Amphibian_species_norway

Occurrence
Latest version published by eDNA solutions on May 11, 2025 eDNA solutions
Publication date:
11 May 2025
Published by:
eDNA solutions
License:
CC0 1.0

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Description

This report summarizes results from water samples collected from 105 ponds in Southern Norway in 2019 to determine amphibian biodiversity in the ponds.

Data Records

The data in this occurrence resource has been published as a Darwin Core Archive (DwC-A), which is a standardized format for sharing biodiversity data as a set of one or more data tables. The core data table contains 61 records.

This IPT archives the data and thus serves as the data repository. The data and resource metadata are available for download in the downloads section. The versions table lists other versions of the resource that have been made publicly available and allows tracking changes made to the resource over time.

Versions

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Rights

Researchers should respect the following rights statement:

The publisher and rights holder of this work is eDNA solutions. To the extent possible under law, the publisher has waived all rights to these data and has dedicated them to the Public Domain (CC0 1.0). Users may copy, modify, distribute and use the work, including for commercial purposes, without restriction.

GBIF Registration

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Keywords

eDNA; water sample; Amphibian species; Occurrence

Contacts

Omneya Osman
  • Metadata Provider
  • Point Of Contact
  • Molecular biologist
eDNA solutions
  • c/o Göteborgs Universitet, , Carl Skottsbergs gata 22B
413 19 Göteborg
SE
  • 0700264843
Omneya Osman
  • Metadata Provider
  • Point Of Contact
eDNA solutions
  • c/o Göteborgs Universitet, , Carl Skottsbergs gata 22B
413 19 Göteborg
SE
  • 0700264843

Geographic Coverage

A selected number of systems was sampled during different seasons to provide the necessary basis for an optimal sampling design for a national monitoring program of BD and amphibian diversity in southern Norway.

Bounding Coordinates South West [36.598, -4.219], North East [77.466, 35.156]

Taxonomic Coverage

Animalia;Chordata;Amphibia;Anura;Bufonidae;Bufo;Bufo_bufo Animalia;Chordata;Amphibia;Caudata;Salamandridae;Lissotriton;Lissotriton_vulgaris Animalia;Chordata;Amphibia;Anura;Ranidae;Rana;Rana_arvalis Animalia;Chordata;Amphibia;Anura;Ranidae;Rana;Rana_temporaria Animalia;Chordata;Amphibia;Anura;Bufonidae;Epidalea;Epidalea_calamita Animalia;Chordata;Amphibia;Anura;Ranidae;Pelophylax;Pelophylax_esculentus Animalia;Chordata;Amphibia;Caudata;Salamandridae;Triturus;Triturus_cristatus

Species Rana_temporaria, Lissotriton_vulgaris, Bufo_bufo, Rana_arvalis, Epidalea_calamita, Pelophylax_esculentus, Triturus_cristatus

Temporal Coverage

Start Date / End Date 2019-05-26 / 2019-09-08

Project Data

The main objectives of this project were to collect samples from a high number of waterbodies to obtain a detailed picture of the presence of BD and amphibians in southern Norway. Furthermore, a selected number of systems was sampled during different seasons to provide the necessary basis for an optimal sampling design for a national monitoring program of BD and amphibian diversity.

Title Monitoring and mapping of amphibian species using environmental DNA
Identifier eDNA
Funding The project was funded by the Norwegian Environmental Agency "Miljødirektoratet"
Study Area Description Samples were obtained in Southern Norway, along the Swedish border, around Oslo, and in the Agder region. Based on the results from the 2019 study (Ahmed et al., 2019), the end of May and beginning of June were chosen for sampling. In total, 91 bodies of water, including forest-, agricultural- and urban ponds, were sampled, and 16 swabs from various amphibian specimens were obtained in 2020.
Design Description 300-500 milliliters of water were filtered through sterivex filters.

The personnel involved in the project:

Omneya Osman

Sampling Methods

Water samples were collected using 50 ml syringe and Stervix filter units. Approximately 100-600 ml of water was injected in Stervix filter.

Study Extent Norway
Quality Control Negative controls were prepared and also positive control. PCRs were run in triplicates.

Method step description:

  1. dx.doi.org/10.17504/protocols.io.973h9qn

Additional Metadata