals in eight common coastal Australian polychaete species collected from uncontaminated locations were measured. The mean concentration range for each trace metal was: Mn: 2.6-13 microg g(-1); Co: 0.8-4.6 microg g(-1); Cu: 3.4-26 microg g(-1); Zn: 47-225 microg g(-1); As: 18-101 microg g(-1); Se: 2.2-20.4 microg g(-1); Ag: 0.03-2.5 microg g(-1); Cd: 0.07-17 microg g(-1); Hg: 0.08-0.88 microg g(-1) and Pb: 0.09-3.2 microg g(-1)dry mass. Principal components analysis of trace metal signatures revealed that the habitat, i.e. exposed coast sand or rock, estuarine sand or estuarine mud substrate in which a polychaete species was found, had a significant influence on the bioaccumulation of six trace metals (Mn, Cu, Zn, Ag, Cd and Pb). However, there is no clear relationship between trace metal concentrations in substrates and polychaetes. The results of the current study contribute to a reference dataset of polychaete species-specific natural background trace metal concentrations for use in determining the extent of trace metal contamination by urban and industrial sources.
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
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.