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Slave-making ant
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Slave-making ants or slaver ants are brood parasites that capture broods of other ant species to increase the worker force of their colony. After emerging in the slave-maker nest, slave workers work as if they were in their own colony, while parasite workers only concentrate on replenishing the labor force from neighboring host nests, a process called slave raiding.
The slave-making ants are specialized to parasitize a single species or a group of related species, and they are often close relatives to their hosts, which is typical for social parasites. The slave-makers may either be permanent social parasites (thus depending on enslaved ants throughout their whole lives) or facultative slave-makers. The behavior is unusual among ants but has evolved several times independently.
Terminology
[edit]Among animals, theft of brood for the purpose of employing the stolen individual's efforts in support of the thief is formally called dulosis (from Greek δοῦλος 'slave'), but the term "slave-making" is considered synonymous.[1]
Slaver ants were first described by the Genevan entomologist Pierre Huber in his 1810 book Recherches sur les mœurs des fourmis indigènes. He referred to the enslaved ants as "auxiliary ants". In 1820 the British translator of this book likened the enslaved ants to "Negro ants", and this naturalist account on slavery in the animal world caused a stir in the proslavery and antislavery discourse in the Atlantic world.[2]
A related type of social parasitism is called inquilinism, in which a reproductive enters a host colony, lays eggs, and relies on the host colony to rear its offspring. Unlike brood parasitism, the inquiline remains within the nest and typically its brood does not outnumber the host's brood.[1]
Obligate and facultative slave-makers
[edit]Slave-making ants may be permanent social parasites, thus depending on enslaved host ants throughout their whole lives and unable to function without them[3] in which case they are termed obligate slave-makers. Alternatively, facultative slave-making ants, like those in the Formica sanguinea complex, represent an intermediate parasitic group, between free-living species and obligatory slave-making species. In laboratory tests, when captured workers were removed from colonies of Formica sanguinea and Polyergus rufescens, the behavior of F. sanguinea changed dramatically within 30 days of their removal, with workers becoming self-sufficient at feeding and brood care. Workers of Polyergus, in contrast, were unable to care for their brood, and experienced high mortality.[4]
Raids
[edit]
Parasitized nests need to replenish the host workers periodically. This is achieved by raiding other nests in a process called slave raiding.[3][5] The parasite workers are specialized for conducting raids in a two-step process. First, scouts individually search for potential host nests. When successful, the scout returns to its nest and recruits nest-mates to initiate the raid, during which slave-maker ants seize a brood and bring it back home.[6] A colony may capture 14,000 pupae in a single season.[7] Most slave-raiders capture only the young, but Strongylognathus sp. also enslave adult workers.[8]
In most parasite species, workers mark the way to their nest with pheromones and afterwards fellow slave-makers are attracted within a few seconds. They then go quickly to the targeted host nest, attack it, and carrying as many larvae and pupae as possible, return to their nest following the same trail marked by the pheromone.[5] Rossomyrmex is the only reported slave-maker that exclusively uses adult transport and single recruitment chain instead of pheromones during raids, a behavior probably constrained by the arid habitat; raids take place in early summer when soil surface temperature can reach up to 30 °C (86 °F), a temperature in which pheromones would quickly evaporate.[5]
Workers of the attacked nest can fight or flee. In the host species Proformica, the most common behavior is flee, probably because hosts almost always lose fights.[5] Most studies on the raiding behavior of species in the F. sanguinea complex confirm that slave raiders usually rout their opponents, who typically flee in a state of panicked alarm, and that aggressive encounters, when they occur, are brief and do not result in the death of adult individuals from either species. However, when large colonies of slave species offer resistance during raids prolonged fighting is possible and many workers of both species can be killed.[9]
Later, host workers emerging in the parasite nest will be imprinted on and integrated into the mixed colony where they will rear the parasite brood, feed and groom the parasite workers, defend the nest against aliens (e.g. other insects or spiders), and even participate in raids,[6] including those against their original colony.[10] Altruistic acts of slaves are thus directed toward unrelated individuals. One hypothesis suggests that slave deception is possible because slaves are captured as pupae and learn the slave-maker colony odor after emergence.[11]
However, in some cases, the enslaved ants rebel against their slave-maker ants, killing a large number of the slave-maker ant offspring.[12] This is because "slaves can gain indirect fitness benefits by reducing parasite pressure on nearby host colonies, because these are often closely related to the slaves".[12] Thus, the slave ants protect their native colonies from further raids by slave-maker ants.[12]
Parasite–host pairs
[edit]- Rossomyrmex–Proformica[13]
- Polyergus–Formica[13]
- Formica–Formica[13]
- Leptothorax–Chalepoxenus[13]
- Leptothorax–Epimyrma[13]
- Leptothorax–Harpagoxenus[13]
- Leptothorax–Leptothorax[13]
- Leptothorax–Protomognathus[13]
- Myrmoxenus–Temnothorax[14]
- Strongylognathus–Tetramorium[13]
Reproduction
[edit]The reproductive behavior of slave-making ants usually consists in synchronous emergence of sexuals followed by a nuptial flight and the invasion of a host nest,[15] but also in some cases females display a mating call around the natal nest to attract males and immediately after mating search for a host nest to usurp.[16]
Only one slave species is usually found in a single Polyergus nest. This is in contrast to related facultative slave-makers of the genus Formica belonging to the F. sanguinea species group, found in the same habitat, whose nests commonly contain two or more species serving as slaves. Choice of a host species can occur both through the colony-founding behavior of queens and through the choice of target nests for slave raids. The parasitic Polyergus queens found colonies either by adoption, where a queen invades the nest of a slave species, killing the resident queen and appropriating workers and brood present, or by "budding", in which a queen invades or is accepted into a host species nest accompanied by workers from her nest of origin.[17]
Evolution
[edit]The first hypothesis concerning the origins of slave-making was Darwin's (1859) suggestion in On the Origin of Species that slavery developed as a by-product of brood predation among related species. Other hypotheses focus on territorial interactions with opportunistic brood predation or brood transport among polydomous colonies (consist of multiple nests) as the main pathway to slave-making.[18][19] Slave-making behavior is unusual among ants but has evolved independently more than ten times in total[8] including in the subfamilies Myrmicinae and Formicinae.[20][21] Slave-makers and their hosts are often close phylogenetic relatives,[22] which is typical for social parasites and their respective hosts (formalized as Emery's rule). This has major evolutionary implications since it may argue for sympatric speciation.[23]
Raids can jeopardize host colony survival, therefore exerting a strong selection pressure upon the hosts. Reciprocally, there is some evidence that hosts also exert a selection pressure on their parasites in return, since resistance by host colonies might prevent enslavement. Coevolutionary processes between slave-making ant species and their hosts then can escalate to an evolutionary arms race.[6]
See also
[edit]References
[edit]- ^ a b Breed, Cook & Krasnec 2012, p. 2
- ^ Minella, Timothy K. “The Enslaved Ants and the Peculiar Institution: Argument by Analogy in the Slavery Question.” Early American Studies, vol. 17, no. 2, 2019, pp. 256–80. JSTOR, https://www.jstor.org/stable/26741208. Accessed 24 Apr. 2025. "The British translator of Huber’s book noted, “I shall take the liberty, when speaking of the dark Ash-coloured Ant, occasionally to use the appellation of Negro . . . a term not inapplicable, when we consider the dark colour of this species, and the situation it holds in the colony, of providing for and administering to, the wants, &c. of the Amazons.” Numerous publications on both sides of the Atlantic retold Huber’s astonishing discoveries, and several made the obvious comparison between the slavery of the ant and America’s “peculiar institution.”"
- ^ a b Ruano et al. 2013, p. 1
- ^ Topoff & Zimmerli 1991, p. 313
- ^ a b c d Ruano et al. 2013, p. 3
- ^ a b c Delattre et al. 2012, p. 2
- ^ Topoff 1999, p. 89
- ^ a b D'Ettorre & Heinze 2001, p. 68
- ^ Topoff & Zimmerli 1991, pp. 313–314
- ^ Miramontes 1993, p. 6
- ^ Blatrix & Sermage 2005, p. 2
- ^ a b c Pennings et al. 2012
- ^ a b c d e f g h i D'Ettorre & Heinze 2001, p. 69
- ^ Delattre et al. 2012, p. 7
- ^ Mori, D'Ettorre & Le Moli 1994, p. 203
- ^ Ruano et al. 2013, p. 2
- ^ Goodloe & Sanwald 1985, p. 297
- ^ Goodloe & Topoff 1987, p. 298
- ^ Topoff & Zimmerli 1991, p. 309
- ^ King & Trager 2007, p. 70
- ^ Goropashnaya et al. 2012, p. 6
- ^ D'Ettorre & Heinze 2001, p. 70
- ^ Fénéron et al. 2013, p. 1
Sources
[edit]- Blatrix, R. S.; Sermage, C. (2005), "Role of early experience in ant enslavement: A comparative analysis of a host and a non-host species", Frontiers in Zoology, 2 13, doi:10.1186/1742-9994-2-13, PMC 1199612, PMID 16076389

- Breed, M. D.; Cook, C.; Krasnec, M. O. (2012), "Cleptobiosis in Social Insects", Psyche: A Journal of Entomology, 2012: 1–7, doi:10.1155/2012/484765

- Delattre, O.; Blatrix, R. S.; Châline, N.; Chameron, S. P.; Fédou, A.; Leroy, C.; Jaisson, P. (2012), "Do host species evolve a specific response to slave-making ants?", Frontiers in Zoology, 9 (38): 1–10, doi:10.1186/1742-9994-9-38, PMC 3551654, PMID 23276325

- D'Ettorre, Patrizia; Heinze, Jürgen (2001), "Sociobiology of slave-making ants", Acta Ethologica, 3 (2): 67–82, doi:10.1007/s102110100038, S2CID 37840769

- Fénéron, R. E.; Poteaux, C.; Boilève, M.; Valenzuela, J.; Savarit, F. (2013), "Discrimination of the Social Parasite Ectatomma parasiticum by Its Host Sibling Species (E. Tuberculatum)", Psyche: A Journal of Entomology, 2013: 1–11, doi:10.1155/2013/573541

- Goodloe, L.; Sanwald, R. (1985), "Host Specificity in Colony-Founding by Polyergus Lucidus Queens (Hymenoptera: Formicidae)", Psyche: A Journal of Entomology, 92 (2–3): 297, doi:10.1155/1985/69513

- Goodloe, L. P.; Topoff, H. (1987), "Pupa Acceptance by Slaves of the Social-Parasitic Ant, Polyergus (Hymenoptera: Formicidae)", Psyche: A Journal of Entomology, 94 (3–4): 293–302, doi:10.1155/1987/48360

- Goropashnaya, A. V.; Fedorov, V. B.; Seifert, B.; Pamilo, P. (2012), Chaline, Nicolas (ed.), "Phylogenetic Relationships of Palaearctic Formica Species (Hymenoptera, Formicidae) Based on Mitochondrial Cytochrome b Sequences", PLOS ONE, 7 (7): 1–7, Bibcode:2012PLoSO...741697G, doi:10.1371/journal.pone.0041697, PMC 3402446, PMID 22911845

- Herbers, J. M. (2007), "Watch Your Language! Racially Loaded Metaphors in Scientific Research", BioScience, 57 (2): 104–105, doi:10.1641/B570203, S2CID 84617477

- King, JR; Trager, JC (2007), "Natural history of the slave making ant, Polyergus lucidus, sensu lato in northern Florida and its three Formica pallidefulva group hosts.", Journal of Insect Science, 7 (42): 1–14, doi:10.1673/031.007.4201, PMC 2999504, PMID 20345317

- Miramontes, Octavio (1993). Complexity and behaviour in Leptothorax ants. CopIt ArXives. ISBN 978-0-9831172-2-3.

- Mori, A.; D'Ettorre, P.; Le Moli, F. (1994), "Mating and post-mating behaviour of the European amazon ant, Polyergus rufescens (Hymenoptera, Formicidae)", Bolletino di Zoologia, 61 (3): 203–206, doi:10.1080/11250009409355886

- Pennings, Pleuni S.; Pamminger, Tobias; Foitzik, Susanne; Metzler, Dirk (4 December 2012). "Oh sister, where art thou? Indirect fitness benefit could maintain a host defense trait". arXiv:1212.0790 [q-bio.PE].
- Ruano, F.; Sanllorente, O.; Lenoir, A.; Tinaut, A. (2013), "Rossomyrmex, the Slave-Maker Ants from the Arid Steppe Environments", Psyche: A Journal of Entomology, 2013: 1–7, doi:10.1155/2013/541804, hdl:10481/98053

- Topoff, H. (1999), "Slave-making queens", Scientific American, 281 (5): 84–90, Bibcode:1999SciAm.281e..84T, doi:10.1038/scientificamerican1199-84

- Topoff, H.; Zimmerli, E. (1991), "Formica Wheeleri: Darwin's Predatory Slave-Making Ant?", Psyche: A Journal of Entomology, 98 (4): 309–317, doi:10.1155/1991/34829

Additional publications
[edit]
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Blatrix, R. S.; Sermage, C. (2005), "Role of early experience in ant enslavement: A comparative analysis of a host and a non-host species", Frontiers in Zoology, 2 13, doi:10.1186/1742-9994-2-13, PMC 1199612, PMID 16076389 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Breed, M. D.; Cook, C.; Krasnec, M. O. (2012), "Cleptobiosis in Social Insects", Psyche: A Journal of Entomology, 2012: 1–7, doi:10.1155/2012/484765 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Delattre, O.; Blatrix, R. S.; Châline, N.; Chameron, S. P.; Fédou, A.; Leroy, C.; Jaisson, P. (2012), "Do host species evolve a specific response to slave-making ants?", Frontiers in Zoology, 9 (38): 1–10, doi:10.1186/1742-9994-9-38, PMC 3551654, PMID 23276325 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Fénéron, R. E.; Poteaux, C.; Boilève, M.; Valenzuela, J.; Savarit, F. (2013), "Discrimination of the Social Parasite Ectatomma parasiticum by Its Host Sibling Species (E. Tuberculatum)", Psyche: A Journal of Entomology, 2013: 1–11, doi:10.1155/2013/573541 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Goodloe, L.; Sanwald, R. (1985), "Host Specificity in Colony-Founding by Polyergus Lucidus Queens (Hymenoptera: Formicidae)", Psyche: A Journal of Entomology, 92 (2–3): 297, doi:10.1155/1985/69513 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Goodloe, L. P.; Topoff, H. (1987), "Pupa Acceptance by Slaves of the Social-Parasitic Ant, Polyergus (Hymenoptera: Formicidae)", Psyche: A Journal of Entomology, 94 (3–4): 293–302, doi:10.1155/1987/48360 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Goropashnaya, A. V.; Fedorov, V. B.; Seifert, B.; Pamilo, P. (2012), Chaline, Nicolas (ed.), "Phylogenetic Relationships of Palaearctic Formica Species (Hymenoptera, Formicidae) Based on Mitochondrial Cytochrome b Sequences", PLOS ONE, 7 (7): 1–7, Bibcode:2012PLoSO...741697G, doi:10.1371/journal.pone.0041697, PMC 3402446, PMID 22911845 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: King, JR; Trager, JC (2007), "Natural history of the slave making ant, Polyergus lucidus, sensu lato in northern Florida and its three Formica pallidefulva group hosts.", Journal of Insect Science, 7 (42): 1–14, doi:10.1673/031.007.4201, PMC 2999504, PMID 20345317 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Ruano, F.; Sanllorente, O.; Lenoir, A.; Tinaut, A. (2013), "Rossomyrmex, the Slave-Maker Ants from the Arid Steppe Environments", Psyche: A Journal of Entomology, 2013: 1–7, doi:10.1155/2013/541804, hdl:10481/98053 Please check the source for the exact licensing terms.
This article incorporates text from a scholarly publication published under a copyright license that allows anyone to reuse, revise, remix and redistribute the materials in any form for any purpose: Topoff, H.; Zimmerli, E. (1991), "Formica Wheeleri: Darwin's Predatory Slave-Making Ant?", Psyche: A Journal of Entomology, 98 (4): 309–317, doi:10.1155/1991/34829 Please check the source for the exact licensing terms.
Slave-making ant
View on GrokipediaTerminology
Obligate and facultative slave-makers
Slave-making ants exhibit two primary strategies of dulosis: obligate and facultative. Obligate slave-makers function as permanent social parasites, depending completely on enslaved host workers for survival and colony maintenance, as their own workers possess severely limited behavioral repertoires incapable of tasks like foraging or brood care.[6] Facultative slave-makers, however, retain the ability to perform essential colony functions independently, using raids opportunistically to supplement their workforce rather than as a necessity.[7] In obligate species, such as those in the genus Polyergus (e.g., P. breviceps and P. lucidus), slaves typically constitute over 90% of the colony's workforce, enabling raids on large host colonies due to specialized morphological adaptations like hooked mandibles for pupae transport.[8] These ants cannot establish or sustain colonies without initial slave acquisition, and experimental removal of slaves leads to colony collapse.[6] Facultative species, exemplified by Formica sanguinea and Formica subnuda, maintain lower slave proportions and activate raiding behaviors seasonally, allowing self-sufficiency outside peak periods.[9] The distinction arises from evolutionary specialization: obligate forms have undergone greater morphological and behavioral degeneration, prioritizing raid efficiency over autonomy, while facultative forms represent less derived parasitism with retained worker functionality.[10] This spectrum reflects varying degrees of host dependence, with obligate slave-makers exhibiting higher raid frequencies and slave integration to compensate for their deficits.[7]Historical origins and terminological debates
The phenomenon of slave-making in ants was first systematically documented by the Swiss entomologist Pierre Huber in his 1810 monograph Recherches sur les mœurs des fourmis indigènes, where he detailed the raiding behavior of Formica (now Polyergus) rufescens in Europe. Huber observed colonies conducting organized raids on nests of host species such as Formica fusca, capturing pupae that eclosed into workers performing all labor for the raiders, who were incapable of sustaining their own colonies without such captives.[11] He also noted similar conduct in the blood-red ant Formica sanguinea, emphasizing the coercive dependency and lack of reciprocity, which he likened to human servitude based on direct field observations.[12] Subsequent 19th-century naturalists, including Charles Darwin in On the Origin of Species (1859), referenced Huber's findings to illustrate natural selection's role in extreme social adaptations, though Darwin avoided endorsing the slavery analogy explicitly to sidestep anthropomorphic overtones. Early 20th-century studies expanded documentation to North American species like Polyergus lucidus, confirming the behavior's prevalence across genera and highlighting its obligate nature in some taxa.[13] Terminologically, Huber introduced "esclavage" (slavery) to describe the raids and enforced labor, a descriptor retained in English as "slave-making" for its precision in capturing the evolutionary strategy of interspecific brood theft and perpetual subjugation. The neologism "dulosis," derived from the Greek doulos (slave), emerged in the late 19th century via entomologist Erich Wasmann to denote this specific parasitism, aiming for a less emotive scientific label while acknowledging the functional equivalence to slavery—raiders depend entirely on host brood for workforce replenishment, with captives exhibiting no voluntary integration or escape.[14] Debates over terminology intensified in the 20th and 21st centuries, with critics arguing that "slavery" imposes anthropocentric moral judgments on non-sentient insects, potentially conflating instinctual behaviors with human institutions laden with ethical baggage; for instance, a 2007 analysis in BioScience urged replacement with neutral terms like "brood parasitism" to avoid racially evocative metaphors in scientific discourse.[15] Proponents of retaining "slave-making," however, contend that the term aptly reflects verifiable causal mechanisms—coerced capture, suppression of host reproduction, and total labor exploitation—distinguishing it from milder parasitisms like temporary egg-laying, and note that alternatives like dulosis have not supplanted it in peer-reviewed literature due to the analogy's heuristic value in elucidating evolutionary costs and benefits.[1] Empirical consistency across species, such as Harpagoxenus and Formicoxenus genera, underscores the term's enduring utility despite such critiques.[16]Evolutionary origins
Phylogenetic evidence for multiple independent evolutions
Phylogenetic analyses of ant taxa demonstrate that slave-making, or dulosis, has evolved independently multiple times, with at least ten documented origins across genera in the subfamilies Myrmicinae and Formicinae.[17] [3] Molecular phylogenies, incorporating mitochondrial and nuclear markers such as COI, 28S rRNA, and long-wavelength opsin, reveal that dulotic behaviors in distantly related lineages like Polyergus (Formicinae) and Rossomyrmex (Myrmicinae) arose separately, as these genera do not form a monophyletic clade with shared slave-making traits inherited from a common ancestor.[18] This polyphyletic distribution underscores convergent evolution driven by ecological pressures favoring parasitic strategies over independent colony founding.[19] Within Formicinae, phylogenomic reconstructions using transcriptomic data from Palearctic Formica species indicate a single origin of dulosis in the Formica sanguinea group, where slave-making parasites diverged from non-parasitic ancestors that retained colony-founding capabilities.[20] [21] However, broader surveys across ant subfamilies, including the "Formicoxenus-group" of Myrmicinae, identify at least five additional independent origins of slavery, supported by gene expression patterns showing parallel but not identical genetic underpinnings for queen-worker dimorphism in slave-makers versus hosts.[17] Genomic comparisons further corroborate multiple origins through convergent reductions in chemoreceptor repertoires; for instance, slave-making species from three independent lineages exhibit approximately 50% fewer gustatory receptors than related non-slave-makers, reflecting adaptations to reliance on host labor rather than direct foraging.[19] These findings, derived from whole-genome sequencing and ortholog mapping, reject monophyly of dulosis and highlight repeated evolutionary transitions from facultative to obligate parasitism in response to competitive environments.[22]Genetic and molecular adaptations
Slave-making ants exhibit convergent genetic adaptations across independent evolutionary origins of dulosis, including reductions in chemoreceptor gene families. Genomic analyses of eight ant species spanning three origins of slavery reveal that slave-makers harbor approximately half as many gustatory receptors as their non-parasitic hosts, correlating with the delegation of foraging and external sensory tasks to enslaved workers.[19] This loss likely reflects relaxed selective pressure on taste perception in parasites reliant on host labor for resource acquisition.[23] Transcriptomic studies further indicate a conserved genetic toolkit for queen-worker dimorphism shared between slave-makers and hosts, with parallel gene expression shifts observed across five independent slavery origins.[17] In slave-makers like Polyergus species, genes regulating caste-specific traits persist despite morphological simplifications in workers, such as specialized raiding mandibles, suggesting retention of core eusocial regulatory networks amid parasitic specialization.[5] At the molecular level, adaptations for chemical integration with hosts involve divergence in cuticular hydrocarbon (CHC) biosynthesis pathways. Host-specific races of Polyergus ants display genetic differentiation linked to CHC profiles that mimic those of targeted Formica hosts, facilitating nest infiltration and reducing rejection.[24] This chemical camouflage, encoded by variations in desaturase and elongase genes, enables effective parasitism without full reliance on aggression alone.[25] Broader genomic erosion characterizes socially parasitic ants, including slave-makers, due to diminished selection on non-essential functions. Comparative genomics show accelerated pseudogenization and contraction of gene families for independent colony maintenance, such as those for brood care and defense, as slaves assume these roles.[26] The reference genome of Polyergus mexicanus, sequenced in 2024, supports investigations into such host-associated adaptations, revealing signatures of selection on stress-response genes amid variable host availability.[27] These patterns underscore how slavery evolves through gene loss and repurposing rather than novel gene acquisition, aligning with causal dependencies on host exploitation.Raid behaviors
Mechanics of slave raids
Slave raids in dulotic ants commence with scouting by individual workers seeking host colonies with abundant brood. In Polyergus breviceps, scouts evaluate potential targets and initiate recruitment only for viable nests, using pheromone trails to summon raiders from the home colony.[4] Scouts in Polyergus rufescens similarly assess host colony size before recruiting, forgoing raids on small nests lacking sufficient workers.[28] Recruitment mobilizes large raiding parties through semiochemicals, enabling mass assembly. For P. breviceps, a single scout can recruit over 2,600 workers, with median raid participation reflecting substantial colony commitment to the assault.[29] In facultative slave-makers like Formica sanguinea, scouts recruit via trails leading to varied attack types, including simple, continuous, or simultaneous incursions on hosts such as F. fusca.[30] The assault phase involves overwhelming host defenses through numerical superiority and specialized aggression. Obligate slave-makers like Polyergus employ falcate mandibles for rapid dispatch of adult hosts, prioritizing pupae theft over larva collection.[31] Raiders kill or expel workers and queens, then seize pupae, which eclose as slaves in the parasite nest.[32] Brood transport follows, with raiders carrying pupae back along recruitment trails, often hooked in mandibles despite ergonomic limitations in Polyergus.[33] In F. sanguinea, 18 of 26 observed raids succeeded in sacking nests and retrieving brood over a 78-day period, yielding a 69% success rate.[30] Raids peak seasonally in summer, driven by host brood availability and slave workforce depletion.[34]Host defenses and slave resistance
Host colonies of ant species targeted by slave-makers exhibit behavioral adaptations to counter raids, including heightened aggression triggered by parasite cues. In the host Temnothorax longispinosus, a brief encounter with a dead worker of the slave-making ant Protomognathus americanus induces elevated aggression levels persisting for up to three days, enhancing post-raid survival probabilities; this response is specific to the parasite and does not occur with non-parasitic competitors like T. curvispinosus.[35] Similarly, host species such as T. unifasciatus demonstrate qualitatively specific aggression toward the slave-maker Myrmoxenus ravouxi, with behavioral responses scaled by chemical similarity showing targeted attacks beyond general heterospecific hostility.[36] Slave-making ants, in turn, preferentially target larger host colonies with stronger defenses, as observed in systems involving Polyergus and Formica hosts, where collective decision-making during scouting favors nests offering higher brood yields despite resistance.[37] During raids, host workers mount direct physical defenses, often through alarm pheromones and coordinated attacks rather than flight responses. For instance, Formica species susceptible to Polyergus raids respond to threats with aggressive alarm behaviors, including biting and ejection, prioritizing colony protection over panic dispersal.[38] These defenses impose selective pressure, as evidenced by geographic variation in host aggression correlating with local parasite prevalence; non-host species like T. nylanderi in parasitized areas exhibit heightened bite and ejection rates toward slave-makers, suggesting convergent evolution of resistance traits.[36] Enslaved host workers, once integrated into the parasite colony, display resistance behaviors that undermine the slave-maker's reproductive success, termed "slave rebellion." In colonies of Protomognathus americanus, enslaved Temnothorax workers (T. longispinosus, T. ambiguus, T. curvispinosus) selectively kill or neglect female pupae of the parasite—achieving 83% mortality for queens and 67% for workers—while sparing males (only 3% mortality), likely via chemical or morphological discrimination.[39] Direct killing accounts for about 30% of failures, with neglect and removal comprising the rest, collectively limiting parasite colony expansion to small sizes (typically 2-5 workers) and reducing raid frequency, thereby benefiting kin-related host populations.[39] Such rebellion decreases the overall fitness cost of parasitism, as slaves systematically eliminate two-thirds of female brood, disrupting the parasite's dependence on host labor for essential tasks like foraging and brood care.[40]Reproduction and colony maintenance
Queen establishment and infiltration
In obligate slave-making ants such as Polyergus breviceps, colony establishment begins with a newly mated queen departing the parental nest following the nuptial flight, actively searching for a suitable host colony of a Formica species, typically one that is queenright and mature to ensure sufficient worker numbers for initial brood care.[41] The queen selects hosts based on chemical cues matching her own cuticular hydrocarbons, facilitating mimicry and reducing immediate detection as a foreign intruder.[42] Upon infiltration, the Polyergus queen, which is morphologically larger than host workers (e.g., body length exceeding that of Formica gnava workers by up to 20-30%), confronts and kills the resident host queen using powerful mandibles, often in direct combat.[3][43] Host workers initially exhibit aggressive behavior toward the invading queen, including biting and stinging attempts, but this hostility diminishes rapidly—within minutes to hours—after the host queen's elimination, allowing the parasite to be tolerated and groomed.[41] A critical mechanism involves secretions from the queen's enlarged, bilobed Dufour's gland, which she applies to the host queen's corpse or directly to workers; these hydrocarbons and other compounds chemically camouflage the intruder, suppressing alarm responses and promoting acceptance as a legitimate reproducer.[44][45] The gland's size decreases post-invasion, correlating with reduced need for defensive secretions once integration occurs.[46] Once adopted, the Polyergus queen begins oviposition, with host workers rearing the initial brood into parasitic workers and slaves obtained from subsequent raids; this dependent founding is obligatory, as Polyergus queens lack the capacity for independent nest initiation due to worker sterility in foraging and non-reproductive tasks.[41] In related species like Polyergus rufescens, similar Dufour's gland-mediated tactics enable infiltration of Formica cunicularia nests, with gland contents showing host-mimicking profiles that enhance long-term tolerance.[45] Success rates vary, but empirical observations indicate that only a fraction of queens achieve establishment, often in host colonies with lower worker density to minimize resistance.[47] This process underscores the parasite's reliance on host social structure for propagation, transitioning the colony to full dulosis once slave numbers dominate.[43]Slave roles in brood care and foraging
In colonies of obligate slave-making ants such as those in the genus Polyergus, enslaved workers from host species like Formica perform the majority of brood care duties, including feeding larvae, cleaning pupae, and transporting brood within the nest, as the parasite workers lack the morphological adaptations for these tasks.[48] These slaves rear both the slave-maker's brood and any surviving host brood integrated into the colony, ensuring the development of new workers despite the absence of functional parasite labor in nest maintenance.[49] Observations indicate that slaves exhibit behavioral plasticity, adapting host-derived instincts to prioritize the mixed brood, though efficiency may vary due to interspecific mismatches in care protocols.[1] Foraging is similarly delegated almost entirely to slaves, who exit the nest to locate and retrieve food resources, compensating for the slave-makers' reduced sensory and manipulative capabilities, such as degenerated antennae and mandibles specialized for combat rather than food handling.[48] In Polyergus rufescens, for instance, parasite workers restrict their activities to raids, leaving slaves to sustain the colony through external provisioning, which includes gathering nectar, insects, and seeds—a division that underscores the parasites' dependence on host-derived labor for survival.[50] This reliance can lead to colony vulnerabilities during periods of low slave numbers, as foraging rates correlate directly with slave abundance.[51] Facultative slave-makers like Formica sanguinea supplement slave foraging with their own workers but still benefit from enhanced efficiency through integrated host labor.[52]Parasite-host interactions
Documented species pairs
Slave-making ants demonstrate host specificity, typically parasitizing one or a few closely related species within the same genus or subgenus, reflecting phylogenetic constraints and coevolutionary adaptations.[53] Obligate slave-makers like those in the genus Polyergus depend exclusively on Formica species for slave labor, with raids targeting pupae from specific host groups such as the Formica fusca, pallidefulva, or montana complexes.[3] For example, Polyergus lucidus primarily enslaves Formica archboldi and Formica incerta in the montana group, as observed in field studies of mixed colonies.[3] Similarly, Polyergus mexicanus raids Formica subsericea, while Polyergus longicornis targets Formica dolosa.[54][55] Facultative slave-makers, such as Formica sanguinea, exploit multiple hosts from the Serviformica subgenus, including Formica fusca, Formica lemani, Formica rufibarbis, Formica cinerea, and Formica gagatoides, allowing flexibility in colony establishment and maintenance.[56][57] In myrmicine slave-makers, Harpagoxenus canadensis parasitizes two Leptothorax species in the subgenus Leptothorax s.str., such as Leptothorax canadensis and related taxa, with host specificity influenced by local abundance and defensive traits.[58] Protomognathus americanus (syn. Temnothorax americanus) primarily uses Temnothorax longispinosus as a host, though it can incorporate up to three Temnothorax species, correlating with geographic distribution and raid success rates.[59][60]| Slave-making species | Primary host species | Geographic range |
|---|---|---|
| Polyergus lucidus | Formica archboldi, F. incerta | North America |
| Polyergus mexicanus | Formica subsericea | North America |
| Formica sanguinea | Formica fusca group (e.g., F. fusca, F. lemani) | Europe, Asia |
| Harpagoxenus canadensis | Leptothorax spp. (two species) | North America |
| Protomognathus americanus | Temnothorax longispinosus | Northeastern North America |
Coevolutionary dynamics and ecological impacts
Slave-making ants and their hosts engage in coevolutionary arms races characterized by escalating adaptations in chemical communication and behavioral defenses. Hosts evolve heightened discrimination against intruders via refined cuticular hydrocarbon (CHC) profiles, enabling recognition of enslaved conspecifics altered by parasite influence, while slave-makers counter with population-specific mimicry that closely approximates host blends to evade detection.[61] In the Protomognathus americanus–Temnothorax system, New York populations of the parasite show tighter chemical convergence to T. longispinosus (Mahalanobis distances of 7.5 for presence-absence and 4.3 for peak area) than Ohio populations facing multiple hosts, indicating specialization-driven escalation.[61] Hosts respond with increased aggression, particularly in high-pressure areas, where T. longispinosus exhibits seasonal peaks in defensive behavior against scouts.[62] Geographic mosaics of coevolution emerge from variable parasite pressure, with local adaptations in host resistance correlating to raid frequency; for example, Temnothorax species under intense dulosis develop specific antiparasite responses absent in unexposed communities.[36] Parasites, in turn, exploit host variability, adjusting raid tactics and slave integration to overcome defenses, as evidenced by interpopulational differences in behavioral interactions consistent with reciprocal selection.[63] Such dynamics extend to tripartite interactions when multiple slave-makers compete for hosts, amplifying evolutionary pressures through resource partitioning and indirect effects on host evolution.[64] Ecologically, slave-making imposes predator-like pressures, with raids causing brood loss, queen mortality, and colony collapse, thereby reducing host fitness by up to 50% annually in vulnerable patches.[62] This leads to depressed host densities, fragmented distributions, and shifts in nest site preferences toward less accessible microhabitats, as documented over two decades in North American forests where slave-makers like P. americanus dictate host demography.[59] Patchy parasitism exacerbates these effects, creating spatial refugia for hosts but overall suppressing population growth and altering community structure by favoring resilient or secondary host species.[62] In sympatric systems, competition among parasites for hosts can stabilize or intensify impacts, potentially driving broader ant assemblage diversity through selection for antipredator traits.[65]Research developments
Key historical studies
The phenomenon of slave-making, or dulosis, in ants was first documented in detail by Pierre Huber in 1810, who described raids by Formica sanguinea workers on colonies of Formica fusca, capturing pupae that eclosed into slaves performing colony labor.[16] Huber's observations, based on field and laboratory experiments in Switzerland, established the core mechanics: raiders paralyze defenders chemically, transport brood, and integrate eclosing slaves without resistance due to imprinting.[66] Auguste Forel expanded on Huber's work in the late 19th century through extensive European field studies, confirming F. sanguinea's facultative dulosis and documenting host defenses like barricades and counterattacks, while noting the slaves' full integration into foraging and brood care.[67] Forel's 1874–1922 publications emphasized the evolutionary puzzle of dulosis, attributing it to innate instincts rather than learned behavior, and identified similar behaviors in Polyergus species, where raids involve organized columns led by scouts.[2] Carlo Emery's 1909 analysis introduced the principle of host-parasite morphological convergence, observing that slave-makers like Polyergus rufescens mimic their Formica hosts in size, color, and cuticular hydrocarbons to evade detection during raids and infiltration.[68] Emery's taxonomic studies across Europe and North America classified dulotic species and hypothesized co-speciation driven by selection pressures, influencing later views on Emery's rule in social parasitism.[69] William Morton Wheeler's early 20th-century American research, including 1900–1910 field observations of Polyergus lucidus enslaving Formica species, detailed obligatory dulosis: queens infiltrate host nests via chemical mimicry, slay rivals, and rely entirely on slaves post-raid.[70] Wheeler's experiments quantified raid frequencies (up to 20 per season per colony) and slave-to-parasite ratios (often 10:1), highlighting ecological dependencies and the parasites' morphological adaptations like hooked mandibles for carrying pupae.[3] These studies laid groundwork for understanding dulosis as a derived social parasitism, distinct from inquilinism.Recent genetic and behavioral findings
Genomic analyses of slave-making ants from independent evolutionary origins have identified convergent reductions in chemoreceptor genes, reflecting adaptations to a parasitic lifestyle where foraging and brood care are delegated to enslaved workers. Specifically, slave-making species possess approximately 311 odorant receptors (Ors), compared to over 400 in non-parasitic relatives, and 41–52 gustatory receptors (Grs), versus 91–128 in hosts. These losses, particularly in Ors associated with social communication and foraging cues, exceed expectations under neutral evolution (P < 0.05 for convergent ortholog losses), suggesting selection for diminished sensory investment in tasks performed by slaves.[19] Parallel gene expression studies across five independent origins of slavery in the Crematogastrini tribe reveal a conserved genetic toolkit underlying queen-worker dimorphism, with 2,321 genes differentially expressed between castes and 1,188 showing consistent patterns across 15 species (slave-makers and hosts). Lifestyle differences account for only 62 genes, far fewer than caste effects, indicating that slave-making evolves primarily through regulatory tweaks rather than wholesale rewiring of caste-determining pathways; no significant caste-lifestyle interaction was detected. This conservation implies that behavioral caste roles, such as queen reproduction versus worker labor, persist despite the parasites' reliance on host workers for nest maintenance.[17] These genetic shifts correlate with observed behavioral traits, including reduced slave-maker involvement in food evaluation and heightened dependence on slave-mediated nest hygiene, as the parasites exhibit limited independent foraging proficiency. Such findings underscore how sensory gene losses facilitate the obligate delegation of survival tasks, enabling efficient raids and colony persistence in host-dependent systems.[19][17]References
- https://www.antwiki.org/wiki/Dulosis
- https://antwiki.org/wiki/images/9/91/Beibl%252C_J.%252C_Stuart%252C_R.J._et_al._2005._Six_origins_of_slavery_in_formicoxenine_ants_%252810.1007%2540s00040-005-0808-y%2529.pdf
- https://www.antwiki.org/wiki/The_Ants_Chapter_12
