Mesozooplankton abundance, biomass and copepod secondary production at the Barents Sea polar front, June 2011

資料紀錄

此資源sampling event的資料已發佈為達爾文核心集檔案（DwC-A），其以一或多組資料表構成分享生物多樣性資料的標準格式。 核心資料表包含 60 筆紀錄。

亦存在 2 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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版本

以下的表格只顯示可公開存取資源的已發布版本。

如何引用

研究者應依照以下指示引用此資源。:

Gawinski C, Dmoch K, Svensen C (2023). Mesozooplankton abundance, biomass and copepod secondary production at the Barents Sea polar front, June 2011. Version 1.6. UiT The Arctic University of Norway. Samplingevent dataset. https://ipt.gbif.no/resource?r=conflux&v=1.6

權利

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此資料的發布者及權利單位為 UiT The Arctic University of Norway。 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: de45ab96-fc20-4d35-ad41-8d25bf7aa22a。  UiT The Arctic University of Norway 發佈此資源，並經由GBIF Norway同意向GBIF註冊成為資料發佈者。

關鍵字

Samplingevent

聯絡資訊

地理涵蓋範圍

Four stations (M1-M4) across the Barents Sea polar front, covering Atlantic to Arctic waters (75-78 °N). M1: Lat 78.097, Lon 28.125, bottom depth: 278 m M2: Lat 76.949, Lon 29.711, bottom depth: 235 m M3: Lat 76.491, Lon: 29.863, bottom depth: 282 m M4: Lat 74.910, Lon 30.003, bottom depth: 371 m M2 M3 M4

時間涵蓋範圍

計畫資料

無相關描述

取樣方法

Mesozooplankton was sampled with a WP-2 net (Hydro-Bios) with 180 µm mesh, 0.57 m diameter net opening and filtering cod-end. Filtration volume was estimated from opening diameter and sampling depth. Three vertical net hauls were taken during day (around noon, WP2-day) and during night (around midnight, WP2-night) at all stations, at fixed depth intervals of 0-50 m, 50-100 m, and 100m-bottom by using a closing mechanism. The content of the cod-end was concentrated over a 90 µm mesh on deck and preserved with buffered formaldehyde at 4 % final concentration. To increase the resolution in the surface and to quantitatively sample the small copepod species and young developmental stages, one GoFlo profile was sampled at daytime at each station in the upper 50 m. Samples were taken from 1, 10, 20, 30, 40 and 50 m depth. The content of the water bottle (30 liters) from each individual depth was concentrated over a 20 µm mesh and preserved with buffered formaldehyde at 4 % final concentration. Mesozooplankton were counted and determined to species and developmental stage under a Leica dissecting microscope at 40x magnification. Mesozooplankton abundance was converted into biomass, based on species and stage-specific carbon weight relationships. Daily copepod secondary production (mg C m−3 d−1) in the upper 50 m water column was calculated as the sum of the product of biomass and weight-specific growth rate of each individual stage within the copepod population. Copepod growth rate was determined using four different growth rate models, namely Hirst & Bunker 2003 (HB_copepod_secondary_production, based on copepod body weight, chlorophyll a concentration, in-situ water temperature), Hirst & Lampitt 1998 (HL_copepod_secondary_productioncopepod, based on body weight, in-situ water temperature), Huntley & Lopez 1992 (HuLo_copepod_secondary_production, based on in-situ water temperature) and Zhou et al. 2010 (Zhou_copepod_secondary_productioncopepod, based on body weight, chlorophyll a concentration, in-situ water temperature, assimilated food input).

方法步驟描述:

1. Daily copepod secondary production (mg C m−3 d−1) in the upper 50 m water column was calculated as the sum of the product of biomass and weight-specific growth rate of each individual stage within the copepod population. Copepod growth rate was determined using four different growth rate models, namely Hirst & Bunker 2003: https://doi.org/10.4319/lo.2003.48.5.1988 Hirst & Lampitt 1998: https://doi.org/10.1007/s002270050390 Huntley & Lopez 1992: https://doi.org/10.1086/285410 Zhou et al. 2010: https://doi.org/10.1093/plankt/fbq054

額外的詮釋資料