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1.
Ecotoxicology ; 31(7): 1169-1188, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-35900710

RESUMO

The present study investigated the effects of rising carbon dioxide levels in nature and the carbon sequestration potential of dominant mangrove species for reducing the toxic effects of ocean acidification. The study was conducted on the east coast of Odisha, in the western Bay of Bengal. To determine the effect of these ambient parameters on the absorption of carbon dioxide by the mangroves, water temperature, salinity, pH levels of seawater along with soil texture and pH, salinity expressed in electrical conductivity, compactness expressed in bulk density, and soil organic carbon were simultaneously monitored. The aboveground biomass and carbon of the selected species were studied for 2 consecutive years at 10 designated stations. The total carbon calculated for the study area varied from 242.50 ± 49.00 to 1321.29 ± 445.52 tons with a mean of 626.68 ± 174.81 tons for Bhitarkanika and Mahanadi mangrove chunks. This is equivalent to 2299.92 ± 641.55 tons of CO2 absorbed from the atmosphere. A total of 27 equations were selected as the best fit models for the study area. The equations between mangrove biomass and carbon along with aquatic and edaphic factors governing the pH of water and soil strongly support the positive influence of mangrove photosynthetic activity in shifting the equilibrium toward alkalinity. This calls for conservation of mangrove ecosystem to minimize the pace of acidification of estuarine water. The results indicate that Excoecariaagallocha and Avicennia marina as are the most capable species for combatting maximum carbon dioxide toxicity from the atmosphere; which will be helpful in REDD + programs and carbon-based payments for ecosystem services (PES).


Assuntos
Ecossistema , Áreas Alagadas , Carbono , Dióxido de Carbono , Concentração de Íons de Hidrogênio , Oceanos e Mares , Água do Mar , Solo , Água
2.
Mar Pollut Bull ; 174: 113203, 2022 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34896755

RESUMO

Increased urea is one of the common nitrogen forms polluting coastal waters and affecting nutrient dynamics. To investigate the effects of urea on sediment phosphorus (P) release, we carried out a 2-month mesocosm experiment with six targeted loadings of urea (0-0.6 mg N L-1 d-1). Results showed that: i) urea was rapidly transformed into ammonium and then nitrate (NO3-). ii) When nitrogen occurred as urea or ammonium, minor P release was observed. iii) After urea were mostly converted to NO3-, P release became clearer. iv) NO3- had a dual effect by promoting P release through decreasing sediment pH and increasing alkaline phosphatase activity or by inhibiting P release through improving sediment oxidation. v) The overall effects of urea on P release depended on the ultimate NO3- concentrations, being prominent when NO3- ≥ 11 mg N L-1. Our findings are of relevance when determining nitrogen reduction targets needed for combating eutrophication.


Assuntos
Fósforo , Poluentes Químicos da Água , Eutrofização , Sedimentos Geológicos , Nitrogênio/análise , Ureia , Poluentes Químicos da Água/análise
3.
Biogeochemistry ; 135(1): 69-88, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-32009692

RESUMO

This study used microelectrodes to record pH profiles in fresh shelf sea sediment cores collected across a range of different sediment types within the Celtic Sea. Spatial and temporal variability was captured during repeated measurements in 2014 and 2015. Concurrently recorded oxygen microelectrode profiles and other sedimentary parameters provide a detailed context for interpretation of the pH data. Clear differences in profiles were observed between sediment type, location and season. Notably, very steep pH gradients exist within the surface sediments (10-20 mm), where decreases greater than 0.5 pH units were observed. Steep gradients were particularly apparent in fine cohesive sediments, less so in permeable sandier matrices. We hypothesise that the gradients are likely caused by aerobic organic matter respiration close to the sediment-water interface or oxidation of reduced species at the base of the oxic zone (NH4 +, Mn2+, Fe2+, S-). Statistical analysis suggests the variability in the depth of the pH minima is controlled spatially by the oxygen penetration depth, and seasonally by the input and remineralisation of deposited organic phytodetritus. Below the pH minima the observed pH remained consistently low to maximum electrode penetration (ca. 60 mm), indicating an absence of sub-oxic processes generating H+ or balanced removal processes within this layer. Thus, a climatology of sediment surface porewater pH is provided against which to examine biogeochemical processes. This enhances our understanding of benthic pH processes, particularly in the context of human impacts, seabed integrity, and future climate changes, providing vital information for modelling benthic response under future climate scenarios.

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