DOI: 10.13102/sociobiology.v61i2.218-224Sociobiology 61(2): 218-224 (June, 2014) Open access journal: http://periodicos.uefs.br/ojs/index.php/sociobiology ISSN: 0361-6525 Reproductive Status of the social wasp Polistes versicolor (Hymenoptera, Vespidae) VO Torres1, D Sguarizi-Antonio2, SM Lima1, LHC Andrade1 & WF Antonialli-Junior1 Introduction An important feature for the ecological success of social insects is the division of labor among individuals in their colonies (Wilson, 1985). For this reason, many investi- gators have devoted their efforts to elucidate the parameters that determine this division, especially the distinction and de- termination of the caste (Robinson, 1992; O’Donnell, 1995; O’Donnell, 1998). The subfamily Polistinae has characteristics that are important to understand how the social behavior has evolved in the wasps (Ross & Matthews, 1991). The degree of mor- phological differences among castes in this group can range from total absence (Richards, 1971; Strassmann et al., 2002) to sharp differences among castes (Jeanne, 1991). This, in- deed, may be a key feature in the evolution of social insects, since the presence of wide differentiation among castes indi- cates a higher degree of sociality (Bourke, 1999). In the basal Polistinae such as Mischocyttarus and Polistes, females are distinguished by their behavior, domi- nance hierarchy, degree of ovarian development and/or their Abstract A fundamental feature in the evolution of social insects is the separation of castes, and the presence of wide differentiation between castes indicates a more advanced degree of sociability. In this study, we evaluated factors indicating the reproductive status of females in colonies of the social wasp Polistes versicolor. The reproductive status of each female was examined by measuring nine morphometric characters, by tracing the cuticular chemical profile, by evidence of insemination and by recording the relative age. We conclude that P. versicolor colonies present 3 female groups according to cu- ticular chemical profile difference. The first group is made of females with filamentous ovarioles, typical of workers; the second one is females with intermediate ovarioles; and the third group is the group of the queens, which are older females, already inse- minated and with the greatest degree of ovarian development. No significant external morphological differences were found among these female groups. Therefore, despite the lack of significant morphological differences among females, there are other factors such as the chemical composition of the cuticula, which are indicative of the reproduc- tive physiological condition of the female in the colony. Sociobiology An international journal on social insects 1 - Universidade Federal da Grande Dourados, Dourados-MS, Brazil. 2 - Universidade Estadual de Mato Grosso do Sul, Dourados-MS, Brazil. Article History Edited by Marcel G Hermes, UFL, Brazil Received 12 November 2013 Initial acceptance 17 February 2014 Final acceptance 06 March 2014 Keywords Cuticular hydrocarbons, Polistinae Ovarian development Corresponding author Viviana de Oliveira Torres Progr. de Pós-graduação em Entomo- logia e Conservação da Biodiversidade Univ. Federal da Grande Dourados Dourados, Mato Grosso do Sul, Brazil 79804-970 E-mail: vivianabio@yahoo.com.br reproductive physiology (Röseler et al., 1985). The dominan- ce status of the individual apparently initiates a physiologi- cal response that directly affects their ovarian development (Wheeler, 1986). The queen shows the highest degree of ovarian development and, by using behavioral strategies to dominate all of the other females, she largely monopolizes reproduction while avoiding energy-consuming tasks such as foraging (Jeanne, 1972; Strassmann & Meyer, 1983). Evidently, on the lack of visible external traits, some other kind of detection mechanism, used by each member of the colony, is needed for the establishment and recognition of this hierarchy, and chemical communication is the most effective way to accomplish this recognition. Among the compounds involved in this process are the cuticular hydro- carbons (CHCs), which are a constituent of the lipid layer that coats the cuticle of insects, and have the primary functions of preventing desiccation (Lockey, 1988) and creating a barrier against microorganisms (Provost et al., 2008). CHCs also act as contact pheromones, allowing conspecific individuals to identify each other, thus assisting in maintaining the colony structure, separating individuals according to their function RESEARCH ARTICLE - WASPS Sociobiology 61(2): 218-224 (June, 2014) 219 in the colony, their physiological status and their hierarchical rank (Provost et al., 2008), functioning, therefore, as a speci- fic chemical signature of the individuals. Sledge et al. (2001) and Monnin (2006) noted that there is a strong correlation between reproductive status and CHC profile of each individual in a colony of wasps. According to Dapporto et al. (2005), in colonies of Polistes dominula (Christ) founded by a single female, the CHC profile of the queen and its brood are different and, when one of those co- lonies becomes orphaned, a worker assumes the queen posi- tion, its ovaries develop, and acquires a CHC profile similar to that of the original queen. Maintenance of a reproductive monopoly by a queen is one of the goals reached by many social insects. In in- dependent-founding species, it was believed that the queen maintains her reproductive status by using aggression toward other females; however, in recent decades many studies have demonstrated the importance and role of CHCs in the com- munication among members of the colonies and in maintai- ning the status of the queen (Bonavita-Cougourdan et al., 1991; Peeters et al., 1999; Liebig et al., 2000; Sledge et al., 2001; Dapporto et al., 2005). This study is focused on analyzing the reproductive status of females of Polistes versicolor (Olivier) through exa- mining morphological and reproductive physiological featu- res and by tracing the chemical profiles of the cuticula. Material and Methods We collected 10 colonies of P. versicolor in the sou- thern region of the state of Mato Grosso do Sul, in the cities of Dourados (22º13’16” S 54º48’20” W) and Mundo Novo (23º56’23” S 54º17’25”W). All of the females from each co- lony were evaluated for morphological, physiological and cuticular chemical profile analyses. The classification of the colonial stage are done according to the system proposed by Jeanne (1972). After collection, the gaster of each female was indivi- dually fixed in an Eppendorf containing absolute ethyl alco- hol (99.8% PA) for later analysis of ovarian development, in- semination and relative age. The remainder of the body was preserved by freezing, for subsequent morphometric measu- rements and analysis of the cuticular chemical profile. We performed nine morphometric measurements, modified from Shima et al. (1994) and Noll et al. (1997), in order to detect morphological diferences: Head: width (HW), minimum interorbital distances (IDx); Mesosoma: width, length and height of mesoscutum (MSW, MSL and MSH, respectively); Metasoma: basal and apical heights of tergite 2 (T2BH and T2AH), length of tergite 2 (T2L); Wing: partial length of the forewing (WL). The gaster was dissected under a Zeiss binocular ste- reomicroscope for evaluation of the degree of ovarian de- velopment, insemination and relative age. The ovaries were classified according to the stage of development of the ova- rioles, based on the observations of Baio et al. (2004). For each female, the spermatheca was removed and put on a slide in a 1:1 solution of acid fucsina (1%) in order to determine the presence of sperm cells under a light mi- croscope. The relative age of all adult females was determined, according to the pigmentation of the transverse apodeme across the hidden base of the fifth sternum, as follows: LY (light yellow), LB (light brown), DB (dark brown) and BA (black). According to Richards (1971) and West-Eberhard (1973), this color sequence indicates a progression in the age of individuals, from younger (LY) to older females (BA). For analysis of the cuticular chemical profile, the tho- rax of each female was submitted to optical spectroscopy by Fourier Transform Infrared Photoacoustic Spectroscopy (FTIR-PAS), after 48 hours in a vacuum oven, in order to minimize the water content. This technique was used by An- tonialli-Junior et al. (2007 and 2008) and Neves et al. (2012) and has proved reliable for assessing the CHCs profiles of ants and wasps, even when compared to gas chromatography (Ferreira et al., 2012). The FTIR-PAS technique measures the radiation absor- bed by the sample. It is advantageous for application on very fragile objects, such as biological materials, because the low- intensity radiation does not destroy the sample. FTIR-PAS uses the infrared spectrum from 400 to 4000 cm-1 (Silverstein et al., 2000; Skoog et al., 2002), which is sensitive to the vibrations and rotations of molecular chemical groups, so it can identify and distinguish molecular radicals and some kinds of chemical bonds in the samples (Smith, 1999). The resulting spectrum for each thorax was obtained from the mean of 64 spectra with a resolution of 8 cm-1, which were separated in absorption lines between 400 and 4000 cm-1, mostly those related to vibrations of CHCs. The degree of ovarian development, morphometric data and the cuticular chemical profile were evaluated by stepwise discriminant analysis, which reveals the group of variables that better explain the groups evaluated in case of a difference. This is indicated by Wilk’s Lambda, a measure of the difference, if any, among the groups (Quinn & Keough, 2002). The chi-square test was performed to test the association between the relative age and the three groups of females (workers 1, workers 2 and queens). For all analyses, the variable was considered signifi- cant when the level reached was <0.05. Results and discussion Four kinds of ovarian development (Fig. 1) were found in females of this species: type A, filamentous ovarioles without visibly developed oocytes; type B, ovarioles containing some oocytes in the initial stage of development; type C, ovarioles with moderately developed oocytes, some in the final phase of vitellogenesis; and type D, well-developed, longer ovario- V.O. Torres et al - Reproductive Status of Polistes versicolor220 lopment were also the inseminated ones. However, Giannotti and Machado (1999), Gobbi et al. (2006) and Murakami et al. (2009) analyzed several independent founding species, Polistes lanio (Fabricius), P. versicolor and Mischocyttarus cassununga (von Ihering) among them, and found six, five and five ova- rian development patterns, respectively. Other studies evaluating the relationship between the degree of ovarian development and the reproductive position occupied by the females were performed on Parachartergus smithii (Saussure) (Mateus et al., 1997), Pseudopolybia vespi- ceps (Ducke) (Shima et al., 1998), Chartergellus communis (Richards) (Mateus et al., 1999), Brachygastra lecheguana (Latreille) (Shima et al., 2000), Parachartergus fraternus (Gribodo) (Mateus et al., 2004) and Protopolybia chartegoides (Gribodo) (Felippotti et al., 2007), all of them species of Epi- ponini. The colonies of P. versicolor contained on average 2.9 ± 1.72 inseminated females, demonstrating the potential of other females to replace the queen; however, only one fe- male had an ovarian condition typical of a laying individual (Fig. 1D). Giannotti & Machado (1999) and Murakami et al. (2009) also reported more than one inseminated female in colonies of P. lanio and M. cassununga, respectively. In fact, the presence of more than one inseminated female in the colony, capable of reproducing, is a common feature in independent-founding species, as is the case for Polistes and Mischocyttarus. This fact shows that the distinction between reproductive and non-reproductive females is quite flexible and complex, depending on physiological, behavioral and ecological factors (Murakami & Shima, 2006). Insemination of two or more females in the same colony can be a strategy to overcome problems encountered during the colony cycle, such as predation or parasitism, as suggested by Murakami et al. (2009) for M. cassununga. Gobbi et al. (2006) found that 75% of P. versicolor females in the aggregate and 85% in the foundation association were inseminated; there- fore, insemination must occur before the formation of aggre- gates. The results from the analyzes of the cuticular chemical profile show that the 4 different types of ovarian development Fig 1. Different degrees of ovarian development found in females of Polistes versicolor. A) type A, filamentous ovarioles without visible developed oocytes; B) type B, ovarioles containing some oocytes in the initial stage of development; C) type C, ovarioles with mode- rately developed oocytes, some in the final phase of vitellogenesis; D) type D, well-developed, longer ovario les, each containing two to several producing oocytes. les, each containing two to several producing oocytes. Type D females were always inseminated. These four physiological conditions were described by Baio et al. (2004) for Brachygastra augusti (Saussure). Noll et al. (2004) also described these same conditions in the species Apoica pallens (Fabricius), Charterginus fulvus (Fox) and Nectarinella championi (Dover). In all of these species, the females with the most advanced ovarian deve- Fig 2. Mean curve for each group of mid-infrared ab- sorption spectra of the thorax of Polistes versicolor females, grouped according to cuticular chemical pro- file and indicating the significant peaks for separation of the groups. Sociobiology 61(2): 218-224 (June, 2014) 221 degree are distributed among three distinct categories of fe- males: a) Workers 1, with filamentous ovarioles, type A; b) Workers 2, with partially developed ovarioles, types B and C; and c) Queens, with fully developed ovarioles, type D (Fig. 1 and 2). These differences were significant (Wilks’ Lambda = 0.476, F = 6.303, P <0.001) (Fig. 3). The spectra analyzed by FTIR-PAS showed significant differences among the cuticular chemical profiles, indicating seven significant peaks for the separation of females groups (Fig. 2 and Table 1). These compounds were linked to chitin (1238, 1523 e 2634 cm-1) and CHCs (667, 1030, 1377 and 1450 cm-1) present in the female cuticle (Table I). Antonialli- Junior et al. (2007) and Neves et al. (2012) discuss the impor- tance of these peaks for distinguishing the groups analysed. However, the most significant peaks for those groups were mainly those corresponding to the hydrocarbon band (Fig. 2 and Table 1). The first canonical root explained 93% of the results, and the second one the reimaning 7%, explaining together 100% of the results. Therefore, it seems that every female within these three groups had a different physiological status within the colony, which leads to a difference in the cuticular chemical profile and probably in the recognition by other fe- males of their position in the colony hierarchy. According to Monnin (2006), there are correlations between reproductive status and the CHC profile in social insects, and that differentiation is important for the establish- ment of a hierarchy in independent-founding species, as it is the case for many Neotropical members of Polistinae. In colonies of P. dominula founded by a single female, the CHC profiles of the queen and workers were different (Dapporto et al., 2005). Bonckaert et al. (2012) investigated colonies of Vespula vulgaris (Linnaeus) and found that laying queens, queens in aggregate, virgin queens, and workers had different degrees of ovarian development, and this was correlated with their respective CHCs profiles. The discriminant analysis of the 3 groups of females with different cuticular chemical profiles, however, showed no significant morphological differences (Wilks’ Lambda = 0.851, F = 3.182, P <0.05), indicating an absence of mor- phological differences among these groups. The absence of morphological differences among castes was also reported by Giannotti & Machado (1999) for P. lanio and by Murakami et al. (2009) for M. cassununga, all of them independent-foun- ding species. However, Gobbi et al. (2006) observed that of P. versicolor female aggregate are significantly larger than first emerged females, foundress association and workers. Tannu- re-Nascimento et al. (2005) suggested that the morphological differences between reproductive and non-reproductive fema- les of Polistes satan (Bequaert) during the colony cycle is due to seasonal nutritional differences. In fact, most studies describe the absence of morpho- logical differences among castes in Polistes and Mischocyt- tarus (Cumber, 1951; Giannotti & Machado, 1999; Tannure- Nascimento et al., 2005; Murakami et al., 2009), supporting the hypothesis of post-imaginal caste determination. How- ever, studies such as those of Gadagkar et al. (1991), Keeping (2002), Dapporto et al. (2008) and Hunt et al. (2011) per- formed with Ropalidia marginata (Fabricius), Belonogaster petiolata (DeGeer), Polistes metricus (Say) e P. dominula, respectively, show that, at least in part, the distinction of cas- tes may be pre-imaginal. By analyzing the relative age of the females we found a higher frequency of young females during the post-emer- gence (pre-male) stage and, as the colony cycle advances, old females become more frequent during the post-emergence Peak Wave number (cm-1) Canonical root 1 Canonical root 2 Functional group Vibration model (1) 667 1.453 3.036 Out-of-plane C-H (benzene) Bending (2) 1030 3.185 -5.432 In plane C-H (benzene) Bending (3) 1238 5.766 -5.481 -C-N Stretching (4) 1377 -15.713 7.655 C-CH3 Symmetric bending (5) 1450 2.659 1.669 C-CH2 and C-CH3 Asymmetric bending scissors (6) 1523 3.216 -1.956 N-H Bending (7) 2634 0.173 1.456 C-N and N-H Overtone bending Table 1. Wave numbers, coefficients of the two canonical roots, functional groups, and vibrations of the peaks identified in the infrared absorption spectra of the thorax of the wasps, for analysis of the cuticular chemical profile. Fig 3. Dispersion diagram of the results of the stepwise discriminant analysis, showing the two canonical roots of differentiation of cuti- cular chemical profile in 3 different groups of females of Polistes versicolor. V.O. Torres et al - Reproductive Status of Polistes versicolor222 (post-male) and decline stages (Fig. 4). The chi-square test (χ2 = 65.594, df = 6, P <0.05) indicated a relationship betwe- en the female age and the degree of ovarian development, in which the queens are always among the older females of the colony. The workers have a range of ages, which is probably related to the stage of the colony cycle. Corroborating these results, Baio et al. (2003), Mu- rakami et al. (2009) and Felippotti et al. (2010), investigating colonies of Metapolybia docilis (Richards), M. cassununga and three species of Clypearia respectively, reported that queens are among the older females in the colony, and that the presence of young and old females varies according to the stage of the colony cycle. Murakami et al. (2009) observed that females with the most advanced ovarian development are older and are also more aggressive in the hierarchical ranking. All of these results agree with the system of ge- rontocracy (Strassmann & Meyer, 1983), common in inde- pendent-founding species, which means that, as the workers grow older, they are subject to more aggressive acts of from the dominant female. Acknowledgments The authors thank Janet W. Reid (JWR Associates) for the revision of the English text, and Orlando T. Silveira (Museu Paraense Emílio Goeldi) for the identification of the species. 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