粗纹举腹蚁蚁巢解剖及其数学建模

为了弄清与排泄蜜露的昆虫有密切关系的粗纹举腹蚁Crematogaster macaoensis Wheeler的生物学特性,于2009年8月至2010年7月在云南省墨江县雅邑乡紫胶园采集并调查了42个粗纹举腹蚁蚁巢。粗纹举腹蚁蚁巢类型为层纸巢,灰黑色,筑于紫胶虫寄主植物树干的中上部,由干枯树叶、杂草、碎屑和蚁分泌物粘结而成;巢内疏松,蚁道纵横交错;单蚁后制,工蚁单型;平均每巢的蚁后、繁殖雌蚁、雄蚁和工蚁的数量分别为(1.00±0.00)头,(488.75±242.59)头,(3 096.86±2 923.75)头和(40 839.07±8 597.98)头;卵、幼虫和蛹的数量分别为(9 936.60±2 448.62)粒,(3 214.83±781.71)头和(4 582.00±656.07)个。粗纹举腹蚁蚁巢体积和每巢工蚁数量的计算公式分别为:V=0.365×(43×πabc)1.056和WN=135.236×V0.660(式中V代表蚁巢体积,a、b、c分别代表蚁巢的长半径、短半径和极半径,WN代表工蚁数量)。这两个公式为监测粗纹举腹蚁的种群数量变化提供了一种手段。     

Centrifugal waste disposal and the optimization of ant nest craters

We considered how ant, Tapinoma simrothi, colonies dispose of the material generated by their nest excavations in nest entrance craters. We developed a model for optimum crater formation on both flat and sloping ground (although we have not solved it in full generality for sloping ground). We found that the ants, when working on flat ground, show a close approximation to this least costly waste disposal. Craters on slopes may not be optimal even though they will be cheaper to make than ones of a similar volume on level ground. We further tested the model with a manipulative experiment, which also suggested the simple rule of thumb that ants might use. In response to having one-quarter of their crater removed, the ants focused most of their further waste disposal in that quarter. This suggests that their rule of thumb may be to deposit material at the nearest point with an angle of elevation less than that of the optimal angle. This should generate symmetrical craters on flat ground. The model also makes certain additional and testable predictions about the fine structure of craters.     

Spatial patterns of granivorous ant nest abundance and nest site selection in agricultural landscapes of Central Spain

Summary Patterns of abundance and site selection of granivorous ant nests were investigated in extensive cereal croplands of Central Spain. Nest densities and distributions were measured in two consecutive summers (1988 and 1989), together with habitat physiognomy and seed availability. Nest site selection patterns were analysed at two spatial scales (landscape and microhabitat) with respect to habitat physiognomy. Results indicate a very constant and predictable pattern of both nest abundance and nest site selection. Granivorous ant nests were most abundant in shrublands, and shrubby microsites were selected for nest placement. Croplands, and microsites with high covers of bare ground and litter, were avoided. These patterns were consistent between years despite a 1.7-fold increase in shrubland nest densities, that was attributed to the exceptionally dry winter between nest censuses. I suggest that winter survivorship of ant nests in the unploughed landscape units, and periodic ploughing in croplands, may be the main factors constraining granivorous ant densities in the landscape studied.     

Interference interactions and nest usurpation between two subordinate ant species

Camponotus foreli (Emery) and Cataglyphis iberica (Emery) are two sympatric, subordinate ant species that have been found to fight in attacks that usually conclude with the death of many workers of both species and with nest abandonment by C. iberica. These harassment episodes have been observed in two different areas and over many years of study. No such attacks of C. foreli were observed in the study areas against any other ant species, nor did any other ants attack C. iberica nests, and laboratory confrontations confirmed this specificity. These attacks neither eliminated C. iberica colonies, nor distanced them from C. foreli nests. Moreover, there was no real competition for food between the species: in an experiment where all C. iberica colonies were eliminated from an area, rates of prey and liquid food collection by C. foreli nests in the exclusion zone were similar to those found in the control zone with C. iberica, and the activity rhythms of C. foreli did not change in the absence of C. iberica. The hypothesis of competition for a nest site is more consistent. Both in the laboratory and the field, the most frequent outcome of these aggressive interactions was the occupation of the C. iberica nest by C. foreli. This behavior may be advantageous for C. foreli, because it is much less skilful at excavating than C. iberica. One of the chief concerns of this study is to show that such interference interactions, typical especially of dominant, very aggressive species, are also found between subordinate, apparently nonaggressive species. Received: 20 March 1997 / Accepted: 29 September 1997     

The relocation of ant nest entrances: Potential consequences for ant-dispersed seeds

The rate at which ant nests relocate may affect the fate of ant-dispersed seeds by influencing nutrient and seed accumulation in localized areas. In this study, the movement of ant nest entrances was monitored in fixed quadrats in dry sclerophyll woodland in Kuringai Chase National Park, NSW. Changes in entrance location were rapid for most species, with few entrances remaining in use for more than 6 months. Approximately 30% of entrances that closed were subsequently re-opened. There was no obvious seasonal pattern in entrance relocation. After 1 year, between 5 and 40% of the ground surface of the quadrats had been within 10 cm of a nest entrance. New nest entrances did not cluster near old entrances, indicating that nest entrance relocation may be accompanied by changes in underlying nest structure. Nutrient levels in soil samples from active nests of Rhytidoponera metallica, Aphaenogaster longiceps, Pheidole sp. 1 and Iridomyrmex sp. 8 did not differ significantly from random locations. The rapid changes in entrance location and the lack of nutrient enrichment may be the result of continual and progressive underground shifts in nest location. Such shifts have three potential consequences for seeds that remain buried within the nests. First, seeds will not benefit following germination by being in a nutrient-rich microsite. Second, a proportion of seeds collected by harvester ant species may escape predation if left in an abandoned section of the nest. Third, concentrations of seeds in localized areas may be reduced, leading to a reduction in competition between establishing seedlings.     

The economics of brood raiding and nest consolidation during ant colony founding

Summary The most dangerous time for an ant colony is during the founding stage when the small colony is vulnerable to predation and competition. Colonies can grow more rapidly when multiple queens cooperate in raising the first worker brood (pleometrosis) or by raiding other incipient colonies for their brood. This brood raiding has been proposed to be the primary force selecting for pleometrosis, i.e. multiple-queen colonies may have a considerable advantage in destroying neighbours by aggressively stealing their brood. An alternative hypothesis is that incipient nests are part of a larger, interconnected population structure and that brood raiding reflects cooperative pleometrosis with subdivided colonies. A simple mathematical model supports the second hypothesis: workers of incipient colonies are especially favoured to peaceably abandon their nest and join with other colonies if the queens are related or queens from raided colonies can infiltrate the raiding colony. The latter condition is often met in ant species that brood raid and particularly exemplified in fire ants (Solenopsis invicta), where brood raiding involves little mortal combat and combines with pleometrosis to rapidly increase colony size. It is proposed that the term nest consolidation should replace brood raiding to more accurately reflect the relatively non-aggressive and potentially apparently cooperative nature of interactions between incipient ant colonies.     

Respiration of wood ant nest material affected by material and forest stand characteristics

We studied differences in respiration of materials from different parts of wood ant nest (top, bottom, and rim) and from the nest surroundings (humus layer and mineral soil). Samples were taken from 8 wood ant (Formica aquilonia) nests in each of the two types of forest (birch and pine) in eastern Finland. The differences were related to material and forest stand characteristics (i.e., moisture, pH, carbon content, and C:N ratio). As a result, the highest respiration per g DW was measured at the top of ant nests in the birch forest. However, respiration did not significantly differ between the parts of ant nests in the pine forest. Respiration of the humus layers in both forest stands was on average higher, whereas respiration of the mineral soils in both forest stands was lower in comparison with respiration of the nest materials. The respiration per g C did not show any significant differences between different parts of nests and surrounding soil. The most important factors influencing respiration of the materials appeared to be moisture, carbon content, and pH. In conclusion, respiration of wood ant nest material is affected by the specific material and forest stand characteristics.     

Some aspects of individual behaviour during nest moving in the ant Tapinoma erraticum

Tapinoma erraticum workers change their nest site if disturbed. Fewer than half of them displace the brood, with varying degrees of efficiency. In order to determine individual reactivity, the following measurements were carried out on each ant during a removal test: (1) seizures of larvae with the mandibles, (2) journeys between the two nests, (3) functional transports.A large number of seizures and a more rapid transport response are poorly correlated with high removal activity. In this situation, the journeys made between the two nests appear independent of transport activity. Each transporting worker was observed to show a characteristic transport rate which may vary during the test period. The extreme heterogeneity of all aspects of individual responses illustrates the probabilistic nature of the behaviour of social insects.     

Defending the nest: variation in the alarm aggression response and nest mound damage in the harvester ant Pogonomyrmex occidentalis

A number of studies have found that ant colonies vary in many colony-level phenotypes, including the level of aggression towards non-nestmates. The extent of a colony’s aggression and defense of the nest in response to attacks by predators is likely to affect its survival and reproduction, but the degree to which colonies vary in their defensive response is poorly known. We documented considerable variation in damage to the external nest mound of Pogonomyrmex occidentalis (Cresson) at our long-term study site in 2012. Heavily damaged colonies formed several spatial clusters, consistent with predation within a home range. We tested two competing hypotheses for the variation in nest damage: (1) colonies vary in their level of aggression, those with stronger defensive responses are better protected, and suffer less damage, versus (2) colonies have similar levels of aggression, but those that suffer predator-induced damage subsequently display a stronger defense response. We measured the alarm/aggression response in colonies exposed to a standardized stimulus and determined whether the level of aggression was correlated to the level of damage. Colonies with strong defensive responses were significantly less likely to exhibit damage than those with weak responses, suggesting that aggression level is a colony phenotype.     

Deterioration in nest quality triggers relocation without affecting its dynamics in an ant

Insectes Sociaux - Nests play an important role in the lives of organisms that occupy them and a suitable nesting site has to be selected carefully. Sometimes, a nest of better quality may be...     

Assessing ant assemblages: pitfall trapping versus nest counting (Hymenoptera, Formicidae)

Pitfall trapping and nest counting are the most common census methods for ant assemblages. We examined the concordance between pitfall catches and nest counts on dry grassland. Spearman rank correlations and non-metric multidimensional scaling of the Bray Curtis similarity index revealed moderate concordance between the data collated by the two methods, but overall method-related differences were considerable. The dissimilarity was influenced by the type of land management, but not by trapping period or plot shape. Trapping success depended on nest density, ground vegetation cover and species-specific traits (inhabited stratum, colony size, foraging distance). Even when these factors were taken into account, the convertibility of pitfall trap and nest density values was unsatisfactory: the census method proved to be crucial in designing ant-ecological studies and interpreting literature data. Received 11 November 2005; revised 9 February 2006; accepted 1 March 2006.     

Utilization of harvester ant nest sites by Persian goitered gazelle in steppes of central Iran

Ants are among the most important elements in many ecosystems and known as famous ecosystem engineers. By changing physical and chemical properties of soil, ants may provide suitable habitats for other species. Based on previous observations, we hypothesized that Persian goitered gazelles (Gazella subgutturosa subgutturosa) exhibit a preference for utilizing sites close to seed harvester ant (Messor spp.) nests. We tested our hypothesis by (1) mapping the occurrence of harvester ant nests and aggregated gazelle pellet groups along 31 strip transects, (2) monitoring pellet group accumulation bimonthly at 56 pairs of permanent plots established on ant nests and at adjacent control sites for a complete year, and (3) comparing vegetation and soil parameters between ant nest sites used by gazelles and paired control plots without ant nests. Although the area of Messor spp. nest sites covered only about 0.29% of the sampled transects, 84% of the gazelle pellet group aggregation sites were positioned upon ant nests, suggesting that gazelles actively selected Messor spp. nest sites. Pair-wise comparisons between ant nest plots and paired control plots also confirmed higher use of ant nest sites by gazelles compared to sites without ant nests in all time periods. Percent soil organic matter, percent cover of gravel, and annual herb vegetation significantly differed between ant nest and paired control plots in all the vegetation communities. We suggest that the alterations brought about by harvester ants on soil and vegetation make these sites attractive to gazelles. Gazelle territoriality behaviour and use of ant nests as bedding sites may be the reasons for selection of ant nest sites by gazelles.     

The capacity of a Myrmica ant nest to support a predacious species of Maculinea butterfly

Summary Caterpillars of Maculinea arion are obligate predators of the brood of Myrmica sabuleti ants. In the aboratory, caterpillars eat the largest available ant larvae, although eggs, small larvae and prepupae are also palatable. This is an efficient way to predate. It ensures that newly-adopted caterpillars consume the final part of the first cohort of ant brood in a nest, before this pupates in early autumn and becomes unavailable as prey. At the same time, the fixed number of larvae in the second cohort is left to grow larger before being killed in late autumn and spring. Caterpillars also improve their feeding efficiency by hibernating for longer than ants in spring, losing just 6% of their weight while the biomass of ant larvae increases by 27%. Final instar caterpillars acquire more than 99% of their ultimate biomass in Myrmica nests, growing from 1.3 mg to an estimated 173 mg. A close correlation was found between the weights of caterpillars throughout autumn and the number of large ant larvae they had eaten. This was used to calculate the number of larvae eaten in spring, allowing both for the loss of caterpillar weight during winter and the increase in the size of their prey in spring. It is estimated that 230 of the largest available larvae, and a minimum nest size of 354 M. sabuleti workers, is needed to support one butterfly. Few wild M. sabuleti nests are this large: on one site, it was estimated that 85% of nests were too small to produce a butterfly, and only 5% could support two or more. This prediction was confirmed by the mortalities of 376 caterpillars in 151 wild M. sabuleti nests there. Mortalities were particularly high in nests that adopted more than two caterpillars, apparently due to scramble competition and starvation in autumn. Survival was higher than predicted in wild nests that adopted one caterpillar. These caterpillars seldom exhaust their food before spring, when there is intense competition among Myrmica for nest sites. Ants often desert their nests in the absence of brood, leaving the caterpillar behind. Vacant nests are frequently repopulated by a neighbouring colony, carrying in a fresh supply of brood. Maculinea arion caterpillars have an exceptional ability to withstand starvation, and sometimes survive to parasitize more than one Myrmica colony. Despite these adaptations, predation is an inefficient way to exploit the resources of a Myrmica nest. By contrast, Maculinea rebeli feeds mainly at a lower trophic level, on the regurgitations of worker ants. Published data show that Myrmica nests can support 6 times more caterpillars of Maculinea rebeli than of M. arion in the laboratory. This is confirmed by field data.     

Leaf-cutting ant workers (Acromyrmex heyeri) trade off nest thermoregulation for humidity control

This study investigated whether workers of the thatching grass-cutting ant Acromyrmex heyeri respond to the competing demands of temperature and humidity control by modifying the architecture of the nest thatch. First, we evaluated whether the opening and closing of nest apertures are thermoregulatory responses. Second, we explored whether the control of nest humidity is compromised by the thermoregulatory responses, and to what extent workers trade off the control of one variable for the other. At temperatures ranging from 20–30°C, workers created more openings in the nest thatch, the higher the internal nest temperature. When the air surrounding the nest was experimentally desiccated at constant temperature, workers were observed to close nest openings at temperatures that previously triggered the opposite response, i.e., opening of apertures. This demonstrates that A. heyeri workers trade off a response related to thermoregulation for the maintenance of internal nest humidity.