Cite this dataset as
White, N., Seaton, F.M., Reinsch, S., Smith, A.R., Brooks, M.R., Emmett, B.A. (2019). Calluna vulgaris root length and fungal colonisation data from the Climoor long-term climate change experiment in Clocaenog forest, UK (2015). NERC Environmental Information Data Centre. (Dataset). https://doi.org/10.5285/3d468857-f5d0-4dc4-88f3-6be6df19608b
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This dataset is available under the terms of the Open Government Licence 
Calluna vulgaris root length and fungal colonisation data from the Climoor long-term climate change experiment in Clocaenog forest, UK (2015)
This dataset contains root length, biomass and fungal colonisation data for Calluna vulgaris from control, drought and warming treated soils from the long term climate change experiment in Clocaenog forest. Soil samples were collected from the climate change experiment in Northeast Wales during April 2015. Roots were separated from the soil, their length and biomass measured and then analysed using microscopy for Ericoid mycorrhizae (ErM) and dark septate endophyte (DSE) colonisation of Calluna vulgaris.
The experimental field site consists of three untreated control plots, three plots where the plant canopy air is artificially warmed during night time hours and three plots where rainfall is excluded from the plots at least during the plants growing season (March to September). The Climoor field experiment intends to answer questions regarding the effects of warming and drought on ecosystem processes and has been running since 1999. The root length and fungal colonisation data aims to understand how changes in soil hydrological and chemical properties have influenced Calluna vulgaris rooting behaviour and interactions with the soil microbiome.
This work was supported by the Natural Environment Research Council award number NE/R016429/1 as part of the UK-SCAPE programme delivering National Capability.
The experimental field site consists of three untreated control plots, three plots where the plant canopy air is artificially warmed during night time hours and three plots where rainfall is excluded from the plots at least during the plants growing season (March to September). The Climoor field experiment intends to answer questions regarding the effects of warming and drought on ecosystem processes and has been running since 1999. The root length and fungal colonisation data aims to understand how changes in soil hydrological and chemical properties have influenced Calluna vulgaris rooting behaviour and interactions with the soil microbiome.
This work was supported by the Natural Environment Research Council award number NE/R016429/1 as part of the UK-SCAPE programme delivering National Capability.
Publication date: 2019-10-11
View record as
Format
Comma-separated values (CSV)
Spatial information
- Study area
-
- Spatial representation type
- Tabular (text)
- Spatial reference system
- WGS 84
Temporal information
- Temporal extent
-
2015-04-01 to 2015-04-01
Provenance & quality
Soil cores of 8cm diameter and depth were collected from each plot near the base of Calluna vulgaris on the 1st April 2015, then transported back to Bangor at 4°C. Cores were cut from the top into 1 cm deep subsections. Each subsection was soaked and agitated to break up the root/soil clumps. Roots confidently identified as C. vulgaris were removed by hand and thoroughly washed in tap water. Necrotic or rotting roots were discarded.
WinRHIZO version 3.2 was used to measure the length and diameter of cleaned subsection roots on a flatbed scanner. Roots were positioned without overlapping, submerged in 5 mm tap water to improve scanning accuracy. Acquisition parameters were set using the TWAIN interface in professional mode: positive film, 24 bit and 300 dpi. Post scanning, ten of the finest roots were manually selected from each subsection for microscopic investigation. The remaining roots were oven dried at 70°C for 24 hours, producing dry weight data for those < and > 2mm in diameter.
All core fragments for microscopic assessment were soaked over 20 hours in 10% Potassium hydroxide (KOH). Roots were thoroughly rinsed in deionised water and heated in a water bath at 90°C for 15 minutes in 5% vinegar-ink solution. Roots were rinsed in three changes of tap water, acidified and de-stained by soaking in tap water with a few drops of vinegar for a further 20 minutes. A compound microscope was used to estimate proportional colonisation using the magnified intersection technique, with a scale bar cuticle instead of cross-hair and at a 40x magnification. Roots were cut approximately 1-2 cm in length, with 2 mm passes made along each root length. All cortical cells were examined for Ericoid mycorrhizae (ErM) and dark septate endophyte (DSE), working through the plane of focus. Each interval was categorised based upon ErM colonisation into 0 %, < 1 %, < 10 %, < 50 %, > 50 % and > 90 % colonisation.
Data were transferred into an Excel spreadsheet. Data were exported as a comma separated value file for ingestion into the EIDC.
WinRHIZO version 3.2 was used to measure the length and diameter of cleaned subsection roots on a flatbed scanner. Roots were positioned without overlapping, submerged in 5 mm tap water to improve scanning accuracy. Acquisition parameters were set using the TWAIN interface in professional mode: positive film, 24 bit and 300 dpi. Post scanning, ten of the finest roots were manually selected from each subsection for microscopic investigation. The remaining roots were oven dried at 70°C for 24 hours, producing dry weight data for those < and > 2mm in diameter.
All core fragments for microscopic assessment were soaked over 20 hours in 10% Potassium hydroxide (KOH). Roots were thoroughly rinsed in deionised water and heated in a water bath at 90°C for 15 minutes in 5% vinegar-ink solution. Roots were rinsed in three changes of tap water, acidified and de-stained by soaking in tap water with a few drops of vinegar for a further 20 minutes. A compound microscope was used to estimate proportional colonisation using the magnified intersection technique, with a scale bar cuticle instead of cross-hair and at a 40x magnification. Roots were cut approximately 1-2 cm in length, with 2 mm passes made along each root length. All cortical cells were examined for Ericoid mycorrhizae (ErM) and dark septate endophyte (DSE), working through the plane of focus. Each interval was categorised based upon ErM colonisation into 0 %, < 1 %, < 10 %, < 50 %, > 50 % and > 90 % colonisation.
Data were transferred into an Excel spreadsheet. Data were exported as a comma separated value file for ingestion into the EIDC.
Related
This dataset is included in the following collections
Data from the Climoor climate change experimental fieldsite in Clocaenog forest, UK
Correspondence/contact details
Fiona Seaton
UK Centre for Ecology & Hydrology
Environment Centre Wales, Deiniol Road
Bangor
Gwynedd
LL57 2UW
UNITED KINGDOM
enquiries@ceh.ac.uk
Bangor
Gwynedd
LL57 2UW
UNITED KINGDOM
Authors
White, N.
Bangor University
https://orcid.org/0000-0002-2022-7451 Other contacts
- Custodian
-
NERC EDS Environmental Information Data Centreinfo@eidc.ac.uk
- Publisher
-
NERC Environmental Information Data Centreinfo@eidc.ac.uk
Additional metadata
- Topic categories
- biota
- INSPIRE theme
- Environmental Monitoring Facilities
- Keywords
- Calluna vulgaris , Climate and climate change , climate change , Clocaenog , drought , fungus , heather , ling , North Wales , soil , UK-SCAPE , Warming
- Funding
- Natural Environment Research Council Award: NE/R016429/1
- Last updated
- 12 March 2024 09:58