Invertebrates from the ANTARXXVII Leg1 expedition to the Bransfield Strait, Antarctica - data

資料紀錄

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亦存在 1 筆延伸集的資料表。延伸集中的紀錄補充核心集中紀錄的額外資訊。 每個延伸集資料表中資料筆數顯示如下。

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如何引用

研究者應依照以下指示引用此資源。:

Salabao L, Claes J, Gan Y, Van de Putte A, Schön I (2022): Invertebrates from the ANTARXXVII Leg1 expedition to the Bransfield Strait, Antarctica - data. v1.6. SCAR - AntOBIS. Dataset/Occurrence. https://ipt.biodiversity.aq/resource?r=antarxxvii-leg1&v=1.6

權利

研究者應尊重以下權利聲明。:

此資料的發布者及權利單位為 SCAR - AntOBIS。 This work is licensed under a Creative Commons Attribution (CC-BY 4.0) License.

GBIF 註冊

此資源已向GBIF註冊，並指定以下之GBIF UUID: 25bf34e6-48ef-41aa-9b62-876ca0c66a2a。  SCAR - AntOBIS 發佈此資源，並經由Ocean Biodiversity Information System同意向GBIF註冊成為資料發佈者。

關鍵字

Occurrence; MYSIDS; RIBBON WORMS; SEA STARS; EARTHWORMS; BRITTLE/BASKET STARS; AMPHIPODS; OSTRACODS; Specimen; Occurrence

聯絡資訊

地理涵蓋範圍

Bransfield Strait, Southern Ocean

分類群涵蓋範圍

無相關描述

時間涵蓋範圍

計畫資料

RECTO applies a multidisciplinary approach in studying evolution and diversity of Southern Ocean faunas. RECTO has 6 main objectives: 1) Reconstruct population histories and phylogenies of selected faunas; 2) Link population histories and refugia to past climate changes; 3) Estimate variation of morphological traits and width of ecological niches; 4) Use physiological and energy limits and traits to model current and future species distributions; 5) Integrate distribution models into hydrodynamic and particle models; and, 6) Develop different scenarios on how target taxa will respond to future climate change. RECTO will focus on six different animal groups, comprising different trophic levels from the micro- over macro-benthos and pelagic crustaceans to fish and seabirds. The selected species differ in their biology, life history traits and dispersal capacities, which are all factors affecting their abilities to cope with environmental changes.

參與計畫的人員:

取樣方法

The amphipod trap was deployed in two different stations close to Machu Picchu base in the Admiralty Bay. About 400 grams of Chilean pickerel fish was used as bait inside the trap. Organisms caught inside the trap were placed in a bucket with cold sea water and sorted. Samples were photographed and immediately preserved and stored in a -20 °C freezer in the laboratory. About 20 amphipod individuals or pleopods were preserved in All protect Tissue reagent as well as DNA/RNA shield for later molecular analyses. A part of the amphipod individuals was also frozen for later flow cytometry and the remaining amphipods were preserved in pure ethanol (99% p.a.) and placed at -20°C for storage. Sorting and processing were done as quickly as possible to prevent degradation of nucleic acids and proteins. Samples were also labelled inside the bottle using ethanol resistant paper and outside the bottle using an ethanol proof marker. Ethanol was replaced after three days. Isaacs-Kidd midwater trawl (IKMT) has a net with a mesh size of 500 µm and was used for pelagic sampling by attaching it on the A-frame crane located at the back of the vessel. The IKMT was deployed at 175 meters and was then towed for 5 minutes. Samples were collected by detaching the cod-end from the net. Amphipods were sorted from the rest of the samples and photos were taken immediately. Organisms were also immediately placed in absolute ethanol (99% purity) afterwards. Van Veen grab sampler allows the sampling of sediments and bottom fauna. Van Veen sampler was deployed at 6 stations in Admiralty Bay and 13 stations along the Bransfield Strait and 1 station within Maxwell Bay. Sampling using the Van Veen grab took approximately 15 minutes from the time it was deployed to the time it came back onboard. In cases where the Van Veen did not close, it was re-deployed up to three trials and only until then was sampling terminated. Large specimens that were visible with the naked eye were immediately collected on board before sieving and were placed in their respective collection bottles with sea water and ice packs on the side to maintain temperature. Any sediment samples collected were sieved onboard using a hand-held kitchen sieve with 1 mm mesh size to collect organisms in the sediment. Further processing and sorting were done in the geological laboratory. To avoid DNA degradation and to keep the organisms alive, sorting was done using a tray with cold sea water with ice packs. Photos were also taken immediately, and organisms directly placed in absolute ethanol (99% purity) afterwards. Processing to storage was done as quickly and as efficiently as possible. All samples that were caught were identified and grouped to the lowest taxonomic level possible using the keys of Marine Wildlife King George Island Antarctica by Schories & Kohlberg (2016) and Rauschert & Arntz (2015). Other taxonomic keys and photographs provided by Cédric d'Udekem d'Acoz were also used for confirmation.

方法步驟描述:

1. - Sampling was carried out at different sites with different sampling devices (baited amphipod trap, Isaacs-Kidd midwater trawl or Van Veen grab sampler). Details of sampling methods are mentioned in the sampling description section. - Samples collected were sorted, photographed and preserved. Preservation method is indicated in the field "preparations" in data. - The quality control of the occurrence records are mentioned in the quality control section.

引用文獻

1. Schories, D., & Kohlberg, G. (Eds.). (2016). Marine Wildlife, King George Island, Antarctica. Dirk Schories Publications.
2. Rauschert, M., & Arntz, W. (2015). Antarctic Macrobenthos: a field guide of the invertebrates living at the antarctic seafloor. Arntz & Rauschert Selbstverlag.
3. Salabao, L., Claes, J., Gan, Y., Van de Putte, A., and Schön, I. 2021. Invertebrates from the ANTARXXVII Leg1 Expedition to the Bransfield Strait, Antarctica - Images (version 2.0). Zenodo. doi:10.5281/zenodo.4942307. https://doi.org/10.5281/zenodo.4942307

額外的詮釋資料