Future levels of climate change depend not only on carbon emissions but also on carbon uptake by the land and the ocean. Here we are using the Earth system model (ESM1) version of the Australian Community Climate and Earth System Simulator (ACCESS) to explore the potential and impact of removing carbon dioxide (CO2) from the atmosphere through the climate and carbon cycle reversibility experiment. This experiment builds on the standard Coupled Model Intercomparison Project (CMIP) experiment, increasing CO2 at 1% per year until 4xCO2 is reached. The atmospheric CO2 levels are then decreased at the same rate which brings the CO2 back to pre-industrial levels. We then continue to run the model with constant CO2 for another 350 years. Our analysis focuses on the response of the land carbon cycle. We find that carbon stores are largely reversible at the global scale over the timescale of changing CO2. However, carbon stores continue to decrease after CO2 returns to its initial value, and the land loses another 40 Pg of carbon (PgC) with the largest change in the tropics. It takes about 300 years beyond the period of changing CO2 for the carbon stores to recover. Interestingly, we saw strong regional variations in the strength of the land response to changing CO2. Australia showed the largest increase/decrease in biomass carbon (about 40%) and the largest variability in productivity, which was strongly correlated with rainfall. This highlights the importance of assessing the regional response to understanding the processes underlying the response and the sensitivity of these processes within each model. This understanding will benefit future multi-model analyses of this reversibility experiment. It also illustrates more generally the potential to use Earth system model experiments as part of the evaluation of proposed applications of carbon dioxide removal (CDR) technologies. As such, we recommend that these types of modelling experiments be included when mitigation policies are developed.
Analytical chemistry is an important tier of environmental protection and has been traditionally linked to compliance and/or exposure monitoring activities for environmental contaminants. The adoption of the risk management paradigm has led to special challenges for analytical chemistry applied to environmental risk analysis. Namely, methods developed for regulated contaminants may not be appropriate and/or applicable to risk management scenarios. This paper contains examples of analytical chemistry applied to risk management challenges broken down by the analytical approach and analyte for some selected work in our laboratory. Specific techniques discussed include stable association complex electrospray mass spectrometry (cESI-MS), gas chromatography-mass spectrometry (GC-MS), split-flow thin cell (SPLITT) fractionation and matrix-assisted laser desorption time of flight mass spectrometry (MALDI-ToF-MS). Specific analytes include haloacetic acids (HAA9), perchlorate, bromate, triazine degradation products, metal-contaminated colloids and Cryptosporidium parvum oocysts. 相似文献
The integrity of social insect colonies is maintained by members recognising and responding to the chemical cues present on the cuticle of any intruder. Nevertheless, myrmecophiles use chemical mimicry to gain access to these nests, and their mimetic signals may be acquired through biosynthesis or through contact with the hosts or their nest material. The cuticular hydrocarbon profile of the myrmecophilous salticid spider Cosmophasis bitaeniata closely resembles that of its host ant Oecophylla smaragdina. Here, we show that the chemical resemblance of the spider does not arise through physical contact with the adult ants, but instead the spider acquires the cuticular hydrocarbons by eating the ant larvae. More significantly, we show that the variation in the cuticular hydrocarbon profiles of the spider depends upon the colony of origin of the ant larvae prey, rather than the parentage of the spider. 相似文献
A measure of soil P status in agricultural soils is generally required for assisting with prediction of potential P loss from agricultural catchments and assessing risk for water quality. The objectives of this paper are twofold: (i) investigating the soil P status, distribution, and variability, both spatially and with soil depth, of two different first-order catchments; and (ii) determining variation in soil P concentration in relation to catchment topography (quantified as the "topographic index") and critical source areas (CSAs). The soil P measurements showed large spatial variability, not only between fields and land uses, but also within individual fields and in part was thought to be strongly influenced by areas where cattle tended to congregate and areas where manure was most commonly spread. Topographic index alone was not related to the distribution of soil P, and does not seem to provide an adequate indicator for CSAs in the study catchments. However, CSAs may be used in conjunction with soil P data for help in determining a more "effective" catchment soil P status. The difficulties in defining CSAs a priori, particularly for modeling and prediction purposes, however, suggest that other more "integrated" measures of catchment soil P status, such as baseflow P concentrations or streambed sediment P concentrations, might be more useful. Since observed soil P distribution is variable and is also difficult to relate to nationally available soil P data, any assessment of soil P status for determining risk of P loss is uncertain and problematic, given other catchment physicochemical characteristics and the sampling strategy employed. 相似文献
Snowmobile use in Yellowstone National Park has been shown to impact air quality, with implications for the safety and welfare
of Park staff and other Park resource values. Localized impacts have been documented at several high-use sites in the Park,
but the broader spatial variability of snowmobile emissions and air quality was not understood. Measurements of 87 volatile
organic compounds (VOCs) were made for ambient air sampled across the Park and West Yellowstone, Montana, during 2 days of
the 2002–2003 winter use season, 1 year before the implementation of a new snowmobile policy. The data were compared with
similar data from pristine West Coast sites at similar latitudes. Backward trajectories of local air masses, alkyl nitrate-parent
alkane ratios, and atmospheric soundings were used to identify the VOC sources and assess their impact. Different oversnow
vehicle types used in the Park were sampled to determine their relative influence on air mass pollutant composition. VOCs
were of local origin and demonstrated strong spatiotemporal variability that is primarily influenced by levels of snowmobile
traffic on given road segments at different times of day. High levels of snowmobile traffic in and around West Yellowstone
produced consistently high levels of benzene, toluene, and carbon monoxide. 相似文献
Previous work has shown that arsenic can accumulate in drinking water distribution system (DWDS) solids (Lytle et~al., 2004) when arsenic is present in the water. The release of arsenic back into the water through particulate transport and/or
chemical release (e.g. desorption, dissolution) could result in elevated arsenic levels at the consumers' tap. The primary
objective of this work was to examine the impact of pH and orthophosphate on the chemical release (i.e. desorption) of arsenic
from nine DWDS solids collected from utilities located in the Midwest. Arsenic release comparisons were based on the examination
of arsenic and other water quality parameters in leach water after contact with the solids over the course of 168~hours. Results
showed that arsenic was released from solids and suggested that arsenic release was a result of desorption rather than dissolution.
Arsenic release generally increased with increasing initial arsenic concentration in the solid and increasing pH levels (in
the test range of 7 to 9). Finally, orthophosphate (3 and 5 mg PO4/L) increased arsenic release at all pH values examined. Based on the study results, utilities with measurable levels of arsenic
present in their water should be aware that some water quality changes can cause arsenic release in the DWDS potentially resulting
in elevated levels at the consumer's tap. 相似文献
Environmental Science and Pollution Research - Vegetated buffer strips (VBSs) are widely encouraged as a cost-effective strategy to address phosphorus (P) pollution associated with agricultural... 相似文献
Brassica juncea, or Indian mustard, was grown in soil artificially contaminated with either a soluble salt, CdCl(2), at 186mg Cdkg(-1), or alternately an insoluble, basic salt, CdCO(3), at 90mg Cdkg(-1). These experiments study the range of Cd uptake by Indian mustard from conditions of very high Cd concentration in a soluble form to the other extreme with an insoluble Cd salt. After plants were established, four different chelating agents were applied. Chelating agents increased plant uptake of Cd from the CdCl(2) soil but did not significantly increase plant uptake of Cd from the CdCO(3) contaminated soil. Addition of ethylenediaminetetraacetic acid (EDTA) increased the plant concentration of Cd by almost 10-fold in soils contaminated with CdCl(2), with a concentration of 1283mg Cdkg(-1) in the dried EDTA-treated plants over a concentration of 131mg Cdkg(-1) in plants without added chelate. However, EDTA increased the aqueous solubility of Cd by 36 times over the soil matrix without added chelator, and thereby, increased the possibility of leaching. Other chelators used in both experiments were ethylenebis(oxyethylenenitrilo)tetraacetic acid, trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid, and diethylenetriaminepentaacetic acid (DTPA) increasing Cd in plants to 1240, 962, and 437mg Cdkg(-1), respectively. The other chelating agents increased the solubility of Cd in the leachate but not to the extent of EDTA. Comparing all chelating agents studied, DTPA increased plant uptake in terms of Cd in dried plant concentration most relative to the solubility of complexed Cd in runoff water. 相似文献
With landfill costs increasing and regulations on landfilling becoming more stringent, alternatives to conventional hazardous waste treatment strategies are becoming more desirable. Incineration Is presently a permanent, proven solution for the disposal of most organic contaminants, but also a costly one, especially in the case of solids which require some auxiliary fuel. The goal of this research is to develop an understanding of the phenomena associated with the evolution of contaminants from solids In the primary combustor of an Incineration system. A four-fold approach is being used. First, a bench-scale particle characterization reactor was developed to study the transport phenomena on a particle basis, where the controlling processes are mainly intraparticle. Second, a bed-characterization reactor was built to examine the controlling transport phenomena within a bed of particles, where the processes are primarily interparticle. The results of these studies can be applied to any primary combustor. A pilot-scale rotary kiln was developed to study the evolution of contaminants from solids within a realistic temperature and rotation environment. Finally, in situ measurements are being obtained from a full-scale rotary-kiln. This paper describes results obtained in a study using a commercial sorbent contaminated with toluene. The data are from the particle-characterization reactor and the rotary-kiln simulator. The results show that the method of contamination and charge size do not have a large effect on desorption, while temperature and contaminant concentration are important parameters In the evolution of contaminants in a rotary kiln. 相似文献