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Available Online at www.ijpba.info
International Journal of Pharmaceutical  Biological Archives 2018; 9(4):255-259
ISSN 2581 – 4303
RESEARCH ARTICLE
Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery
Delta Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India
K. Karunakaran*, Paul Jeevanandham
Department of Zoology, T.B.M.L. College, Porayar, Tamil Nadu, India
Received: 15 September 2018; Revised: 10 October 2018; Accepted: 05 November 2018
ABSTRACT
Amphibian is one of the important ecosystem component, both the ecologically and economically. In
the present study, we intended to analyze the population density based on the temperature in different
months during the year 2016–2017. The data were collected by visual encounter survey method ,and
amphibians were recorded in all 12 months from the study area for 2 years. The monthly variation habitat
temperature was recorded in 2016–2017 using analysis of variance. In different habitat (cultivable,
non-cultivable, pond, and grassland) temperature, the population was maximum at pond followed by
grassland, agriculture, and non-cultivable. The maximum temperature was found in July with 74 numbers
of species which were identified during 2016. Were recorded high number (1600) frog were recorded
in pond 28°C during samba season followed by Thaladi and Kuruvai. Based on this study, we conclude
that the population density may increase and decrease based on the temperature in all the three seasons
with four microhabitats.
Keywords: Anuran, population agroecosystem Cauvery delta region, tranquebar
INTRODUCTION
The physiology of amphibian has received much
attention than that of other vertebrates. The first
investigations of the influence of temperature
during activity have been made only recently.[1,2]
1965 further, amphibians are active even at low
body temperatures.[3]
To investigate the patterns
of anaerobiosis in amphibians, lactate production
was measured during maximal enforced activity
at different temperatures an ecologically
and phylogenetically diverse assemblage of
urodeles and anurans was examined. In South
India, agricultural lands are a complex mixture
of different habitats, namely cultivated, non–
cultivated, pond, grassland, agriculture fields,
and paddy fields, comprising many small pieces
of land owned by different farmers and with
each piece subjected to different methods of
cultivation.As a result, when farmer uses different
agrochemicals, the total habitat gets contaminated
with a mixture of agrochemicals.[4-7]
Agrochemical
contaminants can affect amphibians either by
destroying biodiversity at lower trophic levels
followed by effect at higher trophic levels.[8,9]
Hope to understand further the behavioral and
neuromuscular changes that have accompanied
the evolution of a highly protrusible tongue. In
addition, if frog modulates its feeding behavior
in response to differences in prey type, this
study will be the first to document this ability
among amphibians and the feeding behavior of
anurans also has been considered to be highly
stereotyped.[10,11]
The stereotype of feeding
behavior found in anurans has been attributed
to a limited range of fixed action patterns and
to the animal’s behavioral simplicity.[10]
In
Western Ghats, many amphibians are living and
breeding in shallow waters of rice paddy fields.
In general, their breeding period coincides with
the application of agrochemicals, including
pesticides and fertilizers,[12,13]
Earlier studies have
revealed elevated frequencies of morphological
abnormalities (3.97%) in Fejervarya limnocharis
from rice paddy fields.[14]
Although the Western
Ghats has a diverse amphibian fauna,[15]
few
toxicological studies are available,[16,7]
focusing
on effects of individual or combinations of
agrochemicals on larvae of amphibians.[17]
Recorded 12 species of amphibian in and around
*Corresponding Author:
K. Karunakaran
E-mail: karunaherb@gmail.com
Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta
Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India
IJPBA/Oct-Dec-2018/Vol 9/Issue 4 256
Agarakeerangudi village, Mayiladuthurai taluk
of Nagapattinam district. Freshwater mussels
play a number of important roles in aquatic
ecosystems. As sedentary suspension feeders,
unionoids remove a variety of materials from
the water column, including sediment, organic
matter, bacteria, and phytoplankton.[18]
However,
the effects of agrochemicals on amphibian health
status at field conditions are largely unknown.
Hence, for the 1st
time, we evaluated the anuran
population.
Tropical and monsoonal climates are
characteristics of the study region. The monthly
average temperature is generally low at the
beginning of the year. In the study area, the
temperature reaches 38°C and the minimum
touches even 19.30°C, in January and February
months which are very pleasant with warm days
and cool nights. Heat becomes intense inApril and
increases in May-June and comes down gradually
in June-July when the southwest monsoon sets on.
Very mild winter falls in December and January.
Data on soil temperature are lacking and are
computed by deducting 50°C from atmospheric
temperature. Plant growth as well as chemical and
various biological activities in the soil is greatly
influenced by temperature.
Temperature is an important parameter,
determining the climatic condition of any
region. The climatic condition determines the
agricultural pattern, lifestyle of people, and the
socioeconomic conditions. The Cauvery delta
region of Tranquebar taluk, Nagapattinam district,
falls under the tropical region, so the temperature
here is normally high. Monthly mean temperature
is calculated from the daily temperature observed
from 2016 to 2017 which varies seasonally.
Temperature is very high during the summer
season, low in the winter season, and moderate
during other months.
MATERIALS AND METHODS
Study area
The present study was carried out at 12 places in
Tranquebar taluk, Nagapattinam district, Tamil
Nadu. The study was carried out for 2 years from
January 2016 to December 2017. The study area
is comprised of dry deciduous, grassland rocky
scrub jungle, and agricultural landscapes.
Geographical landscape of tranqubar
Thestudyarea[Figure1]islocatedintheTranqubar
taluk, Nagapattinam district, which lies on the
middle of the coromandel coast. The district lies
between 10°25’ and 11°40’ North Longitude and
76°49’ and 80°01’ East latitude of Tamil Nadu,
India. The Nagapattinam district lies on the shores
of the Bay of Bengal between latitude 10.7906°N
and Longitude 79.8428°E an area of 2715 sq. km
(1048 sq. mi.). The district capital, Nagapattinam,
lies on the eastern coast, 350 km down south of
the state capital Chennai.
Theamphibiansinallthehabitats,suchascultivable,
non-cultivable, pond, dry pond, and grassland,
were studied, and the data collections were done
during morning hours (6.00 am to 12.30 pm).
During the survey periods, parameters such as
population, microhabitat, and water distance from
each species sightings, vegetation type, and soil
types have also been recorded. The four habitats
were classified into two categories, namely
agricultural and non-agricultural areas. The
species were identified using pictorial guides.
Visual encounter survey (VES) method
The selected village ponds were regularly
monitored for diversity and density of amphibian
population, activity, and temperature of the
study area. The area was walked thoroughly
for amphibians. Time-constrained VES method
involves a systematic search of an area or
habitat for a prescribed time.[19]
VES was used as
formalized by Crump and Scott.[20]
The aim of this
study was to maximize the species inventory.
Figure 1: The study area
Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta
Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India
IJPBA/Oct-Dec-2018/Vol 9/Issue 4 257
RESULTS AND DISCUSSION
Amphibian activity observed during this study
revealed the response of the amphibians to their
environmental climate. A total of 9 species of
anurans were recorded [Table 1] during the year
2016.Thetemperaturewasfoundtobehigherinthe
monthofJuly(temp0C±)thatisminimum27°Cand
maximum temperature 31°C (mean value = 29.03,
N = 74, Standard Deviation = 0.875). Similarly,
December month the minimum temperature
26°C and maximum temperature 28°C was
observed (mean value = 27.57, N = 114, Standard
Deviation = 0.764). Table.2 showed the month
variation of anuran population based on the
temperaturein2017.Here,weobservedthatAugust
month minimum temperature 29°C was recorded
and followed by maximum temperature 31°C,
(mean value =12.42, N = 62, Standard Deviation=
14.74).Similarly,2017Decembermonthminimum
temperature 28°C, and maximum temperature
31°C, were recorded (mean value = 29, N = 200,
Standard Deviation=2.25,). From the above two
table clearly indicated that, the population were
decreased during maximum temperature of both
2016 and 2017. This is clearly indicated that the
temperature influencing the anuran population in
all the four habitat during three seasons.
In both the years the lower population was found
to be in the month of august only the population
temperature of amphibian was observed. The
microhabitat environment temperature should be
28°C is optimum for more active for amphibian.
Figure 2 clearly showed the population density
during three seasons at four habitats with
Table 1: The monthly variation of anuran population based on the temperature in 2016
Months Minimum
temperature (°C)
Maximum
temperature (°C)
Total number
of population
Mean±SD
January 27 33 173 29.32±1.653
February 27 31 167 29.69±1.379
March 27 31 127 27.5±4.458
April 27 29 111 26.05±6.286
May 25 33 114 29.03±2.329
June 19 33 120 26.92±4.116
July 27 34 74 29.03±1.26
August 27 30 134 28.04±0.875
September 27 30 96 27.97±4.211
October 26 31 121 27.52±2.835
November 26 29 104 27.41±3.886
December 26 28 114 27.57±0.764
Total 1455 28.15 ± 3.384
SD: Standard deviation
Table 2: The monthly variation of anuran population based on the temperature in 2017
Months Minimum (°C) Maximum (°C) Total number of population Mean±SD
January 27 30 132 26.74±6.881
February 27 30 140 25.58±7.925
March 27 31 129 28.04±5.757
April 27 30 117 25.53±8.695
May 27 29 141 28.3±0.744
June 28 31 147 27.81±6.761
July 28 30 111 25.68±9.831
August 29 31 62 12.42±14.74
September 29 31 86 17.45±14.551
October 27 30 196 28.53±3.047
November 27 30 146 28.62±1.051
December 28 31 200 29.23±2.250
Total 1607 26.44±8.005
SD: Standard deviation
Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta
Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India
IJPBA/Oct-Dec-2018/Vol 9/Issue 4 258
temperature basis. As per the result, we observed
maximum anuran population was observed (1600
numbers) in samba season with 27-30°C. The
grass land occupied the second place of highest
population density during samba followed by
agriculture (600 numbers) and non agriculture
(200 numbers) respectively kuruvai (32°C) and
Thaladi (25°C).Aquatic ecosystem monitoring has
been carried out in India based on either chemical
or biological analysis. The chemical approach is
useful to determine the levels of nutrients, metals,
pesticides,[21]
as per the result present study was
focused in the season of cultivation paddy field
amphibians are temperature changed in these
cultivation periods of Thalady, Samaba, and
Kuruvai seasons. In the non-cultivated season on
field, amphibian observation was very less due to
their indolent temperature. This may be lack of
water and moisture demand on the field. The rest
of the other three season’s water flow was regular
in the cultivation field. Even though the use of
fertilizers is also influenced in the temperature and
in turn the amphibian population during this study.
Hence, it is revealed that various factors such as
microhabitat temperature, availability of water,
and time also to determine the activity behavior
of amphibians in the above-mentioned study area.
Further detailed studies are warranted to delineate
the population density variation during different
temperatures in microhabitat.
ACKNOWLEDGMENT
The authors would like to thank the Management,
Principal, and Head of the Department of
Zoology, TBML College, Porayar, for providing
the adequate facilities to carry out this work.
REFERENCES
1.	 Bennett AF, Licht P. Relative contributions of anaerobic
and aerobic energy production during activity in
amphibia. J Comp Physiol 1973;87:351-60.
2.	 Seymour RS. Physiological correlates of forced activity
and burrowing in the spadefoot toad, Scaphiopus
hammondii. Copeia 1973;1:103-15.
3.	 Brattstrobm H. A 
preliminary review of the thermal
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4.	 Krishnamurthy SV, Meenakumari D, Gurushankara HP,
Griffiths RA. Effects of nitrate on feeding and resting
of tadpoles of Nyctibatrachus Major (Anura: Ranidae).
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5.	 Meenakumari D. Nitrate Tolerance among Anuran
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Vasudev V. Impact of malathion stress on lipid
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7.	 NatarajMB,KrishnamurthySV.Effectsofcombinations
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frog (Fejervarya limnocharis). J Environ Sci Health B
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8.	 Larson SJ, Capel PD, Majewski MS. Pesticides in
Surface Waters: Distribution, Trends, and Governing
Factors. USA, Ann Arbor: CRC Press Inc.; 1997.
9.	 Blaustein AR, Han BA, Relyea RA, Johnson PT,
Buck JC, Gervasi SS, et al. The complexity of
amphibian population declines: Understanding the role
of cofactors in driving amphibian losses. Ann N YAcad
Sci 2011;1223:108-19.
10.	 EwertJP.Neuroethologyofreleasingmechanisms:Prey-
catching in toads. Behav Brain Sci 1987;10:337-405.
11.	 Roth G, Nishikawa KC, Wake DB, Dicke U,
Matsushima T. Mechanics andneuromorphology of
feeding in amphibians. Neth J Zool 1990;40:115-35.
12.	 Vasudev V, Krishnamurthy SV, Gurushankara HP.
Organophosphate pesticides-a major threat to anuran
populations in an agroecosystem of Western Ghats,
India. FrogLog 2007;83:8-9.
13.	 Gurushankara HP, Krishnamurthy SV, Vasudev V.
Effect of malathion on survival, growth, and food
consumption of Indian cricket frog (Limnonectus
limnocharis) tadpoles. Arch Environ Contam Toxicol
2007;52:251-6.
14.	 Gurushankara HP, Krishnamurthy SV, Vasudev V.
Morphological abnormalities in natural populations of
common frogs inhabiting agro ecosystem of the central
Western Ghats. Appl Herpetol 2007b;4:39-45.
15.	 Daniels RJ.Amphibians of Peninsular India. Hyderabad:
Indian Academy of Sciences and University Press;
2005. p. 1-258.
16.	 Krishnamurthy SV, Meenakumari D, Gurushankara HP,
Vasudev V. Nitrate-induced morphological anomalies
in the tadpoles of Nyctibatrachus major and
Fejervarya limnocharis (Anura: Ranidae). Turk J Zool
2008;32:239-44.
17.	 ThenmozhiK,ThangapandianS.Amphibiancommunity
Figure 2: The influence of temperature on the population
density in different habitats
Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta
Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India
IJPBA/Oct-Dec-2018/Vol 9/Issue 4 259
and microhabitat association in agarakeerangudi
agro-ecosystem, Mayiladuthurai, Tamil Nadu. Cobra
2013;8:6-10.
18.	
Vijayan P, Senthilmurugan S, Pugazhendy K,
Tamizhazhagan V. Analysis of physicochemical
parameters water samples from Cauvery river in
Thanjavur district, Tamil Nadu. Analysis 2018;3:223-7.
19.	 Campbell HW, Christman SP. Field Technique for
Herpetofaunal Community Analysis. In: Scott NJ,
editor. Herpetological Communities. Washington, DC:
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Service. Wildlife Research Report No. 13; 1982.
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20.	Crump ML, Scott NJ. Visual encounter survey. In:
Measuring and Monitoring Biological Diversity:
Standard Methods for Amphibians. Washington DC:
Smithsonian; 1994.
21.	Tamizhazhagan V, Pugazhendy K. Physico-chemical
parameters from the manappadaiyur and swamimalai
fresh water ponds. Indo Am J Pharm Sci 2016;3:444-9.

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Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India

  • 1. © 2018, IJPBA. All Rights Reserved 255 Available Online at www.ijpba.info International Journal of Pharmaceutical Biological Archives 2018; 9(4):255-259 ISSN 2581 – 4303 RESEARCH ARTICLE Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India K. Karunakaran*, Paul Jeevanandham Department of Zoology, T.B.M.L. College, Porayar, Tamil Nadu, India Received: 15 September 2018; Revised: 10 October 2018; Accepted: 05 November 2018 ABSTRACT Amphibian is one of the important ecosystem component, both the ecologically and economically. In the present study, we intended to analyze the population density based on the temperature in different months during the year 2016–2017. The data were collected by visual encounter survey method ,and amphibians were recorded in all 12 months from the study area for 2 years. The monthly variation habitat temperature was recorded in 2016–2017 using analysis of variance. In different habitat (cultivable, non-cultivable, pond, and grassland) temperature, the population was maximum at pond followed by grassland, agriculture, and non-cultivable. The maximum temperature was found in July with 74 numbers of species which were identified during 2016. Were recorded high number (1600) frog were recorded in pond 28°C during samba season followed by Thaladi and Kuruvai. Based on this study, we conclude that the population density may increase and decrease based on the temperature in all the three seasons with four microhabitats. Keywords: Anuran, population agroecosystem Cauvery delta region, tranquebar INTRODUCTION The physiology of amphibian has received much attention than that of other vertebrates. The first investigations of the influence of temperature during activity have been made only recently.[1,2] 1965 further, amphibians are active even at low body temperatures.[3] To investigate the patterns of anaerobiosis in amphibians, lactate production was measured during maximal enforced activity at different temperatures an ecologically and phylogenetically diverse assemblage of urodeles and anurans was examined. In South India, agricultural lands are a complex mixture of different habitats, namely cultivated, non– cultivated, pond, grassland, agriculture fields, and paddy fields, comprising many small pieces of land owned by different farmers and with each piece subjected to different methods of cultivation.As a result, when farmer uses different agrochemicals, the total habitat gets contaminated with a mixture of agrochemicals.[4-7] Agrochemical contaminants can affect amphibians either by destroying biodiversity at lower trophic levels followed by effect at higher trophic levels.[8,9] Hope to understand further the behavioral and neuromuscular changes that have accompanied the evolution of a highly protrusible tongue. In addition, if frog modulates its feeding behavior in response to differences in prey type, this study will be the first to document this ability among amphibians and the feeding behavior of anurans also has been considered to be highly stereotyped.[10,11] The stereotype of feeding behavior found in anurans has been attributed to a limited range of fixed action patterns and to the animal’s behavioral simplicity.[10] In Western Ghats, many amphibians are living and breeding in shallow waters of rice paddy fields. In general, their breeding period coincides with the application of agrochemicals, including pesticides and fertilizers,[12,13] Earlier studies have revealed elevated frequencies of morphological abnormalities (3.97%) in Fejervarya limnocharis from rice paddy fields.[14] Although the Western Ghats has a diverse amphibian fauna,[15] few toxicological studies are available,[16,7] focusing on effects of individual or combinations of agrochemicals on larvae of amphibians.[17] Recorded 12 species of amphibian in and around *Corresponding Author: K. Karunakaran E-mail: karunaherb@gmail.com
  • 2. Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India IJPBA/Oct-Dec-2018/Vol 9/Issue 4 256 Agarakeerangudi village, Mayiladuthurai taluk of Nagapattinam district. Freshwater mussels play a number of important roles in aquatic ecosystems. As sedentary suspension feeders, unionoids remove a variety of materials from the water column, including sediment, organic matter, bacteria, and phytoplankton.[18] However, the effects of agrochemicals on amphibian health status at field conditions are largely unknown. Hence, for the 1st time, we evaluated the anuran population. Tropical and monsoonal climates are characteristics of the study region. The monthly average temperature is generally low at the beginning of the year. In the study area, the temperature reaches 38°C and the minimum touches even 19.30°C, in January and February months which are very pleasant with warm days and cool nights. Heat becomes intense inApril and increases in May-June and comes down gradually in June-July when the southwest monsoon sets on. Very mild winter falls in December and January. Data on soil temperature are lacking and are computed by deducting 50°C from atmospheric temperature. Plant growth as well as chemical and various biological activities in the soil is greatly influenced by temperature. Temperature is an important parameter, determining the climatic condition of any region. The climatic condition determines the agricultural pattern, lifestyle of people, and the socioeconomic conditions. The Cauvery delta region of Tranquebar taluk, Nagapattinam district, falls under the tropical region, so the temperature here is normally high. Monthly mean temperature is calculated from the daily temperature observed from 2016 to 2017 which varies seasonally. Temperature is very high during the summer season, low in the winter season, and moderate during other months. MATERIALS AND METHODS Study area The present study was carried out at 12 places in Tranquebar taluk, Nagapattinam district, Tamil Nadu. The study was carried out for 2 years from January 2016 to December 2017. The study area is comprised of dry deciduous, grassland rocky scrub jungle, and agricultural landscapes. Geographical landscape of tranqubar Thestudyarea[Figure1]islocatedintheTranqubar taluk, Nagapattinam district, which lies on the middle of the coromandel coast. The district lies between 10°25’ and 11°40’ North Longitude and 76°49’ and 80°01’ East latitude of Tamil Nadu, India. The Nagapattinam district lies on the shores of the Bay of Bengal between latitude 10.7906°N and Longitude 79.8428°E an area of 2715 sq. km (1048 sq. mi.). The district capital, Nagapattinam, lies on the eastern coast, 350 km down south of the state capital Chennai. Theamphibiansinallthehabitats,suchascultivable, non-cultivable, pond, dry pond, and grassland, were studied, and the data collections were done during morning hours (6.00 am to 12.30 pm). During the survey periods, parameters such as population, microhabitat, and water distance from each species sightings, vegetation type, and soil types have also been recorded. The four habitats were classified into two categories, namely agricultural and non-agricultural areas. The species were identified using pictorial guides. Visual encounter survey (VES) method The selected village ponds were regularly monitored for diversity and density of amphibian population, activity, and temperature of the study area. The area was walked thoroughly for amphibians. Time-constrained VES method involves a systematic search of an area or habitat for a prescribed time.[19] VES was used as formalized by Crump and Scott.[20] The aim of this study was to maximize the species inventory. Figure 1: The study area
  • 3. Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India IJPBA/Oct-Dec-2018/Vol 9/Issue 4 257 RESULTS AND DISCUSSION Amphibian activity observed during this study revealed the response of the amphibians to their environmental climate. A total of 9 species of anurans were recorded [Table 1] during the year 2016.Thetemperaturewasfoundtobehigherinthe monthofJuly(temp0C±)thatisminimum27°Cand maximum temperature 31°C (mean value = 29.03, N = 74, Standard Deviation = 0.875). Similarly, December month the minimum temperature 26°C and maximum temperature 28°C was observed (mean value = 27.57, N = 114, Standard Deviation = 0.764). Table.2 showed the month variation of anuran population based on the temperaturein2017.Here,weobservedthatAugust month minimum temperature 29°C was recorded and followed by maximum temperature 31°C, (mean value =12.42, N = 62, Standard Deviation= 14.74).Similarly,2017Decembermonthminimum temperature 28°C, and maximum temperature 31°C, were recorded (mean value = 29, N = 200, Standard Deviation=2.25,). From the above two table clearly indicated that, the population were decreased during maximum temperature of both 2016 and 2017. This is clearly indicated that the temperature influencing the anuran population in all the four habitat during three seasons. In both the years the lower population was found to be in the month of august only the population temperature of amphibian was observed. The microhabitat environment temperature should be 28°C is optimum for more active for amphibian. Figure 2 clearly showed the population density during three seasons at four habitats with Table 1: The monthly variation of anuran population based on the temperature in 2016 Months Minimum temperature (°C) Maximum temperature (°C) Total number of population Mean±SD January 27 33 173 29.32±1.653 February 27 31 167 29.69±1.379 March 27 31 127 27.5±4.458 April 27 29 111 26.05±6.286 May 25 33 114 29.03±2.329 June 19 33 120 26.92±4.116 July 27 34 74 29.03±1.26 August 27 30 134 28.04±0.875 September 27 30 96 27.97±4.211 October 26 31 121 27.52±2.835 November 26 29 104 27.41±3.886 December 26 28 114 27.57±0.764 Total 1455 28.15 ± 3.384 SD: Standard deviation Table 2: The monthly variation of anuran population based on the temperature in 2017 Months Minimum (°C) Maximum (°C) Total number of population Mean±SD January 27 30 132 26.74±6.881 February 27 30 140 25.58±7.925 March 27 31 129 28.04±5.757 April 27 30 117 25.53±8.695 May 27 29 141 28.3±0.744 June 28 31 147 27.81±6.761 July 28 30 111 25.68±9.831 August 29 31 62 12.42±14.74 September 29 31 86 17.45±14.551 October 27 30 196 28.53±3.047 November 27 30 146 28.62±1.051 December 28 31 200 29.23±2.250 Total 1607 26.44±8.005 SD: Standard deviation
  • 4. Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India IJPBA/Oct-Dec-2018/Vol 9/Issue 4 258 temperature basis. As per the result, we observed maximum anuran population was observed (1600 numbers) in samba season with 27-30°C. The grass land occupied the second place of highest population density during samba followed by agriculture (600 numbers) and non agriculture (200 numbers) respectively kuruvai (32°C) and Thaladi (25°C).Aquatic ecosystem monitoring has been carried out in India based on either chemical or biological analysis. The chemical approach is useful to determine the levels of nutrients, metals, pesticides,[21] as per the result present study was focused in the season of cultivation paddy field amphibians are temperature changed in these cultivation periods of Thalady, Samaba, and Kuruvai seasons. In the non-cultivated season on field, amphibian observation was very less due to their indolent temperature. This may be lack of water and moisture demand on the field. The rest of the other three season’s water flow was regular in the cultivation field. Even though the use of fertilizers is also influenced in the temperature and in turn the amphibian population during this study. Hence, it is revealed that various factors such as microhabitat temperature, availability of water, and time also to determine the activity behavior of amphibians in the above-mentioned study area. Further detailed studies are warranted to delineate the population density variation during different temperatures in microhabitat. ACKNOWLEDGMENT The authors would like to thank the Management, Principal, and Head of the Department of Zoology, TBML College, Porayar, for providing the adequate facilities to carry out this work. REFERENCES 1. Bennett AF, Licht P. Relative contributions of anaerobic and aerobic energy production during activity in amphibia. J Comp Physiol 1973;87:351-60. 2. Seymour RS. Physiological correlates of forced activity and burrowing in the spadefoot toad, Scaphiopus hammondii. Copeia 1973;1:103-15. 3. Brattstrobm H. A  preliminary review of the thermal requirements of amphibians. Ecology 1963;44:238-55. 4. Krishnamurthy SV, Meenakumari D, Gurushankara HP, Griffiths RA. Effects of nitrate on feeding and resting of tadpoles of Nyctibatrachus Major (Anura: Ranidae). Australas J Ecotoxicol 2006;12:123-7. 5. Meenakumari D. Nitrate Tolerance among Anuran Amphibians of Central Western Ghats, Ph. D. Thesis. Western Ghats: Kuvempu University; 2007. p. 171. 6. Gurushankara HP, Meenakumari D, Krishnamurthy SV, Vasudev V. Impact of malathion stress on lipid metabolism in Limnonectus limnocharis. Pestic Biochem Physiol 2007;88:50-6. 7. NatarajMB,KrishnamurthySV.Effectsofcombinations of malathion and cypermethrin on survivability and time of metamorphosis of tadpoles of Indian cricket frog (Fejervarya limnocharis). J Environ Sci Health B 2012;47:67-73. 8. Larson SJ, Capel PD, Majewski MS. Pesticides in Surface Waters: Distribution, Trends, and Governing Factors. USA, Ann Arbor: CRC Press Inc.; 1997. 9. Blaustein AR, Han BA, Relyea RA, Johnson PT, Buck JC, Gervasi SS, et al. The complexity of amphibian population declines: Understanding the role of cofactors in driving amphibian losses. Ann N YAcad Sci 2011;1223:108-19. 10. EwertJP.Neuroethologyofreleasingmechanisms:Prey- catching in toads. Behav Brain Sci 1987;10:337-405. 11. Roth G, Nishikawa KC, Wake DB, Dicke U, Matsushima T. Mechanics andneuromorphology of feeding in amphibians. Neth J Zool 1990;40:115-35. 12. Vasudev V, Krishnamurthy SV, Gurushankara HP. Organophosphate pesticides-a major threat to anuran populations in an agroecosystem of Western Ghats, India. FrogLog 2007;83:8-9. 13. Gurushankara HP, Krishnamurthy SV, Vasudev V. Effect of malathion on survival, growth, and food consumption of Indian cricket frog (Limnonectus limnocharis) tadpoles. Arch Environ Contam Toxicol 2007;52:251-6. 14. Gurushankara HP, Krishnamurthy SV, Vasudev V. Morphological abnormalities in natural populations of common frogs inhabiting agro ecosystem of the central Western Ghats. Appl Herpetol 2007b;4:39-45. 15. Daniels RJ.Amphibians of Peninsular India. Hyderabad: Indian Academy of Sciences and University Press; 2005. p. 1-258. 16. Krishnamurthy SV, Meenakumari D, Gurushankara HP, Vasudev V. Nitrate-induced morphological anomalies in the tadpoles of Nyctibatrachus major and Fejervarya limnocharis (Anura: Ranidae). Turk J Zool 2008;32:239-44. 17. ThenmozhiK,ThangapandianS.Amphibiancommunity Figure 2: The influence of temperature on the population density in different habitats
  • 5. Karunakaran and Jeevanandham: Studies on the Influence of Temperature in Aquatic Anuran Population in Cauvery Delta Region of Tranquebar Taluk of Nagapattinam District, Tamil Nadu, India IJPBA/Oct-Dec-2018/Vol 9/Issue 4 259 and microhabitat association in agarakeerangudi agro-ecosystem, Mayiladuthurai, Tamil Nadu. Cobra 2013;8:6-10. 18. Vijayan P, Senthilmurugan S, Pugazhendy K, Tamizhazhagan V. Analysis of physicochemical parameters water samples from Cauvery river in Thanjavur district, Tamil Nadu. Analysis 2018;3:223-7. 19. Campbell HW, Christman SP. Field Technique for Herpetofaunal Community Analysis. In: Scott NJ, editor. Herpetological Communities. Washington, DC: United States Department of Interior Fish and Wildlife Service. Wildlife Research Report No. 13; 1982. p. 193-200. 20. Crump ML, Scott NJ. Visual encounter survey. In: Measuring and Monitoring Biological Diversity: Standard Methods for Amphibians. Washington DC: Smithsonian; 1994. 21. Tamizhazhagan V, Pugazhendy K. Physico-chemical parameters from the manappadaiyur and swamimalai fresh water ponds. Indo Am J Pharm Sci 2016;3:444-9.