Journal of Threatened Taxa | www.threatenedtaxa.org | 26 October
2019 | 11(13): 14722–14744
SEM study of planktonic
chlorophytes from the aquatic habitat of the Indian Sundarbans and their
conservation status
Gour Gopal Satpati
1 & Ruma
Pal 2
1 Department
of Botany, Bangabasi Evening College, University of
Calcutta, 19 Rajkumar Chakraborty Sarani, Kolkata,
West Bengal 700009, India.
2 Phycology
laboratory, Department of Botany, Center of Advanced
Study (CAS), University of Calcutta, 35, Ballygunge Circular Road, Kolkata,
West Bengal 700019, India.
1 gour_satpati@yahoo.co.in
(corresponding author), 2 rpalcu@rediffmail.com
doi: https://doi.org/10.11609/jott.4422.11.13.14722-14744
Editor: Asheesh Shivam, Nehru Gram Bharati
University, Uttar Pradesh, India. Date of publication: 26
October 2019 (online & print)
Manuscript details: #4422 | Received 21 July 2018 |
Final received 19 July 2019 | Finally accepted 29 September 2019
Citation: Satpati, G.G. & R. Pal (2019). SEM study of planktonic chlorophytes from the aquatic
habitat of the Indian Sundarbans and their conservation status. Journal of Threatened Taxa 11(13): 14722–14744. https://doi.org/10.11609/jott.4422.11.13.14722-14744
Copyright: © Satpati & Pal 2019. Creative Commons Attribution 4.0 International
License. JoTT
allows unrestricted use, reproduction, and distribution of this article in any
medium by adequate credit to the author(s) and the source of publication.
Funding: None.
Competing interests: The authors declare no competing
interests.
Author details: Dr. Gour Gopal Satpati is working as Assistant
Professor in Department of Botany, Bangabasi Evening
College, University of Calcutta, Kolkata. Prof.
Ruma Pal is Professor of Department of Botany,
University of Calcutta, Kolkata. Both the authors are specialized in algal
taxonomy, systematics and bioenergy research.
Author contribution: Both GGS and RP conceived and designed the
study concept, while GGS implemented monitoring and data collection in the
field. GGS lead the writing of the manuscript with significant guidance and
contribution from RP.
Acknowledgements: The authors are thankful to the Centre for Research in
Nanoscience and Nanotechnology (CRNN), University of Calcutta for SEM facilities. We are grateful to Mr. Tridib
Das for SEM studies and Mrs. Mousumi Panda for
English editing of this manuscript respectively.
Abstract: Scanning electron microscopy (SEM) is the most modern
technique for plankton research. The
present paper deals with the taxonomy and morphology of some rare and
endangered planktonic chlorophytes in relation to scanning electron
microscopy. Water samples from the
distinct water body of the Sundarbans have been concentrated and examined by
scanning electron microscopy. A total of
45 species, of which 17 species of Scenedesmaceae, 10
species each of Hydrodictyaceae and Desmidiaceae, five species of Chlorococcaceae,
two species of Selenastraceae and only one species of
Chlorellaceae were recorded from the study site. Some species were recorded as new and rare
from the study area. About 18 species
including nine extremely rare, seven occasional, six frequent, four sporadic
and one abundant was recorded in the present study. A detailed taxonomic description with line
drawings is also included in the present communication.
Keywords:
Conservation, morphology, plankton, scanning electron microscopy, Sundarban, taxonomy, water samples.
Introduction
Planktonic chlorophytes play an important role in the
aquatic ecosystem. They act as the
primary producer of the aquatic food chain.
Several reports have emphasized the importance of small planktonic
chlorophytes in the aquatic habitat such as pond (Anand 1998), river, and sea (Vaulot et al. 2008).
They also function as the progenitor of higher plants because of their
photosynthetic pigments, starch as storage reserve food and chloroplast
morphology (Lewis & McCourt 2004).
They possess simple structural organization and reproduction. They also belong to unicellular and
multicellular form.
The planktonic flora of the Indian Sundarbans was
greatly diversified due to salinity gradient. Phytoplanktons
play an important role in protecting the mangrove vegetation of the
planet. In our earlier reports a few
micro- and macro-chlorophytes were found from different habitats of the Indian
Sundarbans (Satpati & Pal 2015, 2017). The habitats such as mud surface, tree bark,
pneumatophore surface, stone surface, forest floor, water surface, and stilt
root surface were surveyed for filamentous algae collection. A few reports were also available from other
parts of the Sundarbans (Prain 1903; Naskar & Santra 1986; Sanyal & Bal 1986; Maity et
al. 1987; Pal et al. 1988; Santra & Pal 1988; Santra et al. 1991; Mandal & Naskar
1994; Mukhopadhyay & Pal 2002).
Changes in atmospheric temperature and global warming remarkably affect
mangrove vegetation including micro- and macro-flora. The algal species are diminishing with changes
in temperature and increased salinity.
Micro- and pico-planktons are becoming rare and endangered and not
functioning as primary producer of the ecosystem.
The present study was undertaken in order to identify
some rare and endangered planktonic chlorophytes in different water bodies of
the Indian Sundarbans. All taxa were
documented on SEM and illustrations were also made for the same.
Material and methods
Study area
The Sundarbans is the largest tiger inhabiting
mangrove biosphere reserve in India and also a world heritage site designated
by UNESCO. It is the largest chunk of
mangrove ecosystem of the World encompassing many islands and rivers
interconnected with creeks and canals.
The deltaic appearance of the mangrove is formed by the confluence of
three rivers, Ganges, Brahmaputra and Meghna in the Bay of Bengal. The major part of the Sundarbans (60%) lies
in the Bangladesh and the remaining portion (40%) in India. The Hooghly River flows over India’s state of
West Bengal comprising mudflats, multiple tidal streams, open and closed
mangrove systems. The Indian part of the
Sundarbans is distinctive in terms of its vegetation, marine ecosystem and
salinity. Continuous inundation of
saline water into the fresh water ecosystem, greatly affect the floral
diversity. The study area lies between
21.516–22.883 0N and 88.616–89.150 0E of the southeastern part of Bay of Bengal (Image 1).
Sampling site
The sampling site varies from fresh water to brackish
water. A total number of 23 sites were
studied in detail. All the sampling stations belong to the 24 Parganas (South
and North) of the state of West Bengal, India.
The name of the sampling sites and their physico-chemical
parameters are given in Table 1.
Collection of samples
The phytoplanktons were
collected from aquatic habitats during tidal action and also from the brackish
water areas with the help of a truncated plankton net of 25μ mesh size. The samples thus collected were thoroughly
washed with running tap water or saline water and then with double distilled
water to remove soil particles and other debris. The sample material was then washed with
phosphate buffer saline (PBS) 2–3 times and centrifuged at 8000rpm (Satpati & Pal 2017).
Measurement of Physicochemical Parameters
Physicochemical parameters like air and surface water
temperature, pH, and salinity were recorded using digital thermometer (Eurolab ST9269B), pH meter (Eco testr)
and Refractometer (Erma, Japan).
Preparation of voucher specimens
Samples were preserved in 4% (v/v) formalin and stored
as voucher specimen in Calcutta University Herbarium (CUH) for further study.
Scanning Electron Microscopy (SEM)
One drop of washed material was put on a glass cover
slip (Blue Star) and dried at 20°C. The
samples were repeatedly washed with ethanol grade and dried at room
temperature. After complete dehydration
the cover slips were placed on carbon tape and put in Quorum (Q 150 TES) gold coater
to coat the samples with gold. The
scanning electron microscopic (SEM) images have been taken with Carl Zeiss EVO
18 (EDS 8100) microscope and Zeiss Inca Penta FETX 3 (Oxford instruments)
attachment. Photographs were taken in
different magnifications.
Camera Lucida drawing
The hand drawing was made under a compound microscope
with the help of a prism and 0.1- and 0.2- Rotring
isograph pen (Germany). The drawing was
done on transparent tracing paper (A4 size).
The cellular details of vegetative and reproductive parts of different
species were outlined and scale measurement was given under 10X, 40X and 100X
objectives with proper magnification.
The cell length and breadth was measured with ocular lens as ocular
division (O.D.) and standardized using stage micrometer.
Species identification
Identification of taxa was done using standard
research articles and monographs (Smith 1950; Randhawa 1959; Prescott 1982;
Anand 1998; Jaiswal & Tiwari 2003; Sen & Naskar
2003; Shukla et al. 2008; Bellinger & Sigee 2010;
Das & Adhikary 2012; Tripathi et al. 2012; van Geest & Coesel 2012; Baruah
et al. 2013; Keshri & Mallick 2013).
Results
Taxonomic descriptions
A total of 45 species were identified and
detailed descriptions of the species are enumerated below:
Family: Hydrodictyaceae
1. Pseudopediastrum boryanum
(Turpin) E. Hegewald (Image 2A-B and Figure 1A)
Synonym: Pediastrum
boryanum (Turpin) Meneghini
Basionym: Helierella boryana Turpin
[Prescott 1982; Day et al. 1995; Hu & Wei 2006;
Kim & Kim 2012].
Coenobium entire; cells 5–6 sided with smooth or
granular walls; peripheral cells with outer margins extended into two
blunt-tipped processes, cells up to 14μ in diameter and 21μ long; 36 celled
colony 85–90 μ wide. Cells are well
ornamented with pores and wavy margins.
Occurrence: aquatic; voucher number: CUH/Al/MW-171.
2. Pseudopediastrum boryanum
var. perforatum (Raciborski)
Nitardy (Image 2C and Figure 1B)
Basionym: P. boryanum subsp. perforatum Raciborski
[Cambra-Sánchez et al. 1998;
Kim & Kim 2012].
Coenobia are circular in outline and with well
perforations. Coenobia
composed of 4–32 cells. Incisions are
wide and V-shaped. Each cell extended to
two processes. Cell wall ultrastructure
is very distinctly granular having honey comb like appearance. Diameter of the coenobia
is 70–120 μ, cells 3–20 μ wide and 4–20 μ long.
Occurrence: aquatic; voucher number: CUH/Al/MW-172.
3. Stauridium tetras (Ehrenberg)
Hegewald var. apiculatum
(Fritsch) Keshri et Mallick comb. nov.
(Image 2E and Figure 1C)
Synonym: Pediastrum
tetras (Ehrenberg) Ralfs var. apiculatum Fritsch.
[Keshri & Mallick 2013].
Coenobia 4-celled, less rectangular with cells without
intercellular spaces; marginal cells divided into two lobes with deep linear to
cuneate incision on the outer side reaching the middle of the cell and are
trapezoidal in shape; each lobe further divided into two lobes terminating in
an apical nodular thickening; cells 5–15 μ in diameter and colony of four cells
up to 14–28 μ in diameter. Cell wall
ultrastructure varies being irregular net-like or warty.
Occurrence: aquatic; voucher number: CUH/Al/MW-199.
4. Pediastrum obtusum
Lucks (Image 2F and Figure 1D)
[Prescott 1982; Kim & Kim 2012].
Coenobia nearly entire, with minute interstices formed by the retuse margins; Coenobia oblong
to nearly star shaped. Coenobia 8–32 celled with deep narrow sinus forming two
major lobes, lobes incised to form bluntly rounded lobules. The sinus outwardly closed due to the contact
of two central lobules. The
ultrastructure of cell wall shows dotted appearance having minute pores.
Cells are 5–10 μ in diameter and 6–12 μ in
length. Coenobia
15–40 μ in diameter.
Occurrence: aquatic; voucher number: CUH/Al/MW-200.
5. Pediastrum duplex Meyen (Image 2G and Figure 1F)
Synonym: P. napoleonis
Ralfs; P. pertusum Kützing; P. duplex var. reticulatum
Lagerheim
[Bruhl & Biswas 1926;
Prescott 1982; Day et al. 1995; Buchheim et al. 2005;
Hu & Wei 2006; Kim & Kim 2012].
Coenobia 16-celled, arranged more or less compactly, semicircular in outline.
The outer margin is smooth, concave and extended into two blunt tapering
processes. Cells 10–15 μ in diameter and
coenobia are 40–80 μ in diameter. The ultrastructure of cell wall is smooth
with tiny pores.
Occurrence: aquatic; voucher number: CUH/Al/MW-201.
6. Pediastrum araneosum
(Raciborski) Raciborski (Image
2H and Figure 1G)
Synonym: P. angulosum
Ehrenberg ex Meneghini
[Prescott 1982; Day et al. 1995; John & Tsarenko 2002].
Coenobia entire with minute interstices. Central cells packed and peripheral cells
with two minute lobes; margin concave between two lobes. Cell wall smooth and with reticulate
ridges. The ultrastructure of cell wall
shows tiny pores. Cells are 8–12 μ in
diameter.
Occurrence: aquatic; voucher number: CUH/Al/MW-173.
7. Pediastrum integrum Nägeli (Image 2I and Figure 1E)
[Prescott 1982; McManus & Lewis 2005; Hu & Wei
2006; Tsarenko 2011; Kim & Kim 2012].
Coenobia 4, 8, 16 and 32 celled, without or little
perforations. Cell wall reticulates with tiny granules. Shapes of the inner cells are similar to the
peripheral cells. Outer margins of the
peripheral cells with two truncate short processes. The tip of the processes is unequal. Coenobia 14–18 μ in
diameter and cells are 4–8 μ in diameter.
Occurrence: aquatic; voucher number: CUH/Al/MW-174.
8. Parapediastrum biradiatum
(Meyen) E. Hegewald (Image
2J and Figure 1H)
Basionym: Pediastrum biradiatum Meyen
[Prescott 1982; Menezes 2010; McManus & Lewis
2011; Tsarenko 2011].
Coenobia perforated, 16-celled; peripheral cells deeply
bilobed, the lobes incised. Each cell is
bilobed two times. Coenobia 12–16 μ in diameter;
cells are 2–6 μ in diameter. The cell
wall is reticulate and tiny pores are present on it.
Occurrence: aquatic; voucher number: CUH/Al/MW-175.
9. Stauridium tetras (Ehrenberg) E. Hegewald (Image 2K and Figure 1I)
Synonym: Pediastrum
tetras (Ehrenberg) Ralfs; Helierella
renicarpa Turpin; Stauridium
bicuspidatum Corda
Basionym: Micrasterias
tetras Ehrenberg
[Bruhl & Biswas 1926;
Prescott 1982; Tsarenko 2011].
Coenobia oval or circular, 8-celled, marginal cells are deeply
incised and form two lobes, each lobes truncate, generally further divided into
two lobes and are trapezoidal in shape, inner cells 4–6 sided with a single
linear or cuneate incision; cells 5–8 μ in diameter, eight celled colonies
12–18 μ in diameter. The ultrastructure
of cells and coenobia shows presence of granules
throughout. The cell surface is well
wrinkled and folded.
Occurrence: aquatic; voucher number: CUH/Al/MW-81.
10. Pediastrum duplex (Meyen) var. duplex (Image 2L and Figure 1J)
[Prescott 1982; Anand 1998].
Coenobia circular, 40–70 μm in
diameter; 16-32-64 celled. The
peripheral cells are deeply incised to form V-shaped processes. The central and
peripheral cells are of different sizes.
The central cells are 5–8 μ in diameter and marginal cells are 8–12 μ in
diameter. The central cells joined with
each other and leave fine gaps within the coenobia. The ultrastructure of coenobia
shows fine sculpture and granules throughout the cell wall.
Occurrence: aquatic; voucher number: CUH/Al/MW-202.
11. Desmodesmus abundans
var. brevicauda G.M. Smith (Image 3A-B and
Figure 1K–L)
[Menezes 2010; Tsarenko
2011; Tsarenko & John 2011; Gopalakrishnan et al.
2014].
Coenobium composed of four cells, cells smaller with
relatively smaller spines. Cells are 2–4
μ in length and 1–2 μ in diameter.
Spines fewer, 1–3 μ long. The
ultrastructure of the cells shows smooth cell wall with slightly wavy margins.
Occurrence: aquatic; voucher number: CUH/Al/MW-187.
12. Desmodesmus bicaudatus
(Dedusenko) P.M. Tsarenko (Image
3C and Figure 1M)
Basionym: Scenedesmus bicaudatus (Dedusenko)
[Tsarenko 2011; Tsarenko & John 2011].
Coenobium 2–4 celled, with linear or slightly
alternate in arrangement, cells elongated, outer cells with a long curved spine
at alternate poles; inner cells without spines, oval to cylindrical. Cells are 8–12 μ in length and 4–8 μ in
width. The electron microscopic study
revealed folded sculptured wall outside the cell with fine pores.
Occurrence: aquatic; voucher number: CUH/Al/MW-186.
13. Desmodesmus serratus (Corda) S.S.
An, T. Friedl & E. Hegewald
(Image 3D and Figure 2B)
Synonym: Scenedesmus
serratus (Corda) Bohlin
Basionym: Arthrodesmus
serratus Corda
[Prescott 1982; Fawley et al. 2011; Tsarenko 2011; Tsarenko &
John 2011].
Coenobia composed of four ovate, oblong cells arranged in a
single series; the outer and inner cells with longitudinal teeth; apices of all
cells bearing 3–4 small teeth. Cells are
6-10 μ in length and 2–4 μ in width. The
electron microscopic study revealed presence of beads like structure throughout
the cell wall.
Occurrence: aquatic; voucher number: CUH/Al/MW-165.
14. Desmodesmus armatus (R. Chodat) E. Hegewald (Image 3E and
Figure 2D)
Synonym: Scenedesmus
armatus (Chodat) G.M.
Smith
Basionym: Scenedesmus hystrix var. armatus
R. Chodat
[Prescott 1982; Verschoor et al. 2004; Matusiak-Mikulin et al. 2006; Tsarenko
2011; Tsarenko & John 2011].
Coenobia composed of four cells and arranged in single
series. Cells are elongated, ellipsoid;
each cell with abundant uneven spines; each pole of the individual cell
contains 3–6 uneven spines; each cell contains a longitudinal ridge. Cells are 4–8 μ in length and 3–5 μ in width. The sculptured cell wall with folded margin
and granules are shown under scanning electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-166.
15. Scenedesmus quadricauda
(Turpin) de Brébisson (Image 3F and Figure 2A)
Basionym: Achnanthes quadricauda Turpin
[Bruhl & Biswas 1926; Prescott
1982; Day et al. 1995; Hu & Wei 2006].
Coenobia 2–4 celled, cylindrical, sometimes ellipsoid arranged
in a single series. Cells are 6–12 μ
long and 2–4 μ width; cells contain long spines at two opposite poles. Each cell contains a longitudinal ridge
covered by small teeth. Under electron
microscope the cell wall showed several granules and spines.
Occurrence: aquatic; voucher number: CUH/Al/MW-82.
16. Scenedesmus ellipticus Corda (Image 3G and Figure 2C)
Synonym: S. ecornis
var. flexuosus Lemmermann;
S. linearis Komárek
[John & Tsarenko 2002;
Verschoor et al. 2004; Tsarenko 2011; Tsarenko & John 2011].
Coenobia 2-celled, arranged in a single row, cells
cylindrical, bean shaped. Cells are 6–10
μ long and 2–4 μ width. Cell contains numerous small spines throughout the
body. Under electron microscope the cell
wall of each cell showed convoluted margins with numerous granules.
Occurrence: aquatic; voucher number: CUH/Al/MW-191.
17. Scenedesmus bijuga (Turpin) Lagerheim (Image 3H and Figure 2F)
Basionym: Achnanthes bijuga Turpin
[Prescott 1982; Cambra
Sánchez et al. 1998].
Coenobia composed of four cells; cells alternately arranged;
cells round to oblong to cylindrical, without teeth or spines; cells 2–6 μ in
diameter and 3–8 μ long. Electron
microscopic study revealed smooth cell wall with a few convoluted margins and
granules.
Occurrence: aquatic; voucher number: CUH/Al/MW-83.
18. Desmodesmus denticulatus
(Lagerheim) S.S. An, T. Friedl
& E. Hegewald (Image 3I and Figure 2E)
Basionym: Scenedesmus denticulatus Lagerheim
[Prescott 1982; Day et al. 1995; Hu & Wei 2006; Tsarenko 2011; Tsarenko &
John 2011].
Coenobia composed of 4 cells; cells alternately arranged in a
single series; cells are ellipsoid to cylindrical, 4–6 μ long and 1–3 μ width;
each cell with 1–4 small spines and teeth.
Under electron microscope the cells showed wavy margins on the cell wall
and a few apertures.
Occurrence: aquatic; voucher number: CUH/Al/MW-167.
19. Desmodesmus opoliensis
(P.G. Richter) E. Hegewald (Image 3J and Figure 2G)
Basionym: Scenedesmus opoliensis P.G. Richter
[Prescott 1982; Hu & Wei 2006; Menezes 2010; Tsarenko 2011; Tsarenko &
John 2011].
Coenobia composed of 2–4 celled arranged in a single series;
cells 2–6 μ long and 1.5–3 μ width; cells with long spines at the apices. Cell wall is granulated and slightly folded
as shown under electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-168.
20. Desmodesmus subspicatus
(Chodat) E. Hegewald &
A. Schmidt (Image 4A and Figure 2H)
Basionym: Scenedesmus subspicatus Chodat
[Verschoor et al. 2004; Tsarenko
2011; Tsarenko & John 2011; Hilt (nee Korner) et
al. 2012].
Coenobia 2-celled arranged in a single row; cells 6–8 μ in
length and 2–3 μ width; apices of the cells contain 2–4 small teeth or
spines. The cell surface showed numerous
small teeth and granules under scanning electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-169.
21. Desmodesmus brasiliensis (Bohlin) E. Hegewald
(Image 4B)
Basionym: Scenedesmus brasiliensis Bohlin
[Bruhl & Biswas 1926;
Prescott 1982; Menezes 2010; Tsarenko 2011; Tsarenko & John 2011].
Coenobia composed of four cells arranged in a single row;
cells 6–10 μ in length and 1–2 μ in width; apices of each cell with 1–4 small
teeth and with a longitudinal median ridge extending between the apices of each
cell. Median ridge of each cells are
surrounded by folded margins. The outer
two cells are covered with crown like structure shown under electron
microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-170.
22. Comasiella arcuata
var. platydisca (G.M. Smith) E. Hegewald & M. Wolf (Image 4C and Figure 2J)
Synonym: Tetrachlorella
nephrocellularis Komárek
Basionym: S. arcuatus var. platydiscus G.M. Smith
[Prescott 1982; Day et al. 1995; Menezes 2010].
Coenobia composed of eight cells arranged in a flat double
series; no intercellular spaces between the joining of cells; cells are 6–10 μ
long and 3–6 μ width. Numerous small
teeth and granules are found throughout the cell surface of each cell under
electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-196.
23. Scenedesmus acutiformis
Schröder (Image 4D and Figure 2K)
Synonym: Acutodesmus
acutiformis (Schröder) Tsarenko & D.M. John
[Prescott 1982; Day et al. 1995; Cambra
Sánchez et al. 1998; John & Tsarenko, 2002;
Verschoor et al. 2004; Hu & Wei 2006].
Coenobia of 2-celled arranged in a single row; cells 10–16 μ
long and 6-8 μ broad; each cell having 2–3 facial longitudinal ridges covered
by folded margins. The crown-like folded
cell wall with smooth surface was shown under scanning electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-192.
24. Acutodesmus acuminatus
(Lagerheim) Tsarenko (Image
4E and Figure 2I)
Synonym: Scenedesmus acuminatus (Lagerheim) Chodat
Basionym: Selenastrum acuminatum Lagerheim
[Bruhl & Biswas 1926;
Prescott 1982; Tsarenko 2011; Tsarenko
& John 2011].
Coenobia composed of two cells arranged in a curved series;
cells strongly lunate with sharply pointed apices; cells 12–20 μ long and 2–4 μ
width; the concave faces of the cells directed outward. The smooth cell wall is observed under
electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-195.
25. Scenedesmus magnus Meyen (Image 4F and Figure 3A)
Synonym: Desmodesmus
magnus (Meyen) Tsarenko;
Scenedesmus longus Meyen
[Prescott 1982; John & Tsarenko
2002].
Coenobia composed of four cells arranged in a single row;
cells cylindrical 2–6 μ long and 1–3 μ width; apices of both inner and outer
end of each cell with 1–2 sharp spines.
Cells are compactly arranged and contain a median ridge. The convoluted cell wall with tiny pores was
observed under electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-193.
26. Scenedesmus bijuga
var. alternans (Reinsch) Hansgirg
(Image 4G and Figure 3B)
[Prescott 1982; Caraus
2002].
Coenobia 2-celled arranged in a single row; cells oval 6–10 μ
long and 4–6 μ width. Under electron
microscope the ridges were shown well and cell wall covered with tiny pores.
Occurrence: aquatic; voucher number-:CUH/Al/MW-198.
27. Scenedesmus raciborskii
Woloszynska (Image 4H and Figure 3C)
Synonym: Acutodesmus
raciborskii (Woloszynska)
Tsarenko & D.M. John; Scenedesmus
incrassatulus var. mononae
G.M. Smith
[Prescott 1982; John & Tsarenko
2002; Tsarenko 2011].
Coenobia 2-celled arranged in a single row; cells elliptical
or spindle shaped 6–8 μ long and 2–4 μ width; the cells are swollen in the
middle and tapered at the two ends. Fine
ridges and folds were found on the cell wall under electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-194.
Family: Chlorellaceae
28. Chlorella vulgaris Beyerinck
[Beijerinck] (Image 5A)
Synonym: C. pyrenoidosa
var. duplex (Kützing) West; Pleurococcus beijerinckii
Artari
[Shihira & Krauss 1965;
Prescott 1982; Krientez et al. 2004; Rindi & Guiry 2004].
Unicellular, green, free floating planktonic, single
or aggregated form, cells small spherical, single prominent, cup shaped
parietal chloroplast, cells 4–8 μ in diameter.
Occurrence: aquatic; voucher number: CUH/Al/MW-80.
Family: Chlorococcaceae
29. Chlorococcum infusionum (Schrank) Meneghini (Image
4I-K)
Synonym: Cystococcus
humicola Nägeli; Lepra infusionum Schrank; Chlorococcum humicola (Nägeli) Rabenhorst
Basionym: Lepraria infusionum Schrank
[Smith 1950; Prescott 1982; Chrétiennot-Dinet
1990; John & Tsarenko 2011].
Free living, unicellular, green, cells are solitary or
sometimes in colonial form; striking variation in size shows between various
cells when the alga grows in an expanded stratum, young cells are thin walled
and spherical or somewhat compressed, old cells have thick walls that are often
irregular in outline, chloroplasts of young cells are parietal massive cups,
completely filling the cell except for a small hyaline region at one side, they
contain one pyrenoid, as a cell increases in size, the chloroplast usually
becomes diffuse and contains several pyrenoids, young cells are 50–125 μ in
diameter and mature cells are 120–210 μ in diameter. Under electron microscope several groves and
ridges were found on the cell surface.
Many tiny pores were also observed on the cell walls.
Occurrence: aquatic, endozoic; Voucher number:
CUH/Al/MW-190.
30. Tetraëdron caudatum
(Corda) Hansgirg (Image 5B and Figure 3D)
Synonym: Polyedrium
pentagonum Reinsch; Tetraëdron caudatum var.
punctatum Lagerheim
Basionym: Asteriscium caudatum Corda
[Hindák 1980; Prescott 1982;
Cambra Sánchez et al. 1998; Hu & Wei 2006; Tsarenko 2011; Tsarenko &
John 2011].
Cells flat, irregular, 5-sided, the angles rounded and
tipped with a short, sharp spine; the sides between the angles concave; margins
of the cells were narrowly and deeply incised; cells 6–12 μ in diameter. Granulated cell wall with honey comb like
pores were found under electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-176.
31. Tetraëdron minimum (A. Braun) Hansgirg (Image 5C-D and Figure 3E–G)
Synonym: T. platyisthmum
(W. Archer) G.S. West; T. quadratum (Reinsch) Hansgirg
Basionym: Polyedrium
minimum A. Braun
[Hindák 1980; Prescott 1982;
Andreyeva 1998; Hu & Wei 2006; Tsarenko & John 2011].
Cell flat, tetragonal, the angles rounded and without
spines and processes, sometimes very minute process were found on each angles;
cell margin concave; cells 8–16 μ in diameter.
Various apertures and undulating margins were observed under scanning
electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-177.
32. Tetraëdron trigonum (Nägeli) Hansgirg (Image 5E and
Figure 3H–I)
Basionym: Polyedrium trigonum Nägeli
[Prescott 1982; Day et al. 1995; Hu & Wei 2006].
Cell triangular, the angles narrower and tapering at
each corner, each angle was terminated to a small spine or processes, each arm
of the triangle is straight, margins convex; cells 12–20 μ in diameter. Smooth and wavy cell surface was observed
under electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-178.
33. Tetraëdron gracile
(Reinsch) Hansgirg (Image 5F and Figure 3J)
Synonym: T. trigonum
var. gracile (Reinsch) DeToni
Basionym: Polyedrium
gracile Reinsch
[Prescott 1982; Day et al. 1995; Hu & Wei 2006].
Cell triangular, the angles narrower and more curved
like starfish, the angles tapering and terminated to spines; cells 10–22 μ in
diameter; the arms of triangle are not straight and form V-shaped
structure. The electron micrograph showed
wrinkled margins and a triangular ridge on the cell surface.
Occurrence: aquatic; voucher number: CUH/Al/MW-179.
Family: Selenastraceae
34. Selenastrum gracile Reinsch (Image 5G-H and Figure 4A)
[Prescott 1982; Hindák 1988;
Day et al. 1995; John & Tsarenko 2002; Hu &
Wei 2006; Tsarenko 2011; Tsarenko
& John 2011; Das & Keshri 2012].
Cells are found in colonies; cells are sickle shaped
and in irregular arrangement; cells 2–8 μ in diameter; apices of the cells are
sharply pointed. Electron micrograph showed folded and wrinkled cell surface.
Occurrence: aquatic; voucher number: CUH/Al/MW-180.
35. Selenastrum bibraianum
Reinsch (Image 5I and Figure 4B)
Basionym: Kirchneriella bibraiana (Reinsch) E. G.
Williams; Ankistrodesmus bibraianus (Reinsch) Korshikov
[Prescott 1982; Hindák 1988;
Day et al. 1995; John & Tsarenko 2002; Hu &
Wei 2006; Tsarenko 2011; Tsarenko
& John 2011; Das & Keshri 2012].
Cells are found in colonies; cells lunate to sickle
shaped; the apices of the cells are not sharply pointed; cells 12–20 μ long and
2–6 μ width. Small teeth-like
projections on the cell surface were observed under scanning electron
microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-181.
Family: Desmidiaceae
36. Euastrum denticulatum
F. Gay (Image 6A and Figure 4C)
Synonym: E. denticulatum
var. granulatum West; E. amoenum
F. Gay
[Ruzicka 1981; Day et al.
1995; Kouwets 1999; Wei 2003; Martello 2004; Coesel & Meesters 2007; Brook
et al. 2011].
Cell solitary, green, longer than broad, small spine
like projections are found on the surface of the cells; sinus narrow and
linear; cells 18–26 μ long and 13–17 μ broad.
The convoluted cell surface with wrinkled margins was observed under
scanning electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-182.
37. Euastrum dubium Nägeli (Image 6B and Figure 4D)
Synonym: E. dubium
var. triquetrum Nägeli
[Ruzicka 1981; West &
West 1905; Kouwets 1999; Wei 2003; Hu & Wei 2006;
Coesel & Meesters 2007;
Brook et al. 2011].
Cell solitary, green, semi-cells trapezi-form,
basal angles broadly rounded, four very small spines like projections or
processes were shown at each corner of the cell; the margins were denticulate;
cells 18–22 μ long and 12–16 μ broad.
Ornamented cells with wavy margin were observed under scanning electron
microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-183.
38. Teilingia wallichii (D.L. Jacobsen) Bourrelly
(Image 6C and Figure 4H)
Basionym: Sphaerozosma wallichii J. Jacobsen
[Day et al. 1995; Kouwets
1999].
Colonies thread like attached by apices into long
filaments or cells attached by spherical apical processes; apical processes of
cells are very short; individual cells are ‘X’ shaped; cells 2–8 μ in
diameter. Under electron microscope,
smooth cell walls with minute processes were observed.
Occurrence: aquatic; voucher number: CUH/Al/MW-184.
39. Staurastrum pantanale K.R.S. Santos, C.F. da Silva Malone, C. Leite Sant’Anna & C.E. de
Matos Bicudo (Image 6D and Figure 4E)
[Santos et al. 2013].
Cells 3-radiate, 18–24 μ long, 8–12 μ broad with
processes of 8–10 μ long; isthmus 4–8 μ wide; median constriction deep; sinus
acute, angular; margins deeply crenate.
Cell wall provided with minute acute granules in concentric series on
the processes, observed under scanning electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-185.
40. Staurastrum johnsonii West & G.S. West (Image 6E and Figure 4F)
Synonym: S. leptocladum
L.N. Johnson
[Kouwets 1999; Coesel & Meesters 2013].
Cells 3-radiate, composed of two halves called
semi-cells; cells 20–24 μ long and 10–14 μ wide; the processes 10–16 μ long
with small spine like projections. Cell
wall with crenate margins and acute granules were studied under the scanning
electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-159.
41. Staurastrum simonyi var. semicirculare
Coesel (Image
6F and Figure 4K)
[Coesel & Meesters 2007; Coesel & Meesters 2013].
Cell triangular, 14–18 μ long and 8–12 μ wide; cell
wall smooth, small minute apertures were present throughout the surface,
observed under scanning electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-160.
42. Staurastrum oxyacanthum W. Archer (Image 6G and Figure 4G)
[Kouwets 1999; Coesel & Meesters 2007; Brook
et al. 2011; Coesel & Meesters
2013].
Cells 3-radiate, composed of two halves of semi-cells,
cells 30–44 μ long and 20–30 μ broad and isthmus 8–12 μ in diameter; the
processes are deeply incised, 20–30 μ long; cell margin dentate with spine like
projections; each spine is bifurcated to for two daughter spines. Several spines and wavy margins were observed
under electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-161.
43. Cosmarium dubium Borge (Image 6H and Figure 4I)
[Day et al. 1995].
Cell solitary, green, 30–50 μ long and 20–25 μ broad;
isthmus 8–10 μ; the connection between two semi-cells is smooth; the cell wall
is well ornamented with small rounded projections, observed under scanning
electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-162.
44. Cosmarium punctulatum Brébisson (Image 6I and Figure 4J)
Synonym: C. punctulatum
var. granulusculum (Roy & Bissett)
West & West
[West & West 1908; Day et al. 1995; Kouwets 1999; Hu & Wei 2006; Martello 2006; Brook et
al. 2011].
Cell solitary, green, 20-–26 μ long and 18–22 μ broad;
isthmus 4–8 μ; cells ‘dumble’ shaped. Cell wall rough, well ornamented with small
rounded processes observed under scanning electron microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-163.
45. Cosmarium reniforme (Ralfs) W.
Archer (Image 6J and Figure 4L)
Basionym: C. margaritiferum
var. reniforme Ralfs
[West &d West 1908; Day et al. 1995; Kouwets 1999; Hu & Wei 2006; Coesel
& Meesters 2007; Brook et al. 2011].
Cell solitary, green, 20–24 μ long and 12–16 μ broad;
isthmus 6–8 μ; cells ‘dumble’ shaped. Cell wall not so rough, well ornamented with
small rounded globular projections, observed under scanning electron
microscope.
Occurrence: aquatic; voucher number: CUH/Al/MW-164.
Discussion
The present investigation reveals that the Indian
Sundarbans exhibit rare green planktonic diversity. A few studies on planktonic
chlorophytes and diatoms were found in the Gangetic belt and Bhagirathi-Hooghly
estuary of the southern coast (Mukhopadhyay & Pal 2002; Chowdhury & Pal
2008). Mukhopadhyay & Pal (2002)
have reported nine species of chlorophytes and five species of rhodophytes from
the estuarine and coastal region of Bay of Bengal. A detailed systematic account of 19 genera
and 32 species of diatoms has been done so far from the coastal belt (Chowdhury
& Pal 2008). A new planktonic
diatom, Cocconeis gracilariensis
was investigated from the brackish water ecosystem of the Indian Sundarbans as
epiphytic on Gracilaria sp. (Satpati et al. 2017). Continuous inundation of marine water
in the freshwater ecosystem is the major problem for diminishing these
planktonic chlorophytes. A total number
of 46 taxa belonging to six groups have been reported from the Sundarban estuarine ecosystem (Manna et al. 2010). They have reported two green algal taxa Chlorella
and Dunaliella in association with
cyanobacteria and diatom assemblages.
The conservation of these planktonic chlorophytes is suggested to
protect the primary food chain of aquatic ecosystem. A few strains were maintained in the
laboratory in isolated condition with accession number. Planktonic Eugenophytes
were also reported and conserved from different brackish water habitats of the
Indian Sundarbans (Satpati & Pal 2017). A total of 41 species of euglenoids
were reported in our previous study (Satpati &
Pal 2017). Some work was available on
planktonic diatoms from the Sundarbans ecoregion (Choudhury & Bhadury 2014; Satpati et al.
2017). Most of the work was conducted in
the Bangladesh region of the Sundarbans mangrove (Aziz & Rahman 2011). Based on previous literature, Sarkar (2011)
has reported 166 species of phytoplanktons from
estuarine ecosystem and associated brackish water wetlands of the Indian
Sundarbans. Most of the work has been done
on cyanobacteria, diatoms and filamentous chlorophytes. In this study the present group highlighted
on rare green planktonic chlorophytes which were not reported in earlier
studies.
Riverine fresh water run-off and tidal influx of
marine water are two antagonistic hydrological processes resulting in dynamic
changes in phytoplanktons and their community
structure. The continuous anthropogenic
perturbations, nutrient overload, increasing human population density,
globalization and economic development causes vulnerability of phytoplanktons in estuarine ecosystems (Roshith
et al. 2018). Temporal succession of
phytoplankton assemblages of Sundarbans’ mangrove was reported in a tidal creek
system of the Sundarbans mangrove (Bhattacharjee et al. 2013). The phytoplankton assemblage depends on the
physicochemical parameters of water and nutrient availability. The tropical and sub-tropical coastal
ecosystems of the World serve as a great carbon sink due to the presence of
mangroves and phytoplanktons. The biogeochemistry of carbon regulated by
the key functions of genes present in the phytoplanktons
reveals to illustrate their diversity (Bhattacharjee et al. 2013). The availability of phytoplanktons
and mangroves helps to maintain the aquatic food chains of the coastal
environments. Roshith
et al. (2018) have reported the most updated information on the green phytoplanktons of Hooghly-Matla
estuary. They have reported about 44
species of green chlorophytes of which 32 belong to Chlorophyceae,
11 belong to Trebouxiophyceae and 1 to Prasinophyceae. The
Indian part is still less explored and more work is needed to investigate the
different areas of the Sundarbans. The
detailed morphological study of phytoplanktons is
lacking from the Indian Sundarbans to understand their role in primary
productivity.
Conservation Status
In the present study about 18 species including nine
extremely rare, seven occasional, six frequent, four sporadic and one abundant
were recorded. The most abundant species
in the mangrove ecosystem was Scenedesmus quadricauda. On
the basis of sampling, Stauridium tetras,
Pediastrum duplex var. duplex, Chlorella
vulgaris, and Chlorococcum infusionum were found to be sporadic (Table 2). The species recorded as frequent were Pediastrum duplex, Scenedesmus
ellipticus, Scenedesmus
bijuga, Scenedesmus acutiformis, Acutodesmus
acuminatus, and Selenastrum
gracile. The details about the
conservation status of the species including latitude and longitude are given
in Table 2.
Table 1. Name of the sampling station and their
physicochemical parameters.
|
Sampling station |
Physicochemical parameters |
|||
Air temperature (°C) |
Surface water temperature (°C) |
pH |
Salinity (ppt) |
||
1 |
Basanti |
30.8 |
31.2 |
8.2 |
1.2 |
2 |
Jaigopalpur |
31.3 |
31.7 |
7.8 |
1.5 |
3 |
Jharkhali |
29.7 |
30.2 |
8.7 |
4.9 |
4 |
Rajbari |
28.6 |
27.8 |
6.6 |
6.9 |
5 |
Malancha |
27.4 |
26.5 |
6.2 |
7.4 |
6 |
Minakha |
30.3 |
30.8 |
8.3 |
0.8 |
7 |
Canning |
29.4 |
29.7 |
9.4 |
7.8 |
8 |
Bhagabatpur |
27.6 |
28.2 |
9.6 |
3.4 |
9 |
Sandeshkhali |
28.8 |
28 |
9.4 |
8.7 |
10 |
Namkhana |
27.7 |
26.8 |
8.7 |
6.7 |
11 |
Fraserganj |
28.6 |
28 |
8.6 |
11.6 |
12 |
Patibunia Island |
27.6 |
27.4 |
9.8 |
12.3 |
13 |
Dabu |
26.5 |
26.3 |
9.2 |
18.4 |
14 |
Hamanbere Island |
27.5 |
26.8 |
9.6 |
12.5 |
15 |
Bakkhali |
26.5 |
26 |
8.6 |
11.2 |
16 |
Sushni Island |
30.5 |
31.7 |
8.4 |
22.1 |
17 |
Suryamoni Island |
27.8 |
27.3 |
6.8 |
12.5 |
18 |
Kala Jungle |
28.5 |
28.2 |
6.8 |
11.5 |
19 |
Morahero Island |
27.5 |
27.2 |
9.3 |
12.2 |
20 |
Narayanitala |
28.4 |
28.2 |
9.1 |
19.6 |
21 |
Cheramatla |
30.2 |
31.2 |
8.7 |
19.6 |
22 |
Jammudwip |
31.2 |
32 |
9.6 |
16.8 |
23 |
Aamarboni Island |
28.8 |
28 |
9.2 |
15.2 |
Table 2. Name of the identified taxa, their latitude-
longitude and conservation status.
|
Name of the taxa |
Latitude &
Longitude (N, E) |
Conservation status |
1 |
Pseudopediastrum boryanum |
21.893, 88.956 |
Rare |
2 |
Pseudopediastrum boryanum var. perforatum |
21.893, 88.956 |
Rare |
3 |
Stauridium tetras var. apiculatum |
22.328, 88.820 |
Rare |
4 |
Pediastrum obtusum |
22.328, 88.820 |
Occasional |
5 |
Pediastrum duplex |
22.328, 88.820 |
Frequent |
6 |
Pediastrum araneosum |
21.893, 88.956 |
Occasional |
7 |
Pediastrum integrum |
21.893, 88.956 |
Rare |
8 |
Parapediastrum biradiatum |
21.893, 88.956 |
Rare |
9 |
Stauridium tetras |
21.893, 88.956 |
Sporadic |
10 |
Pediastrum duplex var. duplex |
22.328, 88.820 |
Sporadic |
11 |
Desmodesmus abundans var. brevicauda |
22.328, 88.820 |
Rare |
12 |
Desmodesmus bicaudatus |
22.328, 88.820 |
Occasional |
13 |
Desmodesmus serratus |
22.246, 88.819 |
Extremely rare |
14 |
Desmodesmus armatus |
22.246, 88.819 |
Rare |
15 |
Scenedesmus quadricauda |
22.246, 88.819 |
Abundant |
16 |
Scenedesmus ellipticus |
22.327, 88.818 |
Frequent |
17 |
Scenedesmus bijuga |
22.246, 88.819 |
Frequent |
18 |
Desmodesmus denticulatus |
22.246, 88.819 |
Occasional |
19 |
Desmodesmus opoliensis |
22.246, 88.819 |
Extremely rare |
20 |
Desmodesmus subspicatus |
22.246, 88.819 |
Rare |
21 |
Desmodesmus brasiliensis |
22.246, 88.819 |
Rare |
22 |
Comasiella arcuata var. platydisca |
22.327, 88.818 |
Extremely rare |
23 |
Scenedesmus acutiformis |
22.327, 88.818 |
Frequent |
24 |
Acutodesmus acuminatus |
22.327, 88.818 |
Frequent |
25 |
Scenedesmus magnus |
22.327, 88.818 |
Rare |
26 |
Scenedesmus bijuga
var. alternans |
22.246, 88.819 |
Rare |
27 |
Scenedesmus raciborskii |
22.327, 88.818 |
Extremely rare |
28 |
Chlorella vulgaris |
22.328, 88.820 |
Sporadic |
29 |
Chlorococcum infusionum |
22.055, 88.731 |
Sporadic |
30 |
Tetraëdron caudatum |
22.055, 88.731 |
Occasional |
31 |
Tetraëdron minimum |
22.055, 88.731 |
Rare |
32 |
Tetraëdron trigonum |
22.055, 88.731 |
Rare |
33 |
Tetraëdron gracile |
22.055, 88.731 |
Occasional |
34 |
Selenastrum gracile |
22.055, 88.731 |
Frequent |
35 |
Selenastrum bibraianum |
22.055, 88.731 |
Occasional |
36 |
Euastrum denticulatum |
22.055, 88.731 |
Rare |
37 |
Euastrum dubium |
22.055, 88.731 |
Extremely rare |
38 |
Teilingia wallichii |
22.055, 88.731 |
Extremely rare |
39 |
Staurastrum pantanale |
22.055, 88.731 |
Extremely rare |
40 |
Staurastrum johnsonii |
22.246, 88.820 |
Rare |
41 |
Staurastrum simonyi
var. semicirculare |
22.246, 88.820 |
Extremely rare |
42 |
Staurastrum oxyacanthum |
22.246, 88.820 |
Extremely rare |
43 |
Cosmarium dubium |
22.246, 88.820 |
Rare |
44 |
Cosmarium punctulatum |
22.246, 88.820 |
Rare |
45 |
Cosmarium reniforme |
22.246, 88.820 |
Rare |
For
figures & images – click here
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