Table 1. Physico-chemical parameters of
P. quadridentatum bloom area in Cochin
Estuary
Parameters
Water Temperature (oC)
Salinity (psu)
Dissolved Oxygen (ml L-1)
Nitrate (μmol L-1)
Silicate (μmol L-1)
Phosphate (μmol L-1)
Chlorophyll a (mg m-3)
28
20
2.01
10.6
23.3
1.3
27.5
higher turbidity, lower planktonic species richness and discolouration of
water [7-9]. Even though P. quadridentatum has been reported from different
parts of the world, unil now there have
been no records of blooms or harmful
effects of this species in Indian waters.
The study reports the first bloom of P.
quadridentatum along the tropical waters of Cochin estuary (Southwest coast
of India).
Cochin backwater is a productive
estuarine system with a high plankton
diversity. It is highly influenced by the
monsoon run off and inputs from anthropogenic activities which results in
a dynamic change in the overall functioning of the system between seasons
[10,11]. In November 2018, a sudden
discolouration of water was observed
near the Marine Science Jetty (Lat.
09o5751N; Long. 76o1656 E) in
Cochin estuary (Fig.1). Phytoplankton
samples were collected from the bloom
area by filtering ~50 liters of surface
water through 20μm mesh bolting silk
and analysed using a Leica DM2000 microscope. Hydrobiological parameters
such as temperature, salinity and dissolved oxygen were measured immediately and dissolved nutrients (nitrate
and silicate) were estimated according
to standard protocols. Chlorophyll a
was measured spectrophotometrically using a Hitachi U-2900 UV/Visible
spectrophotometer following the ace
tone extraction method.
Microscopic examination of samples
collected from the bloom event revealed
that the discoloration was caused by
the dinoflagellate P. quadridentatum
(Fig. 2). The cells were solitary, small
in size and little longer than wide. The
cell was overall ovoid in shape and divided by a cingulum in the middle. The
12
epitheca was conical with pointed apex
and the hypotheca was round in shape
with four antapical spines, which varied in length. The cells included numerous chloroplasts which were small and
somewhat yellow-greenish in colour.
A number of P. quadridentatum cells
undergoing encystment were also observed (Fig. 2).
During the bloom event, the surface
chlorophyll a concentration was relatively high (27.5 mg m-3) and P. quadridentatum contributed more than 70%
of the overall phytoplankton population
with a cell density 6.2 x 104 cells L-1. As
well as P. quadridentatum, the dinoflagellate community included Noctiluca
scintillans, Tripos muelleri and Protoperidinium sp. Skeletonema costatum and
Nitzschia sigma were the dominant diatom species.
The P. quadridentatum bloom occurred when physical and chemical
conditions during the bloom revealed
the surface water temperature was
28oC, salinity 20 psu, and nitrate and
silicate concentrations were 10.6 μmol
L-1 and 23.3 μmol L-1 respectively. A low
dissolved oxygen concentration (2.01
mg L-1) was recorded during the bloom
event, but there were no reports of fish
mortalities from the bloom area.
This observation is the first bloom
report of P. quadridentatum along
Cochin estuary and further investigation on the bloom dynamics is required.
This information will be useful in planning for potential HAB events along
Cochin estuary.
References
1. Gárate-Lizárraga I & MS MuñetónGómez 2008. Acta Bot Mex 83: 3347
2. Alkawri A et al 2016. Plankton Benthos
Res 11: 75-78
3. Okolodkov Y et al 2016. Mar Pollut Bull
108: 289-296
4. Stein FRv 1883. In: VvW Engelmann
(eds), II Halfte: Die Naturgesichte der
Arthrodelen Flagellaten. Leipzig, pp
130
5. Abé TH 1927. In: Peridiniales. Rep
Tôhoku Imper Univer, 4th Ser Biol,
Sendai, Japan 2: 383438
6. Hansen G 1995. Phycologia 34: 166170
7. Al-Hashmi K et al 2013. J Fish Aquat Sci
8: 595606
8. Gárate-Lizárraga I & MS MuñetónGómez 2008. Acta Bot Mex 83: 3347
9. de Madariaga I et al 1989. Bot Mar 32:
159-165
10. Menon NN et al 2000. Hydrobiologia 4:
149-183
11. Qasim SZ 2003. Indian Estuaries 259 pp
Authors
Twinkle Sathish, Lathika Cicily Thomas &
Kunnatholickal B Padmakumar, Department
of Marine Biology, Microbiology & Biochemistry, School of Marine Sciences, Cochin University of Science and Technology (CUSAT),
Kochi-16, Kerala, India
Email corresponding author:
kbpadmakumar@gmail.com
Continued from page 10
been any reports of toxicity associated
with Mediterranean strains of A. taylorii
[5]. For these reasons, further studies will
be planned to better understand the potential risks associated with this microalga
and its co-occurrence with other phytoplankton species along the Ligurian coast.
Acknowledgements
We are grateful to the ARPAL colleagues
involved in the bathing water monitoring
program and to Susanna Alloisio (ETT
S.p.A., Genoa) for her support. This work
was funded by EU project @lgaWarning (EuroTransBio-Program ID: ETB2017-028).
References
1. Penna A 2002. Mar Ecol 23: 320-328
2. Basterretxea G et al 2005. Estuar Coast
Shelf Sci 62 (1-2): 1-12
3. ISPRA, Quaderni - Ricerca Marina n.
5/2012, ISBN 978-88-448-05586.
4. Katsuo et al 2007. Harmful Algae, 6(6),
790-798.
5. Satta et al 2010. Adv Ocean Limn 1(2):
259-269
Authors
Valentina Giussani, Fabrizia Colonna &
Rosella Bertolotto, Agenzia Regionale per
la Protezione dellAmbiente Ligure (ARPAL),
Genova, Italy
Monica Cangini, Centro Ricerche Marine,
Cesenatico (FC), Italy
Stefano Accoroni & Cecilia Totti, Dipartimento di Scienze della Vita e dellAmbiente,
Università Politecnica delle Marche, Ancona,
Italy
Mariachiara Chiantore, Department for
Earth, Environment and Life Sciences,
University of Genoa, Genoa, Italy
Silvia Casabianca & Antonella Penna,
Department of Biomolecular Sciences,
University of Urbino, Urbino, Italy
Email corresponding author:
valentina.giussani@arpal.liguria.it
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