Wr. Tschinkel, SOCIOMETRY AND SOCIOGENESIS OF COLONIES OF THE FIRE ANT SOLENOPSIS-INVICTA DURING ONE ANNUAL CYCLE, Ecological monographs, 63(4), 1993, pp. 425-457
In social insects, colonies as well as individuals have evolving life
histories. Identification of the life history tactics of a social inse
ct requires data on colony attributes and their development. To this e
nd a full range of fire ant (Solenopsis invicta) colony sizes was samp
led and censused on seven dates throughout 1 yr. Data included: mound
volume; the number, dry masses, and fat contents of sexual and worker
adults and immatures; stratified nest temperatures; worker distributio
n within the nest throughout the year; duration of the pupal stages; a
nd respiration rates. Analysis showed: 1. Colonies reached their annua
l maximum population size in midwinter and their maximum biomass in sp
ring. During the spring sexual production period they declined to a mi
dsummer minimum. Calculations showed that the magnitude of this declin
e increased with colony size. During January to July, worker mortality
exceeded natality, causing colony decline, while from July to Decembe
r, natality predominated, causing growth. 2. Mound volume was closely
related to the total mass of ants in the colony, and varied with seaso
n paralleling the mass of ants. 3. The mean size and variability of wo
rkers, and the percent major workers, increased with colony size and c
hanged over the year. 4. The fat content (percent fat) of workers incr
eased with worker size and colony size. Worker percent fat was lowest
in summer after sexual production, climbed immediately to the annual m
aximum and then declined gradually through winter and spring. 5. Altho
ugh sexual male and female pupae were close in mean dry mass (2.55 mg
and 3. 1 0 mg, respectively), males gained only 6% during adult matura
tion while females gained 290%. Females gained fat more rapidly than l
ean tissue causing their percent fat to increase from 31% to 49%. Mean
mass of male and female sexual adults did not change with colony size
. 6. The cost of worker maintenance declined from nearly 100% of total
colony cost in winter to 46% in late spring when brood production pea
ked. 7. Production rates peaked in spring, with colonies investing 50%
of their daily production in sexuals. This peak production was not su
stained through the summer, and was probably fueled by stored worker f
at. Worker production dominated in the latter part of the summer. All
measures of production rate as well as total annual production increas
ed with colony size, but most did so less rapidly than colony size, re
sulting in a declining efficiency of production and a declining natali
ty rate. 8. The percent of annual production invested in sexuals incre
ased sharply in colonies of between 20 000 and 50 000 workers, then re
mained at almost-equal-to 33% for the remainder of colony growth, show
ing that the transition from the ergonomic to the reproductive stages
is sharp, and that colonies must grow in order to produce more sexuals
. 9. Many quantitative colony attributes were related to one another b
y differential growth, and can thus be seen as isometric or allometric
measures. Rules of relative growth may thus constrain the possible co
mbinations of attributes and their evolution. The methods of morphomet
ric size and shape analysis are discussed as tools for understanding s
uites of colony attributes, and comparing them among species. 10. The
sociometric/sociogenic method is discussed as a way to compile, analyz
e and compare data on social insect colony attributes and their growth
and development.