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USGS2010

Phosphorus and iron cycling in deep saprolite, Luquillo Mountains, Puerto Rico

Rapid weathering and erosion rates in mountainous tropical watersheds lead to highly variable soil and saprolite thicknesses which in turn impact nutrient fluxes and biological populations. In the Luquillo Mountains of Puerto Rico, a 5-m thick saprolite contains high microorganism densities at the surface and at depth overlying bedrock. We test the hypotheses that the organisms at depth are limited by the availability of two nutrients, P and Fe. Many tropical soils are P-limited, rather than N-limited, and dissolution of apatite is the dominant source of P. We document patterns of apatite weathering and of bioavailable Fe derived from the weathering of primary minerals hornblende and biotite in cores augered to 7.5 m on a ridgetop as compared to spheroidally weathering bedrock sampled in a nearby roadcut. Iron isotopic compositions of 0.5 N HCl extracts of soil and saprolite range from about δ 56 Fe = 0 to − 0.1‰ throughout the saprolite except at the surface and at 5 m depth where δ 56 Fe = − 0.26 to − 0.64‰. The enrichment of light isotopes in HCl-extractable Fe in the soil and at the saprolite–bedrock interface is consistent with active Fe cycling and consistent with the locations of high cell densities and Fe(II)-oxidizing bacteria, identified previously. To evaluate the potential P-limitation of Fe-cycling bacteria in the profile, solid-state concentrations of P were measured as a function of depth in the soil, saprolite, and weathering bedrock. Weathering apatite crystals were examined in thin sections and an apatite dissolution rate of 6.8 × 10 − 14 mol m − 2 s − 1 was calculated. While surface communities depend on recycled nutrients and atmospheric inputs, deep communities survive primarily on nutrients released by the weathering bedrock and thus are tightly coupled to processes related to saprolite formation including mineral weathering. While low available P may limit microbial activity within the middle saprolite, fluxes of P from apatite weathering should be sufficient to support robust growth of microorganisms in the deep saprolite.

Puerto Rico↗

USGS2010

Effects of temperature on silicate weathering: Solute fluxes and chemical weathering in a temperate rain forest watershed, Jamieson Creek, British Columbia

Chemical weathering of silicate minerals has long been known as a sink for atmospheric CO 2 , and feedbacks between weathering and climate are believed to affect global climate. While warmer temperatures are believed to increase rates of weathering, weathering in cool climates can be accelerated by increased mineral exposure due to mechanical weathering by ice. In this study, chemical weathering of silicate minerals is investigated in a small temperate watershed. The Jamieson Creek watershed is covered by mature coniferous forest and receives high annual precipitation (4000 mm), mostly in the form of rainfall, and is underlain by quartz diorite bedrock and glacial till. Analysis of pore water concentration gradients indicates that weathering in hydraulically unsaturated ablation till is dominated by dissolution of plagioclase and hornblende. However, a watershed scale solute mass balance indicates high relative fluxes of K and Ca, indicating preferential leaching of these solutes possibly from the relatively unweathered lodgement till. Weathering rates for plagioclase and hornblende calculated from a watershed scale solute mass balance are similar in magnitude to rates determined using pore water concentration gradients. When compared to the Rio Icacos basin in Puerto Rico, a pristine tropical watershed with similar annual precipitation and bedrock, but with dissimilar regolith properties, fluxes of weathering products in stream discharge from the warmer site are 1.8 to 16.2-fold higher, respectively, and regolith profile-averaged plagioclase weathering rates are 3.8 to 9.0-fold higher. This suggests that the Arrhenius effect, which predicts a 3.5- to 9-fold increase in the dissolution rate of plagioclase as temperature is increased from 3.4° to 22 °C, may explain the greater weathering fluxes and rates at the Rio Icacos site. However, more modest differences in K and Ca fluxes between the two sites are attributed to accelerated leaching of those solutes from glacial till at Jamieson Creek. Our findings suggest that under conditions of high rainfall and favorable topography, weathering rates of silicate minerals in warm tropical systems will tend to be higher than in cool temperate systems, even if the temperate system is has been perturbed by an episode of glaciation that deposits regolith high in fresh mineral surface area.

British Columbia↗

USGS2021

The triple argon isotope composition of groundwater on ten-thousand-year timescales

Understanding the age and movement of groundwater is important for predicting the vulnerability of wells to contamination, constraining flow models that inform sustainable groundwater management, and interpreting geochemical signals that reflect past climate. Due to both the ubiquity of groundwater with order ten-thousand-year residence times and its importance for climate reconstruction of the last glacial period, there is a strong need for improving geochemical dating tools on this timescale. Whereas 14 C of dissolved inorganic carbon and dissolved 4 He are common age tracers for Late Pleistocene groundwater, each is limited by systematic uncertainties related to aquifer composition and lithology, and the extent of water-rock interaction. In principle, radiogenic 40 Ar in groundwater acquired from decay of 40 K in aquifer minerals should be insensitive to some processes that impact 14 C and 4 He and thus represent a useful, complementary age tracer. In practice, however, detection of significant radiogenic 40 Ar signals in groundwater has been limited to a small number of studies of extremely old groundwater (>100 ka). Here we present the first high-precision (<1‰) measurements of triple Ar isotopes ( 40 Ar, 38 Ar, 36 Ar) in groundwater. We introduce a model that distinguishes radiogenic 40 Ar from atmospheric 40 Ar by using the non-radiogenic Ar isotopes ( 36 Ar, 38 Ar) to correct for mass-dependent fractionation. Using this model, we investigate variability in radiogenic 40 Ar excess (Δ 40 Ar) across 58 groundwater samples collected from 36 wells throughout California (USA). We find that Δ 40 Ar ranges from ~0‰ (the expected minimum value) to +4.2‰ across three study areas near Fresno, San Diego, and the western Mojave Desert. Based on measurements from a network of 23 scientific monitoring wells in San Diego, we find evidence for a strong dependence of Δ 40 Ar on aquifer lithology. We suggest that Δ 40 Ar is fundamentally controlled by the weathering of old K-bearing minerals and thus reflects both the degree of groundwater-rock interaction, which is related to groundwater age, and the integrated flow through different geological formations. Future studies of Late Pleistocene groundwater may benefit from high-precision triple Ar isotope measurements as a new tool to better interpret 14 C- and 4 He-based constraints on groundwater age and flow.

Chemical Geology↗

USGS2021

Helium-carbon systematics of groundwaters in the Lassen Peak Region

Carbon dioxide emissions from active subaerial volcanoes represent 20–50% of the annual global volcanic CO 2 flux (Barry et al., 2014). Passive degassing of carbon from the flanks of volcanoes, and the associated accumulation of dissolved inorganic carbon (DIC) within nearby groundwater, also represents a potentially important, yet poorly constrained flux of carbon to the surface (Werner et al., 2019). Here we investigate sources and sinks of DIC in groundwaters in the Lassen Peak region of California. Specifically, we report and interpret the relative abundance and isotopic composition of helium ( 3 He, 4 He) and carbon ( 12 C, 13 C, 14 C) in 37 groundwater samples, from 24 distinct wells, collected between 20 and 60 km from Lassen Peak. Measured groundwater samples have air-corrected 3 He/ 4 He values between 0.19 and 7.44 R A (where R A = air 3 He/ 4 He = 1.39 × 10 −6 ), all in excess of the radiogenic production value (~0.05 R A ), indicating pervasive mantle-derived helium additions to the groundwater system in the Lassen Peak region. Stable carbon isotope ratios of DIC (δ 13 C) vary between −12.6 and − 27.7‰ (vs. VPDB). Measured groundwater DIC/ 3 He values fall in the range of 2.2 × 10 10 to 1.1 × 10 12 . Using helium and carbon isotope data, we explore several conceptual models to estimate surface carbon contributions and to differentiate between DIC derived from soil CO 2 versus DIC derived from external (slab and mantle) carbon sources. Specifically, if we use 14 C to identify soil-derived DIC (assuming decadal-to-centennial groundwater ages and a soil CO 2 14 C activity equal to that of the atmosphere), we calculate that a hypothetical external carbon source would have an apparent δ 13 C signature between −10.3 and − 59.3‰ (vs. Vienna Pee Dee Belemnite (VPDB)) and an apparent C/ 3 He between 7.0 × 10 9 and 1.0 × 10 12 . These apparent δ 13 C and C/ 3 He values are substantially isotopically lighter than and greater than canonical MORB values, respectively. We suggest that >95% of any external (non-soil-derived) DIC in groundwater must thus be non-mantle in origin (i.e., slab derived or assimilated organic carbon). We further investigate possible sources of external DIC to groundwater using two idealized conceptual approaches: a pure (unfractionated) source mixing model (after Sano and Marty, 1995) and a scenario that invokes fractionation due to calcite precipitation. Because the former model requires carbon contributions from an organic source component with unrealistically low δ 13 C (~ − 60‰), we suggest that the second scenario is more plausible. Importantly, however, we caution that all conceptual models are dependent on assumptions about initial 14 C activity. Thus, we cannot rule out the possibility that the true fraction of non-surface-derived DIC in these samples is lower or negligible, despite the pervasive mantle-derived He isotope signatures throughout the region. Following the 14 C approach to deconvolving sources of DIC, we determine that the maximum passive carbon flux could be up to ~2.2 × 10 6 kg/yr, which is lower than previous magmatic carbon flux estimates from the Lassen region (Rose and Davisson, 1996). We find that the passive dissolved carbon flux could represent a maximum of ~4–18% of the total Lassen geothermal CO 2 degassing flux (estimated to be ~3.5 × 10 7 kg/yr Rose and Davisson, 1996; Gerlach et al., 2008), which is still more than an order of magnitude smaller than soil gas CO 2 flux estimates (7.3–11 × 10 7 kg/yr) for nearby volcanoes (Sorey et al., 1998; Gerlach et al., 1999; Evans et al., 2002; Werner et al., 2014 ). We conclude that passive dissolved carbon fluxes should be combined with geothermal fluxes and soil gas fluxes to obtain a complete picture of volcanic carbon emissions globally. Our approach highlights the utility of measuring helium isotopes in concert with the full suite of noble gas abundances, tritium, δ 13 C and 14 C, which when interpreted together can be used to better elucidate the various sources of DIC in groundwater.

California↗

USGS2006

Redox potential characterization and soil greenhouse gas concentration across a hydrological gradient in a Gulf coast forest

Soil redox potential (Eh), concentrations of oxygen (O2) and three greenhouse gases (CO2, CH4, and N2O) were measured in the soil profile of a coastal forest at ridge, transition, and swamp across a hydrological gradient. The results delineated a distinct boundary in soil Eh and O2 concentration between the ridge and swamp with essentially no overlap between the two locations. Critical soil Eh to initiate significant CH4 production under this field conditions was about +300 mV, much higher than in the homogenous soils (about -150 mV). The strength of CH4 source to the atmosphere was strong for the swamp, minor for the transition, and negligible or even negative (consumption) for the ridge. Maximum N2O concentration in the soils was found at about Eh +250 mV, and the soil N2O emission was estimated to account for less than 4% for the ridge and transition, and almost negligible for the swamp in the cumulative global warming potential (GWP) of these three gases. The dynamic nature of this study site in response to water table fluctuations across a hydrological gradient makes it an ideal model of impact of future sea level rise to coastal ecosystems. Soil carbon (C) sequestration potential due to increasing soil water content upon sea level rise and subsidence in this coastal forest was likely limited and temporal, and at the expense of increasing soil CH4 production and emission. ?? 2005 Elsevier Ltd. All rights reserved.

Chemosphere↗

USGS2012

Volatilization of polycyclic aromatic hydrocarbons from coal-tar-sealed pavement

Coal-tar-based pavement sealants, a major source of PAHs to urban water bodies, are a potential source of volatile PAHs to the atmosphere. An initial assessment of volatilization of PAHs from coal-tar-sealed pavement is presented here in which we measured summertime gas-phase PAH concentrations 0.03 m and 1.28 m above the pavement surface of seven sealed (six with coal-tar-based sealant and one with asphalt-based sealant) and three unsealed (two asphalt and one concrete) parking lots in central Texas. PAHs also were measured in parking lot dust. The geometric mean concentration of the sum of eight frequently detected PAHs (ΣPAH 8 ) in the 0.03-m samples above sealed lots (1320 ng m -3 ) during the hottest part of the day was 20 times greater than that above unsealed lots (66.5 ng m -3 ). The geometric mean concentration in the 1.28-m samples above sealed lots (138 ng m -3 ) was five times greater than above unsealed lots (26.0 ng m -3 ). Estimated PAH flux from the sealed lots was 60 times greater than that from unsealed lots (geometric means of 88 and 1.4 μg m -2 h -1 , respectively). Although the data set presented here is small, the much higher estimated fluxes from sealed pavement than from unsealed pavement indicate that coal-tar-based sealants are emitting PAHs to urban air at high rates compared to other paved surfaces.

Chemosphere↗

USGS2004

Geologic history of natural coal-bed fires, Powder River basin, USA

Coal-bed fires ignited by natural processes have baked and fused overlying sediments to form clinker, a hard red or varicolored rock, through much of the northern Great Plains of the United States (USA). The gently dipping coal beds in the region burn when regional downwasting brings them above the local water table. The resulting clinker forms a rim along the exposed edge of the coal bed in an ongoing process through geologic time. The resistant clinker is left capping buttes and ridges after the softer unbaked strata erode away. Clinker outcrops cover more than 4100 km2 in the Powder River basin (PRB), which lies in Wyoming (WY) and Montana (MT). The clinker in place records tens of billions of tons of coal that have burned, releasing gases into the atmosphere. The amount of clinker that has eroded away was at least an order of magnitude greater than the clinker that remains in place. Fission-track and uranium-thorium/ helium ages of detrital zircon crystals in clinker, and paleomagnetic ages of clinker, show that coal beds have burned naturally during at least the past 4 million years (Ma). The oldest in-place clinker that has been dated, collected from a high, isolated, clinker-capped ridge, has a fission track age of 2.8??0.6 Ma. Evidence of erosion and downcutting is also preserved by clinker clasts in gravel terraces. One clinker boulder in a terrace 360 m above the Yellowstone River has a fission track age of 4.0??0.7 Ma. Coal-bed fires are caused by lightning, wildfires, spontaneous combustion, or human activity on coal outcrops and in mines. Miners, government agencies, and ranchers have extinguished thousands of coal bed fires, but natural ignition continues where fresh coal has access to air. At any given time, hundreds of fires, mostly small, are burning. In the Powder River basin, the total amount of coal burned by natural fires in the last 2 Ma is one to two orders of magnitude greater than the total amount of coal removed by mining in the past century. However, current annual rates of coal mining are three to four orders of magnitude greater than estimated prehistoric annual rates of coal consumption by natural fires. ?? 2004 Published by Elsevier B.V.

International Journal of Coal Geology↗

USGS2008

Abundance and modes of occurrence of mercury in some low-sulfur coals from China

Mercury (Hg) is one of the hazardous trace elements in coal. Mercury in coal is almost totally emitted into the atmosphere during coal combustion. Especially for utilities burning low-sulfur coals that do not require scrubbers, Hg reduction will be neglected. Hg abundances of 52 low-sulfur coal samples from different coalfields in six provinces of China were determined by a flow injection mercury system (FIMS). The results show that Hg abundances in selected low-sulfur coals range from 0.03??ppm to 0.79??ppm, with an arithmetic mean of 0.24??ppm, which is higher than that of average Chinese coals (0.19??ppm). Correlation analysis and sequential extraction procedures are performed to study possible modes of occurrence of Hg in low-sulfur coals. Modes of occurrence of Hg are variable in low-sulfur coals, and the sulfide-bound and organic-bound Hg may be the dominant forms. In addition, the silicate-bound Hg may be the main form in some of these coals because of magmatic intrusion. ?? 2007 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

USGS2008

Trace element emissions from spontaneous combustion of gob piles in coal mines, Shanxi, China

The emissions of potentially hazardous trace elements from spontaneous combustion of gob piles from coal mining in Shanxi Province, China, have been studied. More than ninety samples of solid waste from gob piles in Shanxi were collected and the contents of twenty potentially hazardous trace elements (Be, F, V, Cr, Mn, Co, Ni, Cu, Zn, As, Se, Mo, Cd, Sn, Sb, Hg, Tl, Pb, Th, and U) in these samples were determined. Trace element contents in solid waste samples showed wide ranges. As compared with the upper continental crust, the solid waste samples are significantly enriched in Se (20x) and Tl (12x) and are moderately enriched in F, As, Mo, Sn, Sb, Hg, Th, and U (2-5x). The solid waste samples are depleted in V, Cr, Mn, Co, Ni, Cu, and Zn. The solid waste samples are enriched in F, V, Mn, Cr, Co, Ni, Cu, Zn, Sb, Th, and U as compared with the Shanxi coals. Most trace elements are higher in the clinker than in the unburnt solid waste except F, Sn, and Hg. Trace element abundances are related to the ash content and composition of the samples. The content of F is negatively correlated with the ash content, while Pb is positively correlated with the ash. The concentrations of As, Mn, Zn, and Cd are highly positively correlated with Fe2O3 in the solid waste. The As content increases with increasing sulfur content in the solid waste. The trace element emissions are calculated for mass balance. The emission factors of trace elements during the spontaneous combustion of the gobs are determined and the trace element concentrations in the flue gas from the spontaneous combustion of solid waste are calculated. More than a half of F, Se, Hg and Pb are released to the atmosphere during spontaneous combustion. Some trace element concentrations in flue gas are higher than the national emission standards. Thus, gob piles from coal mining pose a serious environmental problem. ?? 2007 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

USGS2013

Direct estimation of diffuse gaseous emissions from coal fires: current methods and future directions

Coal fires occur in nature spontaneously, contribute to increases in greenhouse gases, and emit atmospheric toxicants. Increasing interest in quantifying coal fire emissions has resulted in the adaptation and development of specialized approaches and adoption of numerical modeling techniques. Overview of these methods for direct estimation of diffuse gas emissions from coal fires is presented in this paper. Here we take advantage of stochastic Gaussian simulation to interpolate CO 2 fluxes measured using a dynamic closed chamber at the Ruth Mullins coal fire in Perry County, Kentucky. This approach allows for preparing a map of diffuse gas emissions, one of the two primary ways that gases emanate from coal fires, and establishing the reliability of the study both locally and for the entire fire. Future research directions include continuous and automated sampling to improve quantification of gaseous coal fire emissions.

International Journal of Coal Geology↗

USGS2019

Assessment of coal mine methane (CMM) and abandoned mine methane (AMM) resource potential of longwall mine panels: example from Northern Appalachian Basin, USA

"Coal mine methane (CMM) and abandoned mine methane (AMM), are by-products of underground coal mining. The quantity and the emission rate of CMM and AMM may vary depending on the type of mine, gas content of the mined coal seam, and gas sourced from strata and coal beds in overlying and underlying formations affected by mining. Therefore, if a mine has the potential of accumulating gas after being abandoned and sealed properly, methane may be produced and used as an energy source to serve to local communities around the mine. Producing AMM also prevents methane, which is a potent greenhouse gas, from leaking to the atmosphere through seals, shaft plugs or surface cracks. One of the technical barriers in front of investments to economical utilization of CMM and AMM is the difficulty to predict how much methane may be available in the gas emission zone (GEZ) as a resource during mining, and after the panels are sealed and the mine is abandoned. Another difficulty is to estimate how much of the potential methane resource can be produced, and its production feasibility with boreholes, such as gob gas ventholes (GGV) converted to capture AMM. In this study, a comparative assessment is presented to address the issues stated above. The assessment was conducted on two adjacent panels of a longwall mine that operated until 2016 in the Pennsylvania section of the Northern Appalachian Basin. The study is based on two approaches that might be used depending on the availability of data, extensive or minimal. The first approach uses an extensive geological data set, geostatistics, and measured shaft gas emission and GGV production values that were collected while the panel(s) were active to assess the AMM resource. The second approach uses a minimal amount of geologic data and its uncertainty as probabilistic distributions as well as predicted during-mining emissions using a publicly available software. Results showed that both approaches provide relatively comparable estimates of AMM resources and AMM recovery potential using wellbores. The differences in assessed quantities are mostly due to the characteristics of the two methods. In that regard, this paper can be considered as guidance to choose the assessment approach based on data availability. "

Northern Appalachian Basin↗

USGS2021

Insights on the characteristics and sources of gas from an underground coal mine using compositional data analysis

Coal mine gas originates from the gas emission zone (GEZ) of the mine, as well as the longwall face and pillars. Gas emissions are controlled directly at the sources using horizontal or vertical boreholes drilled from surface or from the entries in advance of mining, or it is captured from the fractured and caved zones (gob) using ventholes during mining. The rest of the gas, especially that gas that originates from the longwall face and caved zone, mixes with the ventilation air and travels through bleeder and return entries before being exhausted to atmosphere from air shafts. Although the gas associated with mining mostly focuses on methane, the gas is not pure methane but is a mixture (where both the components and their quantities vary depending on the sampling location). Understanding the evolution of the composition of the gas from source to different sampling and evaluation points in mines using proper statistical analysis and interpretation methods can lead to better designed degasification and ventilation systems and the selection of the most adequate utilization method for generating energy from the gas. In this work, we present the results of compositional data analysis (CoDa) of gases sampled at different locations in a longwall mine operating in Pennsylvanian coal-bearing strata in the Northern Appalachian coal basin. Sampling locations were from accessible parts of the bleeder entries, returns, bleeder evaluation points and shafts within the mine, and also from gob gas ventholes (GGV) and coal degasification boreholes drilled in the panel areas. In addition, desorbed gas samples from seams that are important for the mine were included in the analyses for comparison. The compositional data analysis showed that the gas composition shifts based on the sampling location, putting in-mine and pure coalbed gases on the opposite ends. Removal of air from the samples did not change this observation suggesting that oxygen is depleted especially for in-mine samples, which is due to oxidation. Results also suggested that desorbed gas samples may not represent the composition of the coal seam gas.

International Journal of Coal Geology↗

USGS2023

Predicting methane emissions and developing reduction strategies for a Central Appalachian Basin, USA, longwall mine through analysis and modeling of geology and degasification system performance

Coal mine methane is a safety concern in active mines due to explosion risk and an environmental concern due to the greenhouse gas (GHG) properties of methane emissions to the atmosphere. Depending on the mine design and operation, structural and stratigraphic characteristics of the geology, and the properties of coal beds affected by mining, a significant amount of methane can be released during coal extraction. These emissions may be low and uniform, but they also can be high and abrupt, if not captured by using pre- and post-mining methods of degasification or not controlled by ventilation during mining. Therefore, emissions should be monitored and predicted accurately for underground safety and GHG reduction. Ventilation and degasification systems should be designed accordingly by taking into account the mine geological properties and the degasification system's performance. This paper presents a comprehensive study to predict emissions and proposes alternatives to reduce emissions in a longwall mine extracting metallurgical coal from the Pocahontas No. 3 coal bed in Virginia (Central Appalachian Basin), USA. The work focused on mining activity in four adjacent panels through analysis and modeling of geology and evaluation of the performance of the methane control system. Results showed that the mine geology contained a significant amount of gas within and around the panel areas, which was controlled by utilizing different degasification methods besides ventilation during mining. The study showed that after pre-mining degasification using fractured vertical wells and in-seam horizontal wells, each panel potentially contained ∼19 MMscf and ∼ 2 MMscf of gas remaining to be handled by the gob gas ventholes (GGVs) and the ventilation, respectively, per acre of mining. It was shown that extending the pre-mining degasification duration of vertical wells by as much as 4 years or drilling more horizontal wells with closer spacing could significantly reduce ventilation and gob emissions during the mining of coal.

Kentucky, Virginia, West Virginia↗

USGS2024

Decoding paleomire conditions of Paleogene superhigh-organic-sulfur coals

Superhigh-organic‑sulfur (SHOS) coals (coals with organic sulfur content >4 wt%) are unique coal deposits found at a few notable locations in the world. Specific peat accumulation and preservation conditions must be met to form SHOS coals. Organic sulfur is a major constituent of such coals, and it may have various sources depending on the prevailing paleomire conditions. Understanding such paleomire conditions sheds light on the formation mechanisms of SHOS coals. This investigation decodes the paleomire conditions of the Paleogene SHOS coals from Meghalaya, India, using sulfur isotopic compositions ( δ 34 S) of organic sulfur ( δ 34 S OS ) and pyritic sulfur ( δ 34 S Py ) along with organic petrography, pyrite morphology and trace element ratios. Thirty coal samples were collected from the Jaintia Hills in the east, Khasi Hills in the middle, and Garo Hills in the west of Meghalaya. The organic sulfur content in the Garo, Khasi, and Jaintia coals varies from 1.0 to 3.3 wt%, 1.4 to 13.8 wt%, and 1.0 to 7.2 wt%, respectively. Further, after separation from pyritic sulfur and sulfate sulfur phases, the organic sulfur content ranges from 54.4 to 69.2%, 63.8 to 79.9%, and 59.3 to 73.8%, in the Garo, Khasi, and Jaintia Hills, respectively, suggesting the SHOS nature of these coal samples. The δ 34 S Py varies from −29.3 ‰ to +5.7 ‰, −21.3 ‰ to +27.3 ‰, and −12.1 ‰ to −4.3 ‰, in the Jaintia, Khasi, and Garo Hills, respectively, while the δ 34 S OS fluctuates from −4.6 ‰ to +3.7 ‰, −9.3 ‰ to +7.8 ‰, and − 9.0 ‰ to −5.0 ‰, respectively. The δ 34 S values of pyrite and organic sulfur (OS) in Jaintia coals are 34 S depleted compared to seawater sulfate (+22 ‰), leading to fractionations in the range of −51.3 ‰ to −16.3 ‰ (mean − 31.6 ‰) and − 26.6 ‰ to −18.3 ‰ (mean − 23.1 ‰) for pyritic and organic sulfur (OS), respectively. Pyrite in Khasi coals show a relatively heavier δ 34 S composition averaging at −20.5 ‰, whereas organic sulfur (OS) isotope compositions range from −31.3 ‰ to −14.2 ‰ with a mean of −22.6 ‰. Pyrite and OS in the Garo coals are depleted compared to seawater sulfate. Isotope variations in the Jaintia, Khasi, and Garo coals indicate microbial sulfate reduction (MSR) of seawater sulfate. Large isotopic fractionations between Eocene seawater sulfate and pyritic sulfur ( Δ 34 S SO4Eocene – pyrite = up to −51.3 ‰; mean − 31.6 ‰) in Jaintia coals indicate their possible formation in the water column/near the sediment-seawater interface (open system) and also hint toward dissimilatory sulfate reduction pathways that prevailed under anoxic redox conditions. However, mean values of Δ 34 S SO4Eocene – pyrite (−20.5 ‰) in the Khasi coals imply pyrite formation deeper in the sediments (more closed system) under dysoxic conditions. The dominance of OS over pyritic sulfur, framboidal pyrite, and its microcrystal size distributions in Jaintia coals may suggest syngenetic pyrite formation in open water reducing/anoxic conditions under paralic environments. Elevated Sr/Ba and U/Th values in these coals further confirm the anoxic conditions. Nevertheless, the presence of euhedral pyrite with the alleviated pyrite framboids in the Khasi coals and their complete absence in the Garo coals may suggest dysoxic-suboxic and suboxic-oxic depositional conditions, respectively. The isotopic signatures of the Garo coals suggest sulfur contribution from the parent paleobiota and MSR under a freshwater-oxic environment. Insignificant fractionations between δ 34 S Py and δ 34 S OS indicate limited iron and sulfate availability for additional sulfur cycling and disproportionation reactions, typical of oxic conditions. The absence of framboidal pyrite, elevated sulfate concentration, and mean Sr/Ba and U/Th values of 0.5 and 0.3, respectively, further suggest the freshwater peat deposition in the Garo Hills under limnotelmatic to telmatic freshwater conditions. Moreover, high inertinite content (I mmf = 9.77–33.16 vol%), possibly induced by atmospheric peat exposure, supports the interpretation of suboxic-oxic paleomire conditions in Garo Hills. Gradually decreasing mineral matter content from Jaintia (mean 13.6 vol%) to Garo coals (mean 7.4 vol%) additionally projects a transition from mesotrophic brackish to freshwater limnotelmatic environment, complementing the shift in the paleomire condition from eastern (Jaintia) to western (Garo) Meghalayan Hills.

International Journal of Coal Geology↗

USGS2024

Mitigating climate change by abating coal mine methane: A critical review of status and opportunities

Methane has a short atmospheric lifetime compared to carbon dioxide (CO 2 ), ∼decade versus ∼centuries, but it has a much higher global warming potential (GWP), highlighting how reducing methane emissions can slow the rate of climate change. When considering the contribution of greenhouse gas (GHG) emissions to current global warming (2010–2019) relative to the industrial revolution (1850–1900) levels, methane contributes 0.5 °C or ∼ a third of the total. The most recent post-2023 global estimates of methane emissions by bottom-up (BU) and top-down (TD) approaches for the coal mining sector are in the range of ∼41 ± 3 Tg yr −1 and 33 ± 5 Tg yr −1 , respectively. This divergence, notwithstanding overlapping confidence intervals, is a result of differences between applied TD global inversion models and BU emission inventories. Further research can help to better refine emissions from the various contributing coal mine methane (CMM) emissions sources. The coal mining sector accounts for over 10 % of global anthropogenic methane emissions. The contribution of CMM emissions to the global budget have increased since 2000, although upward and downward regional trends have been observed.

International Journal of Coal Geology↗

USGS2014

Carbon and geochemical properties of cryosols on the North Slope of Alaska

Cryosols contain roughly 1700 Gt of Soil organic carbon (SOC) roughly double the carbon content of the atmosphere. As global temperature rises and permafrost thaws, this carbon reservoir becomes vulnerable to microbial decomposition, resulting in greenhouse gas emissions that will amplify anthropogenic warming. Improving our understanding of carbon dynamics in thawing permafrost requires more data on carbon and nitrogen content, soil physical and chemical properties and substrate quality in cryosols. We analyzed five permafrost cores obtained from the North Slope of Alaska during the summer of 2009. The relationship between SOC and soil bulk density can be adequately represented by a logarithmic function. Gas fluxes at − 5 °C and 5 °C were measured to calculate the temperature response quotient (Q 10 ). Q 10 and the respiration per unit soil C were higher in permafrost-affected soils than that in the active layer, suggesting that decomposition and heterotrophic respiration in cryosols may contribute more to global warming.

Alaska↗

USGS2012

Extension of 239+240 Pu sediment geochronology to coarse-grained marine sediments

Sediment geochronology of coastal sedimentary environments dominated by sand has been extremely limited because concentrations of natural and bomb-fallout radionuclides are often below the limit of measurement using standard techniques. ICP-MS analyses of 239+240 Pu from two sites representative of traditionally challenging (i.e., low concentration) environments provide a "proof of concept" and demonstrate a new application for bomb-fallout radiotracers in the study of sandy shelf-seabed dynamics. A kasten core from the New Zealand shelf in the Southern Hemisphere (low fallout), and a vibracore from the sandy nearshore of North Carolina (low particle surface area) both reveal measurable 239+240 Pu activities at depth. In the case of the New Zealand site, independently verified steady-state sedimentation results in a 239+240 Pu profile that mimics the expected atmospheric fallout. The depth profile of 239+240 Pu in the North Carolina core is more uniform, indicating significant sediment resuspension, which would be expected in this energetic nearshore environment. This study, for the first time, demonstrates the utility of 239+240 Pu in the study of sandy environments, significantly extending the application of bomb-fallout isotopes to coarse-grained sediments, which compose the majority of nearshore regions.

Continental Shelf Research↗

USGS2017

Sand ridge morphology and bedform migration patterns derived from bathymetry and backscatter on the inner-continental shelf offshore of Assateague Island, USA

The U.S. Geological Survey and the National Oceanographic and Atmospheric Administration conducted geophysical and hydrographic surveys, respectively, along the inner-continental shelf of Fenwick and Assateague Islands, Maryland and Virginia over the last 40 years. High resolution bathymetry and backscatter data derived from surveys over the last decade are used to describe the morphology and presence of sand ridges on the inner-continental shelf and measure the change in the position of smaller-scale (10–100 s of meters) seafloor features. Bathymetric surveys from the last 30 years link decadal-scale sand ridge migration patterns to the high-resolution measurements of smaller-scale bedform features. Sand ridge morphology on the inner-shelf changes across-shore and alongshore. Areas of similar sand ridge morphology are separated alongshore by zones where ridges are less pronounced or completely transected by transverse dunes. Seafloor-change analyses derived from backscatter data over a 4–7 year period show that southerly dune migration increases in magnitude from north to south, and the east-west pattern of bedform migration changes ~ 10 km north of the Maryland-Virginia state line. Sand ridge morphology and occurrence and bedform migration changes may be connected to observed changes in geologic framework including topographic highs, deflated zones, and sand availability. Additionally, changes in sand ridge occurrence and morphology may help explain changes in the long-term shoreline trends along Fenwick and Assateague Islands. Although the data presented here cannot quantitatively link sand ridges to sediment transport and shoreline change, it does present a compelling relationship between inner-shelf sand availability and movement, sand ridge occurrence and morphology, geologic framework, and shoreline behavior.

Assateague Island↗