Origin of the Oligocene Tuolangla porphyry-skarn Cu-W-Mo deposit in Lhasa terrane,southern Tibet

Although some porphyry-skarn deposits occur in post-collisional extensional settings,the post-collisional deposits remain poorly understood.Here the authors describe the igneous geology,and mineralization history of Tuolangla,a newly-discovered porphyry-skarn Cu-W-Mo deposit in southern Tibet that belongs to the post-collisional class.The deposit is associated with Lower Cretaceous Bima Formation.It was intruded by granodiorite porphyry intrusions at about 23.1 Ma.Field investigation indicated that mineralization is spatially and temporally associated with granodiorite porphyry.Molybdenite yielded a Re-Os weighted mean age of 23.5±0.3 Ma and is considered to represent the age of skarn mineralization at the deposit.Theδ^34S values of sulfides,concentrated in a range between 0.6‰to 3.4‰,show that the sulfur has a homogeneous source with characteristics of magmatic sulfur.The Pb isotopic compositions of sulfides indicate that ore-forming metal materials were derived from the mantle and ancient crust.The granodiorite porphyry displays high SiO2(68.78%–69.75%)and K2O(3.40%–3.56%)contents,and relatively lower Cr(2.4×10^-6–4.09×10^-6),Ni(2.79×10^-6–3.58×10^-6)contents,and positiveεHf(t)values(7.7–12.9)indicating that the mineralization porphyry was derived from the partial melting of juvenile lower crust.The Tuolangla deposit is located in the central part of Zedang terrane.This terrane was once considered an ancient terrane.This terrane is in tectonic contact with Cretaceous ophiolitic rocks to its south and Mesozoic continental margin arc volcanics and intrusions of the Gangdese batholith of the Lhasa terrane to its north.Thus,the authors proposed that the Oligocene porphyry skarn Cu-W-Mo mineralization is probably associated with the Zedang terrane.This finding may clarify why the Oligocene(about 23 Ma)deposits are found only in the Zedang area and why mineralization types of the Oligocene mineralization are considerably different from those of the Miocene(17–14 Ma)mineralization.

Geology and mineralization of the Tiegelongnan supergiant porphyry-epithermal Cu(Au, Ag) deposit(10 Mt) in western Tibet, China: A review

The Tiegelongnan Cu(Au,Ag)deposit in central Tibet contains more than 10 Mt of copper ranking 29 th in the world.It is characterized by typical porphyry-epithermal alteration and mineralization.In order to improve the understanding of porphyry-epithermal copper deposit in Tibet,new zircon U-Pb age and sulfur isotope data along with published data in the Tiegelongnan are presented to investigate the formation and preservation mechanism.Ore-related intrusive rocks in the Tiegelongnan including Early Cretaceous(about 120 Ma)granodiorite porphyry and diorite porphyry are closely related to the northward subduction of Bangongco-Nujiang ocean.Sulfur mainly comes from deep magma,and ore-forming fluid is affected by both magmatic and meteoric water.The metallogenic setting of Tiegelongnan is consistent with those of Andean porphyry copper deposits in South America.The cover of the Meiriqiecuo Formation volcanic rocks,Lhasa-Qiangtang collision and India-Eurasian collision have significance in the preservation and uplift of the deposit.The formation,preservation and discovery of Tiegelongnan play an important role in exploration of ancient porphyry-epithermal deposits in Tibet.

Risk factors and drug resistance in early-onset neonatal group B streptococcal disease

In recent years,group B streptococcus (GBS) has become an important pathogen that causes infections in many neonatal organs,including the brain, hmg,and eye (Ballard et al.,2016).A series of studies performed on GBS infections in western countries have revealed that GBS is one of the primary patho-gens implicated in perinatal infection,and GBS infections are a major cause of neonatal morbidity and mortality in the United States (Decheva et al.,2013).

Investigation of L/D-threonine substituted L-serine octamer ions by mass spectrometry and infrared photodissociation spectroscopy

Threonine-substituted serine octamer ions were generated by electrospray ionization（ESI） and investigated by mass spectrometry and infrared photodissociation（IRPD） spectroscopy. IRPD spectra of[L-Ser_7＋ L/D-Thr_1]H~＋and [L-Ser_6＋ L/D-Thr_2]H~＋were obtained in the range of 2700–3600 cm^（-1）. Chiral differentiation was achieved by comparing their IRPD spectra. The main difference located in the range of 3300–3500 cm^（-1）. And the results indicate the substitution of L-Ser by D-Thr could weaken the intermolecular H-bonds and loosen the original structures of serine octamers.