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Preemptive circular defence of immature insects: definition and occurrences of cycloalexy revisited.

1. Introduction

Some animals show a remarkable behaviour: they group in a tight circle for defence [1]. This behaviour is reminiscent of Carl von Clausewitz's 1812 Principles of War: "In strategy (...) the side that is surrounded by the enemy is better off than the side which surrounds its opponent, especially with equal or evenweaker forces" [ 2]. Many animal species employ this strategy. For example, among vertebrates, muskoxen (Ovibos moschatus, Blainville, 1816) form a circle enclosing the young calves when attacked by wolves, their principal natural predators [3, 4]. Their circular formation protects the most vulnerable body parts while the extremity that is best defended or involved in attack is at the periphery. Vasconcellos-Neto and Jolivet [5] coinedthe term "cycloalexy (kuklos = circle, alexo = defend)" to describe a particular behaviour of gregarious insect larvae. They defined their new term as "the attitude adopted at rest by some insect larvae, both diurnal and nocturnal, in a tight circle where either the heads or ends of the abdomen are juxtaposed at the periphery, with the remaining larvae at the center of the circle. Coordinated movements such as the adoption of threatening attitudes, regurgitation, and biting, are used to repel predators or parasitoids." [1]. Several elements of the original definition distinguish cycloalexy from other circular formations occurring in nature.

However, as new examples of the behaviour have been proposed in the literature without addressing key aspects of the original definition, the distinctions between cycloalexic behaviour and other circular formations have become imprecise and weakened the concept of cycloalexy. Here, we will review reported examples of cycloalexy and question whether they meet the criteria of a revised definition or are alternative forms of aggregation. Our revised definition strives to adhere to the key aspects of cycloalexy as originally defined, while removing arbitrary and unnecessary criteria. This way, cycloalexy can be recognized as an evolutionarily convergent behaviour rather than several superficially similar behaviours.

1.1. Redefining Cycloalexy. The defensive nature of cycloalexy is paramount as it is found in the etymology of the term: "to defend" [11]. However, this key aspect of the behaviour can be problematic since cycloalexy has often been invoked upon fragmentary observations of groups rather than controlled ecological studies. Nevertheless, until species can be more thoroughly studied, we suggest that three criteria are sufficient to distinguish cycloalexy from other behaviours.

Criterion 1: Individuals Are Arranged in a Circle. The original definition specified "in a tight circle" [1], but we argue that tightness is subjective and should be removed from the definition.

Criterion 2: The Extremity Bearing Defensive Attribute Is Positioned Outwards. In the original definition, the periphery of the circle is uniform: "either the heads or ends of the abdomen are juxtaposed at the periphery" [1], sometimes with individuals at the centre with neither head nor abdomen reaching the periphery. This means that peripheral individuals in a given group face outwards or inwards, but not both. We argue that, in this statement, it was implicit that the best defended extremity is at the periphery since it is unlikely that individuals with their vulnerable side out could ever be at an advantage. Uniformity of the circle in this respect, then, becomes a corollary of our second criterion.

Criterion 3: The Circle Is Adopted as a Resting Formation. Following the original definition, we limit cycloalexy to cases when individuals are in resting or quiescent, nonfeeding periods. This makes cycloalexy a preemptive behaviour.

These criteria allow for the initial identification of cycloalexy by rapid, visual assessment. If later studies disprove defensiveness, then the behaviour studied is not cycloalexy. Additionally, although not specified in the original definition, we suggest adding the distinction that the behaviour is for the defence of the individuals themselves and others within the group, as opposed to the defence of a resource or nest. We also suggest removing the criterion that "Coordinated movements such as the adoption of threatening attitudes, regurgitation, and biting, are used to repel predators or parasitoids" [1], for several reasons. Cycloalexy is notably preemptive, taken regardless of the immediate presence of a threat; in some species, immature animals have passive defences made more efficient by a circular formation; and the second criterion of our amended definition already includes defence, either passive or active. Finally, although the original definition was limited to insect larvae, in this paper, we review all reports of cycloalexy and suggest removing the limitation altogether.

2. Results

See Table 1.

3. Discussion

3.1. Strict Cycloalexy. Among the records in the literature, some species demonstrate behaviour that precisely fit the revised definition and our three essential criteria of cycloalexy (Table 1). This is the case of Coelomera spp. (Coleoptera: Chrysomelidae: Galerucinae) and spitfire grubs Perga dorsalis Leach, 1817 (Hymenoptera: Tenthredinoidea: Pergidae) [1].

Approximately 35 species of genus Coelomera are cycloalexic and feed on Cecropia (Urticaceae). Most Cecropia plants are myrmecophytes protected by mutualistic Azteca ants (Formicidae: Dolichoderinae). The gregarious leaf beetle larvae feed during the day and rest at night, in a tight circular cluster with heads inside and abdomens at the periphery [7, 8]. Their rear end is protected by a supra-anal shield and, when threatened, these larvae excrete a nauseating fluid from the anus. Therefore, the better protected part of the insect, the posterior, is facing outwards in the circle, with the more vulnerable head inside [7, 8]. Thus, by orienting the same way, individual larvae protect themselves and other members of the group (Figures 1 and 2).

Spitfire grubs Perga dorsalis feed on Eucalyptus during the night and rest during the day in a circular formation [47]. The larvae rest with their heads at the periphery of the circle, with some larvae in the middle of the aggregation. When threatened, the larvae rear their heads and abdomens and regurgitate oils sequestered from their host Eucalyptus [47]. The oils are an effective deterrent of potential predators, including ants, birds, and mice [49]. The heads are the better protected part of the insects and, again, form the periphery of the circle.

3.2. Examples of Cycloalexy That Do Not Agree with the Revised Definition

3.2.1. The Oxymoron of Noncircular Cycloalexy. Gregarious caterpillars of genus Arsenura (Saturniidae: Arsenurinae) are reported to "show a kind of cycloalexy when resting on tree trunks during the day" [1]. The caterpillars align side-by-side or head-to-abdomen or both, in an elongated oval cluster [11]. The posture of these caterpillars with their heads, sides, and abdomens at the periphery in a linear mass rather than a circle does not meet the first criterion of the revised definition of cycloalexy. The circle formation with the best defended extremity outwards is an important characteristic of cycloalexic behaviour. Arsenura are gregarious and rest in a tightly aggregated mass, but they are not cycloalexic. Santiago-Blay et al. [11] suggest that, on a tree trunk, "the available background surface makes the shape of the larval aggregation distorted." However, on the scale of a caterpillar, and depending on the diameter of the tree, a tree trunk can be quite large and nearly flat. In addition, probable cycloalexy on tree trunks has been observed in Lonomia sp. (Figure 3(b)). We suggest the caterpillar aggregations described by Santiago-Blay et al. [11] are less circular and compact not because of the shape of tree trunks but because Arsenura caterpillars' resting positions are not cycloalexic.

3.2.2. Mixed Head Orientations. Larvae of the owlfly Ascaloptynx furciger (McLachlan, 1891) (Neuroptera: Ascalaphidae) are gregarious. After eclosion and their first meal of abortive eggs, they settle head-downwards on and around the twig on which they were laid [58]. Jolivet et al. [1] deem the behaviour of A. furciger is "not strictly cycloalexy but related to it" since the owlfly larvae all point in the same downward direction: this does not meet the second criterion of the revised definition. We agree with Jolivet and Verma [12] that cycloalexy exists around twigs and is not restricted to flat surfaces. However, even on small branches, cycloalexic larvae collectively orient their heads either outwards or inwards, but not both. This is true for larvae of Perga sp. (Hymenoptera: Tenthredinoidea: Pergidae) (Figure 3(a)), Omaspides tricolorata (Boheman, 1854) [39], and this arrangement is retained in the pupae of Omaspides pallidipennis (Boheman, 1854) (Chrysomelidae: Cassidinae) [37]. For owlfly larvae, heads form the periphery at the bottom of the aggregation and abdomens are at the periphery on top, but unlike Cassidinae or Coelomera larvae, their abdomens are more vulnerable. It is more accurate to describe the behaviour as unidirectional defence rather than circular defence; larvae are only protected from predators walking up to the group. Secondly, larvae also feed while, in this position, making it a passive hunting formation and not only a resting position [58]. Because they do not meet the second and third criteria, we question reports of cycloalexy in Neuroptera [7, 11, 12, 64].

3.2.3. Nonresting Behaviours. As stated in the third criterion, cycloalexy is adopted preemptively by animals at rest. When immature insects are active and feeding, the circular formation is normally broken (Figure 4). Larvae of Plagiodera versicolora (Laicharting, 1781) and other Plagiodera species form a loose circle when feeding and at rest, with individual larvae not consistently facing outwards or inwards [22, pers. obs.]. Hence their formation is not an example of cycloalexy. Their formation is not only adopted at rest but also while feeding and is often influenced by the shape of the leaf, with multiple "feeding rings" on larger leaves [22]. Some authors [11] feel that cycloalexy facilitates feeding in P versicolora as well as in sawflies. Larval aggregations can increase feeding efficiency through synchronized, coordinated, and spatially concentrated feeding [23-25].The size of P versicolora groups does not influence survival of larvae, but does help with feeding [25]. Thus, available evidence suggests grouping in P. versicolora is related principally to the process of feeding rather than defence.

3.2.4. Nondefensive Behaviour. Cycloalexy is a defensive behaviour; it protects individuals from predation or parasitism. Yet, some reported behaviours are not defensive. Such is the case for huddling in Antarctic penguins, where the huddle is a resting behaviour, usually with heads inwards, but it is for heat conservation rather than defence [63]. For these reasons, we disagree with Jolivet and Verma [12] that penguins are cycloalexic.

To conclusively prove the defensive value of a behaviour, ecological studies are needed. Yet, for many species, the defensive value of cycloalexy has been inferred from anecdotal evidence or personal observations or has simply been presumed. For example, the defensive value of cycloalexy in Phelypera distigma larvae is supported by the following statement: "P distigma larvae are not harvested by polistine wasps, ants, spiders, and other generalist predators that readily harvest caterpillars in dry forest habitats (D. H. Janzen, pers. obs.)" [65].

Rather than rejecting the many reports of cycloalexy on the basis of insufficient ecological studies, we propose that defensive nature of the aggregation can be accepted if the animals meet the other criteria: they are in a circle, taken preemptively with defensive armature uniform at the periphery. When ecological studies are conducted, if defensiveness is disproved, then the behaviour is another type of aggregation and not cycloalexy. This is the case for larval aggregations of Plagiodera versicolora: ecological studies were conducted and the survival of larvae is not significantly influenced by group size [25].

3.2.5. Circular Formations That Do Not React to Threats. The original definition of cycloalexy requires coordinated movements in response to threats [1]. We disagree with this requirement: in some larvae with passive protection, like the exuvial or exuvio-fecal shields of tortoise beetles, the circular groups do not always use coordinated movements when threatened by predators. For example, the larvae of Conchyloctenia punctata (Fabricius, 1787) (Cassidinae) are passively protected by their shields but do not have coordinated reactions to threats [30]. In our opinion, larvae of C. punctata meet the basic criteria of cycloalexy. Although coordinated group reactions to threats are an indication of the defensive nature of the group, we propose it is not an essential criterion for cycloalexy.

The removal of this criterion is also important for several taxa in which the larvae receive maternal care. Cassidinae larvae in maternal care species (e.g., species of genera Acromis, Omaspides, Paraselenis, and Eugenysa) generally have reduced fecal shields and do not always react defensively when threatened. Larval grouping in these species can be considered as increasing the efficiency of maternal guarding. In these cases, all criteria of the revised definition are met: larvae are in a circle, the best defended extremity is always at the periphery, and the circle is the default resting position. Thus, we consider larval aggregations in these maternal care species as further examples of cycloalexy (Table 1).

Similarly, larvae of several chrysomelines rest in tight circular groups with the heads pointing inwards: Doryphora paykulli (Stal, 1859), D. reticulata Fabricius, 1787, Platyphora microspina (Bechyne, 1954),P. selva Daccordi, 1993, Proseicela vittata (Fabricius, 1781), P. spectabilis (Baly, 1858), P.bicruciata Jacoby, 1880 and Pr. sp. nov. "Yasuni" [15]. All these species also have maternal care, and when disturbed, larvae do not have coordinated defensive reactions. Instead, the mother acts as the defensive element of the formation (Figure 5(a)) [15]. Is this behaviour still cycloalexy? In other words, should the defensive element obligatorily be found, at least in part, in the larvae? To this question, our answer is yes, through the second criterion. In Cassidinae larvae, the furca and shield are obvious defensive attributes positioned at the periphery. In Chrysomelinae, the best defended extremity is less obvious. Cycloalexic larvae of nonmaternal care Chrysomelinae face outwards. Their best defended extremity is the head and thorax, through regurgitation and biting [7]. We hypothesize that, in species with maternal care, the individuals face inwards not because the best defended extremity is the abdomen but because of herding by the mother, and thus, these species do not meet the second criterion of the revised definition. Ultimately, only ecological and evolutionary studies will provide a clear answer.

3.2.6. Adult Insects. We use Apoica as an example even though cycloalexy was not explicitly reported in this genus. During the day, these nocturnal wasps rest on the circular or nearly circular lower surface of their nests [52-54]. The wasps rest facing outwards, resulting in a circular formation that could loosely be termed cycloalexy. When disturbed, the formation breaks up as wasps fly off the nest. Even though this behaviour meets several criteria of the revised definition, we argue it is not cycloalexic because the shape of the nest or nest entrance explains the circular formation. In a similar fashion, stingless bees of genus Trigona (Apidae: Meliponinae) are not cycloalexic as suggested by Vasconcellos-Neto and Jolivet [7]. In this case, fully developed individuals are not even at rest: in most Meliponinae, the nest entrance is protected by bees positioned in or around the entrance tube and, at night, the entrance is closed [51]. The bees are not resting but are actively guarding and the ring formation is an artefact of the nest entrance shape.

These examples motivate limiting and specifying cycloalexy as a formation taken by individuals, whether immature or adult, for increased individual and mutual defences, thus excluding formations taken for defence of a nest, brood, or food stores. We argue that evolution of circular nests and resource guarding may have little to do with the evolution of cycloalexy.

3.2.7. Circular Defence in Vertebrates and the Selfish Herd. Several authors compare cycloalexy to the "circle-the-wagons" formation employed by American pioneers to defend themselves against Native Americans [1,11,12, 24]. In Jolivet et al. [1] and Jolivet and Verma [12], the authors discuss behaviours analogous to cycloalexy in vertebrates: muskoxen (Ovibos moschatus), eland (Taurotragus oryx (Pallas, 1766)), elk (Cervus canadensis (Erxleben, 1777)), and penguins. The authors do not provide citations for the behaviour in eland or elk and cite Wilson [4] for descriptions of this behaviour in muskoxen and penguins. Wilson [4] does not mention penguins in this manner but does mention similar behaviours in several terrestrial ungulates and killer whales (Orcinus orca (Linnaeus, 1758)) ([3, 66-69]; all page 45 in [4]). Wilson [4] describes elk grazing in a "windrow" formation but does not mention circular defence [70] and [4, page 45]. We agree that several vertebrates employ defensive circular formations analogous to cycloalexy. However, we would not broaden the definition to include these behaviours. Unlike invertebrates, mammals do not use circular defence when resting but take the formation when threatened. This does not meet the third criterion of the revised definition. In cycloalexic species, the circular formation is the main resting position. The circular defence of vertebrates is reactive, while cycloalexy in invertebrates is largely preemptive.

Hamilton used herding animals as an example of how individuals may form a group to lessen individual chances of falling to a predator without reducing overall predation [71]. Hamilton then cited the circular defence of muskoxen as a potential exception to the selfish herd theory but attributes it to selfish reasons: "they are probably connected on the one hand with the smallness of the risk taken and, on the other, with the closeness of the genetical relationship of the animals benefited" [71]. Because cycloalexy may lessen both overall and individual predation risk, it can also be considered selfish. Cycloalexy can be explained by animals exploiting the best defended extremity of nearby individuals. The preemptive aspect of arthropod cycloalexy also distinguishes it from muskoxen circular defence and Hamilton's selfish herds and may therefore provide interesting systems for study of group defence.

3.2.8. Cycloalexy in Immature Hemimetabolous Insects. We report cycloalexy in Anactinothrips nigricornis Hood, 1936 (Thysanoptera). We observed a group of 14 thrips, in their pupal instar, forming a tight circle with abdomens outwards on a leaf of the woody vine Maripa panamensis Hemsl. (Convolvulaceae) (Figure 5(b)). When disturbed, the threatened individuals and those beside them waved their abdomen. When disturbance continued, a brown liquid was exuded and formed a droplet at the end of the abdomen. The group was then further disturbed and the individuals dispersed. Approximately an hour later, the thrips had reassembled in a circular resting formation. In the lab, after the final moult, the adult thrips dispersed in the container in which they were kept. Similar observations were made in another species of the same genus: the thrips A. gustaviae, Mound and Palmer, 1983, rest in bivouacs and exude a defensive liquid from their abdomen when disturbed 59, 72].

The behaviour was observed in the mobile pupal stage rather than in the larvae. This goes against the original definition but meets all other criteria and assuming it is defensive, we consider the behaviour is cycloalexy. Thus, we propose to remove the taxonomical restriction of the original definition.

3.3. Common Traits of All Cycloalexic Species. When the revised definition of cycloalexy is strictly applied, a set of traits common to all species becomes apparent. Foremost, all cycloalexic species are insects with gregarious immature stages. Gregarious lifestyles have implications in terms of cooperative feeding and continued group cohesion through chemical, tactile, or acoustic communication [24].

To date, all cycloalexic species appear to use chemical defences of one sort or another. The cycloalexic larvae in genera Lema (Criocerinae) and Platyphora (Chrysomelinae) regurgitate when threatened [7, 9]. The larvae of Forcipomyia have paired setae on the head, thorax, and abdomen that exude hygroscopic substances that repel ants [44]. The chemical defences of gregarious Lonomia caterpillars are so potent that the resulting trauma caused by venom injected from their setae can be lethal to humans [73]. Most tortoise beetle larvae carry an exuvial or exuvio-fecal shield on the furca of their eighth abdominal segment which serves as a mechanical or chemical barrier against predators [74-76]. In all cases, the best protected extremity faces outwards.

Furthermore, all the species that exhibit cycloalexic behaviour are miniature grazers, and most feed on leaves. This is the case for cycloalexic caterpillars, and larvae of sawflies [47], weevils, and leaf beetles [7, 40]. Some feed on fungal hyphae, such as Forcipomyia fuliginosa (Meigen, 1818) midge larvae [42], and the rest graze on lichen, like Anactinothrips gustaviae thrips [59].

Gregarious lifestyles, chemical defence, and grazing groups of immature insects are all traits of Costa's [24] "larval herd" syndrome of group living. Like cycloalexy, parental care is only present in some of these larval herds [24]. Possibly, the slow-moving and exposed lifestyle of these immature insects makes them more vulnerable to predators and parasitoids [24, 77]. Increased threats probably explain the multiple defences of insect herbivores, including chemical defence whose evolution generally precedes that of aggregation [78].

4. Conclusion

Several immature insects exhibit cycloalexy, a behaviour whose definition we have amended to: "A preemptive defence employed at rest, where individuals form a circle with their best defended extremity exposed at the periphery. Sometimes remaining individuals rest at the centre of the circle."

In leaf beetles (Chrysomelidae), cycloalexy with abdomens oriented outwards is found in one genus of skeletonizing leaf beetles (Galerucinae: Coelomera spp.), at least fifteen tortoise beetle genera (Cassidinae), two genera of shining leaf beetles (Criocerinae: Lema and probably Lilioceris), and several genera of broad-shouldered leaf beetles (Chrysomelinae: Platyphora, probably Chrysophtharta and tentatively Eugonycha and Pterodunga). Cycloalexy with heads outwards is found in some sawflies (Tenthredinoidea: Pergidae: Perga spp. and Argidae: Themos olfersii (Klug, 1834)) of Australia and Brazil. Social caterpillars often form aggregations, but these aggregations are rarely cycloalexic. However, caterpillars of Lonomia spp. (Saturniidae: Hemileucinae) are probably cycloalexic and Papilio laglaizei Depuiset, 1877 (Papilionidae) are tentatively cycloalexic. One weevil Phelypera distigma (Boheman, 1842) (Curculionidae) is cycloalexic and one midge Forcipomyia fuliginosa (Ceratopogonidae) exhibits cycloalexy. We propose that some immature thrips are also probably cycloalexic and suggest formally changing the definition of cycloalexy to remove taxonomical restrictions so that any animals that meet all other criteria of the definition can be included. New instances of cycloalexy will undoubtedly be discovered. For example, Platydesmid millipedes sometimes aggregate in a tentatively analogous fashion.

Several reports of cycloalexy do not meet one or more of the revised definition criteria, including reports of cycloalexy in feeding aggregations of Hemiptera and larvae of Hymenopteran parasitoids. The behaviour has also been mistakenly attributed to adult Hymenoptera, for example, stingless bees (Apidae: Meliponinae), ants (Formicidae), and wasps (Vespidae), guarding their nest. This is active protection of a nest and not cycloalexy. Similarly, the term has been applied to the circular assembly of an amphipod crustacean which helps the mother herd the larvae. Owlfly larvae (Neuroptera: Ascalaphidae: Ascaloptynx furciger) form unidirectional defensive groups which are not cycloalexic, allowing larvae to feed without changing position. Defensive circles are sometimes observed in mammals: muskoxen, eland, water buffalo, red deer, and killer whales. Contrary to cycloalexy, the defensive formations in these mammals are a reaction to imminent threat. Other vertebrates, like penguins, huddle to reduce heat loss.

Application of a more precise definition of cycloalexy, as provided by Jolivet et al. [1] and revised here, may make unravelling the evolution of cycloalexic behaviour more tractable. Much remains to be learned about whether larval aggregation, cycloalexy, sequestration of plant metabolites, and maternal care are alternative defensive strategies or are honed evolutionary responses to particular threats. Chrysomeline leaf beetles are an ideal group for using phylogenetic reconstruction and character analysis of these behaviours to unravel the number of independent evolutionary origins of cycloalexy and larval aggregation.

http://dx.doi.org/10.1155/2014/642908

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work was funded by the Natural Sciences and Engineering Research Council of Canada (NSERC), the Fonds de recherche du Quebec Nature et technologies (FQRNT), McGill University, the Smithsonian Tropical Research Institute, and the Entomological Society of Quebec. The authors thank Dr. Laurence Mound (CSIRO) for identifying the thrips from Panama.

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Guillaume J. Dury, (1,2) Jacqueline C. Bede, (1) and Donald M. Windsor (2)

(1) Department of Plant Science, McGill University, 21111 Lakeshore Road, Sainte-Anne-de-Bellevue, QC, Canada H9X 3V9

(2) Smithsonian Tropical Research Institute, Apartado 0843-03092, Balboa, Ancon, Panama City, Panama

Correspondence should be addressed to Guillaume J. Dury; guillaume.dury@mail.mcgill.ca

Received 6 December 2013; Accepted 13 February 2014; Published 24 March 2014

Academic Editor: Jacques Hubert Charles Delabie

TABLE 1: Reported cases of cycloalexy and how they fit within the
revised definition.

                                              Criteria

                                                 1
Organism                                      Circular
                                             formation

Coleoptera: Chrysomelidae:
Galerucinae
Coelomera spp.; for example,
C. ruficornis Baly, 1865;                       Yes
C. helenae Jolivet, 1987;
C. raquia Bechyne, 1956; and so forth
Dircema spp.                                Not observed

Coleoptera: Chrysomelidae: Criocerinae
Lema sp.;
Lema apicalis Lacordaire, 1845 and              Yes
L. reticulosa Clark, 1866
Lilioceris nigropectoralis (Pic, 1928),         Yes
L. formosana Heinze, 1943

Coleoptera: Chrysomelidae:
Chrysomelinae                               Not observed
Agrosteomela chinensis (Weise, 1922)
Chrysophtharta obovata (Chapuis, 1877)          Yes
Doryphora paykulli (Stal, 1859), D.             Yes
reticulata Fabricius, 1787
Eugonycha melanostoma (Stal, 1859)              Yes
Gonioctena sibirica Kimoto, 1994              Roughly
Labidomera suturella Guerin-Meneville,          Not
1838                                          observed
Paropsis spp.; for example,
P. aegrota Boisduval, 1835,                 Not circular
P. maculata (Marsham, 1908),
P. atomaria Olivier, 1807 and
P. tasmanica Baly, 1864
Paropsisterna spp.                          Not reported
Plagiodera spp. for example,                Not circular
P. versicolora (Laicharting, 1781)
                                                Not
Phratora spp.                                 observed
Phyllocharis undulata (Linnaeus, 1763)        Roughly
Platyphora selva Daccordi, 1993,                Yes
P. microspina (Bechyne, 1954)
Platyphora conviva (Stal, 1858),
P. anastomozans (Perty, 1832),
P. nigronotata (Stal, 1857),                    Yes
P. nitidissima (Staal, 1857)
P. fasciatomaculata (Staal, 1857),
P. vinula (Stal, 1858)

Proseicela vittata (Fabricius, 1781),           Yes
P. bicruciata Jacoby, 1880,
P spectabilis (Baly, 1858)
Proseicela crucigera (Sahlberg, 1823)           Yes
Pterodunga mirabile Daccordi, 2000              Yes

Coleoptera: Chrysomelidae: Cassidinae
Acromis sparsa (Boheman, 1854)                  Yes
Aspidomorpha puncticosta Boheman,
1854,                                           Yes
A. miliaris (Fabricius, 1775)
Chelymorpha informis Boheman, 1854,
C. alternans Boheman, 1854,                     Yes
C. cribraria (Fabricius, 1875)
Cistudinella foveolata (Champion, 1894)         Yes
Conchyloctenia punctata (Fabricius, 1787)       Yes
Coptocycla dolosa Boheman, 1855                 Yes
Eugenysa columbiana (Boheman, 1850),            Yes
E. coscaroni Viana, 1968
Paraselenis flava (Linnaeus, 1758)              Yes
Nuzonia sp.                                     Yes
Ogdoecosta biannularis (Boheman, 1854)          Yes
Omaspides tricolorata (Boheman, 1854),          Yes
O. pallidipennis (Boheman, 1854),
O. sobrina (Boheman, 1854),
O. bistriata (Boheman, 1854) and
O. convexicollis Spaeth, 1909
Physonota alutacea Boheman, 1854                Yes
Polychalma multicava (Latreille, 1821)          Yes
Stolas sp., Stolas xanthospila                  Yes
(Champion, 1893)

Coleoptera: Curculionidae: Hyperinae
Phelypera distigma (Boheman, 1842)              Yes

Diptera: Ceratopogonidae:
Forcipomyiinae
Forcipomyia fuliginosa (Meigen, 1818)           Yes

Hemiptera Not specified                     Not reported
Ceroplastes sp. (Coccidea),
Potnia sp. (Membracidae),                    Roughly to
Nephesa rosea (Spinola, 1839) (Flatidae),   not circular
Derbe sp. (Derbidae)
Antiteuchus tripterus (Fabricius, 1787)         Yes
(Pentatomidae)
Parastrachiajaponensis (Scott, 1880)            Yes
(Parastrachiidae)

Hymenoptera: Tenthredinoidea Bergiana           Yes
sp. (Cimbicidae)
Perga dorsalis Leach, 1817, P affinis           Yes
Kirby, 1882 (Pergidae)
Pseudoperga guerini (Westwood, 1880)            Yes
(Pergidae)
Themos olfersii (Klug, 1834) (Argidae)          Yes
Dielocerus diasi Smith, 1975 (Argidae)      Not reported

Hymenoptera: other superfamilies                Yes
Trigona sp. (Apidae: Meliponinae)
Adult Hymenoptera, bees (Apidae),               Some
wasps (Vespidae),                            circular,
Conomyrma spp. and numerous other ants        some not
(Formicidae)
Apoica sp. (Vespidae: Polistinae)               Yes
"Parasitic Hymenoptera larvae and               Yes
pupae [on] their host"

Lepidoptera: Papilionidae: Papilioninae         Yes
Papilio laglaizei Depuiset, 1877

Lepidoptera: Saturniidae                      Unclear
Hylesia spp. (Hemileucinae)
Lonomia spp. (Hemileucinae)                     Yes

Arsenura spp. (Arsenurinae)                 Not circular

Lepidoptera: other families Noctuidae and   Not circular
Sphingidae

Neuroptera: Ascalaphidae
Ascaloptynx furciger (McLachlan, 1891)
                                                twig
Thysanoptera: Phlaeothripidae                   Yes
Anactinothrips nigricornis Hood, 1936 and
A. gustaviae Mound & Palmer, 1983

Non-insect arthropods Phronima                  Yes
sedentaria (Forskal, 1775)
(Crustacea: Amphipoda: Hyperiidea)
Platydesmidae, Unidentified sp.                 Yes
(Myriapoda)

Vertebrates
Some ungulates, for example,                    Yes
Muskoxen Ovibos moschatus
(Zimmermann, 1780) Antarctic                    Yes
penguins

                                                    Criteria

                                                       2
Organism                                         Best defended
                                                  extremity at
                                                 the periphery

Coleoptera: Chrysomelidae:
Galerucinae
Coelomera spp.; for example,
C. ruficornis Baly, 1865;                        Yes, abdomens
C. helenae Jolivet, 1987;
C. raquia Bechyne, 1956; and so forth
Dircema spp.                                      Not observed

Coleoptera: Chrysomelidae: Criocerinae
Lema sp.;
Lema apicalis Lacordaire, 1845 and                 Yes, heads
L. reticulosa Clark, 1866
Lilioceris nigropectoralis (Pic, 1928),            Yes, heads
L. formosana Heinze, 1943

Coleoptera: Chrysomelidae:
Chrysomelinae
Agrosteomela chinensis (Weise, 1922)              Not observed
Chrysophtharta obovata (Chapuis, 1877)           Yes, abdomens
Doryphora paykulli (Stal, 1859), D.                 Unclear,
reticulata Fabricius, 1787                          abdomens
Eugonycha melanostoma (Stal, 1859)             Unclear, abdomens
Gonioctena sibirica Kimoto, 1994            Unclear, mostly abdomens
Labidomera suturella Guerin-Meneville,            Not observed
1838
Paropsis spp.; for example,
P. aegrota Boisduval, 1835,                  No, mixed extremities
P. maculata (Marsham, 1908),
P. atomaria Olivier, 1807 and
P. tasmanica Baly, 1864
Paropsisterna spp.                                Not reported
Plagiodera spp. for example,                 No, mixed extremities
P. versicolora (Laicharting, 1781)

Phratora spp.                                     Not observed
Phyllocharis undulata (Linnaeus, 1763)      Unclear, mostly abdomens
Platyphora selva Daccordi, 1993,               Unclear, abdomens
P. microspina (Bechyne, 1954)
Platyphora conviva (Stal, 1858),
P. anastomozans (Perty, 1832),
P. nigronotata (Stal, 1857),                       Yes, heads
P. nitidissima (Staal, 1857)
P. fasciatomaculata (Staal, 1857),
P. vinula (Stal, 1858)

Proseicela vittata (Fabricius, 1781),          Unclear, abdomens
P. bicruciata Jacoby, 1880,
P spectabilis (Baly, 1858)
Proseicela crucigera (Sahlberg, 1823)          Unclear, abdomens
Pterodunga mirabile Daccordi, 2000             Unclear, abdomens

Coleoptera: Chrysomelidae: Cassidinae
Acromis sparsa (Boheman, 1854)                   Yes, abdomens
Aspidomorpha puncticosta Boheman,
1854,                                            Yes, abdomens
A. miliaris (Fabricius, 1775)
Chelymorpha informis Boheman, 1854,
C. alternans Boheman, 1854,                      Yes, abdomens
C. cribraria (Fabricius, 1875)
Cistudinella foveolata (Champion, 1894)          Yes, abdomens
Conchyloctenia punctata (Fabricius, 1787)        Yes, abdomens
Coptocycla dolosa Boheman, 1855                  Yes, abdomens
Eugenysa columbiana (Boheman, 1850),             Yes, abdomens
E. coscaroni Viana, 1968
Paraselenis flava (Linnaeus, 1758)               Yes, abdomens
Nuzonia sp.                                      Yes, abdomens
Ogdoecosta biannularis (Boheman, 1854)           Yes, abdomens
Omaspides tricolorata (Boheman, 1854),           Yes, abdomens
O. pallidipennis (Boheman, 1854),
O. sobrina (Boheman, 1854),
O. bistriata (Boheman, 1854) and
O. convexicollis Spaeth, 1909
Physonota alutacea Boheman, 1854                 Yes, abdomens
Polychalma multicava (Latreille, 1821)           Yes, abdomens
Stolas sp., Stolas xanthospila                   Yes, abdomens
(Champion, 1893)

Coleoptera: Curculionidae: Hyperinae
Phelypera distigma (Boheman, 1842)                 Yes, heads

Diptera: Ceratopogonidae:
Forcipomyiinae
Forcipomyia fuliginosa (Meigen, 1818)            Yes, abdomens

Hemiptera Not specified                           Not reported
Ceroplastes sp. (Coccidea),
Potnia sp. (Membracidae),                          No, mixed
Nephesa rosea (Spinola, 1839) (Flatidae),         extremities
Derbe sp. (Derbidae)
Antiteuchus tripterus (Fabricius, 1787)        Unclear, abdomens
(Pentatomidae)
Parastrachiajaponensis (Scott, 1880)                Unclear,
(Parastrachiidae)                                   abdomens

Hymenoptera: Tenthredinoidea Bergiana             Not reported
sp. (Cimbicidae)
Perga dorsalis Leach, 1817, P affinis              Yes, heads
Kirby, 1882 (Pergidae)
Pseudoperga guerini (Westwood, 1880)               Yes, heads
(Pergidae)
Themos olfersii (Klug, 1834) (Argidae)             Yes, heads
Dielocerus diasi Smith, 1975 (Argidae)            Not reported

Hymenoptera: other superfamilies                   Yes, heads
Trigona sp. (Apidae: Meliponinae)
Adult Hymenoptera, bees (Apidae),
wasps (Vespidae),                              Yes, usually heads
Conomyrma spp. and numerous other ants
(Formicidae)
Apoica sp. (Vespidae: Polistinae)                  Yes, heads
"Parasitic Hymenoptera larvae and                   Unclear,
pupae [on] their host"                              abdomens

Lepidoptera: Papilionidae: Papilioninae          Unclear, heads
Papilio laglaizei Depuiset, 1877

Lepidoptera: Saturniidae                          Not reported
Hylesia spp. (Hemileucinae)
Lonomia spp. (Hemileucinae)                     Probably, heads
                                                   No, mixed
Arsenura spp. (Arsenurinae)                       extremities

Lepidoptera: other families Noctuidae and          No, mixed
Sphingidae                                        extremities

Neuroptera: Ascalaphidae
Ascaloptynx furciger (McLachlan, 1891)             No, mixed
                                                  extremities
Thysanoptera: Phlaeothripidae                    Yes, abdomens
Anactinothrips nigricornis Hood, 1936 and
A. gustaviae Mound & Palmer, 1983

Non-insect arthropods Phronima                  Unclear, heads?
sedentaria (Forskal, 1775)
(Crustacea: Amphipoda: Hyperiidea)
Platydesmidae, Unidentified sp.                Unclear, abdomens
(Myriapoda)

Vertebrates
Some ungulates, for example,                       Yes, heads
Muskoxen Ovibos moschatus
(Zimmermann, 1780) Antarctic                     Unclear, backs
penguins

                                              Criteria

                                                 3
Organism                                    Default rest
                                              position

Coleoptera: Chrysomelidae:
Galerucinae
Coelomera spp.; for example,
C. ruficornis Baly, 1865;                       Yes
C. helenae Jolivet, 1987;
C. raquia Bechyne, 1956; and so forth
Dircema spp.                                Not observed

Coleoptera: Chrysomelidae: Criocerinae
Lema sp.;
Lema apicalis Lacordaire, 1845 and              Yes
L. reticulosa Clark, 1866
Lilioceris nigropectoralis (Pic, 1928),         Yes
L. formosana Heinze, 1943

Coleoptera: Chrysomelidae:
Chrysomelinae                               Not observed
Agrosteomela chinensis (Weise, 1922)
Chrysophtharta obovata (Chapuis, 1877)          Yes
Doryphora paykulli (Stal, 1859), D.             Yes
reticulata Fabricius, 1787
Eugonycha melanostoma (Stal, 1859)          Not reported
Gonioctena sibirica Kimoto, 1994               Mostly
Labidomera suturella Guerin-Meneville,          Not
1838                                          observed
Paropsis spp.; for example,
P. aegrota Boisduval, 1835,                      No
P. maculata (Marsham, 1908),
P. atomaria Olivier, 1807 and
P. tasmanica Baly, 1864
Paropsisterna spp.                          Not reported
Plagiodera spp. for example,                     No
P. versicolora (Laicharting, 1781)
                                                Not
Phratora spp.                                 observed
Phyllocharis undulata (Linnaeus, 1763)           No
Platyphora selva Daccordi, 1993,                Yes
P. microspina (Bechyne, 1954)
Platyphora conviva (Stal, 1858),
P. anastomozans (Perty, 1832),
P. nigronotata (Stal, 1857),                    Yes
P. nitidissima (Staal, 1857)
P. fasciatomaculata (Staal, 1857),
P. vinula (Stal, 1858)

Proseicela vittata (Fabricius, 1781),           Yes
P. bicruciata Jacoby, 1880,
P spectabilis (Baly, 1858)
Proseicela crucigera (Sahlberg, 1823)           Yes
Pterodunga mirabile Daccordi, 2000          Not reported

Coleoptera: Chrysomelidae: Cassidinae
Acromis sparsa (Boheman, 1854)                  Yes
Aspidomorpha puncticosta Boheman,
1854,                                           Yes
A. miliaris (Fabricius, 1775)
Chelymorpha informis Boheman, 1854,
C. alternans Boheman, 1854,                     Yes
C. cribraria (Fabricius, 1875)
Cistudinella foveolata (Champion, 1894)         Yes
Conchyloctenia punctata (Fabricius, 1787)       Yes
Coptocycla dolosa Boheman, 1855                 Yes
Eugenysa columbiana (Boheman, 1850),            Yes
E. coscaroni Viana, 1968
Paraselenis flava (Linnaeus, 1758)              Yes
Nuzonia sp.                                     Yes
Ogdoecosta biannularis (Boheman, 1854)          Yes
Omaspides tricolorata (Boheman, 1854),          Yes
O. pallidipennis (Boheman, 1854),
O. sobrina (Boheman, 1854),
O. bistriata (Boheman, 1854) and
O. convexicollis Spaeth, 1909
Physonota alutacea Boheman, 1854                Yes
Polychalma multicava (Latreille, 1821)          Yes
Stolas sp., Stolas xanthospila                  Yes
(Champion, 1893)

Coleoptera: Curculionidae: Hyperinae
Phelypera distigma (Boheman, 1842)              Yes

Diptera: Ceratopogonidae:
Forcipomyiinae
Forcipomyia fuliginosa (Meigen, 1818)           Yes

Hemiptera Not specified                     Not reported
Ceroplastes sp. (Coccidea),
Potnia sp. (Membracidae),                        No
Nephesa rosea (Spinola, 1839) (Flatidae),
Derbe sp. (Derbidae)
Antiteuchus tripterus (Fabricius, 1787)          No
(Pentatomidae)
Parastrachiajaponensis (Scott, 1880)             No
(Parastrachiidae)

Hymenoptera: Tenthredinoidea Bergiana       Not reported
sp. (Cimbicidae)
Perga dorsalis Leach, 1817, P affinis           Yes
Kirby, 1882 (Pergidae)
Pseudoperga guerini (Westwood, 1880)            Yes
(Pergidae)
Themos olfersii (Klug, 1834) (Argidae)          Yes
Dielocerus diasi Smith, 1975 (Argidae)      Not reported

Hymenoptera: other superfamilies                 No
Trigona sp. (Apidae: Meliponinae)
Adult Hymenoptera, bees (Apidae),
wasps (Vespidae),                                No
Conomyrma spp. and numerous other ants
(Formicidae)
Apoica sp. (Vespidae: Polistinae)               Yes
"Parasitic Hymenoptera larvae and                No
pupae [on] their host"

Lepidoptera: Papilionidae: Papilioninae         Yes
Papilio laglaizei Depuiset, 1877

Lepidoptera: Saturniidae                        Yes
Hylesia spp. (Hemileucinae)
Lonomia spp. (Hemileucinae)                     Yes

Arsenura spp. (Arsenurinae)                     Yes

Lepidoptera: other families Noctuidae and       Not
Sphingidae                                    reported

Neuroptera: Ascalaphidae
Ascaloptynx furciger (McLachlan, 1891)
                                                 No
Thysanoptera: Phlaeothripidae                   Yes
Anactinothrips nigricornis Hood, 1936 and
A. gustaviae Mound & Palmer, 1983

Non-insect arthropods Phronima                  Yes
sedentaria (Forskal, 1775)
(Crustacea: Amphipoda: Hyperiidea)
Platydesmidae, Unidentified sp.             Not reported
(Myriapoda)

Vertebrates
Some ungulates, for example,                     No
Muskoxen Ovibos moschatus
(Zimmermann, 1780) Antarctic                    Yes
penguins

                                               Aggregation is
Organism                                       defensive (not
                                            for nest protection)

Coleoptera: Chrysomelidae:
Galerucinae
Coelomera spp.; for example,
C. ruficornis Baly, 1865;                           Yes
C. helenae Jolivet, 1987;
C. raquia Bechyne, 1956; and so forth
Dircema spp.                                    Not observed

Coleoptera: Chrysomelidae: Criocerinae
Lema sp.;
Lema apicalis Lacordaire, 1845 and                  Yes
L. reticulosa Clark, 1866
Lilioceris nigropectoralis (Pic, 1928),             Yes
L. formosana Heinze, 1943

Coleoptera: Chrysomelidae:
Chrysomelinae
Agrosteomela chinensis (Weise, 1922)            Not observed
Chrysophtharta obovata (Chapuis, 1877)            Probably
Doryphora paykulli (Stal, 1859), D.                 Yes
reticulata Fabricius, 1787
Eugonycha melanostoma (Stal, 1859)              Not reported
Gonioctena sibirica Kimoto, 1994                  Unclear
Labidomera suturella Guerin-Meneville,          Not observed
1838
Paropsis spp.; for example,
P. aegrota Boisduval, 1835,                   Perhaps, unclear
P. maculata (Marsham, 1908),
P. atomaria Olivier, 1807 and
P. tasmanica Baly, 1864
Paropsisterna spp.                              Not reported
Plagiodera spp. for example,                         No
P. versicolora (Laicharting, 1781)

Phratora spp.                                   Not observed
Phyllocharis undulata (Linnaeus, 1763)          Not observed
Platyphora selva Daccordi, 1993,                    Yes
P. microspina (Bechyne, 1954)
Platyphora conviva (Stal, 1858),
P. anastomozans (Perty, 1832),
P. nigronotata (Stal, 1857),                        Yes
P. nitidissima (Staal, 1857)
P. fasciatomaculata (Staal, 1857),
P. vinula (Stal, 1858)

Proseicela vittata (Fabricius, 1781),               Yes
P. bicruciata Jacoby, 1880,
P spectabilis (Baly, 1858)
Proseicela crucigera (Sahlberg, 1823)               Yes
Pterodunga mirabile Daccordi, 2000              Not reported

Coleoptera: Chrysomelidae: Cassidinae
Acromis sparsa (Boheman, 1854)                      Yes
Aspidomorpha puncticosta Boheman,
1854,                                               Yes
A. miliaris (Fabricius, 1775)
Chelymorpha informis Boheman, 1854,
C. alternans Boheman, 1854,                         Yes
C. cribraria (Fabricius, 1875)
Cistudinella foveolata (Champion, 1894)           Probably
Conchyloctenia punctata (Fabricius, 1787)           Yes
Coptocycla dolosa Boheman, 1855                   Probably
Eugenysa columbiana (Boheman, 1850),                Yes
E. coscaroni Viana, 1968
Paraselenis flava (Linnaeus, 1758)                  Yes
Nuzonia sp.                                         Yes
Ogdoecosta biannularis (Boheman, 1854)              Yes
Omaspides tricolorata (Boheman, 1854),              Yes
O. pallidipennis (Boheman, 1854),
O. sobrina (Boheman, 1854),
O. bistriata (Boheman, 1854) and
O. convexicollis Spaeth, 1909
Physonota alutacea Boheman, 1854                  Probably
Polychalma multicava (Latreille, 1821)            Probably
Stolas sp., Stolas xanthospila                    Probably
(Champion, 1893)

Coleoptera: Curculionidae: Hyperinae
Phelypera distigma (Boheman, 1842)                  Yes

Diptera: Ceratopogonidae:
Forcipomyiinae
Forcipomyia fuliginosa (Meigen, 1818)             Probably

Hemiptera Not specified                         Not reported
Ceroplastes sp. (Coccidea),
Potnia sp. (Membracidae),                         Unclear
Nephesa rosea (Spinola, 1839) (Flatidae),
Derbe sp. (Derbidae)
Antiteuchus tripterus (Fabricius, 1787)              No
(Pentatomidae)
Parastrachiajaponensis (Scott, 1880)                 No
(Parastrachiidae)

Hymenoptera: Tenthredinoidea Bergiana           Not reported
sp. (Cimbicidae)
Perga dorsalis Leach, 1817, P affinis               Yes
Kirby, 1882 (Pergidae)
Pseudoperga guerini (Westwood, 1880)                Yes
(Pergidae)
Themos olfersii (Klug, 1834) (Argidae)              Yes
Dielocerus diasi Smith, 1975 (Argidae)            Unclear

Hymenoptera: other superfamilies                     No
Trigona sp. (Apidae: Meliponinae)
Adult Hymenoptera, bees (Apidae),
wasps (Vespidae),                                    No
Conomyrma spp. and numerous other ants
(Formicidae)
Apoica sp. (Vespidae: Polistinae)                    No
"Parasitic Hymenoptera larvae and                    No
pupae [on] their host"

Lepidoptera: Papilionidae: Papilioninae         Not reported
Papilio laglaizei Depuiset, 1877

Lepidoptera: Saturniidae                          Probably
Hylesia spp. (Hemileucinae)
Lonomia spp. (Hemileucinae)                       Probably

Arsenura spp. (Arsenurinae)                     Probably not

Lepidoptera: other families Noctuidae and       Probably not
Sphingidae

Neuroptera: Ascalaphidae
Ascaloptynx furciger (McLachlan, 1891)
                                                    Yes
Thysanoptera: Phlaeothripidae                     Probably
Anactinothrips nigricornis Hood, 1936 and
A. gustaviae Mound & Palmer, 1983

Non-insect arthropods Phronima                       No
sedentaria (Forskal, 1775)
(Crustacea: Amphipoda: Hyperiidea)
Platydesmidae, Unidentified sp.                 Not reported
(Myriapoda)

Vertebrates
Some ungulates, for example,                        Yes
Muskoxen Ovibos moschatus
(Zimmermann, 1780) Antarctic                         No
penguins

                                                    Is the
Organism                                          behaviour
                                                 cycloalexy?

Coleoptera: Chrysomelidae:
Galerucinae
Coelomera spp.; for example,
C. ruficornis Baly, 1865;                            Yes
C. helenae Jolivet, 1987;
C. raquia Bechyne, 1956; and so forth
Dircema spp.                                    None observed

Coleoptera: Chrysomelidae: Criocerinae
Lema sp.;
Lema apicalis Lacordaire, 1845 and                   Yes
L. reticulosa Clark, 1866
Lilioceris nigropectoralis (Pic, 1928),              Yes
L. formosana Heinze, 1943

Coleoptera: Chrysomelidae:
Chrysomelinae                                   None observed
Agrosteomela chinensis (Weise, 1922)
Chrysophtharta obovata (Chapuis, 1877)               Yes
Doryphora paykulli (Stal, 1859), D.                  No *
reticulata Fabricius, 1787
Eugonycha melanostoma (Stal, 1859)               Tentatively
Gonioctena sibirica Kimoto, 1994                   Unclear
Labidomera suturella Guerin-Meneville,               None
1838                                               observed
Paropsis spp.; for example,
P. aegrota Boisduval, 1835,                           No
P. maculata (Marsham, 1908),
P. atomaria Olivier, 1807 and
P. tasmanica Baly, 1864
Paropsisterna spp.                          Not enough information
Plagiodera spp. for example,                          No
P. versicolora (Laicharting, 1781)
                                                     None
Phratora spp.                                      observed
Phyllocharis undulata (Linnaeus, 1763)                No
Platyphora selva Daccordi, 1993,                     No *
P. microspina (Bechyne, 1954)
Platyphora conviva (Stal, 1858),
P. anastomozans (Perty, 1832),
P. nigronotata (Stal, 1857),                         Yes
P. nitidissima (Staal, 1857)
P. fasciatomaculata (Staal, 1857),
P. vinula (Stal, 1858)

Proseicela vittata (Fabricius, 1781),                No *
P. bicruciata Jacoby, 1880,
P spectabilis (Baly, 1858)
Proseicela crucigera (Sahlberg, 1823)       Not enough information
Pterodunga mirabile Daccordi, 2000          Not enough information

Coleoptera: Chrysomelidae: Cassidinae
Acromis sparsa (Boheman, 1854)                      Yes *
Aspidomorpha puncticosta Boheman,
1854,                                                Yes
A. miliaris (Fabricius, 1775)
Chelymorpha informis Boheman, 1854,
C. alternans Boheman, 1854,                          Yes
C. cribraria (Fabricius, 1875)
Cistudinella foveolata (Champion, 1894)              Yes
Conchyloctenia punctata (Fabricius, 1787)            Yes
Coptocycla dolosa Boheman, 1855                      Yes
Eugenysa columbiana (Boheman, 1850),                Yes *
E. coscaroni Viana, 1968
Paraselenis flava (Linnaeus, 1758)                  Yes *
Nuzonia sp.                                          Yes
Ogdoecosta biannularis (Boheman, 1854)               Yes
Omaspides tricolorata (Boheman, 1854),              Yes *
O. pallidipennis (Boheman, 1854),
O. sobrina (Boheman, 1854),
O. bistriata (Boheman, 1854) and
O. convexicollis Spaeth, 1909
Physonota alutacea Boheman, 1854                     Yes
Polychalma multicava (Latreille, 1821)               Yes
Stolas sp., Stolas xanthospila                       Yes
(Champion, 1893)

Coleoptera: Curculionidae: Hyperinae
Phelypera distigma (Boheman, 1842)                   Yes

Diptera: Ceratopogonidae:
Forcipomyiinae
Forcipomyia fuliginosa (Meigen, 1818)                Yes

Hemiptera Not specified                     Not enough information
Ceroplastes sp. (Coccidea),
Potnia sp. (Membracidae),                             No
Nephesa rosea (Spinola, 1839) (Flatidae),
Derbe sp. (Derbidae)
Antiteuchus tripterus (Fabricius, 1787)               No
(Pentatomidae)
Parastrachiajaponensis (Scott, 1880)                  No
(Parastrachiidae)

Hymenoptera: Tenthredinoidea Bergiana       Not enough information
sp. (Cimbicidae)
Perga dorsalis Leach, 1817, P affinis                Yes
Kirby, 1882 (Pergidae)
Pseudoperga guerini (Westwood, 1880)                 Yes
(Pergidae)
Themos olfersii (Klug, 1834) (Argidae)               Yes
Dielocerus diasi Smith, 1975 (Argidae)      Not enough information

Hymenoptera: other superfamilies                      No
Trigona sp. (Apidae: Meliponinae)
Adult Hymenoptera, bees (Apidae),
wasps (Vespidae),                                     No
Conomyrma spp. and numerous other ants
(Formicidae)
Apoica sp. (Vespidae: Polistinae)                     No
"Parasitic Hymenoptera larvae and                     No
pupae [on] their host"

Lepidoptera: Papilionidae: Papilioninae          Tentatively
Papilio laglaizei Depuiset, 1877

Lepidoptera: Saturniidae                    Not enough information
Hylesia spp. (Hemileucinae)
Lonomia spp. (Hemileucinae)                        Probably

Arsenura spp. (Arsenurinae)                           No

Lepidoptera: other families Noctuidae and
Sphingidae                                            No

Neuroptera: Ascalaphidae
Ascaloptynx furciger (McLachlan, 1891)
                                                      No
Thysanoptera: Phlaeothripidae                        Yes
Anactinothrips nigricornis Hood, 1936 and
A. gustaviae Mound & Palmer, 1983

Non-insect arthropods Phronima                       No *
sedentaria (Forskal, 1775)
(Crustacea: Amphipoda: Hyperiidea)
Platydesmidae, Unidentified sp.             Tentatively analogous
(Myriapoda)

Vertebrates
Some ungulates, for example,                          No
Muskoxen Ovibos moschatus
(Zimmermann, 1780) Antarctic                          No
penguins

Organism                                            Reference

Coleoptera: Chrysomelidae:
Galerucinae
Coelomera spp.; for example,
C. ruficornis Baly, 1865;                           [1, 5-8]
C. helenae Jolivet, 1987;
C. raquia Bechyne, 1956; and so forth
Dircema spp.                                          [6,7]

Coleoptera: Chrysomelidae: Criocerinae
Lema sp.;
Lema apicalis Lacordaire, 1845 and            (Figure 1(a)) [9,10]
L. reticulosa Clark, 1866
Lilioceris nigropectoralis (Pic, 1928),           (Figure 1(b))
L. formosana Heinze, 1943                             [11]

Coleoptera: Chrysomelidae:
Chrysomelinae
Agrosteomela chinensis (Weise, 1922)                 [11-13]
Chrysophtharta obovata (Chapuis, 1877)               [11,14]
Doryphora paykulli (Stal, 1859), D.                   [15]
reticulata Fabricius, 1787
Eugonycha melanostoma (Stal, 1859)                   [7,11]
Gonioctena sibirica Kimoto, 1994                   [11,12,16]
Labidomera suturella Guerin-Meneville,             [11,17-19]
1838
Paropsis spp.; for example,
P. aegrota Boisduval, 1835,                    [7, 11, 14, 20, 21]
P. maculata (Marsham, 1908),
P. atomaria Olivier, 1807 and
P. tasmanica Baly, 1864
Paropsisterna spp.                               [11,12,14, 20]
Plagiodera spp. for example,                       [7, 22-25]
P. versicolora (Laicharting, 1781)

Phratora spp.                                        [7,11]
Phyllocharis undulata (Linnaeus, 1763)              [11, 26]
Platyphora selva Daccordi, 1993,                    [15, 27]
P. microspina (Bechyne, 1954)
Platyphora conviva (Stal, 1858),
P. anastomozans (Perty, 1832),
P. nigronotata (Stal, 1857),                      7, 9,10, 28]
P. nitidissima (Staal, 1857)
P. fasciatomaculata (Staal, 1857),
P. vinula (Stal, 1858)

Proseicela vittata (Fabricius, 1781),          (Figure 5(a)) [15]
P. bicruciata Jacoby, 1880,
P spectabilis (Baly, 1858)
Proseicela crucigera (Sahlberg, 1823)                 [7,9]
Pterodunga mirabile Daccordi, 2000                 [11,12,19]

Coleoptera: Chrysomelidae: Cassidinae
Acromis sparsa (Boheman, 1854)                     [7,11, 29]
Aspidomorpha puncticosta Boheman,
1854,                                              [7, 30-32]
A. miliaris (Fabricius, 1775)
Chelymorpha informis Boheman, 1854,
C. alternans Boheman, 1854,                          [7, 8]
C. cribraria (Fabricius, 1875)
Cistudinella foveolata (Champion, 1894)           (Figure 2(a))
Conchyloctenia punctata (Fabricius, 1787)          [7, 30, 33]
Coptocycla dolosa Boheman, 1855                    (Figure 4)
Eugenysa columbiana (Boheman, 1850),              (Figure 2(b))
E. coscaroni Viana, 1968                            [34, 35]
Paraselenis flava (Linnaeus, 1758)                     [8]
Nuzonia sp.                                       (Figure 2(c))
Ogdoecosta biannularis (Boheman, 1854)             [7,11, 36]
Omaspides tricolorata (Boheman, 1854),      [7,11, 32, 35, 37-39] (D.
O. pallidipennis (Boheman, 1854),
O. sobrina (Boheman, 1854),
O. bistriata (Boheman, 1854) and                  observations)
O. convexicollis Spaeth, 1909
Physonota alutacea Boheman, 1854                  (Figure 2(d))
Polychalma multicava (Latreille, 1821)            (Figure 2(e))
Stolas sp., Stolas xanthospila                  (Figure 2(f)) [7]
(Champion, 1893)

Coleoptera: Curculionidae: Hyperinae
Phelypera distigma (Boheman, 1842)                [24, 40, 41]

Diptera: Ceratopogonidae:
Forcipomyiinae
Forcipomyia fuliginosa (Meigen, 1818)             [1,11,42-44]

Hemiptera Not specified                              [11,12]
Ceroplastes sp. (Coccidea),
Potnia sp. (Membracidae),                             [11]
Nephesa rosea (Spinola, 1839) (Flatidae),
Derbe sp. (Derbidae)
Antiteuchus tripterus (Fabricius, 1787)               [45]
(Pentatomidae)
Parastrachiajaponensis (Scott, 1880)                  [46]
(Parastrachiidae)

Hymenoptera: Tenthredinoidea Bergiana                  [1]
sp. (Cimbicidae)
Perga dorsalis Leach, 1817, P affinis         (Figure 3(a)) [7, 11,
Kirby, 1882 (Pergidae)                             12, 47, 48]
Pseudoperga guerini (Westwood, 1880)                  [49]
(Pergidae)
Themos olfersii (Klug, 1834) (Argidae)               [1, 50]
Dielocerus diasi Smith, 1975 (Argidae)               [1, 50]

Hymenoptera: other superfamilies                  [1, 7,11, 51]
Trigona sp. (Apidae: Meliponinae)
Adult Hymenoptera, bees (Apidae),
wasps (Vespidae),                                     [11]
Conomyrma spp. and numerous other ants
(Formicidae)
Apoica sp. (Vespidae: Polistinae)                    [52-54]
"Parasitic Hymenoptera larvae and                     [11]
pupae [on] their host"

Lepidoptera: Papilionidae: Papilioninae             [24, 55]
Papilio laglaizei Depuiset, 1877

Lepidoptera: Saturniidae                               [7]
Hylesia spp. (Hemileucinae)
Lonomia spp. (Hemileucinae)                      (Figure 3(b))
                                                  [11, 56, 57]
Arsenura spp. (Arsenurinae)                          [1,11].

Lepidoptera: other families Noctuidae and             [11]
Sphingidae

Neuroptera: Ascalaphidae
Ascaloptynx furciger (McLachlan, 1891)            [1,11,12, 58]

Thysanoptera: Phlaeothripidae                  (Figure 5(b)) [59]
Anactinothrips nigricornis Hood, 1936 and
A. gustaviae Mound & Palmer, 1983

Non-insect arthropods Phronima                    [24, 60, 61]
sedentaria (Forskal, 1775)
(Crustacea: Amphipoda: Hyperiidea)
Platydesmidae, Unidentified sp.                     [24, 62]
(Myriapoda)

Vertebrates
Some ungulates, for example,                        1,11,12]
Muskoxen Ovibos moschatus
(Zimmermann, 1780) Antarctic                        [12, 63]
penguins

* These taxa are maternally defended and pose a special challenge to
the definitions of cycloalexy (see Section 3.2.5).
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Author:Dury, Guillaume J.; Bede, Jacqueline C.; Windsor, Donald M.
Publication:Psyche (Cambridge, 1874)
Article Type:Report
Date:Jan 1, 2014
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