An account of Faviid Corals of Andaman and Nicobar Islands, India

 

Tamal Mondal1, C. Raghunathan1 and K. Venkataraman2

Zoological Survey of India, Andaman and Nicobar Regional Centre, National Coral Reef Research Institute, Haddo, Port Blair-744 102, Andaman and Nicobar Islands, India

Zoological Survey of India, Prani Vigyan Bhawan, M- Block, New Alipore, Kolkata-700 053, India

 

ABSTRACT:

On global record the family faviidae is the 2nd largest under the order scleractinia. A total of 88 species of faviids were recorded from entire Andaman and Nicobar Islands, of which a maximum of 85 species (H’: 5.96) at South Andaman, whereas the minimum was recorded from Nicobar with 49 species (H’:5.13). Though the variation in species composition, diversity, density and evenness varied between study areas, the results showed significance on the health status of the recorded species under the family faviidae.

 

KEYWORDS: Faviidae, diversity, Andaman and Nicobar

 

INTRODUCTION:

Coral reef ecosystem of Andaman and Nicobar Islands is ecologically important as it harbours more than 60% of the coral species reported world-wide. Faviidae is one of the most important families of hermatypic coral among 18 families of scleractinians [1]. It is the biggest in terms of number of genera, and ranks next to the Acroporidae in species composition and overall abundance in most reef biotopes throughout the Indo-Pacific. Owing to their abundance, the Faviidae have always made up a large part of all taxonomical importance in coral reefs [2]. As most of the species under this family are boulder-like, massive or sub-massive in structural attributes, it shows a great deal of participation towards the shoreline protection measures along with its ecological, ethological, economical etc. importance. This paper deals with the variation and variability in density, diversity, distribution and similarities or dis-similarities of species composition of faviids at three regions.

 

MATERIAL AND METHODS:

Underwater surveys on to quantify the faviids were carried out at 161 sites of Andaman and Nicobar groups of islands by employing Self-Contained Underwater Breathing Apparatus (SCUBA) diving, snorkeling during the period of July, 2009 to January, 2012. Each site was surveyed primarily using “Manta tow” study method [3,4]. A series of 20 m transects were placed at random sampling method to continue Line Intercept Transect Method [5]. As well as Quadrate methods [6] was also applied to investigate the diversity of the scleractinian corals of the surveyed areas. Each quadrate was photographed with a housed digital camera (Sony - Cyber shot, Model-T900, marine pack, 12.1 megapixels) oriented toward the start of transect. Wherever possible, the entire quadrate was photographed in a single image.

Occurrence of coral species in each quadrate was recorded. Corals were photographed within each quadrate when first encounteredv In some cases, corals not recorded inside quadrates were photographed to document their presence in the study area. Species individual photo quadrates were identified in conjunction with Veron et al. [2], Veron [1] and labeled according to the sites.


 

Table-1 Checklist of Scleractinian Corals under the family Faviidae

Sl. No.

Scientific Name

North and Middle Andaman

South Andaman

Nicobar

 

Genus Caulastrea Dana, 1846

 

 

 

1

Caulastrea furcata Dana, 1846

+

+

-

2

Caulastrea echinulata (MED and H, 1849)

-

+

-

 

Genus Favia Oken, 1815

 

 

 

3

Favia helianthoides Wells, 1954

+

+

+

4

Favia speciosa Dana, 1846

+

+

+

5

Favia pallida (Dana, 1846)

+

+

+

6

Favia truncatus Veron, 2000

+

+

+

7

Favia lizardensis Veron and Pichon, 1977

+

+

+

8

Favia danae Verrill, 1872

+

+

+

9

Favia maritima (Nemenzo, 1971)

+

+

-

10

Favia favus (Forskal, 1775)

+

+

-

11

Favia laxa (Klunzinger, 1879)

+

+

+

12

Favia rotundata  (Veron, Pichon and Wijsman-Best, 1977)

+

+

+

13

Favia rotumana (Gardiner, 1899)

+

+

+

14

Favia matthaii Vaughan, 1918

+

+

+

15

Favia albidus Veron, 2000

+

+

+

16

Favia stelligera (Dana, 1846)

+

+

+

17

Favia lacuna Veron, Turak and De Vantier, 2000

-

+

-

18

Favia maxima Veron, pichon and Wijsman-Best, 1977

+

+

-

19

Favia veroni Moll and Best, 1984

+

+

+

20

Favia leptophylla Verrill, 1868

-

+

-

 

Genus Barabattoia Yabe and Sugiyama, 1941

 

 

 

21

Barabattoia amicorum (Milne Edwards and Haime, 1848)

+

+

-

22

Barabattoia laddi (Wells, 1954)

+

+

-

 

Genus Favites Link, 1807

 

 

 

23

Favites bestae Veron, 2000

+

+

-

24

Favites pentagona (Esper, 1794)

+

+

+

25

Favites micropentagona Veron, 2000

+

+

+

26

Favites chinensis (Verrill, 1866)

+

+

-

27

Favites complanata (Hemprich and Ehrenberg, 1834)

+

+

+

28

Favites abdita (Ellis and Solander, 1786)

+

+

+

29

Favites halicora (Hemprich and Ehrenberg, 1834)

+

+

+

30

Favites flexuosa (Dana, 1846)

+

+

-

31

Favites vasta (Klunzinger, 1879)

+

+

-

32

Favites paraflexuosa veron, 2000

+

+

+

33

Favites russelli (Wells, 1954)

+

+

+

34

Favites acuticollis (Ortmann, 1889)

+

+

-

35

Favites spinosa (Klunzinger, 1879)

-

+

+

 

Genus Goniastrea Milne Edwards and Haime, 1848

 

 

 

36

Goniastrea retiformis (Lamarck, 1816)

+

+

+

37

Goniastrea edwardsi Chevalier, 1971

+

+

+

38

Goniastrea aspera Verrill, 1865

+

+

-

39

Goniastrea minuta Veron, 2000

+

+

-

40

Goniastrea pectinata (Hemprich and Ehrenberg, 1834)

+

+

-

41

Goniastrea australensis (Milne Edwards and Haime, 1857)

+

+

-

42

Goniastrea favulus (Dana, 1846)

+

+

-

43

Goniastrea peresi (Faure and Pichon, 1978)

+

+

-

44

Goniastrea palauensis (Yabe and Sugiyama, 1936)

-

-

+

 

Genus Platygyra Ehrenberg, 1834

 

 

 

45

Platygyra lamellina (Hemprich and Ehrenberg, 1834)

+

+

+

46

Platygyra daedalea (Ellis and Solander, 1786)

+

+

+

47

Platygyra crosslandi (matthai, 1928)

+

+

+

48

Platygyra verweyi Wijsman-Best, 1976

+

+

+

49

Platygyra carnosus Veron, 2000

+

+

-

50

Platygyra pini Chevalier, 1975

+

+

+

51

Platygyra ryukyuensis Yabe and Sugiyama, 1936

+

+

+

52

Platygyra sinensis  (Milne Edwards and Haime, 1849)

+

+

+

53

Platygyra acuta Veron, 2000

+

+

+

 

Genus Oulophyllia Edwards and Haime, 1848

 

 

 

54

Oulophyllia bennettae (Veron, Pichon and Wijsman-Best, 1977)

+

+

-

55

Oulophyllia levis (Nemenzo, 1959)

+

+

-

56

Oulophyllia crispa (Lamarck, 1816)

+

+

-

 

Genus Leptoria Milne Edwards and Haime, 1848

 

 

 

57

Leptoria phrygia (Ellis and Solander, 1786)

+

+

+

58

Leptoria irregularis Veron, 1990

+

+

+

 

Genus  Diploria Milne Edwards and Haime, 1848

 

 

 

59

Diploria strigosa (Dana, 1848)

-

+

-

 

Genus Colpophyllia Milne Edwards and Haime, 1848

 

 

 

60

Colpophyllia natans (Houttuyn, 1772)

-

+

-

 

Genus Montastrea de Blainville, 1830

 

 

 

61

Montastrea  curta (Dana, 1846)

+

+

-

62

Montastrea  salebrosa (Nemenzo, 1959)

+

+

-

63

Montastrea  annularis (Ellis and Solander, 1786)

+

+

-

64

Montastrea  valenciennesi (Milne Edwards and Haime, 1849)

+

+

-

65

Montastrea  colemani Veron, 2000

-

+

-

66

Montastrea annuligera (Milne Edwards and Haime, 1850)

+

+

-

67

Montastrea  cavernosa (Linnaeus, 1767)

+

+

+

 

Genus Plesiastrea Milne Edwards and Haime, 1848

 

 

 

68

Plesiastrea veripora (Lamarck, 1816)

+

+

+

 

Genus Oulastrea Milne Edwards and Haime, 1848

 

 

 

69

Oulastrea crispata (Lamarck, 1816)

+

+

+

 

Genus Diploastrea Matthai, 1914

 

 

 

70

Diploastrea helipora (Lamarck, 1816)

+

+

+

 

Genus Leptastrea Milne Edwards and Haime, 1848

 

 

 

71

Leptastrea  purpurea (Dana, 1848)

+

+

+

72

Leptastrea  transversa Klunzinger, 1879

+

+

+

73

Leptastrea bottae (Milne Edwards and Haine, 1849)

+

+

+

74

Leptastrea aequalis Veron, 2000

+

+

-

75

Leptastrea  pruinosa Crossland, 1952

+

+

-

 

Genus Cyphastrea Milne Edwards and Haime, 1848

 

 

 

76

 Cyphastrea chalcidicum (Forskal, 1775)

+

+

+

77

 Cyphastrea serailia (Forskal, 1775)

+

+

-

78

 Cyphastrea microphthalma (Lamarck, 1816)

+

+

+

79

 Cyphastrea ocellina (Dana, 1846)

+

+

+

80

 Cyphastrea japonica Yabe and Sugiyama, 1936

+

+

+

 

Genus Solenastrea Milne Edwards and Haime, 1848

 

 

 

81

Solenastrea bournoni Milne Edwards and Haime, 1849

-

-

+

 

Genus Echinopora Lamarck, 1816

 

 

 

82

Echinopora gemmacea (Lamarck, 1816)

+

+

-

83

Echinopora horrida Dana, 1846

+

+

+

84

Echinopora hirsutissima Milne Edwards and Haime, 1850

+

+

-

85

Echinopora lamellosa (Esper, 1791)

+

+

-

86

Echinopora pacificus Veron, 1990

+

+

+

87

Echinopora fruticulosa Klunzinger, 1879

+

+

+

88

Echinopora forskaliana (Milne Edwards and Haime, 1849)

-

+

-

 

Total Number of Species

77

85

49

 

Pielou’s Evenness Index (J)

0.92

0.93

0.92

 

Shannon-Weaver Diversity Index (H’)

5.80

5.96

5.13

 

Simpson’s Density Index (D)

0.97

0.98

0.96


 


The species diversity of corals was evaluated following Shannon-Weaver diversity index formula as described below [7].

 

               H’= -∑pi loge pi

 

Where, pi = Proportion of number of individual of a particular species and total number of individual of all the species, H’= diversity of a theoretically infinite population.

 

Similarity Index is the simple measure of the extent to which two habitats species in common. The Sørensen index, also known as Sørensen’s similarity coefficient, is a statistic used for comparing the similarity of two  samples [8].

It has been formulated below

 

               QS= (2C/A + B)

 

Where, A and B are the species numbers in station A and B, respectively, and C is the number of species shared by the two stations. This expression is easily extended to abundance instead of incidence of species.

 

Simpson’s diversity index [9] is one of the truthful indices to calculate the species diversity of any study site. It has been applied to calculate the species diversity of scleractinian corals of those islands.

The formula for the Simpson index is:

 

               D=1-

Where S is the number of species, N is the total percentage cover or total number of organisms and n is the percentage cover of a species or number of organisms of a species. In this form, D ranges from 1 to 0, with 1 representing infinite diversity and 0 representing no diversity.

 

Evenness of a community was described by the Pielou’s Evenness Index (J’). The formula of the index  is [10]-

 

J’=H’/H’max

 

Where H' is the number derived from the Shannon diversity.

 

RESULTS:

A total 88 species of faviids were recorded under 18 genera from the study areas. The genus Favia shown a maximum of 18 species followed by Favites where it was 13 species. However the genus Diploria, Colpophyllia, Plesiastrea, Oulastrea, Diploastrea and Solenastrea represented with single species only. Among them, South Andaman region showed maximum number of species composition (85 species) with Shannon-Weaver diversity Index (H’= 5.96), Simpson Density Index (D= 0.98) and Pielou’s Evenness Index (J= 0.93) in comparison with the other two regions of these group of islands (Fig-1). The minimum was recorded at Nicobar region with 49 species of faviids and the species diversity, density and evenness indices are 5.13, 0.96 and 0.92 respectively (Table-1). The similarity of the species composition shows a significant amount of a maximum 0.95 in between North and Middle Andaman and South Andaman regions (Table-2).

 

Table-2 Sorensen’s similarity index

 

South Andaman

Nicobar

North and Middle Andaman

0.95

0.68

Nicobar

0.68

 

 

Fig-1- Comparative study on Species Diversity (H’), Density (D) and Evenness (J)

 

DISCUSSION:

Scleractinian corals are denoted as marine rainforest due to its productivity towards the marine biodiversity from the primary level to tertiary. Due course of time with the exponential efforts of the several expeditions as well as surveys, it was revealed out that scleractinians are widely distributed with varied species composition mostly in tropical regions of the world nevertheless species of the same were also recorded from other parts. Record of 126 species of faviids under 24 genera was made by Veron [1] in global scenario.  In 2003, Venkataraman et al. made a record to describe 36 species of faviids under 13 genera [11]. Ramakrishna et al. (2010) also recorded a checklist of 78 species of faviids under 16 genera from Andaman and Nicobar Islands [12]. The gradual increment on the exploration of species in this group of islands depicts the progressiveness in bio-diversity nodules of these areas. With that extensive effort, present study revealed out 88 species under 18 genera. Finding out of 85 species with Shannon-Weaver diversity Index (H’= 5.96), Simpson Density Index (D= 0.98) and Pielou’s Evenness Index (J= 0.93) is itself a self introductory phenomenon of that place to say about the biogenic habitat of that area. Though the H’, J and D values of other two areas are lesser than the above one, but it can be said that, the species composition, diversity, distribution and evenness of North and Middle Andaman are very closer to South Andaman as it showed 0.95 similarity index. Nicobar region of the study area is relatively less diverse in species with the other two areas with Shannon-Weaver diversity Index (H’= 5.13), Simpson Density Index (D= 0.96) and Pielou’s Evenness Index (J= 0.92), but status of the species is good enough to mean the suitable biogenic environment of that area, which support their recruitment, growth, biological process towards the successive implementation of enriched species compatibility with the surrounding environment.

 

ACKNOWLEDGEMENT:

Authors are grateful to the Ministry of Environment and Forests, Govt. of India for providing financial assistance to undertake the study through the projects of National Coral Reef Research Institute, Zoological Survey of India, Port Blair.

 

REFERENCES

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2.       Veron JEN, Pichon M, Wijsman-Best M. Scleractinia of Eastern Australia. Australian Institute of Marine Science, 1977.

3.       Done TJ, Kenchinton RA, Zell LD. Rapid, large area, reef resource surveys using a manta board. Proceedings of the Fourth International Coral Reef Symposium, Manila 2 ; 1982: 597-600.

4.       Kenchinton RA. Large area surveys of coral reefs, UNESCO Reports in Marine Science 21; 1984: 92-103.

5.       Bradbury RH, Reichelt RE, Meyer DL,. Birtles RA.  Patterns in the distribution of the crinoids community at Davies Reef on the central Great Barrier Reef, Coral Reefs  5; 1886:189-196.

6.       Endean R, Stablum W. A study of some aspects of the crown of thorns starfish (A. planci) infestations of reefs of Australia's Great Barrier Reef, Atoll Res. Bul. 167; 1973:1-60.

7.       Shannon CE. A mathematical theory of communication, Bell System Technical Journal 27; 1948: 379–423 and 623–656.

8.       Sørensen T. A method of establishing groups of equal amplitude in plant sociology based on similarity of species and its application to analyses of the vegetation on Danish commons, Biologiske SkrifterKongelige Danske Videnskabernes Selskab

 (1948) 1–34.

9.       Simpson EH. Measurement of diversity,  Nature 163; 1949: 688.

10.     Pielou EC. The measurement of diversity in different types of biological collections, J. Theor. Biol. 13; 1966: 131-144.

11.     Venkataraman K, Satyanarayan Ch, Alfred JRB, Wolstenholme J. Handbook on Hard Corals of India, 1-266; 2003.

12.     Ramakrishna, Tamal Mondal, Raghunathan C, Raghuraman R, Sivaperuman C. New Records of Scleractinian Corals in Andaman and Nicobar Islands, Rec. zool. Surv. India, Occ. Paper No. 321; 2010: 1-144 (Published by the Director, Zool. Surv. India, Kolkata)

 

Received on 23.01.2012

Modified on 08.03.2012

Accepted on 06.04.2012     

© A&V Publication all right reserved

Research J. Science and Tech.  4(2): March-April 2012: 62-66