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International Journal of Forest, Animal and Fisheries Research (IJFAF)
ISSN: 2456-8791
[Vol-6, Issue-4, Jul-Aug, 2022]
Issue DOI: https://dx.doi.org/10.22161/ijfaf.6.4
Article DOI: https://dx.doi.org/10.22161/ijfaf.6.4.2
Int. J. Forest Animal Fish. Res.
www.aipublications.com/ijfaf Page | 9
Termite Mounds’ Diversity and Distribution: A Study at
Jnanabharathi, Bangalore University
R K Kavyashree*, S Murugan, A Namratha
Department of Zoology, Bangalore University, Bengaluru, India
*Corresponding Author: Kavyashreerk99@gmail.com
Received: 17 Jun 2022; Received in revised form: 11 Jul 2022; Accepted: 16 Jul 2022; Available online: 21 Jul 2022
©2022 The Author(s). Published by AI Publications. This is an open access article under the CC BY license
(https://creativecommons.org/licenses/by/4.0/)
Abstract— Termites work together to modify their surroundings, which in turn influences their behaviour,
leading to the building of termite mounds. The study was designed to assess diversity of termite mounds
present in the Bangalore University Campus, Bengaluru, India. Observations were made on the occurrence,
abundance, evenness and richness of the termite mounds. Mounds were surveyed by field survey and
photographic interpretation method during July 2021 to June 2022. Totally 119 mounds were found, out of
which 18 are ground level mounds, 42 small mounds, 37 medium mounds and 22 tall mounds. To test its
effectiveness and to know about the influence of the mounds on the ecological well-being, termite mounds
were identified, compared and interpreted using google earth map and the results were statistically verified.
Keywords— Termites, Mounds, Diversity Index, Richness index and Evenness index.
I. INTRODUCTION
Termites being eusocial insects are spread widely in sub-
tropics and tropics specially playing key role as
decomposers and engineers of soil [13, 16]. Termite are
having very soft cuticle, they do not sustain in cold regions,
their nests are formed by uniform thermal envelope with
very hard outer shell for protection from predators and
desiccation [33]. Termites feed on various kinds of organic
matter such as dead organic materials, wood, cardboard,
paper etc [15]. Thus, they contribute much to nutrient cycle
and community structuring in any ecosystem [32]. Along
with ants and earthworms, the termites play a major role in
increasing porosity of soil and creates tunnels which are
called mounds. mounds are solid but porous walls made
from soil and termite faeces acting as niche for various
microorganisms and fauna providing protection against
changing environment [10, 20, 27, 34].
The degree of termite contribution for the spatial
heterogeneity in an ecosystem is attached with the mounds’
spatial distribution per unit area and its size and number.
The spatial distribution of mounds is still the concept of
debate as emphasized by findings from various ecosystems
[5, 18, 19, 22, 30, 35]. Earlier studies of mounds are uneven,
focusing on species classification [1] nest building and
foraging activities [2] nutrient cycling [17] and termite-
herbivore interactions [39]. However, understanding the
spatial distribution of termite mounds can be a key
component in predicting habitat utilisation and forage for
herbivores [11, 12, 24]. Hence the present study was
undertaken.
II. METHODOLOGY
The present study was carried out in Jnanabharathi campus
(13º 05” N and 77º 34” E) at an altitude of 924 meters above
the mean sea level with annual rainfall range of 530 mm to
1375 mm (mean 916 mm) spread to an area about 4.5 sq.km
(1100 acres), situated on the elevated plateau at the western
side of Bangalore, Karnataka, India. The study area is
divided into site 1 (North) and site 2 (South) and is partially
inhabited (Fig 1). The major part being un-inhabited,
possesses wide range of vegetation from scrubby jungle,
wild to cultivated trees with fauna such as insects, toads,
reptiles, rodents and birds with a high population of termites
and snakes.
Kavyashree et al. International Journal of Forest, Animal and Fisheries Research (IJFAF)
6(4)-2022
Int. J. Forest Animal Fish. Res.
www.aipublications.com/ijfaf Page | 10
Fig.1: Jnanabharathi campus - Study area (Google map).
The mounds were identified and located in the study area
using global positioning system (GPS) and photographic
interpretation. Field survey was done during July 2021 to
June 2022 for the spatial distribution of different sized
mounds on google earth pro with GPS recordings of each
mound and the same were photographed for further
reference. Data comparison of the mounds between field
reality and photography interpretation was performed by
comparing the marked point corresponding to the location
of mound identified in the field as well as in the image.
Mounds were classified based on considering four standard
heights, ground level mound (0 to 1 feet) (Fig 2A), small
mound (1 to 3 feet) (Fig 2B), medium mound (3 to 7 feet)
(Fig 2C) and tall mounds (7 feet and above) (Fig 2D).
Fig.2: Mounds classification based standard heights
The below mentioned statistical equations were used to
compute the mounds’ diversity, richness and evenness in the
study area [25].
Shannon -Wiener diversity index (H’) [36] was used to
calculate mounds’ diversity index:
𝐻′
= − ∑(𝑃𝑖 ∗ 𝐿𝑛 (𝑃𝑖 ))
𝑠
𝑖=1
where Pi = S / N
S = Number of individuals of one mound type
N = Total number of all individuals in the sample
Ln = Natural logarithm
Kavyashree et al. International Journal of Forest, Animal and Fisheries Research (IJFAF)
6(4)-2022
Int. J. Forest Animal Fish. Res.
www.aipublications.com/ijfaf Page | 11
Margalef’s species richness index (d') [21] was adopted
to measure mounds’ richness index:
d′ =
(𝑆 − 1)
𝐿𝑛(𝑁)
where S = Total number of mounds
N = Total number of individuals in the sample
Ln = Natural logarithm
Pielou’s species evenness index (J’) [28] was used to
analyse the mounds’ evenness index:
J′ =
𝐻′
𝐿𝑛(𝑆)
where H' = Shannon -Wiener diversity index
S = Total number of species in the sample
Ln = Natural logarithm
III. RESULTS AND DISCUSSION
In the present study, out of a total of 119 mounds recorded
(Fig 3), 18 (15%) are ground level mounds, 42 (35%) small
mounds, 37 (31%) medium mounds and 22 (19%) tall
mounds. Out of the 119 mounds identified, 48 (40.34%)
mounds were at site 1(North) and 71 (59.66%) mounds were
at site 2 (South). Site 1 with 48 mounds (Fig 6) had 6
(12.5%) ground level mounds, 12 (25.0%) small mounds,
18 (37.5%) medium sized mounds, 12 (25.0%) tall mounds
(Fig 4) and Site 2 with 71 mounds (Fig 6) had 12 (25.0%)
ground level mounds, 30 (62.5%) small mounds, 19
(39.6%) medium level and 10 (20.8%) large mounds (Fig
5). Significantly lower number of mounds were found in site
1 when compared to site 2, this could be attributed to the
different human activities taking place decreasing the
assemblage of the termite [9, 31].
Forest sites are routinely harvested to satisfy the diverse
demands of the expanding human population. As a result,
the physical complexity of these habitats is reduced, which
lowers the variety and availability of ideal nesting and
feeding sites and alters the microclimate. Termite
microhabitats such as rotting tree stumps, dead logs, humus
soil, etc., will frequently diminish from heavily populated
areas. The succession of alates in creating new colonies is
therefore thought to be reduced as a result of decreasing
biodiversity brought on by human activity [7, 8, 14]. In
addition to disrupting termites' natural adversaries, this
change in microhabitat could make them pests rather than
just a necessary component of the food chain. This is one of
the main effects of this kind of habitat damage, both at micro
and macro level. Despite agricultural intensification, which
results in a trend that is less visible in forests, it is
undoubtedly attributable to the establishment of numerous
colonies [14].
Fig.3: Percentage of different sized mounds in the study
site.
Fig.4: Percentage of different sized mounds at site 1.
Fig.5: Percentage of different sized mounds at site 2.
Diversity index in site 1 and site 2 is found to be 1.32 and
1.29 respectively whereas the overall diversity index in the
study area is 1.33. The mound diversity between the sites in
the study area was not significantly different [26]. The result
falls between 1.29 and 1.33. In comparison to site 2,
diversity was generally greater at site 1 which had open
spaces. This might be due to the denseness of the forest,
15%
35%
31%
19%
Ground level
Small
Medium
Large
12.5%
25.0%
37.5%
25.0% Ground level
Small
Medium
Large
25.0%
62.5%
39.6%
20.8%
Ground level
Small
Medium
Large
Kavyashree et al. International Journal of Forest, Animal and Fisheries Research (IJFAF)
6(4)-2022
Int. J. Forest Animal Fish. Res.
www.aipublications.com/ijfaf Page | 12
which made sampling challenging, or the ecosystem's
potential control over the termite population. This might be
explained by the fact that these locations are found in a less
dry region with moderate rainfall. Resources and
microclimate conditions may not be a constraint to termite
variety in such a setting [31]. The high diversity in site 1
could be due to availability of higher resources from human
made structures and decreased number of predators.
Fig.6: Total number of different sized mounds in the study
site.
Richness index assessed at site 1 is 11.37, out of
which 1.29 ground level mounds, 2.84 small mounds, 4.39
medium mounds and 2.84 tall mounds, while site 2 has
richness index of 15.72 of which 2.58 ground level mounds,
6.80 small mounds, 4.22 medium mounds and 2.11 tall
mounds. Over all the richness index of the study area is
24.06, out of which 3.56 ground level mounds, 8.58 small
mounds, 7.53 medium mounds and 4.39 tall mounds. The
existence or absence of a species in an ecological niche, as
well as the richness or abundance there, are indicators of the
ecosystem's biological and ecological diversity. Termites
are not an exception to this criterion. We may also infer
from this study that where there is substantial human
activity, termite variety is more abundant, this might be
caused by sufficient resources being available and a drop in
natural predators and biodiversity is lost only in areas of
high human interference. The information at hand also
points to human meddling as the cause of the sparse
vegetation in the site 1 area, which has diminished natural
termite control. Because there are fewer natural nutrients
available and predators, termites will infest man-made
structures. Due to the destruction of microhabitat, termite
biomass and richness are reduced. Due to the minimal level
of human influence in the site 2 area, termite biomass and
richness are controlled by nature [31].
Evenness index estimated at site 1 is 0.953, site 2 is 0.933
and for the overall study area it is measured to be 0.958. The
resource ratio theory, according to Tilman [37, 38], predicts
that more species will coexist at low resource levels because
individuals perceive the environment as being more
spatially diverse, which results in more niches and higher
species evenness. Several elements, including fire [6, 7],
rainfall [3, 4] and temperature are known to affect the
richness, diversity, and evenness of mounds [23, 29]. The
loss in mound diversity on this environment is further
exacerbated by the absence of soil feeders. Therefore,
geology could have an indirect effect on the diversity
through soil conditions.
IV. CONCLUSION
The diversity of mound is subjected to change in the pattern
of ecosystem, such study would help in understanding the
ecological well-being. The kind of species, ecological
conditions, clay availability and the degree of termite
disturbance in the environment shall influence
the morphological variations. Soil nutrients build up in
termite mounds and their turnover becomes an essential part
to the ecosystem. The present study provides a baseline data
on the diversity and spatial distribution of the mounds and
helps in taking up mitigation measures to conserve such
areas. Isolating the year effect, as discussed in the
methodological parts of the article, could help uncover
anthropogenic effects on termite presence across time when
employing termite mounds as anthropogenic bio-indicators.
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Termite Mounds’ Diversity and Distribution: A Study at Jnanabharathi, Bangalore University

  • 1. International Journal of Forest, Animal and Fisheries Research (IJFAF) ISSN: 2456-8791 [Vol-6, Issue-4, Jul-Aug, 2022] Issue DOI: https://dx.doi.org/10.22161/ijfaf.6.4 Article DOI: https://dx.doi.org/10.22161/ijfaf.6.4.2 Int. J. Forest Animal Fish. Res. www.aipublications.com/ijfaf Page | 9 Termite Mounds’ Diversity and Distribution: A Study at Jnanabharathi, Bangalore University R K Kavyashree*, S Murugan, A Namratha Department of Zoology, Bangalore University, Bengaluru, India *Corresponding Author: Kavyashreerk99@gmail.com Received: 17 Jun 2022; Received in revised form: 11 Jul 2022; Accepted: 16 Jul 2022; Available online: 21 Jul 2022 ©2022 The Author(s). Published by AI Publications. This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/4.0/) Abstract— Termites work together to modify their surroundings, which in turn influences their behaviour, leading to the building of termite mounds. The study was designed to assess diversity of termite mounds present in the Bangalore University Campus, Bengaluru, India. Observations were made on the occurrence, abundance, evenness and richness of the termite mounds. Mounds were surveyed by field survey and photographic interpretation method during July 2021 to June 2022. Totally 119 mounds were found, out of which 18 are ground level mounds, 42 small mounds, 37 medium mounds and 22 tall mounds. To test its effectiveness and to know about the influence of the mounds on the ecological well-being, termite mounds were identified, compared and interpreted using google earth map and the results were statistically verified. Keywords— Termites, Mounds, Diversity Index, Richness index and Evenness index. I. INTRODUCTION Termites being eusocial insects are spread widely in sub- tropics and tropics specially playing key role as decomposers and engineers of soil [13, 16]. Termite are having very soft cuticle, they do not sustain in cold regions, their nests are formed by uniform thermal envelope with very hard outer shell for protection from predators and desiccation [33]. Termites feed on various kinds of organic matter such as dead organic materials, wood, cardboard, paper etc [15]. Thus, they contribute much to nutrient cycle and community structuring in any ecosystem [32]. Along with ants and earthworms, the termites play a major role in increasing porosity of soil and creates tunnels which are called mounds. mounds are solid but porous walls made from soil and termite faeces acting as niche for various microorganisms and fauna providing protection against changing environment [10, 20, 27, 34]. The degree of termite contribution for the spatial heterogeneity in an ecosystem is attached with the mounds’ spatial distribution per unit area and its size and number. The spatial distribution of mounds is still the concept of debate as emphasized by findings from various ecosystems [5, 18, 19, 22, 30, 35]. Earlier studies of mounds are uneven, focusing on species classification [1] nest building and foraging activities [2] nutrient cycling [17] and termite- herbivore interactions [39]. However, understanding the spatial distribution of termite mounds can be a key component in predicting habitat utilisation and forage for herbivores [11, 12, 24]. Hence the present study was undertaken. II. METHODOLOGY The present study was carried out in Jnanabharathi campus (13º 05” N and 77º 34” E) at an altitude of 924 meters above the mean sea level with annual rainfall range of 530 mm to 1375 mm (mean 916 mm) spread to an area about 4.5 sq.km (1100 acres), situated on the elevated plateau at the western side of Bangalore, Karnataka, India. The study area is divided into site 1 (North) and site 2 (South) and is partially inhabited (Fig 1). The major part being un-inhabited, possesses wide range of vegetation from scrubby jungle, wild to cultivated trees with fauna such as insects, toads, reptiles, rodents and birds with a high population of termites and snakes.
  • 2. Kavyashree et al. International Journal of Forest, Animal and Fisheries Research (IJFAF) 6(4)-2022 Int. J. Forest Animal Fish. Res. www.aipublications.com/ijfaf Page | 10 Fig.1: Jnanabharathi campus - Study area (Google map). The mounds were identified and located in the study area using global positioning system (GPS) and photographic interpretation. Field survey was done during July 2021 to June 2022 for the spatial distribution of different sized mounds on google earth pro with GPS recordings of each mound and the same were photographed for further reference. Data comparison of the mounds between field reality and photography interpretation was performed by comparing the marked point corresponding to the location of mound identified in the field as well as in the image. Mounds were classified based on considering four standard heights, ground level mound (0 to 1 feet) (Fig 2A), small mound (1 to 3 feet) (Fig 2B), medium mound (3 to 7 feet) (Fig 2C) and tall mounds (7 feet and above) (Fig 2D). Fig.2: Mounds classification based standard heights The below mentioned statistical equations were used to compute the mounds’ diversity, richness and evenness in the study area [25]. Shannon -Wiener diversity index (H’) [36] was used to calculate mounds’ diversity index: 𝐻′ = − ∑(𝑃𝑖 ∗ 𝐿𝑛 (𝑃𝑖 )) 𝑠 𝑖=1 where Pi = S / N S = Number of individuals of one mound type N = Total number of all individuals in the sample Ln = Natural logarithm
  • 3. Kavyashree et al. International Journal of Forest, Animal and Fisheries Research (IJFAF) 6(4)-2022 Int. J. Forest Animal Fish. Res. www.aipublications.com/ijfaf Page | 11 Margalef’s species richness index (d') [21] was adopted to measure mounds’ richness index: d′ = (𝑆 − 1) 𝐿𝑛(𝑁) where S = Total number of mounds N = Total number of individuals in the sample Ln = Natural logarithm Pielou’s species evenness index (J’) [28] was used to analyse the mounds’ evenness index: J′ = 𝐻′ 𝐿𝑛(𝑆) where H' = Shannon -Wiener diversity index S = Total number of species in the sample Ln = Natural logarithm III. RESULTS AND DISCUSSION In the present study, out of a total of 119 mounds recorded (Fig 3), 18 (15%) are ground level mounds, 42 (35%) small mounds, 37 (31%) medium mounds and 22 (19%) tall mounds. Out of the 119 mounds identified, 48 (40.34%) mounds were at site 1(North) and 71 (59.66%) mounds were at site 2 (South). Site 1 with 48 mounds (Fig 6) had 6 (12.5%) ground level mounds, 12 (25.0%) small mounds, 18 (37.5%) medium sized mounds, 12 (25.0%) tall mounds (Fig 4) and Site 2 with 71 mounds (Fig 6) had 12 (25.0%) ground level mounds, 30 (62.5%) small mounds, 19 (39.6%) medium level and 10 (20.8%) large mounds (Fig 5). Significantly lower number of mounds were found in site 1 when compared to site 2, this could be attributed to the different human activities taking place decreasing the assemblage of the termite [9, 31]. Forest sites are routinely harvested to satisfy the diverse demands of the expanding human population. As a result, the physical complexity of these habitats is reduced, which lowers the variety and availability of ideal nesting and feeding sites and alters the microclimate. Termite microhabitats such as rotting tree stumps, dead logs, humus soil, etc., will frequently diminish from heavily populated areas. The succession of alates in creating new colonies is therefore thought to be reduced as a result of decreasing biodiversity brought on by human activity [7, 8, 14]. In addition to disrupting termites' natural adversaries, this change in microhabitat could make them pests rather than just a necessary component of the food chain. This is one of the main effects of this kind of habitat damage, both at micro and macro level. Despite agricultural intensification, which results in a trend that is less visible in forests, it is undoubtedly attributable to the establishment of numerous colonies [14]. Fig.3: Percentage of different sized mounds in the study site. Fig.4: Percentage of different sized mounds at site 1. Fig.5: Percentage of different sized mounds at site 2. Diversity index in site 1 and site 2 is found to be 1.32 and 1.29 respectively whereas the overall diversity index in the study area is 1.33. The mound diversity between the sites in the study area was not significantly different [26]. The result falls between 1.29 and 1.33. In comparison to site 2, diversity was generally greater at site 1 which had open spaces. This might be due to the denseness of the forest, 15% 35% 31% 19% Ground level Small Medium Large 12.5% 25.0% 37.5% 25.0% Ground level Small Medium Large 25.0% 62.5% 39.6% 20.8% Ground level Small Medium Large
  • 4. Kavyashree et al. International Journal of Forest, Animal and Fisheries Research (IJFAF) 6(4)-2022 Int. J. Forest Animal Fish. Res. www.aipublications.com/ijfaf Page | 12 which made sampling challenging, or the ecosystem's potential control over the termite population. This might be explained by the fact that these locations are found in a less dry region with moderate rainfall. Resources and microclimate conditions may not be a constraint to termite variety in such a setting [31]. The high diversity in site 1 could be due to availability of higher resources from human made structures and decreased number of predators. Fig.6: Total number of different sized mounds in the study site. Richness index assessed at site 1 is 11.37, out of which 1.29 ground level mounds, 2.84 small mounds, 4.39 medium mounds and 2.84 tall mounds, while site 2 has richness index of 15.72 of which 2.58 ground level mounds, 6.80 small mounds, 4.22 medium mounds and 2.11 tall mounds. Over all the richness index of the study area is 24.06, out of which 3.56 ground level mounds, 8.58 small mounds, 7.53 medium mounds and 4.39 tall mounds. The existence or absence of a species in an ecological niche, as well as the richness or abundance there, are indicators of the ecosystem's biological and ecological diversity. Termites are not an exception to this criterion. We may also infer from this study that where there is substantial human activity, termite variety is more abundant, this might be caused by sufficient resources being available and a drop in natural predators and biodiversity is lost only in areas of high human interference. The information at hand also points to human meddling as the cause of the sparse vegetation in the site 1 area, which has diminished natural termite control. Because there are fewer natural nutrients available and predators, termites will infest man-made structures. Due to the destruction of microhabitat, termite biomass and richness are reduced. Due to the minimal level of human influence in the site 2 area, termite biomass and richness are controlled by nature [31]. Evenness index estimated at site 1 is 0.953, site 2 is 0.933 and for the overall study area it is measured to be 0.958. The resource ratio theory, according to Tilman [37, 38], predicts that more species will coexist at low resource levels because individuals perceive the environment as being more spatially diverse, which results in more niches and higher species evenness. Several elements, including fire [6, 7], rainfall [3, 4] and temperature are known to affect the richness, diversity, and evenness of mounds [23, 29]. The loss in mound diversity on this environment is further exacerbated by the absence of soil feeders. Therefore, geology could have an indirect effect on the diversity through soil conditions. IV. CONCLUSION The diversity of mound is subjected to change in the pattern of ecosystem, such study would help in understanding the ecological well-being. The kind of species, ecological conditions, clay availability and the degree of termite disturbance in the environment shall influence the morphological variations. Soil nutrients build up in termite mounds and their turnover becomes an essential part to the ecosystem. The present study provides a baseline data on the diversity and spatial distribution of the mounds and helps in taking up mitigation measures to conserve such areas. Isolating the year effect, as discussed in the methodological parts of the article, could help uncover anthropogenic effects on termite presence across time when employing termite mounds as anthropogenic bio-indicators. REFERENCES [1] Ahmed (Shiday) B M, Sileshi G W, French J R J, Nkunika P O, Nyeko P and Jain S. 2011. Potential Impact of Climate Change on Termite Distribution in Africa. Br. J. Environ. Clim. Chang. 1, 172–189. [2] Dangerfield J M and Schuurman G. 2000. Foraging by fungus-growing termites (Isoptera: Termitidae, Macrotermitinae) in the Okavango Delta, Botswana 717–731. [3] Davies A B, Eggleton P, van Rensburg B J and Parr C L. 2013. Assessing the Relative Efficiency of Termite Sampling Methods along a Rainfall Gradient in African Savannas. Biotropica. 45, 474–479. [4] Davies A B, Eggleton P, van Rensburg B J and Parr C L. 2015. Seasonal activity patterns of African savanna termites vary across a rainfall gradient. Insectes Soc. 62, 157–165. [5] Davies A B, Levick S R, Asner G P, Robertson M P, van Rensburg B J and Parr C L. 2014. Spatial variability and abiotic determinants of termite mounds throughout a savanna catchment. Ecography 37, 852–862. [6] Davies AB, Eggleton P, Van Rensburg B J and Parr C L. 2012. The pyrodiversity-biodiversity hypothesis: A test with savanna termite assemblages. J. Appl. Ecol. 49, 422–430. [7] Dosso K, Konate S, Aidara D and Linsenmair K E. 2010. Termite diversity and abundance across fire- induced habitat 0 3 6 9 12 15 18 21 24 27 30 Site 1 Site 2 Ground level Small Medium Large
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