scholarly journals Discrete bottle sample measurements for carbonate chemistry, organic alkalinity and organic carbon from samples collected in Waquoit Bay and Vineyard Sound, MA in 2016

Author(s):  
Zhaohui Aleck Wang ◽  
Shuzhen Song ◽  
Meagan Gonneea ◽  
Kevin Kroeger
2009 ◽  
Vol 6 (3) ◽  
pp. 4739-4763 ◽  
Author(s):  
J. Barcelos e Ramos ◽  
M. N. Müller ◽  
U. Riebesell

Abstract. The response of the coccolithophore Emiliania huxleyi to rising CO2 concentrations is well documented in acclimated cultures where cells are exposed to the CO2 treatments for several generations prior to the experiment. Extended acclimation times have generally been applied because of the lack of information about time required to reach a new physiological "equilibrium" (acclimation) in response to CO2-induced changes in seawater carbonate chemistry. Here we show that Emiliania huxleyi's short-term response (hours to 1 day) to increasing CO2 is similar to that obtained with acclimated cultures under comparable conditions in earlier studies. At CO2 concentrations ranging from glacial (190 μatm) to projected year 2100 (750 μatm) levels, calcification decreased and organic carbon fixation increased within 8 h after exposing the cultures to the changed CO2 conditions. This led to a decrease in the ratio of CaCO3 to organic carbon production. Our results show that Emiliania huxleyiapidly alters the rates of various essential processes in response to changes in seawater carbonate chemistry, establishing a new physiological (acclimation) "state" within a matter of hours. If this relatively rapid response applies to other phytoplankton species, it may simplify interpretation of studies with natural communities (e.g. mesocosm studies and ship-board incubations), where often it is not feasible to allow for a pre-conditioning phase before starting experimental incubations.


2021 ◽  
Vol 8 ◽  
Author(s):  
Ariel K. Pezner ◽  
Travis A. Courtney ◽  
Heather N. Page ◽  
Sarah N. Giddings ◽  
Cory M. Beatty ◽  
...  

Spatial and temporal carbonate chemistry variability on coral reefs is influenced by a combination of seawater hydrodynamics, geomorphology, and biogeochemical processes, though their relative influence varies by site. It is often assumed that the water column above most reefs is well-mixed with small to no gradients outside of the benthic boundary layer. However, few studies to date have explored the processes and properties controlling these multi-dimensional gradients. Here, we investigated the lateral, vertical, and temporal variability of seawater carbonate chemistry on a Bermudan rim reef using a combination of spatial seawater chemistry surveys and autonomous in situ sensors. Instruments were deployed at Hog Reef measuring current flow, seawater temperature, salinity, pHT, pCO2, dissolved oxygen (DO), and total alkalinity (TA) on the benthos, and temperature, salinity, DO, and pCO2 at the surface. Water samples from spatial surveys were collected from surface and bottom depths at 13 stations covering ∼3 km2 across 4 days. High frequency temporal variability in carbonate chemistry was driven by a combination of diel light and mixed semi-diurnal tidal cycles on the reef. Daytime gradients in DO between the surface and the benthos suggested significant water column production contributing to distinct diel trends in pHT, pCO2, and DO, but not TA. We hypothesize these differences reflect the differential effect of biogeochemical processes important in both the water column and benthos (organic carbon production/respiration) vs. processes mainly occurring on the benthos (calcium carbonate production/dissolution). Locally at Hog Reef, the relative magnitude of the diel variability of organic carbon production/respiration was 1.4–4.6 times larger than that of calcium carbonate production/dissolution, though estimates of net organic carbon production and calcification based on inshore-offshore chemical gradients revealed net heterotrophy (−118 ± 51 mmol m–2 day–1) and net calcification (150 ± 37 mmol CaCO3 m–2 day–1). These results reflect the important roles of time and space in assessing reef biogeochemical processes. The spatial variability in carbonate chemistry parameters was larger laterally than vertically and was generally observed in conjunction with depth gradients, but varied between sampling events, depending on time of day and modifications due to current flow.


Author(s):  
Dong Chen ◽  
Che-Jen Lin ◽  
R. Gavin Jones ◽  
Sehul Patel ◽  
Rachelle Smith ◽  
...  
Keyword(s):  

2018 ◽  
Vol 18 (3) ◽  
pp. 81-91 ◽  
Author(s):  
C. Lalhriatpuia

Nanopillars-TiO2 thin films was obtained on a borosilicate glass substrate with (S1) and without (S2) polyethylene glycol as template. The photocatalytic behaviour of S1 and S2 thin films was assessed inthe degradation of methylene blue (MB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the SEM, XRD, FTIR and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data confirmed that the TiO2 particles are in its anatase mineral phase. The SEM and AFM images indicated the catalyst is composed with nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of MB was well studied at wide range of physico-chemical parameters. The effect of solution pH (pH 4.0 to 10.0) and MB initial concentration (1.0 to 10.0 mg/L) was extensively studied and the effect of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of MB was demonstrated. The maximum percent removal of MB was observed at pH 8.0 beyond which it started decreasing and a low initial concentration of the pollutant highly favoured the photocatalytic degradation using thin films and the presence of several interfering ions diminished the photocatalytic activity of thin films to some extent. The overall photocatalytic activity was in the order: S2 > S1 > UV. The photocatalytic degradation of MB was followed the pseudo-first-order rate kinetics. The mineralization of MB was studied with total organic carbon measurement using the TOC (total organic carbon) analysis.


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