Steven W. Rissing, Robert A. Johnson, and John W. Martin.
Colony founding behavior of some desert ants: geographic variation in metrosis.
Psyche 103(1-2):95-101, 2000.

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COLONY FOUNDING BEHAVIOR OF SOME DESERT ANTS: GEOGRAPHIC VARIATION IN METROSIS
BY STEVEN W. RISSING~, ROBERT A. JOHN SON^, AND JOHN W. MARTIN^
Social Insect Research Group, Department of Biology, Arizona State University, Tempe, AZ 85287- 1501 ;
Current Address: Department of Evolution, Ecology and Organismal Biology, The Ohio State University, Columbus, OH 43210. Social Insect Research Group, Department of Biology, Arizona State University, Tempe, AZ 85287-1501.
P.O. Box 458, Dolan Springs, AZ 86441.
The ants Pogonornyrrnex californicus and Pheidole tucsonica display cooperative colony foundation with co-foundresses form- ing associations without respect to relatedness. Geographic varia- tion in method of colony foundation [cooperative (pleometrosis) versus non-cooperative (haplometrosis)] occurs in P. californicus, Acromyrmex versicolor, Myrmecocystus rnirnicus and Messor per- gandei. Such variation in colony founding behavior strongly sug- gests that comparative studies of the adaptive value of cooperative colony founding will be extremely rewarding. W. M. Wheeler (1910) believed firmly that, in the vast majority of ant species, new colonies are founded by solitary queens (hap- lometrosis) and retain a single queen throughout the colony life- time (monogyny). This conception was assumed to be generally true until publication of a seminal paper by Holldobler and Wilson (1977). These authors drew attention to the frequent occurrence of multiple fertile queens in mature colonies (polygyny) and identi- fied several species in which multiple founding queens cooperate to start new colonies (pleometrosis). While the number of ant Manuscript received 18 July 1996.
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species displaying cooperative colony foundation has grown steadily (Rissing and Pollock 1988), the discovery and documenta- tion of intraspecific geographical variation in pleometrosis is new and little explored (see Ryti 1988). In this paper we summarize recent observations on geographic variation in colony founding behavior for several species common in the deserts of the south- western United States.
Occurrence of haplometrosis and pleometrosis in the field Nests of newly mated foundresses were excavated and censused in the field following mating flights, which are triggered by sum- merlfall rains for species discussed here except for Messor pergan- dei and Pogonomyrmex californicus which have asynchronous flights apparently triggered by photoperiod. In the field, starting colonies are identifiable by the characteristic coarse grain of soil excavated by foundresses.
Relatedness as a criterion for association formation Queens were brought into the laboratory to determine whether foundress associations formed with respect to kinship, using the assay developed by Rissing and Pollock (1986). Associations (hap- lometrotic and pleometrotic) from a given locale were collected, the queens marked uniquely with paint and then permitted to form new associations in a plastic shoe box half-filled with moistened soil fol- lowed by excavation and identification of all queens in all associa- tions 24 hours later. Similar manipulations revealed a major role for kinship in the formation of foundress associations in the wasp Polistes fuscatus (Noonan 1981) but not the ants M. pergandei (Rissing and Pollock 1986) and Acromyrmex versicolor (Rissing et al. 1986). The lack of close relatedness within foundress associa- tions of these ants was later verified by allozyme electrophoresis (Hagen et al. 1988).
Geographic variation in colony founding behavior The above assay demonstrated that M. pergandei queens col- lected after mating flights from locales that had pleometrotic and haplometrotic foundresses would start colonies pleometrotically when given the chance, even if they were originally collected as a



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haplometrotic foundress (Rissing and Pollock 1986). In fact, they prefer to join associations (Krebs and Rissing 1991). Ryti (1988), however, demonstrated that foundresses collected from a com- pletely haplometrotic population at Deep Canyon, CA, would not form pleometrotic associations when given the chance and would often fight. We used Ryti's (1988) assay on foundresses collected from newly discovered all-haplometrotic populations of species previously known to display pleometrosis in other locales [Myrmecocystus mimicus (Bartz and Holldobler 1982), A. versi- color (Rissing et al. 1986) and P. californicus (see Table 1 for pleometrosis)] .
Haplometrosis and pleometrosis in the field Our field surveys have revealed the first known populations of Pogonomyrmex californicus and Pheidole tucsonica where pleometrosis occurs regularly (Table 1). We have also found popu- lations of Myrmecocystus mimicus and Acromyrmex versicolor, species previously shown to be pleometrotic, where haplometrosis predominates, often exclusively (Table 1). In addition to the species in Table 1, RAJ has documented solitary colony foundation (haplometrosis) in Pogonomyrmex apache Wheeler (N = 22, Cochise Co., AZ), Pogonomyrmex salinus Olsen [N = 60 (Note: 3 additional colonies contained 2 foundresses), Clark Co., NV], Dorymyrmex insanus (Buckley) (N = 35, Pinal Co., AZ), and Myrmecocystus flaviceps Wheeler (N = 25, Pinal Co., AZ). Foundress assortment
Pogonomyrmex californicus, Pheidole tucsonica, Myrmecocys- tus mimicus, and Acromyrmex versicolor all displayed the same patterns in our laboratory tests. Field-caught foundress associa- tions do not retain their original composition when permitted to reform in the presence of other queens from the same population in the laboratory. New, usually larger associations develop in which queens from field-caught foundress associations mix freely. Like- wise, haplometrotic (i.e. solitary) foundresses taken from popula- tions in which pleometrosis occurs readily join pleometrotic groups in the laboratory without conflict. This does not occur in the populations where haplometrosis is the rule: queens fight rather than join groups.



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We add two new species (Pogonomyrmex californicus and Phei- dole tucsonica) to the growing list of ants in which cooperative colony founding is known (see Rissing and Pollock 1988: Table 7.1). Further, while Wheeler (19 10: 190) thought that such behavior occurred only "under very exceptional circumstances [when] a couple of females from the same maternal nest may meet after their marriage flight and together start a colony," we have also shown that relatedness appears unimportant in a foundress' deci- sion to join an association in these same species as well as the others listed in Table 1 (see references cited there). Hymenoptera that display kin-specific foundress associations (e.g. the wasp Polistes fuscatus) normally form associations over several weeks (Noonan 1981). With most ant species, however, including all those displaying cooperative colony founding in Table 1, associations are formed and nest excavation usually begins immediately. This is especially true of ants (e.g. Myrmeco- cystus mimicus, Acromyrmex versicolor, and Pheidole tucsonica) attempting to establish colonies after summer rains in desert envi- ronments as death from heat and desiccation will ensue immedi- ately unless shelter, generally in the form of a newly started nest, is found. Predation threats are similar to desiccation in the desert where even normally granivorous organisms (birds, ants) readily consume reproductive females. In short, under such foreboding abiotic and biotic conditions, a female attempting to form a foundress association simply cannot afford the luxury of limiting the range of potential co-foundresses to only close relatives. Our data also suggest that not all haplometrotic foundresses are the same: those collected from locales that also have pleometrotic associations of the same species will readily form pleometrotic associations in the laboratory while those collected from locales that have no pleometrotic associations will not, and, in fact, will fight.
Hypotheses to explain possible advantages of cooperative colony founding in ants range from crowding due to lack of avail- able nest sites (Tschinkel and Howard 1983), intra-specific brood- raiding and territoriality following clumping of available nest sites by abiotic conditions (Rissing and Pollock 1987), and a need to



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avoid desiccationlpredation (Pfennig 1995). Degree of geo-graphi- cal variation in cooperative colony founding species (Table 1) and the associated variation in mutual tolerance of foundresses in these same species may permit an evaluation of these and related hypotheses.
Supported by NSF grant DEB-89-06319 to SWR. Members of the Social Insect Research Group (SIRG) at Arizona State Univer- sity assisted in field work; J. Weser provided the Maricopa Co., AZ, Pogonomyrmex californicus data; S. Cover and R. Snelling identified Pheidole tucsonica and Myrmecocystus mimicus; S. Cover, S. Cahan and G. Pollock provided helpful comments on the manuscript.
Bartz, S. H. and B. Holldobler. 1982. Colony founding in Myrmecocystus mimicus Wheeler (Hymenoptera: Formicidae) and the evolution of foundress associa- tions. Behav. Ecol. Sociobiol. lO(2): 137-147. Hagen, R. H., D. R. Smith, and S. W. Rissing. 1988. Genetic relatedness among co- foundresses of two desert ants, Veromessor pergandei and Acromyrmex versi- color. Psyche 95(3-4): 191201.
Holldobler, B. and E. 0. Wilson. 1977. The number of queens: an important trait in ant evolution. Naturwissenschaften 64(1): 8-15. Krebs, R. A. and S. W. Rissing. 1991. Preference for larger foundress associations in the desert ant Messorpergandei. Anim. Behav. 41(2): 361-363. Noonan, K. M. 1981. Individual strategies of inclusive-fitness-maximizing in Polistes fuscatus foundresses. In R. D. Alexander and D. W. Tinkle, eds., Nat- ural Selection and Social Behavior, pp. 18-44. New York: Chiron. Pfennig, D. W. 1995. Absence of joint nesting advantage in desert seed harvester ants: evidence from a field experiment. Anim. Behav. 49(3): 567-575. Pollock, G. B. and S. W. Rissing. 1985. Mating season and colony foundation of the seed- harvester ant, Veromessor pergandei. Psyche 92(1): 125-134. Rissing, S. W. and G. B. Pollock. 1986. Social interaction among pleometrotic queens of Veromessor pergandei during colony foundation. Anim. Behav. 34(1): 226-233.
Rissing, S. W. and G. B. Pollock. 1987. Queen aggression, pleometrotic advantage and brood raiding in the ant Veromessor pergandei. Anim. Behav. 35(4): 975- 981.
Rissing, S. W. and G. B. Pollock. 1988. Pleometrosis and polygyny in ants. In R. L. Jeanne, ed., Interindividual Behavioral Variability in Social Insects, pp. 179- 222. Boulder, CO: Westview.




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Rissing, S. W., R. A. Johnson, and G. B. Pollock. 1986. Natal nest distribution and pleometrosis in the desert leaf-cutter ant Acromyrmex versicolor. Psyche 93(3- 4): 177-186.
Ryti, R. T. 1988. Geographic variation in cooperative colony foundation in Veromessorpergandei. Pan-Pac. Entomol. 64(2): 255-257. Tschinkel, W. R. and D. F. Howard. 1983. Colony foundation by pleometrosis in the fire ant, Solenopsis invicta. Behav. Ecol. Sociobiol. 12(2): 103-113. Wheeler, W. M. 1910. Ants. New York: Columbia University Press. 663 pp.



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