2013
DOI: 10.1007/978-4-431-54388-6_6
|View full text |Cite
|
Sign up to set email alerts
|

Molecular Assessment of Benthic Foraminiferal Diversity

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2016
2016
2021
2021

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(3 citation statements)
references
References 19 publications
0
3
0
Order By: Relevance
“…Specimens can be stored either individually, directly in DNA extraction buffer or dried and frozen on cardboard faunal slides (Figure 2, details in Supplementary Data Sheet 1). Preservation in ethanol, a hypothetical third option commonly used for metazoans, is not recommended for foraminifera as it inhibits the amplification of DNA by PCR (Holzmann and Pawlowski, 1996;Lecroq, 2014). Drying and freezing has been used preferably in the last years, since it allows faster handling of foraminiferal specimens (André et al, 2013;Weiner et al, 2014Weiner et al, , 2015.…”
Section: Preservation Of Specimensmentioning
confidence: 99%
“…Specimens can be stored either individually, directly in DNA extraction buffer or dried and frozen on cardboard faunal slides (Figure 2, details in Supplementary Data Sheet 1). Preservation in ethanol, a hypothetical third option commonly used for metazoans, is not recommended for foraminifera as it inhibits the amplification of DNA by PCR (Holzmann and Pawlowski, 1996;Lecroq, 2014). Drying and freezing has been used preferably in the last years, since it allows faster handling of foraminiferal specimens (André et al, 2013;Weiner et al, 2014Weiner et al, , 2015.…”
Section: Preservation Of Specimensmentioning
confidence: 99%
“…williamsoni were present; which comprised up to 80% of the living benthic foraminiferal assemblage. This species is easily identified through the yellow/brown-coloured protoplasm extensively distributed across the entire foraminiferal tests, except in the last chambers [25,44]. Previously, the naturally intense protoplasm colour has been widely used as an indicator of viable foraminiferal individuals [45], and additional observation of pseudopodia activity confirmed that these individuals were alive.…”
Section: Methodsmentioning
confidence: 99%
“…Calcein-labelled specimens were randomly selected and transferred into foraminiferal culture chambers containing a tissue cell culture insert with a silica layer [29,43,44]. As specimens of E .…”
Section: Methodsmentioning
confidence: 99%