Active Termite Nests Research Articles

Opportunistic Occupation of Nests of Microcerotermes spp. Silvestri (Termitidae, Termitinae) by Partamona seridoensis Camargo & Pedro (Apidae, Meliponini) in the Brazilian Tropical Dry Forest

Social bees make use of natural or animal-built structures to protect their colonies from environmental stressors. Here, particularly attractive shelters are active termite nests because they provide a stable climatic environment for inquilines. Several social bee species form obligatory associations with termites, among these the stingless bee Partamona seridoensis (Apidae, Meliponini), whose distribution is limited to the Tropical Dry Forest in the Brazilian Northeast. So far, colonies of this meliponine species have been found mainly in arboreal nests of the termite Constrictotermes cyphergaster, which suggests a tight relationship between these two social insect species. The present study was conducted in an area of the Tropical Dry Forest in the Brazilian State of Rio Grande do Norte, where P. seridoensis naturally occurs albeit the absence of C. cyphergaster. We registered 14 colonies of P. seridoensis, all occupying active arboreal nests of termites of the genus Microcerotermes. The only other termites with arboreal nests present in the study area, Nasutitermes corniger, never housed P. seridoensis. This selective preference of the bees for Microcerotermes nests might be due to differences between termites concerning defense mechanisms or concerning thermal stability within the nests.

Do roost-excavating bats have stronger skulls?

In addition to feeding, many vertebrates use their skulls for other functions that are highly relevant to fitness. One such function is roost excavation by the bat Lophostoma silvicolum. Males of this species use their canines to create cavities inside active termite nests, which are significantly harder than the prey they eat. Here we investigate whether the skull of L. silvicolum is specialized for roost excavation relative to the ecologically similar species Tonatia saurophila and Micronycteris hirsuta, which do not excavate roosts. We conducted a finite element analysis that simulated roost excavating and feeding behaviours. These analyses were informed by our observations of feeding and roost-excavating behaviours, bite force, and dissections of the cranial musculature of the three bat species. During the simulation of roost excavation (bilateral canine biting), our data indicate that most regions of the skull of L. silvicolum exhibit less stress than those of T. saurophila and M. hirsuta; however, the latter exhibited the lowest peak stress at the zygomatic arches. During loads that simulate feeding (bilateral molar biting), the three species exhibit similar stress levels. It is not clear whether L. silvicolum has a skull shape that is stronger under the loads imposed by excavation, but it does exhibit relatively higher bilateral canine bite forces that are generated via relatively larger temporalis muscles. Based on the muscle data, our study suggests that the feeding apparatus of mammals can exhibit performance and morphological adaptations to functions other than feeding. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2011, 102, 1–10.

Roost Making in Bats—Adaptations for Excavating Active Termite Nests

The breadth of an animals’ ecological niche is circumscribed by its morphology, performance, and behavior, 3 factors that can ultimately affect fitness. We investigated potential behavioral and performance adaptations to roost making, a life-history trait associated with high fitness in the insectivorous bat Lophostoma silvicolum. Males of this species use their teeth to excavate roosts in active termite nests, which we found to be much harder than the hardest prey in the bats’ diet (beetles). We compared roost making and feeding behavior in L. silvicolum. We also compared the feeding behavior of L. silvicolum to that of 2 similar species that do not excavate roosts. All 3 species predominantly used bilateral bites centered on the premolar and molar teeth to eat beetles. In contrast, L. silvicolum used mainly bilateral bites involving the incisors and canines for roost excavation. All species generated similar bite forces during biting behaviors associated with feeding, but L. silvicolum generated significantly higher bite forces during biting behaviors used for roost excavation. We found no difference in canine tooth wear between the sexes, but tooth wear was significantly higher in an ecologically similar species that does not excavate roosts. We conclude that the behavior, performance, and possibly morphology of L. silvicolum represent adaptations to roost excavation.

All-offspring dispersal in a tropical mammal with resource defense polygyny

In polygynous mammals, males are usually responsible for gene flow while females are predominantly philopatric. However, there is evidence that in a few mammalian species female offspring may disperse to avoid breeding with their father when male tenure exceeds female age at maturity. We investigated offspring dispersal and local population structure in the Neotropical bat Lophostoma silvicolum. The mating system of this species is resource defense polygyny, with the resource being active termite nests, excavated by single males, which are then joined by females. We combined field observations of 14 harems during 3 years and data about the genetic structure within and between these groups, calculated with one mitochondrial locus and nine nuclear microsatellite loci. The results show that both male and female offspring disperse before maturity. In addition, we estimated life span of excavated termite nests and the duration they were occupied by the same male. Our findings suggest that long male tenure of up to 30 months is indeed a likely cause for the observed dispersal by female offspring that can reach maturity at a low age of 6 months. We suggest that dispersal by offspring of both sexes may occur quite frequently in polygynous tropical bats and thus generally may be more common in mammals than previously assumed.

Roost Structure, Modification, and Availability in the White‐throated Round‐eared Bat,Lophostoma silvicolum(Phyllostomidae) Living in Active Termite Nests1

ABSTRACTWe studied roost structure, modification, and availability inLophostoma silvicolum(Phyllostomidae), an insectivorous gleaning bat, on Barro Colorado Island (BCI), Panamá. Collection of nest material beneath termitaria and infrared video filming indicated that males ofL. silvicolumexcavate and maintain cavities inside active termite nests. A binary logistic regression analysis showed that to be suitable as roosts, termite nests have to be larger than 30 cm in diameter and taller than 30 cm, well shaded, with few transecting branches, and freely accessible from below. Use of active termite nests as roosts may provide several benefits toL. silvicolum, including reduction of competition for roost sites with sympatric bat species, reduced parasite load and a suitable microclimate. A comparison of number of all termite nests in selected forest plots with number of termite nests that are potentially suited as bat roosts and number of termite nests that are actually used by bats suggests thatL. silvicolummay not be roost‐limited on BCI in spite of its highly specialized roost choice.

Mating system of a Neotropical roost-making bat: the white-throated, round-eared bat, Lophostoma silvicolum (Chiroptera: Phyllostomidae)

The vast majority of bats strongly depend on, but do not make, shelters or roosts. We investigated Lophostoma silvicolum, which roosts in active termite nests excavated by the bats themselves, to study the relationship between roost choice and mating systems. Due to the hardness of the termite nests, roost-making is probably costly in terms of time and energy for these bats. Video-observations and capture data showed that single males excavate nests. Only males in good physical condition attracted females to the resulting roosts. Almost all groups captured from excavated nests were single male-multifemale associations, suggesting a harem structure. Paternity assignments based on ten polymorphic microsatellites, revealed a high reproductive success of 46% by nest-holding males. We suggest that the mating system of L. silvicolum is based on a resource-defense polygyny. The temperatures in the excavated nests are warm and stable, and might provide a suitable shelter for reproductive females. Reproductive success achieved by harem males appears to justify the time and effort required to excavate the nests. Reproductive success may thus have selected on an external male phenotype, the excavated nests, and have contributed to the evolution of an otherwise rare behavior in bats.

Ecology of an exceptional roost: Energetic benefits could explain why the bat Lophostoma silvicolum roosts in active termite nests

The ability to create shelters that provide protection from the environment is widespread among animals. However, in spite of the central role roosts play in the life of bats (Chiroptera), only a few species have developed the ability to make their own refuges, one of them being the Neotropical Lophostoma silvicolum. This bat creates and inhabits cavities in active arboreal nests of the termite Nasutitermes corniger. We measured temperature in cavities inside active and dead termite nests, and in tree holes occupied by closely related bats, to determine whether energetic benefits compensate for the cost of excavating the hard nests. The inside temperatures of active termite nests were very stable and 2.1–2.8 °C warmer than those of the other two potential roost types. The observed temperature difference is estimated to allow euthermic L. silvicolum to save about 5% of their daily energy expenditure when roosting in active termite nests instead of dead nests or tree holes. Suitable roosting conditions result from the presence of termites and are independent of nest architecture. Our results indicate that the benefits of higher temperatures may be one of the driving forces promoting the evolution of active roost making in bats.

Meliponini neotropicais: o gênero Partamona Schwarz, 1939 (Hymenoptera, Apidae, Apinae) - bionomia e biogeografia

This work, dedicated to the study of nesting habits of the species of the Neotropical genus Partamona Schwarz, is a sequence to the taxonomic revision recently published elsewhere. A total of 214 nests and nest aggregations of 18 species [Partamona epiphytophila Pedro & Camargo, 2003; P. testacea (Klug, 1807); P. mourei Camargo, 1980; P. vicina Camargo, 1980; P. auripennis Pedro & Camargo, 2003; P. combinata Pedro & Camargo, 2003; P. chapadicola Pedro & Camargo, 2003; P. nhambiquara Pedro & Camargo, 2003; P. ferreirai Pedro & Camargo, 2003; P. pearsoni (Schwarz, 1938); P. gregaria Pedro & Camargo, 2003; P. batesi Pedro & Camargo, 2003; P. ailyae Camargo, 1980; P. cupira (Smith, 1863); P. mulata Moure in Camargo, 1980; P. seridoensis Pedro & Camargo, 2003; P. criptica Pedro & Camargo, 2003; P. helleri (Friese, 1900)] were studied , including data about habitat, substrate, structural characteristics, construction materials and behavior. The descriptions of the nests are illustrated with 48 drawings. Partial data of the nests of P. bilineata (Say, 1837), P. xanthogastra Pedro & Camargo, 1997, P. orizabaensis (Strand, 1919), P. peckolti (Friese, 1901), P. aequatoriana Camargo, 1980, P. musarum (Cockerell, 1917) and P. rustica Pedro & Camargo, 2003 are also presented. Nests of P. grandipennis (Schwarz, 1951), P. yungarum Pedro & Camargo, 2003, P. subtilis Pedro & Camargo, 2003, P. vitae Pedro & Camargo, 2003, P. nigrior (Cockerell, 1925), P. sooretamae Pedro & Camargo, 2003 and P. littoralis Pedro & Camargo, 2003 are unknown. The species of Partamona build notable nest entrance structures, with special surfaces for incoming / exiting bees; some of them are extremely well-elaborated and ornamented, serving as flight orientation targets. All species endemic to western Ecuador to Mexico with known nesting habits (P. orizabaensis, P. peckolti, P. xanthogastra, P. bilineata, P. aequatoriana and P. musarum) build their nests in several substrates, non-associated with termitaria, such as cavities and crevices in walls, among roots of epiphytes and in bases of palm leaves, in abandoned bird nests, under bridges, and in other protected places, except P. peckolti that occasionally occupies termite nests. In South America, on the eastern side of the Andes, only P. epiphytophila and P. helleri nest among roots of epiphytes and other substrates, non-associated with termitaria. All other species studied (P. batesi, P. gregaria, P. pearsoni, P. ferreirai, P. chapadicola, P. nhambiquara, P. vicina, P. mourei, P. auripennis, P. combinata, P. cupira, P. mulata, P. ailyae, P. seridoensis, P. criptica and P. rustica) nest inside active termite nests, whether epigeous or arboreous. The only species that builds obligate subterranean nests, associated or not with termite or ant nests (Atta spp.) is P. testacea. Nests of Partamona have one vestibular chamber (autapomorphic for the genus) closely adjacent to the entrance, filled with a labyrinth of anastomosing pillars and connectives, made of earth and resins. One principal chamber exists for food and brood, but in some species one or more additional chambers are filled with food storage pots. In nests of P. vicina, there is one atrium or false nest, between the vestibule and the brood chamber, which contains involucral sheaths, cells and empty pots. All structures of the nest are supported by permanent pillars made of earth and resins (another autapomorphy of the genus). The characters concerning nesting habits were coded and combined with morphological and biogeographic data, in order to hypothesize the evolutive scenario of the genus using cladistic methodology. The phylogenetic hypothesis presented is the following: (((((P. bilineata (P. grandipennis, P. xanthogastra)) (P. orizabaensis, P. peckolti)) (P. aequatoriana, P. musarum)) P. epiphytophila, P. yungarum, P. subtilis, P. vitae) (((((P. testacea (P. mourei, P. vicina)) (P. nigrior (P. auripennis, P. combinata))) (P. ferreirai (P. pearsoni (P. gregaria (P. batesi (P. chapadicola, P. nhambiquara)))))) ((((P. ailyae, P. sooretamae) P. cupira, P. mulata) P. seridoensis) P. criptica, P. rustica, P. littoralis)) P. helleri))). One area cladogram is presented. Dates of some vicariance / cladogenesis events are suggested. For bilineata / epiphytophila group, which inhabits the Southwestern Amazonia and the Choco-Mexican biogeographical components, the origin of ancestral species is attributed to the Middle Miocene, when the transgressions of the Maracaibo and Paranense seas isolated the tropical northwestern South America from the eastern continental land mass. The next cladogenic event in the history of the bilineata / epiphytophila group is attributed to the Plio-Pleistocene, when the Ecuadorian Andes reached more than 3000 m, and the ancestral species was fragmented in two populations, one occupying the western Andes (ancestral species of the bilineata subgroup) and other the southwestern Amazon (ancestral species of the epiphytophila subgroup). Other aspects of the history of Partamona are also discussed.