Polymorphism in the giant cocoa termite,Neotermes papua (Desneux)

Summary The direct development ofNeotermes papua (Isoptera: Kalotermitidae) comprises four larval and three nymphal instars before the alate. The first five instars can be easily characterized. The second stage nymphs come morphologically close to the pseudergates, characterized by reduced wing buds. These nymphs can moult stationarily, i.e. with little morphological change, or to presoldiers, or proceed to the alate via the third nymphal stage. Pseudergates originate through a late and reversible deviation from the straight development to the alate. Presoldiers may derive from several stages, up to the last nymphal one; their production is subject to an inhibition by extant soldiers. This developmental schema is congruent with those described in other Kalotermitidae and the Termopsidae. By pinpointing the existence of a large pool of pluripotent individuals, in which the penultimate nymphal stage mingles with pseudergates, the present study also reveals a great similarity betweenNeotermes andProrhinotermes, and suggests that this developmental schema might be generally applicable to termites devoid of a permanent worker caste.King Léopold III Biological Station, Laing Island, Papua New Guinea, contribution No. 235     

四川新白蚁属一新种记述(等翅目,木白蚁科)

记述新白蚁属1新种,屏山新白蚁 Neotermes Pingshanensis sp．nov．,新种与长颚新白蚁 Neotermes dolichognathus Xu et Han相近,但体色不同,头长/宽比例不同,触角第2节明显长于第3节,左上颚缘齿4枚,前胸背板前缘具深凹.危害物为潮湿木窗框.模式标本保存于成都市白蚁防治研究所.     

Are the spatio‐temporal dynamics of soil‐feeding termite colonies shaped by intra‐specific competition?

1. Soil‐feeding termites are abundant and diversified in neotropical forests, where they are among the major decomposers of the soil macrofauna. While niche specialisation along the humification gradient may reduce inter‐specific competition, some species are represented by numerous colonies likely to be involved in intra‐specific competition, but the subterranean nesting habits of most species of soil‐feeding termites make direct observations difficult. 2. The soldierless species Anoplotermes banksi Emerson was studied, which, unlike other Anoplotermes‐group species, builds arboreal nests that can be easily detected. To infer the biological processes driving the spatial distribution of this species, we conducted a 3‐year survey of the dynamics of colonisation of a 1‐ha plot by A. banksi. Ripley's L‐function, detecting aggregation or dispersion at various spatial scales, was used to investigate the distribution pattern of A. banksi nests, as well as the distribution of new and established nests. 3. Only one‐fourth of the nests recorded the first year were still alive after 3 years, highlighting a rapid turnover of the A. banksi nest population. Age classes were differentially affected by mortality, which was higher in young nests than in large, established nests. 4. Established nests were overdispersed at a short range, whereas young nests had a random or clumped distribution. Young nests tended to be overdispersed from established ones and were more abundant in areas with recently dead nests. Dead nests predominantly occurred where A. banksi nests were particularly abundant. Altogether, the present results indicate a negative interaction between neighbouring colonies suggesting intra‐specific competition.     

Wood excavations of three species of subterranean termites

We compared the feeding excavations on wood blocks of three species of subterranean termites, Coptotermes formosanus Shiraki, Reticulitermes flavipes (Kollar), and R. virginicus (Banks). Feeding rate followed the order C. formosanus > R. flavipes > R. virginicus. Wood surface area (mm²) exposed per unit feeding was higher for C. formosanus and R. flavipes than for R. virginicus. This was caused by the tendency of C. formosanus and R. flavipes to make internally penetrating tunnels, thereby increasing surface area, whereas R. virginicus made trough- and bowl-like depressions on the outside of blocks, sometimes decreasing the size of blocks outwardly without a corresponding high increase in surface area typical with the tunnels of the other species. Consequently, wood surface area was sometimes reduced, rather than increased as a result of feeding by R. virginicus. Different patterns of wood excavation suggest that these termites have divergent roles in wood decay processes.

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Résumé Les organismes pionniers qui modifient le bois et le rendent acceptable par les insectes qui le perforent sont généralement des champignons du bois pourri. Cependant, une fois que les termites ou autres insectes perforant le bois ont pénétré, leurs galeries favorisent les bactéries fixatrices d'azote, permettent l'invasion d'autres organismes décomposeurs, et de ce fait régularisent la décomposition du bois (Ausmus, 1977). L'exposition de la surface à l'intérieur des perforations jouant un rôle très important dans le processus de pourrissement, il est souhaitable de pouvoir quantifier la surface des galeries dues à l'alimentation des termites. Une courbe type permettant de prédire l'aire de la surface perforée a été construite en perçant 109 morceaux de bois de trous cylindriques de différents diamètres, en calculant l'aire de la surface des morceaux de bois, en appliquant et pesant une couche de vernis pour bois au polyuréthane, et en divisant la masse de polyuréthane par l'aire de la surface. Le modèle prédictif qui en découle est: Y=0,01443×-3,51825 (P=0,0001; r=0,68), y étant la masse de polyuréthane (en g) et x la surface (en mm²) du morceau de bois. En traitant de la même façon au polyuréthane les morceaux de bois perforés par les termites, nous pourrions déduire leur surface.Une expérience a été effectuée avec 3 espèces de rhinotermitides,- Coptotermes formosanus Shiraki, Reticulitermes flavipes (Kollar) et R. virginicus (Banks). Des groupes de chaque espèce se sont alimentés pendant 11 ou 12 jours sur des morceaux de bois non contaminés par des champignons. Nous avons déterminé la survie, la consommation, la modification de la surface du morceau de bois (par utilisation du modèle prédictif) et le changement de surface par terminte.La survie est la même, mais la consommation est dans l'ordre suivant: C. formosanus > R. flavipes > R. virginicus. L'aire de la surface exposée par unité d'alimentation était plus élevée pour C. formosanus et R. flavipes que pour R. virginicus (Tab. 1). Ceci est dû à la tendance de C. formosanus et R. flavipes de creuser des galeries vers l'intérieur, tandis que R. virginicus fait des cuvettes à la surface du bois. Les attaques superficielles de R. virginicus réduisent parfois le volume du morceau de bois sans accroître proportionnellement la surface comme le font les espèces creusant des galeries. Ainsi, avec R. virginicus la surface peut être réduite au lieu d'augmenter. Des différences entre colonies s'observent avec toutes les variables (Tab. 2).Nos résultats suggèrent que C. formosanus et R. flavipes contribuent plus que R. virginicus à exposer le bois aux autres organismes décomposeurs. Cependant, ces résultats peuvent être modifiés par un conditionnement préalable du bois par des champignons.

     

On the origin of termite workers: weighing up the phylogenetic evidence

Resolving the phylogenetic history of a 'true' worker caste in termites is essential to our understanding of termite eusocial evolution. Whether this caste is ancient and monophyletic or derived and polyphyletic will have a tremendous impact on our interpretation of termite eusocial history and remains an outstanding question in termite biology. Recent work has begun to re-examine this question in light of new phylogenetic information, but new questions have now arisen about how best to model character state changes in termite caste systems. In the present paper, we compare the models of Grandcolas and D'Haese [J. Evol. Biol. 15 (2002) 885] and Thompson et al. [J. Evol Biol. 13 (2000) 8691 and attempt to make explicit how these proposals differ with respect to the number of, and homology between, character states. We highlight the support each model has for the two principal, but competing, evolutionary hypotheses outlined above.     

Interspecific variation in the defence secretions of Nasutitermes soldiers

Termite soldiers of the genus Nasutitermes (Isoptera, Termitidae, Nasutitermitinae) eject a viscous, sticky defense secretion composed of non-polar monoterpene hydrocarbons and polyoxygenated diterpenes from the frontal gland. Chemical compositions are described in detail for the East African species, N. kempae and N. infuscatus, and for the Neotropical species N. ephratae. Additional comparisons with the new world species N. costalis, N. rippertii and N. octopilis are presented. The structure of a new monohydroxykempene from N. ephratae is described, and a physicochemical model for the stickiness of the glue is presented. Although the structures of the individual secretion components vary within the genus, the glue-like nature of the secretion remains essentially unchanged. Chemical analysis of soldier defense secretions may be useful in studying the systematic biology of termites.     

Isolation and characterization of 10 microsatellite loci in the magnetic termite,Amitermes meridionalis (Isoptera: Termitidae)

The elongated mounds of the ‘magnetic termite’, Amitermes meridionalis are a prominent feature of the Northern Territory in Australia. They are restricted to habitat patches of seasonally flooded plains which are largely isolated from each other. To investigate the population structure of A. meridionalis, we developed 10 polymorphic microsatellite loci. We tested the variability of the markers on at least 20 individuals from two populations. We found three to 12 alleles per locus with a level of heterozygosity at each locus ranging from 0.05 to 0.74.     

Chemotaxonomy of Subulitermes and Nasutitermes termine soldier defense secretions. Evidence against the hypothesis of diphyletic evolution of the Nasutitermitinae

The soldier defense secretions of advanced neotropical termites of the genus Subulitermes (Isoptera, Nasutitermitinae) contain diterpenes identicalto those found in Nasutitermes species, while soldiers of the primitive mandibulate nasute genera Cornitermes, Armitermes and Rhynchotermes lack diterpenoid compounds. It now appears improbable that the elongate nasus and intimately associated terpenoid defense secretions evolved from a primitive mandibulate ancestor independently along two phyletic branches. An alternate hypothesis is proposed in which morphological divergence from a common diterpene-producing ancestor may have occurred.     

Asexual queen succession in the higher termite Embiratermes neotenicus

Asexual queen succession (AQS), in which workers, soldiers and dispersing reproductives are produced sexually while numerous non-dispersing queens arise through thelytokous parthenogenesis, has recently been described in three species of lower termites of the genus Reticulitermes. Here, we show that AQS is not an oddity restricted to a single genus of lower termites, but a more widespread strategy occurring also in the most advanced termite group, the higher termites (Termitidae). We analysed the genetic structure in 10 colonies of the Neotropical higher termite Embiratermes neotenicus (Syntermitinae) using five newly developed polymorphic microsatellite loci. The colonies contained one primary king accompanied either by a single primary queen or by up to almost 200 neotenic queens. While the workers, the soldiers and most future dispersing reproductives were produced sexually, the non-dispersing neotenic queens originated through thelytokous parthenogenesis of the founding primary queen. Surprisingly, the mode of thelytoky observed in E. neotenicus is most probably automixis with central fusion, contrasting with the automixis with terminal fusion documented in Reticulitermes. The occurrence of AQS based on different mechanisms of ploidy restoration raises the hypothesis of an independent evolutionary origin of this unique reproductive strategy in individual lineages of lower and higher termites.     

Why are so many trees hollow?

In many living trees, much of the interior of the trunk can be rotten or even hollowed out. Previously, this has been suggested to be adaptive, with microbial or animal consumption of interior wood producing a rain of nutrients to the soil beneath the tree that allows recycling of those nutrients into new growth via the trees roots. Here I propose an alternative (non-exclusive) explanation: such loss of wood comes at very little cost to the tree and so investment in costly chemical defence of this wood is not economic. I discuss how this theory can be tested empirically.     

八种白蚁的兵蚁和工蚁消化道形态比较研究(等翅目)

为探讨白蚁消化道形态品级差异及其系统学意义,对4个科8种白蚁兵蚁和工蚁的消化道进行比较形态学研究.结果表明:低等白蚁的兵蚁和(拟)工蚁形态较为相似,高等白蚁的兵蚁与工蚁局部特征存在明显差异.由低等到高等兵蚁和工蚁消化道各部分差异呈增多趋势.前、中、后肠占消化道的百分比在山林原白蚁Hodotermopsis sjoest...     

两种鼻白蚁之间的入侵关系

设计了5个实验以研究台湾乳白蚁(Coptotermes formosanus)和黄肢散白蚁(Reticulitermes flavipes)的种间斗争关系。所试白蚁来自阿拉巴马州。实验1将两组白蚁的兵蚁和工蚁以自然比例混合(台湾乳白蚁工蚁：兵蚁＝20：5,黄肢散白蚁工蚁：兵蚁＝24：1);实验2观察了双方同数量(各25头)工蚁的种间斗争能力;实验3观察两者同数量(各5头)兵蚁的种间斗争关系;实验4、5分别研究双方工蚁与兵蚁的斗争关系。因两种工蚁形态相似,所以在实验前用0．1％Nile blue A染过的滤纸饲喂一方白蚁24h使虫体着色以便观察。所有实验在22℃,65％RH荧光灯下进行。每个实验将两方白蚁同时放入一培养皿中,观察至一方100％受伤,然后把培养皿移到培养箱内,24小时后统计死亡率。结果表明,实验一开始,双方的工蚁和兵蚁都立即进入残酷的厮杀斗争,台湾乳白蚁兵蚁和工蚁的斗争能力都明显强于黄肢散白蚁;兵蚁的斗争行为不受工蚁的影响,工蚁的斗争能力也不受兵蚁的制约。实验中台湾乳白蚁的工蚁与黄肢散白蚁的兵蚁攻击能力相当,但黄肢散白蚁的工蚁却远弱于台湾乳白蚁的兵蚁。上述结果说明,自然界中不可能出现此两种白蚁群体的偶然性融合;外来的台湾乳白蚁很可能在其群体建立的地区占据优势[动物学报49(3)：295—302,2003]。