Investigating the chemistry and biology of porewater and seawater in a site highly influenced by Submarine Groundwater Discharge, SGD (Achziv, northern Israel)

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Autori principali: Yanuka-Golub, Keren, Belkin, Natalia, Weber, Nurit, Mayyani, Meor, Levy, Yehuda, Reznik, Itay J, Rubin-Blum, Maxim, Rahav, Eyal, Kiro, Yael
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Lingua:en
Pubblicazione: PANGAEA 2024
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author Yanuka-Golub, Keren
Belkin, Natalia
Weber, Nurit
Mayyani, Meor
Levy, Yehuda
Reznik, Itay J
Rubin-Blum, Maxim
Rahav, Eyal
Kiro, Yael
author_facet Yanuka-Golub, Keren
Belkin, Natalia
Weber, Nurit
Mayyani, Meor
Levy, Yehuda
Reznik, Itay J
Rubin-Blum, Maxim
Rahav, Eyal
Kiro, Yael
collection Datos científicos de ciencias marinas y ambientales
contents We investigated seawater microbial abundance, activity and diversity in a site strongly influenced by submarine groundwater discharge (SGD). Three sampling campaigns (August 2020, February 2021 and July 2021) were conducted at a field site, highly influenced by SGD (Achziv, northern Israel), Each field campaign lasted 2-5 days and covered at least 2 tidal cycles. Pore-water samples were collected on the shoreline using piezometers (AMS piezometers that reach depths of <2 meters) and a portable peristaltic pump. The density (g cm-3), electric conductivity (mS/cm), temperature (°C) and pH, of surface seawater, porewater and groundwater were measured on-site at the time of the sampling. Samples for microbial analysis were collected from the piezometers and divided to aliquots: 1. For community analysis, samples were immediately filtered through polycarbonate 0.2 μm pore size filters, which were kept on ice and transported to the laboratory on the same day. Filter samples were stored frozen (-20°C) until DNA extraction (filtered pore-water were kept for dissolved nutrient measurements. After thawing, each filter was cut into small pieces using a sterile scalpel blade, which was placed immediately into PowerSoil DNA bead tubes and extracted with the dNeasy PowerSoil Kit (Qiagen, USA) following the standard protocol. 2. For Pico-/nano-phytoplankton and heterotrophic prokaryotic abundance, non-filtered samples were chilled on ice and transported to the laboratory on the same day. Samples (1.8 mL) were fixed with glutaraldehyde (final concentration 0.02 % v:v, Sigma-Aldrich 253 G7651), frozen in liquid nitrogen, and later stored at −80°C until analysis. The abundance of autotrophic pico- and nano-eukaryotes, Synechococcus and Prochlorococcus, and other heterotrophic prokaryotes (bacteria and archaea) was determined using an Attune® Acoustic Focusing Flow Cytometer (Applied Biosystems) equipped with a syringe based fluidic system and 488 and 405 nm lasers. To measure heterotrophic prokaryote abundance, a sample aliquot was stained with SYBR Green (Applied Biosystems). 3. Prokaryotic (bacteria and archaea) heterotrophic production was estimated using the 3H-leucine incorporation method. Photosynthetic carbon fixation rates were estimated using the 14C incorporation method.
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institution PANGAEA
language en
publishDate 2024
publisher PANGAEA
record_format pangaea
spellingShingle Investigating the chemistry and biology of porewater and seawater in a site highly influenced by Submarine Groundwater Discharge, SGD (Achziv, northern Israel)
Yanuka-Golub, Keren
Belkin, Natalia
Weber, Nurit
Mayyani, Meor
Levy, Yehuda
Reznik, Itay J
Rubin-Blum, Maxim
Rahav, Eyal
Kiro, Yael
Acoustic Focusing Flow Cytometer, Applied Biosystems, Attune; equipped with a syringe based fluidic system and 488 and 405 nm lasers; Anton Paar; autotrophic organisms; coastal ecosystem; Conductivity; Conductivity Meter, WTW, ProfiLine Cond 3110; DATE/TIME; Density; DEPTH, water; Event label; Flow injection analyzer, Lachat Instruments, QuikChem 8000; Heterotrophic prokaryotes; LATITUDE; Liquid scintillation counter, Packard, TRI-CARB 2100 TR; Location; LONGITUDE; microbial community; MULT; Multiple investigations; Nitrate; Nitrite; Oxygen, dissolved; pH, total scale; pH-meter, Thermo Scientific, EUTECH; Phosphate; PIEZO; Piezometer; Primary production of carbon; Prochlorococcus; Prokaryotes; Prokaryotes, production as carbon; Salinity; SGD_10; SGD_11; SGD_21; SGD_26; SGD_27; SGD_35; SGD_36; SGD_37; SGD_38; SGD_39; SGD_40; SGD_41; SGD_42; SGD_43; SGD_44; SGD_45; SGD_46; SGD_47; SGD_48; SGD_49; SGD_50; SGD_51; SGD_52; SGD_53; SGD_54; SGD_NW-1; SGD_NW-2; SGD_NW-3; SGD_NW-4; SGD_NW-5; SGD_NW-6; SGD_NW-7; Silicate; Site; Submarine groundwater discharge; subterranean estuary; Synechococcus; Temperature, water
We investigated seawater microbial abundance, activity and diversity in a site strongly influenced by submarine groundwater discharge (SGD). Three sampling campaigns (August 2020, February 2021 and July 2021) were conducted at a field site, highly influenced by SGD (Achziv, northern Israel), Each field campaign lasted 2-5 days and covered at least 2 tidal cycles. Pore-water samples were collected on the shoreline using piezometers (AMS piezometers that reach depths of <2 meters) and a portable peristaltic pump. The density (g cm-3), electric conductivity (mS/cm), temperature (°C) and pH, of surface seawater, porewater and groundwater were measured on-site at the time of the sampling. Samples for microbial analysis were collected from the piezometers and divided to aliquots: 1. For community analysis, samples were immediately filtered through polycarbonate 0.2 μm pore size filters, which were kept on ice and transported to the laboratory on the same day. Filter samples were stored frozen (-20°C) until DNA extraction (filtered pore-water were kept for dissolved nutrient measurements. After thawing, each filter was cut into small pieces using a sterile scalpel blade, which was placed immediately into PowerSoil DNA bead tubes and extracted with the dNeasy PowerSoil Kit (Qiagen, USA) following the standard protocol. 2. For Pico-/nano-phytoplankton and heterotrophic prokaryotic abundance, non-filtered samples were chilled on ice and transported to the laboratory on the same day. Samples (1.8 mL) were fixed with glutaraldehyde (final concentration 0.02 % v:v, Sigma-Aldrich 253 G7651), frozen in liquid nitrogen, and later stored at −80°C until analysis. The abundance of autotrophic pico- and nano-eukaryotes, Synechococcus and Prochlorococcus, and other heterotrophic prokaryotes (bacteria and archaea) was determined using an Attune® Acoustic Focusing Flow Cytometer (Applied Biosystems) equipped with a syringe based fluidic system and 488 and 405 nm lasers. To measure heterotrophic prokaryote abundance, a sample aliquot was stained with SYBR Green (Applied Biosystems). 3. Prokaryotic (bacteria and archaea) heterotrophic production was estimated using the 3H-leucine incorporation method. Photosynthetic carbon fixation rates were estimated using the 14C incorporation method.
title Investigating the chemistry and biology of porewater and seawater in a site highly influenced by Submarine Groundwater Discharge, SGD (Achziv, northern Israel)
topic Acoustic Focusing Flow Cytometer, Applied Biosystems, Attune; equipped with a syringe based fluidic system and 488 and 405 nm lasers; Anton Paar; autotrophic organisms; coastal ecosystem; Conductivity; Conductivity Meter, WTW, ProfiLine Cond 3110; DATE/TIME; Density; DEPTH, water; Event label; Flow injection analyzer, Lachat Instruments, QuikChem 8000; Heterotrophic prokaryotes; LATITUDE; Liquid scintillation counter, Packard, TRI-CARB 2100 TR; Location; LONGITUDE; microbial community; MULT; Multiple investigations; Nitrate; Nitrite; Oxygen, dissolved; pH, total scale; pH-meter, Thermo Scientific, EUTECH; Phosphate; PIEZO; Piezometer; Primary production of carbon; Prochlorococcus; Prokaryotes; Prokaryotes, production as carbon; Salinity; SGD_10; SGD_11; SGD_21; SGD_26; SGD_27; SGD_35; SGD_36; SGD_37; SGD_38; SGD_39; SGD_40; SGD_41; SGD_42; SGD_43; SGD_44; SGD_45; SGD_46; SGD_47; SGD_48; SGD_49; SGD_50; SGD_51; SGD_52; SGD_53; SGD_54; SGD_NW-1; SGD_NW-2; SGD_NW-3; SGD_NW-4; SGD_NW-5; SGD_NW-6; SGD_NW-7; Silicate; Site; Submarine groundwater discharge; subterranean estuary; Synechococcus; Temperature, water
url https://doi.org/10.1594/PANGAEA.962220