Abstract:Strengthening the DNA barcode database is important for a species level identification, which was lacking for seaweeds. We made an effort to collect and barcode seaweeds occurring along Southeast coast of India. We barcoded 31 seaweeds species belonging to 21 genera, 14 family, 12 order of 3 phyla (viz., Chlorophyta, Ochrophyta and Rhodophyta). We found 10 species in 3 phyla and 2 genera (Anthophycus and Chnoospora) of Ochrophyta were barcoded for the first time. Uncorrected p-distance calculated using K2P, nu… Show more
“…Previous nationalised efforts to barcoding the marine diversity (Lakra et al, 2010;Bineesh et al, 2014;Bamaniya et al, 2015) along with localised efforts to barcode the diversity of Vellar estuary (Khan et al, 2010(Khan et al, , 2011PrasannaKumar et al, 2012;Thirumaraiselvi et al, 2015;Rajthilak et al, 2015;Rahman et al, 2013Rahman et al, , 2019Hemalatha et al, 2016;Sahu et al, 2016;Palanisamy et al, 2020;Manikantan et al, 2020;Thangaraj et al, 2020;Narra et al, 2020) resulted in strengthening the reference library which insured that no ambiguous sequences were present in this study (as all sequences were identified to species level). Identification success was likely due to the use of previously generated references sequences from Indian waters from morphologically verified species and published through reference databases (such as GenBank and BOLD).…”
Section: Discussionmentioning
confidence: 99%
“…In addition, to capture potential genetic variation, including undocumented cryptic diversity, it is important to sequence an adequate number of individuals from across a species range (Weigt et al 2012b). We have made considerable efforts in the past decade as part of the Indian Census of Marine Life (ICoML) to recover barcodes in reasonable numbers of marine phyla including fin & shell fishes, invertebrates (Khan et al, 2010(Khan et al, , 2011PrasannaKumar et al, 2012;Thirumaraiselvi et al, 2015;Rajthilak et al, 2015;Rahman et al, 2013Rahman et al, , 2019Hemalatha et al, 2016;Palanisamy et al, 2020;Manikantan et al, 2020;Thangaraj et al, 2020) and plants (Sahu et al, 2016;Narra et al, 2020) occurring in and around the Vellar estuary. Hence we predict a high rate of success in identification of dietary items of A. maculatus occurring in this environment.…”
Identification and quantification of fish diet diversity was the first step in understanding the food web dynamics and ecosystem energetics, where the contribution of DNA barcoding technique has been important. We used DNA barcoding to identify the stomach contents of a euryhaline, benthophagous catfish Ariius maculatus. From 40 catfish stomach items sampled in two different seasons, we barcoded 67 prey items of chordates and macro-invertebrates identified as belonging to 13 species in 4 major phyla (viz., Chordate, Arthropod, Annelida and Mollusca). It is important to note that the mollusc taxa (Meritrix meritrix and Perna viridis) and the species of fish (Stolephorus indicus) could not be found among the gut contents of A. maculatus sampled during the pre- and post-monsoon season, respectively. Among the chordate diets of A. maculatus, Eubleekeria splendens (23.5%) and Stolephorus indicus (23.5%) were the major prey taxa during pre-monsoon season. The hermit crabs forms the major constituents of both pre- and post-monsoon seasons, among invertebrate taxa. Polychaete, Capitella capitata (25.92%) was abundantly consumed invertebrates next to hermit crabs. We noticed that in pre-monsoon A. maculatus was more piscivorous than post-monsoon. As revealed through Kimura-2 parametric pair-wise distance analysis, the diet diversity was relatively higher in post-monsoon. The accumulation curve estimated 57 haplotypes within 14 barcoded species (including the host A. maculatus). Majority of haplotypes were found in Chordates (47.36%) followed by Arthropods (28.07%), Annelids (14.03%) and Mollusca (10.52%), respectively. This study also highlights that there is a growing concern about A. maculatus’s aggressive predation on commercially important stocks of fish and invertebrates. We will continue to expand the coverage of species barcoded in the reference database, which will become more significant as meta- and environmental DNA barcoding techniques become cheaper and prevalent.
“…Previous nationalised efforts to barcoding the marine diversity (Lakra et al, 2010;Bineesh et al, 2014;Bamaniya et al, 2015) along with localised efforts to barcode the diversity of Vellar estuary (Khan et al, 2010(Khan et al, , 2011PrasannaKumar et al, 2012;Thirumaraiselvi et al, 2015;Rajthilak et al, 2015;Rahman et al, 2013Rahman et al, , 2019Hemalatha et al, 2016;Sahu et al, 2016;Palanisamy et al, 2020;Manikantan et al, 2020;Thangaraj et al, 2020;Narra et al, 2020) resulted in strengthening the reference library which insured that no ambiguous sequences were present in this study (as all sequences were identified to species level). Identification success was likely due to the use of previously generated references sequences from Indian waters from morphologically verified species and published through reference databases (such as GenBank and BOLD).…”
Section: Discussionmentioning
confidence: 99%
“…In addition, to capture potential genetic variation, including undocumented cryptic diversity, it is important to sequence an adequate number of individuals from across a species range (Weigt et al 2012b). We have made considerable efforts in the past decade as part of the Indian Census of Marine Life (ICoML) to recover barcodes in reasonable numbers of marine phyla including fin & shell fishes, invertebrates (Khan et al, 2010(Khan et al, , 2011PrasannaKumar et al, 2012;Thirumaraiselvi et al, 2015;Rajthilak et al, 2015;Rahman et al, 2013Rahman et al, , 2019Hemalatha et al, 2016;Palanisamy et al, 2020;Manikantan et al, 2020;Thangaraj et al, 2020) and plants (Sahu et al, 2016;Narra et al, 2020) occurring in and around the Vellar estuary. Hence we predict a high rate of success in identification of dietary items of A. maculatus occurring in this environment.…”
Identification and quantification of fish diet diversity was the first step in understanding the food web dynamics and ecosystem energetics, where the contribution of DNA barcoding technique has been important. We used DNA barcoding to identify the stomach contents of a euryhaline, benthophagous catfish Ariius maculatus. From 40 catfish stomach items sampled in two different seasons, we barcoded 67 prey items of chordates and macro-invertebrates identified as belonging to 13 species in 4 major phyla (viz., Chordate, Arthropod, Annelida and Mollusca). It is important to note that the mollusc taxa (Meritrix meritrix and Perna viridis) and the species of fish (Stolephorus indicus) could not be found among the gut contents of A. maculatus sampled during the pre- and post-monsoon season, respectively. Among the chordate diets of A. maculatus, Eubleekeria splendens (23.5%) and Stolephorus indicus (23.5%) were the major prey taxa during pre-monsoon season. The hermit crabs forms the major constituents of both pre- and post-monsoon seasons, among invertebrate taxa. Polychaete, Capitella capitata (25.92%) was abundantly consumed invertebrates next to hermit crabs. We noticed that in pre-monsoon A. maculatus was more piscivorous than post-monsoon. As revealed through Kimura-2 parametric pair-wise distance analysis, the diet diversity was relatively higher in post-monsoon. The accumulation curve estimated 57 haplotypes within 14 barcoded species (including the host A. maculatus). Majority of haplotypes were found in Chordates (47.36%) followed by Arthropods (28.07%), Annelids (14.03%) and Mollusca (10.52%), respectively. This study also highlights that there is a growing concern about A. maculatus’s aggressive predation on commercially important stocks of fish and invertebrates. We will continue to expand the coverage of species barcoded in the reference database, which will become more significant as meta- and environmental DNA barcoding techniques become cheaper and prevalent.
“…1.6. Barcoding an Entire Regional Marine Flora Previous efforts of DNA barcoding of marine flora have focused either on (1) restricted geographic areas covering the three main macroalgal groups (Chlorophyta, Phaeophyceae, and Rhodophtya; e.g., northern Madagascar [80], Bergen, Norway [81], Boulder Patch, Beaufort Sea [82], southeast coast of India [83], Malta [84]), (2) larger areas (e.g., regional scale) but targeting specific groups (e.g., Rhodophyta in South Africa [85,86] and Qingdao, China [87]; Dumontiaceae [88] and Phyllophoraceae [89] in Canada; Rhodymeniales in Australia [90]; Gracilariaceae [91] and Pyropia [92] in the Republic of Korea), or (3) on lower taxonomic levels (e.g., genus, order, or family) but covering large geographic scales (e.g., Corallinophycidae in Altantic European maerl beds [93]). To our knowledge, no DNA barcoding study has yet been conducted at a regional level encompassing the three macroalgal groups (Chlorophyta, Ochrophyta, Rhodophyta), Cyanobacteria, and the marine phanerogams (seagrasses; marine phanerogams).…”
Located in the heart of the South Pacific Ocean, the French Polynesian islands represent a remarkable setting for biological colonization and diversification, because of their isolation. Our knowledge of this region’s biodiversity is nevertheless still incomplete for many groups of organisms. In the late 1990s and 2000s, a series of publications provided the first checklists of French Polynesian marine algae, including the Chlorophyta, Rhodophyta, Ochrophyta, and Cyanobacteria, established mostly on traditional morphology-based taxonomy. We initiated a project to systematically DNA barcode the marine flora of French Polynesia. Based on a large collection of ~2452 specimens, made between 2014 and 2023, across the five French Polynesian archipelagos, we re-assessed the marine floral species diversity (Alismatales, Cyanobacteria, Rhodophyta, Ochrophyta, Chlorophyta) using DNA barcoding in concert with morphology-based classification. We provide here a major revision of French Polynesian marine flora, with an updated listing of 702 species including 119 Chlorophyta, 169 Cyanobacteria, 92 Ochrophyta, 320 Rhodophyta, and 2 seagrass species—nearly a two-fold increase from previous estimates. This study significantly improves our knowledge of French Polynesian marine diversity and provides a valuable DNA barcode reference library for identification purposes and future taxonomic and conservation studies. A significant part of the diversity uncovered from French Polynesia corresponds to unidentified lineages, which will require careful future taxonomic investigation.
“…Seaweeds are marine macroalgae that inhabit the littoral zone [ 11 ]. Seaweeds are characterized as non-vascular plants, which represent the primary producers in oceans and belong to the Protista not Planta kingdom [ 3 ].…”
Macroalgae are significant biological resources in coastal marine ecosystems. Seasonality influences macroalgae biochemical characteristics, which consequentially affect their ecological and economic values. Here, macroalgae were surveyed from summer 2017 to spring 2018 at three sites at 7 km (south) from El Qusier, 52 km (north) from Marsa Alam and 70 km (south) from Safaga along the Red Sea coast, Egypt. Across all the macroalgae collected, Caulerpa prolifera (green macroalgae), Acanthophora spicifera (red macroalgae) and Cystoseira myrica, Cystoseira trinodis and Turbinaria ornata (brown macroalgae) were the most dominant macroalgal species. These macroalgae were identified at morphological and molecular (18s rRNA) levels. Then, the seasonal variations in macroalgal minerals and biochemical composition were quantified to determine the apt period for harvesting based on the nutritional requirements for commercial utilizations. The chemical composition of macroalgae proved the species and seasonal variation. For instance, minerals were more accumulated in macroalgae C. prolifera, A. spicifera and T. ornata in the winter season, but they were accumulated in both C. myrica and C. trinodis in the summer season. Total sugars, amino acids, fatty acids and phenolic contents were higher in the summer season. Accordingly, macroalgae collected during the summer can be used as food and animal feed. Overall, we suggest the harvesting of macroalgae for different nutrients and metabolites in the respective seasons.
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