How Can Termites Achieve Their Unparalleled Postembryonic Developmental Plasticity? A Test for the Role of Intermolt-Specific High Juvenile Hormone Titers

Termites are “social cockroaches” and amongst the most phenotypically plastic insects. The different castes (i.e., two types of reproductives, workers, and soldiers) within termite societies are all encoded by a single genome and present the result of differential postembryonic development. Besides the default progressive development into winged sexuals of solitary hemimetabolous insects, termites have two postembryonic, non-terminal molts (stationary and regressive; i.e., molts associated, respectively, with no change or reduction of size/morphological differentiation) which allow them to retain workers, and two terminal developmental types to become soldiers and replacement reproductives. Despite this unique plasticity, especially the mechanisms underlying the non-terminal development are poorly understood. In 1982, Nijhout and Wheeler proposed a model how this diversity might have evolved. They proposed that varying juvenile hormone (JH) titers at the start, mid-phase, and end of each intermolt period account for the developmental diversity. We tested this rarely addressed model in the lower termite Cryptotermes secundus using phase-specific pharmacological manipulations of JH titers. Our results partially support the Nijhout and Wheeler model. These data are supplemented with gene expression studies of JH-related genes that characterize different postembryonic developmental trajectories. Our study provides new insights into the evolution of the unique postembryonic developmental plasticity of termites that constitutes the foundation of their social life.

Oceanic dispersal, vicariance and human introduction shaped the modern distribution of the termites Reticulitermes , Heterotermes and Coptotermes

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.

Termite colony ontogeny: supplemental data in the long-term assessment of reproductive lifespan, female neotenic production and colony size in Reticulitermes flavipes (Isoptera: Rhinotermitidae)

Reticulitermes flavipes (Kollar) colonies established by field-collected alates were reared in the laboratory for 11 years. Weights of members of each caste and full-colony censuses were performed regularly; the most recent 2003–2004 data are reported. Colonies averaged 11623.5±910 individuals, and with the exception of primary queens from one genetic lineage, mean weights for all castes had increased since 2001. Female replacement reproductives, or neotenics, developed to replace dead queens in clusters of either few, large individuals or many, small individuals. Regardless of cluster size, female neotenics comprised more reproductive biomass per colony than primary queens. The number and size of female neotenics was independent of colony size or time elapsed since a founding queen's death.

Termite colony ontogeny: a long-term assessment of reproductive lifespan, caste ratios and colony size in Reticulitermes flavipes (Isoptera: Rhinotermitidae)

Thirty Reticulitermes flavipes (Kollar) colonies established by alates collected from two separate field sites were raised in the laboratory for eight years. Twenty-one of the colonies were founded by alates from one field source and nine from another, providing demographic data from two unrelated parental lineages. Colony totals ranged from 3620 to 11641 individuals, with no significant difference in size between lineages. Soldier caste proportion of the colony total and mean wet weights for workers, soldiers and kings were significantly different between the two lineages. This suggests that at least a portion of the variability observed in caste ratios and body size may be heritable. One founding reproductive had died in five of the colonies (17%); none lost both parents. The queenless colonies contained exclusively female replacement reproductives (neotenics); the kingless colony contained a female-skewed mixture of male and female neotenics. All the nests that lost a founding parent contained significantly more pre-alate nymphs than the nests with both a king and a queen. Comparisons with published reports of ontogenetic patterns in other termites and social insects are discussed.