Lagideus podocarpus Smith,

Boeve, Jean-Luc, Marin-Armijos, Diego S., Dominguez, Diego F. & Smith, David R., 2016, Sawflies (Hymenoptera: Argidae, Pergidae, Tenthredinidae) from southern Ecuador, with a new record for the country and some ecological data, Journal of Hymenoptera Research 51, pp. 55-89: 59-63

publication ID

http://dx.doi.org/10.3897/jhr.51.9830

publication LSID

lsid:zoobank.org:pub:062BE137-7933-4E23-AA76-061FB0949E9F

persistent identifier

http://treatment.plazi.org/id/6477481F-37D4-CC1D-1127-52A3386E8E66

treatment provided by

Journal of Hymenoptera Research by Pensoft

scientific name

Lagideus podocarpus Smith
status

sp. n.

Taxon classification Animalia Hymenoptera Pergidae

Lagideus podocarpus Smith  sp. n. Figs 9, 10, 11

Description.

Female. Unknown.

Male. Length 7.0 mm. Antenna and head black; labrum and mouthparts white; mandible dark red brown. Thorax black with posterior corners of pronotum orange. Fore and midlegs light orange; fore coxa black with white stripe on outer surface and extreme apex white; mid coxa black with extreme apex white. Hind legs black with extreme apex of coxa, trochanters, and extreme base of femur white and about basal half of tibia light orange. Wings hyaline; veins and stigma black.

Head with vertex and frons shiny, very few widely scattered punctures; area adjacent to inner orbits slightly dull, micropunctured; with long golden hairs, as long as or longer than second antennomere. Antenna 1.5 × head width; antennomeres 4-8 bipectinate, antennomere 3 unipectinate with inner ramus absent to very slightly indicated ( Smith 2012: fig. 25); apical antennomere with rami less than half length of stem. Malar space linear. Thorax shiny; mesonotum with distinct punctures, separated by flat shiny interspaces more than puncture diameters; with long golden hair on dorsum and grey to white hair on pleurae and sterna. Hindbasitarsomere slightly longer than length of remaining tarsomeres combined; inner hind tibial spur about 0.6 × length of basitarsomere. Genitalia in Fig. 10; parapenis uniformly broad, not distinctly indented on posterior margin; valviceps of penis valve with dorsal margin concave.

Type material.

Holotype labelled "Ad.M, ex-larva," "ECUADOR: Cajanuma, Podocarpus NP, 04°07'S, 079°10'W, 2810 m, X.2014, on Fuchsia vulcanica  , JLBoevé leg. RBINS, EtOH100%, P3898.etc>10" ( RBINS). Paratypes: Same data as for holotype except P3898.etc>01 (1 ♂), P3898.etc>02 (1 ♂), P3898.etc>03 (1 ♂), P3898.etc>04 (1 ♂), P3898.etc>05 (1 ♂), P3898.etc>06 (1 ♂), P3898.etc>07 (1 ♂), P3898.etc>08 (1 ♂), P3898.etc>09 (1 ♂), P3898.etc>11 (1 ♂), P3898.etc>12 (1 ♂), P3898.etc>14 (1 ♂); these specimens are in RBINS, USNM and MUTPL.

Other material.

Cajanuma, Podocarpus NP, 04°07'S, 079°10'W, 2810m, 11.10.2014, on Fuchsia vulcanica  ( Onagraceae  ), P3898 (6 larvae), 14.10.2014, on Fuchsia vulcanica  , P3917 (4 larvae), P3919 (20-30 larvae), 23.10.2014, on Fuchsia vulcanica  , P3968 (>30 larvae), P3969 (6 larvae), P3970 (6 larvae), P3976 (4 larvae), leg. J.-L. Boevé.

Etymology.

Named for Podocarpus National Park, Ecuador, where the collections were made; a noun in apposition.

Comments.

Although only the male is known, it differs from described species, and we prefer to have a name since it was reared and the life history and host plant are known. Only females are known for most species of Lagideus  , and this could be the opposite sex of one of those. However, this won’t be known until the sexes are associated.

The bipectinate antennomeres 4-8 and unipectinate antennomere 3 will take this species to couplet 17c in Smith (2012) which includes Lagideus longicus  Smith and Lagideus tapanti  Smith, both known from Costa Rica. The black antenna and similarity of genitalia will put it closest to Lagideus longicus  .

Lagideus tapanti  has white hairs on the head and body, antennomeres 1-3 or 4 yellowish, thorax black, and legs black with the base of the femora white; the antenna ( Smith 2012: fig. 25) has the rami of the apical antennomere much longer than the stem; and the parapenis of the male genitalia are lobed posteriorly with a central, shallow posterior emargination ( Smith 2012: fig. 28). Lagideus longicus  is entirely black and the apical antennomere has long rami as in Lagideus tapanti  ; the parapenis of the genitalia is distinctly indented posteriorly for at least a third of its medial length ( Smith 2012: fig. 29); and the valviceps of the penis valve have a straight dorsal margin ( Smith 2012: fig. 33).

Lagideus podocarpus  can be distinguished from both these species by light orange posterior corners of the pronotum; the light orange fore and mid legs (except the partly black coxae); basal half of the hind tibia light orange; the antennae, similar to Lagideus longicus  ( Smith 2012: fig. 25) except the rami of the apical antennomere are short, less than half the length of the stem; and the male genitalia (Fig. 10) which has the parapenis nearly uniformly broad, without a central posterior emargination and the valviceps of the penis valve distinctly concave dorsally.

The length varies slightly 6.0-7.5 mm. The tegulae may be black to brown or partly light orange as are posterior corners of the pronotum.

Life history.

The population of Lagideus podocarpus  at Cajanuma (Fig. 11) consisted of larvae found within a circumference of ca. 100 m, on several patches of the host plant, Fuchsia vulcanica  L. ( Onagraceae  ). The larvae were attached to the underside of a leaf and they were generally aggregated in that one or a few individuals occurred per leaf. Younger larvae skeletonised the leaves and made holes in the leaf, whereas larvae of later instars attacked the leaf up to its edge. Larvae fed on both younger and older leaves. One large patch of flowering plants clearly harboured fewer larvae than the smaller and more numerous spots of non-flowering plants. The larvae being kept in rearing still appeared as healthy, despite the fact that the offered leaves (during November 2014) were less fresh and rather decaying. A couple of plant species and varieties were also offered to them to roughly establish their diet breadth. Fuchsia  ‘Koralle’ was rather accepted, whereas only very few small holes were made on leaves of Fuchsia  'Gartenmeister Bonstedt’. These two varieties are cultivars of Fuchsia triphylla  that is related to Fuchsia vulcanica  (Marc Reynders, personal communication). A leaf of Oenothera  sp. ( Onagraceae  ) was also tested, but not accepted.

Larvae of nearly all instars were found in the field, but no adults were collected by sweeping. Among the larvae kept in rearing, several individuals reached the eonymph stage (Fig. 11 g–h), during the first ten days of October 2014. They formed a cocoon between fresh or rather decaying leaves (Fig. 11i), or in an offered layer of moistened sand. At the end of October, prepupae and cocoons occurred in the rearing. A total of 14 adults, all males, emerged from 20.11 to 12.12.2014.

Once disturbed, a larva of Lagideus podocarpus  reacted immediately by raising its abdomen (Fig. 11j), then slowly lowering it. This reaction could be repeated several times, under successive disturbances. After several such behaviours, the larva tended to slightly walk backwards. The prepupa reacted under disturbance by curling its body and making some slow movements. To further investigate the larval defensive behaviour, a dozen workers of the ant species Eciton burchellii  Westwood ( Formicidae  ) were collected in the field (Pueblo Viela, 15.10.2016), held without feeding, and used ca. 36 h later. The bioassay consisted of placing seven ant workers and one larva settled on a host plant leaf in an open box, the interactions being then filmed. As far as no ant contacted the larva, the latter remained merely immobile. But once contacted, the larva instantly raised its abdomen and directed the apical filaments towards the aggressor (Fig. 11 k–l). Thus, these filaments seem to play a major role in defence. Their size is impressive, with a length of 13 mm for a remaining body size of 16 mm. The filaments resemble those of the larvae of Philomastix  ; the two genera are sister-groups ( Schmidt and Walter 2014). However, the filaments protrude from the apical segment in Lagideus  and the ninth one in Philomastix  ( Smith and Bado 2004). Moreover, it seems that they are clearly covered with spines in Lagideus  only (Fig. 11; Smith and Bado 2004). It is unclear whether the defence is only physical, or includes chemical compounds. Larvae of Pergidae  contain toxic peptides which are active against vertebrates and invertebrates ( Boevé et al. 2014), but whether Lagideus  sp. contains such compounds remains unknown.

Note that another sawfly species ( Tenthredinidae  ) was found among the collected leaves (and stems) of Fuchsia vulcanica  , but in much lower numbers (2 individuals: 11.10.2014, P3899, and 14.10.2014, P3919.C1) than Lagideus  sp. (>90 in total). This plant constitutes a host plant, since a larva of the tenthredinid was placed on an intact leaf and the larva ingested significant parts of it.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Order

Hymenoptera

Family

Pergidae

Genus

Lagideus