Acidic drainage drives anomalous rare earth element signatures in intertidal mangrove sediments
- 1. Southern Cross GeoScience, Southern Cross University, Lismore, NSW 2480 (Australia)
- 2. School of Earth, Atmosphere & Environment, Monash University, Clayton, VIC 3800 (Australia)
Description
Sedimentary rare earth element (REE) signatures can provide powerful insights into nearshore biogeochemical processes and anthropogenic influences. Despite this, there is limited research investigating REE behaviour in sediments influenced by coastal acid sulfate soils (CASS). Here, we explore REE abundance and fractionation in intertidal mangrove sediments that received CASS drainage for ~ 15–20 y within the Hastings Catchment in NSW, Australia. Sediments close to the CASS discharge point (< 200 m) were compared with those further downstream (1300–1600 m), and at a nearby control site. Average ΣREE concentrations were highest near the CASS discharge point (148–186 mg/kg), and decreased with distance downstream (111–146 mg/kg) and in control sediments (70 mg/kg). Reactive Fe concentrations (defined by 1 M HCl extractability) were also significantly higher in surface sediments (0–6 cm) near the CASS discharge point. Middle-REE (MREE) enrichments dominated fractionation patterns at all sites (> 1.5), with a high proportion (63–100%) of REEs residing in the reactive (1 M HCl extractable) sediment fraction. Interestingly, the degree of MREE enrichment was significantly correlated with Ce anomalies (r2 = 0.72, P < 0.001) and the heavy-REE (HREE) to light-REE (LREE) ratios (HREE/LREE, r2 = 0.74, P < 0.001) in the reactive sediment fraction, only in those sites situated closest to the CASS drainage. The observed high MREE enrichments, positive Ce anomalies (> 1) and HREE/LREE ratios (> 1) are consistent with reactive Fe(III) oxides/oxyhydroxides driving REE retention in these sediments. This study indicates that CASS drainage alters REE signatures in receiving sediments by (1) providing a source of REEs, thereby enhancing sedimentary REE concentrations, and (2) causing accumulation of reactive Fe(III) phases with a high affinity for REEs. Together, these two factors drive the development of distinctive REE signatures in CASS-impacted sediments. The recognition of such signatures may provide a promising tool for identifying coastal sediments receiving anthropogenic CASS drainage inputs. - Highlights: • REE examined in intertidal sediments exposed to long-term (~ 20 y) acidic drainage • Acidic drainage drives REE enrichment in reactive sediment fraction. • Distinctive REE fractionation observed in sediments closest to acidic source • REE signature reflects sediments rich in reactive Fe(III) due to acidic influence. • Site uninfluenced by CASS has REE fractionation typical of coastal sediments.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.scitotenv.2016.08.172Additional details
Identifiers
- DOI
- 10.1016/j.scitotenv.2016.08.172;
- PII
- S0048-9697(16)31874-5;
Publishing Information
- Journal Title
- Science of the Total Environment
- Journal Volume
- 573
- Journal Page Range
- p. 831-840
- ISSN
- 0048-9697
- CODEN
- STENDL
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49065589
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ACID SOILS; ACID SULFATES; AUSTRALIA; CALCIUM SULFIDES; COMPARATIVE EVALUATIONS; DRAINAGE; ENRICHMENT; FRACTIONATION; HYDROCHLORIC ACID; MANGROVES; OXIDES; PETROLEUM; RARE EARTHS; SEDIMENTS
- Descriptors DEC
- ALKALINE EARTH METAL COMPOUNDS; AUSTRALASIA; CALCIUM COMPOUNDS; CHALCOGENIDES; CHLORINE COMPOUNDS; DEVELOPED COUNTRIES; ELEMENTS; ENERGY SOURCES; EVALUATION; FOSSIL FUELS; FUELS; HALOGEN COMPOUNDS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; MAGNOLIOPHYTA; MAGNOLIOPSIDA; METALS; OXYGEN COMPOUNDS; PLANTS; SEPARATION PROCESSES; SOILS; SULFATES; SULFIDES; SULFUR COMPOUNDS; TREES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.