scholarly journals Isotopic Tracing of Perchlorate Sources in the Environment

2021 ◽  
Vol 2021 ◽  
pp. 1-10
Author(s):  
Mengnan Zhang ◽  
Xiaoqian Li ◽  
Xuxue Cheng ◽  
Xinfeng Wang ◽  
Mian Song ◽  
...  

Perchlorate (ClO4−) is an emerging persistent pollutant that is ubiquitous in the environment at trace concentrations. Perchlorate ingestion poses a risk to human health because it interferes with thyroidal hormone production. The identification of perchlorate sources in groundwater is a primary concern. Chlorine and multi-oxygen isotopic tracing of perchlorate (δ37Cl, 36Cl/Cl, δ18O, and Δ17O) can provide a unique tool for identifying the origin and transport of perchlorate in groundwater. Along with the kinetic fractionation of chlorine and oxygen isotopes, the Δ17O value, 36Cl/Cl ratio, and ε18O/ε37Cl (the fractionation coefficient of oxygen and chlorine isotopes) are constant, potentially indicating the biodegradation of perchlorate, without disguising its source information. Therefore, comprehensive characterization of stable chlorine and poly-oxygen isotopes is expected to provide direct evidence for identifying the source of perchlorate in groundwater. However, further studies are needed to increase the amount of isotopic data of different perchlorate sources, to make the end-member model available to broader regions. It is critically important to understand the range of values and differences of isotopes among natural perchlorate sources and the perchlorate formation mechanisms.

1993 ◽  
Vol 73 (4) ◽  
pp. 633-637 ◽  
Author(s):  
J. J. Miller ◽  
G. J. Beke ◽  
S. Pawluk ◽  
H. R. Krouse

Possible sources of SO4 in soil, drift and bedrock at two saline sites in southern Alberta were investigated using sulfur and oxygen isotope analyses. Slight differences (0.6–5.2 per mil) between δ34S values of SO4 and insoluble S in the geologic material were attributed to kinetic fractionation during oxidation of organic S. Negative δ18O values of SO4 in the shallow (<6 m) bedrock, drift and soil reflected oxidation of reduced S. In contrast, positive δ18O values in the deep (>6 m) bedrock indicated sulfate reduction. The exact source of SO4 could not be determined in this preliminary study. The isotope approach, however, shows promise and warrants more detailed study. Key words: Salinization, sulfates, sulfur isotopes, oxygen isotopes


1998 ◽  
Vol 29 (1) ◽  
pp. 1-20 ◽  
Author(s):  
Peter Raben ◽  
Wilfred H. Theakstone

Marked vertical variations of ions and oxygen isotopes were present in the snowpack at the glacier Austre Okstindbreen during the pre-melting phase in 1995 at sites between 825 m and 1,470 m above sea level. As the first meltwater percolated from the top of the pack, ions were moved to a greater depth, but the isotopic composition remained relatively unchanged. Ions continued to move downwards through the pack during the melting phase, even when there was little surface melting and no addition of liquid precipitation. The at-a-depth correlation between ionic concentrations and isotopic ratios, strong in the pre-melting phase, weakened during melting. In August, concentrations of Na+ and Mg2+ ions in the residual pack were low and vertical variations were slight; 18O enrichment had occurred. The difference of the time at which melting of the snowpack starts at different altitudes influences the input of ions and isotopes to the underlying glacier.


2012 ◽  
Vol 18 ◽  
pp. 167-194 ◽  
Author(s):  
Benjamin H. Passey

Carbon isotopes in Neogene-age fossil teeth and paleosol carbonates are commonly interpreted in the context of past distributions of C3 and C4 vegetation. These two plant types have very different distributions in relation to climate and ecology, and provide a robust basis for reconstructing terrestrial paleoclimates and paleoenvironments during the Neogene. Carbon isotopes in pre-Neogene fossil teeth are usually interpreted in the context of changes in the δ13C value of atmospheric CO2, and variable climate-dependent carbon-isotope discrimination in C3 plants. Carbon isotopes in pre-Neogene soil carbonates can be used to estimate past levels of atmospheric CO2. Oxygen isotopes in fossil teeth and paleosol carbonates primarily are influenced by the oxygen isotopic compositions of ancient rainfall and surface waters. The oxygen isotopic composition of rainfall is has a complex, but tractable, relationship with climate, and variably relates to temperature, elevation, precipitation amount, and other factors. Mammal species that rely on moisture in dietary plant tissues to satisfy their water requirements (rather than surface drinking water) may have oxygen isotopic compositions that track aridity. Thus, oxygen isotopes of fossil mammals can place broad constraints on paleoaridity. Carbonate clumped isotope thermometry allows for reconstruction of soil temperatures at the time of pedogenic carbonate mineralization. The method is unique because it is the only thermodynamically based isotopic paleothermometer that does not require assumptions about the isotopic composition of the fluid in which the archive mineral formed. Soil temperature reflects a complex interplay of air temperature, solar radiative heating, latent heat effects, soil thermal diffusivity, and seasonal variations of these parameters. Because plants and most animals live in and/or near the soil, soil temperature is an important aspect of terrestrial (paleo)climate.


2019 ◽  
Author(s):  
Jingyuan Shao ◽  
Qianjie Chen ◽  
Yuxuan Wang ◽  
Xiao Lu ◽  
Pengzhen He ◽  
...  

Abstract. Air quality models have not been able to reproduce the magnitude of the observed concentrations of fine particulate matter (PM2.5) during wintertime Chinese haze events. The discrepancy has been at least partly attributed to low biases in modeled sulfate production rates due to the lack of heterogeneous sulfate production on aerosols in the models. In this study, we explicitly implement four heterogeneous sulfate formation mechanisms into a regional chemical transport model, in addition to gas-phase and in-cloud sulfate production. We compare the model results with observations of sulfate concentrations and oxygen isotopes (Δ17O(SO42−)) in the winter of 2014–2015, the latter of which is highly sensitive to the relative importance of different sulfate production mechanisms. Model results suggest that heterogeneous sulfate production on aerosols accounts for about 20 % of sulfate production in clean and polluted conditions, partially reducing the modeled low bias in sulfate concentrations. Model sensitivity studies in comparison with the Δ17O(SO42−) observations suggest that heterogeneous sulfate formation is dominated by transition metal ion catalyzed oxidation of SO2.


2020 ◽  
Vol 280 ◽  
pp. 395-422 ◽  
Author(s):  
Ziv Sade ◽  
Ruth Yam ◽  
Aldo Shemesh ◽  
Itay Halevy

2020 ◽  
Author(s):  
Richard Zeebe ◽  
Lauren Yumol ◽  
Joji Uchikawa

&lt;p&gt;A widespread phenomenon in biogenic and inorganic carbonates that are formed out of isotopic equilibrium is a nearly ubiquitous co-variation (slope) of carbon vs. oxygen isotopes, in e.g., speleothem and cryogenic carbonates, shells and skeletons of foraminifera, corals etc. For proxy calibrations, it is critical to understand such isotope variations (often labeled kinetic or vital effects) in proxies widely used for paleo-reconstructions. Given that this phenomenon is observed in inorganic carbonates and biogenic carbonates across different phyla suggest a common underlying mechanism, possibly independent of biological controls, that is, likely of inorganic origin. Here we present results from laboratory experiments on synthetic carbonate precipitation to constrain the kinetic isotope fractionation factor (KFF) of carbon and oxygen during CO2 hydration. We used an experimental setup similar to that of an earlier study but with important modifications and tight temperature and pH control. The average d13C and d18O values of our carbonate samples (BaCO3) produced at 25 deg C and pH = 8.0 (NBS) are -29.7 +- 0.71 per mil (VPDB) and 18.8 +- 0.56 per mil (VSMOW), respectively. From the isotope data, we calculate our experimental 13KFF and 18KFF, which refer to the 13C/12C and 18O/16O fractionation between CO2(g) and BaCO3, where the d13C and d18O values of CO2(g) were calculated using known equilibrium fractionation factors. Our results show that our KFFs are the largest values compared to previously reported experimental KFFs (except for one study), suggesting that our values are closest to the full isotopic disequilibrium during CO2 hydration. Based on our KFFs, we will present the expected slope of carbon vs. oxygen isotopic disequilibrium from kinetic effects during CO2 hydration. We will also discuss the expected slope from equilibrium effects of solution pH on oxygen isotopes. Comparison with field and culture data will reveal the origin of the slope of carbon vs. oxygen isotopic disequilibrium in biogenic and inorganic carbonates.&lt;/p&gt;


2018 ◽  
Vol 40 (2) ◽  
pp. 165-177 ◽  
Author(s):  
Pham Van Long ◽  
Gaston Giuliani ◽  
Anthony E. Fallick ◽  
Andrian J. Boyce ◽  
Vincent Pardieu

Trace elements investigated by electron microprobe analysis (EMPA) have been combined with oxygen isotopic composition of pink, red and other colored spinels (blue, purple, brown, orange, lavender) hosted by marbles and found in placers from Luc Yen and An Phu deposits, Yen Bai province, North Vietnam. The deposits are those from Nuoc Ngap, Cong Troi, Bai Son and different placers from the An Phu area. Trace elements such as Fe-Zn-Cr-V in red and pink gem spinels permit to separate those from Cong Troi and those from the others deposits of the An Phu area. Spinels from Cong Troi have low to extremely low Zn (< 500 ppm) and high Fe contents (3,000 to 16,000 ppm) while those from An Phu area are Zn-rich (up to 11,000 ppm). Iron is the dominant element for the other colored spinels whereas Zn, Cr and V contents are extremely variable. The Bai Son blue spinel is Fe-rich (5,000 to 7,200 ppm) with some V (950 to 1,830 ppm), Cr (270 to 480 ppm), Co (240 to 400 ppm) and Ni (550 to 950 ppm). The O-isotope composition of the whole spinels ranges between 12.1 and 24.2‰ (n = 25). Within each deposit, the range of δ18O values for red, pink and colored spinels is usually similar. However, the red and pink spinels from An Phu present two distinct sets of δ18O values, respectively between  13.2 to 17.0‰  (n = 7) and 22.5< δ18O < 24.2 (n = 5). Those from Cong Troi are from 14.8 to 17.7‰ (n = 3) and their range overlaps that of An Phu. The use of O-isotopes is not useful for distinguishing between the deposits, but the low to extremely low Zn content of the Cong Trois spinels is a discriminant. The variation of δ18O values (12.1 <δ18O < 24.2‰) of the whole spinels indicates that the oxygen isotopic compositions of the metamorphic fluids were probably buffered by the local δ18O values of the impure host marbles.ReferencesChauviré B., Rondeau B., Fritsch E., Ressigeac Ph., Devidal J.-L., 2015. Blue spinel from the Luc Yen district of Vietnam. Gems & Gemology, 51, 2-17.D'Ippolito V., Andreozzi G.B., Hålenius H., Skogby H., Hametner K., Günther D., 2015. Colour mechanisms in spinel: cobalt and iron interplay for the blue colour. Physics and Chemistry of Minerals, 42, 431-439.Garnier V., 2003. Les gisements de rubis associés aux marbres de l’Asie Centrale et du Sud-est: genèse et caractérisation isotopique. PhD thesis INPL, Nancy, France, 373p.Garnier, V., Ohnenstetter, D., Giuliani, G., Maluski, H., Deloule, E., Phan Trong Trinh, Pham Van Long, Hoang Quang Vinh, 2005. Age and significance of ruby-bearing marbles from the Red River shear zone, northern Vietnam. The Canadian Mineralogist, 43, 1315-1329.Garnier V., Giuliani G., Ohnenstetter D., Fallick A.E., Dubessy J., Banks D., Hoang Quang Vinh, Lhomme Th., Maluski H., Pêcher A., Bakhsh K.A., Pham Van Long, Phan Trong Trinh, Schwarz D., 2008. Marble-hosted ruby deposits from central and Southeast Asia: towards a new genetic model. Ore Geology Reviews, 34, 169-191.Giuliani G., Fallick A.E., Garnier V., France-Lanord Ch., Ohnenstetter D., Schwarz D., 2005. Oxygen isotope composition as a tracer for the origins of rubies and sapphires. Geology, 33(4), 249-252.Giuliani G., Fallick A.E., Boyce A.J., Pardieu V., Pham Van Long, 2017. Pink and red spinels in marble: trace elements, oxygen isotopes, and sources. The Canadian Mineralogist, 55, 743-761.Hauzenberger C.A., Häeger T., Baumgartner L.P., Hofmeister W., 2001. High-grade metamorphism and stable isotope geochemistry of N-Vietnamese gem-bearing rocks. In: Proceedings of the Workshop on gems and minerals of Vietnam, Hanoi, 124-138.Hauzenberger C.A., Bagola C., Häeger T., Muellen C., Nguyen Ngoc Khoi, Le Thi Thu Huong, 2014. Mineralogy and petrology of the An Phu marble hosted spinel and corundum deposit, Luc Yen, N-Vietnam. In Proceedings of the 4th International Gem and Jewelry Conference, Chiang Mai, Thailand, 76-78.Kleišmantas A., Daukšyte A., 2016. The influence of Vietnam and Sri Lanka spinel mineral chemical elements on colour. Chemija, 27, 45-51.Kretz R., 1983. Symbols for rock-forming minerals. American Mineralogist, 68, 277-279.Le Thi Thu Huong, Häeger T., Hofmeister W., Hauzenberger C., Schwarz D., Pham Van Long, Wehmeister U., Nguyen Ngoc Khoi, Nguy Tuyet Nhung, 2012. Gemstones from Vietnam: An update. Gems & Gemology, 48, 158-176.Malsy A., Klemm L., 2010. Distinction of gem spinels from the Himalayan mountain belt. Chimia, 64(10), 741-746.Malsy A., Karampelas S., Schwarz D., Klemm L., Armbruster T., Tuan Do Anh, 2012. Orangey-red to orangey-pink gem spinels from a new deposit at Lang Chap (Tan Huong - Truc Lau), Vietnam. The Journal of Gemmology, 33, 19-27.Pham Van Long, Hoang Quang Vinh, Garnier V., Giuliani G., Ohnenstetter D., Lhomme,T., Schwarz D., Fallick A.E., Dubessy J., Phan Trong Trinh, 2004. Gem corundum deposits in Vietnam. Journal of Gemmology, 29, 129-147.Pham Van Long, Pardieu V., Giuliani G., Nguy Tuyet Nhung, Pham Thi Thanh Hien, Pham Duc Anh, Nguyen Ngoc Khoi, Hoang Quang Vinh, 2014. Gemmological characteristics of spinel from Luc Yen, Yen Bai. Journal of Geology, 340, 29-36.Pham Van Long, Pardieu V., Giuliani G., 2014. Update on gemstone mining in Luc Yen, Vietnam. Gems & Gemology, 49, 233-245.Pouchou J.L., Pichoir F., 1991. Quantitative analysis of homogeneous or stratified microvolumes applying "PAP" In Electron Probe Quantification (K.F.J. Heinrich & D.E. Newbury eds.). Plenum Press, New York, USA, 31-75.Valley J.W., 1986. Stable isotope geochemistry of metamorphic rocks. Reviews in Mineralogy, 16, 445-481.Yui T.F., Khin Zaw, Wu C.-M., 2008. A preliminary stable isotope study on Mogok ruby, Myanmar. Ore Geology Reviews, 34, 182-199.


2005 ◽  
Vol 52 (3) ◽  
pp. 229-237 ◽  
Author(s):  
J. De Bénédittis ◽  
J.-L. Bertrand-Krajewski

The paper presents the principle of a method to measure infiltration rates in sewer systems based on the use of oxygen isotopes and its application in Lyon (France). In the urban area of Lyon, significant differences in δ18O that can reach 3‰ are observed between the oxygen isotopic compositions of groundwater originating from Rhone, Saone and from their associated alluvial aquifers. Drinking water supplying Lyon results mainly from pumping in the Rhone alluvial aquifer. Therefore, in some areas, the difference of isotopic composition between wastewater resulting from the consumption of drinking water and local groundwater can be used to measure infiltration in sewer systems. The application in the catchment of Ecully shows that the infiltration flow rate presents strong fluctuations at an hourly scale: it varies between 15 and 40 m3/h. This variability could be explained by non-constant discharges of pumping and by variations of the water level in the sewer.


2018 ◽  
Vol 3 (2) ◽  
pp. 233-239 ◽  
Author(s):  
Hagar Lis ◽  
Tal Weiner ◽  
Frances D. Pitt ◽  
Nir Keren ◽  
Alon Angert

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