scholarly journals The evolution of social parasitism in Formica ants revealed by a global phylogeny

2020 ◽  
Author(s):  
Marek L Borowiec ◽  
Stefan P Cover ◽  
Christian Rabeling
Keyword(s):  
Life History ◽  
New World ◽  
Social Parasitism ◽  
Social Parasite ◽  
Colony Foundation ◽  
Parasite Diversity ◽  
Social Parasites ◽  
Evolutionary Trajectories ◽  
Competing Hypotheses ◽  
Temporary Social Parasitism

Studying the behavioral and life history transitions from a cooperative, eusocial life history to exploitative social parasitism allows for deciphering the conditions under which changes in behavior and social organization lead to diversification. The Holarctic ant genus Formica is ideally suited for studying the evolution of social parasitism because half of its 178 species are confirmed or suspected social parasites, which includes all three major classes of social parasitism known in ants. However, the life-history transitions associated with the evolution of social parasitism in this genus are largely unexplored. To test competing hypotheses regarding the origins and evolution of social parasitism, we reconstructed the first global phylogeny of Formica ants and representative formicine outgroups. The genus Formica originated in the Old World during the Oligocene (~30 Ma ago) and dispersed multiple times to the New World. Within Formica, the capacity for dependent colony foundation and temporary social parasitism arose once from a facultatively polygynous, independently colony founding ancestor. Within this parasitic clade, dulotic social parasitism evolved once from a facultatively temporary parasitic ancestor that likely practiced colony budding frequently. Permanent social parasitism evolved twice from temporary social parasitic ancestors that rarely practiced colony budding, demonstrating that obligate social parasitism can originate from different facultative parasitic backgrounds in socially polymorphic organisms. In contrast to inquiline ant species in other genera, the high social parasite diversity in Formica likely originated via allopatric speciation, highlighting the diversity of convergent evolutionary trajectories resulting in nearly identical parasitic life history syndromes.

scholarly journals The evolution of social parasitism in Formica ants revealed by a global phylogeny

2021 ◽  
Vol 118 (38) ◽  
pp. e2026029118 ◽  
Author(s):  
Marek L. Borowiec ◽  
Stefan P. Cover ◽  
Christian Rabeling
Keyword(s):  
Life History ◽  
Common Ancestor ◽  
Social Parasitism ◽  
Colony Founding ◽  
Colony Foundation ◽  
Social Parasites ◽  
Evolutionary Trajectories ◽  
Dependent Colony Founding ◽  
High Parasite ◽  
Temporary Social Parasitism

Studying the behavioral and life history transitions from a cooperative, eusocial life history to exploitative social parasitism allows for deciphering the conditions under which changes in behavior and social organization lead to diversification. The Holarctic ant genus Formica is ideally suited for studying the evolution of social parasitism because half of its 172 species are confirmed or suspected social parasites, which includes all three major classes of social parasitism known in ants. However, the life history transitions associated with the evolution of social parasitism in this genus are largely unexplored. To test competing hypotheses regarding the origins and evolution of social parasitism, we reconstructed a global phylogeny of Formica ants. The genus originated in the Old World ∼30 Ma ago and dispersed multiple times to the New World and back. Within Formica, obligate dependent colony-founding behavior arose once from a facultatively polygynous common ancestor practicing independent and facultative dependent colony foundation. Temporary social parasitism likely preceded or arose concurrently with obligate dependent colony founding, and dulotic social parasitism evolved once within the obligate dependent colony-founding clade. Permanent social parasitism evolved twice from temporary social parasitic ancestors that rarely practiced colony budding, demonstrating that obligate social parasitism can originate from a facultative parasitic background in socially polymorphic organisms. In contrast to permanently socially parasitic ants in other genera, the high parasite diversity in Formica likely originated via allopatric speciation, highlighting the diversity of convergent evolutionary trajectories resulting in nearly identical parasitic life history syndromes.

scholarly journals The evidence of temporary social parasitism by Polyrhachis lamellidens (Hymenoptera, Formicidae) in a Camponotus obscuripes colony (Hymenoptera, Formicidae)

2021 ◽  
Author(s):  
H. Iwai ◽  
Y. Kurihara ◽  
N. Kono ◽  
M. Tomita ◽  
K. Arakawa
Keyword(s):  
Nestmate Recognition ◽  
Social Parasitism ◽  
Field Observations ◽  
Behavioral Tests ◽  
Colony Foundation ◽  
Social Parasites ◽  
Mixed Brood ◽  
Recognition Ability ◽  
Temporary Social Parasitism ◽  
Rearing Experiment

AbstractPolyrhachis lamellidens is a temporary socially parasitic ant whose new queen utilizes other ant species in the early stages of colony foundation. Field observations and rearing experiments suggest that Camponotus japonicus is a host species of P. lamellidens. It is presumed that Camponotus obscuripes is also a host of P. lamellidens by rearing experiments and field observations; however, there are no records of P. lamellidens workers or brood coexisting in C. obscuripes colonies in field observations, and there is no clear evidence that C. obscuripes is a natural host of P. lamellidens. We conducted detailed field observations, behavioral tests, and rearing experiments to show that C. obscuripes is a host of temporary social parasites. We found colonies with P. lamellidens queens, workers, and larvae intermixed with C. obscuripes workers in the field. Behavioral tests showed that workers of both species in mixed colonies did not attack each other and maintained nestmate recognition ability, which suggests a collaborative nestmate relationship. Furthermore, a rearing experiment confirmed social parasitism by P. lamellidens among C. obscuripes by producing a mixed brood-producing colony. These are the first field and laboratory records of temporary social parasitism involving P. lamellidens and C. obscuripes.

scholarly journals Two new species of socially parasitic Nylanderia ants from the southeastern United States

ZooKeys ◽  
2020 ◽  
Vol 921 ◽  
pp. 23-48
Author(s):  
Steven J. Messer ◽  
Stefan P. Cover ◽  
Christian Rabeling
Keyword(s):  
United States ◽  
Life History ◽  
New Species ◽  
Southeastern United States ◽  
Social Parasitism ◽  
Life History Strategies ◽  
Social Parasite ◽  
Social Parasites ◽  
Two New Species ◽  
Worker Caste

In ants, social parasitism is an umbrella term describing a variety of life-history strategies, where a parasitic species depends entirely on a free-living species, for part of or its entire life-cycle, for either colony founding, survival, and/or reproduction. The highly specialized inquiline social parasites are fully dependent on their hosts for their entire lifecycles. Most inquiline species are tolerant of the host queen in the parasitized colony, forgo producing a worker caste, and invest solely in the production of sexual offspring. In general, inquilines are rare, and their geographic distribution is limited, making it difficult to study them. Inquiline populations appear to be small, cryptic, and they are perhaps ephemeral. Thus, information about their natural history is often fragmentary or non-existent but is necessary for understanding the socially parasitic life history syndrome in more detail. Here, we describe two new species of inquiline social parasites, Nylanderia deyrupisp. nov. and Nylanderia parasiticasp. nov., from the southeastern United States, parasitizing Nylanderia wojciki and Nylanderia faisonensis, respectively. The formicine genus Nylanderia is large and globally distributed, but until the recent description of Nylanderia deceptrix, social parasites were unknown from this genus. In addition to describing the new social parasite species, we summarize the fragmentary information known about their biology, present a key to both the queens and the males of the Nylanderia social parasites, and discuss the morphology of the social parasites in the context of the inquiline syndrome.

scholarly journals The possible role of ant larvae in the defence against social parasites

2019 ◽  
Vol 286 (1898) ◽  
pp. 20182867 ◽  
Author(s):  
Unni Pulliainen ◽  
Heikki Helanterä ◽  
Liselotte Sundström ◽  
Eva Schultner
Keyword(s):  
Host Species ◽  
Social Parasitism ◽  
Social Parasite ◽  
Social Parasites ◽  
Nest Mate ◽  
Formica Fusca ◽  
Before And After ◽  
Key Factor ◽  
Host Worker ◽  
Cuticular Profiles

Temporary social parasite ant queens initiate new colonies by entering colonies of host species, where they begin laying eggs. As the resident queen can be killed during this process, host colonies may lose their entire future reproductive output. Selection thus favours the evolution of defence mechanisms, before and after parasite intrusion. Most studies on social parasites focus on host worker discrimination of parasite queens and their offspring. However, ant larvae can also influence brood composition by consuming eggs. This raises the question whether host larvae can aid in preventing colony takeover by consuming eggs laid by parasite queens. To test whether larvae could play a role in anti-parasite defence, we compared the rates at which larvae of a common host species, Formica fusca , consumed eggs laid by social parasite, non-parasite, nest-mate, or conspecific non-nest-mate queens. Larvae consumed social parasite eggs more than eggs laid by a heterospecific non-parasite queen, irrespective of the chemical distance between the egg cuticular profiles. Also, larvae consumed eggs laid by conspecific non-nest-mate queens more than those laid by nest-mate queens. Our study suggests that larvae may act as players in colony defence against social parasitism, and that social parasitism is a key factor shaping discrimination behaviour in ants.

scholarly journals Inquiline social parasites as tools to unlock the secrets of insect sociality

2019 ◽  
Vol 374 (1769) ◽  
pp. 20180193 ◽  
Author(s):  
Alessandro Cini ◽  
Seirian Sumner ◽  
Rita Cervo
Keyword(s):  
Social Parasitism ◽  
Division Of Labour ◽  
Social Parasite ◽  
Social Parasites ◽  
Insect Societies ◽  
History Of ◽  
Reproductive Division Of Labour ◽  
Insect Sociality ◽  
Taxonomic Groups ◽  
Reproductive Division

Insect societies play a crucial role in the functioning of most ecosystems and have fascinated both scientists and the lay public for centuries. Despite the long history of study, we are still far from understanding how insect societies have evolved and how social cohesion in their colonies is maintained. Here we suggest inquiline social parasites of insect societies as an under-exploited experimental tool for understanding sociality. We draw on examples from obligate inquiline (permanent) social parasites in wasps, ants and bees to illustrate how these parasites may allow us to better understand societies and learn more about the evolution and functioning of insect societies. We highlight three main features of these social parasite–host systems—namely, close phylogenetic relationships, strong selective pressures arising from coevolution and multiple independent origins—that make inquiline social parasites particularly suited for this aim; we propose a conceptual comparative framework that considers trait losses, gains and modifications in social parasite–host systems. We give examples of how this framework can reveal the more elusive secrets of sociality by focusing on two cornerstones of sociality: communication and reproductive division of labour. Together with social parasites in other taxonomic groups, such as cuckoos in birds, social parasitism has a great potential to reveal the mechanisms and evolution of complex social groups. This article is part of the theme issue ‘The coevolutionary biology of brood parasitism: from mechanism to pattern’.

scholarly journals Brood parasitism in eusocial insects (Hymenoptera): role of host geographical range size and phylogeny

2019 ◽  
Vol 374 (1769) ◽  
pp. 20180203 ◽  
Author(s):  
Jukka Suhonen ◽  
Jaakko J. Ilvonen ◽  
Tommi Nyman ◽  
Jouni Sorvari
Keyword(s):  
Brood Parasitism ◽  
Range Size ◽  
Geographical Range ◽  
Social Parasite ◽  
Brood Parasite ◽  
Social Parasites ◽  
Brood Parasites ◽  
Eusocial Insects ◽  
Interspecific Brood Parasitism ◽  
Logistic Regressions

Interspecific brood parasitism is common in many animal systems. Brood parasites enter the nests of other species and divert host resources for producing their own offspring, which can lead to strong antagonistic parasite–host coevolution. Here, we look at commonalities among social insect species that are victims of brood parasites, and use phylogenetic data and information on geographical range size to predict which species are most probably to fall victims to brood parasites in the future. In our analyses, we focus on three eusocial hymenopteran groups and their brood parasites: (i) bumblebees, (ii) Myrmica ants, and (iii) vespine and polistine wasps. In these groups, some, but not all, species are parasitized by obligate workerless inquilines that only produce reproductive-caste descendants. We find phylogenetic signals for geographical range size and the presence of parasites in bumblebees, but not in ants and wasps. Phylogenetic logistic regressions indicate that the probability of being attacked by one or more brood parasite species increases with the size of the geographical range in bumblebees, but the effect is statistically only marginally significant in ants. However, non-phylogenetic logistic regressions suggest that bumblebee species with the largest geographical range sizes may have a lower likelihood of harbouring social parasites than do hosts with medium-sized ranges. Our results provide new insights into the ecology and evolution of host–social parasite systems, and indicate that host phylogeny and geographical range size can be used to predict threats posed by social parasites, as well to design efficient conservation measures for both hosts and their parasites. This article is part of the theme issue ‘The coevolutionary biology of brood parasitism: from mechanism to pattern’.

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