Microbial Fungi in soils on different Sub-Antarctic islands

Versão mais recente publicado por SCAR - Microbial Antarctic Resource System em Mar 22, 2019 SCAR - Microbial Antarctic Resource System

Aplicon sequencing dataset (454 pyrosequencing) of microbial Fungi (ITS) in soils from Bird Island, Signy Island and Leonie Island (Sub-Antarctica)


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Como citar

Pesquisadores deveriam citar esta obra da seguinte maneira:

Cox F, Newsham K, Robinson C (2019): Microbial Fungi in soils on different Sub-Antarctic islands. v1.0. SCAR - Microbial Antarctic Resource System. Dataset/Metadata. https://ipt.biodiversity.aq/resource?r=microbial_fungi_from_3_sub_antarctic_islands&v=1.0


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O editor e o detentor dos direitos deste trabalho é SCAR - Microbial Antarctic Resource System. This work is licensed under a Creative Commons Attribution (CC-BY) 4.0 License.

GBIF Registration

Este recurso foi registrado no GBIF e atribuído ao seguinte GBIF UUID: a5b4d692-96bf-4acf-8809-b546e9938a5d.  SCAR - Microbial Antarctic Resource System publica este recurso, e está registrado no GBIF como um publicador de dados aprovado por Scientific Committee on Antarctic Research.




Quem criou esse recurso:

Filipa Cox
University of Manchester Manchester GB
Kevin Newsham
British Antarctic Survey Cambridge GB
Clare Robinson
University of Manchester Manchester GB

Quem pode responder a perguntas sobre o recurso:

Filipa Cox
University of Manchester Manchester GB

Quem preencher os metadados:

Maxime Sweetlove
Research assistent
Royal Belgian Institute of Natural Sciences Rue Vautier 29 1000 Brussels BE

Quem mais foi associado com o recurso:


Cobertura Geográfica

Soils were sampled in Bird Island, Signy Island and Leonie Island (Sub-Antarctica)

Coordenadas delimitadoras Sul Oeste [-67.598, -68.356], Norte Leste [-54.009, -38.066]

Cobertura Taxonômica

Fungi were profiled by sequencing the ITS gene (454 pyrosequencing)

Filo  Fungi (Fungi)

Dados Sobre o Projeto

Nenhuma descrição disponível

Título Microbial Fungi in soils on different Sub-Antarctic islands
Financiamento Funding was provided by: the Antarctic Funding Initiative grant from the UK Natural Environment Research Council (grant numbers NE/H014098/1, NE/H014772/1 and NE/H01408X/1) and a British Ecological Society Large Research Grant for early career ecologists.

O pessoal envolvido no projeto:

Filipa Cox

Métodos de Amostragem

Soil was collected from under populations of co‐occurring Deschampsia antarctica Desv. and Colobanthus quitensis (Kunth) Bartl., the only two native vascular plant species that occur in Antarctica. On each island, 50 ml sterile centrifuge tubes (Corning Inc, Corning, NY, USA) were used to collect soil samples by hammering them directly into the vertical walls of three pits at three depths (2, 4 and 8 cm). The soil, kept on ice after collection and frozen at −80 °C within 5 h, was freeze dried to preserve fungal nucleotides.

Área de Estudo Soil samples were collected from Bird Island (54.0089°S, 38.0662°W), Signy Island (60.7107°S, 45.5849°W) and Léonie Island (67.5984°S, 68.3561°W) in the sub‐Antarctic, between October and November 2011.

Descrição dos passos do método:

  1. Total DNA and RNA were extracted simultaneously from five individual 50 mg samples, taken from each of the tubes of homogenized soil (representing a total of 27 × 5 = 135 samples), using RNA PowerSoil Total RNA Isolation and DNA Elution Accessory kits (MoBio Laboratories, Carlsbad, CA, USA). Extracted DNA was amplified in triplicate PCR reactions using the primers ITS1F and ITS4 as described by Cox et al. (2016), with conditions matching those described below for cDNA. Extracted RNA was treated with a Turbo DNA‐free kit (Life technologies, Carlsbad, CA, USA), checked for the absence of DNA using PCR, and reverse transcribed using AccuScript High‐Fidelity Reverse Transcriptase (Agilent, Santa Clara, CA, USA) and random nonamers. The resulting cDNA was amplified in triplicate PCR reactions using ITS1F (Gardes and Bruns, 1993) and ITS4 (White et al., 1990) primers. The ITS4 primer was modified with the Roche 454 A adapter and a 10 bp barcode specific to each sample, allowing identification of different samples once pooled, and the ITS1F primer was modified with the 454 B adaptor.
  2. The triplicate PCR products were pooled and subsequently purified using AMPure XP bead purification (Beckman Coulter, Inc, Brea, CA, USA) and quantified using a Qubit dsDNA HS Assay (Life Technologies, Carlsbad, CA, USA) before normalization to consistent concentration. The purified and normalized PCR products were run on a single plate, on the 454 Roche Titanium FLX platform at the Liverpool Centre for Genomic Research, at the same time and under identical conditions to the DNA library.

Citações bibliográficas

  1. Cox, F., Newsham, K. K., & Robinson, C. H. (2019). Endemic and cosmopolitan fungal taxa exhibit differential abundances in total and active communities of Antarctic soils. Environmental microbiology. https://doi.org/10.1111/1462-2920.14533