Strategies of social wasps for thermal homeostasis in light paper nests

1. With the derived free-run temperature of light paper nests the influence of the thermal capacity of the nest or the nest site, respectively, on thermal homeostasis is quantified.

2. Gravimetric information from the continuous investigation of the nest weight coupled with temperature and humidity measurement allows the correlation of the colonies’ foraging behavior with their heat production inside the nest.

3. Wasps (Vespa crabro) do not regulate their nest environment towards a specific and constant temperature but rather build nests adapted to their foraging behavior and general energy budget.

Egg deposition patterns of fig pollinating wasps: implications for studies on the stability of the mutualism

1. Fig pollinating wasps (Agaonidae) enter Ficus inflorescences (figs), oviposit in some of the flowers, and pollinate in the process. Each larva completes its development within a single flower. In most cases, an inflorescence entered by a wasp will represent its only egg‐laying site. The mechanisms that prevent pollinating wasps from exploiting all the flowers inside a fig are not understood. In this study, hypotheses about flower use by pollinating fig wasps were tested by investigating egg deposition patterns in three species. 2. Either one or three wasps were introduced into figs. The figs were then harvested. Serial sections allowed assessment of the presence or absence of a wasp egg in a sample of flowers in each fig. The overall proportion of flowers with eggs and the spatial distribution of eggs were then compared in single wasp figs and three foundress figs. 3. In all species, the proportion of flowers with a wasp egg increased with foundress number but less than three‐fold. 4. In all species, at least in single foundress figs, flowers near the fig cavity were more likely to receive a wasp egg than were flowers near the fig wall. 5. In two species, when the number of foundresses was multiplied by three, there was an increase in the use of flowers near the fig wall, while in the third species, the increase was spread evenly among flowers. 6. Factors affecting wasp egg deposition patterns and the potential of investigating such patterns for studying the stability of the mutualism are discussed.     

钝叶榕(Ficus curtipes)非传粉小蜂交配行为

榕树及其传粉榕小蜂繁殖上相互依存,被认为是生物界中协同进化时间最悠久,相互关系最密切的一对生物;在大多数榕树种类的隐头花序内,除了传粉榕小蜂外,还共存着多种非传粉小蜂,它们的繁殖行为直接影响着榕树和传粉榕小蜂的繁殖和互惠稳定.钝叶榕(Ficus curtipes Corner),是一种雌雄同株的绞杀性榕树.研究在西双版纳热带植物园里共收集钝叶榕100个隐头果内的榕小蜂,获得9493号标本;其中,包括1种传粉小蜂和5种非传粉小蜂,钝叶榕传粉小蜂Eupristina sp.占总数的44.66%,杨氏榕树金小蜂Diaziella yangi 占46.13%,而其它4种非传粉小蜂(Lipothymus sp., Sycobia sp., Philotrypesis sp.和Sycoscopter sp.)仅占9.20%.前3种榕小蜂雌蜂进到果腔产卵,其余3种在果外产卵.观测23个钝叶榕榕果出蜂情况发现,6种榕小蜂在钝叶榕隐头花序内遵循严格的羽化出蜂顺序,首先是Sycobia sp.,次之是Lipothymus sp.,再次之是杨氏榕树金小蜂,最后是钝叶榕传粉小蜂、Philotrypesis sp.和Sycoscopter sp..5种非传粉小蜂的交配场所与雄蜂翅型无关,雄蜂有翅型的杨氏榕树金小蜂大部分交配在果内完成,而且它们的雄蜂为争夺交配机会存在激烈的打斗行为;雄蜂无翅型的Lipothymus sp.有部分雄蜂爬出隐头果,在果壁和附近的叶片背面交配;雄蜂有翅型的Sycobia sp.,其所有交配都发生在果外;Philotrypesis sp.和Sycoscopter sp. 雄蜂均无翅,它们的交配全发生在果内.局域配偶竞争使榕小蜂性比偏雌,杨氏榕树金小蜂雄蜂虽然有翅,但大部分交配发生在榕果内,这将影响其最佳的性比率.因此,依赖雄蜂翅型并不能很好地预测榕小蜂的交配场所和性比率.     

雌花期榕小蜂进入榕果的行为及其活动时间

在西双版纳,钝叶榕传粉榕小蜂Eupristina sp.和杨氏榕树金小蜂Diaziella yangi均在雌花期进入钝叶榕果内繁殖和传粉,比较研究它们进入榕果的行为和活动时间。结果显示:在搜寻苞片处进蜂口时,2种榕小蜂的种内均出现打斗行为,并且杨氏榕树金小蜂的打斗更为激烈,但种间没有打斗行为发生,杨氏榕树金小蜂总是等待钝叶榕传粉榕小蜂先期进入榕果,然后才跟随着进入。在搜寻和进入苞片口通道阶段,钝叶榕传粉榕小蜂均比杨氏榕树金小蜂花费较长时间;而在果腔内产卵、传粉的时间,2种榕小蜂均最多不超过3d。相似的进蜂过程和活动时间,可能是2种榕小蜂与寄主榕树长期协同进化的结果。     

多杀菌素和氟虫睛对瓢虫、寄生蜂和菜缢管蚜选择性的研究

采用药膜法研究了多杀菌素和氟虫睛对3种瓢虫、2种寄生蜂和菜缢管蚜的选择性。与菜缢管蚜相比,2种杀虫剂对3种瓢虫的毒性较低(LC50比值=1.73-41.9),尤其是氟虫睛对3种瓢虫以及多杀菌素对稻红瓢虫均具有较好的选择性(LC50比值大于5)。菜蚜茧蜂和蚜虫宽缘金小蜂对2种杀虫剂的敏感性远高于3种瓢虫和菜缢管蚜,2种杀虫剂对菜蚜茧蜂和蚜虫宽缘金小蜂均是高毒的(LC50比值=0.006-0.05)。3种瓢虫对多杀菌素和氟虫睛具有较高的耐药性,这将有助于其在生物防治中的应用。     

Coevolution of visual signals and eye morphology in Polistes paper wasps

To be effective, signals must propagate through the environment and be detected by receivers. As a result, signal form evolves in response to both the constraints imposed by the transmission environment and receiver perceptual abilities. Little work has examined the extent to which signals may act as selective forces on receiver sensory systems to improve the efficacy of communication. If receivers benefit from accurate signal assessment, selection could favour sensory organs that improve discrimination of established signals. Here, we provide evidence that visual resolution coevolves with visual signals in Polistes wasps. Multiple Polistes species have variable facial patterns that function as social signals, whereas other species lack visual signals. Analysis of 19 Polistes species shows that maximum eye facet size is positively associated with both eye size and presence of visual signals. Relatively larger facets within the eye''s acute zone improve resolution of small images, such as wasp facial signals. Therefore, sensory systems may evolve to optimize signal assessment. Sensory adaptations to facilitate signal detection may represent an overlooked area of the evolution of animal communication.     

Application of the biogenetic law to behavioral ontogeny: a test using nest architecture in paper wasps

General principles derived from studies of morphological ontogeny are useful in ethology. Behavioral ontogeny may be interpreted from an holistic view in which a series of behaviors is treated as an ontogeny toward a larger, complex, behavioral product. If the component behaviors are defined broadly, many taxa may be compared to find general principles that are not evident when behaviors are dissected to their smallest recognizable units. Flow charts can illustrate such general ontogenetic sequences in a manner that shows what sorts of modifications have evolved from the general pattern. Certain changes may illustrate forms of ontogenetic evolution that are well known for morphological development, such as addition or embellishment of terminal ontogenetic steps, or compression of ontogeny by acceleration or deletion of early steps. The major modifications in nest construction behavior of 28 genera of paper wasps are presented to test the predictions of the biogenetic rule with respect to character polarity. Cladistic analyses of separate morphological and behavioral data sets show that polarity is accurately inferred with respect to the five major patterns of nest construction in paper wasps.     

Parasitoid and inquiline attack in the galls of four alien, cynipid gall wasps: host switches and the effect on parasitoid sex ratios

1. Four alien cynipid gall wasps of the genus Andricus are established and still spreading in the British Isles. The order, according to the northerliness of their distribution boundary, is: A. corruptrix→A. quercuscalicis→A. lignicola→A. kollari. All four aliens have a sexual generation in spring on Quercus cerris (introduced to Britain) and an agamic generation in autumn on native oak species. 2. For 2 years 1994 and 1995, galls of both generations of the four alien species were sampled at eight sites from the south of England to the north of Scotland to determine the parasitoid and inquiline species that attack the new galls. The spring generations of the invading species shared a parasitoid complex of four pteromalid species. Five species of inquilines and 11 species of parasitoids emerged from the autumn galls. 3. Two colonisation events were recorded for A. lignicola and A. corruptrix. On both occasions, the spring generations were found first at the new sites, indicating that the agamic generation provides the colonisers for these invading species. After colonisation, the galls of both species were attacked by parasitoids in their first season. 4. In spring, the invading species were among the most abundant cynipids at all eight sites. By sampling the whole local community of cynipid galls, it was found that the parasitoid species attacking the spring galls of the invaders seemed to have shifted their attack to the new hosts. 5. The secondary sex ratios of the parasitoid species emerging from the sexual galls of A. quercuscalicis (the smallest of the four) showed a strong and significant male bias at all sites and in both years. Parasitoid emergence from the galls of the sexual generations of the other three species (all about equal in size) was between 60 and 70% male, and variable among sites and between years.     

Maternal control of offspring sex and male morphology in the Otitesella fig wasps

Models concerning the evolution of alternative mating tactics commonly assume that individuals determine their own strategies. Here we develop a computer-based ESS model that allows mothers, ovipositing in discrete patches, to choose both the sex and the male mating tactics (natal-patch mating or dispersing) of their offspring based only on how many other mothers have used the specific patch before them. Data for three species of nonpollinating fig wasps from the Otitesella genus agree quantitatively with the model's assumptions and predictions. This suggests that females respond to population densities at the level of individual figs. The alternative male tactics in the species we studied are probably a result of a conditional strategy exercised by the mother that laid them. In addition, as females were only allowed to lay one egg per patch, our results suggest a new mechanism that can skew population sex ratios towards a female bias.     

Factors affecting the acceptance of alien conspecifics on nests of the primitively eusocial wasp,Ropalidia marginata (Hymenoptera: Vespidae)

In the primitively eusocial wasp, Ropalidia marginata,individual females are known to drift from one newly founded nest to another. In the laboratory, young (<6- to 8-day-old) alien wasps are accepted onto unrelated colonies, while older (>6- to 8-day-old) wasps are not. Here we have investigated the factors that could influence the acceptance of foreign conspecifics onto unrelated nests. Individually marked wasps of different ages, isolated immediately after eclosion from the natal nest and from each other, were introduced onto unrelated recipient nests. Considered separately, both age and ovarian condition seemed to influence the probability of acceptance as well as the levels of aggression and tolerance received by the introduced wasps. However, partial correlation analysis and multiple regression analysis indicated that only age had a direct influence and that the ovarian condition acts only through age, a variable with which it is highly correlated. The observed acceptance of young aliens and rejection of old aliens are less likely to be due to the perception of older wasps as a reproductive threat rather than some age-related factor, other than ovarian condition, for example, the relative ease with which younger wasps can be molded into desired roles.     

Male morphological variation and the determinants of body size in two Otiteselline fig wasps

The chalcid wasps (Hymenoptera) that develop in fig tree inflorescences(Ficus: Moraceae) have often been used to study alternativereproductive behaviors. However, recent work suggests that suchbehaviors are more complex than previously thought. We investigatedthis in Otitesella longicauda and O. rotunda. In addition toknown dimorphisms in the two species (each have "religiosa"males that use their mandibles to fight for mates in the fig,and "digitata" males that disperse from the fig to mate), wefound that religiosa males below species-specific body sizeswitch points have relatively larger mandibles and are lesssclerotized than those above. Thus, they are actually trimorphic.We suggest that the religiosa morph variation is linked to fighter/nonfighteralternative mating behaviors, with small (nonfighting) maleshaving relatively larger mandibles because they also use themto pull females out of their galls before mating. Also, we investigatedthe determinants of wasp body size, and whether females (foundresses)adjust their offspring allocation strategies according to expectedoffspring size. We found that wasp size is larger in ovariesnear the center of the fig, and more females and fewer religiosamales are laid in such ovaries than in those further away. Thisprobably indicates that foundresses lay females when they areexpected to be large because their fitness is more body size–dependentthan that of religiosa males. We then discuss the implicationsof our findings for the study of alternative reproductive behaviorsand foundress offspring allocation strategies.     

An introduction to parasitic wasps of Drosophila and the antiparasite immune response

Most known parasitoid wasp species attack the larval or pupal stages of Drosophila. While Trichopria drosophilae infect the pupal stages of the host (Fig. 1A-C), females of the genus Leptopilina (Fig. 1D, 1F, 1G) and Ganaspis (Fig. 1E) attack the larval stages. We use these parasites to study the molecular basis of a biological arms race. Parasitic wasps have tremendous value as biocontrol agents. Most of them carry virulence and other factors that modify host physiology and immunity. Analysis of Drosophila wasps is providing insights into how species-specific interactions shape the genetic structures of natural communities. These studies also serve as a model for understanding the hosts'' immune physiology and how coordinated immune reactions are thwarted by this class of parasites.The larval/pupal cuticle serves as the first line of defense. The wasp ovipositor is a sharp needle-like structure that efficiently delivers eggs into the host hemocoel. Oviposition is followed by a wound healing reaction at the cuticle (Fig. 1C, arrowheads). Some wasps can insert two or more eggs into the same host, although the development of only one egg succeeds. Supernumerary eggs or developing larvae are eliminated by a process that is not yet understood. These wasps are therefore referred to as solitary parasitoids.Depending on the fly strain and the wasp species, the wasp egg has one of two fates. It is either encapsulated, so that its development is blocked (host emerges; Fig. 2 left); or the wasp egg hatches, develops, molts, and grows into an adult (wasp emerges; Fig. 2 right). L. heterotoma is one of the best-studied species of Drosophila parasitic wasps. It is a "generalist," which means that it can utilize most Drosophila species as hosts¹. L. heterotoma and L. victoriae are sister species and they produce virus-like particles that actively interfere with the encapsulation response². Unlike L. heterotoma, L. boulardi is a specialist parasite and the range of Drosophila species it utilizes is relatively limited¹. Strains of L. boulardi also produce virus-like particles³ although they differ significantly in their ability to succeed on D. melanogaster¹. Some of these L. boulardi strains are difficult to grow on D. melanogaster¹ as the fly host frequently succeeds in encapsulating their eggs. Thus, it is important to have the knowledge of both partners in specific experimental protocols.In addition to barrier tissues (cuticle, gut and trachea), Drosophila larvae have systemic cellular and humoral immune responses that arise from functions of blood cells and the fat body, respectively. Oviposition by L. boulardi activates both immune arms^1,4. Blood cells are found in circulation, in sessile populations under the segmented cuticle, and in the lymph gland. The lymph gland is a small hematopoietic organ on the dorsal side of the larva. Clusters of hematopoietic cells, called lobes, are arranged segmentally in pairs along the dorsal vessel that runs along the anterior-posterior axis of the animal (Fig. 3A). The fat body is a large multifunctional organ (Fig. 3B). It secretes antimicrobial peptides in response to microbial and metazoan infections.Wasp infection activates immune signaling (Fig. 4)⁴. At the cellular level, it triggers division and differentiation of blood cells. In self defense, aggregates and capsules develop in the hemocoel of infected animals (Fig. 5)^5,6. Activated blood cells migrate toward the wasp egg (or wasp larva) and begin to form a capsule around it (Fig. 5A-F). Some blood cells aggregate to form nodules (Fig. 5G-H). Careful analysis reveals that wasp infection induces the anterior-most lymph gland lobes to disperse at their peripheries (Fig. 6C, D).We present representative data with Toll signal transduction pathway components Dorsal and Spätzle (Figs. 4,5,7), and its target Drosomycin (Fig. 6), to illustrate how specific changes in the lymph gland and hemocoel can be studied after wasp infection. The dissection protocols described here also yield the wasp eggs (or developing stages of wasps) from the host hemolymph (Fig. 8).     

A latitudinal gradient in intensity of applying ant-repellent substance to the nest petiole in paper wasps (Hymenoptera: Vespidae)

Summary Observations on pre-emergence, single-foundress colonies of Japanese paper wasps (Polistes) revealed that there was a latitudinal gradient in intensity of application of an ant-repellent substance (secreted by the metasomal sternum VI glands) to the nest petiole. Thus the lower the latitude, the more frequently a foundress rubbed ant repellent onto the nest petiole. Estimation of potential ant predation on wasp brood using bait traps showed that there was a positive correlation between the frequency of rubbing and potential predation pressure from ants which are guided predominantly by substrate cues for foraging. There was also a latitudinal gradient in the degree of temporal association of rubbing behavior with foraging: the lower the latitude, the more closely foundress departure from the nest was associated with rubbing. Enlargement of the nest petiole by applying oral secretion potentially obliterated previous coats of ant repellent; however, this behavior was not always followed by rubbing behavior. The ant-repellent chemical barrier around the nest petiole may have evolved in tropical regions of the world as a defense against ant predation on wasp brood. I argue that as ant predation pressure diminishes towards the cooler regions, so does selection maintaining the behavioral sequence where foundress departure from the nest is preceded by rubbing behavior.     

Artificial incubation of California condor Gymnogyps californianus eggs removed from the wild

The currrent California condor (Gymnogyps californianus) recovery plan entails increasing the reproductive rate via replacement-clutch manipulation of eggs. During the period from 1983 to 1985, 15 eggs were removed from wild nesting pairs for artificial incubation. The eggs were incubated at a dry bulb temperature of 36.4°C in modified forced-air Lyon Electric incubators. The incubation humidity was adjusted for individual eggs based on weight loss data (water = weight), 25.6–30.0°C wet bulb (41.0–63.0% Relative Humidity (RH)). The chicks were hatched initially under forced-air conditions of 36.1°C dry bulb, 31.1–01.7°C wet bulb (70.0–73.0% RH). In 1984, hatching parameters were changed to still-air conditions, 36.1°C dry bulb (top of the egg), 35.0°C dry bulb (bottom of the egg), 31.1–31.7°C wet bulb (70.0-73.0% RH). Tactile and auditory stimulation was utilized during the pip-to-hatch interval. From among 15 eggs collected, 13 hatched, and 12 condor chicks were raised successfully (hatchability: 86.7%; survivability: 92.3%).     

A comparative study of the ground nests of Centris flavifrons and Centris aethiocesta (Hymenoptera: Anthophoridae)

The nests of Centris aethiocesta Snelling and Centris flavifrons (Friese) are described and compared to published accounts of C. flavofasciata. The three are ground nesting solitary bee species in Costa Rica. Centris aethiocesta, like previously published C. flavofasciata, prefers the beach strand, although C. aethiocesta nests in more shaded areas. Centris flavifrons nests are constructed in the dry forest savanna, often in small depressions. All three construct one cell per tunnel, with the tunnel of completed nests filled with soil. Tunnels of completed nests of C. aethiocesta are unbranched; tunnels of C. flavifrons have 6 to 10 side tunnels also filled with soil, while only one side tunnel is published for C. flavofasciata.     

Within-group aggression and the value of group members: theory and a field test with social wasps

We present a simple, general model of how the optimal levelof intra-group aggression should vary in different social contexts.A key component of this model is the value of the recipientof aggression to a potential aggressor (i.e., the ratio of expectedlong-term group productivity with the recipient present to theexpected group productivity with the recipient absent). Therecipient's value measures its contribution to group reproductivesuccess. We demonstrate theoretically that if aggression increasesthe aggressor's share of the group's expected total reproductiveoutput, but at the same time decreases the magnitude of thisoverall reproductive output, then the optimal level of aggressiontoward a recipient will decrease with increasing recipient'svalue. This proof establishes a rigorous theoretical connectionbetween the level of aggression within a group and the benefitsof belonging to such a group and can be tested by experimentallymanipulating the values of group members to each other. We test,and thus illustrate the utility of, this model by examiningaggression within experimentally-manipulated foundress associationsof social wasps. We show that the value of co-foundresses toeach other in the social wasp Polistes fuscatus lies in theirability to provide insurance against colony failure caused bythe loss of all tending foundresses. Removals of worker-destinedeggs and pupae, which increase the value of co-foundresses,both lead to significant reductions in aggression by the dominantfoundress, despite the fact that the immediate, selfish benefitsof competitive aggression should increase when empty brood cellsare present Removal of reproductive-destined eggs, which doesnot affect co-foundress value, but increases the benefits ofselfish aggression, causes a significant increase in aggressionby beta foundresses. Finally, wing reduction of subordinateco-foundresses significantly increases aggression by dominantfoundresses, as expected since the subordinate's value is reduced.Our results indicate that foundress aggression is sensitiveto the value of future cooperation, as predicted by the optimalaggression model. The model may apply widely to both invertebrateand vertebrate societies     

Reconstruction ofRopalidia fasciata nests by progeny females after a typhoon and its significance in the social evolution of wasps

A strong typhoon, Typhoon 13, which swept through Okinawa on 2 and 3 September 1993, knocked down 57 to 61 of 97Ropalidia fasciata nests. Thirty-five colonies soon reconstructed their nests, and these nests produced 54±46 adults per nest during the remaining two and a half months before winter. The number of females involved in nest reconstruction was 21.3±15.7 per nest. The frequency of foraging activity was significantly higher in nests being reconstructed than in normal nests. As only one out of 205 foundresses marked in spring was found in early September, most cases of nest reconstruction were considered to be made exclusively by females that emerged during the spring and summer of 1993 (progeny females). All of the reconstructed nests but one produced adult females. Many females (31%) collected from the two reconstructed nests were inseminated. As all the reconstructed nests became vacant by early January, indicating completion of the colony cycle, and a large number of nests were established in the spring of 1994, females emerging from reconstructed nests in 1993 probably become foundresses in 1994.Ropalidia fasciata is considered to be, at least partially, bivoltine in Okinawa. The significance of these facts for the evolution of multi-queen social systems in the Polistinae is discussed.     

Euphorine phylogeny: the evolution of diversity in host-utilization by parasitoid wasps (Hymenoptera: Braconidae)

ABSTRACT.

• 1 New data on the phylogeny of the braconid subfamily Euphorinae supports the hypothesis that parasitism of adult insects by Euphorinae originated during parasitism of Chrysomelidae, a group whose larvae are ecologically coincident with adults.
• 2 Evolution of the habit of attacking the adult stage opened a new adaptive zone; subsequently the Euphorinae have diversified on to a phylogenetically greater variety of hosts than any other braconid subfamily.
• 3 Parasitism of eumastacid grasshoppers evolved from beetle parasitism in the tribe Perilitini.
• 4 The tribe Euphorini shows the greatest diversity of hosts utilized. Most attack Heteroptera; however, Chrysopopthorus diversified on to adult Chrysopidae, Euphoriella on to Psocoptera, and Cryptoxilos on to Scolytidae.
• 5 Parasitism of bark beetles (Scolytidae) has evolved independently in three genera: Cosmophorus, Cryptoxilos and Ropalophorus. This is the most specialized form of beetle parasitism by euphorines, since it involves direct parasitism of concealed hosts.
• 6 Parasitism of adult hymenopterans by the tribe Syntretini may be related to attacking hosts while they are foraging at flowers.
• 7 The pattern of diversification in the Euphorinae indicates several adaptive radiations within host orders, as well as a history of major host-shifts between phylogenetically distantly-related host groups: Coleoptera to Orthoptera; Coleoptera to Hymenoptera; Coleoptera to Heteroptera; Heteroptera to Neuroptera, Psocoptera, and back to Coleoptera. Both the‘host taxonomy’and‘host habitat’hypotheses of host-shifting are supported. Host-shifts have involved hosts occurring in the same micro-habitat and usually having similar feeding habits. This is consistent with current theory of host-location by means of host-produced kairomones and visual cues.