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At least 271 records · Page 15Linked to original sources

Linking field-based metabolomics and chemical analyses to prioritize contaminants of emerging concern in the Great Lakes basin

The ability to focus on the most biologically relevant contaminants affecting aquatic ecosystems can be challenging because toxicity-assessment programs have not kept pace with the growing number of contaminants requiring testing. Because it has proven effective at assessing the biological impacts of potentially toxic contaminants, profiling of endogenous metabolites (metabolomics) may help screen out contaminants with a lower likelihood of eliciting biological impacts, thereby prioritizing the most biologically important contaminants. The authors present results from a study that utilized cage-deployed fathead minnows ( Pimephales promelas ) at 18 sites across the Great Lakes basin. They measured water temperature and contaminant concentrations in water samples (132 contaminants targeted, 86 detected) and used 1 H-nuclear magnetic resonance spectroscopy to measure endogenous metabolites in polar extracts of livers. They used partial least-squares regression to compare relative abundances of endogenous metabolites with contaminant concentrations and temperature. The results indicated that profiles of endogenous polar metabolites covaried with at most 49 contaminants. The authors identified up to 52% of detected contaminants as not significantly covarying with changes in endogenous metabolites, suggesting they likely were not eliciting measurable impacts at these sites. This represents a first step in screening for the biological relevance of detected contaminants by shortening lists of contaminants potentially affecting these sites. Such information may allow risk assessors to prioritize contaminants and focus toxicity testing on the most biologically relevant contaminants. Environ Toxicol Chem 2016;35:2493–2502.

Environmental Toxicology and Chemistry

Emerging and historical contaminants detected in desert rodents collected near a low‐level radioactive waste site

In an effort to determine contaminant presence, concentrations, and movement from a low‐level radioactive waste (LLRW) burial disposal site to ecosystems in the surrounding area, a study was developed to assess concentrations of per‐ and polyfluoroalkyl substances (PFAS), polychlorinated biphenyls (PCBs), and tritium. To complete this assessment small mammals, vegetation, soil, and insect samples were collected from areas within and adjacent to the Beatty, Nevada, LLRW site and from a reference area located approximately 3 km south of the LLRW site. Samples underwent analysis via liquid chromatography tandem mass spectrometry, gas chromatography mass spectrometry, or scintillation spectroscopy depending on the analyte of interest. Small mammal tissues showed maximum concentrations of over 1700 ng/g for PFAS, 1600 ng/g for PCBs, and 10 000 Bq/kg for tritium. The primary contaminants found in soil samples were PCBs, with maximum concentrations exceeding 25 ng/g. Trace amounts of PFAS were also detected in soils and insects. Only qualitative data were obtained from vegetation samples because of the complex matrix of the dominant plant species (creosote bush; Larrea tridentata [Sessé & Moc. ex DC.] Coville). Overall, these data indicate the presence of various anthropogenic contaminants in the ecosystem surrounding the LLRW area, but additional analyses are necessary to confirm the sources and migration pathways of PFAS and PCBs in this hyperarid environment. Environ Toxicol Chem 2020;00:1–8. © 2020 SETAC

Nevada

Effects of humic substances on the bioconcentration of polycyclic aromatic hydrocarbons: Correlations with spectroscopic and chemical properties of humic substances

The presence of dissolved humic substances (HS, fulvic and humic acids) generally reduces the up take of hydrophobic organic compounds into aquatic organisms. The extent of this effect depends both on the concentration and on the origin of the HS. The aim of this study was to investigate the role of qualitative differences between HS from different origins. The effects of seven different HS on the bioconcentration of pyrene and benzo[ a ]pyrene (B a P) in the nematode Caenorhabditis elegans were related to the spectroscopic and chemical properties of the HS. The effect of each humic material on the bioconcentration of pyrene or B a P was quantified as a “biologically determined” partition coefficient K DOC . We observed significant linear relationships between K DOC and the atomic H/C ratio, the specific absorptivity at 254 nm, the content of aromatic carbons (as determined by 13 C nuclear magnetic resonance spectroscopy, the copper-complexing capacity, the content of phenolic OH groups, and the molecular weight of the HS. There was no discernible relationship of K DOC with the atomic (N + O)/C ratio, an indicator of the polarity of HS. Taken together, our results show that the variability in the effects of HS from different origins could be related to variations in bulk properties of the HS. Parameters describing the aromaticity of the humic materials seemed to be most useful for estimating effects of HS on the bioconcentration of pyrene and B a P.

Environmental Toxicology and Chemistry

Mineralogical Approaches to Sourcing Pipes and Figurines from the Eastern Woodlands, U.S.A.

Provenance studies of stone artifacts often rely heavily upon chemical techniques such as neutron activation analysis. However, stone specimens with very similar chemical composition can have different mineralogies (distinctive crystalline structures as well as variations within the same mineral) that are not revealed by multielemental techniques. Because mineralogical techniques are often cheap and usually nondestructive, beginning with mineralogy allows the researcher to gain valuable information and then to be selective about how many samples are submitted for expensive and somewhat destructive chemical analysis, thus conserving both valuable samples and funds. Our University of Illinois team of archaeologists and geologists employs Portable Infrared Mineral Analyzer (PIMA) spectroscopy, X-ray diffraction (XRD), and Sequential acid dissolution/XRD/Inductively coupled plasma (SAD-XRD-ICP) analyses. Two case studies of Hopewellian pipes and Mississippian figurines illustrate this mineralogical approach. The results for both studies identify sources relatively close to the sites where the artifacts were recovered: Sterling, Illinois (rather than Ohio) for the (Hopewell) pipes and Missouri (rather than Arkansas or Oklahoma) for the Cahokia figurines. ?? 2002 Wiley Periodicals, Inc.

Geoarchaeology - An International Journal

Microplastic concentrations in two Oregon bivalve species: Spatial, temporal, and species variability

Microplastics are an ecological stressor with implications for ecosystem and human health when present in seafood. We quantified microplastic types, concentrations, anatomical burdens, geographic distribution, and temporal differences in Pacific oysters ( Crassostrea gigas ) and Pacific razor clams ( Siliqua patula ) from 15 Oregon coast, U.S.A. sites. Microplastics were present in organisms from all sites. On average, whole oysters and razor clams contained 10.95 ± 0.77 and 8.84 ± 0.45 microplastic pieces per individual, or 0.35 ± 0.04 pieces g −1 tissue and 0.16 ± 0.02 pieces g −1 tissue, respectively. Contamination was quantified but not subtracted. Over 99% of microplastics were fibers. Material type was determined using Fourier‐transform infrared spectroscopy. Spring samples contained more microplastics than summer samples in oysters but not razor clams. Our study is the first to document microplastics in Pacific razor clams and provides important coast‐wide data to compare microplastic burden across species, seasons, and sites.

Oregon

Three new calcium formate reference materials for δ13C measurements and a redetermination of the R(13C/12C) ratio for VPDB based on proton nuclear magnetic resonance measurements

Rationale Isotope ratio mass spectrometry (IRMS) and proton nuclear magnetic resonance ( 1 H NMR) spectroscopy are independent techniques for determining the isotope ratio R ( 13 C/ 12 C) in organic compounds. However, the lack of suitable reference materials has limited intercalibration of results from these methods. Methods Three high-purity calcium formate isotopic reference materials were developed, each ideal for accurate isotope ratio measurements by both 1 H NMR and isotope-ratio mass spectrometry (IRMS). For each material, R ( 13 C/ 12 C) was determined by 1 H NMR, and the relative isotope abundance ( δ 13 C VPDB-LSVEC ) by IRMS. The combined IRMS and NMR results were used to determine the R ( 13 C/ 12 C) value of Vienna Peedee belemnite (VPDB). Results The combined datasets yield a value for R ( 13 C/ 12 C) of 0.0111050 ± 0.0000047 ( k = 2) for VPDB, which is 6.7‰ lower than the commonly cited value of 0.011180, but similar to other recent determinations. These three calcium formate reference materials exhibit high accuracy across both analytical methods and provide robust tools for instrument calibration, method validation, and inter-laboratory comparison in carbon stable isotope ratio analysis. Conclusions An accurate R ( 13 C/ 12 C) value for VPDB strengthens the link between relative ( δ 13 C VPDB-LSVEC ) values from IRMS and R ( 13 C/ 12 C) isotope ratios from NMR and other techniques. These three calcium formate isotopic reference materials (USGS106, USGS107, and USGS108) are available from the US Geological Survey and provide reference materials for calibration, method validation, and inter-laboratory comparison in carbon isotope ratio analysis.

Rapid Communications in Mass Spectrometry

Spectrally based bathymetric mapping of a dynamic, sand‐bedded channel: Niobrara River, Nebraska, USA

Methods for spectrally based mapping of river bathymetry have been developed and tested in clear‐flowing, gravel‐bed channels, with limited application to turbid, sand‐bed rivers. This study used hyperspectral images and field surveys from the dynamic, sandy Niobrara River to evaluate three depth retrieval methods. The first regression‐based approach, optimal band ratio analysis (OBRA), paired in situ depth measurements with image pixel values to estimate depth. The second approach used ground‐based field spectra to calibrate an OBRA relationship. The third technique, image‐to‐depth quantile transformation (IDQT), estimated depth by linking the cumulative distribution function (CDF) of depth to the CDF of an image‐derived variable. OBRA yielded the lowest depth retrieval mean error (0.005 m) and highest observed versus predicted R 2 (0.817). Although misalignment between field and image data did not compromise the performance of OBRA in this study, poor georeferencing could limit regression‐based approaches such as OBRA in dynamic, sand‐bedded rivers. Field spectroscopy‐based depth maps exhibited a mean error with a slight shallow bias (0.068 m) but provided reliable estimates for most of the study reach. IDQT had a strong deep bias but provided informative relative depth maps. Overprediction of depth by IDQT highlights the need for an unbiased sampling strategy to define the depth CDF. Although each of the techniques we tested demonstrated potential to provide accurate depth estimates in sand‐bed rivers, each method also was subject to certain constraints and limitations.

Nebraska

Using laser micro mass spectrometry with the LAMMA-1000 instrument for monitoring relative elemental concentrations in vitrinite

The variation in relative elemental concentrations among a series of coal macerals belonging to the vitrinite maceral group was determined using laser micro mass spectrometry (LAMMS). Variations in Ba, Cr, Ga, Sr, Ti, and V concentrations among the coals were determined using the LAMM A-1000 instrument. LAMMS analysis is not limited to these elements; their selection illustrates the application of the technique. Ba, Cr, Ga, Sr, Ti, and V have minimal site-to-site variance in the vitrinite macerals of the studied coals as measured by LAMMS. The LAMMS data were compared with bulk elemental data obtained by instrumental neutron activation analysis (INAA) and D. C. arc optical emission spectroscopy (DCAS) in order to determine the reliability of the LAMMS data. The complex nature of the ionization phenomena in LAMMS and the lack of standards characterized on a microscale makes obtaining quantitative elemental data within the ionization microvolume difficult; however, we demonstrate that the relative variation of an element among vitrinites from different coal beds in the eastern United States can be observed using LAMMS in a "bulk" mode by accumulating signal intensities over several microareas of each vitrinite. Our studies indicate gross changes (greater than a factor of 2 to 5 depending on the element) can be monitored when the elemental concentration is significantly above the detection limit. "Bulk" mode analysis was conducted to evaluate the accuracy of future elemental LAMMS microanalyses. The primary advantage of LAMMS is the inherent spatial resolution, ~ 20 ??m for coal. Two different vitrite bands in the Lower Bakerstown coal bed (CLB-1) were analyzed. The analysis did not establish any certain concentration differences in Ba, Cr, Ga, Sr, Ti, and V between the two bands. ?? 1988 Springer-Verlag.

Mikrochimica Acta

Application of epithermal neutron activation in multielement analysis of silicate rocks employing both coaxial Ge(Li) and low energy photon detector systems

The instrumental activation analysis of silicate rocks using epithermal neutrons has been studied using both high resolution coaxial Ge(Li) detectors and low energy photon detectors, and applied to the determination of 23 elements in eight new U.S.G.S. standard rocks. The analytical use X-ray peaks associated with electron capture or internal conversion processes has been evaluated. Of 28 elements which can be considered to be determinable by instrumental means, the epithermal activation approach is capable of giving improved sensitivity and precision in 16 cases, over the normal INAA procedure. In eleven cases the use of the low energy photon detector is thought to show advantages over convertional coaxial Ge(Li) spectroscopy. ?? 1977 Akade??miai Kiado??.

Journal of Radioanalytical Chemistry

Investigation of aggregation in solvent extraction of lanthanides by acidic extractants (organophosphorus and naphthenic acid)

Three acidic extractants (I) di(2-ethylhexyl) phosphoric acid (HDEHP), (II) 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester (HEHPEHE) and (III) naphthenic acid were employed in preparing the samples for the characterization of the coordination structure of lanthanide-extractant complexes and the physicochemica nature of aggregates formed in the organic diluent of the solvent extraction systems. Photo correlation spectroscopy (PCS) results on the aggregates formed by the partially saponified HDEHP in n-heptane showed that the hydrodynamic radius of the aggregates was comparable to the molecular dimensions of HDEHP. The addition of 2-octanol into the diluent, by which the mixed solvent was formed, increased the dimensions of the corresponding aggregates. Aggregates formed from the lanthanide ions and HDEHP in the organic phase of the extraction systems were found very unstable. In the case of naphthenic acid, PCS data showed the formation of w/o microemulsion from the saponified naphthenic acid in the mixed solvent. The extraction of lanthanides by the saponified naphthenic acid in the mixed solvent under the given experimental conditions was a process of destruction of the w/o microemulsion. A possible mechanism of the breakdown of the w/o microemulsion droplets is discussed.

Science in China, Series B: Chemistry

New light on a dark subject: On the use of fluorescence data to deduce redox states of natural organic matter (NOM)

This paper reports the use of excitation-emission matrix fluorescence spectroscopy (EEMS), parallel factor statistical analysis (PARAFAC), and oxidation-reduction experiments to examine the effect of redox conditions on PARAFAC model results for aqueous samples rich in natural organic matter. Fifty-four aqueous samples from 11 different geographic locations and two plant extracts were analyzed untreated and after chemical treatments or irradiation were used in attempts to change the redox status of the natural organic matter. The EEMS spectra were generated and modeled using a PARAFAC package developed by Cory and McKnight (2005). The PARAFAC model output was examined for consistency with previously reported relations and with changes expected to occur upon experimental oxidation and reduction of aqueous samples. Results indicate the implied fraction of total sample fluorescence attributed to quinone-like moieties was consistent (0.64 to 0.78) and greater than that observed by Cory and McKnight (2005). The fraction of the quinone-like moieties that was reduced (the reducing index, RI) showed relatively little variation (0.46 to 0.71) despite attempts to alter the redox status of the natural organic matter. The RI changed little after reducing samples using zinc metal, oxidizing at high pH with air, or irradiating with a Xenon lamp. Our results, however, are consistent with the correlations between the fluorescence indices (FI) of samples and the ratio of PARAFAC fitting parameters suggested by Cory and McKnight (2005), though we used samples with a much narrower range of FI values.

Aquatic Sciences

Vein-type gold formation during late extensional collapse of the Eastern Desert, Egypt: the Gidami deposit

Orogenic gold deposits, though construed to focused fluid flow during orogenesis, commonly post-date the main accretionary events. Several lines of evidence indicate that orogenic gold formation in the Arabian–Nubian Shield continued through the orogen collapse stage and associated rapid exhumation and thermal re-equilibration. The Gidami gold deposit in the Eastern Desert of Egypt is associated with post-foliation, brittle-ductile shear zones that deformed a weakly foliated tonalite-trondhjemite massif dated as ~ 704 Ma (U–Pb zircon age). Gold-sulfide quartz veins exhibit textural features indicative of repeated mylonitization, recrystallization, and muscovite crystallization. New 40 Ar/ 39 Ar ages of muscovite flakes from the auriferous quartz veins and from the altered wallrock overlap within analytical uncertainty at ~ 583 Ma, which corresponds to the climax of extension-related wrenching and rapid exhumation in the region (~ 596 to 582 Ma). Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) data coupled with microtextural characteristics suggest that early formed pyrite generations experienced substantial fluid-mediated recrystallization, and that a set of metals was remobilized by later fluids. A late generation of fibrous pyrite, ubiquitous in microfractures, deposited while the veins re-opened and deformed. The occurrence of free gold particles along with a late-paragenetic assemblage of galena-sphalerite-chalcopyrite(± hessite ± cervelleite) was related to influx of low salinity, metalliferous H 2 O-NaCl-CO 2 -CH 4 fluids as indicated by the fluid inclusion laser Raman spectroscopy and microthermometry results. Au-mobilization and redeposition at T ≤ 350 °C and P ~ 1 to 1.7 kbar, triggered by intermittent fluid pluses and thermal re-equilibration, were most likely stimulated by extensional structures and within-plate magmatism. Coincident province- and deposit-scale pressure–temperature-time data highlight the pivotal role of the orogenic collapse tectonics in gold endowment in the Central Eastern Desert’s crust.

Gidami deposit

Polyphase stratabound scheelite-ferberite mineralization at Mallnock, Eastern Alps, Austria

A peculiar type of stratabound tungsten mineralization in metacarbonate rocks was discovered and explored at Mallnock (Austria) during the late 1980s. It is the only tungsten occurrence in the Eastern Alps in which scheelite is associated with wolframite (96 mol% ferberite). The tungsten prospect is located in the Austroalpine Drauzug-Gurktal Nappe System recording polyphase low-grade regional metamorphism. Raman spectroscopy of carbonaceous material yield maximum metamorphic temperatures of 296 ± 27 °C and 258 ± 27 °C, which are assigned to Variscan and Eoalpine metamorphism, respectively. Scheelite and ferberite occur as polyphase stockwork-like mineralization in Fe-rich magnesite in the northern ore zone (Mallnock North), whereas in the western ore zone (Mallnock West), scheelite-quartz veinlets are exclusively hosted in dolomitic marbles. LA-ICP-MS analyses of scheelite and ferberite yield low contents of Mo, Nb, Ta, and rare earth elements, but high contents of Na and Sr. Uranium is particularly high in scheelite (up to 200 µg/g) and makes this mineral a suitable target for U–Pb dating. In situ U–Pb dating of scheelite yielded an early Permian age (294 ± 8 Ma) for Mallnock West and a Middle Triassic age (239 ± 3 Ma) for Mallnock North. A monzodioritic dike close to Mallnock yielded a U–Pb apatite date of 282 ± 9 Ma and supports the polyphase formation of this mineralization. The U–Pb scheelite ages indicate that a model for tungsten metallogeny in the Eastern Alps must also consider remobilization of tungsten by metamorphic fluids. In the Alps, the Permian to Triassic period (ca. 290–225 Ma) is characterized by an overall extensional geodynamic setting related to the breakup of Pangea. Lithospheric thinning caused higher heat flow, low-P metamorphism, and anatexis in the lower crust, which led to enhanced crustal fluid flow in the upper crust. These processes were not only responsible for the formation of metasomatic hydrothermal magnesite and siderite deposits in the Eastern Alps but also for this unique magnesite-ferberite-scheelite mineralization at Mallnock.

Mount Mallock

Magnesium content within the skeletal architecture of the coral Montastraea faveolata : locations of brucite precipitation and implications to fine-scale data fluctuations

Small portions of coral cores were analyzed using a high-resolution laser ablation inductively coupled plasma mass spectrometer (LA ICP-MS) to determine the geochemical signatures within and among specific skeletal structures in the large framework coral, Montastraea faveolata . Vertical transects were sampled along three parallel skeletal structures: endothecal (septal flank), corallite wall, and exothecal (costal flank) areas. The results demonstrate that trace element levels varied among the three structures. Magnesium (Mg) varied among adjacent structures and was most abundant within the exothecal portion of the skeleton. Scanning electron microscopy (SEM) revealed the presence of hexagonal crystals forming thick discs, pairs or doublets of individual crystals, and rosettes in several samples. High Mg within these crystals was confirmed with energy dispersive spectroscopy (EDS), infrared spectrometry, and LA ICP-MS. The chemical composition is consistent with the mineral brucite [Mg(OH 2 )]. These crystals are located exclusively in the exothecal area of the skeleton, are often associated with green endolithic algae, and are commonly associated with increased Mg levels found in the adjacent corallite walls. Although scattered throughout the exothecal, the brucite crystals are concentrated within green bands where levels of Mg increase substantially relative to other portions of the skeleton. The presence and locations of high-Mg crystals may explain the fine-scale fluctuations in Mg data researchers have been questioning for years.

Florida

Quantifying gas emissions associated with the 2018 rift eruption of Kīlauea Volcano using ground-based DOAS measurements

Starting on 3 May 2018, a series of eruptive fissures opened in Kīlauea Volcano’s lower East Rift Zone (LERZ). Over the course of the next 3 months, intense degassing accompanied lava effusion from these fissures. Here, we report on ground-based observations of the gas emissions associated with Kīlauea’s 2018 eruption. Visual observations combined with radiative transfer modeling show that ultraviolet light could not efficiently penetrate the gas and aerosol plume in the LERZ, complicating SO 2 measurements by differential optical absorption spectroscopy (DOAS). By applying a statistical method that integrates a radiative transfer model with the DOAS retrievals, we were able to calculate sulfur dioxide (SO 2 ) emission rates along with estimates of their uncertainty. We find that sustained SO 2 emissions were highest in June and early July, when approximately 200 kt SO 2 were emitted daily. At the 68% confidence interval, we estimate that 7.1–13.6 Mt SO 2 were released from the LERZ during the entire May to September eruptive episode. Scaling our results with in situ measurements of plume composition, we calculate that 11–21 Mt H 2 O and 1.5–2.8 Mt CO 2 were also emitted. The gas and aerosol emissions caused hazardous conditions in areas proximal to the active vents, but plume dispersion modeling shows that the eruption also significantly impacted air quality hundreds of kilometers downwind. Combined with petrologic studies of the erupted lavas, our measurements indicate that 1.1–2.3 km 3 dense-rock equivalent of lava were erupted from the LERZ, which is approximately twice the concomitant collapse volume of the volcano’s summit.

Hawaii

Fluid inclusion constraints on the geometry of the magmatic plumbing system beneath Mauna Loa – Part I: Lavas and tephras

There are few petrological constraints on magma storage depths at Mauna Loa, Hawai‘i. Yet understanding the geometry of the magmatic plumbing system is critical for interpreting geophysical signals of unrest at this very high-threat volcano. We address this gap by examining CO₂-rich fluid inclusions (FI) in lava and tephra from seven eruptions (8870 ± 56 14C yr BP, 1852, 1855, 1868, 1949, 1950, and 1984), supplemented with published data from 2022. Raman spectroscopy was used to determine FI densities, from which entrapment pressures were calculated using a CO₂-H₂O equation of state. Most FI record pressures of ~ 0.25–1.25 kbar (~ 2–5 km depth below the summit), consistent with geophysical estimates from the past 40 years. In summit eruptions, FI hosted in more evolved olivine and orthopyroxene clots (Fo and Mg# < 84) record slightly shallower pressures than those in more primitive olivines (Fo > 84) from rift zone eruptions, suggesting a crystal-poor evolved cap near the top of the reservoir (~ 2 km). The similarity in storage depths across all eight eruptions indicates that Mauna Loa’s magmas have tapped a quasi-stable reservoir over the past two centuries, and possibly over 10 kyr. Electron backscatter diffraction reveals deformations to the crystal lattice in Fo82-83 olivines, likely due to deformation during storage in mush piles. The intensity of deformation is comparable to that seen at Kīlauea, implying that mush pile stress may be decoupled from edifice size or longevity. Finally, SO₂ contents in FI increase from ~ 2 mol% at 2 kbar to ~ 15 mol% at 0.5 kbar, suggesting sulphur degassing begins far deeper than the 0.2–0.3 kbar commonly assumed for Hawaiian systems. This validates the newest generation of S degassing models (e.g., Sulfur_X), and explains precursory SO2 emissions in the ~3 hours prior to the onset of the 2022 eruption (Esse et al. 2025).

Hawaii

Thermal infrared and ultraviolet remote sensing of sulfur dioxide gas emitted during the 2018 lower East Rift Zone eruption of Kilauea, Hawaiʻi

Ultraviolet (UV) remote sensing is widely used to detect volcanic sulfur dioxide (SO₂) due to its high sensitivity and favorable spatial and temporal resolution. However, significant discrepancies have been reported between ground-based and satellite-based UV observations of dense volcanic plumes. A notable example is the 2018 lower East Rift Zone eruption of Kīlauea, where SO₂ emission rates derived from ground-based Differential Optical Absorption Spectroscopy (DOAS) measurements differed substantially from those obtained by the spaceborne Tropospheric Monitoring Instrument (TROPOMI). In this study, we investigate these differences by applying thermal infrared (TIR) satellite retrievals using a modified version of the SO₂-ALTA algorithm to Moderate Resolution Imaging Spectroradiometer (MODIS) observations. The resulting TIR-derived SO₂ fluxes are compared with ground-based DOAS data, satellite UV observations, and petrological estimates of gas emissions. Our results show strong agreement between TIR-derived fluxes, ground-based DOAS measurements, and petrological estimates, particularly during the peak and plateau phases of the eruption. In contrast, satellite UV-derived SO₂ emissions are systematically lower. We find that TIR observations are more effective in quantifying high-concentration SO₂ plumes in the near-vent region, while UV measurements are more sensitive under lower-concentration conditions but more affected by scattering in optically dense plumes. These findings highlight the complementary strengths of UV and TIR remote sensing techniques and emphasize the importance of accounting for plume density and observation geometry when interpreting satellite SO₂ retrievals.

Hawaii

Linking microbial and ecosystem ecology using ecological stoichiometry: a synthesis of conceptual and empirical approaches

Currently, one of the biggest challenges in microbial and ecosystem ecology is to develop conceptual models that organize the growing body of information on environmental microbiology into a clear mechanistic framework with a direct link to ecosystem processes. Doing so will enable development of testable hypotheses to better direct future research and increase understanding of key constraints on biogeochemical networks. Although the understanding of phenotypic and genotypic diversity of microorganisms in the environment is rapidly accumulating, how controls on microbial physiology ultimately affect biogeochemical fluxes remains poorly understood. We propose that insight into constraints on biogeochemical cycles can be achieved by a more rigorous evaluation of microbial community biomass composition within the context of ecological stoichiometry. Multiple recent studies have pointed to microbial biomass stoichiometry as an important determinant of when microorganisms retain or recycle mineral nutrients. We identify the relevant cellular components that most likely drive changes in microbial biomass stoichiometry by defining a conceptual model rooted in ecological stoichiometry. More importantly, we show how X-ray microanalysis (XRMA), nanoscale secondary ion mass spectroscopy (NanoSIMS), Raman microspectroscopy, and in situ hybridization techniques (for example, FISH) can be applied in concert to allow for direct empirical evaluation of the proposed conceptual framework. This approach links an important piece of the ecological literature, ecological stoichiometry, with the molecular front of the microbial revolution, in an attempt to provide new insight into how microbial physiology could constrain ecosystem processes.

Ecosystems