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Aim The Australian Coptotermes (Family: Rhinotermitidae) are a small monophyletic group of termites, some of which build mounds. In this study, we construct predicted distributions based on environmental data (niche models) for all Australian species of Coptotermes to test whether specific environmental factors have contributed to the evolution of mound-building behaviour and whether the degree of niche similarity and degree of phylogenetic similarity are correlated. Location The Australian mainland, including the known native ranges of all Australian species of Coptotermes. Methods We estimated the phylogenetic relationships between the species of Australian Coptotermes. We then generated and compared environmental niche models in a phylogenetic framework for all study species to test niche conservation. Our analyses were based on location data from our own sampling and from the Atlas of Living Australia, genetic data from a previous study of Australian Coptotermes, and environmental data from WorldClim and ASRIS. Results We found that no environmental variable differed consistently between mound-building and non-mound-building taxa and that the differences in niches between pairs of Australian species of Coptotermes are uncorrelated with time since divergence. The environmental tolerances of the Australian Coptotermes termites are more restricted by rainfall than they are by soil or temperature. Main conclusions Our results show that mound-building behaviour has not necessarily evolved in response to similar abiotic conditions. Our results are consistent with ecological speciation leading to niche divergence since Coptotermes first arrived in Australia ~12.5 million years ago. [ABSTRACT FROM AUTHOR]

Integrative taxonomy, including molecular, morphological, distributional and biological data, is applied in a review of the taxonomy of the Australian species of the pest termite genus Coptotermes. The validity of the previously described species is discussed, and two new species, Coptotermes nanus, sp. nov. and Coptotermes cooloola, sp. nov., are described from the Kimberley region of Western Australia and south-east Queensland respectively. Their delimitation is based on morphological and distributional data, and the results of generalised mixed Yule-coalescent analysis of mitochondrial DNA sequence data. Images of the external view of the two new species are provided, as well as a key, based on soldier characters, for all Australian species of Coptotermes. [ABSTRACT FROM AUTHOR]

Eavesdropping has evolved in many predator-prey relationships. Communication signals of social species may be particularly vulnerable to eavesdropping, such as pheromones produced by ants, which are predators of termites. Termites communicate mostly by way of substrate-borne vibrations, which suggest they may be able to eavesdrop, using two possible mechanisms: ant chemicals or ant vibrations. We observed termites foraging within millimetres of ants in the field, suggesting the evolution of specialised detection behaviours. We found the termite Coptotermes acinaciformis detected their major predator, the ant Iridomyrmex purpureus, through thin wood using only vibrational cues from walking, and not chemical signals. Comparison of 16 termite and ant species found the ants-walking signals were up to 100 times higher than those of termites. Eavesdropping on passive walking signals explains the predator detection and foraging behaviours in this ancient relationship, which may be applicable to many other predator-prey relationships. [ABSTRACT FROM AUTHOR]

The article discusses a study on a global taxonomic road map for species validity and distribution of an economically important subterranean termite genus Coptotermes. Topics discussed include a review of all named species within the genus, their systematic scrutiny according to the region of their original description, and the number of species names within Coptotermes that conformed to the rules of the International Code of Zoological Nomenclature (ICZN).

Reticulitermes, Heterotermes and Coptotermes form a small termite clade with partly overlapping distributions. Although native species occur across all continents, the factors influencing their distribution are poorly known. Here, we reconstructed the historical biogeography of these termites using mitochondrial genomes of species collected on six continents. Our analyses showed that Reticulitermes split from Heterotermes + Coptotermes at 59.5 Ma (49.9-69.5 Ma 95% CI), yet the oldest split within Reticulitermes (Eurasia and North America) is 16.1 Ma (13.4-19.5 Ma) and the oldest split within Heterotermes + Coptotermes is 36.0 Ma (33.9-40.5 Ma). We detected 14 disjunctions between biogeographical realms, all of which occurred within the last 34 Ma, not only after the break-up of Pangaea, but also with the continents in similar to current positions. Land dispersal over land bridges explained four disjunctions, oceanic dispersal by wood rafting explained eight disjunctions, and human introduction was the source of two recent disjunctions. These wood-eating termites, therefore, appear to have acquired their modern worldwide distribution through multiple dispersal processes, with oceanic dispersal and human introduction favoured by the ecological traits of nesting in wood and producing replacement reproductives. [ABSTRACT FROM AUTHOR]

Termite baiting is now one of the two main management tools in developed countries after 20 years of commercial release. It has two main goals: to use small amounts of active ingredient and 'colony elimination', i.e. death of all individuals in the colony. We consider how well baiting has been evaluated from 100 studies in the scientific literature. Studies have included 15 active ingredients, 23 termite species and 16 countries, yet most studies have focused on the chitin synthesis inhibitor hexaflumuron, Reticulitermes and the United States. Baiting has mostly met its goals: typically about 0.5 g of active ingredient was used, and colony elimination achieved, albeit with rates varying from 0 to 100%, and sometimes supplemented with liquid insecticide. Baiting was most successful using chitin synthesis inhibitors against Reticulitermes and Coptotermes (Rhinotermitidae), in temperate locations, although colony elimination was usually inferred indirectly - mostly by termite absence from baits - and was often slow, from 25 to 450 days. Baiting has been less tested and less successful against higher termites in tropical locations, where they are most diverse and abundant. Future research may have to consider greater termite species diversity and other active ingredients to reduce control times in order to fulfil the potential of baiting. © 2014 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

A comparative field study was conducted to evaluate the ability of subterranean termites to damage a set of four different plastic materials (cable sheathings) exposed below- and above-ground. Eight pest species from six countries were included, viz., Coptotermesfonnosantis (Shiraki) in China, Japan, and the United States; Coptotennes gestroi (Wasmann) in Thailand and Malaysia; Coptotennes curvignathiis (Holmgren) and Coptotennes kalshoceni (Kemner) in Malaysia; Coptotennes aeinacifonnis (Froggatt) with two forms of the species complex and Mastotennes darwiniensis (Froggatt) in Australia; and Reticulitennesflavipes (Kollar) in the United States. Termite species were separated into four tiers relative to decreasing ability to damage plastics. The first tier, most damaging, included C. acinaaformis, mound-building form, and M. darwiniensis, both from tropical Australia The second tier included C. acinaaformis, tree-nesting form, from temperate Australia and C. kalshooeni from Southeast Asia, The third tier included C. cwvignathtis and C. gestroi from Southeast Asia and C.fonnosamis from China, Japan, and the United States, whereas the fourth tier included only R. flavipes, which caused no damage. A consequence of these results is that plastics considered resistant to termite damage in some locations will not be so in others because of differences in the termite fauna, for example, resistant plastics from the United States and Japan will require further testing in Southeast Asia and Australia. However, plastics considered resistant in Australia will be resistant in all other locations. [ABSTRACT FROM AUTHOR]

The number of recognized invasive termite species has increased from 17 in 1969 to 28 today. Fourteen species have been added to the list in the past 44 years; 10 have larger distributions and 4 have no reported change in distribution, and 3 species are no longer considered invasive. Although most research has focused on invasive termites in urban areas, molecular identification methods have answered questions about certain species and found that at least six species have invaded natural forest habitats. All invasive species share three characteristics that together increase the probability of creating viable propagules: they eat wood, nest in food, and easily generate secondary reproductives. These characteristics are most common in two families, the Kalotermitidae and Rhinotermitidae (which make up 21 species on the invasive termite list), particularly in three genera, Cryptotermes, Heterotermes, and Coptotermes (which together make up 16 species). Although it is the largest termite family, the Termitidae (comprising 70% of all termite species) have only two invasive species, because relatively few species have these characteristics. Islands have double the number of invasive species that continents do, with islands in the South Pacific the most invaded geographical region. Most invasive species originate from Southeast Asia. The standard control methods normally used against native pest termites are also employed against invasive termites; only two eradication attempts, in South Africa and New Zealand, appear to have been successful, both against Coptotermes species. [ABSTRACT FROM AUTHOR]

The efficacy of bistrifiuron, a chitin synthesis inhibitor, in cellulose bait pellets was evaluated on the mound-building subterranean termite, Coptotermes acinaciformis (Froggatt). Three concentrations of the bistrifluron were used: 0 (untreated control), 0.5, and 1.0% over an 8 wk period. Both doses of bistrifiuron bait eliminated (viz, termites absent from nest or mound) termite colonies: 83% of colonies (10 of 12) were either eliminated or moribund (viz, colony had no reproductive capacity and decreased workforce) after 8 wk, compared with none of the control colonies. The remaining two treated colonies were deemed to be in decline. Early signs that bistrifiuron was affecting the colonies included: 3 wk after baiting mound temperatures showed a loss of metabolic heat, 4 wk after baiting foraging activity in feeding stations was reduced or absent, and dissection of two mounds at 4 wk showed they were moribund. Colony elimination was achieved in around half or less the time, and with less bait toxicant, than other bait products tested under similar conditions in the field, because of either the active ingredient, the high surface area of the pellets, or a combination of both. This suggests the sometimes long times reported for control using baits may be reduced significantly. The use of a mound building species demonstrated clearly colony level effects before and after termites stopped foraging in bait stations. [ABSTRACT FROM AUTHOR]

Competition exclusion, when a single species dominates resources due to superior competitiveness, is seldom observed in nature. Termites compete for resources with deadly consequences, yet more than one species can be found feeding in the same wooden resource. This is especially surprising when drywood species, with colonies of a few hundred, are found cohabiting with subterranean species, with colonies of millions. Termites communicate vibro-acoustically and, as these signals can travel over long distances, they are vulnerable to eavesdropping. We investigated whether drywood termites could eavesdrop on vibration cues from subterranean species. We show, using choice experiments and recordings, that the drywood termite Cryptotermes secundus can distinguish its own species from the dominant competitor in the environment, the subterranean termite Coptotermes acinaciformis. The drywood termite was attracted to its own vibration cues, but was repelled by those of the subterranean species. This response increased with decreasing wood size, corresponding with both increased risk and strength of the cue. The drywood termites appear to avoid confrontation by eavesdropping on the subterranean termites; these results provide further evidence that vibro-acoustic cues are important for termite sensory perception and communication. [ABSTRACT FROM AUTHOR]

Competition is a fundamental process in ecology and helps to determine dominance hierarchies. Competition and dominance hierarchies have been little investigated in wood-eating termites, despite the necessary traits of similar resources, and showing spatial and temporal overlap. Competition and dominance between five species of wood-eating termites found in Huangzhou, China, was investigated in three laboratory experiments of aggression and detection, plus a year-long field survey of termite foraging activity. Dominance depended on body size, with largest species winning overwhelmingly in paired contests with equal numbers of individuals, although the advantage was reduced in paired competitions with equal biomass. The termites could detect different species from used filter papers, as larger species searched through paper used by smaller species, and smaller species avoided papers used by larger species. The largest species maintained activity all year, but in low abundance, whereas the second largest species increased activity in summer, and the smallest species increased their activity in winter. The termite species displayed a dominance hierarchy based on fighting ability, with a temporal change in foraging to avoid larger, more dominant species. The low abundance of the largest species, here Macrotermes barneyi, may be a function of human disturbance, which allows subordinate species to increase. Thus, competitive release may explain the increase in abundance of pest species, such as Coptotermes formosanus, in highly modified areas, such as urban systems. [ABSTRACT FROM AUTHOR]

The termite genus Coptotermes (Rhinotermitidae) is found in Asia, Africa, Central/South America and Australia, with greatest diversity in Asia. Some Coptotermes species are amongst the world’s most damaging invasive termites, but the genus is also significant for containing the most sophisticated mound-building termites outside the family Termitidae. These mound-building Coptotermes occur only in Australia. Despite its economic and evolutionary significance, the biogeographic history of the genus has not been well investigated, nor has the evolution of the Australian mound-building species. We present here the first phylogeny of the Australian Coptotermes to include representatives from all described species. We combined our new data with previously generated data to estimate the first phylogeny to include representatives from all continents where the genus is found. We also present the first estimation of divergence dates during the evolution of the genus. We found the Australian Coptotermes to be monophyletic and most closely related to the Asian Coptotermes , with considerable genetic diversity in some Australian taxa possibly representing undescribed species. The Australian mound-building species did not form a monophyletic clade. Our ancestral state reconstruction analysis indicated that the ancestral Australian Coptotermes was likely to have been a tree nester, and that mound-building behaviour has arisen multiple times. The Australian Coptotermes were found to have diversified ∼13 million years ago, which plausibly matches with the narrowing of the Arafura Sea allowing Asian taxa to cross into Australia. The first diverging Coptotermes group was found to be African, casting doubt on the previously raised hypothesis that the genus has an Asian origin. [ABSTRACT FROM AUTHOR]

Abstract: Cables sheathed with medium density polyethylene or polyamide were exposed together with highly palatable bait wood to termite faunas in south-eastern and northern Australia, Thailand and southern USA using three methods: below-ground exposure, samples buried horizontally at a depth of 15–30 cm; graveyard method, samples inserted vertically 25 cm deep into the ground; ground contact method, samples placed horizontally on the ground surface, covered with soil and a plastic sheet. Samples were inspected for damage and bait wood replaced annually for six years. No polyamide sample was attacked. Damage to polyethylene was most severe at the Australian sites (across all methods) and in the graveyard method (across all sites), although in Australia in the below-ground method samples experienced greatest damage. Exposing samples together with bait wood within containers for one year, and replenishing bait wood up to three times, i.e. an ‘accelerated’ test method, compared to the standard procedure of providing new bait wood only once a year, resulted in only very limited damage to cables at Asian sites (Macrotermitinae, Coptotermes spp., Malaysia; Coptotermes formosanus, Japan), matching the earlier results for Thailand. But 73% of samples were destroyed by Coptotermes acinaciformis in northern Australia. The Australian termite fauna responds more aggressively to plastic samples than major pest species of termite elsewhere. [Copyright &y& Elsevier]