ORCID Profile
0000-0002-8092-3520
Current Organisations
Stony Brook University
,
University of South Australia
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Publisher: Springer Science and Business Media LLC
Date: 08-01-2022
Publisher: Elsevier BV
Date: 12-2021
Publisher: Springer Science and Business Media LLC
Date: 04-03-2013
Publisher: Elsevier BV
Date: 2022
Publisher: Oxford University Press (OUP)
Date: 21-06-2018
DOI: 10.1093/JXB/ERY236
Publisher: American Chemical Society (ACS)
Date: 16-08-2017
Publisher: Public Library of Science (PLoS)
Date: 30-08-2016
Publisher: Wiley
Date: 10-06-2013
DOI: 10.1002/ETC.2246
Abstract: Nanoparticulate cerium dioxide (nano-CeO2 ), when combusted as an additive to diesel fuel, was transformed from 6 nm to 14 nm sizes into particles near 43 nm, with no obvious change in the unit cell dimensions or crystalline form. Cerium sulfate, if formed during combustion, was below detection limits. Ceria nanoparticles were agglomerated within the soot matrix, with a mean aerodynamic diameter near 100 nm. The dissolution of cerium from the dried ceria catalyst in synthetic soft water was extremely small (<0.0006% or <0.2 µg Ce/L), with particles being highly agglomerated (<450 nm). Agglomeration was reduced in the presence of humic acid. In the combusted s les, soot was dominant, and the solubility of cerium in soft water showed an almost 100-fold increase in the <1 nm fraction compared to that before combustion. It appeared that the nano-CeO2 remained agglomerated within the soot matrix and would not be present as dispersed nanoparticles in aquatic or soil environments. Despite the increased dissolution, the solubility was not sufficient for the combusted ceria to represent a risk in aquatic ecosystems. The predicted environmental concentrations were still orders of magnitude below the predicted no effects concentration of near 1 mg/L. In the soil environment, any cerium released from soot materials would interact with natural colloids, decreasing cerium concentrations in soil solutions and further minimizing the potential risk to soil organisms.
Publisher: Elsevier BV
Date: 12-2015
DOI: 10.1016/J.JHAZMAT.2015.08.012
Abstract: Silver nanoparticles (AgNPs) can enter terrestrial systems as sulfidised AgNPs (Ag2S-NPs) through the application of biosolids to soil. However, the bioavailability of Ag2S-NPs in soils is unknown. The two aims of this study were to investigate (1) the bioavailability of Ag to lettuce (Lactuca sativa) using a soil amended with biosolids containing Ag2S-NPs and (2) the effect of commonly used agricultural fertilisers/amendments on the bioavailability of Ag, AgNPs and Ag2S-NPs to lettuce. The study used realistic AgNP exposure pathways and exposure concentrations. The plant uptake of Ag from biosolids-amended soil containing Ag2S-NPs was very low for all Ag treatments (0.02%). Ammonium thiosulfate and potassium chloride fertilisation significantly increased the Ag concentrations of plant roots and shoots. The extent of the effect varied depending on the type of Ag. Ag2S-NPs, the realistic form of AgNPs in soil, had the lowest bioavailability. The potential risk of AgNPs in soils is low even in the plants that had the highest Ag concentrations (Ag(+)+thiosulfate), only 0.06% of added Ag was found in edible plant parts (shoots). Results from the study suggest that agricultural practises must be considered when carrying out risk assessments of AgNPs in terrestrial systems such practises can affect AgNP bioavailability.
Publisher: Elsevier BV
Date: 04-2021
Publisher: Elsevier BV
Date: 12-2020
Publisher: American Chemical Society (ACS)
Date: 13-07-2020
Publisher: Elsevier BV
Date: 10-2013
DOI: 10.1016/J.SCITOTENV.2013.05.089
Abstract: With industrialization and urbanization soils are increasingly exposed to engineered nanoparticles (ENP), yet knowledge regarding the transport of ENP in natural soils is lacking, a process that was examined further in the current study. Saturated columns of 11 natural soils with varying physical and chemical properties were spiked with two pore volumes of a solution containing 1.7 mg Ag L(-1) as polyvinylpyrrolidone (PVP)-coated silver nanoparticles (AgNP) (40 nm actual diameter) and eluted at a constant flow rate of 1 ml min(-1). Breakthrough of Ag was analyzed using filtration theory and a HYDRUS-1D transport model that incorporated two-site kinetic attachment-detachment. Separate kinetic batch studies suggested fast heteroaggregation between negatively charged AgNP and positively charged sites on the common soil colloids maghemite or montmorillonite. The concentration of such sites in the soil correlates positively with the oxalate-extractable aluminum concentration of the soils, a measure that correlated positively with collision efficiency. This correlation thus suggested favorable deposition of AgNP and/or enhanced straining following heteroaggregation of AgNP with mobile soils colloids. Occurrence of heteroaggregation was supported by the batch studies, enhanced size-exclusion in the soil with the highest porosity, and reversible attachment-detachment predicted from HYDRUS modeling, whereas straining and favorable deposition were suggested by irreversible attachment. Our study suggests that under similar experimental conditions, PVP-coated AgNP would rapidly interact with natural colloids in soils significantly reducing their mobility and hence potential risk from off-site transport.
Publisher: Elsevier BV
Date: 08-2023
Publisher: Informa UK Limited
Date: 26-09-2021
Publisher: CSIRO Publishing
Date: 2019
DOI: 10.1071/EN19019
Abstract: Environmental contextZinc, an essential micronutrient often applied to crops as a fertiliser, can be difficult to analyse in plants due to limitations of conventional techniques. Here, we use radiotracers and a non-destructive imaging technique to visualise how zinc applied as a nanofertiliser moves within wheat plants over time. This is an important step towards developing cost-effective fertilisers to help solve one of the world’s most widespread plant deficiencies. AbstractZinc (Zn) deficiency affects half of the world’s arable soil and one-third of the world’s human population. Application of Zn foliar fertilisers to cereal crops can be an effective way to increase grain Zn content however, commonly used formulations can scorch the leaf (e.g. soluble Zn salts) or are prohibitively expensive (e.g. chelated Zn, ZnEDTA). Zinc oxide nanoparticles (ZnO-NPs) may offer an efficient and cost-effective alternative, but little is known regarding the mechanisms of Zn uptake and translocation within the plant. Foliar-applied Zn is analytically challenging to detect, locate and quantify, as it is omnipresent. Furthermore, any single analytical technique does not have the detection limit or spatial resolution required. In this study, the uptake and mobility of foliar-applied ZnEDTA, ZnO-NPs and ZnO microparticles (ZnO-MPs) to wheat (Triticum aestivum L.) were investigated using inductively coupled plasma mass spectroscopy (ICP-MS), synchrotron-based X-ray fluorescence microscopy (XFM) and radiotracing techniques using 65Zn-labelled formulations. The three techniques were compared to highlight limitations and advantages of each. We also report, for the first time, a novel time-resolved invivo autoradiography imaging technique that can be used to visualise 65Zn in live plants treated with foliar applications of 65ZnO-NPs and MPs. The images were supplemented by gamma spectroscopy analysis for quantification. The results of this study provide important insights into the analytical challenges faced when investigating foliar-applied Zn nanofertilisers in plants. Potential solutions using nuclear techniques are also discussed, which in turn may ultimately lead to the development of more efficient foliar fertilisers.
Publisher: Wiley
Date: 05-2012
Publisher: Springer Science and Business Media LLC
Date: 13-05-2021
DOI: 10.1038/S41565-021-00914-3
Abstract: Our knowledge of uptake, toxicity and detoxification mechanisms as related to nanoparticles' (NPs') characteristics remains incomplete. Here we combine the analytical power of three advanced techniques to study the cellular binding and uptake and the intracellular transformation of silver nanoparticles (AgNPs): single-particle inductively coupled mass spectrometry, mass cytometry and synchrotron X-ray absorption spectrometry. Our results show that although intracellular and extracellularly bound AgNPs undergo major transformation depending on their primary size and surface coating, intracellular Ag in 24 h AgNP-exposed human lymphocytes exists in nanoparticulate form. Biotransformation of AgNPs is dominated by sulfidation, which can be viewed as one of the cellular detoxification pathways for Ag. These results also show that the toxicity of AgNPs is primarily driven by internalized Ag. In fact, when toxicity thresholds are expressed as the intracellular mass of Ag per cell, differences in toxicity between NPs of different coatings and sizes are minimized. The analytical approach developed here has broad applicability in different systems where the aim is to understand and quantify cell-NP interactions and biotransformation.
Publisher: Elsevier BV
Date: 11-2022
DOI: 10.1016/J.CHEMOSPHERE.2022.135820
Abstract: Pesticides are known to affect non-targeted soil microorganisms. Still, studies comparing the effect of multiple pesticides on a wide range of microbial endpoints associated with carbon cycling are scarce. Here, we employed fluorescence enzymatic assay and real-time PCR to evaluate the effect of 20 commercial pesticides, applied at their recommended dose and five times their recommended dose, on soil carbon cycling related enzymatic activities (α-1,4-glucosidase, β-1,4-glucosidase, β-d-cellobiohydrolase and β-xylosidase), and on the absolute abundance of functional genes (cbhl and chiA), in three different South Australian agricultural soils. The effects on cellulolytic and chitinolytic microorganisms, and the total microbial community composition were determined using shotgun metagenomic sequencing in selected pesticide-treated and untreated s les. The application of insecticides significantly increased the cbhl and chiA genes absolute abundance in the acidic soil. At the community level, insecticide fipronil had the greatest stimulating effect on cellulolytic and chitinolytic microorganisms, followed by fungicide metalaxyl-M and insecticide imidacloprid. A shift towards a fungal dominated microbial community was observed in metalaxyl-M treated soil. Overall, our results suggest that the application of pesticides might affect the soil carbon cycle and may disrupt the formation of soil organic matter and structure stabilisation.
Publisher: CSIRO Publishing
Date: 20-02-2023
DOI: 10.1071/EN22107
Abstract: Environmental context Nitrate (NO3−) and ammonium (NH4+) are the most important soil nitrogen forms for plant growth. However, conventional extraction techniques may introduce artefacts affecting the measurement of plant-available N concentrations following s ling and s le preparation processes. This is the first study of the DGT technique being used to measure NO3-N and NH4-N in a wide range of soils, compared with conventional KCl extraction, and examined different factors that contribute to the plant-availability of these ions in soils. The knowledge would help to optimise soil nitrogen management practices, increase economic benefits and reduce environmental impacts. Rationale The availability of soil nitrogen for plant uptake can be affected by numerous soil factors such as soil texture, moisture and organic matter content, temperature and microbial activity. Conventional extraction techniques may affect the measurement of plant-available N concentrations following s ling and s le preparation processes, including drying, sieving, homogenising, freezing and thawing. The diffusive gradients in thin-films (DGT) technique can overcome some limitations of the conventional extraction techniques and has been used to successfully estimate the plant-available fractions of nutrients, such as P, K, Zn, Cu and Mn in soils. Therefore, it is important to evaluate the use of DGT for measuring NO3− and NH4+ in a wide variety of soils and examine the factors that contribute to the plant-availability of these ions in soils. Methodology The experiment evaluated the ability of the DGT technique to measure NO3-N and NH4-N in soils using binding layers containing A520E anion exchange resin or Microlite® PrCH cation exchange resin, respectively. The DGT results were compared to those from conventional KCl extraction. Results The A520E- and PrCH-DGTs showed good detection limits for NO3-N (6.90 µg L−1) and NH4-N (6.23 µg L−1) and were able to measure potentially available NO3-N and NH4-N in unfertilised soils. The mass of NO3-N and NH4-N that accumulated on the DGT device increased linearly across soil concentrations ranging from 5 to 300 mg kg−1 NO3-N (depending on soil type) and 5–300 mg kg−1 NH4-N which is equivalent to fertiliser rates of 75–450 kg ha−1 N. DGTs were used to measure potentially available NO3-N and NH4-N in ten soils with various physical and chemical properties. The DGT results were compared with conventional KCl extraction used to determine soil mineral N. DGT and KCl extraction measured values were significantly correlated with each other for NO3-N (R2 = 0.53 P-value 0.001), but the relationship between the two measurements was weaker for NH4-N (R2 = 0.20, P-value = 0.045). Discussion The results suggest that the two methods s le different N pools in the soils, with DGT targeting the NO3-N and NH4-N that are available in soil pore water and attached to labile solid phases.
Publisher: Wiley
Date: 09-09-2020
DOI: 10.1111/PPL.13167
Publisher: Elsevier BV
Date: 02-2022
DOI: 10.1016/J.SCITOTENV.2021.150734
Abstract: The extensive application of pesticides in agriculture raises concerns about their potential negative impact on soil microorganisms, being the key drivers of nutrient cycling. Most studies have investigated the effect of a single pesticide on a nutrient cycling in single soil type. We, for the first time, investigated the effect of 20 commercial pesticides with different mode of actions, applied at their recommended dose and five times their recommended dose, on nitrogen (N) microbial cycling in three different agricultural soils from southern Australian. Functional effects were determined by measuring soil enzymatic activities of β-1,4-N-acetyliglucosaminidase (NAG) and l-leucine aminopeptidase (LAP), potential nitrification (PN), and the abundance of functional genes involved in N cycling (amoA and nifH). Effects on nitrifiers ersity were determined with licon sequencing. Overall, the pesticides effect on N microbial cycling was dose-independent and soil specific. The fungicides flutriafol and azoxystrobin, the herbicide chlorsulfuron and the insecticide fipronil induced a significant reduction in PN and β-1,4-N-acetylglucosaminidase activity (P < 0.05) (NAG) in the alkaline loam soil with low organic carbon content i.e. a soil with properties which typically favors pesticide bioavailability and therefore potential toxicity. For the nitrifier community, the greatest pesticide effects were on the most dominant Nitrososphaeraceae (ammonia-oxidizing archaea AOA) whose abundance increased significantly compared to the less dominant AOA and other nitrifiers. The inhibiting effects were more evident in the soil s les treated with fungicides. By testing multiple pesticides in a single study, our findings provide crucial information that can be used for pesticide hazard assessment.
Publisher: Wiley
Date: 07-2022
DOI: 10.1111/PPL.13761
Abstract: Foliar fertilization delivers essential nutrients directly to plant tissues, reducing excessive soil fertilizer applications that can lead to eutrophication following nutrient leaching. Foliar nutrient absorption is a dynamic process affected by leaf surface structure and composition, plant nutrient status, and ion physicochemical properties. We applied multiple methods to study the foliar absorption behaviors of manganese (Mn) and phosphorus (P) in nutrient‐deficient spring barley ( Hordeum vulgare ) at two growth stages. Nutrient‐specific chlorophyll a fluorescence assays were used to visualize leaf nutrient status, while laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) was used to visualize foliar absorption pathways for P and Mn ions. Rapid Mn absorption was facilitated by a relatively thin cuticle with a low abundance of waxes and a higher stomatal density in Mn‐deficient plants. Following absorption, Mn accumulated in epidermal cells and in the photosynthetically active mesophyll, enabling a fast (6 h) restoration of Mn‐dependent photosynthetic processes. Conversely, P‐deficient plants developed thicker cuticles and epidermal cell walls, which reduced the penetration of P across the leaf surface. Foliar‐applied P accumulated in trichomes and fiber cells above leaf veins without reaching the mesophyll and, as a consequence, no restoration of P‐dependent photosynthetic processes was observed. This study reveals new links between leaf surface morphology, foliar‐applied ion absorption pathways, and the restoration of affected physiological processes in nutrient‐deficient leaves. Understanding that ions may have different absorption pathways across the leaf surface is critical for the future development of efficient fertilization strategies for crops in nutrient‐limited soils.
Publisher: Elsevier BV
Date: 2023
Publisher: Informa UK Limited
Date: 17-11-2019
Publisher: American Chemical Society (ACS)
Date: 26-05-2021
Publisher: Springer Science and Business Media LLC
Date: 14-07-2022
Publisher: Oxford University Press (OUP)
Date: 15-06-2020
DOI: 10.1104/PP.20.00484
Publisher: American Chemical Society (ACS)
Date: 11-03-2022
Location: United States of America
Location: United States of America
No related grants have been discovered for Casey Doolette.