Publications by authors named "Mathew P Johansen"

Three nuclear weapons tests were conducted in the 1950s at the Montebello Islands, an Indian Ocean archipelago in NW Australia. Anthropogenic radionuclides were introduced into the surrounding waters, where little quantification of the marine environment has occurred since. Here, we assess the distribution of anthropogenic radionuclides and plutonium (Pu) atom ratios in marine sediment throughout the Montebello Islands and the Western Australian (WA) coastline.

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Radiological ingestion doses from eating seafood are regularly evaluated near coastal nuclear facilities, following accidents/events and frequently in national studies worldwide. However, a recent global review found that published seafood doses varied greatly depending on which radionuclides were selected for evaluation and that there has been a tendency to omit important radionuclides or focus on less significant ones. This indicates a need for clear guidance on which radionuclides to prioritise in such studies.

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Three nuclear weapons tests were conducted in the 1950s at the Montebello Islands, Western Australia. The detonations were of different yields and configurations (two tower tests, one ship test), and led to substantial radionuclide contamination within the surrounding terrestrial and marine ecosystems. The region possesses great ecological and recreational significance, particularly within the marine environment.

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Low-level radioactive wastes were disposed at the Little Forest Legacy Site (LFLS) near Sydney, Australia between 1960 and 1968. According to the disposal records, U contributes a significant portion of the inventory of actinide activity buried in the LFLS trenches. Although the presence of U in environmental samples from LFLS has been previously inferred from alpha-spectrometry measurements, it has been difficult to quantify because the U and U α-peaks are superimposed.

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Po has been identified as one of the main contributors to ingestion doses to humans, particularly from the consumption of seafood. The amount of Po activity concentration data for various types of seafood has increased greatly in recent times. However, to provide realistic seafood dose assessments, most Po data requires correction to account for losses that can occur before the seafood is actually consumed.

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This study evaluated how the variation in different sorption conditions of beryllium (Be) in soil-water systems (electrolytes; ionic strengths; competing, counter, and co-existing ions; concentrations of Be and soil; and temperature) affected Be's environmental behaviour. For this reason, potentially contaminated soil was collected from a legacy waste site near Sydney, Australia. The sorption-desorption plateau for Be was found at >12.

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Scale residues can accumulate on the interior surfaces of subsea petroleum pipes and may incorporate naturally occurring radioactive materials (NORM). The persistent nature of 'NORM scale' may result in a radiological dose to the organisms living on or near intact pipelines. Following a scenario of in-situ decommissioning of a subsea pipeline, marine organisms occupying the exteriors or interiors of petroleum structures may have close contact with the scale or other NORM-associated contaminated substances and suffer subsequent radiological effects.

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Predictions of radionuclide dose rates to freshwater organisms can be used to evaluate the radiological environmental impacts of releases from uranium mining and milling projects. These predictions help inform decisions on the implementation of mitigation measures. The objective of this study was to identify how dose rate modelling could be improved to reduce uncertainty in predictions to non-human biota.

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Factors influencing the desorption, distribution, and vertical migration behavior of Be in contaminated soils are not fully understood. This study examined the desorption and migration of Be in a soil profile from a legacy radioactive waste disposal site using different batch leaching [monofilled waste extraction procedure (MWEP); synthetic precipitation leaching procedure (SPLP); simulated acid rain solution (SARS); and toxicity characteristic leaching procedure] and sequential leaching [community bureau of reference (BCR)] methods for insights relevant to the application of risk-based management. The results showed that Be desorption was higher in the presence of organic than the inorganic leachate composition (MWEP < SPLP < SARS < TCLP < BCR first-step).

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Inhalation exposure and beryllium (Be) toxicity are well-known, but research on bioaccessibility from soils via different exposure pathways is limited. This study examined soils from a legacy radioactive waste disposal site using in vitro ingestion (Solubility Bioaccessibility Research Consortium [SBRC], physiologically based extraction test [PBET], in vitro gastrointestinal [IVG]), inhalation (simulated epithelial lung fluid [SELF]) and dynamic two-stage bioaccessibility (TBAc) methods, as well as 0.43 M HNO extraction.

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Data on the uptake of elements and radionuclides by flora from soils in arid environments are underrepresented in international databases, especially when comparing across seasons. This study improved the understanding on the uptake of natural uranium-series radionuclides, as well as more than 30 elements, in a range of Australian native flora species that are internationally representative of an arid/semi-arid zone (e.g.

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This study examined the influence of soil physicochemical properties on the sorption, desorption and kinetics of beryllium (Be) uptake and release on soils from a legacy waste site in Australia. This information is needed to help explain the current distribution of Be at the site and evaluate potential future environmental risks. Sorption was determined by a batch study and key soil properties were assessed to explain Be retention.

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Crab has been designated by the ICRP as one of twelve reference/model organisms for understanding the impacts of radionuclide releases on the biosphere. However, radionuclide-crab interaction data are sparse compared with other reference organisms (e.g.

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Plutonium (Pu) has been released in Japan by two very different types of nuclear events - the 2011 Fukushima accident and the 1945 detonation of a Pu-core weapon at Nagasaki. Here we report on the use of Accelerator Mass Spectrometry (AMS) methods to distinguish the FDNPP-accident and Nagasaki-detonation Pu from worldwide fallout in soils and biota. The FDNPP-Pu was distinct in local environmental samples through the use of highly sensitive Pu/Pu atom ratios.

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Radionuclides from 1950s weapons testing at the Montebello Islands, Western Australia, may impact sea turtle embryos incubating within eggs laid in contaminated sands or be taken up into adult body tissues where they can contribute to radiation dose over a turtles' 60+ year lifespan. We measured plutonium in all local samples including turtle skin, bones, hatchlings, eggshells, sea sediments, diet items and beach sands. The amount of Pu in developing embryos/hatchling samples was orders of magnitude lower than that in the surrounding sands.

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This paper examines the distributions of several anthropogenic radionuclides (Pu, Am, Cs, Sr, Co and H) at a legacy trench disposal site in eastern Australia. We compare the results to previously published data for Pu and tritium at the site. Plutonium has previously been shown to reach the surface by a bath-tubbing mechanism, following filling of the former trenches with water during intense rainfall events.

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The adsorption of metals and other elements onto environmental plastics has been previously quantified and is known to be enhanced by surface-weathering and development of biofilms. However, further biofilm-adsorption characterisation is needed with respect to the fate of radionuclides. This study uses spectroscopy, microscopy and radiotracer methods to investigate the adsorption capacity of relatively strong and weak cations onto different microplastic sample types that were conditioned in freshwater, estuarine and marine conditions although marine data were limited.

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Concentration ratios (CRs), expressed by dividing Cs activity in seawater by that in marine biota (mainly fish), were obtained from the monitoring of Cs in coastal areas around Japan between 1984 and 2016. Before the TEPCO Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident (1984-2010), mean CRs of Cs, mainly from global fallout (i.e.

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The dispersion of radionuclides in dust and inhalation dose rates to the public from the planned remediation of the Ranger uranium mine in the wet-dry tropics of Australia was modelled using RESRAD-OFFSITE. Dust inhalation dose rates were predicted to be highest on the remediated site and decrease with an approximate inverse square to inverse cubic dependence with distance from the site. The annual dose above natural background to a hypothetical individual permanently occupying the remediated site (representing the worst case scenario for radionuclide in dust exposure) was estimated to be 5.

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The dispersion of Rn from the planned remediation of the Ranger U mine in the wet-dry tropics of Northern Australia was modelled. Dry and wet season contour maps of Rn dose normalised to Ra activity concentration in the proposed waste rock substrate on the remediated landform were developed. Three example exposure scenarios were assessed based on an anticipated waste rock Ra activity concentration of 800 Bq kg.

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The adsorption of radiocesium and radiostrontium onto a range of natural materials has been well quantified, but not for the new media of environmental plastics, which may have enhanced adsorption due to surface-weathering and development of biofilms. Microplastic samples were deployed in freshwater, estuarine and marine conditions, then characterised using infrared spectroscopy to document changes to the plastic surface (vs interior). Synchrotron elemental mapping data revealed surfaces that were well-covered by accumulation of reactive water solutes and sulphur, but, in contrast, had highly discrete coverage of elements such as Fe and Ti, indicating adhered mineral/clay-associated agglomerates that may increase overall adsorption capacity.

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Article Synopsis
  • A variety of nuclear activities, including weapon tests and reactor accidents, have released radioactive particles like uranium and plutonium into the environment.
  • The properties of these particles, such as their elemental make-up and size, greatly depend on the source and manner of release, which can influence how they interact with ecosystems.
  • Integrating radioactive particles into environmental assessments presents challenges, including linking particle characteristics to their sources and understanding their effects on biological systems and the environment.
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At many legacy radioactive waste sites, organic compounds have been co-disposed, which may be a factor in mobilisation of radionuclides at these sites. Tri-butyl phosphate (TBP) is a component of waste streams from the nuclear fuel cycle, where it has been used in separating actinides during processing of nuclear fuels. Analyses of ground waters from the Little Forest Legacy Site (LFLS) in eastern Australia were undertaken using solid-phase extraction (SPE) followed by gas chromatographic mass spectrometry (GCMS).

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