scholarly journals Molecular Species Delimitation of Icelandic Brittle Stars (Ophiuroidea)

2014 ◽  
Vol 35 (2) ◽  
pp. 243-260 ◽  
Author(s):  
Sahar Khodami ◽  
Pedro Martinez Arbizu ◽  
Sabine Stöhr ◽  
Silke Laakmann

Abstract Brittle stars (Echinodermata: Ophiuroidea) comprise over 2, 000 species, all of which inhabit marine environments and can be abundant in the deep sea. Morphological plasticity in number and shape of skeletal parts, as well as variable colors, can complicate correct species identification. Consequently, DNA sequence analysis can play an important role in species identification. In this study we compared the genetic variability of the mitochondrial cytochrome c subunit I gene (COI) and the nuclear small subunit ribosomal DNA (SSU, 18S rDNA) to morphological identification of 66 specimens of 11 species collected from the North Atlantic in Icelandic waters. Also two species delimitation tools, Automatic Barcode Gap Discovery (ABGD) and General Mixed Yule Coalescence Method (GMYC) were performed to test species hypotheses. The analysis of both gene fragments was successful to discriminate between species and provided new insights into some morphological species hypothesis. Although less divergent than COI, it is helpful to use the SSU region as a complementary fragment to the barcoding gene.

Author(s):  
Caitlin Potter ◽  
Cuong Q Tang ◽  
Vera Fonseca ◽  
Delphine Lallias ◽  
John M Gaspar ◽  
...  

Background: Metabarcoding studies allow a wide variety of taxa to be analysed simultaneously in a fraction of the time taken by morphological identification, but currently metabarcoding studies must rely on sequence similarity-based methodologies to delimit operational taxonomic units (OTUs). Similarity-based OTU clustering methodologies can lead to inaccurate estimates of diversity, species’ distributions or responses to change, meaning that there is a critical need for methods to delimit species in metabarcoding datasets. Methods: We introduce SNAPhy (Species delimitation using Niche And PHYlogeny), a novel approach which utilises ecological and phylogenetic information to delimit de novo OTUs in metabarcoding datasets and avoids the problems associated with current OTU clustering methods. Sequencing reads are first divided into ecological groups based on co-occurrence, thereby reducing data complexity and facilitating the use of evolutionary and phylogenetic models (e.g. BEAST and GMYC) to delimit species-level groupings within discrete ecologically informed phylogenies. The utility of SNAPhy is demonstrated using an 18S rDNA nuclear small subunit (nSSU) dataset representing replicated samples taken along the entire length of an estuarine salinity gradient, and SNAPhy is then compared to existing OTU clustering methods. Results: All of the OTU clustering methods compared yielded different numbers of OTUs and a different taxonomic distribution of OTUs, which we suggest is due to the taxon differences that are known to exist in the degree of intraspecific divergence. SNAPhy and UCLUST (with a 98% similarity threshold) gave the most plausible numbers of OTUs, especially within the Nematoda. Additionally, the degree of variation within nematode OTUs delimited by SNAPhy lies within the range of variation in deeply metabarcoded individuals. Discussion: SNAPhy avoids the static clustering threshold problems associated with current OTU clustering methods and instead focuses on genuine biological diversity delimited according to a general lineage species concept. We suggest that the SNAPhy approach should play a crucial role in future sequencing-based biodiversity assessment by providing more accurate estimates of species diversity and distributions than current methods, thereby enabling more accurate impact assessments and better informing managerial decisions.


2017 ◽  
Author(s):  
Caitlin Potter ◽  
Cuong Q Tang ◽  
Vera Fonseca ◽  
Delphine Lallias ◽  
John M Gaspar ◽  
...  

Background: Metabarcoding studies allow a wide variety of taxa to be analysed simultaneously in a fraction of the time taken by morphological identification, but currently metabarcoding studies must rely on sequence similarity-based methodologies to delimit operational taxonomic units (OTUs). Similarity-based OTU clustering methodologies can lead to inaccurate estimates of diversity, species’ distributions or responses to change, meaning that there is a critical need for methods to delimit species in metabarcoding datasets. Methods: We introduce SNAPhy (Species delimitation using Niche And PHYlogeny), a novel approach which utilises ecological and phylogenetic information to delimit de novo OTUs in metabarcoding datasets and avoids the problems associated with current OTU clustering methods. Sequencing reads are first divided into ecological groups based on co-occurrence, thereby reducing data complexity and facilitating the use of evolutionary and phylogenetic models (e.g. BEAST and GMYC) to delimit species-level groupings within discrete ecologically informed phylogenies. The utility of SNAPhy is demonstrated using an 18S rDNA nuclear small subunit (nSSU) dataset representing replicated samples taken along the entire length of an estuarine salinity gradient, and SNAPhy is then compared to existing OTU clustering methods. Results: All of the OTU clustering methods compared yielded different numbers of OTUs and a different taxonomic distribution of OTUs, which we suggest is due to the taxon differences that are known to exist in the degree of intraspecific divergence. SNAPhy and UCLUST (with a 98% similarity threshold) gave the most plausible numbers of OTUs, especially within the Nematoda. Additionally, the degree of variation within nematode OTUs delimited by SNAPhy lies within the range of variation in deeply metabarcoded individuals. Discussion: SNAPhy avoids the static clustering threshold problems associated with current OTU clustering methods and instead focuses on genuine biological diversity delimited according to a general lineage species concept. We suggest that the SNAPhy approach should play a crucial role in future sequencing-based biodiversity assessment by providing more accurate estimates of species diversity and distributions than current methods, thereby enabling more accurate impact assessments and better informing managerial decisions.


Author(s):  
Dirk Erpenbeck ◽  
Merrick Ekins ◽  
Nicole Enghuber ◽  
John N.A. Hooper ◽  
Helmut Lehnert ◽  
...  

Sponge species are infamously difficult to identify for non-experts due to their high morphological plasticity and the paucity of informative morphological characters. The use of molecular techniques certainly helps with species identification, but unfortunately it requires prior reference sequences. Holotypes constitute the best reference material for species identification, however their usage in molecular systematics and taxonomy is scarce and frequently not even attempted, mostly due to their antiquity and preservation history. Here we provide case studies in which we demonstrate the importance of using holotype material to answer phylogenetic and taxonomic questions. We also demonstrate the possibility of sequencing DNA fragments out of century-old holotypes. Furthermore we propose the deposition of DNA sequences in conjunction with new species descriptions.


2019 ◽  
Author(s):  
◽  
Morgan Gueuning

Wild bees are essential pollinators and therefore play a key role in both natural and agricultural ecosystems. However, bees have often been neglected in conservation studies and policies worldwide, which is surprising given their ecological importance. As a result, little is known on the conservation status of the vast majority of wild bee species in Europe, and even less worldwide. Limited surveys suggest important declines in the abundance and diversity of most wild bee communities worldwide. It is therefore urgent to implement targeted measures for the conservation of these keystone species. Once implemented, the effectiveness of these measures must be evaluated using adequate monitoring programs. To date, wild bee surveys are entirely based on morphological identification, which is both labor intensive and time consuming. Consequently, an affordable, high-throughput identification method is needed to reduce costs and improve bee monitoring. The objective of this thesis was to evaluate novel genetic techniques based on Next Generation Sequencing (NGS) methods for facilitating surveys of wild bees. NGS tools were mainly investigated for bridging two important impediments to wild bee conservation efforts, i.e., the cost of biodiversity assessment schemes and taxonomic incompleteness. With the development of NGS techniques, DNA barcoding has gained enormous momentum, enabling cost-effective, fast and accurate identifications. Before these methods can be routinely used in monitoring programs, there are however still important knowledge gaps to fill. These gaps mainly concern the detection of rare species and the acquisition of accurate quantitative data on species abundance; more generally the cost and labour effectiveness of these methods need to be evaluated. To provide a comprehensive presentation of the advantages and weaknesses of different NGS-based identification methods, we assessed three of the most promising ones, namely metabarcoding, mitogenomics and NGS barcoding. Using a regular monitoring data, we found that NGS barcoding performed best for both species’ presence/absence and abundance data, producing only few false positives and no false negatives. The other methods investigated were less reliable in term of species detection and inference of abundance data, and partly led to erroneous ecological conclusions. In terms of workload and cost, we showed that NGS techniques were more expensive than morphological identification with our dataset, although these techniques would become slightly more economical in large-scale monitoring programs. A second aim of this thesis was to provide an easy and robust genomic solution to alleviate taxonomical incompleteness, one of the major impediments to the effective conservation of many insect taxa. For conservation purposes, having stable and well-delimited species hypotheses is essential. Currently, most species are delimitated based on morphology and/or DNA barcoding. These methods are however associated with important limitations, and it is widely accepted that species delimitation should rely on multi-locus genomic markers. To overcome these limitations, ultraconserved elements (UCEs) were tested as a fast and robust approach using different species-complexes harbouring cryptic diversity, mitochondrial introgression, or mitochondrial paraphyly. Phylogenetic analyses of UCEs were highly conclusive and yielded meaningful species delimitation hypotheses in all cases. These results provide strong evidence for the potential of UCEs as a fast method for delimiting species even in cases of recently diverged lineages. Advantages and limitations of UCEs for shallow phylogenetic studies are further discussed.


2020 ◽  
Vol 59 (2) ◽  
pp. 77-87
Author(s):  
Fernando Gómez ◽  
Luis F. Artigas ◽  
Rebecca J. Gast

The North Sea and the English Channel are regions with a long tradition of plankton studies, where the colony-forming haptophyte Phaeocystis globosa dominates the spring phytoplankton blooms. Among its predators, we investigated an abundant unarmored dinoflagellate (~3000 cells per liter) in the North Sea in May 2019. It has been reported in the literature as Gymnodinium heterostriatum or G. striatissimum, and often identified as Gyrodinium spirale. Phylogenetic analyses using the small-, large subunit- and Internal Transcriber Spacers of the ribosomal RNA (SSU-, LSU-, ITS rRNA) gene sequences indicate that our isolates clustered within the Gyrodinium clade. The new sequences formed a sister group with sequences of the freshwater taxon Gyrodinium helveticum, being one of the infrequent marine-freshwater transitions in the microbial world. This isolate is the first characterized member of a clade of numerous environmental sequences widely distributed from cold to tropical seas. This common and abundant taxon has received several names due to its morphological plasticity (changes of size and shape, often deformed after engulfing prey) and the difficulty in discerning surface striation. We conclude that the priority is for the species name Gymnodinium heterostriatum Kofoid & Swezy 1921, a new name that was proposed for Gymnodinium spirale var. obtusum sensu Dogiel 1906. The species Gyrodinium striatissimum (Hulburt 1957) Gert Hansen & Moestrup 2000 and Gymnodinium lucidum D. Ballantine in Parke & Dixon 1964 (=G. hyalinum M. Lebour 1925) are posterior synonyms. We propose Gyrodinium heterostriatum comb. nov. for Gymnodinium heterostriatum.


2021 ◽  
Vol 9 (08) ◽  
pp. 505-514
Author(s):  
Nguyen Chi Mai ◽  
◽  
NinhThi Ngoc ◽  
Nguyen Xuan Cuong ◽  
Nguyen Hoai Nam ◽  
...  

Vietnam contains diverse marine ecosystems with the high biodiversity of marine organisms, including gorgonian corals of Alcyonacea order. In order to support traditional classification of these corals, in this study mitochondrial barcoding markers msh1 and nuclear 28S rDNA were developed for analysis of 11 specimens collected in 2015 and 2016 from different islands and bays along the North Central coast of Vietnam. Phylogenetic analyses based on msh1 and 28S sequence polymorphism showed that all specimens belonged to Anthozoa class, Octocorallia sub-class and Alcyonacea order. At lower taxa levels, they were divided into 4 sub-orders, 7 families and 7 genera according to 7 distinct clades with bootstrap values from 99-100%.The identifications of 7 out of 11 specimens including Sinularia brassica (2 specimens)and Sinularialeptoclados, Dichotellagemmacea, Annella reticulata, S. conferta and S. nanolobata were in concordance between morphological and molecular methods. The other 4 specimens were only identified at genus levels of Astrogorgia sp., Melithaea sp. Scleronephthya sp. and Muricella sp. by either msh1-morphology or msh1-28S markers. These results highlight the importance of molecular markers to elucidate patterns of biodiversity and species identification of soft coral.


Zootaxa ◽  
2010 ◽  
Vol 2347 (1) ◽  
pp. 37 ◽  
Author(s):  
MARIO TOLEDO ◽  
PAUL J. SPANGLER ◽  
MICHAEL BALKE

The Neotropical Laccophilinae genus Laccodytes Régimbart, 1895 is redefined and revised. We recognize ten species, six of which are described as new. We define two species groups: the Laccodytes apalodes-group (L. apalodes Guignot, 1955, L. rondonia sp.n.), and the L. phalacroides-group (L. americanus Peschet, 1919, L. obscuratus sp.n., L. bassignanii sp.n., L. neblinae sp.n., L. olibroides Régimbart, 1895, L. phalacroides Régimbart, 1895, L. takutuanus sp.n., L. androginus sp.n.). Laccophilus pumilio LeConte, 1878, assigned to Laccodytes by Young (1954), belongs to an undescribed genus. Laccodytes species are lotic and most of them inhabit the north-eastern part of South America, apparently with Venezuela and Guyana as centre of diversity. Descriptions, illustrations and SEM photos of habitus, genitals and other diagnostic features are provided for each species, together with habitat notes, when known. We provide a key for species identification.


2019 ◽  
Vol 7 (11) ◽  
pp. 493 ◽  
Author(s):  
Zhan ◽  
Li ◽  
Xu

Metabarcoding and high-throughput sequencing methods have greatly improved our understanding of protist diversity. Although the V4 region of small subunit ribosomal DNA (SSU-V4 rDNA) is the most widely used marker in DNA metabarcoding of eukaryotic microorganisms, doubts have recently been raised about its suitability. Here, using the widely distributed ciliate genus Pseudokeronopsis as an example, we assessed the potential of SSU-V4 rDNA and four other nuclear and mitochondrial markers for species delimitation and phylogenetic reconstruction. Our studies revealed that SSU-V4 rDNA is too conservative to distinguish species, and a threshold of 97% and 99% sequence similarity detected only one and three OTUs, respectively, from seven species. On the basis of the comparative analysis of the present and previously published data, we proposed the multilocus marker including the nuclear 5.8S rDNA combining the internal transcribed spacer regions (ITS1-5.8S-ITS2) and the hypervariable D2 region of large subunit rDNA (LSU-D2) as an ideal barcode rather than the mitochondrial cytochrome c oxidase subunit 1 gene, and the ITS1-5.8S-ITS2 as a candidate metabarcoding marker for ciliates. Furthermore, the compensating base change and tree-based criteria of ITS2 and LSU-D2 were useful in complementing the DNA barcoding and metabarcoding methods by giving second structure and phylogenetic evidence.


2015 ◽  
Vol 105 (2) ◽  
pp. 210-224 ◽  
Author(s):  
U. Bernardo ◽  
E.J. van Nieukerken ◽  
R. Sasso ◽  
M. Gebiola ◽  
L. Gualtieri ◽  
...  

AbstractThe leafminer Coptodisca sp. (Lepidoptera: Heliozelidae), recently recorded for the first time in Europe on Italian black and common walnut trees, is shown to be the North-American Coptodisca lucifluella (Clemens) based on morphological (forewing pattern) and molecular (cytochrome oxidase c subunit I sequence) evidence. The phylogenetic relatedness of three species feeding on Juglandaceae suggests that C. lucifluella has likely shifted, within the same host plant family, from its original North-American hosts Carya spp. to Juglans spp. Over the few years since its detection, it has established in many regions in Italy and has become a widespread and dominant invasive species. The leafminer completes three to four generations per year, with the first adults emerging in April–May and mature larvae of the last generation starting hibernation in September–October. Although a high larval mortality was recorded in field observations (up to 74%), the impact of the pest was substantial with all leaves infested at the end of the last generation in all 3 years tested. The distribution of the leafminer in the canopy was homogeneous. The species is redescribed and illustrated, a lectotype is designated and a new synonymy is established.


2012 ◽  
Vol 62 (1) ◽  
pp. 427-446 ◽  
Author(s):  
Susana Schönhuth ◽  
David M. Hillis ◽  
David A. Neely ◽  
Lourdes Lozano-Vilano ◽  
Anabel Perdices ◽  
...  

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