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Volume 2012 (2012), Article ID 153862, 7 pages
Division of Labor in Pachycondyla striata Fr. Smith, 1858 (Hymenoptera: Formicidae: Ponerinae)
Departamento de Zoologia, Instituto de Biociências, Universidade Estadual Paulista (UNESP), Campus Rio Claro SP, Caixa Postal 199, 13506-900 Rio Claro, SP, Brazil
Received 26 March 2011; Revised 19 May 2011; Accepted 19 May 2011
Academic Editor: Jacques H. C. Delabie
Copyright © 2012 Adolfo da Silva-Melo and Edilberto Giannotti. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Four colonies of the ant Pachycondyla striata were used to analyze the specie behavioral repertoire. Forty-six behavioral acts were recorded in laboratory. Here, we present the record the division of labor between the castes and the temporal polyethism of monomorphic workers. The queens carried out many of the behavioral traits recorded in this work however; they performed them less frequently compared to the worker. The workers activity involved chasing and feeding on fresh insects and usingthem to nourish larvae besides laying eggs in the C-posture, an activity also performed by queens, which is similar to that of wasps of the subfamily Stenogastrinae. The young workers were involved in activities of brood care, sexuate care, and nest maintenance, and the older workers were involved in defense, exploration, and foraging.
The evolution of social behavior may be defined as the combination of care for young individuals by adults, overlapping generations, and division of labor in the reproductive and nonreproductive castes [1–4]. The ants are eusocial, and their behavior differs from that one of other social insects in three respects: (a) they have a varied diet, (b) nest building retains characteristics unique to this group, parental care in galleries, and workers performing tasks according to their age or size, and (c) adults remaining long time with their brood .
Among the aspects covered in ethologic studies of ants, division of labor (when individuals within a group perform different roles) or polyethism comprehends a widely explored subject and may present two divisions: (a) physical polyethism, when individuals show distinct morphological characteristics to perform specific tasks and (b) temporal polyethism, when the variation of tasks occurs according to age [1, 2, 4, 6]. Therefore, temporal polyethism may occur both in populations of monomorphic workers and in polymorphic workers [7, 8]. The ants of the genus Pachycondyla have a wide pantropical distribution with about 270 species being described . The Pachycondyla species are diverse in their morphology and their behavior .
Pachycondyla striata Smith 1858 , classified into the subfamily Ponerinae , presents relatively large individuals (13.2–16.7 mm long). The castes are slightly different. The workers are different from the queens by the absence of ocelli and wing scars. This species is distributed through northern Argentina, Paraguay, Uruguay, and Brazil [13–15].
The aim of this study was to verify whether there is division of labor among castes and age polyethism in P. striata. The results will contribute to better understanding and interpretation of its social organization and allow comparison with other species of the family Formicidae.
2. Materials and Methods
Four colonies were collected on the campus of the University UNESP—Universidade Estadual Paulista, Rio Claro (22°32′40′′S/47°32′44′′W), São Paulo State. The ethological analysis began two days after the collection. Observations were done in the foraging area and plaster nest.
The colonies selected in field contained queens and/or winged females. The latter were regarded as queens after wing loss. The colonies were transferred to a laboratory and placed in plastic containers (width: 30.0 cm; length: 48.0 cm; height: 12.0 cm). In each container, there was a plaster nest consisting of three chambers in different sizes, interconnected by tunnels of 1.0 cm in width and 3.0 cm in depth, covered with glass to avoid disturbance and red cellophane paper to prevent the passage of the full spectrum of light.
The diet of the ants consisted of sugar and water in a ratio of 1:1 (offered in test tubes, with cotton wool in the opening), termites, worms, cockroaches, larvae of Coleoptera (Tenebrio molitor), flies, and papaya seeds.
Previous observation was performed for 20 hours to obtain behavioral data, with the aim of identifying queens and workers. The ants were differentiated by covering their thorax with quick-drying paint for model airplanes (Revel), allowing the identification of the individuals by age group just after their emergence. Young workers are known for having a paler color in relation to older ones. Later, the scan sampling method described by Altmann  was used to qualify the acts.
The quantitative observation of the behavioral acts of the individuals in each colony was performed for five minutes, with one-minute intervals. The observation time was one hour a day, four times a week, during six months, for a total of 94 hours. A comparative ethogram for the individuals was developed. Sample coverage was defined by the formula , where = number of behavioral acts observed once and = total number of behavioral acts, the more this value approaches to 1, the more complete the sample . The behavioral catalog was divided into ten categories and used to build histograms and a dendrogram with clustering method (UPGMA) of Euclidean distance  (Table 1).
3.1. Division of Labor
When introduced in laboratory, the individuals of P. striata immediately occupied the artificial nest. The ants carried the immature from the foraging area and accommodated them in the first and minor chamber for 12 hours. Only after this, they carried them to the last and bigger chamber. In the nest seven, the workers distributed randomly the immature to the chambers and tunnels of the nest.
As previously announced for this study, we considered the existence of two castes morphologically and subtly differentiated, containing monomorphical workers. In Table 2 the different categories, are distributed and quantified and behavioral acts of queens, workers, winged females, and males of P. striata are defined as well.
The inactivity of the males into the nest suggests their action to be more prevalent in the mating season, but this was not verified in this study (Table 2).
The behavorial acts supposedly regarded as less derived have been identified in the castes, such as feeding larvae and adults on fresh insects, and laying eggs in the C-posture. Furthermore, the queens performed activities that are exclusively carried out by workers in other more derived species, such as brood care, exploring, foraging, and nest maintenance (Table 2).
The dominance behavior involved both individuals for recruiting and reproductive labor. The latter case, the interaction of dominance occurred between queen and worker and among workers. Some workers developed ovaries to lay eggs. However, this data were not quantified.
3.2. Temporal Polyethism
Some activities were preferably carried out by younger workers or older workers. This suggests division of labor by age (Figure 2).
The younger workers (7 to 56 days of age) stayed in the nest for approximately 27.03 ± 12.72 days (7–56, ). For this time, took they care the pupae, larvae, eggs, males, and winged females (Figure 2). However, some newly hatched ants did not taken care for the young individuals. This might be related the presence of physiological problems, because they died within two or three days.
The older workers (those at more than 56 days of age) performed several categories, but they pointed in the activities out of the nest, as defense, foraging, and exploring (Figure 2). Furthermore, the dominance is a category that deserves attention. It may be linked to the maintenance of the colony, as a measure of protection from the nest and obtaining food, or reproduction.
The intermediate group (queens, virgin queens, and winged females), which is regarded as a caste, showed clear transition tasks. The quantitative results of the group are smaller when compared to workers, and the activties have been concentrated within the nest.
It is interesting to note that a small portion of behavioral acts is performed by queens within the nest. This type of occurrence is mentioned to the species of P. (Neoponera) villosa, P. (Neoponera) apicalis, and P. (Neoponera) obscuricornis . The queens of P. striata presented more care for eggs than to the other immature individuals, while P. (Neoponera) villosa spends more energy caring for eggs and pupae, P. (Neoponera) apicalis and P. (Neoponera) obscuricornis invest more energy in caring for larvae and pupae . The involvement of queens in brood care seems to be a little derived characteristic .
Feeding was a behavioral act frequently observed in the queens of P. striata, while the queen of Nothomyrmecia macrops was seen feeding once .
The agonistic behavioral acts were almost always related to reproduction or foraging activities. Antennal boxing occurred with winged females, queens, and workers. This behavior may be related to the recruitment of workers, as the measure was implemented in the nest, and a larger number of workers moved to the foraging arena. The same happens to P. bertholudi .
In nest 8, after the queen’s death, one worker started laying eggs. Afterwards, agonistic encounters became frequent, and another worker that started laying eggs was mutilated. This suggests that P. striata presents a reproductive dominance, as does P. crassinoda . Agonistic encounters were also reported for P. (Neoponera) obscuricornis [29, 30] and P. bertholudi .
Chagas and Vasconcelos  described the fighting behavior between workers of P. striata and P. (Neoponera) obscuricornis in the field. According to these researchers, this event occurred because P. striata invaded the foraging and/or life area of P. obscuricornis.
The agonistic behavioral acts observed in P. striata were also reported for Dinoponera quadriceps , P. (Neoponera) apicalis , P. (Neoponera) obscuricornis , Rhytidoponera sp. 12 , P. inversa , and P. bertholudi .
We checked that the workers ate larvae, pupae, other workers, and males. Some alive males had their abdominal region pulled off by workers. These behaviors may indicate stress or cannibalism. Wilson  reported that dead workers might be used as food or were discarded.
The eggs of P. striata collected from the natural environment and those laid by queens and workers in laboratory did not develop. They were predated by dominant individuals or by the whole group under stress. Egg predation was reported in Ectatomma planidens [22, 23] and E. vizottoi  although it has been absent or not observed in Pachycondyla bertholudi . The eggs laid by workers are usually eaten by queens and larvae, which represents a stereotyped, conspicuous behavior pattern .
Oophagy is indispensable to the social Hymenoptera . It is important because workers do not regurgitate food either for larvae or for queens, so they can use their own resources to produce immature oocytes . This event seems restricted to some genera in the subfamily Ponerinae .
In the presence of a large number of eggs, the workers gathered them and stood still on them. They standing motionless on eggs, pupae, and larvae. This may suggest warming and protection of the immature individuals. When the number of eggs in the nest was small, the ants of this species kept the eggs clustered between their mandibles.
The behavioral act tandem running was carried out to recruit workers into the foraging arena. Medeiros and Oliveira  observed this as well. This behavior is common in several species such as Pachycondyla (Brotoponera) tesserinoda  and Pachycondyla obscuricornis .
The larvae of P. striata display a characteristic behavior to order food. They shake their necks and heads several times towards the ventral region of their body until a worker answers. This behavior is similar to that one of larvae of Gnamptogenys striatula . The workers moved the larvae towards the prey. In some cases, the workers held the prey between their mandibles, while the larvae inserted their head into the sectioned part of the mealworm and fed on hemolymph. The workers feed preferentially larvae closer to them. Asking for food was a behavioral act observed more often in larvae in the last instar. The workers touched the buccal apparatus of the larvae with their mandibles open, but it was not possible to see the food transfer or the projection of the glossa of the workers. A similar behavioral act was described for P. crassinoda .
Small pieces of mealworm were placed in the ventral region of the larvae of ants by the workers. The larvae curved their necks and fed in the same manner as described for Gnamptogenys horni , Ponera pennsylvannica , and Pachycondyla crassinoda . According to Wilson  and Traniello and Jayasuriya , feeding larvae on small fragments of prey is a less derived characteristic.
P. striata use their stinger to paralyze their prey. The sting might be stimulated by sudden movements of the prey, similar to way what happens to workers of P. caffraria . According to Traniello and Jayasuriya , using the stinger to paralyze prey is a less derived characteristic.
The state of inactivity or deep sleep exhibited by P. striata is similar to one that described by Cassill et al. . Many workers remained motionless in foraging area. This category may reflect the restricted space of the arena or, as Miguel and Del-Claro , the state, containment of spent energy. The inactivity behavior was observed in Pachycondyla (Neoponera) villosa, P. (Neoponera) apicalis, P. (Neoponera) obscuricornis , P. crassinoda , Nothomyrmecia macrops , E. planidens [22, 23], and E. opaciventre .
The monomorphic workers of P. striata present specialized task division, forming work groups to performing tasks linking to individuals with similar ages. Young individuals provide parental care, whereas older individuals carry out the activities of defense, exploration, and foraging.
Young workers stayed in the nest for 56 days, but some left earlier. They were recruited into the foraging area according to the necessity of food or to substitute the dead workers. In the first 45 days after emergence, Ectatomma tuberculatum performs tasks progressively according to the age of the individuals . The same happens to workers of Platythyrea lamellosa, which after hatching (0–5 days of age) present association with pupae and later take care of eggs and larvae, performing specific tasks influenced by their age . Unlike P. striata, newly hatched individuals of the species Pachycondyla caffraria (0–5 days of age) present four types of behavioral acts and are capable of foraging early at this age . Each colony of this species has precise requirements as to carbohydrates and proteins, appropriate for labor division, which happens in relatively fixed proportions between hunting foragers and those which collect water with sugar . Workers of P. striata were seen at the carbohydrate source in a very small frequency. This activity was included in the behavioral act of taking water in from the cotton wool. P. striata preferred to capture other insects to provide protein intake.
This research shows the profile of social organization of P. striata. We see that many behavioral acts are common for species of the subfamily Ponerinae. Although there is a narrow dimorphism in castes of P. striata, there is a great difference of division of labour between them. The age is a factor that controls the performance of tasks in workers.
- E. O. Wilson, The Insect Societies, Belknap Press, Cambridge, Mass, USA, 1971.
- E. O. Wilson, Sociobiology The New Synthesis, Belknap Press, Cambridge, Mass, USA, 1975.
- M. Andersson, “The evolution of eusociality,” Annual Review of Ecology and Systematics, vol. 15, pp. 165–189, 1984.
- B. Hölldobler and E. O. Wilson, The Ants, Belknap Press, Cambridge, Mass, USA, 1990.
- H. D. Sudd, “Ants: foragim, nesting, brood behavior and polyethism,” in Social Insects, H. R. Hermann, Ed., vol. 4, pp. 107–155, Academic Press, New York, NY, USA, 1982.
- E. O. Wilson, “The social biology of ants,” Annual Review of Entomology, vol. 8, pp. 345–368, 1963.
- J. H. Sudd and N. R. Franks, The Behavioural Ecology of Ants, Chapman and Hall, New York, NY, USA, 1987.
- A. B. Sendova-Franks and N. R. Franks, “Self-assembly, self-organization and division of labour,” Philosophical Transactions of the Royal Society B, vol. 354, no. 1388, pp. 1395–1405, 1999.
- B. Bolton, A New General Catalogue of the Ants of the World, Harvard University, Cambridge, Mass, USA, 1995.
- A. L. Wild, “The genus Pachycondyla (Hymenoptera: Formicidae) in Paraguay,” Boletin del Museo Nacional de Historia Natural del Paraguay, vol. 14, pp. 1–18, 2002.
- Fr. Smith, Catalogue of the Hymenopterous Insects in the Collection of the British Museum, Part 6, British Museum, London, UK, 1858.
- B. Bolton, Synopsis and Classification of Formicidae, vol. 71 of Memoirs of the American Entomological Institute, American Entomological Institute, 2003.
- W. W. Kempf, “As formigas do gênero Pachycondyla Fr. Smith no Brasil (Hymenoptera: Formicinae),” Revista Brasileira de Entomologia, vol. 10, pp. 189–204, 1961.
- W. W. Kempf, “Catalogo abreviado das formigas da região neotropical (Hymenoptera: Formicidae),” Studia Entomologica, vol. 5, pp. 3–344, 1972.
- W. W. Kempf and K. Lenko, “Levantamento da formicifauna no litoral norte e ilhas adjacentes do Estado de São Paulo, Brasil.I. subfamilias dorylinae, Ponerinae e Pseudomyrmicinae (Hymenoptera: Formicidae),” Studia Entomologica, vol. 19, pp. 45–66, 1976.
- J. Altmann, “Observational study of behavior: sampling methods,” Behaviour, vol. 49, no. 3-4, pp. 227–267, 1974.
- R. M. Fagen and R. Goldman, “Behavioural catalogue analysis methods,” Animal Behaviour, vol. 25, no. 2, pp. 261–274, 1977.
- C. J. Krebs, Ecological Methodology, Benjamin Cummings, Redwood City, Calif, USA, 2nd edition, 1999.
- M. Pérez-Bautista, J. P. Lachaud, and D. Fresneau, “La division del trabajo em la hormiga primitiva Neoponera villosa (Hymenoptera: Formicidae),” Folia Entomológica Mexicana, vol. 65, pp. 119–130, 1985.
- D. Fresneau and P. Dupuy, “A study of polyethism in a ponerine ant: Neoponera apicalis (Hymenoptera, Formicidae),” Animal Behaviour, vol. 36, no. 5, pp. 1398–1399, 1988.
- P. Jaisson, D. Fresneau, and R. W. Taylor, “Social organization in some primitive australian ants. I. Nothomyrmecia macrops Clark,” Insectes Sociaux, vol. 3, no. 4, pp. 425–438, 1992.
- W. F. Antonialli-Junior and E. Giannotti, “Division of labor in Ectatomma edentatum (Hymenoptera, Formicidae),” Sociobiology, vol. 39, no. 1, pp. 37–63, 2002.
- W. F. Antonialli, V. C. Tofolo, and E. Giannotti, “Population dynamics of Ectatomma planidens (Hymenoptera: Formicidae) under laboratory conditions,” Sociobiology, vol. 50, no. 3, pp. 1005–1013, 2007.
- J. Korb and J. Heinze, “Multilevel selection and social evolution of insect societies,” Naturwissenschaften, vol. 91, no. 6, pp. 291–304, 2004.
- S. Turillazzi, “The stenogastrinae,” in The Social Biology of Wasps, K. G. Ross and R. W. Matthews, Eds., pp. 47–98, Cornell University, Ithaca, NY, USA, 1991.
- E. Francescato, A. Massolo, M. Landi, L. Gerace, R. Hashim, and S. Turillazzi, “Colony membership, division of labor, and genetic relatedness among females of colonies of Eustenogaster fraterna (Hymenoptera, Vespidae, Stenogastrinae),” Journal of Insect Behavior, vol. 15, no. 2, pp. 153–170, 2002.
- M. F. Sledge, C. Peeters, and M. R. Crewe, “Reproductive division of labour without dominance interactions in the queenless ponerine ant Pachycondyla (Ophthalmopone) berthoudi,” Insectes Sociaux, vol. 48, no. 1, pp. 67–73, 2001.
- A. Henriques and P. R. S. Moutinho, “Algumas observações sobre a organização social de Pachyconyla crassinoda Latreille,1802 (Hymenoptera: Formicidae: Ponerinae),” Revista Brasileira de Entomologica, vol. 38, pp. 605–611, 1994.
- P. S. Oliveira and B. Hölldobler, “Agonistic interactions and reproductives dominance in Pachycondyla obscuricornis (Hymenoptera: Formicidae),” Psyche, vol. 98, pp. 215–225, 1991.
- B. Gobin, J. Heinze, M. Strätz, and F. Roces, “The energetic cost of reproductive conflicts in the ant Pachycondyla obscuricornis,” Journal of Insect Physiology, vol. 49, no. 8, pp. 747–758, 2003.
- A. C. S. Chagas and V. O. Vasconcelos, “Comparação da freqüência da atividade forrageira da formiga Pachycondyla obscuricornis (Emery, 1890) (Hymenoptera: Formicidae) no verão e no inverno, em condições de campo,” Revista Brasileira de Zoociências, vol. 4, p. 109, 2002.
- T. Monnin and C. Peeters, “Dominance hierarchy and reproductive conflicts among subordinates in a monogynous queenless ant,” Behavioral Ecology, vol. 10, no. 3, pp. 323–332, 1999.
- P. S. Oliveira and B. Hölldobler, “Dominance orders in the ponerine ant Pachycondyla apicalis (Hymenoptera, Formicidae),” Behavioral Ecology and Sociobiology, vol. 27, no. 6, pp. 385–393, 1990.
- W. T. Tay and R. H. Crozier, “Nestmate interactions and egg-laying behaviour in the queenless ponerine ant Rhytidoponera sp. 12,” Insectes Sociaux, vol. 47, no. 2, pp. 133–140, 2000.
- K. Kolmer and J. Heinze, “Rank orders and division of labour among unrelated cofounding ant queens,” Proceedings of the Royal Society B, vol. 267, no. 1454, pp. 1729–1734, 2000.
- A. S. Vieira, W. D. Fernandes, and W. F. Antonialli-Junior, “Temporal polyethism, life expectancy, and entropy of workers of the ant Ectatomma vizottoi almeida, 1987 (Formicidae: Ectatomminae),” Acta Ethologica, vol. 13, no. 1, pp. 23–31, 2010.
- C. P. Peeters and R. M. Crewe, “Male biology in the queenless Ophthalmopone berthoudi (Formicidae: Ponerinae),” Psyche, vol. 93, pp. 227–283, 1986.
- C. Peeters, “Morphologically ‘primitive’ ants; comparative review of social characters, and the importance of queen-worker dimorphism,” in The Evolution of Social Behavior in Insects and Arachnids, J. Choe and B. Crespi, Eds., pp. 372–391, Cambridge University Press, Cambridge, UK, 1997.
- F. N. S. Medeiros and P. S. Oliveira, “Season-dependent foraging patterns case study of a neotropical Forest-dwelling ant (Pachycondyla striata Ponerinae),” in Food Exploitation by Social Insects: Ecological, Behavioral, and Theoretical Approaches, S. Jarau and M. Hrncir, Eds., chapter 4, pp. 81–95, CRC Press, 2009.
- V. U. Maschwitz, B. Hölldobler, and M. Möglich, “Tandelaufen als rekrutierungsverhalten bei Brothroponera tesserinoda forel (Formicidae: Ponerinae),” Zei Tschrift Für Tierpsychologie, vol. 35, pp. 113–123, 1974.
- N. Kaptein, J. Billen, and B. Gobin, “Larval begging for food enhances reproductive options in the ponerine ant Gnamptogenys striatula,” Animal Behaviour, vol. 69, no. 2, pp. 263–299, 2005.
- S. C. Pratt, “Ecology and behavior of Gnamptogenys horni (Formicidae: Ponerinae),” Insectes Sociaux, vol. 41, no. 3, pp. 255–262, 1994.
- C. S. Pratt, F. N. Carlin, and P. Calabi, “Division of labor in Ponera pennsylvannica (Formicidae: Ponerinae),” Insectes Sociaux, vol. 41, no. 1, pp. 43–61, 1994.
- J. F. A. Traniello and A. K. Jayasuriya, “The biology of the primitive ant Aneuretus simoni (Emery) (Formicidae: Aneuretinae) II. the social ethogram and division of labor,” Insectes Sociaux, vol. 32, no. 4, pp. 375–388, 1985.
- C. Agbogba and P. E. Howse, “Division of labor between foraging workers of the ponerine ant Pachycondila caffraria (Smith) (Hymenoptera: Formicidae),” Insectes Sociaux, vol. 39, pp. 455–458, 1992.
- D. L. Cassill, S. Brown, and D. Swick, “Polyphasic wake/sleep episodes in the fire ant, Solenopsis invicta,” Journal of Insect Behavior, vol. 22, no. 4, pp. 313–323, 2009.
- T. B. Miguel and K. Del-Claro, “Polietismo etário e repertório comportamental de Ectatomma opaciventre roger, 1861 (Formicidae: Ponerinae),” Revista Brasileira de Zoociências, vol. 7, pp. 293–310, 2005.
- R. C. S. Brito, Divisão De Trabalho: Aspectos Comportamentais Da Regulação Social Do Cuidado à Prole Em Pachycondyla crassinoda Latreille, 1802 (Hymenoptera: Formicidae: Ponerinae), thesis, USP-Univesidade de São Paulo, 1999.
- A. Champalbert and J. P. Lachaud, “Existence of a sensitive period during the ontogenesis of social behaviour in a primitive ant,” Animal Behaviour, vol. 39, no. 5, pp. 850–859, 1990.
- M. H. Villet, “Social organization of Platythyrea lamellosa (Roger) (Hymenoptera: Formicidae): II division of labour,” Suid-Afrikaanse Tydskrif vir Plantkunde, vol. 25, pp. 254–259, 1990.
- C. Agbogba, “Absence of temporal polyethism in the ponerine ant Pachycondyla caffraria (Smith) (Hymenoptera: Formicidae): early specialization of the foragers,” Behavioural Processes, vol. 32, no. 1, pp. 47–52, 1994.