Chrysis ignita

Chrysis ignita, also known as the ruby-tailed wasp, is a species of cuckoo wasps. Cuckoo wasps are kleptoparasites – they lay their eggs in the nests of other wasp species and their young consume the eggs or larva of the host wasp for sustenance. These wasps have a number of adaptions which have evolved to equip them for their life cycle. Chrysis ignita parasitize mason bees in particular. Ruby-tailed wasps have metallic, armored bodies, and can roll up into balls to protect themselves from harm when infiltrating the nests of host bees and wasps. Unlike most other Hymenopterans, cuckoo wasps cannot sting. Chrysis ignita is found across the European continent.

Chrysis ignita

Least Concern  (IUCN 3.1)
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Chrysididae
Genus: Chrysis
Species:
C. ignita
Binomial name
Chrysis ignita

Taxonomy and phylogeny

Chrysis ignita is a chrysidid wasp with a typical colorful, metallic exoskeleton; the stinger is reduced in size and used as an ovipositor.[1][2]

Description and identification

Chrysidids differ from other Aculeate wasps (stinging Hymenoptera) in their reduction of the number of external body segments, the presence of 11 antennal articles, and wing veins enclosing 5 cells. Chrysis ignita is the most common of a group of very similar ruby-tailed wasps.[3] The head and thorax range from a shiny green to blue, sometimes layered with a golden sheen. The abdomen, a deep ruby color, is its most distinctive feature. The exoskeleton sculpture appears textured, like a golf ball, with dimples, projections, crests, and holes ranging from micrometric to millimetric in size.[1]

Distribution and habitat

Chrysis ignita can be found throughout England, Wales, Scotland, and Ireland, excluding the Orkney and Shetland Islands. Sightings have also been documented on the Isle of Man, Isle of Wight, the isles of Scilly, and the Channel Islands.[4] Other experts record that Chrysis ignita can be found throughout the Palaearctic, spanning Europe, Britain, Germany, Canaries, Italy, Algeria, URSS, and Japan.[5][4] Their habitats overlap with the host wasps they parasitize, and thus they can be found near walls, quarries, bare cliff faces, and around dead wood in sunny places.[6] Since Chrysidids are solitary wasps whose lives are linked to and dependent on their hosts, they live in strict microhabitats. These microhabitats can be further categorized as places of rest and of parasitic activity. The environments in which they are found facilitate their identification and are often characterized by flowers, arid and sandy soil, old wood exposed to sunlight, pebbles, and aphid infested plants.[1]

Life history

Infiltration and egg deposition

Chrysidids are parasitoids, meaning that their parasitic activity, in most cases, kills their hosts. Some species are also cleptoparasites, meaning that they also use the host species’ food supplies as resources to sustain themselves. Chrysis ignita is both a parasite and a cleptoparasite. The female wasp possesses a long, telescopic ovipositor, which evolved from the reduction of the Hymenopteran stinging apparatus. It uses this appendage to deposit its eggs inside the nest of the host wasp. The female ruby-tailed wasp will hide nearby, waiting for an ideal host. She will look for wasps that are in the process of digging burrows or dragging prey or bringing food back to their nests. She will then observe the nest until the host leaves or hitch a ride on the prey to slip in.[1]

Parasitism

There are two basic strategies for parasitizing the host. In the first strategy, the wasp eats the host egg or host young larva as soon as it hatches and moves on to eating the food resources in the nest (cleptoparasitism). In the second strategy, the Chrysidid waits for the host larva to reach its prepupal stage, and it kills it after clearing the nest of food sources.[7] Each strategy has its advantages. The second parasitoid strategy is generally utilized when the host wasp species is a nectar and pollen gatherer. These host wasps stock up their nests with food sources that contain nutrients the Chrysidid wasp cannot synthesize itself.[1] Additionally, if the host mother wasp is able to accumulate enough food resources for both her kin and the host larva, the parasitoid wasp can remain undetected by not killing and eating its adopted siblings.

Morphology

In addition to bold coloration, the Chrysidid head tends to have large, bulging, well developed eyes. The head is generally flat or shallowly convex on the backside, without distinct bumps or grooves. One method of identifying the ruby-tailed wasp is to look for a broad indentation across the back of the head to the neck joint – in these wasps the indentation terminates laterally in a hook like projection.[5] Additionally, in all Chrysidid wasps, the occipital suture, or the groove at the back of the wasp's head, is reduced compared to in other wasp families. The majority of the lateral faces of the ruby-tailed wasp head is taken up by large compound eyes. See the insect anatomy category for vocabulary.

Face

Chrysidid faces, or the front of the head, distinguish them from other Hymenopterans. The antennae are attached low on the face, on the dorsal margin of clypeus.[5] Generally, the clypeus is short and broad, truncating at the apex. The dorsal margin extends around and partly enclose the antennal sockets. Chrysidids have simple mandibles, with usually one or two subapical teeth.

Abdomen

The number of visible Chrysidid segments varies among subfamilies. Chrysis ignita has three segmented abdomens in both sexes, which make sex determination difficult. The morphology of the abdominal anatomy translates into defensive function for the wasp. The visible segments are heavily sclerotized and weakly intermusclated.[5] The abdominal segments I through IV possess spiracles, which the wasp breathes through. The chrysidid stinger is essentially nonfunctional, having been reduced to an ovipositor in females and a genital tube in males.

Coloration

Chrysis ignita is generally colored, and takes on its metallic, iridescent sheen through light interference, and thus varies with the viewing angle. The coloration is most apparent on the body of the wasp, and reduced to spots and stripes on the legs, mandibles, antenna, and abdominal tergites.[5] Identification of Chrysis wasps based on color can be difficult due to the ephemeral nature of their coloration. Chemicals used to kill, preserve, or rehydrate specimens can alter the wasp’s colors.[5] It has also been hypothesized that there may be an environmental relation between the color of the adult and the physical parameters of its developmental environment, like temperature and humidity.[1]

Functional adaptions

Body armor and strategies

Chrysis ignita and its family of Chrysidid wasps have evolved effective defenses for their risky life cycle. While the life of a cuckoo wasp may seem easy, it must drop off its young to be raised by a host wasp species. The ruby-tailed wasp has to infiltrate a nest full of defensive mother wasps, often armed with powerful stingers and jaws. Thus, they have developed defensive, functional body armor to protect themselves. The abdominal segments of their exoskeleton are highly sclerotized on the external surface and concave on the ventral surface.[1] This allows the wasp to tuck in its vulnerable antenna and legs when curling into a defensive sphere. This adaption prevents the ruby-tailed wasp from being stung or mutilated when sneaking around a potential host’s nest. The defense is so effective that even when the mother is caught in the host’s nest, she will simply ball up and become impenetrable to even the strongest stings and mandibles.[1] If they are caught, which happens quite often, they simply tuck and curl. The host wasp has no choice but to grab the balled up ruby-tailed wasp in its jaws and carry it outside to evict it.[8] The ruby-tailed wasp, unharmed, simply makes its way back into the nest again at the next opportunity.

Ovipositor

The ruby-tailed wasp possesses an ovipositor, which evolved from the usual stinging apparatus of most Hymenopterans. Ruby-tailed wasps have been reported to parasitize a variety of hosts, and thus their ovipositor has evolved to be a multi-tool for infiltrating the nests of different wasps. For example, in parasitizing the mud nest of a digger wasp, the female ruby-tailed wasp will first wet a point of the dry mud before attempting to saw through it with her ovipositor.[8] After several repetitions, she will succeed, and can then deposit her egg near or in the host wasp larval cell or cocoon. In the case of parasitizing paper wasp or mason bee, the ruby-tailed wasp’s strong, indented ovipositor is used in a similar fashion to cut through the nest substrate to get to the host young. After the egg is deposited, the ruby-tailed wasp will cover the hole with the original nest material to leave minimal traces of its infiltration. It is essential that both she and her egg remain undetected to ensure the success of her offspring.

Known hosts

Chrysis ignita has been observed to parasitize a wide variety of wasps. Their most common host are from the family Eumenidae, or potter wasps, a cosmopolitan wasp that builds its nests from mud. Their second most preferred host are Megachilidae, or mason and leafcutter bees. Megachilidae nests are usually built in natural or artificial cavities, sometimes embedded in wood, clay, or attached to a plant surface. Although not as frequently, Chrysis ignita also parasitizes Sphecidae (digger wasps, whose nests are burrows in the ground), Colletidae (polyester bees, which build nests from cellophane-like saliva secretion), and very rarely, one species of Vespidae.[4] The commonality among all these hosts, except the one species of Vespidae is that they are all solitary wasps. One can imagine it would be difficult for a cuckoo wasp to infiltrate the nest of a eusocial wasp, filled with tens of worker wasps guarding the nest and tending to food supplies and the larval nursery cells.

Methods of field study

As with other species, study may proceed using a Malaise trap, the more basic Moericke trap, or simply hunting on sight. Alternatively, nests of host wasps can be bred; some will be parasitized by Chrysis ignita.[1]

Research interest

Accessory nuclei

Accessory nuclei (AN) are organelles of mysterious function found in oocytes. Oocytes are highly specialized cells, which not only contain cellular and molecular components that allow for fertilization and embryo development, but also contain food sources for the developing organism. AN are found in the oocytes of several species of wasps, and also in nematodes, other insects, and mammalian embryonic cells.[9] Bilinski and colleagues, in studying AN in Chrysis ignita, have shed light on the possible function of such accessory nuclei. They believe that AN have evolved independently of the rest of the wasp, so they can be used to genetically identify closely related species of Chrysidid.[9] Further research may give us insight into the complexity of AN and its role in oocyte compartmentalization – as well as its importance for early embryonic development.[9]

Cajal bodies homologues

ANs form by budding off the nuclear envelope of the oocyte. They contain structures homologous Cajal Bodies, which are dense inclusions containing proteins and snRNPs. Bilinski and his colleagues have demonstrated that these bodies contain proteins and survival factors essential for the Hymenopteran development, such as survival of motor neuron (SMN) protein. They conjecture that this feature may be characteristic of all Hymenopterans, but further research is required to confirm this.[10]

Mitochondrial phylogeny

The ignita species group of the Chrysis genus includes over 100 cuckoo wasp species.[11] They all live the same parasitic life cycle and are morphologically indistinguishable. The lack of robust morphological features has hindered the construction of the phylogeny of these species of cuckoo wasp.[11] To solve this problem, researchers in Estonia have collected and analyzed the mitochondrial sequences of 41 ingroup and 6 outgroup taxa. By using two simultaneous Bayesian sequence alignment methods, they were able to reconstruct the ignita phylogeny.[11] Their phylogenetic analysis was backed up by maximum-parsimony and maximum-likelihood analyses and formed well-supported and defined clades.[11] Their results suggest that several taxa that are currently grouped together under subspecies may in fact be separate species. This phylogenetic approach will be helpful for further study of not only Chrysis ignita, but other Chrysidids.

Anal teeth and phylogeny

The vast diversity of the cuckoo wasp family, Chrysididae, includes thousands of species, which have individually adapted to their environment and evolved tools uniquely suited to their survival and parasitic activity. This morphological diversity makes it difficult to classify the species. Another breakthrough came through the use of mitochondrial and rRNA sequencing alignment. A group in Germany has identified anal teeth as an early adaptive differentiation, which has potential to be used in phylogenetic reconstruction.[12]

Chemical mimicry

Host-parasite interactions are prime examples of evolutionary arms races. The host evolves methods of detecting the parasite, and the parasite counters by evolving methods of evasion. It has been reported in some specialized Chrysis species that the cuckoo wasp chemically camouflages itself when infiltrating the nest of its host. Field observations indicate that the cuckoo wasp is only attacked when the host wasp visually recognizes it.[13] If the cuckoo wasp can make it into the nest in the dark, research has shown that it can disguise itself chemically by secreting saturated and unsaturated hydrocarbons to match the scent profile of the host wasp. In these situations, even when the host wasp encounters the cuckoo wasp head on in the dark, the cuckoo wasp remains undetected.[13]

gollark: Well, yes.
gollark: eatw.net EATW EATW EATW EATW eggs around the world EATW score = clicks * 12 + uv * 6 + v EATW EATW
gollark: I believe it's mostly to bludgeon down stuff TJ09 happens to disagree with.
gollark: Again, *it's mostly unenforced*.
gollark: EATW EATW EATW EATW!

References

  1. Agnoli G.L. & Rosa P., Chrysis.net website, interim version 20-Sep-2013 , URL: http://www.chrysis.net/
  2. Carpenter, James M. "What Do We Know about Chrysidoid (Hymenoptera) Relationships?" Zoologica Scripta 28.1-2 (1999): 215-31.
  3. "What's That Insect?, Ruby-tailed Wasp | National Insect Week." Royal Entomological Society. N.p., n.d. Web. 16 Oct. 2014.
  4. Agnoli G.L. & Rosa P., 2014 : Chrysis ignita Linnaeus, 1758 . In: Chrysis.net Database of the Italian Chrysididae, interim version 10 October 2014 . URL: http://www.chrysis.net/database/
  5. Kimsey, L. S. & Bohart, R. 1991 (1990). The Chrysidid Wasps of the World. Oxford University Press, New York.
  6. "Chrysis Ignita (Linnaeus,1758)." BWARS. Bees, Wasps & Ants Recording Society, n.d. Web.
  7. Tormos, J., K. V. Krombein, J. D. Asís, and S. F. Gayubo. "A Systematic Study of Larvae of Chrysidini (Hymenoptera: Chrysididae)." Annals of the Entomological Society of America 94.6 (2001): 809-34.
  8. Malyshev S.J., 1911 - Zur biologie der Odynerus Arten und ihre Parasiten. (Chrysis ignita p. 36-39, fig. 16). Horae Societatis Entomologicae Rossicae, XL: 1-54. [in Russian with German summary]
  9. Jaglarz, Mariusz K., Malgorzata Kloc, and Szczepan M. Bilinski. "Accessory Nuclei in Insect Oogenesis: In Search of the Function of Enigmatic Organelles." The International Journal of Developmental Biology 52.2-3 (2008): 179-85.
  10. Jaglarz, Mariusz K., Szczepan M. Bilinski, and M. Kloc. "Assembly and Breakdown of Cajal Bodies in Accessory Nuclei of Hymenoptera." Differentiation 73.2-3 (2005): 99-108.
  11. Soon, Villu, and Urmas Saarma. "Mitochondrial Phylogeny of the Chrysis Ignita (Hymenoptera: Chrysididae) Species Group Based on Simultaneous Bayesian Alignment and Phylogeny Reconstruction."Molecular Phylogenetics and Evolution 60.1 (2011): 13-20.
  12. Niehuis, Oliver, and Johann-Wolfgang Wägele. "Phylogenetic Analysis of the Mitochondrial Genes LSU RRNA and COI Suggests Early Adaptive Differentiation of Anal Teeth in Chrysidine Cuckoo Wasps (Hymenoptera: Chrysididae)." Molecular Phylogenetics and Evolution 30.3 (2004): 615-22.
  13. Strohm, Erhard, Johannes Kroiss, Gudrun Herzner, Claudia Laurien-Kehnen, Wilhelm Boland, Peter Schreier, and Thomas Schmitt. "A Cuckoo in Wolves' Clothing? Chemical Mimicry in a Specialized Cuckoo Wasp of the European Beewolf (Hymenoptera, Chrysididae and Crabronidae)." Frontiers in Zoology 5.1 (2008): 2.
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