Floral diversity in Chilka Lake, Orissa.  

Out of several wetlands in India, Chilka lake in the state of Orissa was designated as Ramsar site in 1991 as an internationally important of waterfowl habitat. Chilka Lake is the largest one and unique of its kind for its magnificent biological diversity, ecological complexity and sustainability.  This vast water body spreading over an area of 1100 sq. km harbours innumerable number of both floral and faunal components. It is a haven for migratory birds, having 159 species/subspecies (Dev, 1997). More than 800 species of animals are reported from this lake and its vicinity by Zoological Survey of India (Ghosh, 1995).  About 225 species of fish have been reported from this lake (Dean & Saaltink, 1991).  On the banks of the lake there are 8 fairly large towns and 122 villages. About 70% of this population depend upon fishing as the only means of livelihood. A population of about 1,27,000 souls are directly dependent on fisheries in the lake and 50,000 cattles may get their fodder need from the margin and bank of the lake (Trisal and Chauhan, 1998).  A revenue of over 70 million rupees, is collected from 24 revenue villages on its banks (Bandyopadhay & Gopal, 1991).  Besides these, the lake attracts several national and international tourists for its pristine beauty and charming environment.  On an average 2.5 lakh tourists visit this lake annually.

Though much information regarding the common ecological and environmental status of the lake exist, still there is a gap in the baseline data on the total plant resources. Little is known of their taxonomy, quantitative ecological status and the mechanism by which they differ in their distributional patterns, their importance in the food chain of different fishes and birds as well as their effective role in protecting soil erosion and purifying the water quality. Not only information on ecological amplitude of algae/phytoplankton and seagrasses, or of aquatic macrophytes but also of the terrestrial plant communities living in the stressed environment of the islands and the shores and their role in this ecosystem are wanting. The detailed survey and studies on the plant resources of the islands and the lake surrounding, it is hoped, will give very important informations on the present status and monitoring the changes, if any, over time. These informations are required for proper planning of management towards sustainability of the ecosystem as a whole. Bandhyapadhya & Gopal (1991) suggested, “The biological and ecological diversity of this unique lagoon ecosystem need an in-depth study.

 

Vegetation  & flora:

The vegetation of the lake ecosystem is broadly classified into aquatic and terrestrial Island vegetation.  The aquatic vegetation is of algal vegetation and macrophytic vegetation.  Phytoplankton and seaweed community is under the algal vegetation.  Phytoplankton is abundant in all over the lake showing their seasonal fluctuation of species component.  Seaweed community is distributed only in brackish and marine water zones.  Aquatic macrophytes are of the Pleustophyte, Epihydate, Vittate, Rosette and Helophytic types. The terrestrial island vegetation is the formation of typical coastal scrubs.

12 seaweeds species are reported from this lake.  72 wetland plants including seagrass species are also collected/reported.  Among the terrestrial vascular plants 305 species are collected/reported.  Pteridophyte, Dicot and Monocot species are respectively 9, 288 and 80 that are reported from this lake.

A total number of 72 genera of phytoplankton and 8 genera of seaweeds have been collected from different sectors of the lake at different seasons. This large-scale diversity has a key role in the food chain of this lake ecosystem. Among the phytoplankton the number of genera under Myxophyceae, Chlorophyceae, Xanthophyceae, Bacillariophyceae and Dinophyceae are 12, 20, 1, 35, 3 respectively. The abundance of phytoplankton genera in the polluted water of the lake has also been studied.

A total number of 12 species of seaweeds under Chlorophyceae and Rhodophyceae are only distributed in marine and brackish water zone.

 

Table – 1: Seasonal and sectorial variation of the number of different phytoplankton groups.

NUMBER OF GENERA

SEASON

SECTOR

 

NORTHERN

CENTRAL

SOUTHERN

OUTER CHANNEL

MY

CH

XA

BA

DI

MY

CH

XA

BA

DI

MY

CH

XA

BA

DI

MY

CH

XA

BA

DI

SUMMER

 

5

3

-

4

-

6

1

-

3

-

5

4

-

21

-

4

9

-

18

2

MONSOON

 

3

4

-

3

-

9

4

-

15

2

3

3

-

13

2

1

2

-

13

3

POST

MONSOON

6

8

-

12

-

7

11

1

13

-

4

3

-

11

-

4

6

-

24

1

WINTER

 

4

1

-

3

-

2

2

-

3

-

3

1

-

6

-

2

-

-

9

-

 

 

 

 

 

 

 

 

 

MY-MYXOPHYCEAE; CH-CHLOROPHYCEAE; XA-XANTHOPHYCEAE; BA-BACILLARIOPHYCEAE; DI-DINOPHYCEAE.

 

Table – 2: Number of genera/genus belonging to different Class associated with different

        Vittate Macrophytes/ Seagrass/ Seaweeds of the lake.

 

No. of Phytoplankton Genera

Macrophytes

 

Myxophyceae

Chlorophyceae

Bacillariophyceae

Dinophyceae

Total

Potamogeton pectinatus

5

6

8

1

20

Najas indica

7

4

6

-

17

Halophila sp.

2

1

5

-

8

Hydrilla verticillata

4

4

11

-

19

Ceratophyllum demersum

4

4

5

-

13

Ruppia maritima

-

1

8

-

8

Enteromorpha intestinalis

3

3

7

-

14

 Distribution of seaweeds varies depending on several factors like season, tidal amplitude, salinity, availability or quality of substrate, etc. 

Table – 3: Distribution of the Seaweeds in the Lake.

CLASS

SEAWEEDS

DISTRIBUTION

 

CHLOROPHYCEAE

Chaetomorpha media

Ramb, P.C., SO, Nal..

Cladophora glomerata

Sat, SO, B.F, P.C..

Enteromorpha intestinalis

Balu, Nal, G.P., Satp, Ramb., P.C., SO, BF., HO., Bird..

PHAEOPHYCEAE

Rosenvingea intricate

Ari., Sat..

 
 
 
 
 
 
RHODOPHYCEAE
Ceramium elegans
Balu, Jat., G.P., Satp, Ramb., SO, BF., HO., Bird.

Gracillaria lichenoides

Balu, Jat., G.P., Satp, Ramb., N.P.,  SO, BF., HO., Bird..

Gracillaria verucosa

Balu, Jat., G.P., Satp, Ramb., N.P., SO, BF., HO. Bird..

Gracillaria confervoides

Nal., Ram., G.P., Sat..

Grateloupia filicina

Balu, Jat., G.P., Satp, Ramb., N.P.,  SO, BF., HO., Bird..

Polysiphonia subtilissima

Balu, Jat., G.P., Satp, Ramb., SO, BF., HO., Bird..

Polysiphonia sertularioides

Balu, Jat., G.P., Satp, Ramb.,S O, BF., HO., Bird..

CHAROPHYCEAE

Chara brachipus

Near Gopekuda Is.

 [Balu = BALUGAON; Nal = NALBAN; Ramb = RAMBHA; So = SOMOLO ISLAND; Bird = BIRD'S ISLAND; Satp = SATPARA; Ari = ARIKUDA; P.C.: PALUR CANAL; B.F.: BREAKFAST ISLAND; G.P.: GARH KRISHNA PRASAD; HO.: HONEYMOON ISLAND; Jat.: JATIA ISLAND; N.P.: NUAPARA]

 Table – 4: Distribution and association of seagrasses with seaweeds and other angiosperms. 

Site

Seagrass

Associates

 

 

Sea weeds

Other angiosperms

Nalban

Halophila ovalis ssp. Ovalis

Halophila ovalis ssp. Ramamurtiana

Halophila beccarii

Ruppia maritima

Enteromorpha intestinalis

Polysiphonia sertullarioides

Gracillaria lichenoides

Potamogeton pectinatus

Rambha

Halophila ovalis ssp. Ovalis

Halophila ovalis ssp. Ramamurtiana

Halophila minor

Halophila beccarii

Enteromorpha intestinalis

Ceramium elegans

Polysiphonia subtilissima

Gracillaria lichenoides

Najas indica

Najas graminea

Potamogeton pectinatus

Somolo

Halophila ovalis ssp. Ramamurtiana

Halophila beccarii

Halophila minor

Ruppia maritima

Enteromorpha intestinalis

Ceramium elegans

Gracillaria verucosa

Gracillaria lichenoides

Potamogeton pectinatus

Palur Canal

Halophila ovalis ssp. Ovalis

Halophila ovalis ssp. Ramamurtiana

Halophila beccarii

Halophila minor

Ruppia maritima

Enteromorpha  intestinalis

Ceramium elegans

Gracillaria lichenoides

Polysiphonia subtilissima

 

Khola Muha

Halophila ovalis ssp. Ovalis

Halophila ovalis ssp. Ramamurtiana

Halophila beccarii

Halophila minor

Ruppia maritima

Enteromorpha intestinalis

Ceramium elegans

Gracillaria lichenoides

Cladophora glomerata

Chetomorpha media

Polysiphonia subtilissima

Potamogeton pectinatus

Satpara

Halophila ovalis ssp. Ovalis

Halophila ovalis ssp. Ramamurtiana

Halophila beccarii

Ruppia maritima

Enteromorpha intestinalis

Ceramium elegans

Gracillaria lichenoides

 

Najas indica

Najas graminea

Potamogeton pectinatus

 Table – 5: Number of species in different growth forms of Aquatic Macrophytes 

Number of  Species

 

Vittate

 

Pleustophyte

 

Epihydate

 

Hyperhydate

 

Rosulate

 

Helophyte

 

9

 

12

 

6

 

6

 

1

 

33

 Table – 6: Macrophytic concentration in the different sectors of the lake:                

Growth form

Northern Sector

Central Sector

Southern Sector

Outer Channel Sector

Vittate

Hydrilla verticillata, Ceratophyllum demersum, Najas graminea, Najas indica

Potamogeton pectinatus, Najas graminea, Najas indica,

 

Potamogeton pectinatus, Najas graminea, Najas indica.

Potamogeton  pectinatus, Potamegeton crispus, Najas indica.

Pleustophyte

Eichornia crassipes, Azolla pinnata sub sp. asiatica, Salvinia nataus, Salvinia cuculata, Pistia stratiotes, Lemna  perpusila Spirodella polyrhiza, Ludwigia adscendens, Ipomoea aquatica, Hygrorhiza aristata, Neptunia olerasia, Utricularia aurea

                Nil.

 

 

 

 

 

 

Nymphoides hydrophylla.

 

 

Nymphoiedes hydrophylla, Potamogeton nodosus, Potamogeton perfoliatus, Potamgeton lucens.

 

Ephydate

Potamogeton nodosus, Nymphaea pubescens, Nymphaea rubra, Nymphaea  nauchali, Nymphoides indica,  Nymphoides hydrophylla, Pasplum vaginatum

 

 

 

Hyperhydate

Arundo donax, Pragmites karka, Typha angustifolia, Monochoria vaginalis,  Schoenoplectus  maritimus, Elaeocharis urticularis

Phragmites karka, Arundo donax, Schoenoplectus maritimus

Arundo donax, Phragmites karka, Schoenoplectus maritimus.

 

Schoenoplectus maritimus

 

Rosulate

Valisnaria spiralis

 

 

 

Helophyte

Bacopa monniera, Alternanthera philexeroides, Alternanthera paranychoides, Commelina suffruticosa, Commelina diffusa, Hygrophylla auriculata, Eragrostis nutans, Paspalum distichum, Paspalidium punctatum, Dentella repens, Mecardonia procumbens, Phylla nodiflora, Marsilea minuta, Persicaria orientale, Persicaria barbata

Salichornia brachiata, Suaeda maritima, Sesuvium portulacustrum, Heliotropium curassivicum (salt marsh), Alloteropsis cimicina, Chenopodium album, Cynodon dactylon, Paspalum vaginatum, Panicum psilopodium, Saccharum spontaneum.

Sesuvium portulacustrum (salt marsh) Commelina suffruticosa,  Murdania spirata, Cyperus rotundus, Ludwigia perennis,  Hemathria  compressa,  Bocopa  monniera, Lindernia ciliata, Lindernia crustacea, Lipia javanica, Phyla nodiflora

Panicum palludosum, Panicum repens, Bocopa monnieri.

 Table – 7: Seasonal variation of Aquatic Macrophytes/Seagrasses in Nalban Island. 

Seasons

Aquatic macrophytes/ seagrass

Summer

Potamogeton pectinatus, Halophila ovalis sub sp. ovalis, Halophila ovalis sub sp. ramamurtiana, Halophila minor,  Halophila beccarii, Panicum  psilopodium, Cyperus rotundus, Schoenoplectus maritimus, Arundo donax, Cressa cretica, Haliotropium curassivicum, Salichonia brachiata, Sesuvium portulacustrum, Sporobolus tremulus, Cynodon dactylon, Fimbristylis cymosa.

Monsoon

Potamogeton pectinatus, Najas graminea, Najas indica, Schoenoplectus maritimus, Arundo donax, Paspalum  vaginatum.

Post Monsoon

Potamogeton pectinatus, Najas indica, Najas graminea, Schoenoplectus maritimus, Cyperus rotundus, Paspalum vaginatum, Chenopodium album, Arundo donax.

Winter

Potamogeton pectinatus, Paspalum vaginatum, Schoenoplectus maritimus, Arundo donax, Cyperus rotundus, Salichornia brachiata, Sesuvium portulacustrum, Suaeda maritima, Heliotropium curassivicum.

   Table – 8: Vegetation type, its nature and distribution in Chilka Lake.

Vegetation type

Nature of the type

Sector

Halophila pure strand

Halophila –Ruppia mixed strand    

Najas-Potamogeton pectinatus mixed strand

Potamogeton  pectinatus pure strand

Vallisneria – Hydrilla mixed strand

Ceratophyllum pure strand

Nymphaea – Nymphoides pure strand

Nymphoides pure strand

Azolla pure strand

Pistia – Eichornia mixed strand

Schoenoplectus-Phragmites mixed strand

Schoenoplectus pure strand

Phragmitis pure strand

Vallisneria-Hydrilla-Nymphaea-Nymphoides  mixed strand

Ipomoea – Nymphoides mixed strand

Submerged

Submerged

Submerged

Submerged

Submerged

Submerged

Floating                

Floating

Floating

Floating

Emergent

Emergent

Emergent

Submerged-Floating

Submerged-Floating

S.S., C.S.

S.S., C.S.

C.S., S.S.

C.S. S.S.

N.S.

N.S.

N.S.

O.S.

N.S.

N.S.

N.S.

N.S.,C.S., S.S.

N.S.

N.S.

N.S

C.S. - Central Sector; N.S. - Northern Sector; S.S. - Southern Sector; O.C.S. -Outer Channel Sector 

Table - 9: Number of economically important plant resources. 

 

 

Vegetable

 

 

Fodder

Paper, Pulp, Fibre and Thatching materials

 
 
Medicine

 

 

Fish Food

 

 

Bird’s Food & Nest

No. of Genera

No. of Sp.

No. of Genera

No. of Sp.

No. of Genera

No. of Sp.

No. of Genera

No. of Sp.

No. of Genera

No. of Sp.

No. of Genera

No. of Sp.

8

10

14

15

6

6

162

185

9

12

37

56

 The landmass of this lake is classified into mainly three categories - viz. 1. Island 2. Shoreline or spit 3. Adjoining areas or bank sites.

Islands: According to different topographic pattern the islands can be divided into four major types on the basis of major edaphic conditions such as. i. Rocky islands, ii. Sand mixed rocky islands, iii. Sand-clay mixed rocky island and iv. Sandy islands. 

Table - 10: Vascular plant diversity of the lake Chilka. 

GROUPS
NUMBER

 

Family

Genus

Species

Sub Species

Variety

Wetland Plants

Climber

DICOTYLEDONS

72

212

284

4

7

25

53

MONOCOTYLEDONS

16

56

81

2

-

42

4

PTERIDOPHYTES

8

8

9

1

-

5

1

SEAWEEDS

8

9

12

-

-

12

-

TOTAL

104

285

386

7

7

84

58

 

Table - 11: Threatened Flora of Lake Chilka:

NAME OF THE SPECIES

STATUS

CAUSE

Cassipourea ceylanica (Gardn.) Alston

Rare

The population of the species has been reduced to countable number

Gloriosa superba L.

Rare

Increasing demand for isolation colchisin.

 Rauvolfia serpentina (L.) Benth. ex Kurz. 

 Rare 

 Overexploitation of roots 

 Capparis roxburghii DC. 

 Rare 

 The population of the species is very reduced.

Commiphora wightii (Arn.) Bhandari 

 Threatened 

 Overexploitation for fuel wood.

Cissus vitiginea L. 

Threatened 

Only restricted in one island and exploited vigorously for fuel.

 Eulophia epidendrea (Retz.) Fischer  

 Threatened

 

 Only single plant observed in the whole area

Sarcostema acidum (Roxb.) Voight 

 Threatened 

 It’s rapid destruction mainly during Commiphora wightii as it is closely associated to it.

 Aegiceras corniculatum (L.) Blanco

 Threatened

 Only a few plants are noted on two islands mainly due to unsuitable condition for multiplication

Aristolochia indica L. 

Threatened 

Overexploitation for medicine 

Halophila beccarii Asch. 

Threatened 

Habitat change mainly for extensive prawn culture and fish catch.

Halophila minor (Zoll. ex Miq.) Hartog

 Threatened  

 Habitat change mainly for extensive prawn culture and fish catch. 

Halophila ovalis (R. Br.) Hook. f.

Threatened

Habitat change mainly for extensive prawn culture and fish catch.

Halophila ovalis (R.Br.) Hook. f. sub sp. ramamurtiana Ravikumar & Ganesan

Threatened

Habitat change mainly for extensive prawn culture and fish catch. 

Ruppia maritima L.

Threatened

Habitat change mainly for extensive prawn culture and fish catch.

Macrotyloma ciliatum (Klein ex Willd.) Verde.

Threatened

Only a few plants are growing on lake bank. Overgrazing caused its thin population.

 Pisonea aculiata L.

 Threatened 

 Population is very thin due to clean up of the scrub jungles. 

Colubrina asiatica (L.) Brogn.  

Threatened 

 

Population is very thin due to clean up of the scrub jungles. 

Chara brachipus Braun 

 

Threatened 

 

Restricted only in one region, can not spread for wave action. 

Rosenvingea intricata (J. Ag.) Boergs  

Threatened

Population of the species has been reduced to countable number.

 

 

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