cr
Ciência Rural
Cienc. Rural
0103-8478
1678-4596
Universidade Federal de Santa Maria
RESUMO:
Os estádios de desenvolvimento pós-embrionário de Marpissa bengalensis (Araneae; Salticidac), a segunda espécie predatória mais abundante no pomar cítrico, foram coletadas no pomar experimental de frutas do Departamento de Horticultura, localizado no campus da Universidade de Agricultura de Faisalabad, onde foram estudados. O ciclo de biológico foi estudado no laboratório, em que iniciou a partir de ovos coletados de fêmeas grávidas e soltas em cativeiro. O período de incubação variou de 5-15 dias. a média de ovos incubados foram 23,8 ovos/casulo e a porcentagem de incubação em condições laboratoriais foi de 73,18%. A duração média da fase imatura a foi de 7 dias. Uma duração geral, média do terceiro estádio da fase imatura, foi de 7,46 dias de todas as fases imaturas incubadas com 8 casulos. A partir do quarto estádio da fase imatura a duração média foi de 10,23 dias. No quinto estádio de imaturação, demorou uma média de 19,82 dias. O sexto e o sétimo estádios de imaturação duraram um total de 23,14 e 25,86 dias, respectivamente. Durante o oitavo estádio de imaturação a duração foi de 28,08 dias, sendo máxima. Em média, desde a incubação até o estádio adulto, o estádio de imaturação duraram 137 dias. A maior mortalidade foi observada nos terciro e quarto estádios de imaturação, diminuindo, a partir de então, e atingindo zero no oitavo estádio de imaturação.
INTRODUCTION:
Spiders possess the characteristics of predators that can contribute to density-independent limitation of prey, including self-damping, high levels of polyphagy and life cycles that are asynchronous to those of prey species. Hunting spider made up 85.5 -91.7% of the spider fauna in peanut agro ecosystem. Spiders may play an important role in stabilizing or regulating insect’s populations because they are one of the most numerous insectivores and exhibit a wide variety of lifestyles and foraging strategies (NYFFELER et al., 1994).
Spider (Arachnidae: Aranae) is a most abundant, diverse and ecologically important group in many cropping systems (HODGE, 1999; SUNDERLAND AND SAMU, 2000; TAHIR et al., 2012; Hitherto 112 families, 3924 genera and 44540 species of spiders are described in the world (PLATNICK, 2014). They live in a variety of habitat like forest, fields, foliage, ground, and even some may live amphibious life (BUKHARI et al., 2012).
They have great importance in reducing and even preventing outbreaks of insect pests in agricultural fields (SUNDERLAND et al., 1986). They are capable of limiting and equilibrating pest populations (NYFFELER, 1982; SUNDERLAND AND SAMU, 2000), because of their abundance and high predatory potential (Tahir and Butt, 2009), prey specialization, polyphagy, top-down effect, numerical and functional responses, and wasteful killing (MALONEY et al., 2003).
Although, the number of prey in the field fluctuate with season, time of day, microhabitat and foraging strategy (UETZ, 1991), but different spiders residing in the same field may exploit same resources (HODGE, 1999). Hunting and web-weavers are the two major clusters of spiders (UETZ 1991; NYFFELER 1982; UETZ et al., 1999) which are further divided into six to eight guilds (i.e., foliage runners, ground runners, stalkers, ambushers, sheet web weavers, wandering sheet weaver, orb weaver and space web builders) based on web use, web type and microhabitat (UETZ et al., 1999). Marpissa bengalensis is a leading species in crop growing areas of Pakistan. It is the true predator and constitutes a heterogeneous group in terms of their feeding strategies, size and activity patterns. Preliminary study on life cycle is essential for ecological work and is of significance importance to investigate the predatory potential of a species.
MATERIALS AND METHODS:
Field collection of Marpissa bengalensis
This specie was collected from the experimental fruit garden of Horticulture department located at University of Agriculture, Faisalabad. Generally spiders were more commonly present at the curly mortal leaves of citrus plants. Marpissa bengalensis females with or without cocoone particularly were present inside the old curled leaves, males were present on fresh and middle aged leaves. Males and the females were captured by direct hand picking jarring method and were placed separately in the polythene bages and were brought to the laboratory. Males and females of Marpissa bengalensis were identified and recognized for the collection of same species in the field. Marpissa bengalensis was identified with the help of field handlens and their hiding places were traced.
Laboratory experiment
Gravid females with or without cocoon were captured from the foliage of citrus trees and kept for the study of their daily activity and other behaviors such as hatching, post hatching developmental stages as spiderlings, their clutch size, brood care survivorship and mortality rate at each developmental stages till the adulthood in the laboratory.
At first hatching all young ones remained inside the cocoon and after 2 -3 days they come out o f the cocoons and ride on their mother back for 5-6 days. At the end of the second spiderling stage, they leave their mother, shed off their skin and attached them to the cage roof, so being able to move freely. Now each spiderling was transferred to the ennumbered cages. Latter on small pres like aphid, Jassid, whiteflies, fruit flies and large prey like mosquitoes, house flies, honey bees, grasshopper were meshed and then given to these young ones for their survival and their molting was also observed till adult. Remaining preys were cleaned and removed daily to avoid fungal and bacterial attacks. Daily observation chart was dully filed in the laboratory for the record of different developmental stages.
Statistical analysis
The data observed was analyzed for survivorship, mortality and life expectancy at different stages up to 8th instar.
The survivourship (Lx) shall be calculated as
Lx = Nx/No
Where Nx = number of individual which were alive in each stage.
No = Total number of eggs which hatched.
Life expectanc (ex) shall be calculated as:
Ex = Tx/Lx
Where Tx = total number of remainder days in the life of an individual that had reached at X, stage
Tx = ∑mxLx
m, being the maximum age which was reached
RESULTS AND DISCUSSION:
Eight Marpissa bengalensis females with cocoon were released in separate cages. An average incubation period range was recorded as 5-15 days. Hatching percentage was recorded as 73.18% (Table 1). No hatching took place in the cocoons without female.
Table 1
Hatching % age of eggs from each cocoons of Marpissa bengalensis.
No of cocoons
1
2
3
4
5
6
7
8
Total
Mean ± SD
Total eggs
35
30
28
25
30
35
38
40
261
32.6±5.18
Eggs Hatched
28
25
20
18
15
20
30
35
191
23.87±6.97
The hatched spiderlings remained inside the cocoon where two moults took place and pre-larva changed into spiderling. Similar findings have been reported by RUBY et al. (2012). ENDERS (1996) studied that Lycosid spiders have higher egg production. After emergence, the spiderlings climbed on mothers back and ride until they able to move independently. This period is known as brood care and female do not feed in this phase. FOELIX AND CHU-WANG (1973) reported that the mother accesses her offspring during hatching and spiderlings climb on her back.
All the spiderlings passed six developmental stages before reaching adulthood. An average duration for 3rd spiderling stage was 7.46 days. For 4th spiderling stage the duration increased to 10.23 days. In the 5th spiderling stage, the spiderling spent an average of 19.82 days.
Similarly for sixth, seventh and eighth spiderling stage the average duration was 23.14, 25.86 and 28.08 respectively (Table 2). Greater mortality was observed in the 3rd and 4th spiderling stages, decreasing thereafter and reaching zero in the 8th spiderling stage (Table 3). Mortality rate at 3rd and 4th stage spiderling was in accordance with MINERVINO (1993). Large body size decreased mortality which is attained by extending growth period (Clader, 1984). The average duration of maturity period for male was recorded as 112 days and ranged from 112- 120 whereas, for female it was 126 days ranging from 121- 134 (Table 2).
Table 2
Average duration (days) and range of life cycle of Marpissa bengalensis.
Developmental stages
Range
Average duration (days)
3rd spiderling stage
5-10
7.38
4th spiderling stage
7-16
10.20
5th spiderling stage
15-25
19.95
6th spiderling stage
18-30
23
7th spiderling stage
22-30
25.59
8th spiderling stage
25-31
28.08
Table 3
Survivershiop (Lx) and life expectancy in different developmental stages of Marpissa bengalensis.
Developmental stages
N
Lx
ex
3rd spiderling stage
137
0.72
3.15
4th spiderling stage
113
0.59
7.12
5th spiderling stage
94
0.49
8.70
6th spiderling stage
86
0.45
9.02
7th spiderling stage
78
0.41
11.25
8th spiderling stage
78
0.41
11.25
There are reports of low mortality rate by Hibana velox, Chiracanthium inclusum and Trachelas volutes on combination of natural diets (AMALIN et al., 2002). Similar trend of comparatively less mortality or in other words better survival rate was observed with combined natural diets. The presence of above discussed nutrients probably explains the higher percent survival and normal development of spiders on the combination diet and also proved that the experimental species is also a nectar feeder as reported by Taylor and Foster (1996).
In conclusion it is suggested that mass rearing of such important predatory species against serious crop pests could be employed.
REFERENCES:
AMALIN, D.M. et al. Comparison of the survival of three species of sac spiders on natural and artificial diets. J. Arachnol. v.29 p.253-262, 2001.
AMALIN
D.M.
Comparison of the survival of three species of sac spiders on natural and artificial diets.
J. Arachnol
29
253
262
2001
BUKHARI, M. et al. Occurrence and distribution of araneid fauna trapped from cotton fields of district Faisalabad, Pakistan. World Appl. Sci. J. v.19 p.714-718, 2012.
BUKHARI
M.
Occurrence and distribution of araneid fauna trapped from cotton fields of district Faisalabad, Pakistan.
World Appl. Sci. J.
19
714
718
2012
CLADER, W.A. Size, function and life history. Harvard University Press, Cambridge. USA, 1984.
CLADER
W.A
Size, function and life history
Harvard University Press
Cambridge. USA
1984
ENDERS, F. Clutch-size related to hunting manners of spider species. Ann. Ent. Soc. Ame. v.69, p.991-998, 1996.
ENDERS
F
Clutch-size related to hunting manners of spider species.
Ann. Ent. Soc. Ame
69
991
998
1996
FOELIX, R.F. et al. The morphology of spider sensilla chemoreceptor. Tiss. Cells. v.5, p44, 1973.
FOELIX
R.F.
The morphology of spider sensilla chemoreceptor.
Tiss. Cells
5
44
44
1973
HODGE, M.A. The implications of intraguild predation for the role of spiders in biological control. J. Arachnol . v.27, p.351-362, 1999.
HODGE
M.A
The implications of intraguild predation for the role of spiders in biological control.
J. Arachnol
27
351
362
1999
MALONEY, D. et al. Spider predation in agroecosystems: Can spiders effectively control pest population. MAFES Tech. Bull. v.190, p.1-32, 2003.
MALONEY
D.
Spider predation in agroecosystems: Can spiders effectively control pest population
MAFES Tech. Bull
190
1
32
2003
MINERVINO, E. Life cycle of Misumenops pallid (Araneae: Thomisidae). Mem. Inst. Oswaldo. Cruz, v.88, p.49-52, 1993.
MINERVINO
E.
Life cycle of Misumenops pallid (Araneae: Thomisidae).
Mem. Inst. Oswaldo. Cruz
88
49
52
1993
NYFFELER, M. Field studies on the ecological role of spiders as insect predators in agro-ecosystems (abandoned grasslands, meadows and cereal fields). Ph.D. thesis. Swiss Fed. Inst. Tech., Zurich, Switzerland, 1982.
NYFFELER
M.
Field studies on the ecological role of spiders as insect predators in agro-ecosystems (abandoned grasslands, meadows and cereal fields)
Ph.D. thesis.
Swiss Fed. Inst. Tech
Zurich, Switzerland
Zurich, Switzerland
1982
NYFFELER, M., W. et al. How spiders make a living. Entomological Society of America, v.23, n.6, p.1357-1367, 1994.
NYFFELER
M.
How spiders make a living
Entomological Society of America
23
6
1357
1367
1994
PLATNICK, N. I. The world spider catalog, Version 14.0. American Museum of Natural History. 2014. <http:/research.amnh.org/entomology/spiders/catalog/index.html>. doi: 10.5531/db.iz.0001.
PLATNICK
N. I
The world spider catalog, Version 14.0.
American Museum of Natural History
2014
http:/research.amnh.org/entomology/spiders/catalog/index.html
10.5531/db.iz.0001.
SUNDERLAND, K. et al. Effects of agricultural diversification on the abundance, distribution, and pest control potential of spiders: a review. Ent. Exp. Appl., v.95, p.1-13, 2000.
SUNDERLAND
K.
Effects of agricultural diversification on the abundance, distribution, and pest control potential of spiders: a review
Ent. Exp. Appl
95
1
13
2000
SUNDERLAND, K. D. et al. Field and laboratory studies on money spiders (Linyphiidae) as predators of cereal aphids. J. Appl. Ecol., v.23, p.433-447, 1986.
SUNDERLAND
K. D.
Field and laboratory studies on money spiders (Linyphiidae) as predators of cereal aphids.
J. Appl. Ecol
23
.433
.447
1986
TAHIR, H. M. et al. Effects of different management practices and field margins on the abundance of ground spiders in rice ecosystems. Pakistan. J. Zool., v.41, p.85-93, 2009.
TAHIR
H. M.
Effects of different management practices and field margins on the abundance of ground spiders in rice ecosystems.
Pakistan. J. Zool
41
85
93
2009
TAHIR, H. M. et al. Effect of tillage practice on the seasonal dynamics of ground spiders. Pakistan. J. Zool ., v.44, p.884-887, 2012.
TAHIR
H. M.
Effect of tillage practice on the seasonal dynamics of ground spiders
Pakistan. J. Zool
44
884
887
2012
RUBY, T. et al. Survivorship of ground spider Pardosa oakleyi (gravely) under laboratory conditions on natural and artificial diets. Pak. J. Agri. Sci. v.49, n.4, p.451-454, 2012.
RUBY
T.
Survivorship of ground spider Pardosa oakleyi (gravely) under laboratory conditions on natural and artificial diets. Pak
J. Agri. Sci
49
4
451
454
2012
TAYLOR, R.M. et al. Spider nectarivory. Ame. Entomol., v.20, p.82-86, 1996.
TAYLOR
R.M.
Spider nectarivory
Ame. Entomol.,
20
82
86
1996
UETZ, G. W. Habitat structure and Spider foraging. In: McCoy, E.D. et al. Habitat structure; the physical Arrangements of objects in space. Chapman and Hall, London, p.325-348, 1991.
UETZ
G. W.
Habitat structure and Spider foraging
McCoy
E.D.
Habitat structure; the physical Arrangements of objects in space
Chapman and Hall
London
325
348
1991
UETZ, G.W. et al. Guild structure of spiders in major crops. J. Arachnl., v.27, p.270- 280, 1999.
UETZ
G.W.
Guild structure of spiders in major crops
J. Arachnl
27
270
280
1999
0
CR-2017-0531
Autoria
Muhammad Nawab
Department of Zoology, Khawaja Fareed Government Post Graduate College, Rahim Yar Khan, Punjab, Pakistan, 64200.Khawaja Fareed Government Post Graduate CollegePakistanRahim Yar Khan, Punjab, PakistanDepartment of Zoology, Khawaja Fareed Government Post Graduate College, Rahim Yar Khan, Punjab, Pakistan, 64200.
Department of Life Sciences, The Islamia University of Bahawalpur, Punjab, Pakistan, 63100. The Islamia University of BahawalpurPakistanPunjab, PakistanDepartment of Life Sciences, The Islamia University of Bahawalpur, Punjab, Pakistan, 63100.
Department of Zoology, Khawaja Fareed Government Post Graduate College, Rahim Yar Khan, Punjab, Pakistan, 64200.Khawaja Fareed Government Post Graduate CollegePakistanRahim Yar Khan, Punjab, PakistanDepartment of Zoology, Khawaja Fareed Government Post Graduate College, Rahim Yar Khan, Punjab, Pakistan, 64200.
Department of Life Sciences, The Islamia University of Bahawalpur, Punjab, Pakistan, 63100. The Islamia University of BahawalpurPakistanPunjab, PakistanDepartment of Life Sciences, The Islamia University of Bahawalpur, Punjab, Pakistan, 63100.
Universidade Federal de Santa MariaUniversidade Federal de Santa Maria, Centro de Ciências Rurais , 97105-900 Santa Maria RS Brazil , Tel.: +55 55 3220-8698 , Fax: +55 55 3220-8695 -
Santa Maria -
RS -
Brazil E-mail: cienciarural@mail.ufsm.br
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