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~ 166 ~
International Journal of Fisheries and Aquatic Studies 2018; 6(6): 166-169
E-ISSN: 2347-5129
P-ISSN: 2394-0506
(ICV-Poland) Impact Value: 5.62
(GIF) Impact Factor: 0.549
IJFAS 2018; 6(6): 166-169
© 2018 IJFAS
www.fisheriesjournal.com
Received: 21-09-2018
Accepted: 22-10-2018
Md Masum Billah
Institute of Marine Sciences and
Fisheries, University of
Chittagong, Chittagong,
Bangladesh
MA Kader
Institute of Marine Sciences and
Fisheries, University of
Chittagong, Chittagong,
Bangladesh
Syed Shoeb Mahmud
Institute of Marine Sciences and
Fisheries, University of
Chittagong, Chittagong,
Bangladesh
Abdulla-Al-Asif
(1) Department of Fisheries and
Marine Bioscience, Faculty of
Biological Science and
Technology, Jessore University
of Science and Technology,
Jessore, Bangladesh
(2) Department of Aquaculture,
Faculty of Fisheries, Bangladesh
Agricultural University,
Mymensingh, Bangladesh
Abdullah Al Mamun Siddiqui
Institute of Marine Sciences and
Fisheries, University of
Chittagong, Chittagong,
Bangladesh
Correspondence
Md Masum Billah
Institute of Marine Sciences and
Fisheries, University of
Chittagong, Chittagong,
Bangladesh
Diversity and distribution of seaweeds in Saint Martin
Island, Bangladesh
Md Masum Billah, MA Kader, Syed Shoeb Mahmud, Abdulla-Al-Asif and
Abdullah Al Mamun Siddiqui
Abstract
This present investigation conducted on diversity and distribution analysis of the sub-littoral seaweed
flora collected from January to June, 2007 from north part and south part of the Saint Martin Island,
Bangladesh has revealed the presence of 37 seaweed taxa, 11 under Chlorophyceae, 14 under
Phaeophyceae and 12 under Rhodophyceae. The distribution, diversity and abundance of seaweed flora
fluctuate due to temperature, locations and species composition variations in Saint Martin Island.
Keywords: Abundance, diversity, distribution, seaweeds, Saint Martin Island
1. Introduction
The floral groups are exemplified by three assemblages of primary producers, the seaweed, sea
grasses, and the mangroves [1]
. Macro benthic algae are significant factor of the marine
ecology. These types of flora reveal vast diversity in size, color, form, and formation of life
and they are tremendously rich in marine ecosystem. As stated by a very coarse approximation
there is more than 17,000 species of sea flora and among them 95% species of them are algae
[2]
. Up to the present time, numerous researches for the exploitation of seaweed in
technologically advanced republics have been completed about biomass and standing crop.
More recently Faveri et al. [3]
studied the chronological variations of seaweeds in Southern
Brazil and its possible reasons. Hay and Villout [4]
studied the seasonality of Undaria
pinnatifida population in New Zealand waters. Jagtap [5]
defined the marine flora of Nicobar
clutch of islands in Andaman Sea. Ballesteros [6]
considered periodic growth and production of
deep-water population of Halimeda tuna in the Northwestern Mediterranean. Pedrini et al. [7]
conveyed the marine algae of Trindade Island, Brazil. Basson et al. [8]
also testified the benthic
flora of Bahrain. Chock and Mathieson [9]
computed the standing crop and biomass
dissimilarity of estuarine seaweed at Cedar point, Dover New Hampshire Maine, UK.
Comparable studies have also been accompanied in other areas of the world such as, North
Carolina [10]
, India [11]
, Dodger channel of Canada [12]
and Central Puget Sound Washington,
U.S.A. [13]
. Josselyn and Mathieson [14]
have stated the biomass deviation of particular
estuarine macrophytes at North temperate estuary, Falmouth Massachusetts, USA. Bangladesh
coast is 710 km long, facing the Bay of Bengal in the south. Bangladesh is a developing
country; the marine resources like seaweeds are under threat due to variety of pollutants. There
are above 4500 industries located in Chittagong at different sites. According to an estimate all
these industries contribute approximately 99% of the total industrial pollution beside the
contamination from oil waste discharge. Chittagong port brings enormous number of ship for
trade material export-import and ocean going vehicle dispose oil, garbage and wastage to the
sea area which is also nearly adjacent with Saint Martin Island, Chittagong. The intertidal and
drifted seaweed flora of these areas, especially the St. Martin’s Island is rich. So far, 197
species of seaweeds (of them 95 are red, 46 greens and 56 brown) have been recorded [15, 16, 17,
18, 19, 20]
. The present investigation covers the status of the submerged seaweeds, while the
species diversity, distribution and abundance of submerged seaweeds of the Saint Martin
Island are also revealed.
~ 167 ~
International Journal of Fisheries and Aquatic Studies
2. Materials and methods
2.1 Study location and periods
Seaweeds species were collected from Saint Martin Island
during January to June, 2007 from two locations; southern
part and northern part. The northern part of island was
coordinate with 20°38'09.0"N 92°19'34.3"E and the southern
part of island was coordinate with 20°35'28.5"N
92°19'53.5"E.
2.2 Sample collection and preservation
Samples are collected from island once a month. The samples
were then preserved in sea water with 5% formalin, and
individual seaweed as herbaria, deposited in the central
laboratory of Institute of Marine Science, University of
Chittagong.
2.3 Data collection
Collected samples were sorted manually, and then identified
by the help of floral chart; after that, species were counted and
thus data collection process was taken place.
2.4 Data analysis
Entire collected data were précised and inspected cautiously
and documented. Afterward assortment of data, these were
revised and notched. In conclusion, significant tables were
prepared in accordance with the objectives of the study. Data
presented mostly in the tabular form because it is simple in
calculation, widely used and easy to understand. Data were
analyzed using the Microsoft excel 2007.
3. Results and Discussions
3.1 Monthly distribution of sea grass species
There are three major class found in Saint Martin island
namely; Chlorophyceae, Phaeophyceae and Rhodophyceae. It
was found that, Phaeophyceae sea weed group is the most
dominant group; on the other hand, Chlorophyceae had the
minimal presence among three groups found in the study
period. January, February and March were the most precious
month for growth of sea weed and their abundance. It was
found Phaeophyceae at the month of March showed the
higher number of species (14 species); along with total
number of species were also mostly abundant in the month of
March. Whereas, with the increase of temperature the number
of species in all classes were decreasing and at the end of the
June the total number of sea weed species were 18 (Table 1).
These present study is more or less similar with the study of
several research work [21, 22, 23, 24]
.
Table 1: number of species found in island (Month wise)
Name of Class January February March April May June Total
Chlorophyceae 11 10 11 8 7 5 52
Phaeophyceae 13 12 14 11 9 7 66
Rhodophyceae 11 10 12 9 7 6 55
Total 35 32 37 28 23 18 173
3.2 Species distribution in North part of island
Phaeophyceae was the most abundant class which is belongs
to the Northern part of the island. Comparatively, species
distribution is high in north than the Sothern part of Saint
Martin Island (Figure 1).
Fig 1: Species abundance in North part of Island
3.3 Species distribution in South part of island
It was found that, Phaeophyceae and Rhodophyceae’s species
were the competitively similar in availability in southern part
of island. It was also appeared that, the species distribution
were decreased in number at the month of April, May and
June while it was higher in the previous months due to
fluctuations of temperature (Figure 2).
~ 168 ~
International Journal of Fisheries and Aquatic Studies
Fig 2: Species abundance in South part of Island
3.4 Diversity and abundance of sea weed
It was found that, class Chlorophyceae had 5 order belongings
5 family, 5 genus and 11 species; in that mean time, class
Phaeophyceae had 3 order belongings 3 family, 6 genus and
14 species; while class Rhodophyceae had 6 order belongings
9 family maintain 10 genus and 12 species. The abundance
varied from time to time and places; (+) sign remark the
intensity of abundance of different species of sea weed. Such
kind of study was conducted by Qari [21]
.
Table 2: Species diversity and abundance of sea weed in Saint Martin Island, Chittagong
Class Order Family Genus Species Abundance
Chlorophyceae
Cladophorales Cladophoraceae Cladophora Cladophora prolifera +++++
Codiales Codiaceae Codium Codium geppei ++++
Siphonales Codiaceae Avrainvillea Avrainvillea amadelpha +++
Caulerpales Caulerpaceae Caulerpa
Caulerpa cactoides ++++
Caulerpa chemnitzschi ++++
Caulerpa chemnitzschi var. occidentalis ++++
Caulerpa racemosa var. clavifera +++++
Caulerpa sertularioides ++++
Caulerpa taxifolia ++++
Caulerpales Udotiaceae Halimeda
Halimeda discoidea +++
Halimeda opuntia +++++
Phaeophyceae
Dictyotales; Dictyotaceae
Dictyota
Dictyota atomaria ++++
Dictyopteris australis +++
Padina
Padina tenuis ++
Padina pavonica +++
Padina gymnospora ++++
Pocockiella Pocockiella variegata +++++
Spatoglossum
Spatoglossum variabile ++++
Spatoglossum asperum ++++
Dictyosiphonales Chnoosporaceae Chnoospora Chnoospora implexa +++++
Fucales Sargassaceae Sargassum
Sargassum coriifolium +++++
Sargassum olygocystum +++++
Sargassum swartzii +++++
Sargassum tenerrimum +++++
Sargassum pallidum +++++
Rhodophyceae
Nemalionales Chaetangiaceae Galaxura Galaxura fastigiata ++++
Cryptonemiales Coralliniaceae Jania Jania ungulata +++
Gigartinales Hypneaceae Hypnea Hypnea musciformis +++++
Bonnemaisoniales Bonnemaisoniaceae Asparagopsis Asparagopsis taxiformis ++++
Ceramiales
Dasyaceae Dasya
Dasya corymbifera ++++
Dasya pedicellata ++++
Rhodomelaceae
Gracilaria Gracilaria spinuligera +++
Neurymenia Neurymenia fraxinifolia ++++
Delesseriaceae Vanvoorstia Vanvoorstia coccinea +++++
Cryptonemiales;
Grateloupiaceae Halymenia
Halymenia floresia ++++
Halymenia floridana +++
Squamariaceae Peyssonnelia Peyssonnelia polymorpha +++++
N.B.: Ascending of (+) sign remarks more availability of species.
~ 169 ~
International Journal of Fisheries and Aquatic Studies
4. Conclusion
The species distribution and abundance denotes the
availability of marine flora especially, sea weed species found
in Saint Martin Island. Although sea weed bearing some
medicinal and food value but proper check of availability and
biodiversity measurement along with conservation could lead
this bio-component to the sustainable status in Bay of Bengal.
This research team, only investigate the diversity and
distribution of sea weed, any further research approach could
be conducted to study the other feature of this bio flora.
5. References
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Philippines and its utilization. Hydro bio logia. 1999;
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2. Chapman VJ, Chapman DJ. Seaweed and their uses.
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3. Faveri C, Scherner F, Farias J, Oliveira EC, Paulo A, et
al. Temporal changes in the seaweed flora in Southern
Brazil and its potential causes, Pan- American. Journal of
Aquatic Science. 2010; 5:350-357.
4. Hay CH, Villouta E. Seasonality of the Adventive Asian
Kelp Undaria pinnatifida in New Zealand. Bot Mar.
1993; 36:461-476.
5. Jagtap TG. Marine flora of Nicobar group of islands in
Andaman Sea. Indian Journal of Marine Science. 1992;
21:56-58.
6. Ballesteros E. Seasonality of growth and production of a
deep-water population of Halimeda tuna (Chlorophyceae,
Caulerpales) in the northwestern Mediterranean. Bot
Marine. 1991; 34:291-301.
7. Pedrini AG, Goncalves JEA, Fonseca MCS, Zau AS,
Lacorte CC. A survey of the marine algae of Trindade
Island, Brazil. Bot Marine. 1989; 32:97-99.
8. Basson PW, Mohamed SA, Arora DK. A survey of the
benthic marine algae of Bahrain. Bot Marine. 1989;
32:27-40.
9. Chock JS, Mathieson AC. Variations of New England
estuarine seaweeds Biomass. Bot Marine. 1983; 26:87-
97.
10. Peckol P. Seasonal occurrence and reproduction of some
marine algae of the continental shelf, North Carolina
USA. Bot Marine. 1982; 25:185-190.
11. Gaur K, Ramakrishna T, Subbaraju DP, Murthy MS.
Ecological studies on Ulva lactuca L. from Veraval,
India. Hydro bio logia. 1982; 89:89-94.
12. Whyte JNC, Englar JR, Saunders RG, landsay JC.
Seasonal variation in the biomass, quantity & quality of
agar from the reproductive and vegetative stages of
Gracilaria (Verrucosa type). Bot Marine. 1981; 24:493-
501.
13. Thom RM. Seasonality in low intertidal benthic marine
algal communities in Central Puget Sound Washington,
USA Bot Marine. 1980; 23:7-11.
14. Josselyn MN, Mathieson AC. Seasonal influx and
decomposition of autochthonous macro phytes litter in a
north temperate estuary. Hydro bio logia. 1980; 71:197-
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15. Ahmed ZU, Begum ZNT, Hassan MA, Khondker M,
Kabir SMH, Ahmad M, Ahmed ATA, Rahman AKA,
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Kabir SMH, Ahmad M, et al. (eds.). Encyclopedia of
Flora and Fauna of Bangladesh. Algae, Charophyta-
Rhodophyta, (Achnanthaceae-Vaucheriaceae). Asiat.
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17. Aziz A, Islam S. Marine algae of the St. Martin's Island,
Bangladesh. VII. Acrochaetium nurulislamii sp. nov.and
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7(4):923-934

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Diversity and distribution of seaweeds in Saint Martin Island, Bangladesh

  • 1. ~ 166 ~ International Journal of Fisheries and Aquatic Studies 2018; 6(6): 166-169 E-ISSN: 2347-5129 P-ISSN: 2394-0506 (ICV-Poland) Impact Value: 5.62 (GIF) Impact Factor: 0.549 IJFAS 2018; 6(6): 166-169 © 2018 IJFAS www.fisheriesjournal.com Received: 21-09-2018 Accepted: 22-10-2018 Md Masum Billah Institute of Marine Sciences and Fisheries, University of Chittagong, Chittagong, Bangladesh MA Kader Institute of Marine Sciences and Fisheries, University of Chittagong, Chittagong, Bangladesh Syed Shoeb Mahmud Institute of Marine Sciences and Fisheries, University of Chittagong, Chittagong, Bangladesh Abdulla-Al-Asif (1) Department of Fisheries and Marine Bioscience, Faculty of Biological Science and Technology, Jessore University of Science and Technology, Jessore, Bangladesh (2) Department of Aquaculture, Faculty of Fisheries, Bangladesh Agricultural University, Mymensingh, Bangladesh Abdullah Al Mamun Siddiqui Institute of Marine Sciences and Fisheries, University of Chittagong, Chittagong, Bangladesh Correspondence Md Masum Billah Institute of Marine Sciences and Fisheries, University of Chittagong, Chittagong, Bangladesh Diversity and distribution of seaweeds in Saint Martin Island, Bangladesh Md Masum Billah, MA Kader, Syed Shoeb Mahmud, Abdulla-Al-Asif and Abdullah Al Mamun Siddiqui Abstract This present investigation conducted on diversity and distribution analysis of the sub-littoral seaweed flora collected from January to June, 2007 from north part and south part of the Saint Martin Island, Bangladesh has revealed the presence of 37 seaweed taxa, 11 under Chlorophyceae, 14 under Phaeophyceae and 12 under Rhodophyceae. The distribution, diversity and abundance of seaweed flora fluctuate due to temperature, locations and species composition variations in Saint Martin Island. Keywords: Abundance, diversity, distribution, seaweeds, Saint Martin Island 1. Introduction The floral groups are exemplified by three assemblages of primary producers, the seaweed, sea grasses, and the mangroves [1] . Macro benthic algae are significant factor of the marine ecology. These types of flora reveal vast diversity in size, color, form, and formation of life and they are tremendously rich in marine ecosystem. As stated by a very coarse approximation there is more than 17,000 species of sea flora and among them 95% species of them are algae [2] . Up to the present time, numerous researches for the exploitation of seaweed in technologically advanced republics have been completed about biomass and standing crop. More recently Faveri et al. [3] studied the chronological variations of seaweeds in Southern Brazil and its possible reasons. Hay and Villout [4] studied the seasonality of Undaria pinnatifida population in New Zealand waters. Jagtap [5] defined the marine flora of Nicobar clutch of islands in Andaman Sea. Ballesteros [6] considered periodic growth and production of deep-water population of Halimeda tuna in the Northwestern Mediterranean. Pedrini et al. [7] conveyed the marine algae of Trindade Island, Brazil. Basson et al. [8] also testified the benthic flora of Bahrain. Chock and Mathieson [9] computed the standing crop and biomass dissimilarity of estuarine seaweed at Cedar point, Dover New Hampshire Maine, UK. Comparable studies have also been accompanied in other areas of the world such as, North Carolina [10] , India [11] , Dodger channel of Canada [12] and Central Puget Sound Washington, U.S.A. [13] . Josselyn and Mathieson [14] have stated the biomass deviation of particular estuarine macrophytes at North temperate estuary, Falmouth Massachusetts, USA. Bangladesh coast is 710 km long, facing the Bay of Bengal in the south. Bangladesh is a developing country; the marine resources like seaweeds are under threat due to variety of pollutants. There are above 4500 industries located in Chittagong at different sites. According to an estimate all these industries contribute approximately 99% of the total industrial pollution beside the contamination from oil waste discharge. Chittagong port brings enormous number of ship for trade material export-import and ocean going vehicle dispose oil, garbage and wastage to the sea area which is also nearly adjacent with Saint Martin Island, Chittagong. The intertidal and drifted seaweed flora of these areas, especially the St. Martin’s Island is rich. So far, 197 species of seaweeds (of them 95 are red, 46 greens and 56 brown) have been recorded [15, 16, 17, 18, 19, 20] . The present investigation covers the status of the submerged seaweeds, while the species diversity, distribution and abundance of submerged seaweeds of the Saint Martin Island are also revealed.
  • 2. ~ 167 ~ International Journal of Fisheries and Aquatic Studies 2. Materials and methods 2.1 Study location and periods Seaweeds species were collected from Saint Martin Island during January to June, 2007 from two locations; southern part and northern part. The northern part of island was coordinate with 20°38'09.0"N 92°19'34.3"E and the southern part of island was coordinate with 20°35'28.5"N 92°19'53.5"E. 2.2 Sample collection and preservation Samples are collected from island once a month. The samples were then preserved in sea water with 5% formalin, and individual seaweed as herbaria, deposited in the central laboratory of Institute of Marine Science, University of Chittagong. 2.3 Data collection Collected samples were sorted manually, and then identified by the help of floral chart; after that, species were counted and thus data collection process was taken place. 2.4 Data analysis Entire collected data were précised and inspected cautiously and documented. Afterward assortment of data, these were revised and notched. In conclusion, significant tables were prepared in accordance with the objectives of the study. Data presented mostly in the tabular form because it is simple in calculation, widely used and easy to understand. Data were analyzed using the Microsoft excel 2007. 3. Results and Discussions 3.1 Monthly distribution of sea grass species There are three major class found in Saint Martin island namely; Chlorophyceae, Phaeophyceae and Rhodophyceae. It was found that, Phaeophyceae sea weed group is the most dominant group; on the other hand, Chlorophyceae had the minimal presence among three groups found in the study period. January, February and March were the most precious month for growth of sea weed and their abundance. It was found Phaeophyceae at the month of March showed the higher number of species (14 species); along with total number of species were also mostly abundant in the month of March. Whereas, with the increase of temperature the number of species in all classes were decreasing and at the end of the June the total number of sea weed species were 18 (Table 1). These present study is more or less similar with the study of several research work [21, 22, 23, 24] . Table 1: number of species found in island (Month wise) Name of Class January February March April May June Total Chlorophyceae 11 10 11 8 7 5 52 Phaeophyceae 13 12 14 11 9 7 66 Rhodophyceae 11 10 12 9 7 6 55 Total 35 32 37 28 23 18 173 3.2 Species distribution in North part of island Phaeophyceae was the most abundant class which is belongs to the Northern part of the island. Comparatively, species distribution is high in north than the Sothern part of Saint Martin Island (Figure 1). Fig 1: Species abundance in North part of Island 3.3 Species distribution in South part of island It was found that, Phaeophyceae and Rhodophyceae’s species were the competitively similar in availability in southern part of island. It was also appeared that, the species distribution were decreased in number at the month of April, May and June while it was higher in the previous months due to fluctuations of temperature (Figure 2).
  • 3. ~ 168 ~ International Journal of Fisheries and Aquatic Studies Fig 2: Species abundance in South part of Island 3.4 Diversity and abundance of sea weed It was found that, class Chlorophyceae had 5 order belongings 5 family, 5 genus and 11 species; in that mean time, class Phaeophyceae had 3 order belongings 3 family, 6 genus and 14 species; while class Rhodophyceae had 6 order belongings 9 family maintain 10 genus and 12 species. The abundance varied from time to time and places; (+) sign remark the intensity of abundance of different species of sea weed. Such kind of study was conducted by Qari [21] . Table 2: Species diversity and abundance of sea weed in Saint Martin Island, Chittagong Class Order Family Genus Species Abundance Chlorophyceae Cladophorales Cladophoraceae Cladophora Cladophora prolifera +++++ Codiales Codiaceae Codium Codium geppei ++++ Siphonales Codiaceae Avrainvillea Avrainvillea amadelpha +++ Caulerpales Caulerpaceae Caulerpa Caulerpa cactoides ++++ Caulerpa chemnitzschi ++++ Caulerpa chemnitzschi var. occidentalis ++++ Caulerpa racemosa var. clavifera +++++ Caulerpa sertularioides ++++ Caulerpa taxifolia ++++ Caulerpales Udotiaceae Halimeda Halimeda discoidea +++ Halimeda opuntia +++++ Phaeophyceae Dictyotales; Dictyotaceae Dictyota Dictyota atomaria ++++ Dictyopteris australis +++ Padina Padina tenuis ++ Padina pavonica +++ Padina gymnospora ++++ Pocockiella Pocockiella variegata +++++ Spatoglossum Spatoglossum variabile ++++ Spatoglossum asperum ++++ Dictyosiphonales Chnoosporaceae Chnoospora Chnoospora implexa +++++ Fucales Sargassaceae Sargassum Sargassum coriifolium +++++ Sargassum olygocystum +++++ Sargassum swartzii +++++ Sargassum tenerrimum +++++ Sargassum pallidum +++++ Rhodophyceae Nemalionales Chaetangiaceae Galaxura Galaxura fastigiata ++++ Cryptonemiales Coralliniaceae Jania Jania ungulata +++ Gigartinales Hypneaceae Hypnea Hypnea musciformis +++++ Bonnemaisoniales Bonnemaisoniaceae Asparagopsis Asparagopsis taxiformis ++++ Ceramiales Dasyaceae Dasya Dasya corymbifera ++++ Dasya pedicellata ++++ Rhodomelaceae Gracilaria Gracilaria spinuligera +++ Neurymenia Neurymenia fraxinifolia ++++ Delesseriaceae Vanvoorstia Vanvoorstia coccinea +++++ Cryptonemiales; Grateloupiaceae Halymenia Halymenia floresia ++++ Halymenia floridana +++ Squamariaceae Peyssonnelia Peyssonnelia polymorpha +++++ N.B.: Ascending of (+) sign remarks more availability of species.
  • 4. ~ 169 ~ International Journal of Fisheries and Aquatic Studies 4. Conclusion The species distribution and abundance denotes the availability of marine flora especially, sea weed species found in Saint Martin Island. Although sea weed bearing some medicinal and food value but proper check of availability and biodiversity measurement along with conservation could lead this bio-component to the sustainable status in Bay of Bengal. This research team, only investigate the diversity and distribution of sea weed, any further research approach could be conducted to study the other feature of this bio flora. 5. References 1. Trono GC. Jr. Diversity of the seaweeds flora of the Philippines and its utilization. Hydro bio logia. 1999; 398:1-6. 2. Chapman VJ, Chapman DJ. Seaweed and their uses. Chapman and Hall London. New York, 1980. 3. Faveri C, Scherner F, Farias J, Oliveira EC, Paulo A, et al. Temporal changes in the seaweed flora in Southern Brazil and its potential causes, Pan- American. Journal of Aquatic Science. 2010; 5:350-357. 4. Hay CH, Villouta E. Seasonality of the Adventive Asian Kelp Undaria pinnatifida in New Zealand. Bot Mar. 1993; 36:461-476. 5. Jagtap TG. Marine flora of Nicobar group of islands in Andaman Sea. Indian Journal of Marine Science. 1992; 21:56-58. 6. Ballesteros E. Seasonality of growth and production of a deep-water population of Halimeda tuna (Chlorophyceae, Caulerpales) in the northwestern Mediterranean. Bot Marine. 1991; 34:291-301. 7. Pedrini AG, Goncalves JEA, Fonseca MCS, Zau AS, Lacorte CC. A survey of the marine algae of Trindade Island, Brazil. Bot Marine. 1989; 32:97-99. 8. Basson PW, Mohamed SA, Arora DK. A survey of the benthic marine algae of Bahrain. Bot Marine. 1989; 32:27-40. 9. Chock JS, Mathieson AC. Variations of New England estuarine seaweeds Biomass. Bot Marine. 1983; 26:87- 97. 10. Peckol P. Seasonal occurrence and reproduction of some marine algae of the continental shelf, North Carolina USA. Bot Marine. 1982; 25:185-190. 11. Gaur K, Ramakrishna T, Subbaraju DP, Murthy MS. Ecological studies on Ulva lactuca L. from Veraval, India. Hydro bio logia. 1982; 89:89-94. 12. Whyte JNC, Englar JR, Saunders RG, landsay JC. Seasonal variation in the biomass, quantity & quality of agar from the reproductive and vegetative stages of Gracilaria (Verrucosa type). Bot Marine. 1981; 24:493- 501. 13. Thom RM. Seasonality in low intertidal benthic marine algal communities in Central Puget Sound Washington, USA Bot Marine. 1980; 23:7-11. 14. Josselyn MN, Mathieson AC. Seasonal influx and decomposition of autochthonous macro phytes litter in a north temperate estuary. Hydro bio logia. 1980; 71:197- 208. 15. Ahmed ZU, Begum ZNT, Hassan MA, Khondker M, Kabir SMH, Ahmad M, Ahmed ATA, Rahman AKA, Haque EU (eds.) Encyclopedia of Flora and Fauna of Bangladesh. Algae, Chlorophyta (Aphanochaetaceae- Zygnemataceae). Asiatic Society of Bangladesh, Dhaka. 2008; 3:812. 16. Ahmed ZU, Khondker M, Begum ZNT, Hassan MA, Kabir SMH, Ahmad M, et al. (eds.). Encyclopedia of Flora and Fauna of Bangladesh. Algae, Charophyta- Rhodophyta, (Achnanthaceae-Vaucheriaceae). Asiat. Soc. Bangladesh, Dhaka. 2009; 4:543. 17. Aziz A, Islam S. Marine algae of the St. Martin's Island, Bangladesh. VII. Acrochaetium nurulislamii sp. nov.and new records of Acrochaetium (Rhodophyceae). Bangladesh Journal of Botany. 2009; 38(2):145-151. 18. Islam S, Aziz A, Chowdhury AH. Marine algae of St. Martin's Island, Bangladesh. VIII. New records of Red algae (Rhodophyceae). Bangladesh Journal of Botany. 2010; 39(1):87-96. 19. Aziz A, Rahman MT. Marine algae of the St. Martin's Island, Bangladesh. XI. Red algae (Rhodophyceae). Bangladesh Journal of Botany. 2010; 39(2):161-168. 20. Aziz A, Rahman MT. Marine algae of the St. Martin's Island, Bangladesh. XII. New records of Red and green algae. Bangladesh Journal of Botany. 2011; 40(1):41-45. 21. Qari R. An Assessment of Seaweeds Diversity and Distribution at the Beach of Nathia Gali, Karachi, Pakistan Journal of Marine Science Research and Development. 2017; 7:228. 22. Aziz A, Towhidy S, Alfasane MA. Sublittoral seaweed flora of the St. Martin’s Island, Bangladesh. Bangladesh Journal of Botany. 2015; 44(2):223-236. 23. Palanisamy M, Yadav SK, Murthy GVS. Distribution and Diversity of Seaweeds at Thikkodi Coast, Kerala, South India. Botanical Survey of India, Southern Regional Centre, Coimbatore - 641 003, Tamil Nadu, India, 2015. 24. Bhagyaraj I, Kunchithapatham VR. Diversity and distribution of seaweeds in the shores and water lagoons of Chennai and Rameshwaram coastal areas, South- Eastern coast of India. Biodiversity Journal. 2016; 7(4):923-934