Ulva intestinalis and Ulva compressa are two bloom-forming morphologically-cryptic species of green seaweeds widely accepted as cosmopolitan in distribution. Previous studies have shown that these are two distinct species that exhibit great morphological plasticity with changing seawater salinity. Here we present a phylogeographic assessment of tubular Ulva that we considered belonging to this complex collected from various marine and estuarine green-tide occurrences in a ca. 600 km stretch of the Indian west coast. Maximum Likelihood and Bayesian Inference phylogenetic reconstructions using ITS nrDNA revealed strong endemism of Indian tubular Ulva, with none of the Indian isolates forming part of the already described phylogenetic clades of either U. compressa or U. intestinalis. Due to the straightforward conclusion that Indian isolates form a robust and distinct phylogenetic clade, a description of a new bloom-forming species, Ulva paschima Bast, is formally proposed. Our phylogenetic reconstructions using Neighbor-Joining method revealed evolutionary affinity of this new species with Ulva flexuosa. This is the first molecular assessment of Ulva from the Indian Subcontinent.
Citation: Bast F, John AA, Bhushan S (2014) Strong Endemism of Bloom-Forming Tubular Ulva in Indian West Coast, with Description of Ulva paschima Sp. Nov. (Ulvales, Chlorophyta). PLoS ONE 9(10): e109295. https://doi.org/10.1371/journal.pone.0109295
Editor: Ross Frederick Waller, University of Cambridge, United Kingdom
Received: June 4, 2014; Accepted: August 22, 2014; Published: October 15, 2014
Copyright: © 2014 Bast et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. All data are available through GenBank and LabArchives; accession numbers and URLs and DOIs are included in the paper.
Funding: Supported by INSPIRE Faculty award (IFA-LSPA-02) from Department of Science and Technology, Government of India. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Genus Ulva (Linnaeus), commonly known as “Sea Lettuce”, encompasses some of the most ubiquitous green seaweeds distributed throughout the world, with habitats ranging from marine to freshwater. This algal genus is both beneficial and disadvantageous; beneficial as some species of this genus, including Ulva prolifera  and Ulva intestinalis , are commercially cultivated worldwide for its culinary use and disadvantageous as this genus is notorious for its ability to cause massive green-tides  and marine fouling . Species of this genus are well known for having highly plastic morphologies, and that the habits can change from tube-form to blade-form or vice versa in response to changing environmental conditions . Therefore, morphology-based classifications, which have been routinely used since the inception of this genus, are now being replaced with molecular systematics , . For example, the genus Enteromorpha- which had been separated from Ulva based on tubular morphology by Link (Link in Nees 1820)- has recently been merged back to Ulva based on DNA sequence evidence –. Due to taxonomic confusions in morphology-based species delineation, concept of Operational Taxonomic Units (OTUs) have been used in recent phylogeographic assessments of Ulva from Hawaii  and USA .
Tubular Ulva in Indian Coast is believed to be comprised mainly of two species; Ulva intestinalis Linnaeus and Ulva compressa Linnaeus (personal observation). These two species are so closely related that they are regarded as cryptic species in a number of molecular phylogenetic studies , . These species are separated from each other based on microscopic and macroscopic morphological characters . Microscopic characters include distinct cell arrangement in U. compressa consisting of rosettes of cells (“Cell islands”) and longitudinal rows of cells in contrast to U. intestinalis, where there are no obvious arrangement of cells. Macroscopic characters include branching pattern and compression of thallus, in which U. intestinalis is mostly unbranched with hollow tubular monostromatic thalli, with very few branches for algae growing on low-saline environments, and U. compressa is highly branched with compressed thalli . Taxonomic validity of these character states have been repeatedly questioned (see  for review). Morphological and phylogenetic variation in these two species has been investigated from the Baltic Sea Area  and the British Isles , and both of these reports concluded that U. intestinalis and U. compressa are distinct, monophyletic species. In recent phylogenetic assessments of Ulva from North Adriatic sea  and temperate Australia ,  these two species together formed strongly supported clade, confirming their evolutionary relatedness.
The genus Ulva from India has never been subjected to extensive taxonomic scrutiny to date. While phylogeographic assessments of Ulva have been conducted in various parts of the world, including Japan , Australia , China , North-East Pacific  and Hawaii , sequence-based assessment of Ulva from Indian subcontinent have not yet been done. Objectives of the present study are to understand morphological and molecular variation of tubular Ulva occurring on the Indian west coast. Almost all of the previous phylogeographic assessments in genus Ulva were based on nucleoribosomal Internal Transcribed Spacer (ITS). ITS is one of the well-represented loci at Genbank and therefore we selected this locus for our molecular assessment.
Materials and Methods
During our 2012 expedition to the west coast of India, a particular tubular Ulva was detected causing massive blooms in a number of freely accessible locations (Table 1). Bloom specimens of tubular Ulva, either attached to intertidal substrates (including rocks, pebbles, wooden dinghies, mooring lines and breakwaters), or drifting while attached to a variety of floating objects were subsequently collected (Table 1). Collection coordinates were acquired with a handheld GPS device (eTrex 30, Garmin, USA). A map overlay of sampling locations with an accuracy of ± 10 meters is accessible at http://bit.ly/UlvaBloom. Photographs of the bloom were taken using a GPS-enabled digital camera (CyberShot DSC HX20V, Sony, Japan) and these photographs, with embedded GPS data, are available as online-only supplementary data (Figs. S1–10 in File S1). Seawater salinity was measured at the collection locations using a handheld salinometer (PCTTestr 35, Eutech Instruments, Singapore). Collected specimens were transported to the laboratory in zip-lock polythene bags under cold conditions (4–10°C). After washing the thalli in tap water to remove sediments and other contaminants, morphological characterization of the specimens was made using an upright microscope (BX53, Olympus, Japan) with an attached digital camera (E450, Olympus, Japan). Public domain software ImageJ (http://rsbweb.nih.gov/ij/) was used for scale calibration and size measurements. Pressed vouchers were prepared and deposited in the Central National Herbarium, Botanical Survey of India, Calcutta (Index Herbariorum code: CAL). Samples for molecular analyses were stored at -80°C awaiting further analysis.
DNA extraction, PCR amplification, purification and DNA sequencing
The frozen specimens were thawed in artificial sea water . Total genomic DNA was extracted from the specimens using a HiPurA Algal Genomic Extraction Kit (HiMedia Laboratories Pvt. Ltd., Mumbai) following manufacturer's protocol. Tissues from the apical thalli were selected to increase DNA yield. The quality of DNA was checked on 0.8% agarose gel and the quantity of DNA was checked with spectrophotometer. Isolated DNA was stored at −20°C.
A DNA working solution of 25 ng/µl was prepared for polymerase chain reaction (PCR) in a separate tube. The 20 µl PCR reaction mix contained 2 µl of 10× reaction buffer with 15 mM MgCl2 (Applied Biosystems, India), 4 µl each of 10 µM primer, 2 µl of 1 µM dNTPs (Imperial Life sciences, India), 0.6 unit of rTaq DNA polymerase (Imperial Life sciences, India), 4 µl of template DNA and sterile water. The four universal primers used for amplifying the ITS regions and the 5.8S gene (fragment length = 639 bp) were: ITS1 (5'-TCCGTAGGTGAACCTGCGG-3'), ITS2 (5'- GCTGCGTTCTTCATCGATGC-3'), ITS3 (5'- GCATCGATGAAGAACGCAGC-3') and ITS4 (5'- TCCTCCGCTTATTGATATGC-3') . PCR amplifications were carried out in programmable thermal cycler (Veriti, ABI, USA) and reaction profile included an initial denaturation at 94°C for 5 minutes, followed by 35 cycles of 94°C for 1 minute, 52°C for 2 minutes and 72°C for 2 minutes, and a final extension of 72°C for 10 minutes.
Purification of PCR product
Amplicons were purified using ExoSAP-IT PCR clean-up kit following manufacturer's instructions (USB Corporation, Cleveland, OH, USA). A working solution of 1∶10 (DNA: water) was prepared as sequencing template. PCR amplification reactions (as well as its sequencing) were carried out in duplicate for each target sequence of each isolate using the same set of primers as a quality control.
Purified PCR products were subjected to bidirectional Sanger sequencing using a dideoxy chain termination protocol with ABI BigDye Terminator Cycle Sequencing Ready Reaction Kit v3.1 (Applied Biosystems, Foster City, CA, USA) and a programmable thermal cycler (Veriti, ABI, USA), as per .DNA sequences were assembled using the computer program CodonCodeAligner (CodonCode Corporation, USA). Sequences were deposited in Genbank (Table 1).
We followed the step-by-step protocol for phylogenetic analysis, including alignment construction, Maximum Likelihood test to find best-fitting substitution models , phylogeny reconstruction using Maximum Likelihood (ML), Bayesian Inference (BI) and distance analysis as outlined in Bast . In summary, six sequences of tubular Ulva from India were aligned with other published accessions of Ulva intestinalis and Ulva compressa obtained from Genbank (Table S1) by MUSCLE algorithm inside computer program Geneious v6.1.6 (available at http://www.genious.com) and alignments were edited by eye. Phylogenetic analysis using ML algorithm was conducted in MEGA (www.megasoftware.net/) with starting tree generated by BioNJ. Substitution bias was modelled by Tamura-3-Parameter  (T3P) model with Gamma distribution (that was the best model in our test to find best fitting substitution models  with BIC (Bayesian Information Criterion) score of 5626.537).Heuristic searches were performed with tree bisection-reconnection, MULTREES and steepest descent options in effect. 1000 bootstrap replicates were performed under ML criterion to estimate interior branch support . Phylogenetic analysis with BI was conducted using the MrBayes plug-in v3  within Geneious. Analyses were run with four Markov chains using the T3P model with Gamma distribution for 106 generations with a tree saved every 100th generation. The first 1000 trees were discarded as burn-in, as determined by “burnin <number>“ function of MrBayes plug-in. A consensus tree was constructed using the consensus tree builder within Geneious. In order to investigate relative phylogenetic position of our isolates in genus Ulva, a separate ITS dataset was constructed with 120 sequences obtained from Genbank, spanning all major species represented in the database. Due to the computational limitations, we used Neighbor-Joining (NJ) method for this dataset. All of our scientific datasets, including cell area measurements, DNA sequence alignment in FASTA format, results of ModelTest, T3P pairwise distances, tree in nexus format and original electropherograms of DNA sequences with contig assembly instructions are freely available at LabArchives (http://dx.doi.org/10.6070/H4639MP5).
The electronic version of this article in Portable Document Format (PDF) in a work with an ISSN or ISBN will represent a published work according to the International Code of Nomenclature for algae, fungi, and plants, and hence the new names contained in the electronic publication of a PLOS ONE article are effectively published under that Code from the electronic edition alone, so there is no longer any need to provide printed copies. The online version of this work is archived and available from the following digital repositories: PubMed Central, LOCKSS and Research Gate.
Seawater salinity ranged between 35PSU and 24PSU. As expected, exposed shores had higher salinity than inlets and river mouth areas. On external morphology, all six isolates had their own unique features (Fig 1, and Figs S1–S10 in File S1). All isolates were grass green in color, erect filamentous, and had a parietal chloroplast with more than three pyrenoids inside each cell (Arrowheads in Figs 1 D, H, L, P, T and X). Isolates ANJ, MAN and PON had some part of their thallus flattened (indicated by Arrowheads in Figs 1A, M and U, respectively) and had thicker thalli (Figs 1B, N and V), comparing with other isolates. In terms of thalli branching character state, isolate KUN was unique in that it was branched, up to two lateral branch orders (Arrowheads in Fig 1J), while the other isolates were unbranched. In terms of cell arrangement, isolates KAR and KAN were similar, with more or less linear arrangement of cells (cell layers accentuated with pairs of lines in Figs 1G and S, respectively). In terms of cell size, isolates ANJ and MAN were the largest and PON was the smallest (Table 1). A comparison of taxonomically relevant morphological characters for our isolates with U. intestinalis, U. compressa and U. flexuosa is presented (Table 2). As per thallus branching character and thallus compression character, isolates ANJ, KAR, MAN, KAN and PON were arbitrarily classified as U. intestinalis (unbranched, hollow) and isolate KUN as Ulva compressa (branched, compressed).
A–D ANJ Isolate, E–H KAR isolate, I–L KUN isolate, M-P MAN isolate, Q–T KAN Isolate and U–X PON Isolate. Arrowheads in M and U indicate flat portions of thalli, J indicate branching pattern and D, H, L, P, T and X indicate pyrenoids. Scale bars are 2 mm for A, E, I, M, Q and U; 200 µm for B, F, J, N, R and V; 100 µm for C, G, K, O, S and W; and 50 µm for D, H, L, P, T and X.
While we primarily employed ITS sequence data for barcoding, phylogenetic reconstruction using this locus revealed a number of evolutionary trends. Phylogenetic reconstruction using the ML (Fig 2) and BI (Fig 3) methods resulted in moderately-resolved phylograms, with three clades. All Indian isolates of tubular Ulva formed a single clade (highlighted “Paschima”). Our isolate KUN (U. compressa morphotype) seems to have been much diverged from Indian isolates of U. intestinalis morphotype as evidenced by long branch-length. This isolate clustered within U. intestinalis accessions from India in BI, but was basal to U. intestinalis accessions from India in ML. Other monophyletic clades included that of non-Indian isolates of U. compressa (highlighted “Compressa”) and U. intestinalis (highlighted “Intestinalis). Within-group mean T3P distance was 0.5352 for “Paschima” and 0.000 for both “Intestinalis” and “Compressa”, which indicates a very high genetic heterogeneity for the “Paschima” clade. In one study , within-group JC (Jukes-Cantor) distance for Enteromorpha had been reported to range between 0.09 to 0.16. As within- group distance for “Paschima” clade observed in the present study being much higher, possibility that our isolate KUN belonging to another unique taxon from India cannot be ruled out.
Numbers near nodes represent bootstrap support (1000 replicates), exceeding 50. This phylogram is rooted with Ulva prolifera as outgroup. Scale bar given on bottom is in the units of average nucleotide substitutions per site.
Numbers near nodes represent Bayesian Posterior Probabilities, exceeding 0.5. This phylogram is rooted with Ulva prolifera as outgroup. Scale bar given on bottom is in the units of average nucleotide substitutions per site.
Phylogenetic analysis with NJ conducted for 121 sequences of Ulva resulted in a moderately-resolved phylogram (Fig.4). Paschima clade showed evolutionary affinity to Flexuosa clade, albeit with weak bootstrap support (36, not shown in figure). Ulva flexuosa, Ulva compressa, and Ulva intestinalis formed respective monophyletic clades. A clade comprising of Ulva rigida, Ulva laetevirens, Ulva scandinavica, Ulva fenestrata, Ulva armoricana and Ulva lactuca had strong bootstrap support, indicating phylogenetic affinity of these species. Ulva fasciata formed a strongly supported clade with Ulva ohnoi (clade “fasciata”) and Ulva linza clustered within a strongly supported clade comprising of Ulva prolifera (clade “prolifera”). For a definitive phylogenetic assessment of these taxa, additional genetic loci need to be employed.
The present study made several interesting revelations, the most significant of which is the apparent endemism of a bloom-forming Indian tubular Ulva that is morphologically plastic and indistinguishable from U. intestinalis and U. compressa. Contrary to our expectations, the five isolates that had hollow, unbranched thalli did not group within the already described U. intestinalis clade in our phylogenetic analyses, nor did the single identified isolate that had compressed, branched thalli show affiliation to the U. compressa clade. Instead, all of our isolates formed a strongly supported clade, which showed affinity to a previous sample identified as Ulva intestinalis from Gopnath, Gujarat, India (personal communication). This clearly indicates a high degree of endemism for the Indian tubular Ulva. Interestingly, Japanese isolates of either Ulva compressa, or Ulva intestinalis, were described to have very little pair-wise distance from European Isolates at ITS loci. Given the vast geographical distance of ca. 10,000 km, this earlier report could either be suggestive of a recent introduction of these species to either of these locations or existence of temperate haplotypes. A recent report on the molecular assessment of Ulva from Australia concluded that the genus encompasses a number of endemic potentially cryptic species in addition to cosmopolitan species . In the light of these findings, assumptions of cosmopolitanism among certain species of Ulva can cause novel and endemic species to be overlooked.
Our identification of the KUN isolate as U. compressa was based on the previously described character states of branching pattern of thallus and compressed state of the filament . However, phylogeny reconstruction clustered our U. compressa specimen within a clade comprised chiefly of hollow, unbranched tubular Ulva from India (similar to U. intestinalis morphospecies). These two tubular Ulva morphospecies from India might indeed be conspecific. Low salinity at the habitat of the KUN isolate might have influenced the species to acquire this morphotype as suggested by previous studies . Alternately, non-Indian accessions of U. intestinalis and U. compressa might indeed be unique species with yet-to-discover synapomorphic character state/s, as observed in our phylogenetic analyses. In summary, without molecular data, Indian species of bloom-forming Ulva most closely resemble with either/both U. intestinalis and U. compressa, two species that are shown in the literature to be difficult to distinguish between.
Results from our phylogenetic reconstructions strongly argue in favor of species-level taxonomic treatment for the OTUs from India, which is evolutionarily unrelated to either Ulva intestinalis or Ulva compressa. We therefore formally propose a new species of bloom-forming tubular Ulva as per the following description, congruent with Phylogenetic Species Concept :
Ulva paschima Bast sp. nov. (Fig 1)
Primary diagnosis is the phylogenetic affiliation of OTUs with ITS clade “Paschima” as per this report. Fronds erect filamentous and grass green in color; 5 cm–40 cm in length; mostly unbranched tubular with some parts of the thalli compressed or flat, ribbon-like; tufts of filamentous thalli attached via rhizoid. Morphotype in low-saline inlets and estuaries might have branched, compressed thalli. Cells are more or less quadrilateral; some have linear cell arrangement. Parietal chloroplast with>2 pyrenoids per cell.
Collected from intertidal rocks at a splash zone near Paraiso de Goa, Anjuna Beach, Goa, India (15.58419N, 73.73683E). Deposited at Central National Herbarium, Botanical Survey of India, Calcutta (Index Herbariorum code: CAL) under voucher # CAL-CUPVOUCHER-UP-2013-3. DNA sequences of nrDNA ITS1-5.8S-ITS2 complete region of the holotype deposited at Genbank under accession # KF385504.
Deposited at Herbarium, the Central University of Punjab under voucher No.: CUPVOUCHER-UP-2013-3. Frozen voucher maintained at Centre for Biosciences, the Central University of Punjab under voucher No.: CUPFVOUCHER-UP-2013-1.
Compressed file containing Figure S1 to Figure S10. Figure S1, Photograph of algal bloom specimen of Ulva intestinalis isolate ANJ. Figure S2, Photograph of drifting algal bloom specimen of Ulva intestinalis isolate KAR, attached on mooring line. Figure S3, Photograph of algal bloom specimen of Ulva compressa isolate KUN. Figure S4, Photograph of algal bloom specimen of Ulva compressa isolate KUN. Figure S5, Photograph of algal bloom specimen of Ulva compressa isolate KUN. Figure S6, Photograph of algal bloom specimen of Ulva intestinalis isolate MAN. Figure S7, Photograph of algal bloom specimen of Ulva intestinalis isolate MAN, attached on wooden dinghy. Figure S8, Photograph of algal bloom specimen of Ulva intestinalis isolate MAN, attached on wooden dinghy. Figure S9, Photograph of algal bloom specimen of Ulva intestinalis isolate KAN. Figure S10, Photograph of algal bloom specimen of Ulva intestinalis isolate PON.
We thank Dr. Chris Yesson, Natural History Museum for his help with phylogenetics, especially refining the alignment. We are also thankful for the Vice chancellor, the Central University of Punjab for his support with respect to the execution of this research.
Conceived and designed the experiments: FB. Performed the experiments: FB AAJ SB. Analyzed the data: FB. Contributed reagents/materials/analysis tools: FB. Wrote the paper: FB.
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