Journal of Threatened Taxa | www.threatenedtaxa.org | 26 July 2021 | 13(8): 19108–19117

 

ISSN 0974-7907 (Online) | ISSN 0974-7893 (Print) 

https://doi.org/10.11609/jott.6375.13.8.19108-19117

#6375 | Received 08 July 2020 | Final received 21 January 2021 | Finally accepted 07 July 2021

 

 

Diversity of ants in Aarey Milk Colony, Mumbai, India

 

Akshay Gawade 1 & Amol P. Patwardhan 2

 

1 B.N. Bandodkar College of Science, Thane 400601. Maharashtra. India.

2 Department of Zoology, K.J. Somaiya College of Science and Commerce, Mumbai, Maharashtra 400077, India.

1 akki.gawade2@gmail.com, 2 amolppatwardhan@gmail.com (corresponding author)

 

 

Editor: Anonymity requested.   Date of publication: 26 July 2021 (online & print)

 

Citation: Gawade, A. & A.P. Patwardhan (2021). Diversity of ants in Aarey Milk Colony, Mumbai, India. Journal of Threatened Taxa 13(8): 19108–19117. https://doi.org/10.11609/jott.6375.13.8.19108-19117

 

Copyright: © Gawade & Patwardhan 2021. Creative Commons Attribution 4.0 International License.  JoTT allows unrestricted use, reproduction, and distribution of this article in any medium by providing adequate credit to the author(s) and the source of publication.

 

Funding: None.

 

Competing interests: The authors declare no competing interests.

 

Acknowledgements: We gratefully thank the C.E.O. of Aarey Milk Dairy Pvt. Ltd, Aarey Milk Colony, Goregaon, Mumbai and senior police inspector, Aarey Police Station, AMC Goregaon, Mumbai for giving AG permission to carry out the research project in AMC and for supporting throughout the study. We would like to thank Dr. Poonam Kurve and Ashutosh Joshi of the Department of Environmental science of B.N. Bandodkar College of Science, Thane, for there valuable inputs. AG is grateful to Anand Pendharkar for suggesting the topic, valuable inputs, and help rendered during the pilot study.

 

 

 

Abstract: Aarey Milk Colony (AMC) is 16km2 of forested area, acts as a buffer to the Sanjay Gandhi National Park, Mumbai. It has gardens, lakes, recreation spots, and a nursery. It also harbors 32 cattle farms, animal husbandry centers. Apart from urbanization and forest degradation, this forest harbors great biodiversity which includes the leopard as a top predator and also lesser-known species of amphibians, reptiles, and arthropods. Considering ants as important bio indicators and the vulnerability of AMC to development plans, a study on the diversity of ants was conducted from January 2016 to May 2016. Four methods were used for data collection of ants—pitfall trap, line-transect, quadrate, and all-out search. A total of 35 species under 24 genera under six subfamilies– Myrmicinae, Formicinae, Ponerinae, Dolichoderinae, Pseudomyrmecinae, and Cerapachyinae were recorded during this study. The Simpson’s diversity index (0.88) for the pit fall trap indicates that the diversity of ants in the AMC is fairly high. This increases the importance of this forest land which is presently facing a mass destruction of trees.

 

Keywords: Bio indicator, data collection, Maharashtra, Sanjay Gandhi National Park.

 

 

Aarey Milk Colony (AMC) was notified in 1949 which covers an area of 16km2. It is situated on the southwestern boundary of Sanjay Gandhi National Park, Mumbai. The colony acts as a buffer zone for the densely forested national park. The colony faces heavy anthropogenic pressure such as illegal encroachment, change in land use, which converted it into a garden, nursery, picnic spots, restaurants, and milk processing units.

Among invertebrates, insects are the most abundant and diverse organisms on Earth, as most of the insects are highly mobile, their presence in an ecosystem may be temporary which limits their use to detect environmental changes (Khot et al. 2013). On the other hand, the ants being more local than other insects they can be efficiently used as a bio-indicator (Stephens & Wagner 2006; Underwood & Fisher 2006; Jonathan et al. 2007; Abril & Gomez 2013).

Andersen et al. (2002) suggested that ants can provide valuable information about the environment in which they occur and considerably more than could traditional wildlife (vertebrate) surveys. According to Wilson (1990) and Gadagkar et al. (1993), the biomass of ants is approximately four times greater than the biomass of all of the vertebrates. Due to their abundance, high species richness, occupancy of high topographic level and being highly responsive to environmental changes ants are considered as excellent bio-indicators (Jonathan 1983). According to Bharti (2011), there are 652 species/subspecies that are known to occur in India. Khot et al. (2012) recorded 28 species representing six subfamilies from Maharashtra Nature Park and Quadros et al. (2009) recorded 19 species of ants from IIT Bombay campus; 163 species of ants, in 52 genera, were reported by Mathew & Tiwari (2000) from Meghalaya. Kharbani & Hajong (2009) recorded 28 species from 18 genera from the West Khasi hills, Meghalaya.  Bharti et al. (2009) recorded 40 species of ants from eight genera from Punjab Shivalik.

The forest of AMC is of mixed moist deciduous type and is dominated by Tectona grandis, Bombax ceiba, Butea monosperma, Pongamia pinnata, Cassia fistula, Ziziphus sp., heavily intermixed with exotic/invasive species such as Eucalyptus, Gliricidia sepium as well as Delonix regia and Lantana sp. (Mirza & Sanap 2010). According to Mirza & Sanap (2010) the faunal diversity of AMC includes 13 species of amphibians, 46 species of reptiles, 76 species of avifauna, 16 species of mammals, 86 species of butterflies, five species of scorpions, and 19 families of spiders. There is no reported work on the ants of this area.

AMC (Image 1) is under immense anthropogenic pressure. Hence the study on ants might be helpful in throwing some light on the diversity of invertebrates that are about to get lost or displaced.

 

Material and Methods

The survey was carried out from January 2016 to May 2016.

Four sampling methods were deployed as follows.

Pitfall trap (n= 52): Transparent plastic glasses having 7.5 cm diameter and 7.5 cm height were used for pitfall traps buried at ground level. In each trap four plastic glasses were kept at the corner of 4 x 4 m quadrate. The traps were set up for 24 hr. The total area covered was 832 m2. The trap was observed regularly to avoid predation on ants, if any. Ants were released from the trap after photo documentation.

Line transect (n= 9): Line transects of 100 m were plotted in the study site so that maximum area and different habitats were covered. This method was used three times a day (morning, afternoon, and evening). The total area covered by line transects was 1,800 m.

Quadrat method (n= 13):  Four quadrates of 4 x 4 m were placed in the selected study site. Each quadrat was observed for 10 min.

All-out search method (n= 30): This method was used to collect data opportunistically.

All the individuals recorded by the above four methods were photographed using Canon 600D camera body with a 90mm macro lens and identified using Bingham (1903), Narendra & Kumar (2006), antweb (http://antweb.org/), and antwiki (http://www.antwiki.org/wiki/).

To have a basic idea of richness, pit fall trap data was utilized for calculating Simpson’s diversity index.

 

Results

A total of 35 species under 24 genera and six subfamilies were recorded from the study area (Table 1). Table 2 represents the dominance of the subfamilies. Myrmicinae (9 genera and 13 species) and Formicinae (6 genera and 11 species) were the most dominant subfamilies followed by Poneriane (5 genera and 6 species); Dolichoderinae (2 genera and 2 species), Pseudomyrmicinae (1 genus and 2 species), and Cerapachynae (1 species).

Pitfall trap, line transects, quadrate, and all-out search methods were used to collect this data (Table 3). Solenopsis geminata, Crematogaster subnuda, Crematogaster ransonneti, Monomarium pharaonis, Camponotus compressus, Paratrechina longicornis, Polyrachis lacteipennis, Diacama rugosum, and Tapinoma melanocephalum were recorded from all four sampling methods. Oecophylla smaragdina, Anochetes graffei, Platythyrea sagei, Leptogenys chinensis, Leptogenys processionalis, and Cerapachys longitarsus were recorded only by one of the methods.

A comparison of sampling methods (Table 4) suggests that the pitfall method was the most productive yielding 27 of 35 species recorded. All-out search method was the second most productive yielding 24 of 35 species which was high probably because a larger area was covered in opportunistic visits. Pitfall and all-out search methods shared 16 species in common. The line transact was substantially productive in terms of recording the number of individuals. This can be attributed to the foraging habits of the ants.

 

The Simpson’s diversity index for pitfall trap data.

D= 1 - ∑ n(n-1)/N(N-1) = 1 - ∑ 29292/250500 = 0.88

The Simpson’s diversity index of 0.88 indicates the diversity of ants on the higher side. Further,  a long time assessment and detailed analyses of different sampling methods might reveal more comprehensive results.

Aarey colony is under pressure from human developmental activities hence further study is required so as to use ant as an effective indicator for highly disturbed forest habitats.

 

Table 1. Ant diversity in Aarey Milk Colony, Mumbai, Maharashtra.

 

Species

Subfamily

Figure number

1

Aphaenogaster beccarii

Myrmicinae

2

2

Cardiocondyla nuda

Myrmicinae

3

3

Cataulacus taprobanae

Myrmicinae

4

4

Crematogaster ransonneti

Myrmicinae

5

5

Crematogaster subnuda

Myrmicinae

6

6

Meranoplus bicolor

Myrmicinae

7

7

Monomorium criniceps

Myrmicinae

8

8

Monomorium pharaonis

Myrmicinae

9

9

Myrmicaria brunnea

Myrmicinae

10

10

Pheidole watsoni

Myrmicinae

11

11

Solenopsis geminata

Myrmicinae

12

12

Tetramorium smithi

Myrmicinae

13

13

Tetramorium walshi

Myrmicinae

14

14

Camponotus angusticollis

Formicinae

15

15

Camponotus compressus

Formicinae

16

16

Camponotus irritans

Formicinae

17

17

Camponotus parius

Formicinae

18

18

Camponotus sericeus

Formicinae

19

19

Oecophylla smaragdina

Formicinae

20

20

Paratrechina longicornis

Formicinae

21

21

Polyrhachis exercita

Formicinae

22

22

Polyrhachis lacteipennis

Formicinae

23

23

Polyrhachis rastellata

Formicinae

24

24

Camponotus angusticollis

Formicinae

25

25

Anochetus graeffei

Ponerinae

26

26

Brachyponera lutipes

Ponerinae

27

27

Diacamma rugosum

Ponerinae

28

28

Leptogenys chinensis

Ponerinae

29

29

Leptogenys processionalis

Ponerinae

30

30

Platythyrea sagei

Ponerinae

31

31

Tapinoma melanocephalum

Dolichoderinae

32

32

Technomyrmex albipes

Dolichoderinae

33

33

Tetraponera rufonigra

Pseudomyrmicinae

34

34

Tetraponera allaborans

Pseudomyrmicinae

35

35

Cerapachys longitarsus

Cerapachyinae

36

 

 

Table 2. Family-wise diversity of ant species.

 

Sub-families

Species

Percentage (%)

1

Myrmicinae

13

37

2

Formicinae

11

31

3

Ponerinae

6

17

4

Dolichoderinae

2

6

5

Pseudomyrmicinae

2

6

6

Cerapachyinae

1

3

 

Total

35

100

 

 

Table 3. Sampling methods deployed for collecting data on ants. PT—Pitfall trap | LT—Line transect | Q—Quadrate | AO—All-out search.

 

Species

PT

LT

Q

AL

1

Aphaenogaster beccarii

+

-

-

-

2

Cardiocondyla nuda

-

-

-

+

3

Cataulacus taprobanae

-

+

-

+

4

Crematogaster ransonneti

+

+

+

+

5

Crematogaster subnuda

+

+

+

+

6

Meranoplus bicolor

-

-

-

+

7

Monomorium criniceps

+

-

+

-

8

Monomorium pharaonis

+

+

+

+

9

Myrmicaria brunnea

+

-

+

-

10

Pheidole watsoni

+

+

+

+

11

Solenopsis geminata

+

+

+

+

12

Tetramorium smithi

+

-

-

+

13

Tetramorium walshi

-

+

+

-

14

Camponotus angusticollis

+

+

-

+

15

Camponotus compressus

+

+

+

+

16

Camponotus irritans

+

+

-

+

17

Camponotus parius

-

+

-

+

18

Camponotus sericeus

+

-

-

+

19

Oecophylla smaragdina

-

-

-

+

20

Paratrechina longicornis

+

+

+

+

21

Polyrhachis exercita

-

-

-

+

22

Polyrhachis lacteipennis

+

+

+

+

23

Polyrhachis rastellata

+

-

-

+

24

Camponotus angusticollis

+

+

-

+

25

Anochetus graeffei

+

-

-

-

26

Brachyponera lutipes

+

-

-

+

27

Diacamma rugosum

+

+

+

+

28

Leptogenys chinensis

+

-

-

-

29

Leptogenys processionalis

+

-

-

-

30

Platythyrea sagei

+

-

-

-

31

Tapinoma melanocephalum

+

+

+

+

32

Technomyrmex albipes

+

+

-

-

33

Tetraponera rufonigra

-

+

+

+

34

Tetraponera allaborans

+

+

-

+

35

Cerapachys longitarsus

+

-

-

-

 

Total

27

18

14

24

 

 

Table 4. Species and total individuals recorded in sampling methods.

 

Trapping method

Species recorded

Individuals recorded

1

Pitfall trap

27

501

2

Line transect

18

889

3

Quadrate

14

225

4

All-out search

24

534

 

 

For images - - click here

 

References

 

Abril, S. & C. Gomez (2013). Rapid assessment of ant assemblages in public pine forests of the central Iberian Peninsula. Forest Ecology and Management 293: 79–84.

Andersen, A., B.D. Hoffman, W.J. Muller & A.D. Griffiths (2002). Using Ants as Bioindicators in Land management: Simplifying Assessment of Ant Community Responses. Journal of applied Ecology 39(1): 8–17.

Bharti, H., Y.P. Sharma & A. Kaur (2009). Seasonal patterns of ants (Hymenoptera: Formicidae) in Punjab Shivalik. Haltere 1: 36–47.

Bharti, H. (2011). List of Indian Ants. Halteres 2: 79–87.

Bingham, C.T. (1903). The Fauna of British India, including Ceylon and Burma. Hymenoptera, Vol. ll. Ants and Cuckoo-wasps. London: Taylor and Francis, 506pp.

Gadagkar, R., P. Nair, C. Chandrashekhara & D.M. Bhat (1993). Ant species richness and diversity in some selected localities in Western Ghats, India. Hexapoda 5(2) : 79–94.

http://antweb.org/ ( visited June 2016; Revisited 20th June 2020)

http://www.antwiki.org/  (visited June 2016; Revisited 20 June 2020)

Jonathan, D.M. (1983). Ants: Bio-indicators of minesite rehabilitation, land-use, and land conservation. Environmental Management 7(4): 375–383.

Jonathan, D.M., G. Oraby & L. Bisevac (2007). Ants (Hymenoptera: Formicidae) pass the bioindicator scorecard. Myrmecological News 10: 69–76.

Kharbani, H. & S.R. Hajong (2013). Seasonal patterns in ant (Hymenoptera: Formicidae) activity in a forest habitat of the West Khasi Hills, Meghalaya, India. Asian Myrmecology 5: 103–112.

Khot, K., G. Quadros & V.U. Somani (2013).  Ant diversity in an urban garden at Mumbai, Maharashtra, pp. 121–125. Proceedings of the National Conference of Biodiversity: Status and Challenges in Conservation.

Mathew, R. & R.N. Tiwari (2000). Insecta: Hymenoptera: Formicidae Zoological Survey of India, State Fauna Series 4: Fauna of Meghalaya Part-7: 251–409pp. 

Mirza, Z. & R. Sanap (2010). Biodiversity of Aarey Milk Colony and Film City (2007–2009). A report submitted to the Government of Maharashtra and the Forest Department of Maharashtra, 51pp.

Narendra, A. & M.S. Kumar (2006). On Trail with Ants. A Handbook of the Ants of Peninsular India. Self published, 193pp.

Quadros, G., G. Gurav, K. Bhagat, A. Chorghe, A. Dhamorikar, K. Khot & M. Nagarkar (2009). Report on the Study of the Biodiversity of Indian Institute of Technology Bombay Campus. By WWF-India MSO for IIT Bombay, 158pp.

Stephens, S.S. & M.R. Wagner (2006). Using Ground Foraging Ant (Hymenoptera: Formicidae) Functional Groups as Bioindicators of Forest Health in Northern Arizona Ponderosa Pine Forests. Environmental Entomology 35(4): 937–949

Underwood, E.C. & B.L. Fisher (2006). The role of ants in conservation monitoring: If, when and how. Biological conservation 132: 166–182.

Wilson, E.O. (1990). Success and Dominance in Ecosystems: The Case of the Social Insects. In: Kinne, O. (Ed.). Excellence in Ecology. Vol. 2. Ecology Institute, Oldendorf/Luhe, Germany, 104pp+15figs.