<< Chapter < Page Chapter >> Page >

Similarly, Damaraland mole-rats have a dispersive morph made up of bigger mole-rats who do less work (Hazell et al. 2000, Scantlebury et al. 2006). Scantlebury et al. (2006) found that these mole-rats work little until after rains, when they substantially increase their work in comparison to normal workers. The disperser mole-rats are also significantly bigger than the queen, who is significantly larger than the workers (Scantlebury et al. 2006). The disperser morph in both species has an advantage that allows it to attempt the second strategy, dispersing and gaining direct reproduction. Its larger fat stores allow it to travel longer distances without starving and provide a good reserve of energy when beginning reproduction (Scantlebury et al. 2006). Overall, the disperser morph, while costly to its natal colony in terms of energy consumed and not used (O’Riain et al. 1996, Scantlebury et al. 2006), benefits itself through the potential for direct reproduction and provides gene flow for these highly unusual and fascinating mammalian species (Faulkes et al. 1997a).

Conclusion

The evolution of eusociality in mole-rats can be explained primarily by the Aridity Food Distribution Hypothesis which uses the environmental factors of aridity and unequal food distribution to explain why certain species of mole rats evolved to be eusocial. This also accounts for the separate evolution of eusociality in two different species. As a eusocial species, the mole-rat has tiers of breeders, workers, and dispersers. The situations in which mole-rats will and will not breed is not entirely understood, but appears to be more socially or hormonally driven, as even mole-rats who are not mole-rats do preserve their ability to reproduce, even if they do not use it. The dispersal tier of the mole-rat eusocial hierarchy is essential to allowing for enough outbreeding to sustain healthy offspring, and allows large, successful colonies to spread their genes even further. The entire hierarchy of eusociality in mole-rats is certainly intricately evolved, from intrinsic differences to social cues that allow the mole-rat to survive in harsh conditions.

Discussion questions

  1. In mole-rats, non-breeders do not lose reproductive capabilities. If non-breeder tiers of the mole rat did engage in reproductive behavior, how might this interfere with the eusocial structure of the colony? Would this behavior increase that individual’s fitness, why or why not?
  2. Eusociality appears to have evolved twice separately in the mole-rat. What conditions would likely allow for eusocial evolution in other mole-rat species, or even in other organisms that are typically solitary?

Glossary

  • Arid climate - characterized by severe lack of available water
  • Basal clade - the first to diverge from the lineage in a cladogram
  • Dimorphism - two distinct body forms of an individual within a species
  • Eusocial - applies to a society with reproductive division of labor, overlapping generations, and cooperative care of young
  • Fractal dimension - the extent that the burrow fills the area it inhabits
  • Fitness - ability of an individual to stay alive and pass on genes
  • Inbreeding - breeding with relatives, leads to less genetic variation
  • Inbreeding depression - a decrease in offspring size, fertility, and fitness due to inbreeding as recessive deleterious traits are more likely to manifest themselves in homozygous individuals
  • Inclusive fitness - the combination of direct fitness and indirect fitness gained
  • Indirect fitness - the fitness gained by helping a relative and impacted by the degree of relatedness
  • Kin Selection - altruistic acts directed towards kin that lead to greater overall inclusive fitness because of an increase in indirect fitness
  • Mesic - having a moderate supply of moisture.
  • Shoving - nose-to-nose pushing for protracted periods of time
  • Outbreeding - reproduction between two different populations , leading to more genetic variation
  • Reproductive skew - distribution of breeding between members of a population where some members hold more breeding rights than others

References

  • Alexander RD, Noonan KM, Crespi BJ. 1991. The evolution of eusociality. In: Sherman PW, Jarvis JUM, Alexander RD. The Biology of the Naked Mole Rat. Princeton (NJ): Princeton University Press. p. 3-44.
  • Allard MW, Honeycutt RL. 1992. Nucleotide sequence variation in the mitochondrial 12S rRNA gene and the phylogeny of African mole-rats (Rodentia: Bathyergidae). Mol Biol Evol. 9:27–40.
  • Braude S. 2000. Dispersal and new colony formation in wild naked mole-rats: evidence against inbreeding as the system of mating. Behav Ecol. 11:7–12.
  • Burda H. 1995. Individual recognition and incest avoidance in eusocial common mole-rats rather than reproductive suppression by parents. Experientia. 51:411–413.
  • Burland TM, Bennett NC, Jarvis JUM, Faulkes CG. 2002. Eusociality in African mole-rats: new insights from patterns of genetic relatedness in the Damaraland mole-rat (Cryptomys damarensis). Proc R Soc Lond B. 269:1025-1030.
  • Burland TM, Bennett NC, Jarvis JUM, Faulkes CG. 2004. Colony structure and parentage in wild colonies of cooperatively breeding Damaraland mole-rats suggest incest avoidance alone may not maintain reproductive skew. Mol Ecol. 13:2371-2379.
  • Ciszek D. 2000. New colony formation in the “highly inbred” eusocial mole-rat: outbreeding is preferred. Behavioral Ecology. 11:1-6.
  • Clarke FM, Faulkes CG. 1999. Kin discrimination and female mate choice in the naked mole-rat Heterocephalus glaber. Proc R Soc Lond B. 266:1995-2002.
  • Faulkes CG, Abbott DH. 1993. Evidence that primer pheromones do not cause social suppression of reproduction in male and female naked mole-rats (Heterocephalus glaber). J Reprod Fert. 99:225-230
  • Faulkes CG, Abbott DH, O’Brien HP, Lau L, Roy MR, Wayne RK, Bruford MW. 1997a. Micro- and macro-geographic genetic structure of colonies of naked mole-rats, Heterocephalus glaber. Mol Ecol. 6:615–628.
  • Faulkes CG, Bennett NC, Bruford MW, O’Brien HP, Aguilar GH, Jarvis JUM. 1997b. Ecological constraints drive social evolution in the African mole-rats. Proc R Soc Lond B. 264:1619–1627.
  • Faulkes CG, Verheyen E, Verheyen W, Jarvis JUM, Bennett NC. 2004. Phylogeographic patterns of speciation and genetic divergence in African mole-rats (Family Bathyergidae). Mol Ecol. 13:613–629.
  • Hazell RWA, Bennett NC, Jarvis JUM, Griffin M.  2000. Adult dispersal in the co-operatively breeding Damaraland mole-rat (Cryptomys damarensis): a case study from the Waterberg region of Namibia. J Zool Lond. 252:19-25
  • Hughes WOH, Oldroyd BP, Beekman M, Ratnieks FLW. 2008. Ancestral Monogamy Shows Kin Selection Is Key to the Evolution of Eusociality. Science. 320:1213-1216.
  • Jacobs DS, Jarvis JUM. 1996. No evidence for the work conflict hypothesis in the eusocial naked mole-rat (Heterocephalus glaber). Behav Ecol. 39:401–409.
  • Jarvis JUM, Bennett NC, Spinks AC. 1998. Food availability and foraging by wild colonies of Damaraland mole-rats (Cryptomys damarensis): implications for sociality. Oecologia. 113:290–298.
  • Jarvis JUM, Bennett NC. 1993. Eusociality has evolved independently in two genera of bathyergid mole-rats – but occurs in no other subterranean mammal. Behav Ecol Sociobiol. 33:253–260.
  • Jarvis JUM, O’Riain MJ, Bennett NC, Sherman PW. 1994. Mammalian eusociality: a family affair. Trends Ecol. Evol. 9:47-51.
  • Le Comber SC, Spinks AC, Bennett NC, Jarvis JUM, Faulkes CG. 2002. Fractal dimension of African mole-rat burrows.  Canadian Journal of Zoology. 80(3):436-441.
  • Lovegrove BG, Wissel C. 1988. Sociality in mole-rats: metabolic scaling and the role of risk sensitivity. Oecologia. 74:600–606.
  • Lovegrove BG. 1991. The evolution of eusociality in mole-rats, Bathyergidae: a question of risks, numbers, and costs. Behav Ecol Sociobiol. 28:37–45.
  • O’Riain MJ, Jarvis JUM, Buffenstein R, Alexander R, Peeters C. 2000. Morphological castes in a vertebrate. Proc Natl Acad Sci USA. 97:13194–13197.
  • O’Riain MJ, Jarvis JUM, Faulkes CG. 1996. A dispersive morph in the naked mole-rat. Nature. 380:619–621.
  • O’Riain MJ, Jarvis JUM. 1997. Colony member recognition and xenophobia in the naked mole-rat (Heterocephalus glaber). Anim Behav. 53:487–498.
  • Queller DC, Strassmann JE. 1998. Kin Selection and Social Insects. BioScience. 48:165-175.
  • Reeve HK, Westneat DF, Noon WA, Sherman PW, Aquadro CF. 1990. DNA ‘fingerprinting’ reveals high levels of inbreeding in colonies of the eusocial naked mole-rat. Proc Natl Acad Sci USA. 87:2496–2500.
  • Rickard CA, Bennett NC. 1997. Recrudescence of sexual activity in a reproductively quiescent colony of the Damaraland mole-rat, by the introduction of a genetically unrelated male — A case of incest avoidance in ‘queenless’ colonies. J Zool London. 241:185–202.
  • Scantlebury M, Speakman JR, Oosthuizen MK, Roper TJ, Bennett NC. 2006. Energetics reveals physiologically distinct castes in a eusocial mammal. Nature. 440:795-797.
  • Sichilima AM, Bennett NC, Faulkes CG, Le Comber SC. 2008. Evolution of African mole-rat sociality: burrow architecture, rainfall and foraging in colonies of the cooperatively breeding Fukomys mechowii. J Zool Lond. 275:276-282.
  • Spinks AC, Jarvis JUM, Bennett NC. 2000. Comparative patterns of philopatry and dispersal in two common mole-rat populations: implications for the evolution of mole-rat sociality. Journal of Animal Ecology. 69:224-234.
  • Walton AH, Nedbal MA, Honeycutt RL. 2000. Evidence from Intron 1 of the nuclear tranthyretin (Prealbumin) gene for the phylogeny of African mole-rats (Bathyergidae). Mol Phylo Evol. 16(3):467–474.

About the author

A portrait of the author.

Sheena Shah-Simpson is an undergraduate from Arlington, Texas, majoring in Biochemistry and Cell Biology. In her free time she likes to play, or attempt to play, musical instruments, read, hang out with her friends, listen to good music, and dance. While studying animal behavior she learned fascinating things about conflicts of interest, between species, within species, within individual families (parent-offspring conflict is particularly interesting), etcetera. Writing this chapter, Sheena also learned many extraordinary things about such varied topics as incest and different morphologies within just one family of animals, the ever-fascinating mole-rats.

Questions & Answers

Discuss the differences between taste and flavor, including how other sensory inputs contribute to our  perception of flavor.
John Reply
taste refers to your understanding of the flavor . while flavor one The other hand is refers to sort of just a blend things.
Faith
While taste primarily relies on our taste buds, flavor involves a complex interplay between taste and aroma
Kamara
which drugs can we use for ulcers
Ummi Reply
omeprazole
Kamara
what
Renee
what is this
Renee
is a drug
Kamara
of anti-ulcer
Kamara
Omeprazole Cimetidine / Tagament For the complicated once ulcer - kit
Patrick
what is the function of lymphatic system
Nency Reply
Not really sure
Eli
to drain extracellular fluid all over the body.
asegid
The lymphatic system plays several crucial roles in the human body, functioning as a key component of the immune system and contributing to the maintenance of fluid balance. Its main functions include: 1. Immune Response: The lymphatic system produces and transports lymphocytes, which are a type of
asegid
to transport fluids fats proteins and lymphocytes to the blood stream as lymph
Adama
what is anatomy
Oyindarmola Reply
Anatomy is the identification and description of the structures of living things
Kamara
what's the difference between anatomy and physiology
Oyerinde Reply
Anatomy is the study of the structure of the body, while physiology is the study of the function of the body. Anatomy looks at the body's organs and systems, while physiology looks at how those organs and systems work together to keep the body functioning.
AI-Robot
what is enzymes all about?
Mohammed Reply
Enzymes are proteins that help speed up chemical reactions in our bodies. Enzymes are essential for digestion, liver function and much more. Too much or too little of a certain enzyme can cause health problems
Kamara
yes
Prince
how does the stomach protect itself from the damaging effects of HCl
Wulku Reply
little girl okay how does the stomach protect itself from the damaging effect of HCL
Wulku
it is because of the enzyme that the stomach produce that help the stomach from the damaging effect of HCL
Kamara
function of digestive system
Ali Reply
function of digestive
Ali
the diagram of the lungs
Adaeze Reply
what is the normal body temperature
Diya Reply
37 degrees selcius
Xolo
37°c
Stephanie
please why 37 degree selcius normal temperature
Mark
36.5
Simon
37°c
Iyogho
the normal temperature is 37°c or 98.6 °Fahrenheit is important for maintaining the homeostasis in the body the body regular this temperature through the process called thermoregulation which involves brain skin muscle and other organ working together to maintain stable internal temperature
Stephanie
37A c
Wulku
what is anaemia
Diya Reply
anaemia is the decrease in RBC count hemoglobin count and PVC count
Eniola
what is the pH of the vagina
Diya Reply
how does Lysin attack pathogens
Diya
acid
Mary
I information on anatomy position and digestive system and there enzyme
Elisha Reply
anatomy of the female external genitalia
Muhammad Reply
Organ Systems Of The Human Body (Continued) Organ Systems Of The Human Body (Continued)
Theophilus Reply
what's lochia albra
Kizito
Got questions? Join the online conversation and get instant answers!
Jobilize.com Reply

Get Jobilize Job Search Mobile App in your pocket Now!

Get it on Google Play Download on the App Store Now




Source:  OpenStax, Mockingbird tales: readings in animal behavior. OpenStax CNX. Jan 12, 2011 Download for free at http://cnx.org/content/col11211/1.5
Google Play and the Google Play logo are trademarks of Google Inc.

Notification Switch

Would you like to follow the 'Mockingbird tales: readings in animal behavior' conversation and receive update notifications?

Ask