Characterization Of Organic Matter Research Articles

Evaluation of characterization and adsorption kinetics of natural organic matter onto nitric acid modified activated carbon

Natural organic substances (NOM) found in drinking water are a major contributor to disinfectant by-product formation and are potentially toxic to humans. Traditional water treatment techniques may not always effectively treat NOMs. Therefore, an advanced treatment method such as adsorption can be inexpensive, simple and efficient. The selected adsorbent's and the NOMs properties both affect the removal effectiveness of the adsorption method. Activated carbon (AC), which is widely used in real-scale water treatment plants, has been modified and used in recent years In order to oxidize the porous carbon surface, raise its acidic qualities, eliminate mineral components, and enhance the surface's hydrophilic qualities. In this research, AC was modified with nitric acid (M-PAC) and NOM removal was investigated. In addition, it is discussed how the modification with nitric acid changes the adsorbent structure and chemistry. A morphology with smooth and irregular voids was observed as a result of nitric acid modification of the original AC by SEM analysis. The particle size increased from 387.65 nm to 502.07 nm for the M-PAC adsorbent. The FTIR spectrum indicates that structures connected to aromatic rings get formed in the M-PAC adsorbent as a result of the modification. The highest NOM removal for the original powdered activated carbon (PAC), 47%, was observed at 36 hours of contact time. On the other hand, M-PAC adsorbent achieved 40% NOM removal at contact times of 72 hours and above. It was concluded that the pseudo-second order kinetic model better represented NOM adsorption for both adsorbents.

Regional differences in lead (Pb) and tetracycline (TC) binding behavior of sediment dissolved organic matter (SDOM): Effects of DOM heterogeneity and microbial degradation

Lake Nansi, primarily dominated by macrophytes, faces threats from heavy metals and antibiotics due to human activity. This study investigated sediment dissolved organic matter (SDOM) characteristics and complexation of lead (Pb) and tetracycline (TC) in barren zone (BZ) and submerged macrophytes zone (PZ). Additionally, a microbial degradation experiment was conducted to examine its impact on the regional variations in complexation. SDOM abundance and protein-like materials in PZ was significantly greater than in BZ, indicating a probable contribution from the metabolism and decomposition of submerged macrophytes. Both zones exhibited a higher affinity of SDOM for Pb compared to TC, with all four components participating in Pb complexation. Protein-like materials in PZ had a higher binding ability (LogKPb=4.19 ± 1.07, LogKTC=3.89 ± 0.67) than in BZ (LogKPb=3.98 ± 0.61, LogKTC=3.69 ± 0.13), suggesting a potential presence of organically bound Pb and TC due to the higher abundance of protein-like materials in PZ. Although microbial communities differed noticeably, the degradation patterns of SDOM were similar in both zones, affecting the binding ability of SDOM in each. Notably, the fulvic-like component C4 emerged as the dominant binding material for both Pb and TC in both zones. Degradation might increase the amount of organically bound TC due to the increase in the LogKTC.

Effects of UV/Cl2 and UV/PDS advanced oxidation on chemical characteristics of typical organic matter in reclaimed water

In this research, humic acid was selected as a typical organic substance in reclaimed water, and the effects of higher oxidation of UV/Cl2 and UV/PDS on its chemical composition, including aromaticity, molecular weight and fluorescence characteristics were investigated. Results showed that under the same oxidation conditions, the UVA254 removal rate of UV/Cl2 was higher than that of UV/PDS, but with the increase of pH, the UVA254 removal rate of both decreased. Increasing the oxidant concentration could improve the UVA254 removal rate, but UVA254 would not continue to decrease after a certain concentration (Cl2 0.5mM, PDS 0.75mM). After oxidation, organics whose molecular weight >6520 Da significantly decreased, molecular weight 350-1690 Da significantly increased, with increasing UV dose, the molecular weight of 350-1690 Da decreased in UV/Cl2, but continued to increase in UV/PDS. The fluorescent regions of fulic acids under different treatments were effectively degraded after oxidation. The degradation efficiency of UV/Cl2 and UV/PDS reached 87.6% and 83.3% respectively with 0.75mM oxidant and 1500 mJ/cm2 UV light.

Deciphering dissolved organic matter characteristics and its fate in a glacier-fed desert river—the Tarim river, China

The bioavailable diverse dissolved organic matter (DOM) present in glacial meltwater significantly contributes to downstream carbon cycling in mountainous regions. However, the comprehension of molecular-level characteristics of riverine DOM, from tributary to downstream and their fate in glacier-fed desert rivers remains limited. Herein, we employed spectroscopic and high-resolution mass spectrometry techniques to study both optical and molecular-level characteristics of DOM in the Tarim River catchment, northwest China. The results revealed that the DOC values in the downstream were higher than those in the tributaries, yet they remained comparable to those found in other glacier-fed streams worldwide. Five distinct components were identified using EEM-PARAFAC analysis in both tributary and downstream samples. The dominance of three protein-like components in tributary samples, contrasting with a higher presence of humic-like components in downstream samples, which implied that the dilution and alterations of the glacier DOM signature and overprinting with terrestrial-derived DOM. Molecular composition revealed that thousands of compounds with higher molecular weight and increased aromaticity were transformed, generated and introduced from terrestrial inputs during downstream transportation. The twofold rise in polycyclic aromatic and polyphenolic compounds observed downstream compared to tributaries indicated a greater influx of terrestrial organic matter introduced into the downstream during water transportation. The study suggests that the glacier-sourced DOM experienced minimal photodegradations, with limited influence from human activities, while also being shaped by terrestrial inputs during its transit in the alpine-arid region. This unique scenario offers valuable insights into comprehending the fate of DOM originating from glacial meltwater in arid mountainous regions.

Experimental Open Air Burning of Vegetation Enhances Organic Matter Chemical Heterogeneity Compared to Laboratory Burns.

Wildfires produce solid residuals that have unique chemical and physical properties compared to unburned materials, which influence their cycling and fate in the natural environment. Visual burn severity assessment is used to evaluate post-fire alterations to the landscape in field-based studies, yet muffle furnace methods are commonly used in laboratory studies to assess molecular scale alterations along a temperature continuum. Here, we examined solid and leachable organic matter characteristics from chars visually characterized as low burn severity that were created either on an open air burn table or from low-temperature muffle furnace burns. We assessed how the different combustion conditions influence solid and dissolved organic matter chemistries and explored the potential influence of these results on the environmental fate and reactivity. Notably, muffle furnace chars produced less leachable carbon and nitrogen than open air chars across land cover types. Organic matter produced from muffle furnace burns was more homogeneous than open air chars. This work highlights chemical heterogeneities that exist within a single burn severity category, potentially influencing our conceptual understanding of pyrogenic organic matter cycling in the natural environment, including transport and processing in watersheds. Therefore, we suggest that open air burn studies are needed to further advance our understanding of pyrogenic organic matter's environmental reactivity and fate.

Source rock assessment and organic matter characterization of the Oligocene upper Shahejie and Dongying formations in the Nanpu depression of the saline lacustrine Bohai Bay basin, China: Geochemical, palynological, and mineralogical perspectives

The Bohai Bay Basin, located in eastern China, is a significant petroliferous, non-marine rift basin, underwent intricate tectonic activities throughout the Cenozoic. The Nanpu Depression in the Huanghua sub-basin in the northern part of the basin was controlled by Paleogene rifting and increased subsidence. These geological processes resulted in the deposition of the Shahejie and Dongying formations, which exhibited varying quantities and qualities of organic matter. Eighty drill cuttings samples of the Paleogene First Member (Es1) and the overlying Third (Ed3) and Second (Ed2) members of the Shahejie and Dongying formations, respectively, were investigated. An integrated approach including organic and inorganic geochemistry, palynology, and mineralogy was employed to assess the paleoredox and marine incursion conditions, source rock quality and levels of thermal maturity, and factors that governed organic matter accumulation. Results indicated that the Es1 Member was deposited under anoxic conditions, resulting in the accumulation of organic matter-rich mudstones in the Nanpu Depression. Abundant pollen grains and acritarchs were found in the Es1 Member yielded along with minor occurrences of dinoflagellate cysts, freshwater algae, and spores. Terrestrial palynomorph composition provided evidence of increased terrestrial runoff, while the high abundance of acritarchs, accompanied by some dinoflagellate cysts, confirmed episodes of marine incursion and deposition under hypersaline conditions in the lacustrine Bohai Bay Basin. The Ed2 Member exhibited poor to fair amounts of organic matter and a limited potential of hydrocarbon generation with a variety of kerogen Types, including IV, III, II/III, and II. The Ed3 Member shows fair to good organic matter richness and hydrocarbon potential of kerogen Types III, II/III, and II. The Es1 Member emerged as the most promising source rock within the studied interval, boasting good to excellent organic matter richness, and fair to good hydrocarbon generation potential of kerogen Types III and II/III. Evaluating the thermal maturity of organic matter, based on Tmax and VRo-Eq% and related cross-plots, revealed that the Shahejie and Dongying formations are still in the immature to the early stage of the oil window. The mineralogical composition of the Es1 Member primarily consists of clay and quartz with some carbonate and accessory minerals, such as epigenetic halite, dolomite, and plagioclase. Weak correlations observed between the total organic carbon (TOC) and mineral components indicated that the availability of organic matter was primarily controlled by enhanced production and preservation rather than limited dilution under saline lacustrine, oxygen-deprived, and well-stratified water column conditions. Regional investigations of the Es1 Member confirmed the widespread anoxia and deposition of organic-rich source rocks in the Bohai Bay Basin during the Oligocene.

Palaeodepositional environment, implications of Glossopteris flora, and organic matter characteristics from the Lower Permian, Karo Open Cast Mine, East Bokaro Coalfield, Damodar Basin, India

The present study deals with the Early Permian floral diversity, palaeoenvironment, palaeoclimate and depositional setting using a multiproxy approach that includes morphotaxonomy, palynology, and organic geochemistry of Karo OCM (Open Cast Mine), East Bokaro Coalfield, Damodar Gondwana Basin, India. The Permian sediments of Peninsular India are widely regarded as fluvial, along with some marine incursions. The macroplant fossil assemblage exhibits the presence of Glossopteridales, comprising Glossopteris, Gangamopteris, and Vertebraria, as well as Coniferales, which includes Noeggerathiopsis. The palynological assemblage encompasses the dominance of the striate bisaccate pollen Faunipollenites sp. and the sub-dominance of the non-striate bisaccate pollen Scheuringipollenites sp. with glossopterid affinities. The megafloral and palynofloral assemblage confirms the biostratigraphical age to be Late Barakar palynoflora of Kungurian affinity. The studied morphological characteristics, including small to large Glossopteris leaves exhibiting a lanceolate shape, acute apices, and acute cuneate or tapering bases, as well as entire margins with narrower lamina and narrow meshes, suggest the existence of a dense forest with the prevalence of a warm and humid climate during their deposition. The organic geochemical characterization based on functional group and biomarker analyses reveals the diagenetic effects on organic matter. Aliphatic symmetric (∼2865–2855 cm-1) and asymmetric stretching (∼2930–2910 cm-1) peaks are identifiable in coal samples, whereas they are absent in carbonaceous shale. The A-factor vs. C-factor plot suggests that the kerogen type is type III, which can generate mainly gaseous kerogen. The vitrinite reflectance studies (Rr av. 1.1%) show increased maturity of the samples, which is supported by the n-alkane distribution pattern and the absence of hopane terpenoids. The Indian floral assemblages in contemporary of southern Gondwana continents reveal a stronger inclination/affinity with the flora of Africa than that of South America, thereby supporting the age to be of Artinskian–Kungurian.

Organic geochemical investigation of cretaceous source rocks with varying thermal maturity levels in the East Andes (Boyacá, Colombia)

This study encompasses a geochemical investigation of Cretaceous source rocks from the Eastern Cordillera (Colombia). This basin represents an interesting area for geochemical studies due to its abundance of organic matter-rich levels, some of which exhibit mild to extremely high thermal maturities, enabling discussion on long-term carbon sinks. This research work focuses on the study of organic-rich shaly sediments of Barremian to Campanian age from seven (7) outcrop locations in two areas of the Boyacá Department. A set of seventy (70) rock samples have been analysed using several organic geochemical techniques and have shown to cover thermal maturity ranges from the early oil window to the metagenesis stage (measured reflectance values from 0.6% to 2.1%). The OAE2 event was identified based on a 2.5‰–3‰ carbon isotopic excursion in the distal Guaguaquí Group from the section along the Guaquaquí River. Maturity was not found to correlate with depositional burial depths in the so-called distal study area, suggesting that other tectonic events may have played an important role in the genetic history of hydrocarbons particularly in this part of the Boyacá Department. During the mid-to late Cretaceous times, the two study areas consisted of a marine margin with a terrestrial input from the east, which is reflected in a higher terrestrial character of sediments in the eastern foothills (V/Ni < 0.7) compared to the others. Finally, fluorene- and diamondoid-based components were used for enhancing the characterization of the mid-to late Cretaceous organic matter in terms of source in the study sub-region (three-fluorenes and dimethyl-/trimethyl-adamantanes ratios above or below 0.25 and 0.85).

Organic geochemical characteristics of the Late Cretaceous coal and carbonaceous shale succession from the Taranaki Basin, New Zealand: Implications for sedimentary environmental setting and petroleum generation potential

This comprehensive study investigates the organic matter characteristics within the Late Cretaceous Rakopi and Taniwha formations, based on data from four exploration wells situated in New Zealand's Taranaki Basin. It employs a multifaceted approach, integrating bulk geochemical analyses, biomarker measurements and carbon isotopes to unveil the geological history of these formations. Analytical results include total organic carbon content, ranging from 7.27 to 75.78 wt%, and generation potentials spanning from 28.24 to 309.16 mg hydrocarbon/g rock. These observations underscore the source rock potential of these Late Cretaceous strata. These rocks show a mixed organic matter of hydrogen‐rich Type II and Type II/III kerogens, as evidenced by hydrogen index values (HI) between 237 to 428 mg hydrocarbon/g rock. These formations demonstrate promise potential for both oil and gas generation. Biomarker analysis uncovers distinct signatures, featuring a pristane/phytane (Pr/Ph) ratio ranging from 3.27 to 10.91, a Tm/Ts ratio surpassing 7 and elevated concentrations of C29 regular steranes relative to C27 and C28 regular steranes. These biomarker characteristics suggest a composite organic matter composition, influenced by terrigenous organic matter, likely deposited in oxygenated fluvial deltaic environments. Bulk carbon isotopic data corroborate these findings, highlighting the abundance of terrigenous organic matter. Collectively, these insights reveal that the coal and carbonaceous shale intervals in the examined wells are in the early stages of oil generation. Therefore, the Rakopi and Taniwha formations have not yet yielded commercially viable oil and/or gas quantities. In this case, these formations hold substantial promise for future exploration activities in relatively deep wells, with limited oil expulsion from coals.

Nanoscale Spectroscopic Identification and Characterization of Minerals and Organic Matter in Ryugu Particles

AbstractCarbonaceous asteroids are leftover materials from the early solar system. They did not undergo planetary differentiation processes and thus still retained signatures and clues of the origin and evolution of the solar system. Thus, samples of carbonaceous asteroids provide significant potential for deciphering the origin of the solar system. The Hayabusa2 spacecraft returned the first samples of a carbonaceous asteroid (162173) Ryugu. In this work, we report the nanoscale mineralogy and organic matter content of two Ryugu particles, A0030 and C0034. These were analyzed by highly novel scattering‐type scanning near‐field optical microscopy (s‐SNOM)‐based nanoscale‐Fourier transform infrared (nano‐FTIR) spectroscopy with ∼20 nm spatial resolution. The nano‐FTIR measurements were supported by confocal micro‐Raman imaging and spectroscopy (∼500 nm/pixel spatial sampling). Our investigations show that the two Ryugu particles (a) contain different silicate mineralogies, indicating heterogeneous and incomplete aqueous alteration and (b) are highly rich in organic matter, consisting a variety of molecular functional groups. The spatial distributions of chemical functional groups and their associations based on pseudo‐heterodyne (PsHet) SNOM imaging show that the organic matter is distributed as either diffused or discrete grains. Micro‐Raman spectra show that the Ryugu particles experienced minimal thermal metamorphism, although A0030 was slightly more heated than C0034. The identification of abundant nanoscale organic molecules within the Ryugu grains that could not be identified via micrometer‐scale investigations emphasizes the importance of using nanoscale nondestructive methods for studying primitive solar system materials, such as Ryugu and OSIRIS‐Rex particles and those that will be returned in the future (such as MMX samples).

Effect of pyrolysis temperature and molecular weight on characterization of biochar derived dissolved organic matter from invasive plant and binding behavior with the selected pharmaceuticals

A comprehensive understanding of the characteristics of biochar released-dissolved organic matter (BDOM) derived from an invasive plant and its impact on the binding behavior of pharmaceuticals is essential for the application of biochar, yet has received less attention. In this study, the binding behavior of BDOM pyrolyzed at 300–700 °C with sulfathiazole, acetaminophen, chloramphenicol (CAP), and carbamazepine (CMZ) was investigated based on a multi-analytical approach. Generally, the pyrolysis temperature exhibited a more significant impact on the spectral properties of BDOM and pharmaceutical binding behavior than those of the molecular weight. With increased pyrolysis temperature, the dissolved organic carbon decreased while the proportion of the protein-like substance increased. The highest binding capacity towards the drugs was observed for the BDOM pyrolyzed at 500 °C with the molecular weight larger than 0.3 kDa. Moreover, the protein-like substance exhibited higher susceptive and released preferentially during the dialysis process and also showed more sensitivity and bound precedingly with the pharmaceuticals. The active binding points were the aliphatic C–OH, amide II N–H, carboxyl CO, and phenolic-OH on the tryptophan-like substance. Furthermore, the binding affinity of the BDOM pyrolyzed at 500 °C was relatively high with the stability constant (logKM) of 4.51 ± 0.52.

Organic Petrologic Characterization and Paleoenvironmental Analysis of Permian Shale in Northeast Sichuan Province, China

The Permian shale in Northeast Sichuan is an important shale oil and gas resource potential area, and the study of its organic matter characteristics and paleoenvironmental analysis is of great significance for revealing the shale oil and gas formation mechanism and resource evaluation. In this study, the organic matter of Permian shales in northeast Sichuan was carefully studied based on various analytical tools, such as petrology, laser Raman, microscopy, and principal trace elements, and the paleoenvironmental parameters of the shales were comprehensively analysed. A detailed study of the organic matter characteristics of Permian shales in northeast Sichuan reveals important features such as organic matter fractions, structural characteristics, maturity and sources. The results show that the organic matter of the shale consists mainly of solid bitumen, putrescine group, specular group and multicellular planktonic algae. Petrological observations and laser Raman analyses indicate a high maturity of the organic matter and a high content of organic carbon (TOC), showing good hydrocarbon potential. In this study, we reconstructed the palaeoenvironmental parameters and inferred the palaeoenvironmental evolution through palaeoenvironmental analyses of Permian shales in northeast Sichuan. The results of the comprehensive multi-indicator study show that the type of palaeoenvironment at the time of shale deposition was mainly an anoxic-reducing environment, and the depositional conditions were favourable to the enrichment and preservation of organic matter. In summary, the organic matter characteristics and paleoenvironmental analyses of the Permian shales in Northeast Sichuan provide important geological background information for an in-depth understanding of the formation mechanism, exploration potential and development prospect of shale hydrocarbons in this area. The results of this study can provide a scientific basis for the evaluation and development of shale oil and gas resources in this area, which is of great significance to geologists and the energy industry.

Characterization and function of particulate organic matter: Evidence from lakes undergoing ecological restoration

Particulate organic matter (POM) plays a crucial role in the organic composition of lakes; however, its characteristics remain poorly understood. This study aimed to characterize the structure and composition of POM in Lake Baiyangdian using many kinds of techniques and investigate the effects of different extracted forms of POM on water quality. The suspended particulate matter in the lake had complex compositions, with its components primarily derived from aquatic plants and their detritus. The organic matter content of the suspended particulate matter was relatively high (organic carbon content 27.29–145.94 g/kg) for the sum of three extractable states (water-extracted organic matter [WEOM], humic acid, and fulvic acid) and one stable bound state (humin). Spatial distribution analysis revealed that the POM content in the water increased from west to east, which was consistent with the water flow pattern influenced by the Baiyangdian water diversion project. Fluorescence spectroscopy analysis of the WEOM showed three prominent peaks with excitation/emission wavelengths similar to those of dissolved organic matter peaks. These peaks were potentially initial products of POM conversion into dissolved organic matter. Furthermore, the intensity of the WEOM fluorescence peak (total fluorescence peak intensity) was negatively correlated with the inorganic nitrogen concentration in water (p < 0.01), while the intensity of the HA fluorescence peak showed a positive correlation with the inorganic nitrogen concentration (p < 0.01). This suggested that exogenous organic matter inputs led to the diffusion of alkaline dissolved nitrogen from sediment into water, while degradation processes of aquatic plant debris contributed to the decrease in inorganic nitrogen concentrations in the water column. These findings enhance our understanding of POM characteristics in shallow lakes and the role of POM in shallow lake ecosystems.

The complex relationships between diatoms, bacterial communities, and dissolved organic matter: Effects of silicon concentration

Complex relationships exist between diatoms, bacterial communities and dissolved organic matter in aquatic ecosystems. Clarifying their relationships is essential to reveal biogeochemical cycles. In this study, the diatom Cyclostephanos invisitatus was cultured in standard silicon (SS), no silicon (NS), and excessive silicon (ES). Integrated 16S rDNA high-throughput sequencing and excitation-emission matrix parallel factor analysis (EEM-PARAFAC) were used to investigate diatom growth, bacterial community and dissolved organic matter (DOM) characteristics. It was found that the abundance of diatoms decreased in no silicon and excessive silicon conditions. Further, the composition and function of the associated bacterial communities were affected. The Proteobacteria and Cyanobacteria were more highly represented in the attached bacteria, whereas the Proteobacteria and Bacteroidetes were more highly represented in the free-living bacteria. Alpha diversity showed different trends with incubation time in all treatments. Moreover, genes (K01995 to K01998) involved in environmental information processing were more abundant in diatoms during the stationary phase in attached bacterial community. Stochastic processes play a key role in the formation of bacterial communities, both for attached and free-living bacteria. In addition, the differences in fluorescence components (protein and humic-like) and spectral indices (fluorescence index, biological index, freshness index, and humification index) revealed intricate relationship between microalgae and bacteria. Overall, this work confirmed the importance of silicon concentration in regulating diatom-associated bacterial communities and DOM characteristics.

Degrading surface-water-based natural organic matter and mitigating haloacetonitrile formation during chlorination: Comparison of UV/persulfate and UV/hydrogen peroxide pre-treatments

Haloacetonitriles (HANs) are unregulated disinfection by-products that are more toxic than regulated species. Therefore, efficient decomposition of HAN precursors prior to disinfection is crucial for allaying the potential HAN-induced health risks. This study investigated the key roles of ultraviolet-activated persulfate (UV/PS) treatment in alleviating HAN formation. The effects of UV/PS treatment were evaluated by correlating with the characteristics of organic matter in surface water and comparing with conventional UV/H2O2 treatment. Upon irradiating raw water samples and a Suwannee River humic acid solution spiked with 10 mM PS or H2O2 with 254 nm UV light, UV/PS treatment was found to be more potent than UV/H2O2 in mitigating the HAN production and degrading organic substances; moreover, UV/PS treatment effectively decreased the dissolved organic nitrogen (DON) content. In contrast, UV/H2O2 treatment did not induce any noticeable reduction in DON level. Furthermore, both UV/PS and UV/H2O2 treatments reduced the dichloroacetonitrile (DCAN) formation potential (FP), leading to strong correlations with the degradation of aromatic and humic-acid-like compounds. Notably, UV/PS treatment efficiently decreased the FP of bromochloroacetonitrile (BCAN) and dramatically reduced that of dibromoacetonitrile (DBAN) after a sharp increase; however, UV/H2O2 treatment gradually increased the DBAN-FP. Bromide was activated by sulfate radicals during UV/PS treatment, negatively correlating with the BCAN-FP and DBAN-FP, indicating that the formation of reactive bromine species increased the DBAN-FP; however, excessive oxidation possibly led to the recovery of inorganic bromine for decreasing the BCAN-FP and DBAN-FP. Additionally, UV/PS treatment effectively suppressed toxicity owing to its high reduction rate for brominated HANs; in contrast, UV/H2O2 treatment resulted in less significant BCAN and DBAN reductions, leading to minimal net reduction in toxicity. Overall, UV/PS treatment was remarkably effective at diminishing the toxicity of brominated HANs, underscoring its potential to mitigate drinking-water-related health risks.

Study on the effect of alkali on the production of volatile fatty acids from rhamnolipid‐alkali‐thermal pretreated waste activated sludge

AbstractThis article systematically explores the strengthening effect of NaOH dosage on the fermentation acid production of Waste Activated Sludge (WAS) by the rhamnolipids‐alkali‐thermal combined pretreatment. Analyzed the dissolution characteristics of organic matter in sludge, changes in total volatile fatty acids (VFAs) content and components, and microbial community structure. Research has shown that increasing the amount of NaOH can promote the dissolution of sludge extracellular polymeric substances (EPS) and cell lysis. When NaOH dose was 60 mg/g VS, the dissolution of SCOD was the largest, reaching 5427.78 mg/L. It provides high‐quality substrate for anaerobic flora through the decomposition of refractory humus‐like substances and macromolecular substances, thus improving the production of VFAs. When NaOH dose was 80 mg/g VS, the maximum VFAs yield was 1663.76 mg C/L, and the fermentation type was butyric acid. The increase of NaOH dose promotes the effective enrichment of bacteria, and the dominant bacteria are Proteobacteria, Firmicutes, and Bacteroides at the gate level, with different abundance. The fermentation time plays a decisive role in the evolution of microbial population, and the increase of NaOH dose promotes the enrichment of acid‐producing bacteria, thus improving the production of VFAs.

Computational tools and algorithms for ion mobility spectrometry-mass spectrometry.

Ion mobility spectrometry-mass spectrometry (IMS-MS or IM-MS) is a powerful analytical technique that combines the gas-phase separation capabilities of IM with the identification and quantification capabilities of MS. IM-MS can differentiate molecules with indistinguishable masses but different structures (e.g., isomers, isobars, molecular classes, and contaminant ions). The importance of this analytical technique is reflected by a staged increase in the number of applications for molecular characterization across a variety of fields, from different MS-based omics (proteomics, metabolomics, lipidomics, etc.) to the structural characterization of glycans, organic matter, proteins, and macromolecular complexes. With the increasing application of IM-MS there is a pressing need for effective and accessible computational tools. This article presents an overview of the most recent free and open-source software tools specifically tailored for the analysis and interpretation of data derived from IM-MS instrumentation. This review enumerates these tools and outlines their main algorithmic approaches, while highlighting representative applications across different fields. Finally, a discussion of current limitations and expectable improvements is presented.

Disentangling the effects of temperature and reactive minerals on soil carbon stocks across a thermal gradient in a temperate native forest ecosystem

Effects of global warming on soil organic carbon (C) can be investigated by comparing sites experiencing different temperatures. However, observations can be affected by covariance of temperature with other environmental properties. Here, we studied a thermal gradient in forest soils derived from volcanic materials on Mount Taranaki (New Zealand) to disentangle the effects of temperature and reactive minerals on soil organic C quantity and composition. We collected soils at four depths and four elevations with mean annual temperatures ranging from 7.3 to 10.5 °C. Soil C stocks were not significantly different across sites (average 162 MgC ha−1 to 85 cm depth, P > .05). Neither aluminium (Al)-complexed C, nor mineral-associated C changed significantly (P > .05) with temperature. The molecular characterisation of soil organic matter showed that plant-derived C declined with increasing temperature, while microbial-processed C increased. Accompanying these changes, soil short-range order (SRO) constituents (including allophane) generally increased with temperature. Results from structural equation modelling revealed that, although a warmer temperature tended to accelerate soil organic C decomposition as inferred from molecular fingerprints, it also exerted a positive effect on soil total C presumably by enhancing plant C input. Despite a close linkage between mineral-associated C and soil organic C, the increased abundance of reactive minerals at 30–85 cm depth with temperature did not increase soil organic C concentration at that depth. We therefore propose that fresh C inputs, rather than reactive minerals, mediate soil C responses to temperature across the thermal gradient of volcanic soils under humid-temperate climatic conditions.

Chemical characterization of soil organic matter in differents management practices in the Cerrado-Pantanal ecotone

Different land uses and occupations have a direct impact on edaphic attributes, which can be identified by soil quality indicators, with organic matter being an excellent edaphic quality indicator. The objective of the work was to chemically characterize soil organic matter (SOM) in different management systems in the municipality of Aquidauana, Mato Grosso do Sul, Brazil. Soil samples were collected in five areas with different management practices, in addition to an area of native Cerrado forest (NF), and the managed areas were: exposed soil (ES), conventional tillage system (CTS), no-tillage (NTS), permanent pasture (PP) and sugarcane (SC). In addition to the determination of bulk density (Bd), total organic carbon (TOC) contents and stocks were quantified, as well as carbon (C) contents and stocks of the humified fractions: humic acid (AH), fulvic acid (AF) and humin (HUM), with subsequent calculation of HA/FA and alkaline extract/humin (AE/HUM) and TOC stratification index (SI). There were no significant changes for Ds after six years of implementation of management systems. TOC levels and stocks were higher in PP and NTS areas. The HUM fraction was predominant, with higher contents and stocks of all fractions for the PP and NTS areas, demonstrating the greater intensity of the humification process in these management systems, with greater stability of C in the soil after six years of experiment. The PCA indicated a difference between the areas that present conservation practices in the ES and CTS areas. The NF, NTS, PP and SC areas contribute to SOM stabilization.

Dissolved organic matter characteristics linked to bacterial community succession and nitrogen removal performance in woodchip bioreactors

Woodchip bioreactors are an eco-friendly technology for removing nitrogen (N) pollution. However, there needs to be more clarity regarding the dissolved organic matter (DOM) characteristics and bacterial community succession mechanisms and their association with the N removal performance of bioreactors. The laboratory woodchip bioreactors were continuously operated for 360 days under three influent N level treatments, and the results showed that the average removal rate of TN was 45.80 g N/(m3·day) when the influent N level was 100 mg N/L, which was better than 10 mg N/L and 50 mg N/L. Dynamic succession of bacterial communities in response to influent N levels and DOM characteristics was an important driver of TN removal rates. Medium to high N levels enriched a copiotroph bacterial module (Module 1) detected by network analysis, including Phenylobacterium, Xanthobacteraceae, Burkholderiaceae, Pseudomonas, and Magnetospirillaceae, carrying N-cycle related genes for denitrification and ammonia assimilation by the rapid consumption of DOM. Such a process can increase carbon limitation to stimulate local organic carbon decomposition to enrich oligotrophs with fewer N-cycle potentials (Module 2). Together, this study reveals that the compositional change of DOM and bacterial community succession are closely related to N removal performance, providing an ecological basis for developing techniques for N-rich effluent treatment.