TL;DR: The colony structure and reproduction of C. damarensis are compared with those of the eusocial Heterocephalus glaber and mole-rats from the incomplete colonies were maintained in captivity for more than 2 years.
Abstract: Cryptomys damarensis occurs in semiarid regions of southwestern and central Africa. It lives in colonies in which reproduction is restricted to one or two of the largest-sized males and the largest female in the colony. Some division of labor, into frequent and infrequent workers, occurs within the remaining colony members. Reproduction and details of colony size and the number of breeding animals in a colony are described for two complete and five incomplete wild-captured colonies; one of the complete colonies and mole-rats from the incomplete colonies were maintained in captivity for more than 2 years. The breeding female initiated precopulatory behavior, mating occurred for about 2 weeks, the gestation length was 78–92 days, mean litter size was 2.8 ( n = 10), and a maximum of four pups was born. The pups were precocial, wandered out of the nest within 24 h after birth, began to eat solids when 6 days old, and were fully weaned when 3 weeks old. When 6 weeks old, pups began to spar with each other and with some colony members, but levels of aggression were never high and the pups were incorporated into the colony. In the colony, subordinate and frequent-worker mole-rats weighed less than dominant animals and infrequent workers; mass, therefore, was not necessarily indicative of the age of the animal. During the 2-year study period, three mole-rats that were frequent workers on capture changed their castes to infrequent workers, two of them showed a concomitant increase in body mass. The colony structure and reproduction of C. damarensis are compared with those of the eusocial Heterocephalus glaber .
TL;DR: It is argued that eusociality in mole-rats evolved from a monogamous mating system where cooperative brood care was already established, and a tendency for group living is considered to be an ancestral (plesiomorph) trait among African bathyergid mole- rats, linking them to other hystricognath rodents.
Abstract: Eusociality in mammals is defined in the present paper by the following criteria: reproductive altruism (which involves reproductive division of labor and cooperative alloparental brood care), overlap of adult generations, and permanent (lifelong) philopatry. We argue that additional criteria such as the existence of castes, colony size, reproductive skew, and social cohesion are not pertinent to the definition of eusociality in mammals. According to our definition of mammalian eusociality, several rodent species of the African family Bathyergidae can be considered eusocial, including the naked mole-rat (Heterocephalus glaber), Damaraland mole-rat (Cryptomys damarensis), and several additional, if not all, species in the genus Cryptomys. Furthermore, some species of social voles (like Microtus ochrogaster) may also fulfill criteria of mammalian eusociality. Understanding the evolution of eusociality in mole-rats requires answers to two primary questions: (1) What are the preconditions for the development of their eusocial systems? (2) Why do offspring remain in the natal group rather than dispersing and reproducing? Eusociality in mammals is by definition a special case of monogamy (more specifically: monogyny one female breeding), involving prolonged pair bonding for more than one breeding period. We argue that eusociality in mole-rats evolved from a monogamous mating system where cooperative brood care was already established. A tendency for group living is considered to be an ancestral (plesiomorph) trait among African bathyergid mole-rats, linking them to other hystricognath rodents. A solitary lifestyle seen in some genera, such as Bathyergus, Georychus, and Heliophobius, is assumed to be a derived trait that arose independently in different lineages of bathyergids, possibly as a consequence of selective constraints associated with the subterranean environment. In proximate terms, in eusocial mole-rats either puberty is assumed to be developmentally delayed so that under natural conditions most animals die before dispersal is triggered (e.g., in the case of Heterocephalus) or dispersal is induced only by an incidental encounter with an unfamiliar, yet adequate sexual partner (e.g., in the case of Cryptomys). Ultimately, a combination of strategies involving either dispersal and/or philopatry can be beneficial, especially in a highly unpredictable environment. If genetic relatedness among siblings is high (e.g., a coefficient of relatedness of 0.5 or more), then philopatry would not invoke an appreciable loss of fitness, especially if the cost of dispersing is higher than staying within the natal group. High genetic relatedness is more likely in a monogamous mating system or a highly inbred population. In this paper, we argue that the preconditions for eusociality in bathyergid mole-rats were a monogamous mating system and high genetic relatedness among individuals. We argue against the aridity food-distribution hypothesis (AFDH) that suggests a causal relationship between cooperative foraging for patchily distributed resources and the origin of eusociality. The AFDH may explain group size dynamics of social mole-rats as a function of the distribution and availability of resources but it is inadequate to explain the formation of eusocial societies of mole-rats, especially with respect to providing preconditions conducive for the emergence of eusociality.
TL;DR: This study uses an extensive molecular phylogeny and mitochondrial cytochrome b and 12s rRNA molecular clocks to examine in detail the divergence times, and patterns of speciation of the five extant genera in the context of rift valley formation in Africa.
Abstract: African mole-rats are subterranean Hystricomorph rodents, distributed widely throughout sub-Saharan Africa, and displaying a range of social and reproductive strategies from solitary dwelling to the ‘insect-like’ sociality of the naked mole-rat, Heterocephalus glaber . Both molecular systematic studies of Rodentia and the fossil record of bathyergids indicate an ancient origin for the family. This study uses an extensive molecular phylogeny and mitochondrial cytochrome b and 12s rRNA molecular clocks to examine in detail the divergence times, and patterns of speciation of the five extant genera in the context of rift valley formation in Africa. Based on a value of 40–48 million years ago (Myr) for the basal divergence of the family ( Heterocephalus ), we estimate divergence times of 32–40 Myr for Heliophobius , 20–26 Myr for Georychus / Bathyergus and 12–17 Myr for Cryptomys , the most speciose genus. While early divergences may have been independent of rifting, patterns of distribution of later lineages may have been influenced directly by physical barriers imposed by the formation of the Kenya and Western Rift, and indirectly by accompanying climatic and vegetative changes. Rates of chromosomal evolution and speciation appear to vary markedly within the family. In particular, the genus Cryptomys appears to have undergone an extensive radiation and shows the widest geographical distribution. Of the two distinct clades within this genus, one exhibits considerable karyotypic variation while the other does not, despite comparatively high levels of sequence divergence between some taxa. These different patterns of speciation observed both within the family and within the genus Cryptomys may have been a result of environmental changes associated with rifting.
TL;DR: In a captive male the onset of drumming was accompanied by a rise in urinary testosterone concentrations and the enlargement of testes and accessory reproductive glands, and the male appeared to drum with a different frequency to the female.
Abstract: Georychus capensis is a seasonal breeder with the reproductive potential of producing two litters during the summer breeding season (August to December). These solitary mole-rats signal to each other through the soil, by drumming with their hind feet. This drumming is probably important in spacing the burrow systems and in triggering the onset of reproductive behaviour. In a captive male the onset of drumming was accompanied by a rise in urinary testosterone concentrations and the enlargement of testes and accessory reproductive glands. The male appeared to drum with a different frequency to the female. Courtship is initiated by the male and copulation involves brief multiple intromissions. The gestation period is about 44 days and the mean litter size is 5.9 with a maximum of 10 pups. Development of the pups is relatively rapid. Inter-sibling aggression begins to develop at 35 days, eventually resulting in the pups dispersing when about 60 days old. Body mass increases exponentially from birth to day 60 and the asymptote is reached around day 260. These features are compared with those of other solitary subterranean rodents and with those of the social Bathyergidae (Cryptomys hottentotus, Cryptomys damarensis and Heterocephalus glaber).
TL;DR: Non-reproductive females in families of eusocial common mole-rats (Cryptomys sp., Rodentia) are not suppressed by their mother, (either behaviourally or pheromonally) as is generally assumed.
Abstract: Non-reproductive females in families of eusocial common mole-rats (Cryptomys sp., Rodentia) are not suppressed by their mother, (either behaviourally or pheromonally) as is generally assumed. They do not mate with their father and brothers simply because they are not sexually attractive for them (and vice versa). The incest avoidance is based on the capability to recognize (and keep in memory for up to three weeks) each family member individually. A ‘sterile’ daughter may conceive and deliver young in her parental family if given the opportunity to mate with an unfamiliar mate in a separate cage. In this way, two females may breed side by side in one family.