Sexual and asexual colony foundation and the mechanism of facultative parthenogenesis in the termite Reticulitermes speratus (Isoptera, Rhinotermitidae)

2004 ◽  
Vol 51 (4) ◽  
pp. 325-332 ◽  
Author(s):  
K. Matsuura ◽  
M. Fujimoto ◽  
K. Goka
Keyword(s):  
Colony Foundation ◽  
Reticulitermes Speratus ◽  
Facultative Parthenogenesis

scholarly journals The lose-to-win strategy of the weak: intraspecific parasitism via egg abduction in a termite

2021 ◽  
Vol 17 (12) ◽  
Author(s):  
Chihiro Tamaki ◽  
Mamoru Takata ◽  
Kenji Matsuura
Keyword(s):  
Genomic Imprinting ◽  
Social Insects ◽  
Animal Species ◽  
Colony Foundation ◽  
Reticulitermes Speratus ◽  
Major Threat ◽  
Incipient Colonies ◽  
Intraspecific Parasitism

Predation by larger conspecifics poses a major threat to small juveniles in many animal species. However, in social insects, raids perpetrated by large colonies may provide smaller colonies with opportunities for parasitization. Herein, in the termite Reticulitermes speratus , we demonstrate that small incipient colonies parasitize large mature colonies through egg abduction when attacked by raiding conspecifics. We observed that the eggs of incipient colonies were brought into raiding colonies while their parents were killed during the attack. In this species, unmated females found new colonies with female–female (FF) cooperation, in addition to the typical monogamous colony foundation. Interestingly, the abducted eggs of FF pairs developed into nymphs (reproductive caste) in the raiding colonies, whereas the eggs of male–female (MF) pairs developed into workers (non-reproductive caste). Parthenogenetic eggs are known to be developmentally predisposed to becoming female reproductives owing to genomic imprinting in termites. This study demonstrates that the plundering of small colonies by larger conspecific colonies not only results in the extinction of the weaker colonies, but also serves as a strategy that incipient colonies use to obtain the reproductive position in large colonies by stealth. The results elucidate the diversity and complexity of inter-colonial interactions in social insects.

scholarly journals Cellulolytic Protist Numbers Rise and Fall Dramatically in Termite Queens and Kings during Colony Foundation

2013 ◽  
Vol 12 (4) ◽  
pp. 545-550 ◽  
Author(s):  
Keisuke Shimada ◽  
Nathan Lo ◽  
Osamu Kitade ◽  
Akane Wakui ◽  
Kiyoto Maekawa
Keyword(s):  
Nutrient Transfer ◽  
Reproductive Tissue ◽  
Colony Foundation ◽  
Dynamic Nature ◽  
Termite Species ◽  
Reticulitermes Speratus ◽  
Content Type ◽  
Trade Offs ◽  
Critical Phase ◽  
Incipient Colonies

ABSTRACTAmong the best-known examples of mutualistic symbioses is that between lower termites and the cellulolytic flagellate protists in their hindguts. Although the symbiosis in worker termites has attracted much attention, there have been only a few studies of protists in other castes. We have performed the first examination of protist population dynamics in queens and kings during termite colony foundation. Protist numbers, as well as measurements of hindgut and reproductive tissue sizes, were undertaken at five time points over 400 days in incipient colonies ofReticulitermes speratus, as well as in other castes of mature colonies of this species. We found that protist numbers increased dramatically in both queens and kings during the first 50 days of colony foundation but began to decrease by day 100, eventually disappearing by day 400. Hindgut width followed a pattern similar to that of protist numbers, while ovary and testis widths increased significantly only at day 400. Kings were found to contain higher numbers of protists than queens in incipient colonies, which may be linked to higher levels of nutrient transfer from kings to queens than vice versa, as is known in some other termite species. Protists were found to be abundant in soldiers from mature colonies but absent in neotenics. This probably reflects feeding of soldiers by workers via proctodeal trophallaxis and of reproductives via stomodeal trophallaxis. The results reveal the dynamic nature of protist numbers during colony foundation and highlight the trade-offs that exist between reproduction and parental care during this critical phase of the termite life cycle.

scholarly journals Fisher vs. The Worms: Extraordinary Sex Ratios in Nematodes and the Mechanisms That Produce Them

Cells ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1793
Author(s):  
Justin Van Goor ◽  
Diane C. Shakes ◽  
Eric S. Haag
Keyword(s):  
Sex Ratio ◽  
Sperm Competition ◽  
Sex Chromosomes ◽  
Sex Ratios ◽  
Environmental Sex Determination ◽  
Fitness Advantage ◽  
Selection For ◽  
Facultative Parthenogenesis ◽  
Multicellular Organisms ◽  
Inbred Populations

Parker, Baker, and Smith provided the first robust theory explaining why anisogamy evolves in parallel in multicellular organisms. Anisogamy sets the stage for the emergence of separate sexes, and for another phenomenon with which Parker is associated: sperm competition. In outcrossing taxa with separate sexes, Fisher proposed that the sex ratio will tend towards unity in large, randomly mating populations due to a fitness advantage that accrues in individuals of the rarer sex. This creates a vast excess of sperm over that required to fertilize all available eggs, and intense competition as a result. However, small, inbred populations can experience selection for skewed sex ratios. This is widely appreciated in haplodiploid organisms, in which females can control the sex ratio behaviorally. In this review, we discuss recent research in nematodes that has characterized the mechanisms underlying highly skewed sex ratios in fully diploid systems. These include self-fertile hermaphroditism and the adaptive elimination of sperm competition factors, facultative parthenogenesis, non-Mendelian meiotic oddities involving the sex chromosomes, and environmental sex determination. By connecting sex ratio evolution and sperm biology in surprising ways, these phenomena link two “seminal” contributions of G. A. Parker. 

scholarly journals Colony Foundation in an Oceanic Seabird

PLoS ONE ◽  
2016 ◽  
Vol 11 (2) ◽  
pp. e0147222 ◽  
Author(s):  
Ignacio Munilla ◽  
Meritxell Genovart ◽  
Vitor H. Paiva ◽  
Alberto Velando
Keyword(s):  
Colony Foundation

SYSTEMATICS OF THE TRICHADENOTECNUM ALEXANDERAE SPECIES COMPLEX (PSOCOPTERA: PSOCIDAE) BASED ON AN INVESTIGATION OF MODES OF REPRODUCTION AND MORPHOLOGY

1983 ◽  
Vol 115 (10) ◽  
pp. 1329-1354 ◽  
Author(s):  
B. W. Betz
Keyword(s):  
Life History ◽  
North America ◽  
Sibling Species ◽  
Species Complex ◽  
Morphological Analysis ◽  
Geographic Range ◽  
Eastern North America ◽  
Facultative Parthenogenesis

AbstractTrichadenotecnum alexanderae Sommerman is shown to represent one biparental (= euphrasic) species capable of facultative parthenogenesis (thelytoky) and three uniparental (= obligatorily parthenogenetic) sibling species, as determined by tests for mating, life history observations, and morphological analysis of specimens over the geographic range of the species complex. The name T. alexanderae is restricted to the biparental species because the holotype is a male. The three uniparental species are here named and described as T. castum n. sp., T. merum n. sp., and T. innuptum n. sp. The female of T. alexanderae is redescribed to allow its separation from the three uniparental species. A key to females of the species complex is supplied. All three uniparental species were derived from the biparental ancestor of T. alexanderae. Most collections of populations represented only by females consist of one or more uniparental species. Facultative parthenogenesis is shown to maintain a population of T. alexanderae through one generation only. The biparental species is found not to be restricted geographically to a relictual or peripheral range within the species complex, but to occupy a rather wide, north-temperate distribution across eastern North America.

scholarly journals The evolution of social parasitism in Formica ants revealed by a global phylogeny

2020 ◽  
Author(s):  
Marek L Borowiec ◽  
Stefan P Cover ◽  
Christian Rabeling
Keyword(s):  
Life History ◽  
New World ◽  
Social Parasitism ◽  
Social Parasite ◽  
Colony Foundation ◽  
Parasite Diversity ◽  
Social Parasites ◽  
Evolutionary Trajectories ◽  
Competing Hypotheses ◽  
Temporary Social Parasitism

Studying the behavioral and life history transitions from a cooperative, eusocial life history to exploitative social parasitism allows for deciphering the conditions under which changes in behavior and social organization lead to diversification. The Holarctic ant genus Formica is ideally suited for studying the evolution of social parasitism because half of its 178 species are confirmed or suspected social parasites, which includes all three major classes of social parasitism known in ants. However, the life-history transitions associated with the evolution of social parasitism in this genus are largely unexplored. To test competing hypotheses regarding the origins and evolution of social parasitism, we reconstructed the first global phylogeny of Formica ants and representative formicine outgroups. The genus Formica originated in the Old World during the Oligocene (~30 Ma ago) and dispersed multiple times to the New World. Within Formica, the capacity for dependent colony foundation and temporary social parasitism arose once from a facultatively polygynous, independently colony founding ancestor. Within this parasitic clade, dulotic social parasitism evolved once from a facultatively temporary parasitic ancestor that likely practiced colony budding frequently. Permanent social parasitism evolved twice from temporary social parasitic ancestors that rarely practiced colony budding, demonstrating that obligate social parasitism can originate from different facultative parasitic backgrounds in socially polymorphic organisms. In contrast to inquiline ant species in other genera, the high social parasite diversity in Formica likely originated via allopatric speciation, highlighting the diversity of convergent evolutionary trajectories resulting in nearly identical parasitic life history syndromes.

scholarly journals Cuticular hydrocarbon profile for queen recognition in the termite Reticulitermes speratus

2021 ◽  
Author(s):  
Yuki Mitaka ◽  
Tadahide Fujita
Keyword(s):  
Cuticular Hydrocarbon ◽  
Gas Chromatography Mass Spectrometry ◽  
Reticulitermes Speratus ◽  
Recognition Mechanism ◽  
The Social ◽  
Queen Succession ◽  
Queen Recognition ◽  
And Function ◽  
Reproductive Division Of Labor ◽  
Reproductive Division

Abstract Chemical communication underlies the sophisticated colony organization of social insects. In these insects, cuticular hydrocarbons (CHCs) play central roles in nestmate, task, and caste recognition, which contribute to maintenance of the social and reproductive division of labor. Queen-specific CHCs reflect queen fertility status and function as a queen recognition pheromone, triggering aggregation responses around the queens. However, there are only a few studies about the royal recognition mechanism in termites, and particularly, no study has reported about queen-specific CHCs in the species using asexual queen succession (AQS) system, in which the primary queen is replaced by neotenic queens produced parthenogenetically. In this study, we identified the CHC pheromone for neotenic queen recognition in the AQS termite species Reticulitermes speratus. Gas chromatography-mass spectrometry analyses revealed that the relative amount of n-pentacosane was disproportionately greater in the CHC profiles of queens than in the CHC profiles of kings, soldiers, and workers. Furthermore, we investigated the cuticular chemicals of the queen aggregate workers; bioassays demonstrated that n-pentacosane shows a worker arrestant activity in the presence of workers’ cuticular extract. These results suggest that R. speratus workers identify whether each individual is a neotenic queen by recognizing the relatively higher ratio of n-pentacosane in the conspecific CHC background. Moreover, they suggest that termites have evolved queen recognition behavior, independently of social hymenopterans.

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