Iron is prone to change its form and speciation in phases. Thus, several methods have been developed to estimate iron partitioning in the mineral phases of soils. However, the accuracy of these methods to evaluate the iron contribution from minor phases, such as actinolite, almandine, biotite, chlorite, epidote, hornblende, muscovite, and Fe-diospide, remains low. Furthermore, most of the current iron speciation research is focused on bulk samples, and only applies to soil samples that are mostly composed of clays or clay minerals, without a wide-ranging evaluation of soil particles with different grain sizes. In this study, we classified several iron phases using a mineral liberation analyzer on desert soil particles with diameters ranging from silt- to fine-sand (5–20 µm, 20–45 µm, 45–63 µm, 63–75 µm, and > 75 µm). The iron containing minor phases were identified, the modal mineral abundances were determined via matching with the standard energy dispersive spectra library, and a particle size analysis was performed using mineral processing tools on each of the examined 40,000 particles. The iron partition results were ultimately established based on the standard iron concentration in the mineral phases and the modal mineral abundances. This new method could be automated, thereby facilitating high efficiency identification of iron-containing phases that would allow, for the first time, the generation of a dataset for iron partitioning in soil particles. This method allows the identification of minor iron phases in soil particles, and permits in situ mapping of iron mineralogy in fine sand- to silt-sized soil particles. Not restricted by single mineral particles, this method considers multi-phase complex particles. Thus, it largely improves the accuracy for estimating the iron partition parameter.
The sources of the sediments in distinct areas of the Chinese Loess Plateau (CLP) are still disputed, starting with the particle formation in the original desert areas, as well as the neighboring river systems. The formation of loess particles in the southern CLP was investigated using Scanning Electron Microscopy (SEM) and combined material modal composite analysis. Here, we determined the mineralogy in the Duanjiapo (DJP) section on the southernmost CLP and the last glacial‐interglacial samples on the central and north CLP. The results reveal that the samples plot along the N‐S transect, which is very likely the result of differential weathering. The SEM observations of the internal textures of soil aggregates from DJP suggest that precipitation mediated dissolution led to the formation of the fine particle fraction (5–10 μm). The most dissolution was observed for the hornblende particles. The further evolution of these smaller particles followed a decrease (2.6–0 Ma) in the grain size up section. Our record of the changes in and trend of the hornblende concentrations suggests an imbalance in the budget of the hornblende influx via sub‐aerosol wind transport versus the mineral dissolution, which provides robust evidence for a sediment provenance in the deserts north and west of CLP. Understanding the sediment source is critical to trace Asian monsoon evolution. The hornblende record suggests a coeval change in the trends of the summer monsoon and winter monsoon, and this contemporaneous change may not support the recently proposed Pacific Walker Circulation mechanism in the interpretation of Asian monsoon.
Klebsiella pneumoniae is a global public health concern due to the rising myriad of hypervirulent and multi-drug resistant clones both alarmingly associated with high mortality. The molecular microbial genetics underpinning these recalcitrant K. pneumoniae infections is unclear, coupled with the emergence of lineages resistant to nearly all present day clinically important antimicrobials. In this study, we performed a genome-wide screen in K. pneumoniae ECL8, a member of the endemic K2-ST375 pathotype most often reported in Asia, to define genes essential for growth in a nutrient-rich laboratory medium (Luria-Bertani medium), human urine and serum. Through transposon directed insertion-site sequencing (TraDIS), a total of 427 genes were identified as essential for growth on LB agar, whereas transposon insertions in 11 and 144 genes decreased fitness for growth in either urine or serum, respectively. Genome-wide functional studies like these provide further knowledge on the genetics of this pathogen but also provide a strong impetus for discovering new antimicrobial targets to improve current therapeutic options for K. pneumoniae infections.
Klebsiella pneumoniae is a global public health concern due to the rising myriad of hypervirulent and multi-drug resistant clones both alarmingly associated with high mortality. The molecular microbial genetics underpinning these recalcitrant K. pneumoniae infections is unclear, coupled with the emergence of lineages resistant to nearly all present day clinically important antimicrobials. In this study, we performed a genome-wide screen in K. pneumoniae ECL8, a member of the endemic K2-ST375 pathotype most often reported in Asia, to define genes essential for growth in a nutrient-rich laboratory medium (Luria-Bertani medium), human urine and serum. Through transposon directed insertion-site sequencing (TraDIS), a total of 427 genes were identified as essential for growth on LB agar, whereas transposon insertions in 11 and 144 genes decreased fitness for growth in either urine or serum, respectively. Genome-wide functional studies like these provide further knowledge on the genetics of this pathogen but also provide a strong impetus for discovering new antimicrobial targets to improve current therapeutic options for K. pneumoniae infections.
Klebsiella pneumoniae is a global public health concern due to the rising myriad of hypervirulent and multi-drug resistant clones both alarmingly associated with high mortality. The molecular microbial genetics underpinning these recalcitrant K. pneumoniae infections is unclear, coupled with the emergence of lineages resistant to nearly all present day clinically important antimicrobials. In this study, we performed a genome-wide screen in K. pneumoniae ECL8, a member of the endemic K2-ST375 pathotype most often reported in Asia, to define genes essential for growth in a nutrient-rich laboratory medium (Luria-Bertani medium), human urine and serum. Through transposon directed insertion-site sequencing (TraDIS), a total of 427 genes were identified as essential for growth on LB agar, whereas transposon insertions in 11 and 144 genes decreased fitness for growth in either urine or serum, respectively. Genome-wide functional studies like these provide further knowledge on the genetics of this pathogen but also provide a strong impetus for discovering new antimicrobial targets to improve current therapeutic options for K. pneumoniae infections.
There are over 70 types of mineral species in desert soils. Previous data have focused on major mineral contents and thus, the identification of minor mineral species is lacking. The diversity of minor mineral species was investigated in 19 surficial sediments from deserts in China and Mongolia. A modern scanning electron microscope (SEM)-based in-situ mineral mapping technique was used to determine the minor mineral species concentrations. For further analysis and interpretation, the identified species were grouped into felsic, mica, carbonate, heavy, rare earth, and salt-type minerals. The data in this article demonstrate that the concentrations of felsic, mica, and carbonate minerals are higher than those of the other mineral groups, and thus can be used to provide evidence of sediment provenance. The obtained mineral concentrations were converted from the relative area percentage for each mineral species using standard mineral density data. Mineral mapping was performed using the mineral liberation analysis platform, and on average, approximately 40,000 single particles per sample were analyzed to achieve an accurate quantification of the mineral concentrations. For each of the analyzed single particles, the particle shape parameters, such as particle length and width, were stored and can be used to trace the sediment transport process. For a deeper interpretation of the data presented herein, please see the related research article “Provenance of Fe in Chinese Deserts: Evidence from the geochemistry and mineralogy of soil particles” [1] .
Diphtheria is a respiratory disease caused by Corynebacterium diphtheriae. While the toxin-based vaccine has helped control outbreaks of the disease since the mid-20th century there has been an increase in cases in recent years, including systemic infections caused by non-toxigenic C. diphtheriae strains. Here we describe the first study of gene essentiality in C. diphtheriae, providing the most-dense Transposon Directed Insertion Sequencing (TraDIS) library in the phylum Actinobacteriota. This high-density library has allowed the identification of conserved genes across the genus and phylum with essential function and enabled the elucidation of essential domains within the resulting proteins including those involved in cell envelope biogenesis. Validation of these data through protein mass spectrometry identified hypothetical and uncharacterized proteins in the proteome which are also represented in the vaccine. These data are an important benchmark and useful resource for the Corynebacterium, Mycobacterium, Nocardia and Rhodococcus research community. It enables the identification of novel antimicrobial and vaccine targets and provides a basis for future studies of Actinobacterial biology.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.