研究目的
To reveal the characteristics of the linking optical (FDOMC, FDOMT) and chemical signatures (TDCHO, TDAA) of dissolved organic matter in the southern end of the Argentine shelf, and to provide insights about the factors driving and affecting their relationship, such as bacterial biomass and hydrology in the complex system of the Pacific-Atlantic connection.
研究成果
The comparison of FDOMC and FDOMT distributions with DOM composition indicated substantial input of terrestrial, humic-rich DOM into the shelf region, with carbohydrates behaving as a refractory component in the estuarine environment. Heterotrophic activity played a key role in modulating amino acids distribution, with tight coupling between microbial production and consumption in the Beagle Channel. The study highlights the importance of combining chemical and optical approaches to evaluate DOM sources and fate in marine environments.
研究不足
The study is limited to surface waters (3-10 m depth) and a single sampling period (austral summer 2012), which may not capture seasonal or depth variations. Potential interference in TDCHO quantification from humic phenolic aldehydes is noted, and the spatial coverage is restricted to the southern Argentine shelf.
1:Experimental Design and Method Selection:
The study involved field sampling in the southern Argentine shelf during late austral summer 2012. Optical properties (fluorescence spectroscopy) and chemical analyses (TDCHO, TDAA, DOC) were used to assess DOM signatures. Relationships were analyzed using correlation methods.
2:Optical properties (fluorescence spectroscopy) and chemical analyses (TDCHO, TDAA, DOC) were used to assess DOM signatures. Relationships were analyzed using correlation methods. Sample Selection and Data Sources:
2. Sample Selection and Data Sources: Surface water samples (3-10 m depth) were collected from 16 stations in three sectors (BCW, CW, OW) based on bathymetry, temperature, and salinity. Samples were filtered and stored for analysis.
3:List of Experimental Equipment and Materials:
CTD (Sea Bird model 911 plus with General Oceanic rosette), spectrofluorometer (Shimadzu RF-5301), HPLC (Shimadzu 1OAS with Beckman C-18 column and Shimadzu RF-551 fluorometer), GF/F filters (Whatman), glass ampoules, quinine sulfate standard, amino acid standard mix (Thermo Scientific Pierce, standard code: N° 20088), D-glucose analytical standard, phosphoric acid, HCl, NaOH, TPTZ reagent.
4:Experimental Procedures and Operational Workflow:
Continuous CTD profiles recorded temperature and salinity. Water samples were filtered, aliquoted, and stored. Fluorescence measurements were performed with inner filter corrections and normalization to quinine sulfate units. TDAA were quantified via HPLC after hydrolysis and derivatization. TDCHO were measured spectrophotometrically after hydrolysis and oxidation. DOC was analyzed after acidification and storage.
5:Data Analysis Methods:
Parametric Pearson’s rank correlation coefficient was applied using PAST 2.17c software to assess inter-relations among parameters (e.g., salinity, Chla, TDAA, TDCHO, DOC, FDOMC, FDOMT, HB).
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CTD
911 plus
Sea Bird
Recording continuous profiles of temperature and salinity in the water column.
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Spectrofluorometer
RF-5301
Shimadzu
Determining spectral properties of DOM, including fluorescence measurements for FDOMC and FDOMT.
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HPLC
1OAS
Shimadzu
Separating and quantifying amino acids after derivatization, with fluorescence detection.
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Fluorometer
RF-551
Shimadzu
Fluorescence detection for amino acid analysis in HPLC.
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Filter
GF/F
Whatman
Filtering seawater samples to remove particulates for DOM analysis.
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Amino Acid Standard
N° 20088
Thermo Scientific Pierce
Calibrating amino acid concentrations in TDAA analysis.
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Glucose Standard
Calibrating carbohydrate concentrations in TDCHO analysis.
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