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J. Bio. Env. Sci. 2016
104 | Rana et al.
RESEARCH PAPER OPEN ACCESS
Distribution of ground dwelling spider genera among berseem
crop at Okara district, Pakistan
Muhammad Arshad Rana1*
, Munaza Shabnam2
, Naureen Rana3
, Tayyba Sultana4
,
Salma Sultana4
, Sobia Kanwal3
, Imran Ahmad4
1
Department of Zoology, Govt. Postgraduate College Okara, Pakistan
2
Department of Biology, Govt. Postgraduate College for Women Sahiwal, Pakistan
3
Department of Zoology, Wildlife and Fisheries, UAF, Pakistan
4
Department of Zoology, Govt. College University Faisalabad, Pakistan
Article published on February 11, 2016
Key words: Ground dwelling, Spider, Pitfall, Population, Transect.
Abstract
The present study was designed to record the distribution of ground dwelling spider genera among berseem crop
at Okara district. Sampling was made from Trifolium crop on fortnight basis through pitfall traps. Equal number
of traps were placed in three rows e.g. along the boundary, middle of the field and centre of the field. Each trap
was filled with mixture solution of alcohol and glycerin (70:30%) along with few drops of kerosene oil. After 5
days interval sample traps was collected and spider specimens were washed with distilled water and permanently
stored in labeled glass vials, and brought into the Pest Control Laboratory, Departmentof Zoology, Wildlife and
Fisheries, University of Agriculture, Faisalabad. Thereafter, each spider specimen was identified according to the
taxonomic material and internet source. Identified data was analyzed statistically to quantify their spatial
distribution. Overall maximum spatial distribution of spider population was documented in middle transect than
boundary and centre of the berseem crop. It was also observed that temperature, humidity, vegetation and prey
availability were the major factors that effecting the spider population. Population variations were recorded
during the months of February, March and April in 2015, due to rise of temperature, decrease of humidity and
availability of prey. It was concluded that despite to cosmopolitan nature, spiders have some correlation with
suitable local conditions or habitat. More over, spiders are cost effective, functionally significant and play a key
role in regulating decomposer population.
*Corresponding Author: Muhammad Arshad Rana  marshadrana719@gmail.com
Journal of Biodiversity and Environmental Sciences (JBES)
ISSN: 2220-6663 (Print) 2222-3045 (Online)
Vol. 8, No. 2, p. 104-113, 2016
http://www.innspub.net
J. Bio. Env. Sci. 2016
105 | Rana et al.
Introduction
Fodder crops are particularly refer to food for animals
or live-stock. They comprise of straw, hay, pelleted
feed, silage, oils, legumes and sprouted grains.
Currently in Pakistan, various fodder crops are
cultivated over 15 million hectares with 52 million ton
annual fodder production (Anonymous, 2013).
However, suitable rainfall and temperature range can
enhance the present outcomes (Hussain et al., 2010).
Because, in many parts of Pakistan, there is abrupt
shortage of fodder for live-stock, and also the
available fodder is of poor quality.
The farmers are facing a lot of problems to get
maximum forage yield to meet the feed requirements.
Improved fodder varieties along with control of
damage by invading insect pest can overcome the
situation. In this context, berseem provides valuable
supplemental food to live-stock community e.g.
nitrogen, energy, minerals and vitamins.
Consequently, it increase the availability of nutrients
for maintenance and ideal production status.
(Douglas et al., 2000).
However, fodder crops especially, berseem provide
more than 80% feeding to live-stock from October to
April (Younas and Yaqoob, 2005). But, its production
is low due to serious insect damage. Berseem
(Trifolium alexandrinum) is important Rabi legume
grown for green fodder. It is able to prepare about
seven cuts of forages. (Khalil and Jan, 2000).
To enhance the yield, control of insect pests is a major
issue and use of spiders to control these insect pests is
of profound importance. Spiders have globally more
than 40,000 identified species (Platnick, 2012). They
have remarkable abundance and are highly
diversified terrestrial predator especially in agro-
ecosystems (Wise, 1993).
They can play a pivotal role in keeping insect and pest
populations in check and balance and they are also
serve as food for birds, snakes, fish and other animals.
They eat insects and bugs which destroy different
crops and consequently safeguard the agro-
ecosystems. By habitat management. We can
conserve the diversity of natural enemies (including
spiders) of arthropod pest
(Douglas et al., 2000).
Spider’s abundance and diversity vary in different
agro-ecosystems and they have temporo-spatial
distribution in all agricultural lands to effectively
destruct the insect pest population (Seyfulina and
Tshernyshev, 2001; Seyfulina, 2003). Their breeding
success is directly related to amount of precipitation
which act as potential factors to affect the abundance
and species richness (Thomas et al., 2014). They are
most important arthropods for economic point of
view playing role as biological control agent and their
adaptation towards different habitats (Kazim et al.,
2014).
Keeping in view the importance of spider densities
and role of berseem in live-stock sector, the present
study was designed to record the population
dynamics and spatial distribution of ground dwelling
spider families and genea among berseem crop at
Okara district.
Materials and methods
Study area
The present study was designed to record spatial
distribution of ground dwelling spiders among
berseem crop at Okara district. Because information
about their distribution in any agro-ecosystem was
pre-requisite to formulate any strategy to use them
for bio-control purposes.
Presently, these informations were recorded from
Okara district. Trifolium crop was cultivated in one
acre rectangular field. The sampling field was
surrounded by wheat fields from two sides, where as
on third side, it was surrounded by a Trifolium and
Mustard field.
Okara district
Okara district is situated in Punjab province at 30,
J. Bio. Env. Sci. 2016
106 | Rana et al.
8081 (304829.160”N) latitude and 73, 4458
(732644.880”E) longitude. This district is bounded
on the East by Kasur district, Sahiwal and Pakpattan
districts on the West, Sheikhupura and Faisalabad
districts on the North and Bahawalnagar district on
the South. The Indian border also lies on the South-
Eastern side of the district. Okara district has a total
area of 4,377 square kilometres and comprises of
three tehsils i.e. Okara, Depalpur and Renala Khurd.
Climate
The climate of the Okara district is hot in summer and
cold in winter. May and June are hottest months and
January is the coldest one.Temperature ranges
between 36-440C in summer and 2-280C in winter.
Soil of the district is loamy and sandy loamy with
annual rainfall up to 200 mm.
Sampling design and techniques
The sampling was carried out from October, 2014
through April, 2015 to collect the ground dwelling
spider fauna in berseem crop.Total thirty traps were
set in the field for five successive days. The two
successive traps were at equal distance from each
other and the distance from outer boundary of the
field was 5m. Pitfall traps were 12cm long glass jars
with 6cm (diameter) wide mouths. Each trap
contained 150 ml of 70% ethyl alcohol and a small
amount of kerosene oil which served as preservative
and killing agent.Ten pitfall traps were laid along
each transect line i.e. boundary, middle and centre at
an equal interval from each other.
Collection of data
For berseem crop, ideal field measuring 7200 sq. ft.
were selected to observe the spatial distribution of
ground dwelling spiders through pitfall trap method.
However, trapping was made by three layers inside
the field radius wise to observe the infestation along
the entire field. Data was collected fortnightly and
collected specimens were brought into the Pest
Control Laboratory, Departmentof Zoology, Wildlife
and Fisheries, University of Agriculture, Faisalabad.
All the specimens were identified according to the
reference material. The field of berseem was sampled
after 5 days intervals right from the pre-harvest stage.
More over, minimum and maximum temperature and
humidity of area was also recorded.
Preservation
All traps were taken to Pest Control Laboratory,
Department of Zoology, Wildlife and Fisheries,
University of Agriculture, Faisalabad. Where the
specimens were washed with xylene and preserved
in 95% ethanol containing few drops of glycerin.
Specimens were preserved separately in small glass
vials indicating with trap number and the date of
capture.
Identification
The collected samples were identified with the aid of
naked eye, magnifying glass and under the
microscope. All the specimens were identified up to
species level according to the taxonomic and
reference material (Tikader and Malhotra (1982),
Tikader and Biswas (1981), Barrion and Litsinger
(1995), Zhu et al. (2003), Platnick (2012), other
relevant literature and internet source.
Statistical analysis
Thereafter, all the identified specimens were arranged
in table form according to their morphological
characters e.g. family, genus. To determine the
various aspects of diversity, Shannon Diversity Index
was used (Magurran, 1988). Analysis of Variance was
made to compare the population means between
three transects, i.e. Boundary, middle and centre of
berseem crop. The richness, diversity and evenness
indices were computed by using the Programme
SPDIVERS.BAS.
Results
The present study was conducted to highlight the
spatial distribution of ground dwelling spiders among
berseem crop at Okara district. A total number of 463
specimen pertaining to 25 genera and 7 families
among berseem crop were identified from Okara
district (Table 1).
J. Bio. Env. Sci. 2016
107 | Rana et al.
Table 1. The number of families, specimen and genera recorded from berseem field at Okara district.
Sr.No. Families No. of Specimen No. of Genera
1 Araneidae 34 4
2 Clubionidae 20 1
3 Gnaphosidae 122 5
4 Linyphiidae 63 3
5 Lycosidae 165 5
6 Salticidae 37 4
7 Thomisidea 22 3
Total 7 463 25
Table 2. Monthly record of spider families captured from berseem crop at Okara district.
Families No.of spiders in
Nov-14
No.of spiders in
Dec-14
No.of spiders in
Jan-15
No.of spiders in
Feb-15
No.of spiders in
Mar-15
No.of spiders in
Apr-15
Total No. of
spiders
Araneidae 2 2 0 4 9 17 34
Clubionidae 0 0 0 3 5 12 20
Gnaphosidae 9 3 1 18 31 60 122
Linyphiidae 5 3 3 7 14 31 63
Lycosidae 11 4 3 25 50 72 165
Salticidae 3 1 0 8 10 15 37
Thomisidea 3 1 1 3 6 8 22
Grand Total 33 14 8 68 125 215 463
Population variations among families in berseem
crop
Data presented in Table 2, is pertaining to family’s
wise comparison of spiders’ population recorded from
two fodder crops during the study. In Berseem crop,
the population of wolf spiders – family Lycosidae was
recorded with highest population (N = 165), followed
by Flat bellied ground spiders – family Gnaphosidae
(N = 122), Sheat weaver spiders – family Linyphiidae
(N = 63), Jumping spiders – family Salticidae (N =
37), Orb-weaver spiders – family Araneidae (N = 34),
Crab spiders-- family--Thomisidea (N = 22) and Sac
spiders-- family—Clubionidae (N = 21) respectively.
Table 3. Population variations of spider genera among berseem field at Okara district.
Family Genera Nov-14 Dec-14 Jan-15 Feb-15 Mar-15 Apr-15 Total
Araneidae Araneus Clerck, 1757 1 0 0 3 2 5 11
Gea C. L. Koch, 1843 0 2 0 0 2 4 8
Neoscona Simon, 1864 1 0 0 1 3 3 8
Cyclosa Menge, 1866 0 0 0 0 2 5 7
Clubionidae Clubiona latreille,1804 0 0 0 3 5 12 20
Gnaphosidae Drassodes 4 2 1 8 12 20 47
Gnaphosa Latreille, 1804 2 0 0 3 6 11 22
Scotophaeus Simon, 1893 2 0 0 3 5 10 20
Zelotes Gistel, 1848 1 1 0 4 6 14 26
Micaria Westring, 1851 0 0 0 0 2 5 7
Linyphiidae Tapinocyboides Wiehle, 1960 1 1 0 2 5 16 25
Tchatkalophantes Tanasevitch, 2001 2 1 2 3 4 8 20
Tiso Simon, 1884 2 1 1 2 5 7 18
Lycosidae Evippa Simon, 1882 5 2 1 14 21 36 79
Hogna Simon,1885 1 1 1 2 3 8
Lycosa Latreille, 1804 3 1 0 8 18 20 50
Pardosa C. L. Koch, 1847 2 1 1 2 8 12 26
Trochosa C. L. Koch, 1847 0 0 0 0 1 1 2
Salticidae Myrmarachne MacLeay, 1839 2 0 0 2 4 5 13
Phlegra Simon, 1876 1 0 2 2 4 9
Plexippus C. L. Koch, 1846 1 0 0 1 2 3 7
Sitticus Simon, 1901 0 0 0 3 2 3 8
Thomisidea Runcinia Simon, 1875 1 1 1 2 2 7
Thomisus Walckenaer, 1805 1 0 0 3 2 4 10
Xysticus 1 0 0 0 2 2 5
Grand Total 33 14 8 68 125 215 463
J. Bio. Env. Sci. 2016
108 | Rana et al.
The maximum population of wolf spiders – family
Lycosidae was recorded due to that they were strictly
ground dwelling spiders. Second and third highest
population recorded were of Flat bellied ground
spiders – family Gnaphosidae and Sheat weaver
spiders – family Linyphiidae respectively due to the
reason that they were also ground living and live in
high vegetation density, therefore the existing
environment was supportive for them. However
minimum population of identified spiders in case of
Jumping spiders – family Salticidae followed by Orb-
weaver spiders – family Araneidae, Crab spiders--
family Thomisidea and Sac spiders -- family
Clubionidae was recorded from berseem field.Their
low population was recorded due to that they live in
leaf litter and shaddy areas. The study area was
surrounded by wheat crops from north and east side
and mustard crop from west side. Whole cultivated
area was comprised of crop land and there was no
shaddy tree near the study area. Another reason for
their least collection was that, they were foliage
spiders and pitfall method was applied for the
collection of spiders.
Table 4. Number of genera (S), total number of samples (N), Shannon diversity index, Lambda value and
Evenness for transect-wise monthly data of berseem crop for different genera.
Site Month S N H' Shannon Lambda Evenness Dominance
Boundary Nov. 11 17 2.2624 0.1211 0.9435 0.0565
Dec. 6 6 1.7918 0.1667 1.0000 0.000
Jan. 3 3 1.0986 0.3333 1.0000 0.000
Feb. 15 24 2.5209 0.0972 0.9309 0.0691
Mar. 19 45 2.6839 0.0884 0.9115 0.0885
Apr. 25 73 2.9098 0.0696 0.9040 0.096
Middle Nov. 9 12 2.0947 0.1389 0.9534 0.0466
Dec. 5 5 1.6094 0.2000 1.0000 0.000
Jan. 5 5 1.6094 0.2000 1.0000 0.000
Feb. 18 40 2.6485 0.0938 0.9163 0.0837
Mar. 25 66 2.8543 0.0804 0.8868 0.1132
Apr. 23 103 2.8428 0.0755 0.9067 0.0933
Center Nov. 5 5 1.6094 0.2000 1.0000 0.000
Dec. 2 2 0.6932 0.5000 1.0000 0.000
Jan. - - - - - -
Feb. 4 4 1.3863 0.2500 1.0000 0.000
Mar. 11 14 2.3420 0.1020 0.9767 0.0233
Apr. 16 39 2.4830 0.1059 0.8956 0.1044
Where S = Number of species
N = Total number of samples (sum).
Population variations among genera in berseem
crop
Data presented in Table 3, is regarding the
comparison of spider’s population among genera
recorded in berseem field during the study. Out of 25
genera, maximum population of identified genera was
recorded in case of genus Evapa (N=79) followed by
Lycosa (N=50) and Drassodes (N=47) respectively.
Minimum population of identified spider genera was
recorded in case of genus Cyclosa (N=7), Micaria
(N=7), Plexipus (N=7), Runcinia (N=7), Xysticus
(N=5), and Trochosa (N=2) respectively.
Least population was recorded in case of genus
Cyclosa, Micaria, plexipus, Runcinia, Xysticus, and
Trochosa respectively. Because they were ground
dwelling spiders and live in shelter places while in
berseem field, fodder was cut down again and again
that’s why their minimum population was recorded.
J. Bio. Env. Sci. 2016
109 | Rana et al.
Table 5. Number of genera(S), total number of samples(N), Shannon diversity index, Lambda value, Evenness
and dominance for transect-wise monthly record of berseem crop for different genera.
Month S N H Shannon Lambda Evenness Dominance
November 18 33 2.7327 0.0762 0.9455 0.0545
December 11 14 2.342 0.102 0.9767 0.0233
January 7 8 1.9062 0.1563 0.9796 0.0204
February 19 68 2.6641 0.0921 0.9048 0.0952
March 25 125 2.8624 0.0788 0.8893 0.1107
April 25 215 2.8859 0.0728 0.8966 0.1034
Spatial diversity of spider genera in berseem
cropData presented in Tabl 4, is pertaining the month
wise comparison of diversity indices among species at
three trasects i.e. boundary, middle and centre of the
berseem crop. During the month of November
maximum diversity (H) at boundary recorded was
2.2624, eveness 0.9435 and dominance was 0.0565
when compared with middle, maximum diversity was
2.0947, eveness 0.9534, and dominance 0.0466. and
at centre, maximum diversity 1.6094, eveness 1.0000
and dominance 0.0000.During the month of
December maximum diversity (H) at boundary
recorded was 1.7918, eveness 1.0000 and dominance
was 0.0000, when compared with middle, maximum
diversity was 1.6094, eveness 1.0000, and
dominance 0.000. and at centre, maximum diversity
0.6932, eveness 1.0000 and dominance
0.0000.During the month of January maximum
diversity (H) at boundary recorded was 1.0986,
eveness 1.0000 and dominance was 0.0000 when
compared with middle, maximum diversity was
1.6094, eveness 1.0000, and dominance 0.000. and
no diversity was recorded in centre.During the month
of February maximum diversity (H) at boundary
recorded was 2.5209, eveness 0.9309 and dominance
was 0.0691 when compared with middle, maximum
diversity was 2.6485, eveness 0.9163, and dominance
0.0837. and at centre, maximum diversity 1.3863,
eveness 1.0000 and dominance 0.0000.During the
month of March maximum diversity ( H”) at
boundary recorded was 2.6839, eveness 0.9115 and
dominance was 0.0885 when compared with middle,
maximum diversity was 2.8543, eveness 0.8868, and
dominance 0.1132 and at centre, maximum diversity
2.3420, eveness 0.9767 and dominance
0.0233.During the month of April, maximum
diversity (H) at boundary recorded was 2.9098,
eveness 0.9040 and dominance was 0.096 when
compared with middle, maximum diversity was
2.8428, eveness 0.9067, and dominance 0.0933 and
at centre, maximum diversity 2.4830, eveness 0.8956
and dominance 0.1044. Overall maximum diversity
(H”) recorded in the month of April at the boundary
was 2.9098, eveness 0.9040 and dominance was
0.096 respectively, when compared with boundary
and centre of the berseem crop.
Overall comparison of diversity indices among
berseem crop
Data presented in Table 5, is pertaining the month
wise comparison of diversity indices among genera
from Berseem crop. Overall genera wise maximum
diversity (H”) recorded in Berseem crop during the
month of November was 3.7327, evenness 0.9455 and
dominance 0.0545 respectively. During the month of
December maximum diversity 2.3420, evenness
0.9767 and dominance 0.0233 was recorded. During
the month of January maximum diversity 1.9062,
evenness 0.9796 and dominance 0.0204 was
recorded. During the month of February maximum
diversity 2.6641, evenness 0.9048 and dominance
0.0952 was recorded. During the month of March
maximum diversity 2.8624, evenness 0.8893 and
dominance 0.1107 was recorded. During the month of
April maximum diversity 2.8859, evenness 0.8966
and dominance 0.1034 was recorded.
J. Bio. Env. Sci. 2016
110 | Rana et al.
Table 6. Analysis of variance table for transect-wise abundance of different genera for different crops.
Source of variation Degrees of
freedom
Sum of squares Mean squares F-value
Months
Crop
Transect
Crop x Transect
Error
Total
5
1
2
2
25
35
16332.6
49.0
4423.7
24.5
3893.1
24722.9
3266.51
49.00
2211.86
12.25
155.72
20.98**
0.31NS
14.20**
0.08NS
NS = Non-significant (P>0.05); * = Significant (P<0.05); ** = Highly significant (P<0.01).
Month wise mean ± SE.
Month Mean ± SE
November-14
December-14
January-15
February-15
March-15
April-15
11.50±3.03
4.00±0.82
2.33±0.71
26.33±6.73
42.33±9.22
60.83±11.79
CD
D
D
C
B
A
Means sharing similar letters are statistically non-significant (P>0.05).
Crops x Transect interaction mean ± SE.
Transect Berseem Crop
Mean ± SE
Boundary 28.00 ± 10.89A
Middle 38.50 ± 16.19A
Center 10.67 ± 6.00B
Mean 25.72 ± 6.97A
Means sharing similar letter in a row or in a column are statistically non-significant (P>0.05).
Maximum diversity 2.8859 was recorded during the
month of April .while evenness 0.9796, and
dominance 0.1107 were recoded during the month of
January and March respectively.
Relative abundance
Pie graph (Fig. 1) represent the relative abundance of
identified spider families in berseem crop at Okara
district. Maximum abundance of spiders was
recorded in case of family Lycosidae 36% followed by
Gnaphosidae 26% and Lyniphiidae 14%. Minimum
abundance of spiders was recorded in family
Araneidae 7% followed by Thomisidae 5% and
Clubionidae 4% respectively.
Ecological distribution
Temperature of the country is increasing day by day
due to global warming. Consequently, the change in
temperature also alter the humidity of the
environment. Due to change of temperature and
humidity, imbalanece the relation ship between
organism and the environment (Table 7). This issue
was observed on scientific basis among ground
dwelling spiders to record the effect of ecological
changes. It was recorded that population of spiders
was increased with the increase in temperature and
J. Bio. Env. Sci. 2016
111 | Rana et al.
decreasing tendency was recorded in case of
humidity. Because, breeding season of spiders started
during April and peaks were recorded with the
increase in temperature. Temperature also affects the
body processes and egg development. They concluded
that females may be able to protect themselves
against temperatures that are prohibitively low for
reproduction. From these results, it was concluded
that variations in population density were due to
effect of temperature, humidity, availability of prey,
nature of crop rotation and pesticides uses instead of
ecological successions.
Table 7. Monthly average temperature (maximum and minimum), percentage of humidity recorded from Okara
district.
Month Average maximum temperature °C Average minimum temperature °C Average relative humidity
Novermber 27.2 8.7 85%
December 18.9 4.1 90.50%
January 16.6 4.1 93.00%
February 22.3 6.7 78.50%
March 25.1 10 77.00%
April 32.5 16.6 78.00%
Analysis of variance
Data represented in Table 6, pertaining to Analysis of
variance for transect-wise abundance of different
genera of spiders for berseem crop.The mean number
of spider genera in berseem at district Okara was
statistically similar. The mean number of spider’s
population month wise and transect wise were
statistically highly significant (P<0.01). The mean
number of spider’s population during the month of
December (4.00±0.82) and January (2.33±0.71) were
statistically non significant (P>0.05), when compared
with mean number in November (11.50±3.03),
February (26.33±6.73), March (42.33±9.22) and
April (60.83±11.79) was statistically significan
(P<0.05). Crop x Transect-wise mean number of
spider genera in boundary (27.75±6.68) and middle
(36.25±9.89) were statistically non significant
(P>0.05) when compared with mean number in
centre (9.63±3.38) was statistically significant
(P<0.05) among berseem crop. Overall mean number
of spider genera in berseem (25.72±6.97) crop was
statistically non significant (P>0.05).
It is obvious from the indices calculations that spiders
abundance decrease with the decrease in temperature
and increase in humidity. Resultantly, ecological
imbalance of prey verses predators develops which
upset the all ecological pyramids and natural cycling.
Sustainable prey and predator status is limiting for
integrity of any natural system for long term
functions.
Discussion
Seasonal variations in spider population
Evidences regarding sesaonal variations of spider
population was underlined by considering the
findings of previous researchers because field type,
management pattern, agronomic operations and use
of pesticides, soil culture and floral structures
significantly affect spider’s population (Liljesthrom et
al., 2002; Ahmad et al., 2005; Pradeep et al., 2015).
It was also estimated that start of breeding season,
enhancment in growth and acceleration in maturity
were proportional to temperature and humidity. As
temperature reached above 25°C, start in breeding
occur and with decrease in temperature up to the
same situation and increase in humidity, it comes to
the end. Findings of present study are in agreement
with Rajeswaran et al. (2005); Dippenaar-Schoeman
(2006); Mushtaq et al. (2003 & 2005); Kazim et al.
(2014), Pradeep et al. (2015).
It is obvious from the indices calculations that
spider’s abundance decrease with the decrease in
J. Bio. Env. Sci. 2016
112 | Rana et al.
temperature and increase in humidity. These findings
support the earlier reports of Mushtaq et al. (2003 &
2005); Iqbal et al. (2009) and Pradeep et al. (2015).
Resultantly, ecological imbalance of prey verses
predators develops which upset the all ecological
pyramids and natural cycling. Sustainable prey and
predator status is limiting for integrity of any natural
system for long term functions. These findings are in
same cotext as reported by Rajeswaran et al. (2005);
Dippenaar-Schoeman (2006); Mushtaq et al. (2003 &
2005); Kazim et al. (2014), Pradeep et al. (2015).
Fig. 1. Pie graph represent the relative abundance of spider families in berseem crop.
Conclusion
Hence, it was concluded from the present work that
despite to cosmopolitan nature, spiders have some
correlation with suitable local conditions or habitat.
However, it was also observed that spider’s
population in the same study region were also
effected by increase or decrease in temperature and
humidity. So, there is necessity of future research for
the proper use of spider fauna as biological control
agent in IPM programmes.
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Distribution of ground dwelling spider genera among berseem crop at Okara district, Pakistan

  • 1. J. Bio. Env. Sci. 2016 104 | Rana et al. RESEARCH PAPER OPEN ACCESS Distribution of ground dwelling spider genera among berseem crop at Okara district, Pakistan Muhammad Arshad Rana1* , Munaza Shabnam2 , Naureen Rana3 , Tayyba Sultana4 , Salma Sultana4 , Sobia Kanwal3 , Imran Ahmad4 1 Department of Zoology, Govt. Postgraduate College Okara, Pakistan 2 Department of Biology, Govt. Postgraduate College for Women Sahiwal, Pakistan 3 Department of Zoology, Wildlife and Fisheries, UAF, Pakistan 4 Department of Zoology, Govt. College University Faisalabad, Pakistan Article published on February 11, 2016 Key words: Ground dwelling, Spider, Pitfall, Population, Transect. Abstract The present study was designed to record the distribution of ground dwelling spider genera among berseem crop at Okara district. Sampling was made from Trifolium crop on fortnight basis through pitfall traps. Equal number of traps were placed in three rows e.g. along the boundary, middle of the field and centre of the field. Each trap was filled with mixture solution of alcohol and glycerin (70:30%) along with few drops of kerosene oil. After 5 days interval sample traps was collected and spider specimens were washed with distilled water and permanently stored in labeled glass vials, and brought into the Pest Control Laboratory, Departmentof Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad. Thereafter, each spider specimen was identified according to the taxonomic material and internet source. Identified data was analyzed statistically to quantify their spatial distribution. Overall maximum spatial distribution of spider population was documented in middle transect than boundary and centre of the berseem crop. It was also observed that temperature, humidity, vegetation and prey availability were the major factors that effecting the spider population. Population variations were recorded during the months of February, March and April in 2015, due to rise of temperature, decrease of humidity and availability of prey. It was concluded that despite to cosmopolitan nature, spiders have some correlation with suitable local conditions or habitat. More over, spiders are cost effective, functionally significant and play a key role in regulating decomposer population. *Corresponding Author: Muhammad Arshad Rana  marshadrana719@gmail.com Journal of Biodiversity and Environmental Sciences (JBES) ISSN: 2220-6663 (Print) 2222-3045 (Online) Vol. 8, No. 2, p. 104-113, 2016 http://www.innspub.net
  • 2. J. Bio. Env. Sci. 2016 105 | Rana et al. Introduction Fodder crops are particularly refer to food for animals or live-stock. They comprise of straw, hay, pelleted feed, silage, oils, legumes and sprouted grains. Currently in Pakistan, various fodder crops are cultivated over 15 million hectares with 52 million ton annual fodder production (Anonymous, 2013). However, suitable rainfall and temperature range can enhance the present outcomes (Hussain et al., 2010). Because, in many parts of Pakistan, there is abrupt shortage of fodder for live-stock, and also the available fodder is of poor quality. The farmers are facing a lot of problems to get maximum forage yield to meet the feed requirements. Improved fodder varieties along with control of damage by invading insect pest can overcome the situation. In this context, berseem provides valuable supplemental food to live-stock community e.g. nitrogen, energy, minerals and vitamins. Consequently, it increase the availability of nutrients for maintenance and ideal production status. (Douglas et al., 2000). However, fodder crops especially, berseem provide more than 80% feeding to live-stock from October to April (Younas and Yaqoob, 2005). But, its production is low due to serious insect damage. Berseem (Trifolium alexandrinum) is important Rabi legume grown for green fodder. It is able to prepare about seven cuts of forages. (Khalil and Jan, 2000). To enhance the yield, control of insect pests is a major issue and use of spiders to control these insect pests is of profound importance. Spiders have globally more than 40,000 identified species (Platnick, 2012). They have remarkable abundance and are highly diversified terrestrial predator especially in agro- ecosystems (Wise, 1993). They can play a pivotal role in keeping insect and pest populations in check and balance and they are also serve as food for birds, snakes, fish and other animals. They eat insects and bugs which destroy different crops and consequently safeguard the agro- ecosystems. By habitat management. We can conserve the diversity of natural enemies (including spiders) of arthropod pest (Douglas et al., 2000). Spider’s abundance and diversity vary in different agro-ecosystems and they have temporo-spatial distribution in all agricultural lands to effectively destruct the insect pest population (Seyfulina and Tshernyshev, 2001; Seyfulina, 2003). Their breeding success is directly related to amount of precipitation which act as potential factors to affect the abundance and species richness (Thomas et al., 2014). They are most important arthropods for economic point of view playing role as biological control agent and their adaptation towards different habitats (Kazim et al., 2014). Keeping in view the importance of spider densities and role of berseem in live-stock sector, the present study was designed to record the population dynamics and spatial distribution of ground dwelling spider families and genea among berseem crop at Okara district. Materials and methods Study area The present study was designed to record spatial distribution of ground dwelling spiders among berseem crop at Okara district. Because information about their distribution in any agro-ecosystem was pre-requisite to formulate any strategy to use them for bio-control purposes. Presently, these informations were recorded from Okara district. Trifolium crop was cultivated in one acre rectangular field. The sampling field was surrounded by wheat fields from two sides, where as on third side, it was surrounded by a Trifolium and Mustard field. Okara district Okara district is situated in Punjab province at 30,
  • 3. J. Bio. Env. Sci. 2016 106 | Rana et al. 8081 (304829.160”N) latitude and 73, 4458 (732644.880”E) longitude. This district is bounded on the East by Kasur district, Sahiwal and Pakpattan districts on the West, Sheikhupura and Faisalabad districts on the North and Bahawalnagar district on the South. The Indian border also lies on the South- Eastern side of the district. Okara district has a total area of 4,377 square kilometres and comprises of three tehsils i.e. Okara, Depalpur and Renala Khurd. Climate The climate of the Okara district is hot in summer and cold in winter. May and June are hottest months and January is the coldest one.Temperature ranges between 36-440C in summer and 2-280C in winter. Soil of the district is loamy and sandy loamy with annual rainfall up to 200 mm. Sampling design and techniques The sampling was carried out from October, 2014 through April, 2015 to collect the ground dwelling spider fauna in berseem crop.Total thirty traps were set in the field for five successive days. The two successive traps were at equal distance from each other and the distance from outer boundary of the field was 5m. Pitfall traps were 12cm long glass jars with 6cm (diameter) wide mouths. Each trap contained 150 ml of 70% ethyl alcohol and a small amount of kerosene oil which served as preservative and killing agent.Ten pitfall traps were laid along each transect line i.e. boundary, middle and centre at an equal interval from each other. Collection of data For berseem crop, ideal field measuring 7200 sq. ft. were selected to observe the spatial distribution of ground dwelling spiders through pitfall trap method. However, trapping was made by three layers inside the field radius wise to observe the infestation along the entire field. Data was collected fortnightly and collected specimens were brought into the Pest Control Laboratory, Departmentof Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad. All the specimens were identified according to the reference material. The field of berseem was sampled after 5 days intervals right from the pre-harvest stage. More over, minimum and maximum temperature and humidity of area was also recorded. Preservation All traps were taken to Pest Control Laboratory, Department of Zoology, Wildlife and Fisheries, University of Agriculture, Faisalabad. Where the specimens were washed with xylene and preserved in 95% ethanol containing few drops of glycerin. Specimens were preserved separately in small glass vials indicating with trap number and the date of capture. Identification The collected samples were identified with the aid of naked eye, magnifying glass and under the microscope. All the specimens were identified up to species level according to the taxonomic and reference material (Tikader and Malhotra (1982), Tikader and Biswas (1981), Barrion and Litsinger (1995), Zhu et al. (2003), Platnick (2012), other relevant literature and internet source. Statistical analysis Thereafter, all the identified specimens were arranged in table form according to their morphological characters e.g. family, genus. To determine the various aspects of diversity, Shannon Diversity Index was used (Magurran, 1988). Analysis of Variance was made to compare the population means between three transects, i.e. Boundary, middle and centre of berseem crop. The richness, diversity and evenness indices were computed by using the Programme SPDIVERS.BAS. Results The present study was conducted to highlight the spatial distribution of ground dwelling spiders among berseem crop at Okara district. A total number of 463 specimen pertaining to 25 genera and 7 families among berseem crop were identified from Okara district (Table 1).
  • 4. J. Bio. Env. Sci. 2016 107 | Rana et al. Table 1. The number of families, specimen and genera recorded from berseem field at Okara district. Sr.No. Families No. of Specimen No. of Genera 1 Araneidae 34 4 2 Clubionidae 20 1 3 Gnaphosidae 122 5 4 Linyphiidae 63 3 5 Lycosidae 165 5 6 Salticidae 37 4 7 Thomisidea 22 3 Total 7 463 25 Table 2. Monthly record of spider families captured from berseem crop at Okara district. Families No.of spiders in Nov-14 No.of spiders in Dec-14 No.of spiders in Jan-15 No.of spiders in Feb-15 No.of spiders in Mar-15 No.of spiders in Apr-15 Total No. of spiders Araneidae 2 2 0 4 9 17 34 Clubionidae 0 0 0 3 5 12 20 Gnaphosidae 9 3 1 18 31 60 122 Linyphiidae 5 3 3 7 14 31 63 Lycosidae 11 4 3 25 50 72 165 Salticidae 3 1 0 8 10 15 37 Thomisidea 3 1 1 3 6 8 22 Grand Total 33 14 8 68 125 215 463 Population variations among families in berseem crop Data presented in Table 2, is pertaining to family’s wise comparison of spiders’ population recorded from two fodder crops during the study. In Berseem crop, the population of wolf spiders – family Lycosidae was recorded with highest population (N = 165), followed by Flat bellied ground spiders – family Gnaphosidae (N = 122), Sheat weaver spiders – family Linyphiidae (N = 63), Jumping spiders – family Salticidae (N = 37), Orb-weaver spiders – family Araneidae (N = 34), Crab spiders-- family--Thomisidea (N = 22) and Sac spiders-- family—Clubionidae (N = 21) respectively. Table 3. Population variations of spider genera among berseem field at Okara district. Family Genera Nov-14 Dec-14 Jan-15 Feb-15 Mar-15 Apr-15 Total Araneidae Araneus Clerck, 1757 1 0 0 3 2 5 11 Gea C. L. Koch, 1843 0 2 0 0 2 4 8 Neoscona Simon, 1864 1 0 0 1 3 3 8 Cyclosa Menge, 1866 0 0 0 0 2 5 7 Clubionidae Clubiona latreille,1804 0 0 0 3 5 12 20 Gnaphosidae Drassodes 4 2 1 8 12 20 47 Gnaphosa Latreille, 1804 2 0 0 3 6 11 22 Scotophaeus Simon, 1893 2 0 0 3 5 10 20 Zelotes Gistel, 1848 1 1 0 4 6 14 26 Micaria Westring, 1851 0 0 0 0 2 5 7 Linyphiidae Tapinocyboides Wiehle, 1960 1 1 0 2 5 16 25 Tchatkalophantes Tanasevitch, 2001 2 1 2 3 4 8 20 Tiso Simon, 1884 2 1 1 2 5 7 18 Lycosidae Evippa Simon, 1882 5 2 1 14 21 36 79 Hogna Simon,1885 1 1 1 2 3 8 Lycosa Latreille, 1804 3 1 0 8 18 20 50 Pardosa C. L. Koch, 1847 2 1 1 2 8 12 26 Trochosa C. L. Koch, 1847 0 0 0 0 1 1 2 Salticidae Myrmarachne MacLeay, 1839 2 0 0 2 4 5 13 Phlegra Simon, 1876 1 0 2 2 4 9 Plexippus C. L. Koch, 1846 1 0 0 1 2 3 7 Sitticus Simon, 1901 0 0 0 3 2 3 8 Thomisidea Runcinia Simon, 1875 1 1 1 2 2 7 Thomisus Walckenaer, 1805 1 0 0 3 2 4 10 Xysticus 1 0 0 0 2 2 5 Grand Total 33 14 8 68 125 215 463
  • 5. J. Bio. Env. Sci. 2016 108 | Rana et al. The maximum population of wolf spiders – family Lycosidae was recorded due to that they were strictly ground dwelling spiders. Second and third highest population recorded were of Flat bellied ground spiders – family Gnaphosidae and Sheat weaver spiders – family Linyphiidae respectively due to the reason that they were also ground living and live in high vegetation density, therefore the existing environment was supportive for them. However minimum population of identified spiders in case of Jumping spiders – family Salticidae followed by Orb- weaver spiders – family Araneidae, Crab spiders-- family Thomisidea and Sac spiders -- family Clubionidae was recorded from berseem field.Their low population was recorded due to that they live in leaf litter and shaddy areas. The study area was surrounded by wheat crops from north and east side and mustard crop from west side. Whole cultivated area was comprised of crop land and there was no shaddy tree near the study area. Another reason for their least collection was that, they were foliage spiders and pitfall method was applied for the collection of spiders. Table 4. Number of genera (S), total number of samples (N), Shannon diversity index, Lambda value and Evenness for transect-wise monthly data of berseem crop for different genera. Site Month S N H' Shannon Lambda Evenness Dominance Boundary Nov. 11 17 2.2624 0.1211 0.9435 0.0565 Dec. 6 6 1.7918 0.1667 1.0000 0.000 Jan. 3 3 1.0986 0.3333 1.0000 0.000 Feb. 15 24 2.5209 0.0972 0.9309 0.0691 Mar. 19 45 2.6839 0.0884 0.9115 0.0885 Apr. 25 73 2.9098 0.0696 0.9040 0.096 Middle Nov. 9 12 2.0947 0.1389 0.9534 0.0466 Dec. 5 5 1.6094 0.2000 1.0000 0.000 Jan. 5 5 1.6094 0.2000 1.0000 0.000 Feb. 18 40 2.6485 0.0938 0.9163 0.0837 Mar. 25 66 2.8543 0.0804 0.8868 0.1132 Apr. 23 103 2.8428 0.0755 0.9067 0.0933 Center Nov. 5 5 1.6094 0.2000 1.0000 0.000 Dec. 2 2 0.6932 0.5000 1.0000 0.000 Jan. - - - - - - Feb. 4 4 1.3863 0.2500 1.0000 0.000 Mar. 11 14 2.3420 0.1020 0.9767 0.0233 Apr. 16 39 2.4830 0.1059 0.8956 0.1044 Where S = Number of species N = Total number of samples (sum). Population variations among genera in berseem crop Data presented in Table 3, is regarding the comparison of spider’s population among genera recorded in berseem field during the study. Out of 25 genera, maximum population of identified genera was recorded in case of genus Evapa (N=79) followed by Lycosa (N=50) and Drassodes (N=47) respectively. Minimum population of identified spider genera was recorded in case of genus Cyclosa (N=7), Micaria (N=7), Plexipus (N=7), Runcinia (N=7), Xysticus (N=5), and Trochosa (N=2) respectively. Least population was recorded in case of genus Cyclosa, Micaria, plexipus, Runcinia, Xysticus, and Trochosa respectively. Because they were ground dwelling spiders and live in shelter places while in berseem field, fodder was cut down again and again that’s why their minimum population was recorded.
  • 6. J. Bio. Env. Sci. 2016 109 | Rana et al. Table 5. Number of genera(S), total number of samples(N), Shannon diversity index, Lambda value, Evenness and dominance for transect-wise monthly record of berseem crop for different genera. Month S N H Shannon Lambda Evenness Dominance November 18 33 2.7327 0.0762 0.9455 0.0545 December 11 14 2.342 0.102 0.9767 0.0233 January 7 8 1.9062 0.1563 0.9796 0.0204 February 19 68 2.6641 0.0921 0.9048 0.0952 March 25 125 2.8624 0.0788 0.8893 0.1107 April 25 215 2.8859 0.0728 0.8966 0.1034 Spatial diversity of spider genera in berseem cropData presented in Tabl 4, is pertaining the month wise comparison of diversity indices among species at three trasects i.e. boundary, middle and centre of the berseem crop. During the month of November maximum diversity (H) at boundary recorded was 2.2624, eveness 0.9435 and dominance was 0.0565 when compared with middle, maximum diversity was 2.0947, eveness 0.9534, and dominance 0.0466. and at centre, maximum diversity 1.6094, eveness 1.0000 and dominance 0.0000.During the month of December maximum diversity (H) at boundary recorded was 1.7918, eveness 1.0000 and dominance was 0.0000, when compared with middle, maximum diversity was 1.6094, eveness 1.0000, and dominance 0.000. and at centre, maximum diversity 0.6932, eveness 1.0000 and dominance 0.0000.During the month of January maximum diversity (H) at boundary recorded was 1.0986, eveness 1.0000 and dominance was 0.0000 when compared with middle, maximum diversity was 1.6094, eveness 1.0000, and dominance 0.000. and no diversity was recorded in centre.During the month of February maximum diversity (H) at boundary recorded was 2.5209, eveness 0.9309 and dominance was 0.0691 when compared with middle, maximum diversity was 2.6485, eveness 0.9163, and dominance 0.0837. and at centre, maximum diversity 1.3863, eveness 1.0000 and dominance 0.0000.During the month of March maximum diversity ( H”) at boundary recorded was 2.6839, eveness 0.9115 and dominance was 0.0885 when compared with middle, maximum diversity was 2.8543, eveness 0.8868, and dominance 0.1132 and at centre, maximum diversity 2.3420, eveness 0.9767 and dominance 0.0233.During the month of April, maximum diversity (H) at boundary recorded was 2.9098, eveness 0.9040 and dominance was 0.096 when compared with middle, maximum diversity was 2.8428, eveness 0.9067, and dominance 0.0933 and at centre, maximum diversity 2.4830, eveness 0.8956 and dominance 0.1044. Overall maximum diversity (H”) recorded in the month of April at the boundary was 2.9098, eveness 0.9040 and dominance was 0.096 respectively, when compared with boundary and centre of the berseem crop. Overall comparison of diversity indices among berseem crop Data presented in Table 5, is pertaining the month wise comparison of diversity indices among genera from Berseem crop. Overall genera wise maximum diversity (H”) recorded in Berseem crop during the month of November was 3.7327, evenness 0.9455 and dominance 0.0545 respectively. During the month of December maximum diversity 2.3420, evenness 0.9767 and dominance 0.0233 was recorded. During the month of January maximum diversity 1.9062, evenness 0.9796 and dominance 0.0204 was recorded. During the month of February maximum diversity 2.6641, evenness 0.9048 and dominance 0.0952 was recorded. During the month of March maximum diversity 2.8624, evenness 0.8893 and dominance 0.1107 was recorded. During the month of April maximum diversity 2.8859, evenness 0.8966 and dominance 0.1034 was recorded.
  • 7. J. Bio. Env. Sci. 2016 110 | Rana et al. Table 6. Analysis of variance table for transect-wise abundance of different genera for different crops. Source of variation Degrees of freedom Sum of squares Mean squares F-value Months Crop Transect Crop x Transect Error Total 5 1 2 2 25 35 16332.6 49.0 4423.7 24.5 3893.1 24722.9 3266.51 49.00 2211.86 12.25 155.72 20.98** 0.31NS 14.20** 0.08NS NS = Non-significant (P>0.05); * = Significant (P<0.05); ** = Highly significant (P<0.01). Month wise mean ± SE. Month Mean ± SE November-14 December-14 January-15 February-15 March-15 April-15 11.50±3.03 4.00±0.82 2.33±0.71 26.33±6.73 42.33±9.22 60.83±11.79 CD D D C B A Means sharing similar letters are statistically non-significant (P>0.05). Crops x Transect interaction mean ± SE. Transect Berseem Crop Mean ± SE Boundary 28.00 ± 10.89A Middle 38.50 ± 16.19A Center 10.67 ± 6.00B Mean 25.72 ± 6.97A Means sharing similar letter in a row or in a column are statistically non-significant (P>0.05). Maximum diversity 2.8859 was recorded during the month of April .while evenness 0.9796, and dominance 0.1107 were recoded during the month of January and March respectively. Relative abundance Pie graph (Fig. 1) represent the relative abundance of identified spider families in berseem crop at Okara district. Maximum abundance of spiders was recorded in case of family Lycosidae 36% followed by Gnaphosidae 26% and Lyniphiidae 14%. Minimum abundance of spiders was recorded in family Araneidae 7% followed by Thomisidae 5% and Clubionidae 4% respectively. Ecological distribution Temperature of the country is increasing day by day due to global warming. Consequently, the change in temperature also alter the humidity of the environment. Due to change of temperature and humidity, imbalanece the relation ship between organism and the environment (Table 7). This issue was observed on scientific basis among ground dwelling spiders to record the effect of ecological changes. It was recorded that population of spiders was increased with the increase in temperature and
  • 8. J. Bio. Env. Sci. 2016 111 | Rana et al. decreasing tendency was recorded in case of humidity. Because, breeding season of spiders started during April and peaks were recorded with the increase in temperature. Temperature also affects the body processes and egg development. They concluded that females may be able to protect themselves against temperatures that are prohibitively low for reproduction. From these results, it was concluded that variations in population density were due to effect of temperature, humidity, availability of prey, nature of crop rotation and pesticides uses instead of ecological successions. Table 7. Monthly average temperature (maximum and minimum), percentage of humidity recorded from Okara district. Month Average maximum temperature °C Average minimum temperature °C Average relative humidity Novermber 27.2 8.7 85% December 18.9 4.1 90.50% January 16.6 4.1 93.00% February 22.3 6.7 78.50% March 25.1 10 77.00% April 32.5 16.6 78.00% Analysis of variance Data represented in Table 6, pertaining to Analysis of variance for transect-wise abundance of different genera of spiders for berseem crop.The mean number of spider genera in berseem at district Okara was statistically similar. The mean number of spider’s population month wise and transect wise were statistically highly significant (P<0.01). The mean number of spider’s population during the month of December (4.00±0.82) and January (2.33±0.71) were statistically non significant (P>0.05), when compared with mean number in November (11.50±3.03), February (26.33±6.73), March (42.33±9.22) and April (60.83±11.79) was statistically significan (P<0.05). Crop x Transect-wise mean number of spider genera in boundary (27.75±6.68) and middle (36.25±9.89) were statistically non significant (P>0.05) when compared with mean number in centre (9.63±3.38) was statistically significant (P<0.05) among berseem crop. Overall mean number of spider genera in berseem (25.72±6.97) crop was statistically non significant (P>0.05). It is obvious from the indices calculations that spiders abundance decrease with the decrease in temperature and increase in humidity. Resultantly, ecological imbalance of prey verses predators develops which upset the all ecological pyramids and natural cycling. Sustainable prey and predator status is limiting for integrity of any natural system for long term functions. Discussion Seasonal variations in spider population Evidences regarding sesaonal variations of spider population was underlined by considering the findings of previous researchers because field type, management pattern, agronomic operations and use of pesticides, soil culture and floral structures significantly affect spider’s population (Liljesthrom et al., 2002; Ahmad et al., 2005; Pradeep et al., 2015). It was also estimated that start of breeding season, enhancment in growth and acceleration in maturity were proportional to temperature and humidity. As temperature reached above 25°C, start in breeding occur and with decrease in temperature up to the same situation and increase in humidity, it comes to the end. Findings of present study are in agreement with Rajeswaran et al. (2005); Dippenaar-Schoeman (2006); Mushtaq et al. (2003 & 2005); Kazim et al. (2014), Pradeep et al. (2015). It is obvious from the indices calculations that spider’s abundance decrease with the decrease in
  • 9. J. Bio. Env. Sci. 2016 112 | Rana et al. temperature and increase in humidity. These findings support the earlier reports of Mushtaq et al. (2003 & 2005); Iqbal et al. (2009) and Pradeep et al. (2015). Resultantly, ecological imbalance of prey verses predators develops which upset the all ecological pyramids and natural cycling. Sustainable prey and predator status is limiting for integrity of any natural system for long term functions. These findings are in same cotext as reported by Rajeswaran et al. (2005); Dippenaar-Schoeman (2006); Mushtaq et al. (2003 & 2005); Kazim et al. (2014), Pradeep et al. (2015). Fig. 1. Pie graph represent the relative abundance of spider families in berseem crop. Conclusion Hence, it was concluded from the present work that despite to cosmopolitan nature, spiders have some correlation with suitable local conditions or habitat. However, it was also observed that spider’s population in the same study region were also effected by increase or decrease in temperature and humidity. So, there is necessity of future research for the proper use of spider fauna as biological control agent in IPM programmes. References Ahmad S, Ghafoor A, Iqbal MZ. 2005. Biodiversity of Gnaphosid spiders of Triticum vulgare from District Okara, Punjab, Pakistan. Indus Journal Biological Science 2(4), 477-482. Anonymous. 2012-13. Agricultural Statistics of Pakistan. Ministry of Food and Agriculture (Economic Wing), Government of Pakistan. Islamabad. Barrion AT, Litsinger TA. 1995. Riceland spider of South and South Asia. International Rice Research Institute Philphines. Dippenaar-Schoeman A. 2006. Spiders - The African Farmer's Best Friend. Science in Africa - Africa's First On-Line Science Magazine, 1-4 P. Douglas AL, Stephen DW, Geoff MG. 2000. Habitat management to conserve natural enemies of arthropod pests in agriculture. Annu. Rev. Ent., 45: 175-201. Ghaffar A, Musthaq S, Rana SA, Khalil-ur- Rehman. 2011. Influence of Citrus and Guava Branch Architecture on Foliage Spider Fauna. Journal of Agriculture Biology 13, 406-410. Govt. of Pakistan. 2010. Agriculture Statistics, Federal Bureau of Statistics, Ministry of Economics Affairs and Statistics, Pakistan. Hussain A, Khan S, Bakhsh A, Imran M, Ansar M. 2010. Variability in fodder production potential of
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