Skip to main content

Population and colony structure of an ant with territorial males, Cardiocondyla venustula



Many species of social insects have large-scale mating and dispersal flights and their populations are therefore often relatively homogenous. In contrast, dispersal on the wing appears to be uncommon in most species of the ant genus Cardiocondyla, because its males are wingless and the winged queens mate in their natal nests before dispersing on foot. Here we examine the population structure of C. venustula from South Africa. This species is of particular interest for the analysis of life history evolution in Cardiocondyla, as it occupies a phylogenetic position between tropical species with multi-queen (polygynous) colonies and fighting males and a Palearctic clade with single-queen colonies and mutually peaceful males. Males of C. venustula exhibit an intermediate strategy between lethal fighting and complete tolerance – they mostly engage in non-lethal fights and defend small territories inside their natal nests. We investigated how this reproductive behavior influences colony and population structure by analyzing samples on two geographic scales in South Africa: a small 40 × 40m2 plot and a larger area with distances up to 5 km between sampling sites in Rietvlei Nature Reserve near Pretoria.


Colonies were found to be facultatively polygynous and queens appear to mate only with a single male. The extraordinarily high inbreeding coefficient suggests regular sib-mating. Budding by workers and young queens is the predominant mode of colony-founding and leads to high population viscosity. In addition, some queens appear to found colonies independently or through adoption into foreign nests.


While C. venustula resembles tropical Cardiocondyla in queen number and mating frequency, it differs by the absence of winged disperser males. Dispersal by solitary, mated queens on foot or by short flights and their adoption by alien colonies might promote gene flow between colonies and counteract prolonged inbreeding. The abundance of suitable habitat and the high density of nests facilitate the spread of this species by budding and together with the apparent resistance against inbreeding make it a highly successful pioneer species and invader of degraded and man-made habitats.


The population structure of social insects is strongly shaped by their specific life-histories, in particular their mating behavior, dispersal abilities, and mode of colony founding. Many ant species are characterized by large-scale mating and dispersal flights and lack strong spatial population structure (e.g., [1,2,3]). In others, young queens mate in or near their natal nests and establish new colonies close by. This leads to high differentiation among populations at least at the level of maternally inherited mtDNA (e.g., [4,5,6,7]). Gene flow and outbreeding in the latter case are typically promoted by the dispersal of winged males [8, 9].

Winged males have been replaced by wingless “ergatoid” males in most species of the ant genus Cardiocondyla [10,11,12,13]. Mating occurs inside the nest and mostly involves sibs, and the frequent occurrence of solitarily walking winged and dealate queens (which have lost their wings after mating) [13] suggests limited dispersal capability and a highly viscous population structure. This stands in striking contrast to reports that Cardiocondyla are often among the first ants colonizing disturbed or rehabilitated habitats and that several species are highly successful “tramp species” with an almost worldwide distribution [14,15,16,17]. While the reproductive behavior of Cardiocondyla has been studied in detail in a number of species (e.g., [18,19,20,21], little is known about the genetic structure of populations and how far queens disperse.

The African species Cardiocondyla venustula is of particular interest in this context because of its placement in the phylogeny of the genus: it is positioned between tropical taxa, where colonies typically contain multiple, singly-mated queens and wingless males engage in fatal fighting over access to freshly emerging virgin queens, and a Palearctic clade where colonies have a single, multiply-mated queen per colony and mutually tolerant males [12, 13]. Analyzing the social and genetic structure of C. venustula colonies and populations therefore is of considerable importance for unravelling the evolution of different life histories in this genus.

Behavioral studies revealed that males of C. venustula are always ergatoid and show an “intermediate” behavior between fatal fighting and complete tolerance: they defend small areas in the nest against nestmate males, engaging in regular, but typically non-lethal fighting with nestmate males [22, 23]. Female sexuals (young, winged queens) were observed interacting with several males, but it remained unclear if they mated multiply. However, from male territoriality we hypothesized that queen mating frequencies would be low as in species with lethally fighting males.

Field studies gave conflicting results concerning queen number: while Wheeler [24] reported on regular single-queening in an introduced population in Puerto Rico, our own observations revealed the regular presence of multiple queens per colony both in introduced and native populations [23, 25]. The finding of dense populations of C. venustula near Pretoria and Bergville, South Africa, allowed us to conduct detailed analyses of the genetic structure of colonies and populations and how they are influenced by male territoriality and female dispersal on foot.


Sampling and field observations

Samples for DNA analysis were collected in Rietvlei Nature Reserve, Pretoria, Gauteng, South Africa, and Hlalanathi Drakensberg Resort, Bergville, KwaZulu-Natal, South Africa, in February and March 2013. Workers were easily spotted when foraging on bare or sparsely vegetated ground, e.g., on unpaved parking lots. They were followed back to their nests, which consisted of two or three pea-sized holes in the ground down to a depth of 20 cm [25]. Subsequently, these nests were carefully excavated and the ants were either directly transferred into a tube with 100% ethanol or transferred to the laboratory alive for behavioral experiments. Of the latter colonies, a few individuals were also stored in 100% ethanol immediately after collection.

To analyze genetic population structure, relatedness and dispersal on a small scale, we measured the distances between all 57 colonies found in February 2013 in an area of 40 × 40 m2 at the main gate of Rietvlei Nature Reserve (Riet: S 25.88250, E 28.26417, 1515 m). A few colonies from sampling areas in and near Rietvlei Nature Reserve, 0.5 to 5.5 km away from the plot at the entrance building, were used to estimate gene flow and population structure on a larger scale (C: Rietvlei Coffee Shop, n = 13, S 25.87722, E 28.30083, 1511 m; CC: Coots Corner Bird Hide parking lot, n = 4, S 25.88139, E 28.26861, 1477 m; IV: Island View Bird Hide parking lot, n = 8, S 25.87639, E 28.28056, 1481 m; MD: Marais Dam parking lot, n = 8, S 25.90528, E 28.30833, 1511 m; PH: Pheasant Hill B&B, n = 2, S 25.88722, E 28.25778, 1508 m). Additionally, colonies from Hlalanathi Drakensberg Resort were used for estimation of relatedness and inbreeding (n = 82, S 28.65903, E 29.03136, 1288 m).

DNA extraction, microsatellite genotyping, and mt DNA sequencing

Before DNA extraction, samples were frozen in liquid nitrogen and crushed with a pestle in order to destroy the hard cuticle. Thereafter, DNA was extracted from older or damaged whole ants or pupae using a CTAB protocol [26] and from fresh and intact specimens using the Macherey Nagel XS Tissue Kit following the protocol for tissue samples.

Seven microsatellite markers developed for Cardiocondyla were found to be sufficiently polymorphic for population genetic analysis in C. venustula (CE2-3A, CE2-4E, CE2-5D, CE2-12D [27]; Card 8 [28]; Cobs 3 and Cobs 13 [29], see Table 1 for details). PCRs were conducted with a total volume of 15 μl using 7.5 μl GoTaq PCR mix (Promega, Madison, WI), 5 μl water, 0.5 pm/μl of each primer, and 1 μl of the DNA solution. Forward primers were end-labelled with fluorescent dye (FAM, Eurofin Genomics, Ebersberg). PCRs were run using an initial denaturation step at 94 °C for 4 min followed by 36 cycles with 70 s at 94 °C for denaturation, 45 s at the specific annealing temperature, and 25 s at 72 °C for elongation, and a final elongation step at 72 °C for 3 min. Fragment lengths were determined on an ABI PRISM using a TAMRA labelled size standard. Alleles were scored using Genescan 3.1 software (PR Biosystems).

Table 1 Number of alleles NA, allele sizes, expected (Hexp) and observed heterozygosity (Hobs), and inbreeding coefficient for microsatellite markers in the ant Cardiocondyla venustula from two populations in South Africa

We analyzed a 795 bp-fragment of the COI/COII gene. Amplification of mtDNA was conducted in a total volume of 25 μl using 12.5 μl GoTaq PCR mix, 8.5 μl water, 0.5 pm/μl of each primer, and 1.5 μl of the DNA solution. Due to amplification problems with standard primers, we designed new primers using conserved regions in the previously obtained COI/COII-sequences: COICv-f (5′-ATTATCGCCGTCCCTACAGG-3′) and COICv-r (5′-TCGGATGGGGAAGTTATAAGGT-3′). PCRs were run using an initial denaturation step at 94 °C for 4 min followed by 39 cycles with 75 s at 94 °C for denaturation, 45 s at the specific annealing temperature, and 90 s at 72 °C for elongation, and a final elongation step at 72 °C for 7 min. PCR products were purified using the Macherey-Nagel Gel and PCR clean-up kit following the manufacturer’s instructions and sent to LGC Genomics, Berlin, for sequencing. The trace files of obtained sequences were checked by eye for sequence quality.

Analysis of mating frequency

Field observations and dissections suggested that colonies of C. venustula might contain multiple, fertile queens. Polygyny was additionally corroborated by the analysis of workers by microsatellite genotyping. In addition, we investigated by COI sequencing whether colonies may contain individuals belonging to several unrelated lineages.

Queens and their worker offspring from natural colonies were genotyped to determine queen mating frequencies. However, these genotypes did not always allow determining whether workers were offspring of one queen, which had mated with several related males, or offspring of multiple related queens sharing the same mitochondrial haplotype, of which several might have been missed during or had died before collection. We therefore investigated whether female sexuals mate with multiple males in the laboratory. We set up experimental colonies, each consisting of ten workers, brood, and a queen pupa, in small nests (diameter appr. 1.5 cm) and later added one male each from two unrelated colonies with different genotypes, using colonies from both the populations at Rietvlei and at Hlalanathi, KwaZulu-Natal. To avoid males killing each other we first kept male pupae separately in nests with some brood and workers from their natal colony. After they had eclosed and hardened their cuticula, they were transferred into the experimental colonies with the young queen pupae. Experimental colonies, in which one of the males had died prematurely, were excluded from the analysis. Thus, each female sexual was provided with simultaneous access to two males until it was mated. Mating events are inconspicuous and difficult to observe [23]. We therefore waited for several days until all queens had shed their wings – which they usually do only after mating - and then stored them in 100% before genotype analysis of stored sperm following Lenoir et al. [30].

As the small amount of sperm DNA might not always give a reliable estimate of mating frequencies (because of large allele dropout or non-detection of alleles due to varying amounts of sperm from individual males), we also determined mating frequency from offspring genotypes. To do so we transferred ten additional, dealate queens into small colonies containing 20 workers and large larvae or worker pupae. From six of these queens we managed to collect and genotype five to eight 2nd instar or larger larvae. Thereafter, the queens were killed and genotyped.

Population genetic analyses

We used the software STRUCTURE [31] to find potential population structure on two scales, the 40 × 40m2 plot and the whole Rietvlei Reservation Area. The results were analyzed with STRUCTURE harvester [32] in order to find the optimal number of clusters (K). In addition, we assessed K with the function find.clusters implemented in the package “adegenet” [33] in R [34]. Population genetic parameters, intra- and intercolonial relatedness were calculated in SpaGeDi 1.5a [35]. Isolation by distance was tested via Mantel test comparing genetic and geographic distance matrices with the software Arlequin 3.1 [36] with 10,000 permutations. As a measure for genetic distance in the 40 × 40m2 plot codominant pairwise distances were calculated in GenAlEx 6.5 [37], for the inter-population test, Slatkin’s linearized FST [38] was calculated as implemented in Arlequin. F-statistics were calculated using GDA 1.1 with bootstrapping over loci to obtain confidence intervals [39]. Significance of pairwise differentiation between sampling sites was calculated by permutation in Arlequin [36]. Microsatellites were tested for the existence and frequencies of null-alleles using INEST 2.2 [40].


Field observations

Solitary queens, both winged and dealate, were regularly seen walking on the ground; one winged queen was observed flying for approximately 20 cm from the top of a blade of grass. These observations and dissections of winged, dispersing queens in the lab suggest short-range dispersal by queens both before and after mating (see also [25]).

Of the 92 colonies collected in Rietvlei Nature Reserve, 30 contained a single dealate queen, 17 contained multiple, up to seven dealate queens, and the rest were queenless. The latter were probably incompletely sampled and were directly transferred into EtOH for genetic analyses.

Population structure

We obtained microsatellite genotypes of one worker each for 92 colonies from Rietvlei Nature Reserve (57 colonies from main gate, 13 colonies from C, four colonies from CC, eight colonies from IV, eight colonies from MD, two colonies from PH). Estimation of null allele frequencies in INEST did not support the existence of null alleles in any of the markers.

Mean FST-values indicated considerable differentiation between collecting sites (mean FST = 0.308, 95% confidence interval 0.136–0.456; Table 2). FST-values were positive for all pairs of sites, and permutation tests revealed significant differences in 11 of 15 pairwise comparisons. STRUCTURE analysis proposed two clusters in the intensively sampled 40 × 40 m2 plot. While the “find.clusters” algorithm in DAPC did not provide clear clustering, manually setting the number of clusters to two revealed the same grouping as the one calculated by STRUCTURE. Plotting genetic clusters against sampling location in the 40 × 40 m2 plot showed that cluster 1 (blue squares in Fig. 1) appeared to be mostly concentrated in two distinct spots in the sampling area while cluster 2 (black circles in Fig. 1) was distributed relatively evenly over the whole sampling area.

Table 2 Pairwise FST-values and geographic distance between sampling sites of the ant Cardiocondyla venustula at Rietvlei Nature Reserve, South Africa.
Fig. 1
figure 1

Distribution of clusters (K = 2) found by STRUCTURE among nests of the ant Cardiocondyla venustula in the 40 × 40 m2 grid at the main gate of Rietvlei nature reserve, South Africa. Coordinate points (circles and triangles) represent one sampled colony each

Across all collecting sites in Rietvlei, STRUCTURE suggested six clusters. Similar to the analysis in the smaller plot, “find.clusters” in DAPC did not reveal clear clustering. However, when K was set to six, results were concordant with those from STRUCTURE. While FST-values suggested significant differentiation among sampling sites, individuals from different sampling sites clustered together in structure analysis (Fig. 2). A comparison of pairwise genetic and geographic distances suggested a weak trend of isolation by distance in the 40 × 40 m2 plot (p = 0.06, r2 = 0.01). When comparing pairwise FST-values and geographic distances within the whole sampling area, no such effect was visible (p = 0.40, r2 = 0.01).

Fig. 2
figure 2

Location of sample sites with distribution of clusters (K = 6) found by STRUCTURE among nests of the ant Cardiocondyla venustula at Rietvlei nature reserve, South Africa. Pie charts represent sample sites (not to scale) with the relative abundance of samples assigned to the respective cluster. Rietvlei nature reserve is depicted in light gray, water surfaces are depicted in darker grey. Sample site abbreviations: PH = Pheasant Hill B&B, CC = Coots Corner Bird Hide parking lot, IV = Island View Bird Hide parking lot, C = Rietvlei Coffee Shop, MD = Marais Dam parking lot

Due to amplification problems, mtDNA sequences were available only for a subset of 44 individuals from 35 colonies (21 from main gate, two from C, four from CC, four from IV, three from MD, one from PH). In the 40 × 40m2 plot we found six haplotypes, one of which, h2, exhibited a similar distribution to that observed in microsatellite cluster 1, occurring mainly in two spots in the sampling area. The other haplotypes were scattered (Fig. 3). Across all sampling sites, seven haplotypes were found (GenBank Accession numbers MK138574 – MK138580). Interestingly, we found only a single haplotype at several of the less intensively sampled sites (Fig. 4). Comparison of genetic clusters found by STRUCTURE analysis of the microsatellite genotypes with those found in mitochondrial haplotypes revealed an independent distribution of both marker types (Mantel test for correlation between FST-values: p = 0.42, r2 = 0.005).

Fig. 3
figure 3

Distribution of mtDNA-haplotypes of the ant Cardiocondyla venustula in the 40 x 40 m2 grid at main gate of Rietvlei nature reserve, South Africa. Coordinate points represent one sampled colony each, dots represent samples used in microsatellite, but not in mtDNA analysis

Fig. 4
figure 4

Haplotype network for the 795-bp fragment of the COI-gene of the ant Cardiocondyla venustula at Rietvlei nature reserve, South Africa. Pie charts represent one haplotype each, sample sites are represented by the respective color/signature. Sample site abbreviations: PH = Pheasant Hill B&B, CC = Coots Corner Bird Hide parking lot, IV = Island View Bird Hide parking lot, C = Rietvlei Coffee Shop, MD = Marais Dam parking lot

Isolation by distance was similarly low in mtDNA markers as in microsatellite markers. For the 40 × 40 m2 plot, isolation by distance was significant but weak (p = 0.05, r2 = 0.02). Between the sampling sites, no significant effect was found (p = 0.40, r2 = 0.005). Maternally inherited mtDNA and the bi-parentally inherited genomic microsatellites and their spatial distribution thus revealed only subtle differences, suggesting a female-biased dispersal and supporting the observations of dispersing queens in the field.

Relatedness and colony structure

For the analysis of relatedness and colony structure, we obtained microsatellite genotypes from 8 to 23 workers per colony, analyzing ten colonies from Rietvlei (117 genotypes in total) and twelve colonies from Hlalanathi (112 genotypes in total). FIS and background allele frequencies were calculated using one individual per colony for all sampled colonies in the respective populations (91 colonies from Rietvlei, 82 colonies from Hlalanathi). Microsatellite genotypes showed high levels of inbreeding in all sampled areas in Rietvlei (overall FIS = 0.608, 95% confidence interval 0.366–0.562) as well as in Hlalanathi (overall FIS = 0.551, 95% confidence interval 0.422–0.614), suggesting 86.1 and 83.1% sib-mating, respectively (following [41]). Though field observations revealed the frequent presence of multiple queens within a single colony (see above), relatedness was usually high (Rietvlei: mean 0.867 ± S.E. 0.079, ranging from 0.030 ± 0.291 to 1 ± 0; 5 colonies only from Rietvlei main gate: mean 0.767 ± S.E. 0.133, ranging from 0.567 ± 0.175 to 0.983 ± 0.018; Hlalanathi: mean 0.786 ± S.E. 0.096, ranging from 0.456 ± 0.185 to 1 ± 0). This matches the high inbreeding coefficient and the assumption that workers may occasionally be offspring of multiple, usually related queens, most of which have mated with the same or several closely related males. Correction for inbreeding [42] yielded a mean relatedness of 0.454 (Rietvlei) and 0.261 (Hlalanathi). The co-occurrence of two different mtDNA haplotypes in workers of a previously studied colony [25] indicates that colonies may contain multiple unrelated queens or occasionally adopt alien workers.

The non-detection error arising from the low variability of microsatellites typical for most Cardiocondyla, the high inbreeding coefficient, and the fluidity of colony structure all make it difficult to exactly determine the number of matrilines and patrilines. We therefore staged mating experiments in the lab to determine whether female sexuals (young, winged queens) mate with multiple or single males. In the spermathecae of queens that had been given the possibility to mate with two genetically different males, we did never find more than one paternal allele, i.e., there was no evidence of multiple inseminations. Similarly, the five to eight offspring larvae produced each by the six queens that had been exposed to two males were all offspring of only one father (total number 36 larvae).


The reproductive biology of ants of the genus Cardiocondyla with stationary wingless males, mating in the nest, and dispersal on foot by winged, mated and / or unmated queens is quite unusual for ants and social insects in general [13]. As we here show specifically for C. venustula from Rietvlei Nature Reserve in South Africa, this leads to high levels of inbreeding and nestmate relatedness.

Unfortunately, the low genetic diversity, already known from previous studies in other Cardiocondyla species (e.g. [29, 43, 44]) together with sib-mating and the short lifespan and rapid turnover of queens [45] makes it difficult to resolve colony and population structure to a high degree of accuracy. Nevertheless, our findings are in agreement with previous assumptions about the dispersal biology of this genus, with local mating, short-range dispersal by queens, colony budding, and occasional long-range dispersal by queens on the wing or mediated by human activities. Population viscosity was surprisingly small both at the level of nuclear microsatellites and mtDNA haplotypes, and no significant structure was seen when colonies from more distant collecting sites were included in the analysis.

A detailed survey in a 40 × 40 m2 plot with almost 60 colonies showed that colonies with similar microsatellite genotypes and mtDNA haplotypes may occasionally cluster. This matches our field observations: while wingless males are only very rarely observed outside the nest (e.g., [30, 46]), winged and wingless queens are regularly seen walking over distances of a few meters. Winged queens may even be drifted over longer distances by wind [13], explaining the relatively weak isolation by distance. The clumped distribution of cluster 1 and haplotype 2 in the 40 × 40 m2 plot suggest that new colonies may be founded by budding, i.e., young queens disperse together with several workers from their natal nest after mating. In the laboratory, new colonies are easily produced by splitting multi-queen colonies (e.g., [19]), supporting the hypothesis that budding is a regular mode of founding in this genus. Whether colonies of C. venustula may inhabit several neighboring nests (polydomy), as suggested for populations of this species introduced to Puerto Rico [24, 47], remains unclear. Workers in Rietvlei exhibited aggression or backed off when confronted with a worker from an adjacent nest in a small confined space in the field (S. Jacobs, unpublished observations), making it unlikely that buds remain connected to the natal nest.

The rare co-occurrence of different mtDNA-haplotypes within the same colony [25] might suggest that in addition to colony founding by budding solitarily dispersing queens occasionally may be adopted into alien nests. This would explain the lack of a strong correlation between mtDNA and microsatellite clusters and also promote gene flow between colonies. In the laboratory, groups of multiple queens of C. venustula and other Cardiocondyla were able to rear larvae ([48], S.J., unpubl. observations). Hence, cooperative founding by unrelated dispersing queens provides an alternative way of colony founding and might also contribute to the existence of multiple mtDNA haplotypes in one colony.

Though FST-values were significant, we could not reveal a clear genetic structure across all sampling sites in Rietvlei Nature Reserves. The population from Island View (IV) did not show any variability in the analyzed markers despite a sufficiently large sample size at least for microsatellite genotyping. This might indicate that populations are occasionally founded by only one or a few related queens (with or without workers). Isolated patches might be colonized via several stepping stones of small, sparsely vegetated patches. In addition, the worldwide spread of several Cardiocondyla tramp species [13, 49,50,51], including C. venustula, suggests that the accidental transfer of solitary queens or colony fragments with soil, seedlings, or garbage may ease the colonization of new habitat and may have contributed to these apparent founder effects. The network of unpaved roads in Rietvlei Nature Reserve may also have facilitated the dispersal of C. venustula as such roads provide the ideal habitat for these ants.

The inbreeding and relatedness coefficients obtained by microsatellite genotyping for nestmates of C. venustula were higher than in other Cardiocondyla species [28,29,30, 44], including the related C. shuckardi from Madagascar [43]. The inbreeding coefficient suggests more than 80% sib-mating. Generally, Cardiocondyla show a high tolerance to inbreeding. In C. obscurior, no diploid males were found even after several generations of sib-mating in the lab [52]. In contrast to honeybees and presumably also other social Hymenoptera [53], Cardiocondyla does not exhibit single-locus complementary sex determination and inbreeding therefore does not lead to the production of non-viable or sterile diploid males. Resistance towards inbreeding and genetic impoverishment has previously been suggested to facilitate the successful establishment of small propagules in novel environments [16, 54,55,56,57], and our study again highlights that sib-mating in Cardiocondyla is not a consequence but a precondition of invasiveness (see also [58]).

Nevertheless, exclusive inbreeding may occasionally have adverse effects also in Cardiocondyla, including reduced queen life span and a lower fecundity of males [52]. These are presumably lessened by occasional outbreeding events, e.g., through the adoption of alien queens as described above. Winged queens have regularly been observed to disperse on foot, and some of them may enter and mate in alien nests, similar to what has been observed in Palearctic Cardiocondyla [30, 44]. Wingless males of C. venustula may therefore not only compete for mating with their sisters [22, 23] but also for mating with alien queens. The presence of multiple fertile queens in field and also lab colonies (unpublished data) suggests that C. venustula is facultatively polygynous, in contrast to the obligatorily monogynous Palearctic clade. While workers typically are expected to oppose the adoption of alien queens on relatedness grounds (e.g., [59, 60]), C. venustula workers would be closely related to an adopted queen’s offspring in case it has mated with one of the colony’s males.

The low variability of genetic markers and the presumed high relatedness among nestmate males did not allow determining the mating frequency of field-collected queens. Sperm and offspring analyses suggest that queens, which in the lab had been given the chance to mate with two genotypically distinct males, mated only once. Monogamy in C. venustula is in accordance with males successfully increasing their fitness by defending small “territories” inside the nests and monopolizing mating with female sexuals inside the nest. While obligatorily monogynous Cardiocondyla are polyandrous [28, 30, 44], facultatively polygynous C. obscurior [29] and, as we here show, C. venustula appear to be monandrous. This matches previous observations of the correlation between queen number and mating frequency in other ants (e.g., [61]).


Our study shows that C. venustula resembles other tropical species of the genus in the presence of multiple queens per nest and single mating by queens. Though lethal fighting among C. venustula males appears to be uncommon, the aggressive defense of small areas in the nest appears to allow them to monopolize mating with many female sexuals. The very high levels of inbreeding and nestmate relatedness indicate that most matings involve siblings, but the co-occurrence of multiple mtDNA haplotypes in a single colony suggests that dispersing queens may occasionally be adopted by alien colonies. This can promote gene flow and alleviate the negative effects of prolonged inbreeding. Dispersal by young queens over short distances and budding appear to be the prevalent modes of colony founding. Though it still remains to be clarified how long-range dispersal is achieved, the preference of C. venustula for ruderal, degraded patches with sparse vegetation certainly facilitates the colonization of novel habitats, such as rehabilitated mines, parks, or roadsides. Human-assisted transfer in potted plants may have allowed it to spread from its Afrotropical origin to Florida and several Caribbean and Pacific Islands [11, 17] and may also have contributed to the limited isolation by distance across all collecting sites in Rietvlei.

Availability of data and materials

mtDNA sequences have been uploaded to GenBank (accession numbers MK138574 – MK138580).

The results from microsatellite analyses are available as Additional file 1 Material.


  1. Sundström L. Genetic population structure and sociogenetic organisation in Formica truncorum (Hymenoptera; Formicidae). Behav Ecol Sociobiol. 1993;33:345–54.

    Article  Google Scholar 

  2. Seppä P, Pamilo P. Gene flow and population viscosity in Myrmica ants. Heredity. 1995;74:200–9.

    Article  Google Scholar 

  3. Ross KG, Krieger MJ, Shoemaker DD, Vargo EL, Keller L. Hierarchical analysis of genetic structure in native fire ant populations: results from three classes of molecular markers. Genetics. 1997;147:643–55.

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Chapuisat M, Goudet J, Keller L. Microsatellites reveal high population viscosity and limited dispersal in the ant Formica paralugubris. Evolution. 1997;51:475–82.

    Article  PubMed  Google Scholar 

  5. Doums C, Cabrera H, Peeters C. Population genetic structure and male-biased dispersal in the queenless ant Diacamma cyaneiventre. Mol Ecol. 2002;11:2251–64.

    Article  CAS  PubMed  Google Scholar 

  6. Sundström L, Keller L, Chapuisat M. Inbreeding and sex-biased gene flow in the ant Formica exsecta. Evolution. 2003;57:1552–61.

    Article  PubMed  Google Scholar 

  7. Jaffé R, Moritz RF, Kraus FB. Gene flow is maintained by polyandry and male dispersal in the army ant Eciton burchellii. Pop Ecol. 2009;51:227–36.

    Article  Google Scholar 

  8. Boomsma JJ, Baer B, Heinze J. The evolution of male traits in social insects. Annu Rev Entomol. 2005;50:395–420.

    Article  CAS  PubMed  Google Scholar 

  9. Helms JA IV. The flight ecology of ants (Hymenoptera: Formicidae). Myrmecol News. 2018;26:19–30.

    Google Scholar 

  10. Kugler J. The males of Cardiocondyla Emery (Hymenoptera: Formicidae) with the description of the winged male of Cardiocondyla wroughtoni (Forel). Isr J Entomol. 1983;17:1–21.

    Google Scholar 

  11. Seifert B. The ant genus Cardiocondyla (Insecta: Hymenoptera: Formicidae) - a taxonomic revision of the C. elegans, C. bulgarica, C. batesii, C. nuda, C. shuckardi, C. stambuloffi, C. wroughtoni, C. emery, and C. minutior species groups. Ann Naturhist Mus Wien Ser B Bot Zool. 2003;104:203–338.

    Google Scholar 

  12. Oettler J, Suefuji M, Heinze J. The evolution of alternative reproductive tactics in male Cardiocondyla ants. Evolution. 2010;64:3310–7.

    Article  Google Scholar 

  13. Heinze J. Life-history evolution in ants: the case of Cardiocondyla. Proc R Soc B. 2017;284:20161406.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Hoffmann BD, Andersen AN. Responses of ants to disturbance in Australia, with particular reference to functional groups. Austral Ecol. 2003;28:444–64.

    Article  Google Scholar 

  15. Van Hamburg H, Andersen AN, Meyer WJ, Robertson HG. Ant community development on rehabilitated ash dams in the south African Highveld. Restor Ecol. 2004;12:552–8.

    Article  Google Scholar 

  16. Heinze J, Cremer S, Eckl N, Schrempf A. Stealthy invaders: the biology of Cardiocondyla tramp ants. Insect Soc. 2006;53:1–7.

    Article  Google Scholar 

  17. Wetterer JK. Geographic origin and spread of cosmopolitan ants (Hymenoptera: Formicidae). Halteres. 2015;6:66–78.

    Google Scholar 

  18. Kinomura K, Yamauchi K. Fighting and mating behaviors of dimorphic males in the ant Cardiocondyla wroughtoni. J Ethol. 1987;5:75–81.

    Article  Google Scholar 

  19. Heinze J, Kühnholz S, Schilder K, Hölldobler B. Behavior of ergatoid males in the ant Cardiocondyla nuda. Insect Soc. 1993;40:273–82.

    Article  Google Scholar 

  20. Heinze J, Hölldobler B, Yamauchi K. Male competition in Cardiocondyla ants. Behav Ecol Sociobiol. 1998;42:239–46.

    Article  Google Scholar 

  21. Yamauchi K, Ishida Y, Hashim R, Heinze J. Queen-queen competition by precocious male production in multiqueen ant colonies. Curr Biol. 2006;16:2424–7.

    Article  CAS  PubMed  Google Scholar 

  22. Frohschammer S, Heinze J. Male fighting and “territoriality” within colonies of the ant Cardiocondyla venustula. Naturwissenschaften. 2009;96:159–63.

    Article  CAS  PubMed  Google Scholar 

  23. Jacobs S, Heinze J. Between fighting and tolerance: reproductive biology of wingless males in the ant Cardiocondyla venustula. Insect Sci. 2017;24:818–28.

    Article  PubMed  Google Scholar 

  24. Wheeler WM. The ants of Puerto Rico and the Virgin Islands. Bull Am Mus Nat Hist. 1908;24:117–58.

    Google Scholar 

  25. Heinze J, Aumeier V, Bodenstein B, Crewe RM, Schrempf A. Wingless and intermorphic males in the ant Cardiocondyla venustula. Insect Soc. 2013;60:43–8.

    Article  Google Scholar 

  26. Sambrook J, Russell D. Molecular cloning: a laboratory manual. New York: Cold Spring Harbor Laboratory Press; 2001.

    Google Scholar 

  27. Lenoir J-C, Schrempf A, Lenoir A, Heinze J, Mercier J-L. Five polymorphic microsatellite markers for the study of Cardiocondyla elegans (Hymenoptera: Myrmicinae). Mol Ecol Notes. 2005;5:565–6.

    Article  CAS  Google Scholar 

  28. Schrempf A, Reber C, Tinaut A, Heinze J. Inbreeding and local mate competition in the ant Cardiocondyla batesii. Behav Ecol Sociobiol. 2005;57:502–10.

    Article  Google Scholar 

  29. Schmidt CV, Schrempf A, Trindl A, Heinze J. Microsatellite markers for the tramp ant Cardiocondyla obscurior (Formicidae: Myrmicinae). J Genet. 2016;95:1–4.

    Article  CAS  Google Scholar 

  30. Lenoir J-C, Schrempf A, Lenoir A, Heinze J, Mercier J-L. Genetic structure and reproductive strategy of the ant Cardiocondyla elegans: strictly monogynous nests invaded by unrelated sexuals. Mol Ecol. 2007;16:345–54.

    Article  PubMed  Google Scholar 

  31. Pritchard JK, Stephens M, Donnelly P. Inference of population structure using multilocus genotype data. Genetics. 2000;155:945–59.

    CAS  PubMed  PubMed Central  Google Scholar 

  32. Earl DA, von Holdt BM. STRUCTURE HARVESTER: a website and program for visualizing STRUCTURE output and implementing the Evanno method. Conserv Genet Resour. 2012;4:359–61.

    Article  Google Scholar 

  33. Jombart T. Adegenet: a R package for the multivariate analysis of genetic markers. Bioinformatics. 2008;24:1403–5.

    Article  CAS  PubMed  Google Scholar 

  34. R Development Core Team. R: A language and environment for statistical computing 2008.

    Google Scholar 

  35. Hardy OJ, Vekemans X. SPAGeDi: a versatile computer program to analyse spatial genetic structure at the individual or population levels. Mol Ecol Resour. 2002;2:618–20.

    Article  Google Scholar 

  36. Excoffier L, Lischer HE. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and windows. Mol Ecol Resour. 2010;10:564–7.

    Article  PubMed  Google Scholar 

  37. Peakall R, Smouse PE. GENALEX 6: genetic analysis in excel. Population genetic software for teaching and research. Mol Ecol Resour. 2006;6:288–95.

    Article  Google Scholar 

  38. Slatkin M. A measure of population subdivision based on microsatellite allele frequencies. Genetics. 1995;139:457–62.

    CAS  PubMed  PubMed Central  Google Scholar 

  39. Lewis PO, Zaykin D. Genetic data analysis: computer program for the analysis of allelic data. 2001.

  40. Chybicki IJ, Burczyk J. Simultaneous estimation of null alleles and inbreeding coefficients. J Hered. 2009;100:106–13.

    Article  CAS  PubMed  Google Scholar 

  41. Suzuki Y, Iwasa Y. A sex ratio theory of gregarious parasitoids. Res Popul Ecol. 1980;22:366–82.

    Article  Google Scholar 

  42. Pamilo P. Effect of inbreeding on genetic relatedness. Hereditas. 1995;103:195–200.

    Article  Google Scholar 

  43. Heinze J, Schrempf A, Wanke T, Rakotondrazafy H, Rakotondranaivo T, Fisher BL. Polygyny, inbreeding, and wingless males in the Malagasy ant Cardiocondyla shuckardi Forel (Hymenoptera, Formicidae). Sociobiology. 2014;61:300–6.

    Article  Google Scholar 

  44. Schrempf A. Inbreeding, multiple mating and foreign sexuals in the ant Cardiocondyla nigra (Hymenoptera: Formicidae). Myrmecol News. 2014;20:1–5.

    Google Scholar 

  45. Oettler J, Schrempf A. Fitness and aging in Cardiocondyla obscurior ant queens. Curr Opin Insect Sci. 2016;6:58–63.

    Article  Google Scholar 

  46. Bolton B. Afrotropical species of the myrmicine ant genera Cardiocondyla, Leptothorax, Melissotarsus, Messor and Cataulacus (Formicidae). Bull Br Mus Nat His Entomol Ser. 1982;45:307–70.

    Google Scholar 

  47. Wilson EO. Communication by tandem running in the ant genus Cardiocondyla. Psyche. 1959;66:29–34.

    Article  Google Scholar 

  48. Schrempf A, Heinze J. Back to one: consequences of derived monogyny in an ant with polygynous ancestors. J Evol Biol. 2007;20:792–9.

    Article  CAS  PubMed  Google Scholar 

  49. Wetterer JK. Worldwide spread of Emery’s sneaking ant, Cardiocondyla emeryi (Hymenoptera: Formicidae). Myrmecol News. 2012;17:13–20.

    Google Scholar 

  50. Wetterer JK. Worldwide spread of the Moorish sneaking ant, Cardiocondyla mauritanica (Hymenoptera: Formicidae). Sociobiology. 2014;59:985–97.

    Google Scholar 

  51. Wetterer JK. Worldwide spread of the lesser sneaking ant, Cardiocondyla minutior (Hymenoptera: Formicidae). Fla Entomol. 2014;97:567–74.

    Article  Google Scholar 

  52. Schrempf A, Aron S, Heinze J. Sex determination and inbreeding depression in an ant with regular sib-mating. Heredity. 2006;97:75–80.

    Article  CAS  PubMed  Google Scholar 

  53. Van Wilgenburg E, Driessen G, Beukeboom LW. Single locus complementary sex determination in Hymenoptera: an" unintelligent" design? Front Zool. 2006;3:1.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Baker HG. Self-compatibility and establishment after “long-distance” dispersal. Evolution. 1005;9:337–49.

    Google Scholar 

  55. Yamauchi K, Ogata K. Social structure and reproductive systems of tramp versus endemic ants (Hymenoptera: Formicidae) of the Ryukyu Islands. Pac Sci. 1995;49:55–68.

    Google Scholar 

  56. Passera L. Characteristics of tramp species. In: Williams DF, editor. Exotic ants. Biology, impact, and control of introduced species. Boulder: Westview Press; 1994. p. 23–43.

    Google Scholar 

  57. Evans TA, Inta R, Lai JCS. Foraging choice and replacement reproductives facilitate invasiveness in drywood termites. Biol Invasions. 2011;13:1579–87.

    Article  Google Scholar 

  58. Eyer P-A, Matsuura K, Vargo EL, Kobayashi K, Yashiro T, Suehiro W, Himuro C, Yokoi T, Guénard B, Dunn RR, Tsuji K. Inbreeding tolerance as a pre-adapted trait for invasion success in the invasive ant Brachyponera chinensis. Mol Ecol. 2018;27:4711–24.

    PubMed  Google Scholar 

  59. Stuart RJ, Gresham-Bissett L, Alloway TM. Queen adoption in the polygynous and polydomous ant, Leptothorax curvispinosus. Behav Ecol. 1993;4:276–81.

    Article  Google Scholar 

  60. Gadau J, Gertsch PJ, Heinze J, Pamilo P, Hölldobler B. Oligogyny by unrelated queens in the carpenter ant, Camponotus ligniperdus. Behav Ecol Sociobiol. 1998;44:23–33.

    Article  Google Scholar 

  61. Hughes WOH, Ratnieks FLW, Oldroyd BP. Multiple paternity or multiple queens: two routes to greater intracolonial genetic diversity in the eusocial Hymenoptera. J Evol Biol. 2008;21:1090–5.

    Article  CAS  PubMed  Google Scholar 

Download references


We thank Sonja Dorfner, Lukas Schrader, and Tina Wanke for help in the field, Riaan Marais for permission to work at Rietvlei Nature Reserve (SP 16-10-2012) and the administration for Hlalanathi Drakensberg Resort for permission to collect ants on their property. Robin Crewe helped obtaining permits for collecting and exporting ants from the Premier of the province of Gauteng (CPF6 0173 and CPB5 003499) and Ezemvelo KZN Wildlife (OP 4720/2012). Two reviewers and Qiao Wang made helpful suggestions on the manuscript.

Ethics approval and consent to esparticipate

All experiments comply with national and international guidelines. Approval by an appropriate ethics committee was not needed.


This study was supported by DFG (He 1623/34). The funding agency had no role in study design, data collection, analysis and interpretation, or writing the manuscript.

Author information

Authors and Affiliations



SJ and JH conceived and designed the experiments. SJ conducted molecular experiments and analyzed the data, SJ and JH wrote the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Jürgen Heinze.

Ethics declarations

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Additional file

Additional file 1:

Raw data of the population genetic analysis of the ant Cardiocondyla venustula from South Africa. (XLSX 40 kb)

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jacobs, S., Heinze, J. Population and colony structure of an ant with territorial males, Cardiocondyla venustula. BMC Evol Biol 19, 115 (2019).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: