Eutrichosoma mirabile Ashmead,

Baker, Austin J. & Heraty, John M., 2020, Larval morphology and life history of Eutrichosoma mirabile Ashmead and description of a new species of Eutrichosoma (Hymenoptera, Chalcidoidea), Journal of Hymenoptera Research 75, pp. 67-85: 67

publication ID

http://dx.doi.org/10.3897/jhr.75.47880

publication LSID

lsid:zoobank.org:pub:2D542983-8FC8-4616-834F-47625EDBB5F0

persistent identifier

http://treatment.plazi.org/id/7A076909-5289-528E-BB8E-2DA208D71238

treatment provided by

Journal of Hymenoptera Research by Pensoft

scientific name

Eutrichosoma mirabile Ashmead
status

 

Eutrichosoma mirabile Ashmead  Fig. 1A-HView Figure 1

Eutrichosoma mirabile  Ashmead 1904: 375. Lectotype designated by Gahan and Peck (1946: 315): USA: Montana: Helena (female). Deposited in USNM.

Eutrichosoma albipes  Crawford 1908: 158-159. Synonymy by Bouček, 1975. Holotype: USA: Texas: Dallas (female). Deposited in USNM.

E. mirabile  ; Bouček 1975: 132-133. Redescription and identification key.

Biology and life history.

Eggs and first-instar larvae were found inside the early (green) seedpods of Vachellia constricta  and associated with the presence of weevil eggs and larvae ( Curculionidae  ). Eutrichosoma mirabile  eggs are laid among the host eggs inside the seedpods between the ovule and the inner wall of the pod. Hatching of the parasitoid seems to coincide with or precede hatching of the host because parasitoid eggs were never observed without host eggs. The majority of planidia found were parasitizing first- or second-instar weevils (~85%). Typically, only one planidium was found per host, positioned anterodorsally on the body just behind the head attached by the mandibles; always on the external surface and never penetrating the cuticle. The remaining unattached planidia were observed crawling around near clusters of host eggs. Eggs and planidia were the only life stages of the wasps observed in the seedpods. While there may be several eggs and early instars of weevil (up to ~10) per ovule within a seedpod, by the time the weevils are in their fourth instar, there is only one individual per ovule remaining. Considering the wasps are ectoparasitic koinobionts, they are likely detaching then reattaching and repositioning themselves on their hosts between host molts or transferring between individual host larvae. Given the similarities between E. mirabile  and chrysolampines (discussed below), it is assumed that the E. mirabile  planidia remain attached externally to the weevil when it leaves the seedpod to pupate in the soil, where the parasitoid likely finishes development. We were not able to keep the weevil larvae alive outside of the pods to allow the parasitoid to develop further. Parasitism rates shown in Suppl. material 1: Table S3.

Egg (Fig. 1AView Figure 1). Egg body length approximately 0.2 mm, maximum width approximately 0.07 mm; ovoid; caudal stalk about half as long as the body of the egg. Eggs separate, not forming tight clusters.

Planidium (Fig. 1B-HView Figure 1). Length approximately 0.13 mm, maximum width approximately 0.05 mm; fusiform in shape. Body and cranium white, darkened around mouth (Fig. 1CView Figure 1). Cranium with one pair of short, papilliform antennae (ant), one pair of longer, thinner pleurostomal setae (plst), and one pair of minute, lateral cranial spines (cs); postlabium (psl) large, flat, circular, and surrounding prelabium (prl); labial palp (lp) present; pleurostomal bridge (psb) present and connected by thin integument (Fig. 1EView Figure 1). Thirteen body segments beyond head; terga lightly sclerotized and ring-like, encircling the body; band of 1-2 irregular rows of tubercles (tbs) on anteroventral side of terga II-XII; prominent dorsolateral spines (spn) on terga I and III-XI; setae (set) present on terga I-VIII and XII, with three pairs on tergum II and two pairs on tergum III; short cerci present on XIII (cer); spiracles on terga II, IV-VI (spi) (Fig. 1B, D, F-GView Figure 1).

Determining if a first-instar larva is a type I planidium (i.e. undergoes hypermetamorphosis sensu Pinto (2009)) requires examination of subsequent instars, which we did not find for Eutrichosoma  . However, the mobility of the larvae observed in the seedpods and inferred from their koinobiont ectoparasitc behavior suggests that Eutrichosoma  behavior is congruent with other PLC larvae, even if their morphology is not as derived as Eucharitidae  , Perilampinae  , or Philomidinae  , which are all more heavily sclerotized and generally lack ventral fusion of the terga. Larvae of Eutrichosomatinae  and Chrysolampinae  appear to be somewhat intermediate between typically hymenopteriform first instars of other chalcidoid taxa and the highly derived planidial larvae in the PLC.

Material examined.

USA: Arizona: Cochise Co.: Canadian Lane, Portal , 1426m, 31°55'1"N, 109°07'37"W, 28.viii.2016, A. Baker & S. Heacox, AB16.024 [2 larvae slide mounted, UCRCENT00513221-2]GoogleMaps  ; 4.viii.2018, A. Baker, S. Heacox, L. Kresslein, AB18.007 [larvae in alcohol, UCRCENT00513223] deposition UCRC.GoogleMaps 

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hymenoptera

Family

Pteromalidae

Genus

Eutrichosoma

Loc

Eutrichosoma mirabile Ashmead

Baker, Austin J. & Heraty, John M. 2020
2020
Loc

Eutrichosoma albipes

Crawford 1908
1908
Loc

Eutrichosoma mirabile

Ashmead 1904
1904