Bacteria and Archaea biodiversity in Arctic and Subarctic terrestrial ecosystems in Alaska

版本 1.1 published by SCAR - Microbial Antarctic Resource System on 十二月 4, 2018 SCAR - Microbial Antarctic Resource System
發布日期:
2018年12月4日
授權條款:
CC-BY-NC 4.0

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說明

Methane emissions from aquatic and terrestrial ecosystems play a crucial role in global warming, which is particularly affecting high-latitude ecosystems. As major contributors to methane emissions in natural environments, the microbial communities involved in methane production and oxidation deserve a special attention. Microbial diversity and activity are expected to be strongly affected by the already observed (and further predicted) temperature increase in high-latitude ecosystems, eventually resulting in disrupted feedback methane emissions. The METHANOBASE project has been designed to investigate the intricate relations between microbial diversity and methane emissions in Arctic, Subarctic and Subantarctic ecosystems, under natural (baseline) conditions and in response to simulated temperature increments. We report here a small subunit ribosomal RNA (16S rRNA) analysis of lake, peatland and mineral soil ecosystems.

版本

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如何引用

請注意,此資料集為舊版本。  研究者應依照以下指示引用此資源。:

Cabrol L, Barret M, Thalasso F, Gandois L, Lavergne C, Martinez Cruz K, Sepulveda Jaureguy A, Fochesatto G J (2018): Bacteria and Archaea biodiversity in Arctic and Subarctic terrestrial ecosystems in Alaska. v1.1. SCAR - Microbial Antarctic Resource System. Dataset/Metadata. http://ipt.biodiversity.aq/resource?r=methanobasealaska&v=1.1

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此資料的發布者及權利單位為 SCAR - Microbial Antarctic Resource System。 This work is licensed under a Creative Commons Attribution Non Commercial (CC-BY-NC 4.0) License.

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此資源已向GBIF註冊,並指定以下之GBIF UUID: 0ea51b6e-d02f-495e-a29b-73783e4060c0。  SCAR - Microbial Antarctic Resource System 發佈此資源,並經由Scientific Committee on Antarctic Research同意向GBIF註冊成為資料發佈者。

關鍵字

metadata; methane; greenhouse gas; bacteria; archaea; procaryote; peatland; wetland; soil; lake; sediment; metabarcoding; 16S rRNA; MiSeq

聯絡資訊

Léa Cabrol
  • 出處
  • 連絡人
Researcher
Institut méditerranéen d'Océanologie
Marseille
FR
Maialen Barret
  • 元數據提供者
  • 出處
  • 使用者
  • 連絡人
Associate professor
ECOLAB, Université de Toulouse
Toulouse
FR
Frederic Thalasso
  • 出處
Professor
CINVESTAV
Mexico
MX
Laure Gandois
  • 出處
Researcher
ECOLAB, Université de Toulouse
Toulouse
FR
Céline Lavergne
  • 出處
Postdoc
Pontificia Universidad Catholica de Valparaiso
Valparaiso
CL
Karla Martinez Cruz
  • 出處
Associate professor
Universidad de Magallanes
Punta Arenas
CL
Armando Sepulveda Jaureguy
  • 出處
Postdoc
Universidad de Magallanes
Punta Arenas
CL
Gilberto Javier Fochesatto
  • 出處
Associate professor
University of Alaska Fairbanks
Fairbanks
US

地理涵蓋範圍

Alaska

界定座標範圍 緯度南界 經度西界 [63.21, -150.8], 緯度北界 經度東界 [68.62, -147.65]

分類群涵蓋範圍

Bacteria and Archaea

時間涵蓋範圍

起始日期 2016-06-27

計畫資料

METHANOgenic Biodiversity and activity in Arctic, subarctic and Subantarctic Ecosystems affected by climate change

計畫名稱 Methanobase
辨識碼 METHANOBASE ELAC2014-DCC092
經費來源 ERANET-LAC joint call 2014
研究區域描述 Alaska Lakes (water, sediments), peatlands (hollows, edges, hummocks) and mineral soils
研究設計描述 The METHANOBASE project has been designed to investigate the intricate relations between microbial diversity and methane emissions in Arctic, Subarctic and Subantarctic ecosystems, under natural (baseline) conditions and in response to simulated temperature increments.

參與計畫的人員:

Maialen Barret

取樣方法

Water samples were collected with a Van Dorn bottle. Sediments were sampled thanks to a grab-sampler, peat monoliths (approximately 30*30*30cm) were cut with a bread-knife and soil monoliths with a shovel.

研究範圍 Samples were collected in summer 2015, without any temporal replication. A total of 19 ecosystems were studied in Alaska, USA. The selected sites are representative of this Subantarctic region: lakes, peatlands, Nothofagus forest, pampa In each site, various samples were collected to take into account the local heterogeneity: different depths in water column and sediments, soil horizons, hollows/edges/hummocks.

方法步驟描述:

  1. After collection, samples were stored at 4°C prior to further processing. Liquid samples were filtered at 0.45µm until clogging and the filters were stored at -20°C. DNA was extracted from these filters using the PowerWater DNA isolation kit (MOBIO) while DNA was extracted from solid samples using the PowerSoil DNA isolation kit (MOBIO). DNA extracts were kept at -20°C. The V4-V5 region of 16S rRNA gene was amplified in the following conditions: 515F and 928R primers (Wang & Qian, 2009. doi:10.1371/journal.pone.0007401), 2min at 94°C, 30 cycles of 60s at 94°C, 40s at 65°C and 30s at 72°C, and 10 min at 72°C. Amplicon sequencing was carried out with Illumina MiSeq technology (2x250pb, V3). Denoising of the sequences dataset and OTU clustering was carried using the FROGS pipeline (Auer et al., 2017. doi:10.1093/bioinformatics/btx791). BLAST was used for taxonomic affiliation.

額外的詮釋資料