Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543211
Title: Defining marine meiofaunal genetic diversity using 454 sequencing
Author: da Fonseca Batista, Vera Alexandra Garcia
ISNI:       0000 0004 2712 2550
Awarding Body: Prifysgol Bangor University
Current Institution: Bangor University
Date of Award: 2011
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Abstract:
Biodiversity is the product of millions of years of evolution and forms the basis of earth‘s life support system, but the magnitude and relative diversity of global species richness remains unknown. On earth there may be over 100 million speciesbut fewer than 2 million have been formally described. Coverage across different biological groups is very uneven with a known taxonomic deficit especially marked for microfauna and meiofauna due to problematic identification and hyper abundant representatives. Soft-bottom benthic meiofauna are ubiquitous, highly abundant organisms that play a crucial role in marine ecosystem functioning. Nevertheless, quantifying community structure using standard morphological approaches requires highly skilled taxonomists that are in short supply, and is very time consuming. The development of massively parallel sequencing has paved the way to explore microbial and meiofaunal diversity in time and space. Several studies have used pyrosequencing to assess the diversity of bacteria and archaea in the marine environment but there has been comparatively limited focus on eukaryotes. Moreover, diversity estimates derived from earlier second-generation sequencing studies are now known to be artificially inflated and skewed, due to several problems ranging from DNA manipulation and PCR amplifications to bioinformatic analyses. Here, I initially provide an overview of the emerging field of meiofaunal biodiversity assessment, using 454 Roche sequencing. The field differs substantially from environmental sequencing of prokaryotes and even some protists and so warrants separate attention. Empirically, meiobenthic richness of numerous phyla was estimated at alpha (local) and beta (European) scales, illustrating the extensive, but also spatial nature of meiofaunal richness and putative distribution patterns. Further to this, I sequenced carefully constructed artificial nematode control communities to assess the drivers (richness and genetic diversity) of DNA recombinant (or chimera) formation in environmental DNA PCR reactions. Theseadvancesprovide a fast, objective and cost-effective wayof accuratelyexploring and elucidating biodiversity in environmental samples.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.543211  DOI: Not available
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