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USGS2018

Assessing historical and projected carbon balance of Alaska: A synthesis of results and policy/management implications

We summarize the results of a recent interagency assessment of land carbon dynamics in Alaska, in which carbon dynamics were estimated for all major terrestrial and aquatic ecosystems for the historical period (1950–2009) and a projection period (2010–2099). Between 1950 and 2009, upland and wetland (i.e., terrestrial) ecosystems of the state gained 0.4 Tg C/yr (0.1% of net primary production, NPP), resulting in a cumulative greenhouse gas radiative forcing of 1.68 × 10 −3 W/m 2 . The change in carbon storage is spatially variable with the region of the Northwest Boreal Landscape Conservation Cooperative (LCC) losing carbon because of fire disturbance. The combined carbon transport via various pathways through inland aquatic ecosystems of Alaska was estimated to be 41.3 Tg C/yr (17% of terrestrial NPP). During the projection period (2010–2099), carbon storage of terrestrial ecosystems of Alaska was projected to increase (22.5–70.0 Tg C/yr), primarily because of NPP increases of 10–30% associated with responses to rising atmospheric CO 2 , increased nitrogen cycling, and longer growing seasons. Although carbon emissions to the atmosphere from wildfire and wetland CH 4 were projected to increase for all of the climate projections, the increases in NPP more than compensated for those losses at the statewide level. Carbon dynamics of terrestrial ecosystems continue to warm the climate for four of the six future projections and cool the climate for only one of the projections. The attribution analyses we conducted indicated that the response of NPP in terrestrial ecosystems to rising atmospheric CO 2 (~5% per 100 ppmv CO 2 ) saturates as CO 2 increases (between approximately +150 and +450 ppmv among projections). This response, along with the expectation that permafrost thaw would be much greater and release large quantities of permafrost carbon after 2100, suggests that projected carbon gains in terrestrial ecosystems of Alaska may not be sustained. From a national perspective, inclusion of all of Alaska in greenhouse gas inventory reports would ensure better accounting of the overall greenhouse gas balance of the nation and provide a foundation for considering mitigation activities in areas that are accessible enough to support substantive deployment.

Alaska↗

USGS2011

Mars Global Digital Dune Database (MGD3): North polar region (MC-1) distribution, applications, and volume estimates

The Mars Global Digital Dune Database (MGD 3 ) now extends from 90°N to 65°S. The recently released north polar portion (MC‐1) of MGD 3 adds ~844 000 km 2 of moderate‐ to large‐size dark dunes to the previously released equatorial portion (MC‐2 to MC‐29) of the database. The database, available in GIS‐ and tabular‐format in USGS Open‐File Reports, makes it possible to examine global dune distribution patterns and to compare dunes with other global data sets (e.g. atmospheric models). MGD 3 can also be used by researchers to identify areas suitable for more focused studies. The utility of MGD 3 is demonstrated through three example applications. First, the uneven geographic distribution of the dunes is discussed and described. Second, dune‐derived wind direction and its role as ground truth for atmospheric models is reviewed. Comparisons between dune‐derived winds and global and mesoscale atmospheric models suggest that local topography may have an important influence on dune‐forming winds. Third, the methods used here to estimate north polar dune volume are presented and these methods and estimates (1130 km 3 to 3250 km 3 ) are compared with those of previous researchers (1158 km 3 to 15 000 km 3 ). In the near future, MGD 3 will be extended to include the south polar region.

Earth Surface Processes and Landforms↗

USGS2007

Carbon isotope fractionation of dissolved inorganic carbon (DIC) due to outgassing of carbon dioxide from a headwater stream

The stable isotopic composition of dissolved inorganic carbon (??13C-DIC) was investigated as a potential tracer of streamflow generation processes at the Sleepers River Research Watershed, Vermont, USA. Downstream sampling showed ?? 13C-DIC increased between 3-5??? from the stream source to the outlet weir approximately 0??5 km downstream, concomitant with increasing pH and decreasing PCO2. An increase in ??13C-DIC of 2.4 ?? 0??1??? per log unit decrease of excess PCO2 (stream PCO2 normalized to atmospheric PCO2) was observed from downstream transect data collected during snowmelt. Isotopic fractionation of DIC due to CO2 outgassing rather than exchange with atmospheric CO2 may be the primary cause of increased ?? 13C-DIC values downstream when PCO2 of surface freshwater exceeds twice the atmospheric CO2 concentration. Although CO2 outgassing caused a general increase in stream ??13C-DIC values, points of localized groundwater seepage into the stream were identified by decreases in ??13C-DIC and increases in DIC concentration of the stream water superimposed upon the general downstream trend. In addition, comparison between snowmelt, early spring and summer seasons showed that DIC is flushed from shallow groundwater flowpaths during snowmelt and is replaced by a greater proportion of DIC derived from soil CO2 during the early spring growing season. Thus, in spite of effects from CO2 outgassing, ??13C of DIC can be a useful indicator of groundwater additions to headwater streams and a tracer of carbon dynamics in catchments. Copyright ?? 2007 John Wiley & Sons, Ltd.

Hydrological Processes↗

USGS1995

Hydrological and thermal response of lakes to climate: Description and modeling

Lake systems continually respond to climatic conditions that vary over broad scales of space and time. The spatial distribution of lakes on the Earth’s surface is indicative of long-term patterns of atmospheric circulation, and the annual cycle of climate over lake basins is reflected in seasonal change in the size and temperature of lakes. Lake size is determined by the balance of water inputs and outputs, and lake temperature is governed by the balance of heat inputs and outputs. The lake hydrological and energy balances are coupled to the atmosphere. In response to the inputs of mass, energy, and momentum (precipitation, radiation, and wind stress), lakes return heat and moisture to the atmosphere through conduction and evaporation. Global, regional, or local change in the hydrological or thermal states of lakes thus represent interactive responses to climatic variation in the supply of water and energy.

Book chapter↗

USGS2024

Microbial communities in standing dead trees in ghost forests are largely aerobic, saprophytic, and methanotrophic

Standing dead trees (snags) are recognized for their influence on methane (CH 4 ) cycling in coastal wetlands, yet the biogeochemical processes that control the magnitude and direction of fluxes across the snag-atmosphere interface are not fully elucidated. Herein, we analyzed microbial communities and fluxes at one height from ten snags in a ghost forest wetland. Snag-atmosphere CH 4 fluxes were highly variable (− 0.11–0.51 mg CH 4 m −2 h −1 ). CH 4 production was measured in three out of ten snags; whereas, CH 4 consumption was measured in two out of ten snags. Potential CH 4 production and oxidation in one core from each snag was assayed in vitro. A single core produced CH 4 under anoxic and oxic conditions, at measured rates of 0.7 and 0.6 ng CH 4 g −1 h −1 , respectively. Four cores oxidized CH 4 under oxic conditions, with an average rate of − 1.13 ± 0.31 ng CH 4 g −1 h −1 . Illumina sequencing of the V3/V4 region of the 16S rRNA gene sequence revealed diverse microbial communities and indicated oxidative decomposition of deadwood. Methanogens were present in 20% of the snags, with a mean relative abundance of < 0.0001%. Methanotrophs were identified in all snags, with a mean relative abundance of 2% and represented the sole CH 4 -cycling communities in 80% of the snags. These data indicate potential for microbial attenuation of CH 4 emissions across the snag-atmosphere interface in ghost forests. A better understanding of the environmental drivers of snag-associated microbial communities is necessary to forecast the response of CH 4 cycling in coastal ghost forest wetlands to a shifting coastal landscape.

Current Microbiology↗

USGS2025

Avian navigation: Comparing the olfactory navigational “map” and the infrasound direction-finding hypotheses to aeronautics

Animal navigation has long been a fascinating but bewildering subject. Humans and animals might well share similar navigational strategies because they developed within the same physical environments. A “map-and-compass” model has been proposed to explain the two-step avian navigational process, but the “map” step has remained elusive. Although scalar values from bicoordinate geomagnetic or atmospheric olfactory gradients have been considered foundational to the avian map, neither has proved convincing engendering decades of controversy. The olfactory map, and an alternative infrasound direction-finding (IDF) hypothesis, are discussed in this review. The olfactory map hypothesis currently requires extensive stable gradients of trace-odor ratios, but such gradients are highly unlikely within a turbulent and rapidly mixed lower atmosphere. The IDF hypothesis, on the other hand, postulates a two-step navigational model analogous to the maritime and aeronautical radio direction-finding technique. This review was also written to encourage further investigation, and direct testing, of the acoustic navigational process. The IDF hypothesis, at present, appears the better explanation of observed avian navigational behavior and accuracy within the atmosphere’s physical environment.

Journal of Comparative Physiology A↗

USGS1996

The initial cooling of pahoehoe flow lobes

In this paper we describe a new thermal model for the initial cooling of pahoehoe lava flows. The accurate modeling of this initial cooling is important for understanding the formation of the distinctive surface textures on pahoehoe lava flows as well as being the first step in modeling such key pahoehoe emplacement processes as lava flow inflation and lava tube formation. This model is constructed from the physical phenomena observed to control the initial cooling of pahoehoe flows and is not an empirical fit to field data. We find that the only significant processes are (a) heat loss by thermal radiation, (b) heat loss by atmospheric convection, (c) heat transport within the flow by conduction with temperature and porosity-dependent thermal properties, and (d) the release of latent heat during crystallization. The numerical model is better able to reproduce field measurements made in Hawai'i between 1989 and 1993 than other published thermal models. By adjusting one parameter at a time, the effect of each of the input parameters on the cooling rate was determined. We show that: (a) the surfaces of porous flows cool more quickly than the surfaces of dense flows, (b) the surface cooling is very sensitive to the efficiency of atmospheric convective cooling, and (c) changes in the glass forming tendency of the lava may have observable petrographic and thermal signatures. These model results provide a quantitative explanation for the recently observed relationship between the surface cooling rate of pahoehoe lobes and the porosity of those lobes (Jones 1992, 1993). The predicted sensitivity of cooling to atmospheric convection suggests a simple field experiment for verification, and the model provides a tool to begin studies of the dynamic crystallization of real lavas. Future versions of the model can also be made applicable to extraterrestrial, submarine, silicic, and pyroclastic flows.

Bulletin of Volcanology↗

USGS2013

On the twenty-first-century wet season projections over the Southeastern United States

This paper reconciles the difference in the projections of the wet season over the Southeastern United States (SEUS) from a global climate model (the Community Climate System Model Version 3 [CCSM3]) and from a regional climate model (the Regional Spectral Model [RSM]) nested in the CCSM3. The CCSM3 projects a dipole in the summer precipitation anomaly: peninsular Florida dries in the future climate, and the remainder of the SEUS region becomes wetter. The RSM forced with CCSM3 projects a universal drying of the SEUS in the late twenty-first century relative to the corresponding twentieth-century summer. The CCSM3 pattern is attributed to the “upped-ante” mechanism, whereby the atmospheric boundary layer moisture required for convection increases in a warm, statically stable global tropical environment. This criterion becomes harder to meet along convective margins, which include peninsular Florida, resulting in its drying. CCSM3 also projects a southwestward expansion of the North Atlantic subtropical high that leads to further stabilizing of the atmosphere above Florida, inhibiting convection. The RSM, because of its high (10-km grid) resolution, simulates diurnal variations in summer rainfall over SEUS reasonably well. The RSM improves upon CCSM3 through the RSM’s depiction of the diurnal variance of precipitation, which according to observations accounts for up to 40 % of total seasonal precipitation variance. In the future climate, the RSM projects a significant reduction in the diurnal variability of convection. The reduction is attributed to large-scale stabilization of the atmosphere in the CCSM3 projections.

Alabama;Arkansas;Florida;Georgia;Kentucky;Louisian↗

USGS2020

Decadal-scale decoupling of soil phosphorus and molybdenum cycles by temperate nitrogen-fixing trees

Symbiotic nitrogen- (N) fixing trees can influence multiple biogeochemical cycles by fixing atmospheric N, which drives net primary productivity and soil carbon (C) and N accumulation, as well as by mobilizing soil phosphorus (P) and other nutrients to support growth and metabolism. The soil micronutrient molybdenum (Mo) is essential to N-fixation, yet surprisingly little is known of whether N-fixing trees alter soil Mo cycling, and if changes to soil Mo are coupled to soil C, N, and P. We compared how symbiotic N-fixing red alder and non-N-fixing Douglas-fir trees modified surface soil C, N, P, and Mo across variation in climate and other site factors in the Pacific Northwest. We found that after two decades, N-fixing trees drove coupled increases in surface soil C, N, total P, and organic P. Consistent with contributions of N-fixing trees to soil organic matter, increased soil C and N were accompanied by lower δ13C in all sites, and lower δ15N in sites where non-fixer plots exhibited elevated soil δ15N. However, N-fixing trees did not affect surface soil Mo concentrations or fractions, suggesting that different factors control the cycling of P versus Mo over decadal timescales. Random forest analysis revealed that surface soil P was most strongly influenced by factors related to soil C accumulation, whereas surface soil Mo was related primarily to environmental factors, including potential differences in atmospheric Mo deposition across sites. Ratios of surface soil P:Mo were higher in extractable pools than in total soil digests, reinforcing the idea of stronger biotic cycling of P than Mo. Overall, our multi-site, multi-decadal field study found surprisingly small effects of N-fixing trees on soil Mo, despite rapid increases in soil organic C, N, and P. We hypothesize that, rather than direct effects of N-fixing vegetation, abiotic or indirect biotic factors such as soil sorption of atmospheric Mo inputs can link C–N–P–Mo cycles in terrestrial ecosystems on longer timescales.

British Columbia, Washington↗

USGS2025

Seasonal synchronicity and multi-decadal stability of headwater biogeochemistry in the northern temperate zone

Temporal patterns in chemistry of headwater streams reflect responses of water and elemental cycles to perturbations occurring at local to global scales. We evaluated multi-scale temporal patterns in up to 32 y of monthly observations of stream chemistry (ammonium, calcium, dissolved organic carbon, nitrate, total dissolved phosphorus, and sulfate) in 22 reference catchments within the northern temperate zone of North America. Multivariate autoregressive state-space (MARSS) models were applied to quantify patterns at multi-decadal, seasonal, and shorter intervals during a period that encompassed warming climate, seasonal changes in precipitation, and regional declines in atmospheric deposition. Significant long-term trends in solute concentrations within a subset of the catchments were consistent with recovery from atmospheric deposition (e.g., calcium, nitrate, sulfate) and increased precipitation (e.g., dissolved organic carbon). Lack of evidence for multi-decadal trends in most catchments suggests resilience of northern temperate ecosystems or that subtle net effects of simultaneous changes in climate and disturbance regimes do not result in directional trends. Synchronous seasonal oscillations of solute concentrations occurred across many catchments, reflecting shared climate and biotic drivers of seasonality within the northern temperate zone. Despite shared patterns among catchments at a seasonal scale, multi-scale temporal patterns were statistically distinct among even adjacent headwater catchments, implying that local attributes of headwater catchments modify the signals imparted by atmospheric phenomena and regional disturbances. To effectively characterize hydrologic and biogeochemical responses to changing climate and disturbance regimes, catchment monitoring programs could include multiple streams with contributing areas that encompass regional heterogeneity in vegetation, topography, and elevation. Overall, detection of long-term patterns and trends requires monitoring multiple catchments at a frequency that captures periodic variation (e.g., seasonality) and a duration encompassing the perturbations of interest.

Biogeochemistry↗

USGS1985

Sulphur in char and char desulphurization by acid leaching and hydropyrolysis

Sulphur compounds volatilized during pyrolysis of acid-leached char were measured to determine characteristics of char desulphurization reactions. Pyrolysis of char in a hydrogen atmosphere (hydropyrolysis) produced a much higher concentration of thiophenic organics compared with that produced during pyrolysis in a nitrogen atmosphere. Hydrogen sulphide gas evolution, at progressively increasing pyrolysis temperature in a helium atmosphere, was measured on five char samples: untreated char, hydrochloric acid-leached char, and three model chars: a demineralized char and two demineralized chars incorporated with sulphur via reactions with elemental sulphur. Hydrogen sulphide gas evolution in untreated char and acid-leached char was found to peak in three temperature regions; the maxima are thought to relate to sulphur in different bonding environments. The amounts of hydrogen sulphide volatilized were much higher for acid-leached char than for untreated char. The gas evolved from each of the remaining three samples showed a single peak region corresponding closely to one of the three peak regions observed for the first two chars. The results of this study indicate that elemental sulphur was produced during hydrochloric acid leaching of the untreated char and suggested that the improved rate of desulphurization observed in the char that had been acid-leached before hydropyrolysis was due in part to the conversion of strongly bound mineral sulphur forms to more weakly bound sulphur forms that are predominantly elemental sulphur in character, and are more easily removed by hydrogen.

Fuel↗

USGS1976

Studies of quaternary saline lakes-II. Isotopic and compositional changes during desiccation of the brines in Owens Lake, California, 1969-1971

Owens Lake is an alkaline salt lake in a closed basin in southeast California. It is normally nearly dry, but in early 1969, an abnormal runoff from the Sierra Nevada flooded it to a maximum depth of 2·4 m. By late summer of 1971, the lake was again nearly dry and the dissolved salts recrystallized. Changes in the chemistry, pH, and deuterium content were monitored during desiccation. During flooding, salts (mostly trona, halite, and burkeite) dissolved slowly from the lake floor. Their concentration in the lake waters increased as evaporation removed water and salts again crystallized, but winter temperatures caused precipitation of some salts and the following summer warming caused their solution, resulting in seasonal variations in the concentration patterns of some ions. The pH values (9·4–10·4) changed with time but showed no detectable diurnal pattern. The deuterium concentration increased during evaporation and appeared to be in equilibrium with vapor leaving the lake according to the Rayleigh equation. The effective α(D/H in liquid/D/H in vapor) decreased as salinity increased; the earliest measured value was 1·069 [as total dissolved solids (TDS) of lake waters changed from 136,200 to 250,400 mg/1]and the last value (calc.) was 1·025 (as TDS changed from 450,000 to 470,300 mg/1). Deuterium exchange with the atmosphere was apparently small except during late desiccation stages when the isotopic contrast became great. Eventually, atmospheric exchange, combined with decreasing α and lake size and increasing salinity, stopped further deuterium concentration in the lake. The maximum contrast between atmospheric vapor and lake deuterium contents was about 110%.

Geochimica et Cosmochimica Acta↗

USGS1995

The geochemical cycling of stable Pb, 210Pb, and 210Po in seasonally anoxic Lake Sammamish, Washington, USA

The geochemical processes controlling the behavior of stable Pb, 210 Pb, and 210 po in seasonally anoxic Lake Sammamish, Washington were identified from water column distributions and box model calculations. Total (sum of dissolved and particulate) inventories of stable Pb, 210 Pb, and 210 Po increased in the whole lake during the latter part of the oxic stage of the lake and were attributed to diffusion from sediments. Large decreases in the total inventories of these elements occurred during the transition from oxic to anoxic conditions, and the lowest inventories were observed during the sulfidic stage of stratification. The cycling of stable Pb and 210 Pb during oxic periods appeared to be linked to Fe cycling while 210 Po cycling was more closely linked to the cycling of Mn. The behavior of stable and radioactive Pb and, possibly, 210 Po during anoxia was influenced by sulfur cycling. Thermodynamic calculations indicated that dissolved Pb concentrations might be controlled by PbS precipitation during anoxia. Flux balance calculations during stratification indicated that atmospheric deposition was the major source of both 210 Pb and 210 Po to the lake and fluvial input was more important for 210 Po than for 210 Pb. 210 Pb and 210 Po supplied by atmospheric deposition were scavenged and removed by sedimentation from the epilimnion. Residence times with respect to scavenging and sedimentation in the epilimnion were 1–3 and 617 days, respectively, for 210 Pb and 9–22 and 9–26 days for 210 Po. Model results in the hypolimnion indicated that at certain times the radionuclides diffused out of the sediments and at other times into the sediments. Residence times with respect to sedimentation of particulate nuclides in the hypolimnion were 2–124 days for 210 Pb and 8–48 days for 210 Po. The behavior of 210 Pb and 210 Po in Lake Sammamish was compared to that in B~' kford Reservoir, Massachusetts. Although the comparison indicated similarities (e.g., links to Fe and Mn cycling, larger scavenging rates for 210 Pb than for 210 Po), the major differences between the systems were that atmospheric inputs were greater than fluvial inputs, activities of the radionuclides were lower, and the presence of sulfide in the hypolimnion during anoxia affected the cycling of stable Pb, 210 Pb, and 210 Po in Lake Sammamish.

Washington↗

USGS2016

Iron oxide minerals in dust-source sediments from the Bodélé Depression, Chad: Implications for radiative properties and Fe bioavailability of dust plumes from the Sahara

Atmospheric mineral dust can influence climate and biogeochemical cycles. An important component of mineral dust is ferric oxide minerals (hematite and goethite) which have been shown to influence strongly the optical properties of dust plumes and thus affect the radiative forcing of global dust. Here we report on the iron mineralogy of dust-source samples from the Bodélé Depression (Chad, north-central Africa), which is estimated to be Earth’s most prolific dust producer and may be a key contributor to the global radiative budget of the atmosphere as well as to long-range nutrient transport to the Amazon Basin. By using a combination of magnetic property measurements, Mössbauer spectroscopy, reflectance spectroscopy, chemical analysis, and scanning electron microscopy, we document the abundance and relative amounts of goethite, hematite, and magnetite in dust-source samples from the Bodélé Depression. The partition between hematite and goethite is important to know to improve models for the radiative effects of ferric oxide minerals in mineral dust aerosols. The combination of methods shows (1) the dominance of goethite over hematite in the source sediments, (2) the abundance and occurrences of their nanosize components, and (3) the ubiquity of magnetite, albeit in small amounts. Dominant goethite and subordinate hematite together compose about 2% of yellow-reddish dust-source sediments from the Bodélé Depression and contribute strongly to diminution of reflectance in bulk samples. These observations imply that dust plumes from the Bodélé Depression that are derived from goethite-dominated sediments strongly absorb solar radiation. The presence of ubiquitous magnetite (0.002–0.57 wt%) is also noteworthy for its potentially higher solubility relative to ferric oxide and for its small sizes, including PM < 0.1 μm. For all examined samples, the average iron apportionment is estimated at about 33% in ferric oxide minerals, 1.4% in magnetite, and 65% in ferric silicates. Structural iron in clay minerals may account for much of the iron in the ferric silicates. We estimate that the mean ferric oxides flux exported from the Bodélé Depression is 0.9 Tg/yr with greater than 50% exported as ferric oxide nanoparticles (<0.1 μm). The high surface-to-volume ratios of ferric oxide nanoparticles once entrained into dust plumes may facilitate increased atmospheric chemical and physical processing and affect iron solubility and bioavailability to marine and terrestrial ecosystems.

Aeolian Research↗

USGS2012

Recent paleorecords document rising mercury contamination in Lake Tanganyika

Recent Lake Tanganyika Hg deposition records were derived using 14 C and excess 210 Pb geochronometers in sediment cores collected from two contrasting depositional environments: the Kalya Platform, located mid-lake and more removed from watershed impacts, and the Nyasanga/Kahama River delta region, located close to the lake’s shoreline north of Kigoma. At the Kalya Platform area, pre-industrial Hg concentrations are 23 ± 0.2 ng/g, increasing to 74 ng/g in modern surface sediment, and the Hg accumulation rate has increased from 1.0 to 7.2 μg/m 2 /a from pre-industrial to present, which overall represents a 6-fold increase in Hg concentration and accumulation. At the Nyasanga/Kahama delta region, pre-industrial Hg concentrations are 20 ± 3 ng/g, increasing to 46 ng/g in surface sediment. Mercury accumulation rate has increased from 30 to 70 μg/m 2 /a at this site, representing a 2–3-fold increase in Hg concentration and accumulation. There is a lack of correlation between charcoal abundance and Hg accumulation rate in the sediment cores, demonstrating that local biomass burning has little relationship with the observed Hg concentration or Hg accumulation rates. Examined using a sediment focusing-corrected mass accumulation rate approach, the cores have similar anthropogenic atmospheric Hg deposition profiles, suggesting that after accounting for background sediment concentrations the source of accumulating Hg is predominantly atmospheric in origin. In summary, the data document an increase of Hg flux to the Lake Tanganyika ecosystem that is consistent with increasing watershed sediment delivery with background-level Hg contamination, and regional as well as global increases in atmospheric Hg deposition.

Tanzania, the Democratic Republic of the Congo , B↗

USGS2005

234Th, 210Pb, 210Po and stable Pb in the central equatorial Pacific: Tracers for particle cycling

Samples were collected during the 1992 US JGOFS EqPac Survey I and II cruises from 12??N to 12??S at 140??W in the central equatorial Pacific for water column profiles of dissolved, particulate and total 234Th, 210Pb and 210Po and total acid soluble stable Pb and sediment trap fluxes of 234Th, 210Pb and 210Po. Survey I occurred in February/March with moderate El Nino conditions while Survey II was conducted in September/October when there was a well developed cold-tongue. 234Th, 210Pb and 210Po are all particle reactive yet they partition differently between dissolved and particulate phases. Fractionation factors (the ratios of the distribution coefficients) show that the selectivity for suspended and sediment trap particles follows Th>Po>Pb. Scavenging residence times (??) for 234Th, 210Pb and 210Po ranged from 25 to 100 d, 3 to 8 years and 100 to 500 d, respectively. These particle reactive tracers have very different distributions in the water column, which reflect differences in their sources and sinks. The deficiency of 234Th relative to 238U was fairly uniformly distributed meridionally, though deficiencies were higher during Survey II when there was higher new production. Excess 210Pb relative to 226Ra was very asymmetrical with much higher excess values north of the equator. The distributions were similar for Surveys I and II. The deficiency of 210Po relative to 210Pb had a symmetrical distribution about the equator for both Survey I and II but the deficiencies were larger during Survey I when upwelling was smaller. Stable Pb was generally higher at the surface than at 250 m and there was no meridional trend from 12??N to 12??S. A mass balance for 210Pb was used to determine the atmospheric input of 210Pb. The average values for Surveys I and II were 0.12 and 0.32 dpm cm-2 year-1, respectively. There was no general increase in atmospheric input of 210Pb north of the equator but there was a strong maximum at 2-3??N during Survey I coincident with the location of the intertropical convergence zone (ITCZ), suggesting a large role for wet deposition. A mass balance for stable Pb was used to determine the atmospheric input of stable Pb. Results ranged from 110 to 140 pmol cm-2 year-1. This flux was low in the southern hemisphere and increased steadily north of the equator. We evaluated use of 210Po as a tracer for export of particulate organic matter during Survey I. Organic carbon and 210Po were highly correlated in suspended matter and sediment trap samples. Average values of organic carbon fluxes determined from the deficiencies of 210Po times the orgC/210Po ratio agreed well with those determined from the deficiencies of 234Th times the organic carbon/234Th ratio and 15N-new production, but had a much larger variability because of the more variable advection corrections. ?? 2005 Elsevier Ltd. All rights reserved.

Deep-Sea Research Part I: Oceanographic Research P↗

USGS2016

Species and tissue type regulate long-term decomposition of brackish marsh plants grown under elevated CO2 conditions

Organic matter accumulation, the net effect of plant production and decomposition, contributes to vertical soil accretion in coastal wetlands, thereby playing a key role in whether they keep pace with sea-level rise. Any factor that affects decomposition may affect wetland accretion, including atmospheric CO 2 concentrations. Higher CO 2 can influence decomposition rates by altering plant tissue chemistry or by causing shifts in plant species composition or biomass partitioning. A combined greenhouse-field experiment examined how elevated CO 2 affected plant tissue chemistry and subsequent decomposition of above- and belowground tissues of two common brackish marsh species, Schoenoplectus americanus (C 3 ) and Spartina patens (C 4 ). Both species were grown in monoculture and in mixture under ambient (350-385 μL L -1 ) or elevated (ambient + 300 μL L -1 ) atmospheric CO 2 conditions, with all other growth conditions held constant, for one growing season. Above- and belowground tissues produced under these treatments were decomposed under ambient field conditions in a brackish marsh in the Mississippi River Delta, USA. Elevated CO 2 significantly reduced nitrogen content of S. americanus , but not sufficiently to affect subsequent decomposition. Instead, long-term decomposition (percent mass remaining after 280 d) was controlled by species composition and tissue type. Shoots of S. patens had more mass remaining (41 ± 2%) than those of S. americanus (12 ± 2 %). Belowground material decomposed more slowly than that placed aboveground (62 ± 1% vs. 23 ± 3% mass remaining), but rates belowground did not differ between species. Increases in atmospheric CO 2 concentration will likely have a greater effect on overall decomposition in this brackish marsh community through shifts in species dominance or biomass allocation than through effects on tissue chemistry. Consequent changes in organic matter accumulation may alter marsh capacity to accommodate sea-level rise through vertical accretion.

Louisiana↗

USGS2015

Global patterns and environmental controls of perchlorate and nitrate co-occurrence in arid and semi-arid environments

Natural perchlorate (ClO 4 − ) is of increasing interest due to its wide-spread occurrence on Earth and Mars, yet little information exists on the relative abundance of ClO 4 − compared to other major anions, its stability, or long-term variations in production that may impact the observed distributions. Our objectives were to evaluate the occurrence and fate of ClO 4 − in groundwater and soils/caliche in arid and semi-arid environments (southwestern United States, southern Africa, United Arab Emirates, China, Antarctica, and Chile) and the relationship of ClO 4 − to the more well-studied atmospherically deposited anions NO 3 − and Cl − as a means to understand the prevalent processes that affect the accumulation of these species over various time scales. ClO 4 − is globally distributed in soil and groundwater in arid and semi-arid regions on Earth at concentrations ranging from 10 −1 to 10 6 μg/kg. Generally, the ClO 4 − concentration in these regions increases with aridity index, but also depends on the duration of arid conditions. In many arid and semi-arid areas, NO 3 − and ClO 4 − co-occur at molar ratios (NO 3 − /ClO 4 − ) that vary between ∼10 4 and 10 5 . We hypothesize that atmospheric deposition ratios are largely preserved in hyper-arid areas that support little or no biological activity (e.g. plants or bacteria), but can be altered in areas with more active biological processes including N 2 fixation, N mineralization, nitrification, denitrification, and microbial ClO 4 − reduction, as indicated in part by NO 3 − isotope data. In contrast, much larger ranges of Cl − /ClO 4 − and Cl − /NO 3 − ratios indicate Cl − varies independently from both ClO 4 − and NO 3 − . The general lack of correlation between Cl − and ClO 4 − or NO 3 − implies that Cl − is not a good indicator of co-deposition and should be used with care when interpreting oxyanion cycling in arid systems. The Atacama Desert appears to be unique compared to all other terrestrial locations having a NO 3 − /ClO 4 − molar ratio ∼10 3 . The relative enrichment in ClO 4 − compared to Cl − or NO 3 − and unique isotopic composition of Atacama ClO 4 − may reflect either additional in-situ production mechanism(s) or higher relative atmospheric production rates in that specific region or in the geological past. Elevated concentrations of ClO 4 − reported on the surface of Mars, and its enrichment with respect to Cl − and NO 3 − , could reveal important clues regarding the climatic, hydrologic, and potentially biologic evolution of that planet. Given the highly conserved ratio of NO 3 − /ClO 4 − in non-biologically active areas on Earth, it may be possible to use alterations of this ratio as a biomarker on Mars and for interpreting major anion cycles and processes on both Mars and Earth, particularly with respect to the less-conserved NO 3 − pool terrestrially.

Geochimica et Cosmochimica Acta↗