Estimation of residence time of groundwater, particularly in regions with inadequate surface waters are very important for formulating sustainable groundwater management policies. We developed a technique for extracting dissolved inorganic carbon (DIC) quantitatively from water for measuring its 14C contents and presented the analytical details here. We also measured stable carbon isotope ratio (δ13C) in soil CO2 and groundwater DIC to correct the groundwater 14C ages. In addition, 14C in soil CO2 were measured for making necessary correction in the initial activity of the recharging water. The corrected 14C contents in the groundwater samples were used to estimate their residence times employing Lumped Parameter Models (LPM), a set of mathematical models to account for the processes that take place during transport from the recharge to the sampling spots. We present a case study focused on the calculation of radiocarbon ages and residence times for a groundwater sample collected from the campus of Physical Research Laboratory in Ahmedabad, Gujarat, India. The study also includes estimations of groundwater residence times using previously measured 14C ages of groundwater samples from Gujarat, India. Various factors controlling the groundwater ages in the LPM and their applicability are discussed.

Radiocarbon observations (Δ14C) in dissolved inorganic carbon (DIC) of seawater provide useful information about ocean carbon cycling and ocean circulation. To deliver high-quality observations, the Laboratory of Ion Beam Physics (LIP) at ETH-Zurich developed a new simplified method allowing the rapid analysis of radiocarbon in DIC of small seawater samples, which is continually assessed by following internal quality controls. However, a comparison with externally produced 14C measurements to better establish an equivalency between methods was still missing. Here, we make the first intercomparison with the National Ocean Sciences Accelerator Mass Spectrometry (NOSAMS) facility based on 14 duplicate seawater samples collected in 2020. We also compare with prior deep-water observations from the 1970s to 1990s. The results show a very good agreement in both comparisons. The mean Δ14C of 12 duplicate samples measured by LIP and NOSAMS were statistically identical within one sigma uncertainty while two other duplicate samples agreed within two sigma. Based on this small number of duplicate samples, LIP values appear to be slightly lower than the NOSAMS values, but more measurements will be needed for confirmation. We also comment on storage and preservation techniques used in this study, including the freezing of samples collected in foil bags.

The importance of studying the radiocarbon content of dissolved inorganic carbon (DI14C) in the oceans has been recognized for decades. Starting with the GEOSECS program in the 1970s, 14C sampling has been a part of most global survey programs. Early results were used to study air-sea gas exchange while the more recent results are critical for helping calibrate ocean general circulation models used to study the effects of climate change. Here we summarize the major programs and discuss some of the important insights the results are starting to provide.

We report on an initial long-term study of dissolved inorganic and organic carbon (DIC) from Sabino Creek, located in Sabino Canyon, Pima County, Arizona. The purpose of this study was to monitor changes in dissolved radiocarbon (14C) with time and to understand the processes contributing to these variations. Our results span the period 2009–2016 and show a mixing trend between dissolved inorganic and organic carbon modern end-members with an older component. This study provides preliminary information for more detailed research on recycling of organic components in this stream system.

Radiocarbon (14C) generated by the thermonuclear tests in the late 1950s to early 1960s has been used as a tracer to study atmospheric and oceanic circulations, carbon exchange between different reservoirs, and fossil fuel emissions. Here we report the first measurements of 14C in atmospheric CO2 of maritime air collected over the South China Sea (SCS) during July 2014. We also present 14C of the dissolved inorganic carbon (DIC) in the sea surface water in the same region. Most of the Δ14C values of the atmospheric CO2 vary in the range of 15.6±1.6‰– 22.0±1.6‰, indicating that the central SCS maritime air is well-mixed and consistent with the clean background air in the Northern Hemisphere. The 14C values of the DIC (DI14C) in the surface seawater vary between 28.3±2.5‰ and 40.6±2.7‰, mainly due to the lateral mixing between the SCS and western Pacific. The average surface seawater DI14C is 15.4 ± 5.1‰ higher than that of the maritime air 14CO2. The reversal of the sea–air Δ14C gradient occurred at ∼2000, marking the start of the upper ocean transferring bomb 14C back to the atmosphere in the SCS.

Radiocarbon (14C) in dissolved inorganic carbon (DIC) was measured for water samples collected from six deep stations in the Kuroshio Extension (KE) region in the northwestern North Pacific in April–May 2015. Vertical profiles of Δ14C-DIC indicate that bomb-produced 14C was present from the surface to ~1500 m water depth. Large variations in Δ14C-DIC values (300‰) were observed at 500 m water depth among the stations and the differences were likely controlled by transport and mixing dynamics of different water masses in the region. The major Pacific western boundary currents, such as Kuroshio and Oyashio and regional mesoscale eddies, could play important roles affecting the observed Δ14C-DIC variability. The depth profiles of both Δ14C-DIC and DIC concentrations can be predicted by the solution mixing model and can be used as conservative tracers of water mass movement and water parcel homogenization in the ocean.

We present radiocarbon (14C) measurements of dissolved inorganic carbon (DIC) from surface waters of 11 lakes, widely distributed in China. Surface lake water DIC F14C values show distinct differences, and we relate these to the physical exchange character (“open” or “closed”) of each lake. Open lakes studied here generally have lower DIC F14C values than closed lakes. We present a simple model of a lake water cycle to calculate an average residence time for each lake. Comparisons between lake DIC F14C and average residence time shows that the DIC F14C increases with the average residence time and reflects a steady-state.

Terrestrial plant remains in the sediments of lakes from semi-arid and arid regions are rare and therefore the establishment of a sediment chronology depends on accurate assessment of the reservoir effect of the lake water. In a study of Genggahai Lake in the Gonghe Basin, northeastern Qinghai-Tibetan Plateau, we used accelerator mass spectrometry radiocarbon (AMS 14C) dating to determine the age of (1) dissolved inorganic carbon in the water (DICLW), (2) macrophyte remains in the uppermost samples of core sediments, (3) living P. pectinatus in the lake, and (4) dissolved inorganic carbon of spring water in the catchment. The results show that the ages of the DICLW (910 14C yr BP on average) were much younger than the ages of the groundwater (6330 14C yr BP on average), which may result mainly from CO2 exchange between the lake water and the atmosphere. In addition, the 14C ages of DICLW and macrophyte remains in the uppermost core sediments varied from site to site within the lake, which we ascribe to the different photosynthesis rates of Chara spp. and vascular plants. The higher photosynthesis rate of Chara spp. decreases lake-water pCO2, which leads to more atmospheric CO2 being absorbed by the lake water, and thereby greatly reducing the age of carbon species in areas dominated by Chara spp. Although Genggahai Lake is well mixed, the differences between the apparent ages of the lake water are significantly modulated by the photosynthesis intensity of submerged plants.

In order to map the freshwater reservoir effect (FRE) variability of the Loire River and its tributaries, spatial and temporal carbon isotope (13C and 14C) analyses of the dissolved inorganic carbon (DIC) were conducted. Sites were selected to represent the diversity of geological settings, soil type, and land use. Results show a large spatial variability of 14C FRE ranging between 135 and 2251±30 yr, objectively correlated to DIC contents and alkalinity. Deeper investigations of the relationship between 14C activity of DIC and environmental variables show that the geological substrate is the dominant factor in the 14C reservoir effect, and far more influential than the river flow discharge.

Dissolved inorganic carbon (DIC) in groundwater is used to estimate the residence time based on radiocarbon concentration. DIC is usually extracted by a gas-strip or precipitation (SrCO3 or BaCO3) method. In this study, the gas-strip and precipitation methods of DIC were applied to both artificially prepared NaHCO3 solutions and natural groundwater to estimate the certainty of the two methods for 14C dating. 14C values obtained by the gas-strip method for NaHCO3 solutions with distinct salinity, DIC, and 14C concentrations were close to the theoretically predicted 14C value based on the 14C value of NaHCO3 powder. Conversely, the 14C value obtained by the precipitation method always showed higher values than the predicted values. The difference in 14C value between the gas-strip and precipitation methods was assumed to be caused by the contamination of modern carbon in the NaOH solution used in the precipitation method. The contamination of modern carbon derived from the NaOH solution during precipitation was found to range from less than 1 mg/L to about 1 mg/L. The applicability of the precipitation method for groundwater should be considered carefully according to the DIC, 14C concentration of groundwater, and purpose of the study being conducted.

This article presents a modified method for extraction of dissolved inorganic carbon (DIC) from seawater for radiocarbon measurement by accelerator mass spectrometry (AMS). Standard tests indicate that the extraction efficiencies of DIC are >96%, and the respective precisions of Δ14C-DIC and δ13C-DIC analyses are 6‰ and 0.1‰ or better. Using the method, we report Δ14C-DIC profiles collected from the shelf and slope in the East China Sea (ECS) of the northwest Pacific Ocean. Both the DIC concentration and Δ14C-DIC in the shelf and slope regions seem primarily affected by the Kuroshio Current. It is estimated that 54–65% of the bottom water in the shelf region could be from the intrusion of Kuroshio intermediate water, which carries a high concentration and low Δ14C values of DIC, and which influenced the DIC and its 14C signature on the shelf. Compared with the Δ14C-DIC profiles at other sites in the northwest Pacific reported previously, it appears that the Δ14C-DIC distributions are mainly controlled by the major oceanic currents in the region, and large variations in Δ14C-DIC occurred mostly in the upper 800 m of the water column. The similarity of Δ14C-DIC at depth suggests that the deep-water circulation patterns have been relatively stable in the northwest Pacific Ocean in the last 20 yr.

We performed an artificial pool experiment in the Antarctic multi-year land-fast ice to examine and simulate the effect of sea ice melting on physical and biogeochemical components of the sea ice field. The input of snow and ice meltwater resulted in warmer, low salinity water at the surface of the pool and probably stratification of the less dense water. Current speed measurements also pointed to water stratification within the pool. Rapid phytoplankton growth in the pool resulted in drastic decreases in concentrations of dissolved inorganic carbon and nutrients (NO3- and Si(OH)4) in the surface waters of the pool, particularly depleted for NO3-. There was high correlation between variations of dissolved inorganic carbon and nutrient concentrations, but the apparent uptake ratios of these components deviated from that generally applied to marine phytoplankton. The sequence of changes in the physical and biogeochemical components of the pool water suggests that the onset of rapid phytoplankton growth was closely related to the water stratification, which provided stable conditions for phytoplankton bloom even though the supply of nutrients from under-ice water would have declined.

A range of marine photosynthetic picoeukaryote phytoplankton species grown in culture were screened for the presence of extracellular carbonic anhydrase (CAext), a key enzyme in inorganic carbon acquisition under carbon- limiting conditions in some larger marine phytoplankton species. Of the species tested, extracellular carbonic anhydrase was detected only in Micromonas pusilla Butcher. The rapid, light-dependent development of CAext when cells were transferred from carbon-replete to carbon-limiting conditions was regulated by the available free- CO2 concentration and not by total dissolved inorganic carbon. Kinetic studies provided support for a CO2- concentrating mechanism in that the K0.5[CO2] (i.e. the CO2 concentration required for the half-maximal rate of photosynthesis) was substantially lower than the Km [CO2] of Rubisco from related taxa, whilst the intracellular carbon pool was at least seven fold greater than the extracellular DIC concentration, for extracellular DIC values [les ]1.0 mm.

It is proposed that when the flux of CO2 into the cell is insufficient to support the photosynthetic rate at an optimum photon irradiance, the development of CAext increases the availability of CO2 at the plasma membrane. This ensures rapid acclimation to environmental change and provides an explanation for the central role of M. pusilla as a carbon sink in oligotrophic environments.

The presence of extracellular carbonic anhydrase (CA) in relation to medium composition was investigated using cultures of the marine diatom Phaeodactylum tricornutum Bohlin. Large-volume cultures, with low initial cell inocula were grown on ASP-2 (no dissolved inorganic carbon (DIC), 550 μM NO3−), f/2 (2·0 mM DIC, 880 μM NO3−) and modified f/2 (2·0 mM DIC, 20 μM NO3− media. Cells growing on ASP-2 showed extracellular CA in the early stages of growth, whereas extracellular CA was not detected until partial depletion of total DIC in the stationary phase for cultures on f/2 or modified f/2. Both HCO3− and CO2 were important in carbon limitation, extracellular CA being present when the free-CO2 concentration fell below 5 μM, but the HCO3− concentration needed to be below 1 mM. When carbon-replete cells were transferred to carbon-limited conditions, extracellular CA was recorded within minutes, the process being light-dependent and completely inhibited by 3,3,4-dichlorophenyl-1,1-dimethylurea (DCMU). The addition of DIC to carbon-limited cells resulted in a rapid decrease in extracellular CA activity. The membrane-impermeable inhibitor of carbonic anhydrase, dextran-bound sulphonamide (DBS) was used to inhibit extracellular CA activity in relation to photosynthetic rate in carbon-replete and carbon-limited cells. At the lowest DIC concentration (0·10 mM), for cells with maximum external CA activity, DBS gave over 80% inhibition of the photosynthetic rate, demonstrating the key role of external CA in maintaining high photosynthetic rate under conditions of carbon limitation.

It is proposed that the key factor in the regulation of extracellular CA activity is the total flux of inorganic carbon (Ci) into the cell. This determines the Ci flux into the chloroplast and when this is inadequate to support the photosynthetic rate attained by a carbon-replete chloroplast at optimum photon flux density, extracellular CA is activated. This mechanism would explain the observed interaction of CO2 and HCO3− in the regulation of extracellular CA activity.