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We present relativistic magnetohydrodynamic modelling of jets running into hydrostatic, spherically symmetric cluster atmospheres. For the first time in a numerical simulation, we present model cluster atmospheres based upon the universal pressure profile (UPP), incorporating a temperature profile for a 'typical' self-similar atmosphere described by only one parameter – M 500. We explore a comprehensive range of realistic atmospheres and jet powers and derive dynamic, energetic, and polarimetric data which provide insight into what we should expect of future high-resolution studies of AGN outflows. From the simulated synchrotron emission maps which include Doppler beaming we find sidedness distributions that agree well with observations. We replicated a number of findings from our previous work, such as higher power jets inflating larger aspect-ratio lobes, and the cluster environment impacting the distribution of energy between the lobe and shocked regions. Comparing UPP and β-profiles we find that the cluster model chosen results in a different morphology for the resultant lobes with the UPP more able to clear lobe material from the core; and that these different atmospheres influence the ratio between the various forms of energy in the fully developed lobes. This work also highlights the key role played by Kelvin–Helmholtz instabilities in the formation of realistic lobe aspect ratios. Our simulations point to the need for additional lobe-widening mechanisms at high jet powers, for example jet precession. Given that the UPP is our most representative general cluster atmosphere, these numerical simulations represent the most realistic models yet for spherically symmetric atmospheres. [ABSTRACT FROM AUTHOR]

Premise: The Aptian-Albian (121.4-100.5 Ma) was a greenhouse period with global temperatures estimated as 10-15°C warmer than pre-industrial conditions, so it is surprising that the most reliable CO 2 estimates from this time are <1400 ppm. This low CO 2 during a warm period implies a very high Earth-system sensitivity in the range of 6 to 9°C per CO 2 doubling between the Aptian-Albian and today., Methods: We applied a well-vetted paleo-CO 2 proxy based on leaf gas-exchange principles (Franks model) to two Pseudotorellia species from three stratigraphically similar samples at the Tevshiin Govi lignite mine in central Mongolia (~119.7-100.5 Ma)., Results: Our median estimated CO 2 concentration from the three respective samples was 2132, 2405, and 2770 ppm. The primary reason for the high estimated CO 2 but with relatively large uncertainties is the very low stomatal density in both species, where small variations propagate to large changes in estimated CO 2 . Indeed, we found that at least 15 leaves are required before the aggregate estimated CO 2 approaches that of the full data set., Conclusions: Our three CO 2 estimates all exceeded 2000 ppm, translating to an Earth-system sensitivity (~3-5°C/CO 2 doubling) that is more in keeping with the current understanding of the long-term climate system. Because of our large sample size, the directly measured inputs did not contribute much to the overall uncertainty in estimated CO 2 ; instead, the inferred inputs were responsible for most of the overall uncertainty and thus should be scrutinized for their value choices., (© 2024 Botanical Society of America.)

In the last decades, the increase in global industrialization and the consequent technological progress have damaged the quality of the environment. As a consequence, the high levels of hazardous compounds such as metals and gases released in the atmosphere and water, have raised several concerns about the health of living organisms. Today, many analytical techniques are available with the aim to detect pollutant chemical species. However, a lot of them are not affordable due to the expensive instrumentations, time-consuming processes and high reagents volumes. Last but not least, their use is exclusive to trained operators. Contrarily, colorimetric sensing devices, including paper-based devices, are easy to use, providing results in a short time, without particular specializations to interpret the results. In addition, the colorimetric response is suitable for fast detection, especially in resource-limited environments or underdeveloped countries. Among different chemical species, transition and heavy metals such as iron Fe(II) and copper Cu(II) as well as volatile compounds, such as ammonia (NH3) and acetaldehyde (C2H4O) are widespread mainly in industrialized geographical areas. In this work, we developed a colorimetric paper-based analytical device (PAD) to detect different contaminants, including Fe2+ and Cu2+ ions in water, and NH3 and C2H4O in air at low concentrations. This study is a “proof of concept” of a new paper sensor in which the intensity of the colorimetric response is proportional to the concentration of a detected pollutant species. The sensor model could be further implemented in other technologies, such as drones, individual protection devices or wearable apparatus to monitor the exposure to toxic species in both indoor and outdoor environments.

Rationale: The analysis of chemical warfare agents (CWAs) from ambient atmosphere presents an analytical challenge due to their ease of degradation and volatility. Herein is described a method for derivatizing CWAs directly onto a paper spray substrate prior to analysis. This derivatization allows for much longer times of analysis without sample degradation and with little to no sample preparation. Methods: Derivatization was performed using 2‐[(dimethylamino)methyl] phenol both in‐vial and directly on paper spray cartridges. Solution studies were carried out over time and samples were analyzed via liquid chromatography/tandem mass spectrometry (LC/MS/MS) operated in positive ion mode. Paper spray substrates impregnated with the derivatizing agent prior to CWA vapor capture were also analyzed over time using a mass spectrometer operated in positive ion mode. Results: Use of 2‐[(dimethylamino)methyl] phenol as a paper spray substrate dopant enables derivatization of G‐series compounds into lower volatility complexes. The reaction occurs in solution and in the vapor phase. This new technique effectively traps and captures G‐series agents for analysis while extending the time for which the compound remains absorbed. The complex is highly suitable for direct analysis via paper spray mass spectrometry. Conclusions: Derivatization of paper spray substrates was shown to greatly increase the time for analysis of CWAs. This technique, combined with the vapor phase capture stage outlined previously, allows for rapid, quantitative CWA detection by paper spray ionization with little or no sample preparation. [ABSTRACT FROM AUTHOR]

In order to study the effects of different atmospheres ( nitrogen and air) and temperature ranges (300 ~ 500 °C, 300 ~ 700 °C and 300 ~ 900 °C ) on the composition and amount of pyrolysis products in paper-making reconstituted tobacco substrates, solid phase microextraction, adsorption-desorption and gas chromatography-mass spectrometry methods were used for analysis. The results showed that under the nitrogen and air atmospheres, the pyrolysis products of substrates at the range of 300 ~ 700 °C and 300 ~ 900 °C obviously increased when compared with those at the range of 300 ~500 °C . A large number of polycyclic aromatic hydrocarbons and olefins were produced in these two temperature ranges. Nicotine was only found in the pyrolysis products of substrates at the range of 300 ~ 500 °C. The contents of furfural and phytadiene were higher at these three temperature ranges. In the same temperature range,under the air atmosphere,the release amount of important cleavage products such as crotonaldehyde, 2-methyl-furan and furfural with relatively low molecular weight was higher than that under nitrogen atmosphere. The relative release of alcohols increased, and the presence of oxygen in air promoted the full combustion of substrates, thereby resulting in the reduction of total pyrolysis products. [ABSTRACT FROM AUTHOR]

We report and discuss the challenges to realize a nanoLED based display from the perspective of materials and processes. Additionally, we report on an active‐matrix nanoLED display using cadmium free Quantum Dots (QDs) patterned by photolithography in the atmosphere. [ABSTRACT FROM AUTHOR]

Atmospheric oxygen levels control the oxidative side of key biogeochemical cycles and place limits on the development of high-energy metabolisms. Understanding Earth's oxygenation is thus critical to developing a clearer picture of Earth's long-term evolution. However, there is currently vigorous debate about even basic aspects of the timing and pattern of the rise of oxygen. Chemical weathering in the terrestrial environment occurs in contact with the atmosphere, making paleosols potentially ideal archives to track the history of atmospheric O 2 levels. Here we present stable chromium isotope data from multiple paleosols that offer snapshots of Earth surface conditions over the last three billion years. The results indicate a secular shift in the oxidative capacity of Earth's surface in the Neoproterozoic and suggest low atmospheric oxygen levels (<1% PAL pO 2 ) through the majority of Earth's history. The paleosol record also shows that localized Cr oxidation may have begun as early as the Archean, but efficient, modern-like transport of hexavalent Cr under an O 2 -rich atmosphere did not become common until the Neoproterozoic., (© 2019 John Wiley & Sons Ltd.)

Research reported during the past decade has shown that global warming is roughly proportional to the total amount of carbon dioxide released into the atmosphere. This makes it possible to estimate the remaining carbon budget: the total amount of anthropogenic carbon dioxide that can still be emitted into the atmosphere while holding the global average temperature increase to the limit set by the Paris Agreement. However, a wide range of estimates for the remaining carbon budget has been reported, reducing the effectiveness of the remaining carbon budget as a means of setting emission reduction targets that are consistent with the Paris Agreement. Here we present a framework that enables us to track estimates of the remaining carbon budget and to understand how these estimates can improve over time as scientific knowledge advances. We propose that application of this framework may help to reconcile differences between estimates of the remaining carbon budget and may provide a basis for reducing uncertainty in the range of future estimates.

The critical comments to the publications by the authors ofthe present paper that were given in [10] (the publications deal with the possible effects of gravity field inhomogeneities in the atmosphere and ocean) are discussed. In the authors' opinion, some remarks are groundless. At the same time, the authors agree with one of the important remarks that the results of their paper concerning studies of the ocean disturbances are to be reconsidered. [ABSTRACT FROM AUTHOR]

A low-cost and simple-arranged paper-based microplasma array device made by tape and Xerox paper was presented. Uniform array of discharge can be sustained in Ar, He, and ambient air atmosphere. Stable discharge can be sustained for at least 55 min when plasma is ignited in Ar ambient, based on the examination of time-resolved optical emission spectra. Throughout the conditions investigated, the power consumed by the device was well below 0.3 W. We also demonstrated that stable and uniform discharge can be generated when the device was bent to a radius of curvature of 2.5 mm. [ABSTRACT FROM PUBLISHER]

This article contributes to scholarship in Muslim geographies to show how the Prevent Duty is a racializing and securitizing policy, which exists in an already unequal school space. Through the concept of 'stickiness', it shows how the Prevent Duty creates associations of violence and extremism with gendered Muslim bodies and considers the spatial politics of Prevent Duty training. By attending to the effective nature of Prevent, this paper considers how these policy documents create negative attachments that shape how Muslim teachers experience the school space, as both the implementers and potential targets of the policy. In-depth interviews with current and former teachers working in London schools were conducted in 2018, with a particular focus on the experiences of Muslim teachers. The results indicate that when the Prevent Duty is in circulation, it creates an atmosphere in which 'Muslimness' feels under surveillance, lingering beyond the training space. [ABSTRACT FROM AUTHOR]

Atmospheric carbon dioxide enrichment (eCO 2 ) can enhance plant carbon uptake and growth 1-5 , thereby providing an important negative feedback to climate change by slowing the rate of increase of the atmospheric CO 2 concentration 6 . Although evidence gathered from young aggrading forests has generally indicated a strong CO 2 fertilization effect on biomass growth 3-5 , it is unclear whether mature forests respond to eCO 2 in a similar way. In mature trees and forest stands 7-10 , photosynthetic uptake has been found to increase under eCO 2 without any apparent accompanying growth response, leaving the fate of additional carbon fixed under eCO 2 unclear 4,5,7-11 . Here using data from the first ecosystem-scale Free-Air CO 2 Enrichment (FACE) experiment in a mature forest, we constructed a comprehensive ecosystem carbon budget to track the fate of carbon as the forest responded to four years of eCO 2 exposure. We show that, although the eCO 2 treatment of +150 parts per million (+38 per cent) above ambient levels induced a 12 per cent (+247 grams of carbon per square metre per year) increase in carbon uptake through gross primary production, this additional carbon uptake did not lead to increased carbon sequestration at the ecosystem level. Instead, the majority of the extra carbon was emitted back into the atmosphere via several respiratory fluxes, with increased soil respiration alone accounting for half of the total uptake surplus. Our results call into question the predominant thinking that the capacity of forests to act as carbon sinks will be generally enhanced under eCO 2 , and challenge the efficacy of climate mitigation strategies that rely on ubiquitous CO 2 fertilization as a driver of increased carbon sinks in global forests.

In the last decades, the increase in global industrialization and the consequent technological progress have damaged the quality of the environment. As a consequence, the high levels of hazardous compounds such as metals and gases released in the atmosphere and water, have raised several concerns about the health of living organisms. Today, many analytical techniques are available with the aim to detect pollutant chemical species. However, a lot of them are not affordable due to the expensive instrumentations, time-consuming processes and high reagents volumes. Last but not least, their use is exclusive to trained operators. Contrarily, colorimetric sensing devices, including paper-based devices, are easy to use, providing results in a short time, without particular specializations to interpret the results. In addition, the colorimetric response is suitable for fast detection, especially in resource-limited environments or underdeveloped countries. Among different chemical species, transition and heavy metals such as iron Fe(II) and copper Cu(II) as well as volatile compounds, such as ammonia (NH3) and acetaldehyde (C2H4O) are widespread mainly in industrialized geographical areas. In this work, we developed a colorimetric paper-based analytical device (PAD) to detect different contaminants, including Fe2+ and Cu2+ ions in water, and NH3 and C2H4O in air at low concentrations. This study is a "proof of concept" of a new paper sensor in which the intensity of the colorimetric response is proportional to the concentration of a detected pollutant species. The sensor model could be further implemented in other technologies, such as drones, individual protection devices or wearable apparatus to monitor the exposure to toxic species in both indoor and outdoor environments. [ABSTRACT FROM AUTHOR]

Due to the complexity of the multiple scattering problem for shortwave radiative transfer in Earth's atmosphere, operational physical retrieval algorithms commonly use a plane parallel Radiative Transfer Model (RTM). This so-called One-Dimensional (1-D) assumption allows practical retrieval algorithms to be implemented. In order to understand the impacts of this assumption for low altitude, unresolved clouds observed by OCO-2, the Three-Dimensional (3-D) radiative transfer model SHDOM is used to generate synthetic observations which are then processed by the operational retrieval algorithm based on a 1-D RTM. Simulations are performed over three realistic surface spectral albedos, corresponding to snow, vegetation, and bare soil. The results show that the existing cloud screening algorithm has difficulty identifying sub-Field of View (FOV), unresolved clouds that fill less than half of the FOV. The unresolved clouds introduce a bias in the retrieved CO2 concentration, as quantified by the dry air mole fraction (XCO2). The biases are relatively small (less than 1 ppm) when the albedo at 2.1 µm is high, which is common over bare land surfaces. For cases with low 2.1 µm albedo, such as snow, the bias becomes much larger, up to 5 ppm. These results indicate that the XXCO2 retrieval appears robust to 3-D scattering effects from unresolved low level clouds when the short wave infrared surface albedo is large, but for darker surfaces these clouds can introduce significant biases. [ABSTRACT FROM AUTHOR]

This paper reviews how excessive lighting in historical sites can negatively affect the enjoyment of social gatherings. Because light pollution has the potential to affect socialization negatively, we need the appropriate tools to handle these effects. As part of this research, three techniques were used to analyze these effects: a bibliographical examination of relevant concepts, field measurements of illumination levels at historical sites in Cairo, Egypt, as well as questionnaires sent out to users around the world to determine what influences their perceptions of historical sites at night. Based on the results of a systematic review, we developed the concept of toolkits for creating a lively ambiance for evening events. Furthermore, based on the spatial measurements made in the case study, it was determined that the challenge of visual pollution hinders creating a vibrant atmosphere at historical sites. An online survey that investigated the factors influencing the enjoyment of historical sites at night around the world found that positioning the lighting fixtures and illumination is one of the most critical factors. The results of the current study confirm that the urban form of the context provides a pleasant visual and perceptual experience at night as well. The findings of this study have led to three design considerations that can help urban planners and designers when it comes to implementing lighting in public spaces. As a result of these considerations, the historical site in the case study, Al-Hussein Square, Cairo, presents a livelier ambiance at night; hence they can be used by urban designers to enhance the ambiance in similar settings to the present case study. This toolkit provides valuable insights into how local authorities and citizens can work together to reduce lighting pollution by examining the causes of the pollution. [ABSTRACT FROM AUTHOR]

This paper is intended to summarize the research conducted during the first 2 years of the Dragon 5 project 59,332 (geophysical and atmospheric retrieval from Synthetic Aperture Radar (SAR) data stacks over natural scenarios). Monitoring atmospheric phenomena, encompassing both tropospheric and ionospheric conditions, holds pivotal significance for various scientific and practical applications. In this paper, we present an exploration of advanced techniques for estimating tropospheric and ionospheric phase screens using stacks of Synthetic Aperture Radar (SAR) images. Our study delves into the current state-of-the-art in atmospheric monitoring with a focus on spaceborne SAR systems, shedding light on their evolving capabilities. For tropospheric phase screen estimation, we propose a novel approach that jointly estimates the tropospheric component from all the images. We discuss the methodology in detail, highlighting its ability to recover accurate tropospheric maps. Through a series of quantitative case studies using real Sentinel-1 satellite data, we demonstrate the effectiveness of our technique in capturing tropospheric variability over different geographical regions. Concurrently, we delve into the estimation of ionospheric phase screens utilizing SAR image stacks. The intricacies of ionospheric disturbances pose unique challenges, necessitating specialized techniques. We dissect our approach, showcasing its capacity to mitigate ionospheric noise and recover precise phase information. Real data from the Sentinel-1 satellite are employed to showcase the efficacy of our method, unraveling ionospheric perturbations with improved accuracy. The integration of our techniques, though presented separately for clarity, collectively contributes to a comprehensive framework for atmospheric monitoring. Our findings emphasize the potential of SAR-based approaches in advancing our knowledge of atmospheric processes, thus fostering advancements in weather prediction, geophysics, and environmental management. [ABSTRACT FROM AUTHOR]

In the Earth's atmosphere, greenhouse gases (GHGs) and reactive trace gases are essential components of chemistry–climate interactions. These trace gases are emitted from both natural and anthropogenic sources over terrestrial and marine regions. Air–sea exchange is the dominant process controlling the distribution of several important trace gases over remote marine regions. Although the ocean–atmosphere interface covers ~70% of the Earth's surface, the quantitative air–sea exchange of reactive trace gases is estimated over the limited oceanic regions. The production and air–sea exchange of trace gases are controlled by physical conditions at both sides of the interface and ocean biogeochemistry. The northern Indian Ocean (NIO) experiences strong seasonal monsoon winds and intense tropical cyclones. Consisting of the Arabian Sea and the Bay of Bengal, it is one of the most biologically productive regimes of the world ocean and home to the intense oxygen minimum zone (OMZ) of the Arabian Sea with dissolved oxygen concentrations. Thus, the NIO offers a unique system to investigate the air–sea exchange processes of reactive trace gases. So far, most of the studies of air–sea exchange of trace gases is focused on the Atlantic and Pacific Oceans, while studies over the northern Indian Ocean are very limited and reported mainly for CH4, CO2 and N2O. Although progress has been made in recent years, studies of air–sea exchange of reactive trace gases such as non-methane hydrocarbon (NMHCs), oxygen-, sulfur- and halogen-containing hydrocarbons remain scarce. This paper addresses the current understanding of air–sea exchange processes and fluxes of reactive trace gases, including NMHCs, dimethyl sulfide (DMS), oxygenated volatile organic compounds (OVOCs), halocarbons, carbon monoxide (CO) and ozone (O3) in the northern Indian Ocean. This review summarizes the studies on the air–sea exchange of trace gases over the northern Indian Ocean and common parametrization approaches used to estimate the air–sea flux of gases. Flux range for ethene (3–10.35 µmol m–2 d–1), isoprene (0.215–0.172 µmol m–2 d–1), acetaldehyde (–6.75–11.35 µmol m–2 d–1), acetone (–9–9 µmol m–2 d–1), DMS (0.03–41.4 µmol m–2 d–1) and CO (1.4–5.4 µmol m–2 d–1) over the NIO were summarized from various in-situ and modelling studies. The paper addresses the importance of the northern Indian Ocean apropos the production and exchange of reactive trace gases, the knowledge gaps and the future scientific scope. Additionally, it emphasizes the need for a multidisciplinary study of oceanic reactive trace gas cycling and its impact on regional atmospheric chemistry over the northern Indian Ocean. [ABSTRACT FROM AUTHOR]

A new one‐dimensional variational (1D‐Var) retrieval method for ionospheric GNSS radio occultation (GNSS‐RO) measurements is described. The forward model implicit in the retrieval calculates the bending angles produced by a one‐dimensional ionospheric electron density profile, modeled with multiple "Vary‐Chap" layers. It is demonstrated that gradient based minimization techniques can be applied to this retrieval problem. The use of ionospheric bending angles is discussed. This approach circumvents the need for Differential Code Bias (DCB) estimates when using the measurements. This new, general retrieval method is applicable to both standard GNSS‐RO retrieval problems, and the truncated geometry of EUMETSAT's Metop Second Generation (Metop‐SG), which will provide GNSS‐RO measurements up to about 600 km above the surface. The climatological a priori information used in the 1D‐Var is effectively a starting point for the 1D‐Var minimization, rather than a strong constraint on the final solution. In this paper the approach has been tested with 143 COSMIC‐1 measurements. We find that the method converges in 135 of the cases, but around 25 of those have high "cost at convergence" values. In the companion paper (Elvidge et al., 2023), a full statistical analysis of the method, using over 10,000 COSMIC‐2 measurements, has been made. Plain Language Summary: This paper presents a new way of estimating the density of electrons in the ionosphere—the part of the Earth's atmosphere in which atoms are ionized by radiation from the Sun. Radio signals sent between GNSS navigational satellites and receivers in a low orbit around the Earth are delayed, and their paths are bent, by the presence of electrons in the ionosphere. Previous attempts to use these observations to estimate the electron density have been based on the delay of the signals. The new approach outlined in this paper uses the bending incurred by the radio waves instead. Such "bending angles" have been used to infer some properties of the lower atmosphere for many years, and are widely available. We demonstrate that by extending these measurements to greater heights, they can provide useful information about the ionosphere as well. Key Points: A new method of deriving ionospheric electron densities, using the difference between bending angles at two different frequenciesIt is based on a 1D variational retrieval, the solution of which is the best fit to the a priori background and the observationsThe forward model assumes the ionosphere to consist of several idealized "Vary‐Chap" electron density layers [ABSTRACT FROM AUTHOR]

The ability of plants to uptake nutrients from mineral dust lying on their foliage may prove to be an important mechanism by which plants will cope with increasing CO 2 levels in the atmosphere. This mechanism had only recently been reported and was shown to compensate for the projected dilution in plants ionome. However, this phenomenon has yet to be thoroughly studied, particularly in terms of the expected trends under different dust types and varying atmospheric CO 2 concentrations, as projected by the IPCC. We treated plants grown under ambient (415 ppm) and elevated CO 2 (850 ppm) conditions with either desert dust, volcanic ash, and fire ash analogues by applying it solely on plant foliage and studied their Rare Earth Elements concentrations and patterns. The Rare Earth Elements compositions of the treated plants originated from the dust application, and their incorporation into the plants led to a significant increase in plants vitality, evident in increased photosynthetic activity and biomass. Two trends in the foliar nutrient uptake mechanism were revealed by the Rare Earth Elements, one is that different treatments affected the plant in decreasing order volcanic ash > desert dust > fire ash. The second trend is that foliar intake becomes more significant under elevated CO 2 , an observation not previously seen. This testifies that the use of Rare Earth Elements in the study of foliar nutrient uptake, and other biological mechanisms is fundamental, and that foliar pathways of nutrient uptake will indeed become more dominant with increasing CO 2 under expected atmospheric changes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Per- and polyfluoroalkyl substances (PFAS), often referred to as "forever chemicals", are a class of man-made, extremely stable chemicals, which are widely used in industrial and commercial applications. Exposure to some PFAS is now known to be detrimental to human health. By virtue of PFAS long residence times, they are widely detected in the environment, including remote locations such as the Arctics, where the origin of the PFAS is poorly understood. It has been suggested that PFAS may be transported through contaminated waters, leading to accumulation in coastal areas, where they can be aerosolised via sea spray, thereby extending their geographical distribution far beyond their original source regions. The aim of this work is to investigate, for the first time, whether "forever chemicals" could be transported to areas considered to be pristine, far from coastal sites. This study was performed at the Amazonian Tall Tower Observatory (ATTO), a unique remote site situated in the middle of the Amazon rainforest, where a restricted PFAS, perfluorooctanoic acid (PFOA), was observed with concentrations reaching up to 2 pg/m 3 . A clear trend of increasing concentration with sampling height was observed and air masses from the south over Manaus had the highest concentrations. Atmospheric lifetime estimations, removal mechanisms supported by measurements at two heights (320 and 42 m above the rainforest), and concentration spikes indicated a long-range transport of PFOA to pristine Amazon rainforest. Potential sources, including industrial activities in urban areas, were explored, and historical fire management practices considered. This research presents the first measurements of PFAS in the atmosphere of Amazon rainforest. Remarkably, even in this remote natural environment, appreciable levels of PFAS can be detected. This study provides valuable insights into the long-range transport of the anthropogenic "forever chemical" into a remote natural ecosystem and should raise awareness of potential environmental implications., Competing Interests: Declaration of competing interest The authors declare they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)

β-caryophyllonic acid (BCA), as an important precursor of aqueous secondary organic aerosols (aqSOA), has adverse effects on the atmospheric environment and human health. However, the key atmospheric chemical reaction process in which BCA participates in the formation of aqueous secondary organic aerosols is still unclear. In this study, the reaction mechanism and kinetics of BCA with ·OH and O 3 were investigated by quantum chemical calculations. The initiation reactions between BCA and ·OH include addition and H-abstraction reaction pathways, subsequent intermediates will also react with O 2 , ultimately undergo a cracking reaction to generate small molecular substances. The reaction of BCA with O 3 can generate primary ozone oxides and the Criegee Intermediates oIM3, subsequent main reaction products include keto-BCA, as well as other small molecule aqSOA precursors. The entire reaction process increases the O/C ratio of aqSOA in the aqueous phase and generates products of small molecules such as 4-formylpropionic acid, which plays an important role in the formation of aqSOA. At 298K, the transformation rate constants of BCA initiated by ·OH and O 3 are 1.47 × 10 10  M -1  s -1 and 3.16 × 10 5  M -1  s -1 , respectively, the atmospheric lifetimes of BCA reacting with ·OH range from 0.86 h-5.40 h, while the lifetimes of BCA reacting with O 3 range from 0.44 h-10.04 years. This suggests that BCA primarily reacts with ·OH. However, under higher O 3 concentrations, its ozonolysis becomes significant, promoting the formation of aqSOA. According to the risk assessment, the toxicity of most transformation products (TPs) gradually decreased, but the residual developmental toxicity could not be ignored. In this paper, the atmospheric liquid phase oxidation mechanisms of sesquiterpene unsaturated derived acid were studied from the microscopic level, which has guiding significance for the formation and transformation of aqSOA in atmosphere., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

In this study, we statistically demonstrated that an anomalous high of 40 K fallout in the atmospheric fallout in Kagoshima City is caused by heavy ashfall associated with eruptions of Sakurajima volcano. Sakurajima is one of the most active volcanoes in Japan, and its repeated explosive eruptions cause large amounts of ash to fall on Kagoshima City. The fallout of crust-derived natural radionuclides, 40 K, 212 Pb, and 214 Bi, from the atmosphere in Kagoshima City showed a significant correlation with the number of eruptions of Sakurajima volcano and the amount of ashfall in Kagoshima City. In contrast, no significant correlation was found between 40 K and 7 Be fallout. The 40 K fallout indicates that almost all of the atmospheric fallout in Kagoshima City is composed of volcanic ash particles. The contribution from mineral and sea salt particles other than volcanic ash is minimal. The mass balance of the observed 40 K fallout, ashfall, and atmospheric fallout yield indicates that there is a significant amount of volcanic ash deposition that is not accounted for as ashfall. In most cases, the ash deposition observed as ashfall is only 30-70 wt% of the total deposition collected as atmospheric fallout samples, and the remaining portion is fine-grained and behaves as suspended volcanic ash particles, which significantly impact the atmospheric environment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Here we present the UCI Fluxtron, a cost-effective multi-enclosure dynamic gas exchange system that provides an adequate level of control of the experimental conditions for investigating biosphere-atmosphere exchange of trace gases. We focus on the hardware and software used to monitor, control, and record the air flows, temperatures, and valve switching, and on the software that processes the collected data to calculate the exchange flux of trace gases. We provide the detailed list of commercial materials used and also the software code developed for the Fluxtron, so that similar dynamic enclosure systems can be quickly adopted by interested researchers. Furthermore, the two software components -Fluxtron Control and Fluxtron Process- work independently of each other, thus being highly adaptable for other experimental designs. Beyond plants, the same experimental setup can be applied to the study of trace gas exchange by animals, microbes, soil, or any materials that can be enclosed in a suitable container., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Glacial bodies in the Peruvian Andes Mountains store and supply freshwater to hundreds of thousands of people in central Peru. Atmospheric black carbon (BC) is known to accelerate melting of snow and ice, in addition to contributing to air pollution and the health of people. Currently there is limited understanding on the sources and temporal variability of BC in valley and mountain environments in Peru. To address this problem, this study combined surface observations of BC collected during 2022-2023 with WRF model simulations and HYSPLIT trajectories to analyze the dispersion and sources of BC in valley and high elevation environments and the associated local atmospheric circulations. Results show high BC concentrations are associated with the valley-mountain wind system that occurs on both sides of the Huaytapallana mountain range. A pronounced circulation occurs on the western slopes of Huaytapallana when concentrations of BC increase during daylight hours, which transports atmospheric pollutants from cities in the Mantaro River Valley to the Huaytapallana mountain range. Low concentrations of BC are associated with circulations from the east that are channeled by the pronounced ravines of the Andes-Amazon transition. On average, during the season of highest BC concentrations (July-November), the relative contributions of fossil fuels are dominant to biomass burning at the valley observatory and are slightly lower at the Huaytapallana observatory. These results demonstrate the need to promote mitigation actions to reduce emissions of BC and air pollution associated with forest fires and local anthropogenic activity., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Elver Villalobos Puma reports was provided by National Institute for Research on Glaciers and Mountain Ecosystems. Elver Villalobos-Puma reports a relationship with National Institute for Research on Glaciers and Mountain Ecosystems that includes: employment. Elver Villalobos-Puma has patent pending to Lincensee. co-author previously employed by INAIGEM Company-A.M If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Lake Erhai is a potentially phosphorus (P)-limited lake and its water quality may have been affected by atmospheric P deposition. However, there have been few studies on atmospheric P deposition in this lake. In this study, we established five wet deposition monitoring sites and two dry deposition monitoring sites around Lake Erhai to quantify the wet and dry deposition of total phosphorus (TP), including dissolved inorganic phosphorus (DIP), dissolved organic phosphorus (DOP) and particulate phosphorus (PP) from July 2022 to June 2023. Wet deposition fluxes of P species were collected by automatic rainfall collection instrument, and dry deposition fluxes were estimated using airborne concentration measurements and inferential models. The results reveal that among the different P components, DOP had the highest contribution (50%) to wet TP deposition (average all sites 12.7 ± 0.7 mg P m 2 /yr), followed by PP (40%) and DIP (10%). Similarly, DOP (51%) was the major contributor to dry TP deposition (average two sites 2.4 ± 0.9 mg P m 2 /yr), followed by DIP (35%) and PP (14%). Wet deposition dominated the annual total TP deposition (wet plus dry), accounting for approximately 83%. The key seasons for dry deposition were spring and autumn, which accounted for 64% of the annual total dry TP deposition. In comparison, wet deposition was significantly higher in the summer, accounting for 73% of the annual total wet TP deposition. The results of the potential source contribution function and concentration-weighted trajectories analysis indicate that local source emission and long-range transport from surrounding cities jointly exerted a substantial influence on aerosol P concentrations, particularly in the eastern and northwestern regions of the lake. These findings provide a comprehensive understanding of the different P components in atmospheric deposition, which is beneficial for developing effective strategies to manage the P cycle in Lake Erhai., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Triphenyl phosphate (TPhP) and transition metal elements have been ubiquitously detected in the atmosphere, which can participate in atmospheric chemical reactions and induce damage to human health. Currently the understanding of TPhP degradation, transformation and cytotoxicity on atmospheric particles surface are still limited. Therefore, this study used laboratory simulation methods to investigate the influence of irradiation time, transition metal salts, relative humidity (RH) to TPhP degradation, transformation and relative cytotoxicity. TPhP was coated on particle surfaces of four transition metal salts (MnSO 4 , CuSO 4 , FeSO 4 and Fe 2 (SO 4 ) 3 ) in the experiment. Within 12 h irradiation, the significant TPhP photodegradation can be observed on all particles surface. Among these influence factors, the irradiation and RH were the crucial aspects to TPhP degradation, which primarily affect the OH concentration in the atmosphere. The transition metal elements only exhibited slightly catalytic effect to TPhP degradation. The mechanism study indicated that the major degradation products of TPhP are diphenyl hydrogen phosphate (DPhP) and OH-DPhP, which originated from the phenoxy bond cleavage and hydroxylation of TPhP induced by OH. As for the cytotoxicity to A549 cells, all the transition metal particles coated with TPhP can cause cellular injury, which was chiefly induced by the transition metal salt. The possible cytotoxicity mechanism of these particles to A549 cells can be attributed to the excessive reactive oxygen species (ROS) production. This study may provide a further understanding of TPhP degradation and related cytotoxicity with the coexistent transition metal salts in the atmosphere., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The Earth's atmosphere contains ultrafine particles known as aerosols, which can be either liquid or solid particles suspended in gas. These aerosols originate from both natural sources and human activities, termed primary and secondary sources respectively. They have significant impacts on the environment, particularly when they transform into ultrafine particles or aerosol nanoparticles, due to their extremely fine atomic structure. With this context in mind, this review aims to elucidate the fundamentals of atmospheric-derived aerosol nanoparticles, covering their various sources, impacts, and methods for control and management. Natural sources such as marine, volcanic, dust, and bioaerosols are discussed, along with anthropogenic sources like the combustion of fossil fuels, biomass, and industrial waste. Aerosol nanoparticles can have several detrimental effects on ecosystems, prompting the exploration and analysis of eco-friendly, sustainable technologies for their removal or mitigation.Despite the adverse effects highlighted in the review, attention is also given to the generation of aerosol-derived atmospheric nanoparticles from biomass sources. This finding provides valuable scientific evidence and background for researchers in fields such as epidemiology, aerobiology, and toxicology, particularly concerning atmospheric nanoparticles., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The main purpose of this study is to evaluate the near-zero wind velocity measurement performance of two separate 1.5 μm all-fiber coherent Doppler lidars (CDL). The performance characterization is performed through the presentation of the results from two separate atmospheric field campaigns. In one campaign, a recently developed continuous wave (CW) CDL benefiting from an image-reject front-end was deployed. The other campaign utilized a different CW CDL, benefiting from a heterodyne receiver with intermediate frequency (IF) sampling. In both field campaigns the results are compared against a sonic anemometer, as the reference instrument. The measurements clearly show that the image-reject architecture results in more accurate measurements of radial wind velocities close to zero. Close-to-zero velocities are usually associated with the vertical component of the wind and are important to characterize. [ABSTRACT FROM AUTHOR]

This work presents a new iterative method for optimally selecting a vertical retrieval grid based on the location of the information content while accounting for inter-level correlations. Sample atmospheres initially created to parametrise the RTTOV forward model are used to compare the presented iterative vertical selection method with two other common approaches, which are using levels of equal vertical spacing and selecting levels based on the cumulative trace of the averaging kernel matrix (AKM). This new method is shown to outperform compared methods for synthesized profile retrievals with IASI of temperature, H2O, O3, CH4, and CO. However, the benefits of using the more complicated iterative approach compared to the simpler method of referencing the cumulative trace of the AKM are slight and may not justify the added effort. Furthermore, comparing retrievals using a globally optimized static grid vs. an atmosphere specific one shows that a static grid is likely appropriate for retrievals of O3, CH4, and CO. However, developers of temperature and H2O retrieval schemes may at least consider using adaptive or location specific vertical retrieval grids. [ABSTRACT FROM AUTHOR]

Carbon dioxide exchange between the atmosphere and forested subtropical wetlands is largely unknown. Here we report a first step in characterizing this atmospheric-ecosystem carbon (C) exchange, for cypress strands and pine forests in the Greater Everglades of Florida as measured with eddy covariance methods at three locations (Cypress Swamp, Dwarf Cypress and Pine Upland) for one year. Links between water and C cycles are examined at these three sites, and methane emission measured only at the Dwarf Cypress site. Each forested wetland showed net C uptake (retained in the soil and biomass or transported laterally via overland flow) from the atmosphere monthly and annually. Net ecosystem exchange (NEE) of carbon dioxide (CO2) (difference between photosynthesis and respiration, with negative values representing net ecosystem uptake) was greatest at the Cypress Swamp (-1000 gCm-2 year-1), moderate at the Pine Upland (-900 gCm-2 year-1), and least at the Dwarf Cypress (-500 gCm-2 year-1). Methane emission was a negligible part of the C (12 gCm-2 year-1) budget when compared to NEE. However, methane (CH4) production was considerable in terms of global warming potential, as about 20 g CH4 emitted per m² year was equivalent to about 500 g CO2 emitted per m² year. Changes in NEE were clearly a function of seasonality in solar insolation, air temperature and water availability from rainfall. We also note that changes in the satellite-derived enhanced-vegetation index (EVI) served as a useful surrogate for changes in net and gross atmospheric-ecosystem C exchange at these forested wetland sites. [ABSTRACT FROM AUTHOR]

This article explores the overlooked history of atmospheric electricity in the last third of the nineteenth century, delineating the work of Austrian physicist Franz Exner and German schoolteachers Julius Elster and Hans Geitel, and identifying the consequences of their work for twentieth-century physics. Since the earliest days of electrical science, the constant electrification of the atmosphere had been a persistent puzzle, with histories by historians and physicists alike typically focusing on what came after the discovery of gaseous ions in the atmosphere in 1899: cosmic rays, radioactivity, particle physics, and quantum phenomena. I argue that Exner and Elster and Geitel's creative work in atmospheric electricity before 1899 provided the essential conditions for these twentieth-century discoveries. Their divergent theories, experiments, instruments, and environments, developed to understand the origins of the atmosphere's electrification, provided a setting for new ideas about charge, determinism, and measurement to arise. This paper expands on the existing scholarship that has pointed to the fruitful interactions between physics and meteorology in British contexts in this period. In disentangling Exner's and Elster and Geitel's differing views on geographical and meteorological conditions I offer a new perspective on the recent vertical turn in the history of science. The paper concludes by suggesting that while the ionic revolution of 1899 was foundational for much of twentieth-century physics, it constituted a significant theoretical undoing for atmospheric electricians, leaving the field with even less understanding of the atmosphere's electrification than before. [ABSTRACT FROM AUTHOR]

The annual average CO2 difference between baseline data from Mauna Loa and the southern Hemisphere increased by ~ 0.8 µmolmol-1 (0.8 ppm) between 2009 and 2010, a step unprecedented in over 50 years of reliable data. We find no evidence for coinciding, sufficiently large and rapid, source/sink changes. A statistical anomaly is unlikely due to the highly systematic nature of the variation in observations. An explanation for the step, and the subsequent 5 year stability in this north-south difference, involves inter-hemispheric atmospheric exchange variation. The selected data describing this episode provide a critical test for studies that employ atmospheric transport models that interpret global carbon budgets and inform management of anthropogenic emissions. [ABSTRACT FROM AUTHOR]

The atmospheric boundary layer (ABL) exhibit multilayered thermal structure especially in polar atmosphere during extreme winters. These thermal inversions are originated based on the combined forcing of local and large scale synoptic meteorology. At the local scale the thermal inversion layer forms near the surface and plays a central role in controlling the surface radiative cooling; however, depending upon the large scale synoptic meteorological forcing, an upper level thermal inversion can also exist topping the local ABL. In this article a numerical methodology is developed to determine all-thermal inver sion layers present in a given temperature profile and deduce some of their thermodynamic properties. The algorithm extract from the temperature profile the most important temperature variations defining thermal layers. This is accomplished by a linear interpolation function of variable length that minimizes an error function. The algorithm functionality is demonstrated on actual radiosonde profiles to deduce all-present inversion layers with an error fraction set independently. [ABSTRACT FROM AUTHOR]

This paper describes an attempt to use data obtained from sodar (sound detection and ranging) for short-term forecasting of PM 10 concentration levels in Krakow. Krakow is one of the most polluted cities in central Europe (CE) in terms of PM 10 concentration. This is due to the high municipal emissions. Thanks to intensive corrective actions taken by the city authorities, these are being effectively eliminated, but the unfavourable topographic location of the city limits natural ventilation. The article describes all these conditions, focusing on presenting the method of short-term correction of air quality for the time needed to take quick corrective actions by the city authorities in the event of anticipated exceedances of the permissible values. Based on several years of measurements of the physical properties of the atmosphere with sodar, the authors of the paper suggest that sodar data could be considered for operational use to generate short-term predictions. The proposed method is based on the use of the spectrum, i.e. the set of amplitudes of signals returning to the sodar receiver from the reflection of a single-frequency sound transmission and its characteristic properties depending on the physical state of the atmosphere. Similar spectra were parameterised with a single numerical value using statistical methods. It was found that, in some cases preceding high concentrations of PM 10 , the spectral parameters had similar values. This made it possible to develop a forecasting method for such concentrations by using data mining to search for conditions in historical data closest to the state of the atmosphere at the time of forecasting. In this part of the study, data from 2017–2018 were used. In the next step, three methods of using the sodar data developed for PM 10 prediction were proposed, comparing them with the method without sodar use. The study results were tested on independent material using data concerning the episodes of high concentrations of pollutants from October 2021 to March 2022 in Krakow. The findings were considered to be encouraging, also taking into account the speed and low cost of preparing the forecast. [ABSTRACT FROM AUTHOR]

This paper presents research results on CO2 emissions originating from maritime vessels with various main engine settings. The impact (i.e., the volume and amount) of gas emissions into the environment is shown, along with the characteristics of the marine fuel used. This research was carried out on a container vessel sailing on a fixed route between Rotterdam and St. Petersburg. It covered mainly two different engine operations, at 124 RPM and 100 RPM settings, in the Kiel Canal area. The purpose of this study is to demonstrate that the engine setting of 100 RPM compared to the same voyage through the Kiel Canal, with an engine setting of 124 RPM, leads to a significant reduction of CO2 emissions. Though proving such a thesis seems to be evident, the analysis in the paper shows that, in practice, mainly due to time constraints and engineers' assumptions of engine technical status, the higher speeds are still preferred over lower ones. In studies not related to passive use or active methods, only specific and simplest methods of obtaining CO2 emissions are presented. [ABSTRACT FROM AUTHOR]

Optical beam propagation through the atmosphere is suffering from turbulence condition and scattering due to the refractive index effects on propagation. In this paper, we study optical beam propagation under the UAE's weather conditions. An outdoor test was carried out to gather the atmosphere parameters (temperature, wind, humidity, and refractive index) and feed them to a beam propagation model. The beam centroid was determined to study and predict the effects on it at different periods of the day. [ABSTRACT FROM AUTHOR]

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The paper aims to analyze the influence of the stand characteristics in two areas of the Lunca Mureşului Natural Park, on the main greenhouse gases in the atmosphere (O3, NH3, NO2). In the first part, an extensive bibliographic study was carried out, regarding similar research referring to greenhouse gases in generally and O3, NH3 and NO2 in specially, and the relation of these greenhouse gases to forest vegetation. The working method regarding data collection in the period 2014-2019, the types of gases analyzed, the types of collection pads used, the exposure times of the collection pads were presented, together with the working method for data processing. The results were obtained by analyzing relation of certain characteristics of the stand (age, volume, stand density) with concentration of studied greenhouse gases on vegetation season from the period 2014-2019. The obtained results were discussed in the context of other current research in the field and the most important aspects were presented as conclusions at the end of the paper. [ABSTRACT FROM AUTHOR]

Understanding the transport of 137 Cs emitted during the Fukushima accident is challenging because the critical emissions that produced the high-deposition area are not adequately resolved in existing source terms. This paper presents an objective inverse reconstruction of these emissions by fusing atmospheric concentrations with a-priori emissions extracted from total depositions. This extraction, previously considered impossible for complex real-world accidents, is achieved by identifying the critical temporal formation process of depositions in the high-deposition area and estimating the corresponding emissions by using an atmospheric transport model. The reconstructed source term reveals two emission peaks from 10:00-11:00 and 14:00-15:00 on March 15, which agree with the in situ pressure measurements and accident analysis, suggesting that they came from pressure drops in the primary containment vessels of Units 3 and 2, respectively. This finding explains the environmental observations of spherical 137 Cs particles. The source term also objectively and independently confirms the widely used reverse estimate. The corresponding 137 Cs transport simulations better match the various observations than those produced by other source terms, proving that the two-peak emission creates a high-deposition area. The proposed method outperforms the direct fusion of deposition and atmospheric concentration observations, providing a robust tool for multiobservation fusion.

Beryllium-7 activity concentrations in the atmosphere and precipitation were continuously measured every day between April 2011 and December 2015 in Dazaifu, western Japan. The measured data were quantitatively analyzed to determine the precipitation-induced variation in 7 Be activity concentrations. The average concentrations on nonprecipitation and precipitation days were 5.5 and 3.8 mBq/m 3 , respectively. This difference of 31% (1.7 mBq/m 3 ) on average, was attributable to the washout effect, which was more significant in the summer. Regarding the association between 7 Be activity concentration and precipitation, the concentration remained at a similar level for the small precipitation amount of <5.0 mm/day and showed a decreasing trend (but was insignificant) for the precipitation of 5.0-10.0 mm/day. A significant decrease in the concentration was observed for ≥10 mm/day. Furthermore, when precipitation occurred on two successive days, the 7 Be activity concentrations on the second day significantly decreased regardless of precipitation., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Plutonium, as well as fission products such as 137 Cs, had been released into the earth environment in 1945 after the first atmospheric nuclear explosion of plutonium bomb in the desert of New Mexico (USA, July 16) and later over Nagasaki (August 9), followed then by many other explosions. Thus, plutonium cycling in the atmosphere and ocean has become a major public concern as a result of the radiological and chemical toxicity of plutonium. However, plutonium isotopes and 137 Cs are important transient tracers of biogeochemical and physical processes in the environment, respectively. In this review, we show that both physical and chemical approaches are needed to comprehensively understand the behaviors of plutonium in the atmosphere and ocean. In the atmosphere, plutonium and 137 Cs attach with aerosols; thus, plutonium moves according to physical and chemical processes in connection with aerosols; however, since plutonium is a chemically reactive element, its behavior in an aqueous environment is more complicated, because biogeochemical regulatory factors, in addition to geophysical regulatory factors, must be considered. Meanwhile, 137 Cs is chemically inert in aqueous environments. Therefore, the biogeochemical characteristics of plutonium can be elucidated through a comparison with those of 137 Cs, which show conservative properties and moves according to physical processes. Finally, we suggest that monitoring of both plutonium and 137 Cs can help elucidate geophysical and biogeochemical changes from climate changes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)

The interactions of the micro-mechanism of hydroxymethanesulfonic acid (HMSA) with the typical small organic molecule in atmospheric (X = methanol, formaldehyde, formic acid, methyl formate, dimethyl ether, acetone) has been investigated by density functional theory (DFT), quantum theory of atoms in molecules (QTAIM), Generalized Kohn-Sham Enery Decomposition Analysis (GKS-EDA) and the atmospheric clusters dynamic code (ACDC). The results of DFT show that the stable six- to eight-membered ring structures are easily formed in HMSA-X clusters. According to the topological analysis results of the AIM theory and the IRI method, a strong hydrogen bonding interaction is present in the complex. GKS-EDA results show that electrostatic energy is the main contributor to the interaction energy as it accounts for 51 %-55 % of the total attraction energy. The evaporation rates of HMSA-HMSA and HMSA-HCOOH clusters were much lower than those of the other HMSA complexes. In addition, the Gibbs energy of formation (ΔG) of HMSA-X dimers is investigated under atmosphere temperature T = 217-298 K and p = 0.19-1.0 atm, the ΔG decreased with decreasing of the atmosphere temperature and increased with the decrease of atmospheric pressure, indicating that the low temperature and high pressure may significantly facilitate to the formation of dimers., Competing Interests: Declaration of competing interest First of all, thank you very much for your busy schedule to view the submitted manuscripts. I confirm that this manuscript has not been submitted to some other journal. There are no financial conflicts to declare, I guarantee that the above statement is true, and I shall bear corresponding responsibilities arising from any violation of the statement therefrom. All data is provided in full in the results section of this paper. I guarantee that the above statement is true, and I shall bear corresponding responsibilities arising from any violation of the statement therefrom., (Copyright © 2024 Elsevier Inc. All rights reserved.)

CH 4 serves as an important greenhouse gas, yet limited knowledge is available in global and regional CH 4 cycling, particularly in widely distributed karst terrain. In this study, we investigated an upland in Puding Karst Ecosystem Research Station, and explored CH 4 concentration and/or flux in atmosphere, soil and cave using a closed static chamber method and an eddy covariance system. Meanwhile, we monitored atmospheric temperature, precipitation, temperature and wind velocity in the cave entrance. The results demonstrated that atmospheric CH 4 and actual soil CH 4 fluxes in the source area of eddy covariance system were -0.19 ± 8.64 nmols -1 m -2 and -0.16 nmols -1 m -2 respectively. The CH 4 concentrations in Shawan Cave exhibited 10 ∼ 100-fold lower than that of the external atmosphere. CH 4 oxidation rate dominated by methane-oxidizing bacteria was 1.98 nmols -1 m -2 in Shawan Cave when it combined with temperature difference between cave and external atmosphere. Therefore, CH 4 sink in global karst subterranean spaces was estimated at 106.2 Tg CH 4 yr -1 . We supplemented an understanding of CH 4 cycling paths and fluxes in karst terrain, as well as CH 4 sinks in karst subterranean space. Further works require to establish a karst ecosystem observation network to conduct long-term integrated studies on CH 4 fluxes regarding atmosphere, soils, plants and caves., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Anthropogenic shifts in seas are reshaping fishing trends, with significant implications for aquatic food sources throughout this century. Examining a 21-year abundance dataset of Argentine shortfin squids Illex argentinus paired with a regional oceanic analysis, we noted strong correlations between squid annual abundance and sea surface temperature (SST) in January and February and eddy kinetic energy (EKE) from March to May in the Southwest Atlantic. A deeper analysis revealed combined ocean-atmosphere interactions, pinpointed as the primary mode in a rotated empirical orthogonal function analysis of SST. This pattern produced colder SST and amplified EKE in the surrounding seas, factors crucial for the unique life stages of squids. Future projections from the CMIP6 archive indicated that this ocean-atmosphere pattern, referred to as the Atlantic symmetric pattern, would persist in its cold SST phase, promoting increased squid abundance. However, rising SSTs due to global warming might counteract the abundance gains. Our findings uncover a previously unrecognized link between squids and specific environmental conditions governed by broader ocean-atmosphere interactions in the Southwest Atlantic. Integrating these insights with seasonal and decadal projections can offer invaluable information to stakeholders in squid fisheries and marine conservation under a changing climate., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.)