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A Study on Species distribution and Diversity of Macro-Fauna of River Tawa - A Tributary of River Narmada in Madhya Pradesh, India

Charu Tiwari1 * , Vipin Vyas2 and Manik Sharma3

Corresponding author Email: charuzoology05@gmail.com

DOI: http://dx.doi.org/10.12944/CWE.16.1.27

This study is aimed to collect information about the macrofauna diversity of Tawa River. The Tawa River joins to Narmada at district Hoshangabad (Madhya Pradesh). During the study 8 sites were selected for the investigation . collections of samples were done from the eight sampling sites of the river. Collected samples were identified up to species level and their diversity and richness were analyzed. Shannon index for diversity and margalef index for richness were used for the study.Total 48 taxa of macrofauna have been recorded from the identified sampling stations. Benthic fauna of phylum Arthropoda was found in dominant position in the study and phylum Mollusca was found in second position.

Benthos, Distribution and Diversity, Macrofauna, Margalef Index, Shannon Index, Tawa River

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Tiwari C, Vyas V, Sharma M. A Study on  Species distribution and Diversity of Macro-Fauna of River Tawa - A Tributary of River Narmada in Madhya Pradesh, India. Curr World Environ 2021;16(1). DOI:http://dx.doi.org/10.12944/CWE.16.1.27

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Tiwari C, Vyas V, Sharma M. A Study on  Species distribution and Diversity of Macro-Fauna of River Tawa - A Tributary of River Narmada in Madhya Pradesh, India. Curr World Environ 2021;16(1). Available From : https://bit.ly/2Z8cqL5


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Article Publishing History

Received: 16-07-2020
Accepted: 10-02-2021
Reviewed by: Orcid Orcid Y. Vasudeva Rao
Second Review by: Orcid Orcid Manoj Kumar
Final Approval by: Dr. Hiren B. Soni


Introduction

River ecosystems are most important lotic fresh water habitats for many aquatic animals and benthic animals are one of these animal. Benthic animals are generally found in both of fresh water habitats i.e. – lotic habitats and lentic habitats. Benthos spends their whole life in bottom of aquatic ecosystem because of their feeding nature. Basically they are detritus feeders and divided in to two types – microzoobenthos and macrozoobenthos. Macro benthos are those animals which can be seen with naked eyes. Their diversity and distribution are good indicators of water quality of an ecosystem that’s why they are known as bioindicators. In the present investigation diversity and distribution of Macroinvertebrates were recorded for the period of two years from July 2017 to June 2019. The study was focused on two main phyla of macrozoobenthos community of arthropoda and mollusca. Macrozoobenthos show sessile and sedentary behavior .Aquatic organisms are common indicator of aquatic environmental conditions.1 Macrozoobenthic fauna serve as a biological indicator of aquatic ecosystem.2 Physicochemical quality of water is the factors that influence species composition of a water body.3 Macrobenthos are good source of fish food and their food chain.4 They are Ecological engineers of ecosystems.5 Fresh water ecosystem was the conservation priority during International decade Action 6 and in the present time also. Periodical bioassessment of taxonomic diversity of aquatic ecosystem play an important role for nature and ecological protection. Different measures are used in bioassessment for fresh water.7 Macrozoobenthos due to their special characteristics are indicator of the water quality of an aquatic ecosystem.8,9 The abundance of macrozoobenthos are depending on its surrounding environment.2 composition of benthic community is directly related to water quality10 .The present research was aimed to study the distribution of benthic macro fauna of Tawa river.

Material and Methods

Study Area


Tawa River is one of the major tributaries of Narmada in the central India.The Tawa originates from Satpura hills of Betul district and flows towards Hoshangabad District of (Madhya Pradesh).The Tawa joins to Narmada river at Bandrabhan village of Hoshangabad. The preserve forest BORI is situated along the Tawa. Bori sanctuary of the preserve forest is very famous part of Biosphere of Panchmarhi of Hoshangabad district.

Figure 1: Map Showing Position of Tawa River.

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Figure 2: Map Showing Catchment Area of River – Tawa.

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Study Sites

Total 8 sites were identified for the research. Their geographical positions are shown in the Table 1. These sites arranged from upstream to downstream and joins to Narmada in Bandrabhan village at district Hoshangabad.

Table 1: Position of Sampling Stations.

Sampling station

Name of sites

Latitude

Longitude

S1

Sarni  (power plant area)

22.05068

78.1300

S2

Ghoradondri (banspur)

22.1610

77.996

S3

Bhoura (khapa)

22.2620

77.927

S4

Ranipur(dam area)

22.5747

77.98004

S5

Maharghat

22.684

77.831

S6

Babai bridge

22.7104

77.83144

S7

Raipur

22.71785

77.7254

S8

Bandrabhan (Tawa-Narmada confluence point)

22.7441

77.7369

 


Protocoll

Selected sites were visited periodically to gather samples of benthic macro-fauna. To collect samples, various types of gears like surber sampler, D-net sampler, kick net sampler, and grab sampler etc. were used according to river bed of the sites. 0.5 to 0.6 micron mesh sized sieve were used to collect benthic macro fauna. Separated fauna were washed carefully and stored in labeled plastic bottles. 4% formalin were used for benthos preservation. Collected  animals were identified upto the species level. Microscope and hand lens were used to observe detailed features of the animals.   

Diversity and Richness Index

Collected samples were recorded in a manner of tabulation chart. After the collection of data, statistical analysis was done. In the present paper two important diversity index were analysed.

Diversity Index of Shannon

Shannon index is very common index which is used for diversity calculation of a habitat.11 The index value ranges between 0.0 and 5.00.

Table 3: Index Value and Diversity of Shannon Index.

Index value

Diversity

1.5 to 3.5

Common

3.6 to 4.5

Rich

4.5 to 5.0

Very rich

H’= ∑ [(ni / N)*(ln ni / N)]

H’= Shannon Diversity Index

ni = number of individuals belonging to i species

N = Total number of individuals of all species

Richness Index of Margalef

The margalef index formula is used to calculate richness of species.12 This index shows richness of species in a habitat.r

d = (S -1) / ln N

d = Margalef Diversity Index

S = Total number of species

N = Total number of individuals

Result and Discussion

During the study, total 48 taxa of macrozoobenthos belonging to phylum Mollusca and Arthropoda were noted form eight sampling station of the study area. Out of these 48 taxa, 17 taxa of class Gastropoda represented by two orders Megastropoda and Hygrophila with 4 and 1 families respectively. Class Bivalvia was represented by three orders with four families  Amblemidae, Unionidae, Corbiculidae and Lymnaeidae. Phylum Arthropoda has been recorded with two classes Insecta and Malacostraca. Class Insecta  were represented by 6 orders and 17 families with 25 taxa while class Malacostraca represented by one order with a family. Class Insecta of phylum Arthropoda and class Gastropoda of phylum Mollusca were main representatives of macrozoobenthos of the river. Similar observations were recorded at Ganjal River, Ken River and Streams of Yedigoller National Park 14, 15, 16. Bellamya bengalensis of mollusca is a dominant species and found at all eight sampling stations and Total 41 individuals were collected. More than 20 taxa of phylum arthropoda and mollusca were recorded from four sampling sites S-1, S-2, S-3, and S-5. Maximum taxa varieties were noted from site1 and 5. Lowest number of taxa was observed from site 4 and 6. Bellamya bengalensis (family-Viviparidae) and Brotia costula (family-Thiaridae) of phylum   mollusca were recorded from all the sampling stations. Phylum Arthropoda are dominant in position than Mollusca. Dominancy of phylum arthropoda in the river ecosystem was reported by Vyas, et.al.  ,Sharma, et.al. and Khan 17, 18, 19. It may be due to favorable habitat conditions and food availability for Arthropods in the river.  The finding of this study reports the current position of macrozoobenthos diversity of river Tawa.

Figure 3: Composition of Taxonomic Group of Macrozoobenthos.

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Figure 4: Species Level Distribution of  Macrozoobenthos at Different Sampling Sites.

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Table 2: Diversity of Macrozoobenthos of Tawa River.

S.No.

Taxa

Sampling Stations

   

S1

S2

S3

S4

S5

S6

S7

S8

Phylum

Mollusca

               

Class

Gastropoda

               

Order

Megastropoda

               

Family

Viviparidae

               

1

Bellamya bengalensis

+

+

+

+

+

+

+

+

2

Bellamya dissimilis

-

+

-

+

+

+

+

+

3

Bellamya heliciformis

-

+

+

-

-

-

+

+

4

Bellamya crassa

-

-

+

-

+

-

-

-

5

Angulyagra microchaetophora

-

-

+

-

+

-

+

-

Family

Thiaridae

               

6

Melanoides tuberculata crebra

+

+

-

+

+

+

-

+

7

T.Melanoides tuberculata

-

+

+

+

+

-

+

-

8

Tarebia granifera

-

-

+

-

-

+

-

-

9

Thiara (M.) tigrina raoi

+

+

+

-

+

-

-

+

10

Brotia costula

+

+

+

+

+

+

+

+

11

Brotia costula juvenile

+

+

+

-

-

+

-

+

Family

Bithyniidae

               

12

Gabbia travancorica

-

+

+

+

-

-

+

-

13

Digoniostoma cerameopoma

-

-

+

-

-

-

-

+

Family

Pilidae

               

14

Pila globosa

+

-

-

+

+

-

-

-

Order

Hygrophila

               

Family

Planorbidae

               

15

Gyraulus velifer

+

+

+

+

+

-

-

+

16

Gyraulus rotula

+

-

+

+

+

-

-

+

17

Indoplanorbis exustus

-

-

-

+

-

-

-

-

Class

Bivalve

               

Order

Trigoinoida

               

Family

Amblemidae

               

18

Parreysia radiatula crispisulcata

+

+

+

+

+

-

-

-

19

Parreysia R. caerulea

+

+

+

+

+

+

-

+

Family

Unionidae

               

20

Lamellidens narainporensis

+

-

-

+

-

+

-

-

Order

Veneroida

               

Family

Corbiculidae

               

21

Corbicula striatella

+

+

-

-

+

+

+

-

Order

Basomatophora

               

Family

Lymnaeidae

               

22

Lymnaea accuminata

+

-

+

+

+

+

+

+

Phylum     

Arthropoda

               

Class

Insecta

               

Order

Odonata

               

Family

Gomphidae

               

23

Gomphus vastus

-

+

-

-

-

-

-

-

24

progomphus larva

+

+

-

-

-

-

-

-

Family

Aeshnidae

               

25

Anux sps.

-

+

-

+

+

+

-

-

 

Lestidae

               

26

Lestes sps

-

+

-

-

-

-

-

-

Family

Libellulidae

               

27

Libellula luctuosa

-

+

-

+

-

-

-

-

28

Libellula larva

-

-

-

-

+

+

-

-

Family

Cordulegastridae

               

29

Cordulegaster larva

-

-

-

-

-

-

-

+

Family

Petalurdaei

               

30

Tachopteryx larva

-

-

+

-

-

-

-

-

Family

Coenagrionidae

               

31

Enallagma sps.

-

-

+

+

-

-

-

-

32

Enallagma larva

-

-

+

+

+

-

+

+

Family

Macromiidae

               

33

Macromia larva

+

-

-

-

+

+

+

-

Order

Hemiptera

               

Family

Nepidae

               

34

Ranatra sp.

-

+

+

-

+

-

+

-

35

Nepa sp.

-

-

+

+

+

-

-

+

Family

Corixidae

               

36

Sigara sp.

-

+

-

-

-

-

-

-

Order

Diptera

               

Family

Culicidae

               

37

Culicinae larva

-

-

-

-

-

+

-

-

38

Culex pipiens larva

-

-

-

-

-

-

+

-

39

wyeomyia larva

-

-

-

+

-

-

-

-

Order

Lepidoptera

               

Family

Noctuidae

               

40

Bellura larva

-

+

+

-

-

-

-

-

Order

Ephemeroptera

               

Family

Baetidae

               

41

callibaetis larva

-

-

-

+

-

-

+

-

Family

Siphlonuridae

               

42

ameletus larva

-

-

+

+

-

-

-

+

Family

Behningiidae

               

43

Dolamia larva

-

-

-

-

+

-

-

-

Order

Coleoptera

               

Family

Carabidae

               

44

Omophron adult

-

-

-

+

-

-

+

+

45

Bembidion adult

-

-

-

+

-

-

-

-

Family

Elmidae

               

46

Optioservus adult

-

-

-

-

+

+

+

-

47

Stenelmis adult

-

-

+

-

+

-

-

-

Class

Malacostraca

               

Order

Decapoda

               

Family

Palaemonidae

               

48

Palaemonetes sp.

-

-

-

-

-

-

+

-

                   



In the study, Diversity index was from 2.22 to 2.93.The diversity value of site no. 5 was highest and lowest value of index was noted at site 6. Site1 and 2 shows similar diversity composition of species with index value 2.7. The Margalef index shows richness of species. The value margalef diversity index ranges between 5.53 to 2.26 and highest value was recorded at site 5.Taxonomic richness at sampling site 1 and 5 may be due to favorable habitats for macrozoobenthos. Similar conclusion was made by Vyas at Barna Stream13 and Mouri River by Khan et.al 20.

Table 3: Shannon and Margalef Index of the Sampling Sites.

Sampling Sites

No. of Species

No. of Individual

Shannon Diversity Index

Margalef Diversity Index

Site-1

24

87

2.74

5.15

Site-2

23

96

2.72

4.82

Site-3

21

111

2.29

4.24

Site-4

15

132

2.23

2.26

Site-5

24

64

2.93

5.53

Site-6

15

62

2.22

3.39

Site-7

17

61

2.28

3.89

Site-8

18

131

2.35

3.48

 

Figure 5: Graphical Presentation of Species Level Distribution.

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Figure 6: Graphical Presentation of Shannon and Margalef Diversity Index of Sampling Sites.

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Conclusion

In the present study of macrozoobenthos diversity of Tawa river, dominant phylum was Arthropoda followed by Mollusca. The range of Shannon diversity index was lies between 2.93 to 2.22 which are indicating moderate pollution level in the sampling sites. Species diversity value in the range of 1.00 to 3.00 indicates moderate pollution in the water. Margalef diversity index value varied from 2.26 to 5.53 in the study and indicates low species richness. Road connectivity  increased human activities in the study area. Moreover, Agriculture activities, dam, activity of power plant, over exploitation and human disturbance in the study area may be cause to change habitat structure and low of species richness.

Acknowledgement

The authors are thankful to the Department of zoology and aquaculture and Department of Bioscience, Barkatullah University, Bhopal, (M.P) India, for providing necessary facilities for study as well as laboratory analysis. I also thank to my co-workers who helped in all the field studies. I am grateful to my Guide and Co-Guide for their guidance.

Funding Source

The author(s) received no financial support for the research, authorship, and/or publication of this article.

Conflict of Interest

The authors do not have any conflict of interest.

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