Search USGS⌕ Search

SEARCH · Search USGS

Results for “Carbon”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 703 records · Page 39Linked to original sources
USGS2013

Alternative ways of using field-based estimates to calibrate ecosystem models and their implications for carbon cycle studies

Model-data fusion is a process in which field observations are used to constrain model parameters. How observations are used to constrain parameters has a direct impact on the carbon cycle dynamics simulated by ecosystem models. In this study, we present an evaluation of several options for the use of observations in modeling regional carbon dynamics and explore the implications of those options. We calibrated the Terrestrial Ecosystem Model on a hierarchy of three vegetation classification levels for the Alaskan boreal forest: species level, plant-functional-type level (PFT level), and biome level, and we examined the differences in simulated carbon dynamics. Species-specific field-based estimates were directly used to parameterize the model for species-level simulations, while weighted averages based on species percent cover were used to generate estimates for PFT- and biome-level model parameterization. We found that calibrated key ecosystem process parameters differed substantially among species and overlapped for species that are categorized into different PFTs. Our analysis of parameter sets suggests that the PFT-level parameterizations primarily reflected the dominant species and that functional information of some species were lost from the PFT-level parameterizations. The biome-level parameterization was primarily representative of the needleleaf PFT and lost information on broadleaf species or PFT function. Our results indicate that PFT-level simulations may be potentially representative of the performance of species-level simulations while biome-level simulations may result in biased estimates. Improved theoretical and empirical justifications for grouping species into PFTs or biomes are needed to adequately represent the dynamics of ecosystem functioning and structure.

Alaska↗
USGS2023

An assessment of HgII to preserve carbonate system parameters in organic-rich estuarine waters

This work assesses the effectiveness of sample preservation techniques for measurements of pH T (total scale), total dissolved inorganic carbon (C T ), and total alkalinity (A T ) in organic-rich estuarine waters as well as the internal consistency of measurements and calculations (e.g., A T , pH T , and C T ) in these waters. Using mercuric chloride (HgCl 2 )-treated and untreated water samples, measurements of these carbonate system parameters were examined over a period of 3 months. Respiration of dissolved organic matter in untreated samples created large discrepancies in C T concentrations (~37 μ mol kg −1 increase, p < 0.0001), while C T was effectively constant in treated samples (3095.0 ± 1.14 μ mol kg −1 ). A T changes were observed for both treated and untreated samples, with HgCl 2 -treated samples showing the greatest variation (~ 26 μ mol kg −1 decrease, p < 0.001). In response to changing A T /C T ratios, pH T changes occurred in both treated and untreated samples but were relatively small in treated samples. Results in organic-rich estuarine waters that reflect the in situ carbonate system characteristics of the samples at the time of collection can be improved when samples obtained for C T and A T analysis are collected and stored separately. Accurate analyses of C T can be obtained by filtration and preservation with HgCl 2 . Accuracy of A T analyses can be improved by filtration and storage without adding HgCl 2 . The quality of pH T measurements can be improved by prompt analysis in the field and, if this cannot be accomplished, then samples can be preserved with HgCl 2 and measured in the laboratory within 1 week.

Limnology and Oceanography: Methods↗
USGS2013

Characterisation of the Permafrost Carbon Pool

The current estimate of the soil organic carbon (SOC) pool in the northern permafrost region of 1672 Petagrams (Pg) C is much larger than previously reported and needs to be incorporated in global soil carbon (C) inventories. The Northern Circumpolar Soil Carbon Database (NCSCD), extended to include the range 0–300 cm, is now available online for wider use by the scientific community. An important future aim is to provide quantitative uncertainty ranges for C pool estimates. Recent studies have greatly improved understanding of the regional patterns, landscape distribution and vertical (soil horizon) partitioning of the permafrost C pool in the upper 3 m of soils. However, the deeper C pools in unconsolidated Quaternary deposits need to be better constrained. A general lability classification of the permafrost C pool should be developed to address potential C release upon thaw. The permafrost C pool and its dynamics are beginning to be incorporated into Earth System models, although key periglacial processes such as thermokarst still need to be properly represented to obtain a better quantification of the full permafrost C feedback on global climate change.

Permafrost and Periglacial Processes↗
USGS2010

The effects of land cover and land use change on the contemporary carbon balance of the arctic and boreal terrestrial ecosystems of northern Eurasia

Recent changes in climate, disturbance regimes and land use and management systems in Northern Eurasia have the potential to disrupt the terrestrial sink of atmospheric CO 2 in a way that accelerates global climate change. To determine the recent trends in the carbon balance of the arctic and boreal ecosystems of this region, we performed a retrospective analysis of terrestrial carbon dynamics across northern Eurasia over a recent 10-year period using a terrestrial biogeochemical process model. The results of the simulations suggest a shift in direction of the net flux from the terrestrial sink of earlier decades to a net source on the order of 45 Tg C year −1 between 1997 and 2006. The simulation framework and subsequent analyses presented in this study attribute this shift to a large loss of carbon from boreal forest ecosystems, which experienced a trend of decreasing precipitation and a large area burned during this time period.

Book chapter↗
USGS1994

Hydrological controls on dissolved organic carbon during snowmelt in the Snake River near Montezuma, Colorado

A quantitative understanding of the factors controlling the variation of dissolved organic carbon (DOC) in headwater streams is of scientific concern for at least two reasons. First, quantifying the overall carbon budgets of lotic systems is needed for a fundamental understanding of these systems. Second, DOC interacts strongly with other dissolved substances (heavy metals in particular) and plays an important role in the transport of contaminants. In the Snake River near Montezuma, Colorado, measurements of DOC from 1980 to 1986 show rapid decreases in concentration from a peak very early in the snowmelt period. Peak DOC concentrations occur approximately one month prior to peak discharge in the stream. The decline in DOC with time is approximately exponential, suggesting that a simple flushing mechanism can explain the response. We examined hydrological mechanisms to explain the observed variability of DOC in the Snake River by simulating the hydrological response of the catchment using TOPMODEL and routing the predicted flows through a simple model that accounted for temporal changes in DOC. Conceptually the DOC model represents a terrestrial (soil) reservoir in which DOC builds up during low flow periods and is flushed out by infiltrating meltwaters. The model reproduces the main features of the observed variation in DOC in the Snake River and thus lays the foundation for quantitatively linking hydrological processes with carbon cycling through upland catchments. Model results imply that a significant fraction of the soils in the Snake River catchment contribute DOC to the stream during peak discharge. Our work represents one of the first attempts to quantitatively describe the hydrological controls on DOC dynamics in a headwater stream. These controls are studied through the model by imposing mass balance constraints on both the flux of water through the various DOC source areas and the amount of DOC that can accumulate in these areas.

Colorado↗
USGS1993

Alternative solution model for the ternary carbonate system CaCO3 - MgCO3 - FeCO3 - I. A ternary Bragg-Williams ordering model

The minerals of the ternary carbonate system CaCO3 - MgCO3 - FeCO3 represent a complex series of solid solutions and ordering states. An understanding of those complexities requires a solution model that can both duplicate the subsolidus phase relationships and generate correct values for the activities. Such a solution model must account for the changes in the total energy of the system resulting from a change in the ordering state of the individual constituents. Various ordering models have been applied to binary carbonate systems, but no attempts have previously been made to model the ordering in the ternary system. This study derives a new set of equations that allow for the equilibrium degree of order to be calculated for a system involving three cations mixing on two sites, as in the case of the ternary carbonates. The method is based on the Bragg-Williams approach. From the degree of order, the mole fractions of the three cations in each of the two sites can be determined. Once the site occupancies have been established, a Margules-type mixing model can be used to determine the free energy of mixing in the solid solution and therefore the activities of the various components. ?? 1993 Springer-Verlag.

Physics and Chemistry of Minerals↗
USGS1993

Alternative solution model for the ternary carbonate system CaCO3 - MgCO3 - FeCO3 - II. Calibration of a combined ordering model and mixing model

Earlier attempts at solution models for the ternary carbonate system have been unable to adequately accommodate the cation ordering which occurs in some of the carbonate phases. The carbonate solution model of this study combines a Margules type of interaction model with a Bragg-Williams type of ordering model. The ordering model determines the equilibrium state of order for a crystal, from which the cation distribution within the lattice can be obtained. The interaction model addresses the effect that mixing different cation species within a given cation layer has on the total free energy of the system. An ordering model was derived, based on the Bragg-Williams approach; it is applicable to ternary systems involving three cations substituting on two sites, and contains three ordering energy parameters (WCaMg, WCaFe, and WCaMgFe). The solution model of this study involves six Margules-type interaction parameters (W12, W21, W13, W31, W23, and W32). Values for the two sets of energy parameters were calculated from experimental data and from compositional relationships in natural assemblages. ?? 1993 Springer-Verlag.

Physics and Chemistry of Minerals↗
USGS2002

Carbon budget for a subtropical seagrass dominated coastal lagoon: How important are seagrasses to total ecosystem net primary production?

It has been assumed that because seagrasses dominate macrophyte biomass in many estuaries they also dominate primary production. We tested this assumption by developing three carbon budgets to examine the contribution of autotrophic components to the total ecosystem net primary production (TENPP) of Lower Laguna Madre, Texas. The first budget coupled average photosynthetic parameters with average daily irradiance to calculate daily production. The second budget used average photosynthetic parameters and hourly in situ irradiance to estimate productivity. The third budget integrated temperature-adjusted photosynthetic parameters (using Q 10 =2) and hourly in situ irradiance to estimate productivity. For each budget TENPP was calculated by integrating production from each autotroph based on the producers’ areal distribution within the entire Lower Laguna Madre. All budgets indicated that macroalgae account for 33–42% of TENPP and seagrasses consistently accounted for about 33–38%. The contribution by phytoplankton was consistently about 15–20%, and the contribution from the benthic microalgae varied between 8% and 36% of TENPP, although this may have been underestimated due to our exclusion of the within bed microphytobenthos component. The water column over the seagrass beds was net heterotrophic and consequently was a carbon sink consuming between 5% and 22% of TENPP, TENPP ranged between 5.41×10 10 and 2.53×10 11 g C yr −1 , depending on which budget was used. The simplest, most idealized budget predicted the highest TENPP, while the more realistic budgets predicted lower values. Annual production rates estimated using the third budget for Halodule urightii and Thalassia testudinum compare well with field data. Macroalgae and microalgae contribute 50–60% of TENPP, and seagrass may be more important as three-dimensional habitat (i.e., structure) than as a source of organic carbon to the water column in Lower Laguna Madre.

Texas↗
USGS2020

Seasonal and individual event-responsiveness are key determinants of carbon exchange across plant functional types

Differentiation in physiological activity is a critical component of resource partitioning in resource-limited environments. For example, it is crucial to understand how plant physiological performance varies through time for different functional groups to forecast how terrestrial ecosystems will respond to change. Here, we tracked the seasonal progress of 13 plant species representing C 3 shrub, perennial C 3 and C 4 grass, and annual forb functional groups of the Colorado Plateau, USA. We tested for differences in carbon assimilation strategies and how photosynthetic rates related to recent, seasonal, and annual precipitation and temperature variables. Despite seasonal shifts in species presence and activity, we found small differences in seasonally weighted annual photosynthetic rates among groups. However, differences in the timing of maximum assimilation ( A net ) were strongly functional group-dependent. C 3 shrubs employed a relatively consistent, low carbon capture strategy and maintained activity year-round but switched to a rapid growth strategy in response to recent climate conditions. In contrast, grasses maintained higher carbon capture during spring months when all perennials had maximum photosynthetic rates, but grasses were dormant during months when shrubs remained active. Perennial grass A net rates were explained in part by precipitation accumulated during the preceding year and average maximum temperatures during the past 48 h, a result opposite to shrubs. These results lend insight into diverse physiological strategies and their connections to climate, and also point to the potential for shrubs to increase in abundance in response to increased climatic variability in drylands, given shrubs’ ability to respond rapidly to changing conditions.

Oecologia↗
USGS2011

The effects of permafrost thaw on soil hydrologic, thermal, and carbon dynamics in an Alaskan peatland

Recent warming at high-latitudes has accelerated permafrost thaw in northern peatlands, and thaw can have profound effects on local hydrology and ecosystem carbon balance. To assess the impact of permafrost thaw on soil organic carbon (OC) dynamics, we measured soil hydrologic and thermal dynamics and soil OC stocks across a collapse-scar bog chronosequence in interior Alaska. We observed dramatic changes in the distribution of soil water associated with thawing of ice-rich frozen peat. The impoundment of warm water in collapse-scar bogs initiated talik formation and the lateral expansion of bogs over time. On average, Permafrost Plateaus stored 137 ± 37 kg C m -2 , whereas OC storage in Young Bogs and Old Bogs averaged 84 ± 13 kg C m -2 . Based on our reconstructions, the accumulation of OC in near-surface bog peat continued for nearly 1,000 years following permafrost thaw, at which point accumulation rates slowed. Rapid decomposition of thawed forest peat reduced deep OC stocks by nearly half during the first 100 years following thaw. Using a simple mass-balance model, we show that accumulation rates at the bog surface were not sufficient to balance deep OC losses, resulting in a net loss of OC from the entire peat column. An uncertainty analysis also revealed that the magnitude and timing of soil OC loss from thawed forest peat depends substantially on variation in OC input rates to bog peat and variation in decay constants for shallow and deep OC stocks. These findings suggest that permafrost thaw and the subsequent release of OC from thawed peat will likely reduce the strength of northern permafrost-affected peatlands as a carbon dioxide sink, and consequently, will likely accelerate rates of atmospheric warming.

Alaska↗
USGS1992

Chemical changes and carbon isotope variations in a cross-section of a large Miocene gymnospermous log

The cross-sectional radius of a 3-m (diam.) brown coal gymnospermous log of Miocene age, previously analyzed for carbohydrate and lignin methoxyl content by solid-state 13 C nuclear magnetic resonance spectroscopy, was examined using stable carbon isotopic ratios in order to determine if the isotopic composition could be related to chemical changes or to radial position. This study found a possible relationship between δ 13 C-values and radial position; however, these changes cannot be linked to carbohydrate content and are probably attributable to changing growth conditions during the lifetime of the tree. An apparent linear relationship between the changes in carbohydrate content after sodium para-periodate treatment and corresponding changes in the δ 13 C-values indicates constant isotopic fractionation between lignin and carbohydrates along the cross-sectional radius. This result indicates that diagenesis has not produced any significant change in the lignin-carbohydrate carbon isotopic fractionation or, alternatively, that diagenesis has erased any fractionation pattern that once existed. A sample of fresh wood from another gymnospermous species was analyzed by the same methods and found to have lignin-carbohydrate carbon isotopic fractionation significantly different from that of the Miocene log section samples, suggesting that differences may be species-related or that the complex mixture of carbohydrates in the fresh wood was isotopically different from that of the degraded wood, and the whole Miocene log was uniformly altered.

Chemical Geology↗
USGS1969

Hydrology of carbonate rock terranes — A review: With special reference to the United States

Limestone and other carbonate rocks are characterized by many unusual features and extreme conditions, either involving the hydrologic system within them or wrought by hydrologic conditions on them or through them. Perhaps there could be little agreement as to what is typical or average for the many features of carbonate rocks, as indicated by the following conditions: bare rock and thin soils are common, but so are thick soils; very highly permeable limestones are common, but so are poorly permeable ones; and rugged karst topographic features with underlying solution caverns are common, but so are flat, nearly featureless topographic conditions. Some conditions of carbonate terranes are suitable to man's needs and interests, such as the use of some permeable aquifers for water supply and the exploitation of caves for tourist attractions. On the other hand, many problems may exist, including: permeability too low for adequate water supply or so high that the aquifer retains too little water for use during periods of fair weather, soils too thin for growing of crops and for adequate filtration of wastes near the ground surface, instability of the ground for buildings and foundations in sinkhole areas, and unusually rugged topography. Some of the many variable conditions are readily observable, but others can be determined only by careful geologic and hydrologic studies. The need for knowing the specific geologic and hydrologic conditions at various places in limestone terranes, as well as the variations in hydrologic conditions with changing conditions and time, has resulted in many published reports on local areas and on special topical problems of limestone hydrology. Many of these reports have been used to advantage by the present writers in preparing this paper. The concept that secondary permeability is developed by circulation of water through openings with the accompanying enlargement of these openings by solution is now universally accepted in limestone terranes. Emphasis is placed on the hydrogeologic framework, or structural setting, in relation to the ease or difficulty of water to move from a source of recharge, through a part of the limestone, to a discharge area. Parts of the limestone favored by circulating ground water tend to develop solution openings, commonly in the upper part of the zone of saturation; as base level is lowered (sea level or perennial stream level), the related water table lowers in the limestone leaving air-filled caverns above the present zone of saturation in sinkhole areas. Reconstruction of the geologic and hydrologic history of a limestone area aids in determining the extent of development and the positions of fossil and present permeability. References are made to the hydrology of many limestone regions, especially those of the United States.

Journal of Hydrology↗
USGS1976

Bicarbonate content of groundwater in carbonate rock in eastern North America

In carbonate-rock terrane the most effective solution occurs where soil and vegetative cover facilitate biogenic production and storage of CO 2 in the soil until part of it is carried downward in percolating water. Bicarbonate data for groundwater in eastern North America are examined in the light of these conditions, of the CO 2 content of soil gas, and of the timing of groundwater recharge relative to seasonal changes in soil temperature. There appears to be no well-marked relation between latitude and bicarbonate content of groundwater in this region. Interplay of all the factors listed above, and of lithology and soil types, is evidently such that under optimum conditions the amount of solution of carbonate rock is roughly comparable, per unit of groundwater recharge, over the region from Ohio to Florida (and, perhaps, to Puerto Rico and Yucatan). Relatively low HCO 3 concentrations observed in much of the southern United States are attributed to low production and storage of CO 2 in sandy soil that is poor in organic matter. On the other hand, concentrations observed in Ontario, New York and Michigan are markedly higher than is to be expected from interrelations of the factors considered. These high values, apparently anomalous, are attributed in part to solution of granular glacial drift derived largely from carbonate rock.

Journal of Hydrology↗
USGS1981

Tertiary carbonate-dissolution cycles on the Sierra Leone Rise, eastern equatorial Atlantic Ocean

Most of the Tertiary section on Sierra Leone Rise off northwest Africa consists of chalk, marl, and limestone that show cyclic alterations of clay-rich and clay-poor beds about 20–60 cm thick. On the basis of biostratigraphic accumulation rates, the cycles in Oligocene and Miocene chalk have periods which average about 44,000 years, and those in Eocene siliceous limestone have periods of 4000–27,000 years. Several sections were sampled in detail to further define the cycles in terms of content of CaCO 3 , clay minerals, and relative abundances of calcareous nannofossils. Extending information gained by analyses of Pleistocene cores from the continental margin of northwest Africa to the Tertiary cycles on Sierra Leone Rise, both dilution by noncarbonate material and dissolution of CaCO 3 could have contributed to the observed relative variations in clay and CaCO 3 . However, dissolution of CaCO 3 as the main cause of the carbonate-clay cycles on the Sierra Leone Rise, rather than dilution by clay, is suggested by the large amount of change (several thousand percent) in terrigenous influx required to produce the observed variations in amount of clay and by the marked increase in abundance of dissolution-resistant discoasters relative to more easily dissolved coccoliths in low-carbonate parts of cycles. The main cause of dissolution of CaCO 3 was shoaling of the carbonate compensation depth (CCD) during the early Neogene and climatically induced fluctuations in the thickness of Antarctic Bottom Water.

Marine Geology↗
USGS2009

Simulated dynamics of carbon stocks driven by changes in land use, management and climate in a tropical moist ecosystem of Ghana

Sub-Saharan Africa is large and diverse with regions of food insecurity and high vulnerability to climate change. This project quantifies carbon stocks and fluxes in the humid forest zone of Ghana, as a part of an assessment in West Africa. The General Ensemble biogeochemical Modeling System (GEMS) was used to simulate the responses of natural and managed systems to projected scenarios of changes in climate, land use and cover, and nitrogen fertilization in the Assin district of Ghana. Model inputs included historical land use and cover data, historical climate records and projected climate changes, and national management inventories. Our results show that deforestation for crop production led to a loss of soil organic carbon (SOC) by 33% from 1900 to 2000. The results also show that the trend of carbon emissions from cropland in the 20th century will continue through the 21st century and will be increased under the projected warming and drying scenarios. Nitrogen (N) fertilization in agricultural systems could offset SOC loss by 6% with 30 kg N ha −1 year −1 and by 11% with 60 kg N ha −1 year −1 . To increase N fertilizer input would be one of the vital adaptive measures to ensure food security and maintain agricultural sustainability through the 21st century.

Agriculture, Ecosystems and Environment↗
USGS2013

Tracing groundwater with low-level detections of halogenated VOCs in a fractured carbonate-rock aquifer, Leetown Science Center, West Virginia, USA

Measurements of low-level concentrations of halogenated volatile organic compounds (VOCs) and estimates of groundwater age interpreted from 3 H/ 3 He and SF 6 data have led to an improved understanding of groundwater flow, water sources, and transit times in a karstic, fractured, carbonate-rock aquifer at the Leetown Science Center (LSC), West Virginia. The sum of the concentrations of a set of 16 predominant halogenated VOCs (TDVOC) determined by gas chromatography with electron-capture detector (GC–ECD) exceeded that possible for air–water equilibrium in 34 of the 47 samples (median TDVOC of 24,800 pg kg −1 ), indicating that nearly all the water sampled in the vicinity of the LSC has been affected by addition of halogenated VOCs from non-atmospheric source(s). Leakage from a landfill that was closed and sealed nearly 20 a prior to sampling was recognized and traced to areas east of the LSC using low-level detection of tetrachloroethene (PCE), methyl chloride (MeCl), methyl chloroform (MC), dichlorodifluoromethane (CFC-12), and cis-1,2-dichloroethene (cis-1,2-DCE). Chloroform (CHLF) was the predominant VOC in water from domestic wells surrounding the LSC, and was elevated in groundwater in and near the Fish Health Laboratory at the LSC, where a leak of chlorinated water occurred prior to 2006. The low-level concentrations of halogenated VOCs did not exceed human or aquatic-life health criteria, and were useful in providing an awareness of the intrinsic susceptibility of the fractured karstic groundwater system at the LSC to non-atmospheric anthropogenic inputs. The 3 H/ 3 He groundwater ages of spring discharge from the carbonate rocks showed transient behavior, with ages averaging about 2 a in 2004 following a wet climatic period (2003–2004), and ages in the range of 4–7 a in periods of more average precipitation (2008–2009). The SF 6 and CFC-12 data indicate older water (model ages of 10s of years or more) in the low-permeability shale of the Martinsburg Formation located to the west of the LSC. A two-a record of specific conductance, water temperature, and discharge recorded at 30-min intervals demonstrated an approximately 3-month lag in discharge at Gray Spring. The low groundwater ages of waters from the carbonate rocks support rapid advective transport of contaminants from the LSC vicinity, yet the nearly ubiquitous occurrence of low-level concentrations of halogenated VOCs at the LSC suggests the presence of long-term persistent sources, such as seepage from the closed and sealed landfill, infiltration of VOCs that may persist locally in the epikarst, exchange with low-permeability zones in fractured rock, and upward leakage of older water that may contain elevated concentrations of halogenated VOCs from earlier land use activities.

West Virginia↗
USGS2012

A land-use and land-cover modeling strategy to support a national assessment of carbon stocks and fluxes

Changes in land use, land cover, disturbance regimes, and land management have considerable influence on carbon and greenhouse gas (GHG) fluxes within ecosystems. Through targeted land-use and land-management activities, ecosystems can be managed to enhance carbon sequestration and mitigate fluxes of other GHGs. National-scale, comprehensive analyses of carbon sequestration potential by ecosystem are needed, with a consistent, nationally applicable land-use and land-cover (LULC) modeling framework a key component of such analyses. The U.S. Geological Survey has initiated a project to analyze current and projected future GHG fluxes by ecosystem and quantify potential mitigation strategies. We have developed a unique LULC modeling framework to support this work. Downscaled scenarios consistent with IPCC Special Report on Emissions Scenarios (SRES) were constructed for U.S. ecoregions, and the FORE-SCE model was used to spatially map the scenarios. Results for a prototype demonstrate our ability to model LULC change and inform a biogeochemical modeling framework for analysis of subsequent GHG fluxes. The methodology was then successfully used to model LULC change for four IPCC SRES scenarios for an ecoregion in the Great Plains. The scenario-based LULC projections are now being used to analyze potential GHG impacts of LULC change across the U.S.

Applied Geography↗
USGS2004

Feasibility of measuring dissolved carbon dioxide based on head space partial pressures

We describe an instrument prototype that measures dissolved carbon dioxide (DC) without need for standard wetted probe membranes or titration. DC is calculated using Henry's Law, water temperature, and the steady-state partial pressure of carbon dioxide that develops within the instrument's vertical gas-liquid contacting chamber. Gas-phase partial pressures were determined with either an infrared detector (ID) or by measuring voltage developed by a pH electrode immersed in an isolated sodium carbonate solution (SC) sparged with recirculated head space gas. Calculated DC concentrations were compared with those obtained by titration over a range of DC (2, 4, 8, 12, 16, 20, 24, and 28mg/l), total alkalinity (35, 120, and 250mg/l as CaCO3), total dissolved gas pressure (-178 to 120 mmHg), and dissolved oxygen concentrations (7, 14, and 18 mg/l). Statistically significant (P < 0.001) correlations were established between head space (ID) and titrimetrically determined DC concentrations (R2 = 0.987-0.999, N = 96). Millivolt and titrimetric values from the SC solution tests were also correlated (P < 0.001, R 2 = 0.997, N = 16). The absolute and relative error associated with the use of the ID and SC solution averaged 0.9mg/l DC and 7.0% and 0.6 mg/l DC and 9.6%, respectively. The precision of DC estimates established in a second test series was good; coefficients of variation (100(SD/mean)) for the head space (ID) and titration analyses were 0.99% and 1.7%. Precision of the SC solution method was 1.3%. In a third test series, a single ID was coupled with four replicate head space units so as to permit sequential monitoring (15 min intervals) of a common water source. Here, appropriate gas samples were secured using a series of solenoid valves (1.6 mm bore) activated by a time-based controller. This system configuration reduced the capital cost per sample site from US$ 2695 to 876. Absolute error averaged 2.9, 3.1, 3.7, and 2.7 mg/ l for replicates 1-4 (N = 36) during a 21-day test period (DC range, 36-40 mg/l). The ID meter was then modified so as to provide for DO as well as DC measurements across components of an intensive fish production system. ?? 2003 Elsevier B.V. All rights reserved.

Aquacultural Engineering↗