DOI: 10.13102/sociobiology.v62i4.396Sociobiology 62(4): 604-606 (December, 2015) Open access journal: http://periodicos.uefs.br/ojs/index.php/sociobiology ISSN: 0361-6525 Differential Nest Parasitism in Three Sympatric Social Wasps (Hymenoptera: Vespidae: Polistes spp.) in the West Indies Introduction Social wasps of the subfamily Polistinae (Hymenoptera: Vespidae) are host to nest parasitoids from at least 14 families of insects (Makino, 1985; Nelson, 1968). Social wasps with open-comb nests would seem especially vulnerable to parasitoid invasion. In most of the records compiled by Makino (1985), the host is a species of Polistes or Mischocyttarus, whose nests are of this type. However, this bias may partly be due to the ease with which such parasitism is noted and the overall greater study devoted to these genera. Wasps have a number of tactics to limit penetration by nest parasitoids. The presence of a parasitoid near the nest is likely to elicit prolonged, agitated patrolling of the comb surface by the wasps (Lutz et al., 1984; pers. obs.), and Starr (1990) and Gadagkar (1991) suggest that constant vigilance and active repulsion by adult females are the most important guard against parasitism. If a parasitoid succeeds in laying eggs in the nest, most Polistes and Mischocyttarus make little apparent effort to remove parasitoid brood at any stage Abstract Jamaica’s three species of social wasps were found nesting together in a suburban area. Their nests gave evidence of markedly different parasitoid loads in the sequence Polistes crinitus > P. dorsalis > P. major. Based on larval and pupal silk remains, the moth Chalcoela pegasalis appears to be the main nest parasitoid at this locality. Despite widely different parasitoid loads, the estimated per-nest production of adults was similar among the three species. This suggests a trade-off between investment in anti-parasitoid tactics and in other brood-care activities. Sociobiology An international journal on social insects CK Starr1, JM Nelson2 Article History Edited by Fernando Barbosa Noll, UNESP, Brazil Received 13 April 2014 Initial acceptance 11 June 2014 Final acceptance 17 June 2015 Keywords Chalcoela pegasalis, Jamaica, nest symbionts. Corresponding author Christopher K. Starr Dep’t of Life Sciences University of the West Indies St Augustine, Trinidad & Tobago E-Mail: ckstarr@gmail.com (Gadagkar, 1991). One apparent recourse is to excavate cells with parasitoid larvae and/or pupae, although we have seen evidence of this tactic in few species. Nest parasitoids are very often made conspicuous by the larval silk and pupal cases that they leave behind, which may remain visible long after the wasps have left the nest. Our observations over the years indicate that regions and localities can differ a great deal in the parasitoid load seen in nests, so that the wasps in some places are subject to heavy parasitoid pressure, while those in others are relatively parasitoid-free. What has not been examined up to now is whether co- occurring, closely-related species may differ in this respect. Our purpose here is to compare nest-parasitoid load in three congeneric species at a single neotropical locality. Materials and Methods Jamaica is an oceanic island with just three species of social wasps, all in the genus Polistes (Richards, 1978). One of us (CKS) found all three species nesting abundantly RESEARCH ARTICLE - WASPS 1 - University of the West Indies, St Augustine, Trinidad & Tobago 2 - Oral Roberts University, Tulsa, Oklahoma, USA Sociobiology 62(4): 604-606 (December, 2015) 605 on buildings and other human-made structures in suburban Mona, near the city of Kingston. Nests are easily identifiable to species in the absence of wasps. Among other features, the petiole is excentric in P. crinitus (Felton) nests, centric is those of P. dorsalis (Fabr.) and P. major Beauvois, and the cells are notably larger in P. major than the other two species. The three species all nested in much the same places at our site, often interspersed, with no evident nest-site separation among them. All old nests that could conveniently be reached were collected from buildings on the University of the West Indies campus, up to 100 nests per species. These were then examined in the laboratory with an ordinary dissecting microscope. Cocoons spun by the wasp larvae just before pupating are closely applied to the cell walls (resembling a coat of varnish) and close the cell with a smooth cap. Silk from parasitoids, in contrast, clutters the cell interior and renders it unserviceable for brood rearing. We counted a nest as parasitized if at least one cell was fouled by such foreign silk. Adult wasps sometimes cut away parts of cells walls in an apparent attempt to remove the very tough, resistant parasitoid silk. We counted a nest as showing excavation if there was removal of at least a significant part of any cell wall. The number of larvae that have pupated (and presumably emerged as adults) in a given cell can be determined with confidence by dissecting the cell and counting the fecal pellets deposited in the cell base after the cocoon is spun. Pellets are of fairly uniform size, and where there are two or (rarely) more in a cell base they are separated by a silk layer and therefore distinct (Yamane & Yamane, 1975). Results and Discussion Nests of all three species varied widely in size in our samples from fewer than 25 to at least 250 cells. Average nest size was significantly greater in P. dorsalis than P. crinitus and P. major (Kruskal-Wallis test, p<0.01), while the latter two showed no average difference (p>0.05) (Table 1). (CKS) found a high incidence of P. crinitus nests with evidence of nest parasitoids, while no P. major appeared affected. Based on remains of larval and pupal silk, the predominant parasitoid appeared to be the widespread Chalcoela pegasalis (Walker) (Lepidoptera: Crambidae), previously recorded from P. crinitus (Nelson, 1968). In contrast, no nest showed the pupae characteristic of Pachysomoides (Hymenoptera: Ichneumonidae), although members of this genus are important parasitoids of several New World Polistes spp. (Nelson, 1968; Makino, 1985). As seen in Table 2, P. crinitus had the highest incidence of cells showing C. pegasalis infestation, P. major the lowest (X2>100, p<0.01), consistent with the relative fractions of nests with parasitoids in Table 1. Because the three species nest in much the same places at this one locality, it is reasonable to believe that they are equally exposed to searching nest parasitoids. Nonetheless, the data show that P. crinitus colonies suffer the greatest impact and P. major the least. Most cells of all species had at most one fecal pellet, with a very small number having two or three. Mean per- cell production of adults differed significantly among species (Kruskal-Wallis test; p<0.01). Combining nest size with per- cell production does not significantly alter this pattern. Although species differ significantly in per-cell and per-nest production of adults, the differences were quite modest and showed no evident correlation with differences in parasitoid load. It is our interpretation that differences in losses of brood to parasitoids are offset by differences in another, unknown parameter to produce a trade-off. It is a plausible hypothesis that successful anti-parasitoid vigilance by adult females is so demanding that it markedly diminishes their attention to foraging and other aspects of brood-care. Table 1. Mean size (number of cells) of old nests, frequency of nests with parasitoid silk, and frequency of nests with evidence of cell excavation in three Jamaican social wasps. Further explanation in text. Polistes crinitus n=100 Polistes dorsalis n=100 Polistes major n=74 Mean size + SD 75.2+52.2 95.5+58.8 73.4+77.4 With silk 75 (75%) 21 (21%) 3 (4%) With excavation 24 (24%) 7 (7%) 7 (10%) The species show significant differences (p<0.01) in both the frequency of parasitized nests and frequency of nests with excavation (Table 1; X2 = 108.4 and 13.7, respectively), although there is no significant difference between P. dorsalis and P. major in the latter parameter. Consistent with this, at Villa Altagracia, San Cristóbal, Dominican Republic one of us Polistes crinitus n=7523 Polistes dorsalis n=10,204 Polistes major n=5428 Cells with C. pegasalis silk 2042 (27.1%) 571 (5.6%) 27 (0.5%) Per-cell production of adult wasps 0.69 0.72 0.59 Table 2. Frequency of cells with apparent Chalcoela pegasalis silk and per-cell production of adult wasps in old nests of three Jamaican social wasps. Total numbers of cells below each species are from the nests enumerated in Table 1. Per-cell production of adults is based on counts of fecal pellets in cells bases; e.g. the 7523 cells of the P. crinitus nests contained an estimated 5203 pellets, a mean of 0.69 per cell. Acknowledgements Financial support for this study came from a University of the West Indies travel grant to CKS. We thank Peter & Tyra Bacon for facilitation in Jamaica and the journal’s reviewers for improving criticism. CK Starr, JM Nelson – Polistes nest parasitoids606 References Gadagkar, R. (1991). Belonogaster, Mischocyttarus, Parapolybia and independent-founding Ropalidia. In KG Ross & RW Matthews (Eds.), The Social Biology of Wasps. Ithaca: Cornell Univ. Press (pp 149-190). Lutz, GG, Strassmann, JE, Hughes, CR (1984). Nest defense by the social wasps Polistes exclamans and P. instabilis (Hymenoptera: Vespidae) against the parasitoid Elasmus polistis (Hymenoptera: Chalcidoidea: Eulophidae). Entomological News, 95: 47-50. Makino, S. (1985). List of parasitoids of polistine wasps. Sphecos, 10: 19-25. Nelson, J.M. (1968). Parasites and symbionts of nests of Polistes wasps. Annals of the Entomological Society of America, 61: 1528-1539. Richards, OW (1978). The Social Wasps of the Americas, Excluding the Vespinae. London: British Museum (Natural History) 580 p. Starr, CK (1990). Holding the fort: Colony defense in some primitively social wasps. In DL Evans & JO Schmidt (Eds.), Insect Defenses. Albany: State Univ. of New York Press (pp 421-463). Yamane, Sô, Yamane, Sk. (1975). [Investigating methods for dead vespine nests (Hymenoptera, Vespidae).] Seibutsu Kyôzai (Kikonia), 10: 18-39.