Research Article (Open access) |
---|
SSR
Inst. Int. J. Life Sci., 7(6): 2921-2930, November 2021
Study of External
Nest Appearances and Foraging Behavior
of Tetragonula nr. pagdeni
Manjunatha
Basanna1*, Magdaline Christina Rajanand2
1Assistant
Professor, Department of Zoology, Government Science College (Autonomous),
Bengaluru, Karnataka, India
2Student,
Department of Post Graduate Studies in Zoology, Government Science College
(Autonomous), Bengaluru, Karnataka, India
*Address for Correspondence: Mr. Manjunatha Basanna, Assistant professor, Department of Zoology,
Government Science College (Autonomous), Bengaluru Karnataka, India
E-mail: manjunatha.b01@gmail.com
ABSTRACT-
Background: The eusocial stingless
bees (family Apidae: dammer bees) are found everywhere. They exhibit different
nesting habits and also diverse habitat preferences. The nest entrance plays a
very important role towards nest characters. The nest entrance prevents
airstreams but allows slow gas exchange.
Methods: A
study was conducted to elucidate data on the nesting sites, external nest
characteristics, foraging behaviour
at three selected study areas, pollen sources and identification and determination of the percentage of
drone bees of T nr. pagdeni at Bengaluru during
the months of summer in the year 2019.
The selected three study areas are Campus of the University of Agricultural
Science (GKVK), Government Science College and DGQA Residential Complex (CQAL campus).
Results:
Of
the 28 stingless bee nests, twenty were found in stone walls at a mean height of 1537.7 mm from the
ground. The entrance of the colony was either made of mud or a waxy dark coloured substance called resin. The most
preferred substance used for building the
entrance tube was found to be resin. The activity of foragers was observed from
7:00 hours to 17:00 hours at GKVK, Bengaluru.
The highest activity was observed at 1100 hours (37.38 bees per 5 mins).
Conclusion:
Study area has given the relevance of ecologically
sustainable, economically viable scope as it interlinks the conservation of
plant species for the continuity of the generations of stingless bees. Knowledge of bee flora vis-à-vis bee diet is
essential for sustainable meliponiculture, management, and proper
conservation strategies for a sustainable livelihood in our
region.
Key-words- Foraging, Stingless bee, Sustainable livelihood,
Tetragonula
INTRODUCTION-
The
eusocial stingless bees (family Apidae: dammer bees) are found everywhere.
Their size can range from 2 to 16 mm. Tetragonula is a genus of
stingless bees. There are more than 500 species worldwide [1,2]
and nine have been reported from India [3].
They are Lepidotrigona arcifera [4] Lisotrigona
cacciae [5], L. mohandasi [6], Tetragonula aff. laeviceps
(Smith), T. bengalensis [7],
T. gressitti [8],
T. iridipennis [9],
T. ruficornis [10]
and T. fuscobalteata Cameron [7].
The stingless bees visit the male flowers as well as female flowers [11].
The Colonies are perennial and societal
structure is also interesting [12].
Different stingless
bee species nest in various cavities in the trees. A
few species live in termite nests. Stingless bees collect several
types of material on their foraging
flights [2]. Their nests are usually not seen
easily, but their service as pollinators is appreciated in the scientific
community. Honey also possesses medicinal values.
Stingless bees are mainly associated with tropical
dry and humid forests, in low and warm lands [13], but the
metropolitan cities have made the situation worst by polluting the environment.
There are reports of declining populations of honey bees including the
stingless bees due to the heavy traffic,
which has contributed to decreased air quality.
Man has been spraying a large number of highly poisonous
pesticides in the environment and on crops which
removes stingless bees or due to this. The food sources of these
tiny creatures get poisoned [14]. The talk is to conserve
ecologically relevant animal species whose real role in the future of humankind
is immense [15]. Natural calamities such as epidemics may end the
human population as we are witnessing in this Covid-19 daunted situation
everywhere. Similarly, the animals may be deprived of the essential food
sources in the future if important insect pollinators of the crops are
destructed due to the tremendous non-degradable pesticide use. In this regard,
we planned to explore eco-behavioural aspects of T. nr. pagdeni,
in three regions of Bengaluru. Thus, preliminary information about this
stingless bee could be assessed in these surroundings.
MATERIALS AND METHODS-
This study was conducted to elucidate data on the nesting sites, external nest
characteristics, foraging behaviour
at three selected study areas, pollen sources and identification and determination of the percentage of
drone bees of T. nr. pagdeni at Bengaluru, Karnataka, India, during
the months of summer in the year 2019.
The selected three study areas are Campus of University of Agricultural Science (GKVK),
Government Science College
and DGQA Residential Complex (CQAL campus).
Study
area- The study was conducted at three different areas in Bengaluru each distanced 8 km apart from the other.
Fig. 1: Satellite view of study area
around the Department of Apiculture, University of Agricultural Science (GKVK),
Hebbal, Bengaluru (Source: Google maps,
Internet)
Fig. 2: Satellite view of the study area
near Biotechnology department, Government Science College (Autonomous),
Nrupathunga road, Bengaluru (Source: Google maps,
Internet)
Fig. 3: Satellite view of study area
around DGQA Residential Complex, Gunata Vihar, CQAL Campus, J.C. Nagar,
Bengaluru (Source: Google maps,
Internet)
RESULTS- Investigations have been carried
out on stingless bee Tetragonula
nr. pagdeni around Bengaluru. The
results are enumerated in this chapter.
Nesting sites and external
nest characteristics- 28 stingless bee colonies have been
studied for nesting sites and external nest characteristics in the selected
study sites in Bengaluru. To analyze the nesting habitats of stingless bee Tetragonula
nr. pagdeni, 28 colonies were studied (Table 1). Of the 28 stingless bee nests, twenty were found in stone
walls at a mean height of 1537.7 mm
from the ground. Five colonies were seen nesting
in materials made out of metals at a mean height of 1446.0 mm. Other nesting places were cement walls,
PVC pipes and tree cavities where one colony
in each of them was found. Among nesting sites,
stone walls were found to be the most preferred
nesting place or site for Tetragonula nr. pagdeni.
At one study area, seven colonies
were found to be aggregated in a single stone wall (at Government Science College, Bengaluru).
The
entrance of the colony was either made of mud or a waxy dark coloured substance called resin. The most
preferred substance used for building the
entrance tube was found to be resin. In three colonies nested in metal poles or metal doors, the entrance
tube was not distinct. In those colonies which had an entrance tube, the length of the entrance tube of colonies nested in stone walls ranged from
17.52 mm to 24.18 mm with a mean length of 20.85
mm while the width ranged
from 8.28 mm to 7.22 mm
with a mean width of 7.75 mm. Similarly, the length of the entrance tube of colonies nested in metal frames
ranged from 1.95 mm to 9.25 mm with a
mean of 5.6 mm and the width ranged from 3.27 mm to 4.73 mm with a mean of 4.0 mm. The dimensions of
the entrance tube of the colonies nested in other sites are presented in Table 1.
Table 1: Nesting sites
of Stingless bee, Tetragonula nr. pagdeni in Bengaluru
Nesting places |
Number of colonies observed |
Height from the ground (mm) |
Entrance tube dimensions |
|
Width (mm) |
Length (mm) |
|||
Stone wall |
20 |
1537.70±205.60 |
7.75±0.53 |
20.85±3.33 |
Metal material |
5 |
1446.00±228.07 |
4.00±0.73 |
5.60±3.65 |
Cement
wall |
1 |
7500.00 |
6.00 |
5.00 |
PVC
pipe |
1 |
2700.00 |
6.00 |
12.00 |
Tree
cavity |
1 |
690.00 |
9.00 |
23.00 |
Fig. 4: Nesting elevation of T. nr. pagdeni colonies at different nesting
sites
According
to the graph (Nesting sites vs Height
from the ground level in millimeters),
the highest nesting elevation from the ground was recorded in the colony found in the cement wall (7500 mm),
followed by that of the PVC pipes (2700
mm). The least nesting elevation from the ground was recorded in that of the tree cavities
(690 mm).
Table 2: Activity of
outgoing foragers at GKVK Bengaluru
Months/
Hours |
Mean
number of bees/ 5 minutes/ colony |
Mean |
|||||
700 |
900 |
1100 |
1300 |
1500 |
1700 |
||
March |
6.20 |
25.02 |
40.37 |
39.20 |
22.53 |
8.46 |
23.63 |
April |
5.48 |
13.10 |
34.80 |
27.75 |
20.85 |
8.90 |
18.48 |
May |
5.40 |
12.70 |
32.17 |
27.79 |
21.13 |
6.63 |
17.64 |
Mean |
5.70 |
16.94 |
35.78 |
31.58 |
21.50 |
7.99 |
|
Observations
were made on the activity of foragers from 0700 hours to 1700 hours at GKVK,
Bengaluru. The lowest number of outgoing bees was observed
in the morning at 0700 hours with 5.70 bees per
5 mins and evening at 1700 hours with
7.99 bees per 5 mins.
The
activity was at its peak at 1100 hrs with 35.78 bees per 5 mins. While examining the foraging activity
month by month, the highest activity was seen
in March with 23.63 bees per 5 mins, which declined to 18.48 bees per
5 mins during April which further declined to 17.64 bees
per 5 mins during May.
Table 3: Activity of
Incoming foragers without pollen load at GKVK, Bengaluru
Months/
Hours |
Mean
number of bees/ 5 minutes/ colony |
Mean |
|||||
700 |
900 |
1100 |
1300 |
1500 |
1700 |
||
March |
5.20 |
21.65 |
37.90 |
28.75 |
22.90 |
6.90 |
20.55 |
April |
3.40 |
10.93 |
24.90 |
17.78 |
16.95 |
9.07 |
13.84 |
May |
2.19 |
5.82 |
13.17 |
16.18 |
17.04 |
9.43 |
10.64 |
Mean |
3.59 |
12.80 |
25.32 |
20.90 |
18.96 |
8.46 |
|
The
activity of foragers was observed from 0700 hours to 1700 hours at GKVK,
Bengaluru. The number of bees without
pollen load was the lowest (3.59 bees per 5 mins) at 0700 hours. The significant heightened activity
was recorded at 1100
hours (25.32 bees per 5 mins).
However, at 1700 hours, the activity decreased to the level of 8.46 bees per 5
mins. When foraging activity was reviewed
every month, higher activity was noticed in March with 20.55 bees per 5 mins
and a gradual decline in May with the lowest number of bees without pollen load
(10.64 bees per 5 mins).
Table 4: Activity of
Incoming foragers with pollen load at GKVK, Bengaluru
Months/ Hours |
Mean
number of bees/ 5 minutes/ colony |
Mean |
|||||
700 |
900 |
1100 |
1300 |
1500 |
1700 |
||
March |
2.82 |
5.10 |
11.80 |
11.17 |
5.30 |
2.37 |
6.43 |
April |
1.82 |
4.72 |
10.70 |
10.31 |
4.48 |
2.47 |
5.75 |
May |
1.52 |
4.76 |
9.05 |
9.01 |
4.12 |
2.19 |
5.11 |
Mean |
2.05 |
4.86 |
10.51 |
10.16 |
4.63 |
2.34 |
|
Observations
were made on the activity of foragers from 700 hours to 1700 hours at GKVK,
Bengaluru (Table 4). The least number of bees with pollen (2.05 bees per
5 mins) was noticed at 0700 hours.
The activity gradually increased,
peaking at 10.51 bees per 5 minutes at 1100 hours. Subsequently, the foragers
gradually decreased to 2.34 bees
per 5mins at 1700 hours by the end of the day. When the activity
of foragers was pooled month by month, maximum activity was recorded in March
(6.43 bees per 5 mins) which reached
a minimum of 5.75 to 5.11 bees per 5 mins from April to May.
Fig. 5: Foraging activity of T nr.
pagdeni during the months of summer at different intervals of time at GKVK,
Bengaluru
Table 5: Activity of
Outgoing foragers at Government Science College, Bangalore
Months/
Hours |
Mean number of bees/
5 minutes/ colony |
Mean |
|||||
700 |
900 |
1100 |
1300 |
1500 |
1700 |
||
March |
6.55 |
29.25 |
43.17 |
40.62 |
24.25 |
9.02 |
25.48 |
April |
6.10 |
13.44 |
35.82 |
28.75 |
21.93 |
9.18 |
19.20 |
May |
5.97 |
13.23 |
33.16 |
28.76 |
21.70 |
7.30 |
18.35 |
Mean |
6.21 |
18.64 |
37.38 |
32.71 |
22.63 |
8.50 |
|
The
activity of foragers was recorded at Government Science College, Bengaluru,
from 0700 hours to 1700 hours. The number
of bees leaving their respective nests was the lowest in the morning at 0700
hours with 6.21 bees per 5 mins and in the evening at 1700 hours with 8.50 bees per 5 mins.
The
highest activity was observed at 1100 hours (37.38 bees per 5 mins). When the activity of foragers was analyzed
month-wise, the highest activity was recorded in March with 25.48 bees per
5mins, which reduced to 19.20 bees per 5 mins
in April which further reduced to 18.35 bees per 5mins in May.
Table 6: Activity of
Incoming foragers without pollen load at Government Science College, Bengaluru
Months/
Hours |
Mean
number of bees/ 5 minutes/ colony |
Mean |
|||||
|
0700 |
0900 |
1100 |
1300 |
1500 |
1700 |
|
March |
5.85 |
22.36 |
39.85 |
29.49 |
24.08 |
7.05 |
21.45 |
April |
4.07 |
11.78 |
26.19 |
19.17 |
17.20 |
9.60 |
14.67 |
May |
2.75 |
6.15 |
13.68 |
16.56 |
17.88 |
9.83 |
11.14 |
Mean |
4.22 |
13.43 |
26.57 |
21.74 |
19.72 |
8.83 |
|
The following are the observations made on the activity
of foragers at Government Science College, Bengaluru from 0700 to 1700 hours.
The least number of incoming bees without pollen load (4.22 bees per 5 mins) was recorded at 0700 hrs.
A markedly increased activity of 26.57 bees
per 5 mins was recorded at 1100 hrs. Nevertheless, the activity reduced
significantly to the level of 8.83
bees per 5 mins at 1700 hours. When the activity of foragers was studied
month-wise, the activity was at
its peak in March with 21.45 bees/ 5 mins, which gradually decreased to 11.14
bees per 5 mins during
May.
Table 7: Activity of
Incoming foragers with pollen load at Government Science College, Bengaluru
Months/ Hours |
Mean number of bees/
5 minutes/ colony |
Mean |
|||||
|
0700 |
0900 |
1100 |
1300 |
1500 |
1700 |
|
March |
2.83 |
5.77 |
13.33 |
13.19 |
6.35 |
3.45 |
7.48 |
April |
2.25 |
5.37 |
11.10 |
10.68 |
4.70 |
2.45 |
6.09 |
May |
1.58 |
4.97 |
9.30 |
9.24 |
4.98 |
2.61 |
5.45 |
Mean |
2.22 |
5.37 |
11.24 |
11.04 |
5.34 |
2.83 |
|
The activity of foragers returning to their
respective nests with pollen load was recorded
from 0700 hours to 1700 hours at Government Science College, Bengaluru (Table 7). The least number of bees with pollen was recorded (2.22 bees per 5
mins) at 0700 hrs. The activity was highest at 1100 hours with 11.24 bees per 5
mins. However, there was a steep
decline in the activity at 1700 hours (2.83 bees per 5 mins).
While
examining the activity of foragers month by month, it was found that extreme
activity was noticed during March (7.48 bees per 5 mins) and the lowest
activity (5.45 bees per 5 mins) was recorded during May.
Fig. 6: Foraging activity of T. nr. pagdeni during the months of summer
at different intervals of time at
Government Science College,
Bengaluru
DISCUSSION-
There can be seen a slight increase in the foraging activity of the bees at Government Science College, Bengaluru
compared to that of GKVK, Bengaluru. Hence, foraging
activity of T. nr.
pagdeni at Government Science
College, Bengaluru is
comparatively higher than that of GKVK, Bengaluru. The graph 5 was a plot of number of foragers (X-axis)
against the mean of the types of foragers at
different months of summer (Y-axis)
irrespective of the time of
foraging.
Unlike
Apis dorsata and Apis florea that construct their nests in open
places [17], stingless bees prefer closed
structures [18] to construct their nests. The
nests of T. nr. Pagdeni were found in
the cavities of hollow trees, mud walls, cement walls, stone walls, crevices of
metal doors and electrical metal
pipes in the three areas studied in Bengaluru. Similar observations were
reported by Gajanan et al. [19]; Danaraddi et al. [20] and Vijayakumar et
al. [21].
While reporting on the stingless bees of Bhutan, Nidup
mentioned that T.
gressit do not make any nest entrance like L. arcifera; however, it coats the nest tunnel with yellowish
substances (likely resin or resin mixed with wax) [22]. The mean length, mean width of the entrance tube of
nests found in stone walls and tree cavities measured 20.85 mm, 7.75 mm and
23.00 mm, 9.00 mm respectively (Table 1). Thangjam
et al.
[23] reported similar findings in 2005. At
Bankura, the tree nested colonies had a mean entrance tube length of 3.5 mm ranging
from 3-4 mm and the width of the entrance tube. Each species prefers to build
entrance tubes of differing lengths which may depend on the type of nesting
site. In Sulawesi (Indonesia), high variations in the type of entrance opening
(irregular, round, oval, ellipse, and triangle) and three different brood cells
arrangements (semi-cluster, cluster, and semi-comb) for Tetragonula sapiens has
been reported. In addition, the nest structure of the endemic stingless bee W. incisa, which had a slit longitudinal
entrance with lamellate pillar structures in a 2 m cavity of a tree trunk.
Many
different types of plant resources are searched to meet the required food
resources for a variety of functions to be executed. The pollen supplies
protein to the larvae stingless bees differ somewhat from honey bees in those
non-floral resources (e.g. resinous materials, fruit juice and carrion also
account for a significant proportion of foraging trips [24].
Significant variations were observed in the foraging behavior of T nr. pagdeni during different
times of the day and the dynamics of activity were similar in the two study
areas selected (Table 2 to 7). The
lowest activity of the foragers was observed during the beginning of the day
(700 hours), which gradually rose to attain a peak at 1100 and 1300 hours
following which a significant drop in the activity was noticed at 1700 hours (Graph
3 and 4). The exact reason for this behaviour can not be elucidated.
The queen loss changes behaviour and increases
longevity in a stingless bee of a particular type [25].
The
study was conducted in the months of summer. The highest activity of foragers leaving their nests and returning
to their nests with and without pollen load was recorded in March. Two significant peaks of outgoing foragers at
1200 to 1300 hours and 1600 to 1700 hours; and of pollen foragers at 1000 to
1100 hours and 1300 to 1400 hours were recorded respectively by Roopa [26]
in Bengaluru. The difference in colony conditions, climatic factors and
foraging sources can be the possible reasons for the variations found in the
present study.
Also, the foraging activity
was found to be comparatively higher at Government Science College, Bengaluru than
that found at GKVK, Bengaluru. This can
be attributed predominantly to the occurrence of deforestation at a slower rate in GKVK, Bengaluru which can be the
most possible reason for comparatively decreased
foraging activity of these bees at GKVK, Bengaluru than Government Science
College, Bengaluru. Also, at the Government Science College campus the range of foraging
areas is less as the pollen and nectar sources
are near the nesting site.
This can be one of the causes for the increased foraging behaviour of these bees when compared to that of
GKVK, Bengaluru. Some new
insights were reported about foraging by stingless bees like drinking tear and sweat [27].
CONCLUSIONS-
T. nr.
pagdeni nested in the walls of stones
and cement, Metal door frames and lamp
posts, PVC pipe and tree cavities at Bengaluru. The nest entrance plays a very
important role towards nest characters. The nest entrance
prevents airstreams but allows slow gas exchange.
The nest entrance revealed that bees prefer nest
opening of smaller size over the medium and larger
opening. The
stingless bee identification is now also done through the help of
biotechnology- DNA barcoding. The
ecologically sustainable, economically viable plants if potted, the
stingless bees may try to populate in the diverse habitats even in the urban
areas.
In the future, meliponiculture
can be planned in the cities by knowing the specific stingless bees abounding
in that locality. This can give the added avenue for the income generations as
the honey of the stingless bee is in great demand in the market.
CONTRIBUTION OF AUTHORS
Research
concept- Manjunatha B
Research
design- Manjunatha B and Magdaline Christina R
Supervision-
Manjunatha
B
Materials-
Manjunatha
B and Magdaline Christina R
Data collection- Magdaline
Christina R
Data analysis and Interpretation- Magdaline Christina R
Literature search- Magdaline
Christina R
Writing article- Manjunatha
B
Critical review- Manjunatha
B
Article editing- Manjunatha
B
Final approval- Manjunatha
B
REFERENCES
1.
Oliveira RC, Contrera
FA , Arruda H , Jaffe R, Costa L, et al.
Foraging and Drifting Patterns of the Highly Eusocial Neotropical Stingless Bee
Melipona fasciculata Assessed by
Radio-Frequency Identification tags. Front
Ecol Evol., 2021; 517.
2.
Choudhary A, Singh
J,Chhuneja PK. Nest Architecture and Nesting Site Preference of Smith in
North-Western Plains of India. J Apic Sci., 2021; 65 (1): 49-59.
3.
Singh HK,Chauhan A.
Beekeeping in Nagaland with Stingless Bees: Present and Future. Rassa
J Sci Soc., 2020; 2(1): 41-45.
4.
Bui M, Singh HK,
Aleminla AO, Chauhan A, Behere GT. Diagnostics of wild stingless bees from
northeast India. Indian J Entomol.,2020; 82(2): 337-42.
5.
Thangjam R, Rao S,
Viraktamath S, Devarishi Sharma L. First report of drinking tear and sweat by Lisotrigona
bees (Apidae: Meliponini) from India. J Apic Res., 2021; pp. 1-3.
6.
Prakash AS, Jobiraj T,
Bijoy CA. Checklist of bees (Insecta: Hymenoptera: Apoidea) of Kerala.
Entomon., 2021; 45(3): 189-200.
7.
Kunal G, Das R,
Nagulapalli SL, Layek A, Jha S. Nesting habitat and comb geometry of stingless
bee Tetragonula bengalensis Cameron in west Bengal. Ind J Entomol., 2020;
82(3): 445-51.
8.
Chauhan
A, Singh HK. Nest architecture of stingless bee Tetragonula gressitti Sakagami from Nagaland India. International Journal of Tropical
Insect Scienc., 2021; 22: 1-6
9.
Tej MK, Srinivasan MR
,Vijayakumar K, Natarajan N, Kumar SM.
Morphometry Analysis of Stingless Bee
Tetragonula iridipennis Smith (1854). Int J Curr Microbiol App Sci., 2017; 6 (10):
2963-70.
10. Shanas S, Faseeh P. A new subgenus and three new species of
stingless bees (Hymenoptera: Apidae: Apinae: Meliponini) from India. Entomon.,
2019; 44(1): 33-48.
11.
Krishna
S, Somanathan H. Intersexual mimicry and flowering phenology facilitate pollination
in a dioecious habitat specialist species, Myristica fatua (Myristicaceae).
Plant Ecol., 2018; 219(10): 1247-57.
12.
Bhatta CP, Gonzalez VH,
MayesD, Simões M, Smith DR. Nesting biology and niche modelling of Tetragonula
iridipennis (Smith) (Hymenoptera: Apidae (Meliponini) in Nepal. J Apic Res.,
2019; 58 (4): 501-11.
13.
Reyes-González
A, Camou-Guerrero A, Reyes-Salas O, Argueta A, Casas A. Diversity, local
knowledge and use of stingless bees (Apidae: Meliponini) in the municipality of
Nocupétaro, Michoacan, Mexico. J Ethnobiol Ethnomed., 2014; 10(1): 1-2.
14.
Cham
KO, Nocelli RC, Borges LO, Viana-Silva FE, Tonelli CA, et al. Pesticide
exposure assessment paradigm for stingless bees. Environ entomol., 2019; 48(1):
36-48.
15.
Kopnina HN. Half the
earth for people (or more)? Addressing ethical questions in conservation. Biol
Conserv., 2016; 203: 176-85.
16. Erdtman
G. The acetolysis method: a revised description. Svensk Bot. Tidskr, 1960; 54:
561- 64.
17. Young AM,
Kodabalagi S, Brockmann A, Dyer FC. A hard day’s night: Patterns in the diurnal
and nocturnal foraging behavior of Apis dorsata across lunar cycles and
seasons. PloS one., 2021; 16(10): e0258604.
18. Li YR,
Wang ZW, Yu ZR, Corlett RT. Species diversity, morphometrics, and nesting
biology of Chinese stingless bees (Hymenoptera, Apidae, Meliponini). Api.,
2021; pp. 1-7.
19. Gajanan S,
Mohite GC, Kuberappa GC, Kencharaddi RN. The nest architecture of stingless
bee, Trigona iridipennis. Indian Bee
J., 2005; 67(1&2): 36-40.
20. Danaraddi CS,
Manjunath T, Sangamesha H, Biradar SB, Satyareddi SA. Nesting habits and nest
structure of stingless bee, Trigona
iridipennis Smith at Dharwad, Karnataka. Int J Plant Prot., 2012; 5 (1):
96-98.
21. Vijayakumar
K, Jeyaraaj R. Taxonomic notes on Tetragonula pagdeni Schwarz (Apidae:
Meliponini) from India. Int J Adv Life Sci., 2020.
22. Nidup T.
Report on the stingless bees of Bhutan (Hymenoptera: Apidae: Meliponini). J
Threatened Taxa, 2021; 13(5): 18344-48.
23. Thangjam
R, Rao S, Viraktamath S, Devarishi SL. First report of drinking tear and sweat
by Lisotrigona bees (Apidae: Meliponini) from India. J Api Res., 2021; pp. 1-3.
24. Sayusti T,
Raffiudin R, Kahono S, Nagir T. Stingless bees (Hymenoptera: Apidae) in South
and West Sulawesi, Indonesia: morphology, nest structure, and molecular
characteristics. J Api Res., 2021; 60(1): 143-56.
25. Lopes BD,
Campbell AJ, Contrera FA. Queen loss
changes behavior and increases longevity in a stingless bee. Behavioral Ecol
Sociobiol., 2020; 74(3): 1-9.
26. Roopa CA.
Bioecology of stingless bees, Trigona iridipennis Smith, M. Sc. (Ag.) Thesis,
University of Agricultural Sciences, GKVK, Bangalore, Karnataka (India), 2002.
27. Trinkl M,
Kaluza BF, Wallace H, Heard TA, Keller A, et al. Floral species richness
correlates with changes in the nutritional quality of larval diets in a
stingless bee. Insects, 2020; 11(2): 125. doi: 10.3390/insects11020125.