Applications of Inorganic Mass Spectrometry By John R. DeLaeter (Curtin University of Technology, Perth, Western Australia). Wiley-Interscience:  New York. 2001. xx + 474 pp. $99.95. ISBN:  0-471-34539-3.

2002 ◽  
Vol 124 (18) ◽  
pp. 5251-5252
Author(s):  
Jack M. Miller
2021 ◽  
Author(s):  
Jordan A. McDivitt ◽  
Steffen G. Hagemann ◽  
Anthony I.S. Kemp ◽  
Nicolas Thébaud ◽  
Christopher M. Fisher ◽  
...  

Abstract Different genetic and timing models for gold mineralization in the Kalgoorlie gold camp (Yilgarn craton, Western Australia) suggest either broadly synchronous, late-stage mineralization related to metamorphic fluids at ca. 2640 Ma or a punctuated mineralization history from ca. 2675 to 2640 Ma with the involvement of early magmatic-hydrothermal systems (represented by the Fimiston, Hidden Secret, and Oroya gold-telluride lodes) and late metamorphic fluids (represented by the Mt. Charlotte gold stockwork veins). The results of U-Pb and Sm-Nd geochronological studies of zircon, apatite, and titanite from pre-ore dikes and syn-ore dikes constrain the absolute timing of mineralization and provide new evidence to this timing controversy. Emplacement ages constrained by U-Pb sensitive high-resolution ion microprobe (SHRIMP) zircon data are interpreted to be similar for both the pre-ore dikes (n = 10) and syn-ore dikes (n = 7) at ca. 2675 Ma. An inferred emplacement age of ca. 2675 Ma for the syn-ore dikes is supported by a Sm-Nd isochron age from apatite (laser ablation-inductively coupled plasma-mass spectrometry; LA-ICP-MS) of 2678 ± 15 Ma and by a U-Pb titanite age (LA-ICP-MS) of 2679 ± 6 Ma. The results of chemical abrasion-isotope dilution-thermal ionization mass spectrometry U-Pb zircon analysis from the pre- and syn-ore dikes are complicated by multistage Pb loss, reverse discordance, and potential inheritance. However, the data are compatible with the emplacement of Fimiston/Hidden Secret gold mineralization at ca. 2675 Ma and suggest a younger age for Oroya mineralization at ca. 2665 Ma. These results contrast with models for orogenic gold deposits that invoke broadly synchronous, late-stage mineralization related to metamorphic fluids at ca. 2640 Ma. The bulk of the Kalgoorlie gold camp’s estimated 2,300 t Au endowment was emplaced at ca. 2675 Ma as Fimiston/Hidden Secret Au mineralization. This early Au mineralization was deformed and overprinted twice by subordinate Au mineralization at ca. 2665 (Oroya mineralization) and ca. 2640 Ma (Mt. Charlotte mineralization). Gold mineralization in the Kalgoorlie gold camp was protracted in nature from ca. 2675 to 2640 Ma and reflects the interplay of early magmatic (Fimiston, Hidden Secret, Oroya) and late metamorphic (Mt. Charlotte) hydrothermal fluid systems in the formation of hybrid intrusion-related and metamorphic orebodies.


2020 ◽  
Vol 32 (5) ◽  
pp. 722-726
Author(s):  
Elisha A. Frye ◽  
Christina Egan ◽  
Michael J. Perry ◽  
Esther E. Crouch ◽  
Kyle E. Burbank ◽  
...  

Twenty-eight lactating dairy cattle in New York State were exposed to botulism toxin; 12 died and 16 recovered but never returned to full productivity. Pieces of a raccoon carcass were found in the total mixed ration on the first day of the outbreak. Clinical signs included anorexia, decreased milk production, decreased tongue tone, profound weakness, and recumbency. Clostridium botulinum type A (BoNT/A) was detected in rumen contents from 2 deceased cows via matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). In addition, C. botulinum type C was cultured from the liver of a third cow, and C. botulinum neurotoxin-producing type C gene ( bont/C) was detected via real-time PCR. On postmortem examination, 4 cows had findings suggestive of toxic myopathy, but the cause and significance of these lesions is unknown given that botulism is typically not associated with gross or histologic lesions. This outbreak of BoNT/A in cattle in North America was diagnosed via MALDI-TOF MS, a rapid and sensitive modality for detection of botulinum preformed neurotoxin.


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