Environmental long read amplicons of soil fungi across Podzol soil profile

Occurrence
Последняя версия опубликовано Biology Section, Uppsala University июн. 13, 2024 Biology Section, Uppsala University
Дата публикации:
13 июня 2024 г.
Опубликовано:
Biology Section, Uppsala University
Лицензия:
CC-BY 4.0

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Описание

Soil samples were collected in mid-October 2013 from Ivantjärnsheden field station in Jädraås (60°49‘N, 16°30’E, altitude 185 m), a well-documented field site in central Sweden (Persson, 1980) with Pinus sylvestris L. overstory and an understory of ericaceous dwarf shrubs (Calluna vulgaris (L.) Hull and Vaccinium vitis-ideae L.) and mosses (Dicranum majus Turner and Pleurozium schreberi (Bridel) Mitten). To account for small-scale variability in soil fungal communities we collected 5 soil cores (5 cm diameter and 15 cm deep) in each of 12 plots in the since terminated experiment IhII (9802) (Axelsson & Bråkenhielm, 1980). After visually dividing the plot into four quadrats one core were taken from the middle of each quadrat and from the middle of the plot after peeling back the top shrub and moss layer (incl. most of the litter layer). Soil cores were separated into visually distinct podzol soil layers: organic soil (O), mineral elluvial soil (E) and mineral illuvial soil (B) before pooling the layers for each plot. From each composite soil sample two sub-samples of approximately 0.5 g wet weight were collected for DNA extraction. Approximately 1500 bp of the rDNA from all soil DNA extracts was amplified using the primer set ITS1F (Gardes & Bruns, 1993) and LR5 (Hopple Jr & Vilgalys, 1994). A total of 5, 8 and 3 samples successfully amplified for O, E and B horizons, respectively (Table S1). PCR products from the separate soil horizons were pooled to generate three amplicon libraries (SwO, SwE and SwB) for sequencing at SciLifeLab/NGI (Uppsala, Sweden) on a PacBio RS II system (Pacific Biosciences, Menlo Park, CA, USA). This dataset was published via the SBDI ASV portal.

Записи данных

Данные этого occurrence ресурса были опубликованы в виде Darwin Core Archive (DwC-A), который является стандартным форматом для обмена данными о биоразнообразии в виде набора из одной или нескольких таблиц. Основная таблица данных содержит 611 записей.

Также в наличии 2 таблиц с данными расширений. Записи расширений содержат дополнительную информацию об основной записи. Число записей в каждой таблице данных расширения показано ниже.

Occurrence (core)
611
dnaDerivedData 
611
ExtendedMeasurementOrFact 
611

Данный экземпляр IPT архивирует данные и таким образом служит хранилищем данных. Данные и метаданные ресурсов доступны для скачивания в разделе Загрузки. В таблице версий перечислены другие версии ресурса, которые были доступны публично, что позволяет отслеживать изменения, внесенные в ресурс с течением времени.

Версии

В таблице ниже указаны только опубликованные версии ресурса, которые доступны для свободного скачивания.

Как оформить ссылку

Исследователи должны дать ссылку на эту работу следующим образом:

Rosling A, Urbina H, Kluting K, Eshghi Sahraei S (2024). Environmental long read amplicons of soil fungi across Podzol soil profile. Version 1.11. Biology Section, Uppsala University. Occurrence dataset. https://www.gbif.se/ipt/resource?r=sbdi-asv-1&v=1.11

Права

Исследователи должны соблюдать следующие права:

Публикующей организацией и владельцем прав на данную работу является Biology Section, Uppsala University. Эта работа находится под лицензией Creative Commons Attribution (CC-BY 4.0).

Регистрация в GBIF

Этот ресурс был зарегистрирован в GBIF, ему был присвоен следующий UUID: 2148b949-ef4e-465c-b706-48e9f29e0a15.  Biology Section, Uppsala University отвечает за публикацию этого ресурса, и зарегистрирован в GBIF как издатель данных при оподдержке GBIF Sweden.

Ключевые слова

Occurrence

Контакты

Anna Rosling
  • Originator
  • Point Of Contact
Associate Professor
Department of Ecology and Genetics, Uppsala University
Evolutionsbiologiskt centrum, Norbyvägen 18D
752 36 Uppsala
SE
+46184716444
Hector Urbina
  • Metadata Provider
Post doc
Department of Ecology and Genetics, Uppsala University
Evolutionsbiologiskt centrum, Norbyvägen 18D
752 36 Uppsala
SE
+46184716444
Kerri Kluting
  • Metadata Provider
PhD student
Department of Ecology and Genetics, Uppsala University
Evolutionsbiologiskt centrum, Norbyvägen 18D
752 36 Uppsala
SE
+46184716444
Shadi Eshghi Sahraei
  • Metadata Provider
PhD student
Department of Ecology and Genetics, Uppsala University
Evolutionsbiologiskt centrum, Norbyvägen 18D
752 36 Uppsala
SE
+46184716444

Географический охват

Soil samples were collected from Ivantjärnsheden field station in Jädraås (60°49‘N, 16°30’E, altitude 185 m), in an area of around 150x150 m.

Ограничивающие координаты Юг Запад [60,815, 16,506], Север Восток [60,816, 16,508]

Временной охват

Дата начала / Дата окончания 2013-10-01 / 2013-10-31

Данные проекта

Soil samples were collected in mid-October 2013 from Ivantjärnsheden field station in Jädraås (60°49‘N, 16°30’E, altitude 185 m), a well-documented field site in central Sweden (Persson, 1980) with Pinus sylvestris L. overstory and an understory of ericaceous dwarf shrubs (Calluna vulgaris (L.) Hull and Vaccinium vitis-ideae L.) and mosses (Dicranum majus Turner and Pleurozium schreberi (Bridel) Mitten). To account for small-scale variability in soil fungal communities we collected 5 soil cores (5 cm diameter and 15 cm deep) in each of 12 plots in the since terminated experiment IhII (9802) (Axelsson & Bråkenhielm, 1980). After visually dividing the plot into four quadrats one core were taken from the middle of each quadrat and from the middle of the plot after peeling back the top shrub and moss layer (incl. most of the litter layer). Soil cores were separated into visually distinct podzol soil layers: organic soil (O), mineral elluvial soil (E) and mineral illuvial soil (B) before pooling the layers for each plot. From each composite soil sample two sub-samples of approximately 0.5 g wet weight were collected for DNA extraction. Approximately 1500 bp of the rDNA from all soil DNA extracts was amplified using the primer set ITS1F (Gardes & Bruns, 1993) and LR5 (Hopple Jr & Vilgalys, 1994). A total of 5, 8 and 3 samples successfully amplified for O, E and B horizons, respectively (Table S1). PCR products from the separate soil horizons were pooled to generate three amplicon libraries (SwO, SwE and SwB) for sequencing at SciLifeLab/NGI (Uppsala, Sweden) on a PacBio RS II system (Pacific Biosciences, Menlo Park, CA, USA). Ref Axelsson B, Bråkenhielm S. 1980. Investigation sites of the Swedish coniferous forest project - biological and physiological features. In: Persson T ed. Structure and Function of Northern Coniferous Forests - An Ecosystem Study. Arlöv, Sweden: Berlings, 25 - 64. Gardes M, Bruns TD. 1993. ITS primers with enhanced specificity for basidiomycetes‐application to the identification of mycorrhizae and rusts. Molecular Ecology 2(2): 113-118. Hopple Jr JS, Vilgalys R. 1994. Phylogenetic relationships among coprinoid taxa and allies based on data from restriction site mapping of nuclear rDNA. Mycologia 86(1): 96-107. Persson, T, ed . 1980. Structure and function of northern coniferous forests – an ecosystem study. Ecological Bulletins 32. Stockholm, Sweden.

Название Environmental long read amplicons of soil fungi across Podzol soil profile

Исполнители проекта:

Anna Rosling
  • Principal Investigator
Jeanette Tångrot
  • Processor

Методы сбора

We collected 5 soil cores (5 cm diameter and 15 cm deep) in each of 12 plots after peeling back the top shrub and moss layer (incl. most of the litter layer). Soil cores were separated into visually distinct podzol soil layers: organic soil (O), mineral elluvial soil (E) and mineral illuvial soil (B) before pooling the layers for each plot. This sampling rendered a total of 36 soil samples that were separately homogenized in ziplock bags before separating a 15 mL sample from each that was transported back to the laboratory on ice and stored at -20°C. Approximately 1500 bp of the rDNA from all soil DNA extracts was amplified using the primer set ITS1F (Gardes & Bruns, 1993) and LR5 (Hopple Jr & Vilgalys, 1994). PCR products from the separate soil horizons were pooled to generate three amplicon libraries (SwO, SwE and SwB) for sequencing at SciLifeLab/NGI (Uppsala, Sweden) on a PacBio RS II system (Pacific Biosciences, Menlo Park, CA, USA).

Охват исследования Soil samples were collected in mid-October 2013 from Ivantjärnsheden field station in Jädraås (60°49‘N, 16°30’E, altitude 185 m)

Описание этапа методики:

  1. Data analysis is described in more detail in Kalsoom-Khan et al. 2020 (DOI: 10.1186/s43008-020-00045-9). In short, raw sequence reads were filtered and trimmed using the tool cutadapt (Martin 2011; version 1.18) to de-multiplexed reads based on the forward and reverse barcodes, to keep only reads with both primers present, and to remove the actual primer sequences from the reads. Amplicons sequenced in reverse were reverse complemented before continuing the analyses. Amplified sequence variants (ASVs) were generated using DADA2 (Callahan et al. 2016; version 1.9.3). Default parameters were used for filtering the reads, but discarding sequences with more than 12 "expected errors" (maxEE=12). The tool ITSx (Bengtsson-Palme et al. 2013; version 1.1-beta) was used to extract the ITS2 region of ribosomal rDNA within each ASV, which was then used for taxonomy assignment.

Библиографические ссылки

  1. Kalsoom Khan, F., Kluting, K., Tångrot, J. et al. Naming the untouchable – environmental sequences and niche partitioning as taxonomical evidence in fungi. IMA Fungus 11, 23 (2020). https://doi.org/10.1186/s43008-020-00045-9

Дополнительные метаданные

Альтернативные идентификаторы 2148b949-ef4e-465c-b706-48e9f29e0a15
https://www.gbif.se/ipt/resource?r=sbdi-asv-1