Data on the morphology of the egg, mature larva (L₃) and pupa of Squamapion elongatum (Germar, 1817) are presented. The development cycle of this species lasts 51–54 days: a 12-day egg period, a 30-day larval period, and a 12-day pupal period, on average. The larvae are attacked by parasitic hymenopterans of the superfamily Chalcidoidea.

Weevil, Apionidae , Squamapion , egg, mature larva, pupa, life cycle, Salvia , Lamiaceae

The genus Squamapion Bokor, 1923 is distributed in the Palaearctic and Afrotropical regions and includes 33 species (Alonso-Zarazaga 2011). In Poland it is represented by 9 species: Squamapion atomarium (Kirby, 1808), S. cineraceum (Wencker, 1864), S. elongatum (Germar, 1817), S. flavimanum (Gyllenhal, 1833), S. serpyllicola (Wencker, 1864), S. mroczkowskii (Wanat, 1997), S. oblivium (Schilsky, 1902), S. samarense (Faust, 1891) and S. vicinum (Kirby, 1808) (Petryszak 2004; Mokrzycki and Wanat 2005). These are mono- or oligophagous herbivores feeding on species from the family Lamiaceae, mainly of the genera Salvia, Thymus, Thymbra, Mentha, Origanum, Prunella and Saccocalyx. Their larvae burrow tunnels inside roots or stems, occasionally causing galls (Alonso-Zarazaga 1990). These insects are quite similar in terms of external morphology, which causes many problems in identification. As yet no attempts have been made to divide the taxon into subgenera or species groups (Wanat 1997).

Squamapion elongatum is a species inhabiting the southern and central part of Europe, as well as East Asia and Algeria. It inhabits lowland and submontane areas. In Poland it is recorded in the Masurian Lake District, the Wielkopolsko-Kujawska Lowland, Upper and Lower Silesia, the Krakowsko-Wieluńska Upland, the Małopolska Upland, the Świetokrzyskie Mountains, the Lublin Upland, Roztocze and Eastern Beskid (Burakowski et al. 1992). This species is characteristic of xerothermic grasslands, where it feeds on plants of the genus Salvia – S. pratensis and S. nemorosa (Cmoluch 1962). Its life cycle has not yet been described.

Squamapion elongatum eggs, larvae, pupae and adults were collected from two patches of xerothermic grasslands in Gródek (50°46'58.18"N, 23°56'47.04"E) near Hrubieszów and in Łęczna (51°18'9.7"N, 22°51'47.8"E) (SE Poland). The material was collected during one growing season from July to September 2011 at 3–7 day intervals between 10 a.m. and 2 p.m. Adults were collected using an entomological net in an association of Thalictro-Salvietum pratensis. To obtain the other development stages for breeding, whole plants of the genus Salvia were collected. In total 67 specimens of meadow sage were collected. A delicate cut was made along the stem and root of the plants and then they were dissected with needles to find the eggs, larvae, pupae and even adults located inside. Some of the larvae were used to begin breeding and others for microscopic slides, to be used in making drawings showing the morphology of the developmental stages. To prepare the drawings we used an OLYMPUS BX61 microscope at magnifications from 200 × to 400 × and a TESCAN VEGA3LMU scanning microscope at magnifications from 500 × to 4,500 ×. The figures were made based on the biological preparations using Corel Draw 12 software. Metric sizes are the average value of 10 measurements (Table 1).

Larval specimens in successive developmental stages were transferred in vitro to Petri dishes after the larval stadium was determined on the basis of morphological characteristics and the number of exuvia of head capsules. Breeding of larvae was carried out to the L₃ stage. Breeding of preimaginal stages was carried out according to Scherf (1964) and Łętowski (1991). Petri dishes were transferred to a breeding chamber with the following conditions: temperature during the day 30 °C, temperature at night 20 °C, humidity during the day 60%, humidity at night 80%. Adults were kept in glass containers covered with a fine mesh. As in the case of the larvae, filter paper saturated with distilled water was placed at the bottom to maintain humidity and as a possible reservoir of drinking water for the beetles. They were fed with fragments of fresh sage shoots, which were replaced on average every three days. The used stems were examined to search for eggs. Microscope slides with the developmental stages and their morphological structures were prepared according to Łętowski (1991) and Gosik et al. (2010). The terminology of Scherf (1964), May (1993, 1994), Marvaldi (2003) and Wang et al. (2013) was used in the morphological description of the larva and pupa. The morphology of the egg, L₃ and pupa and the developmental cycle from egg to adult were described.

Setae of thorax and abdomen of larva (L₃) and pupa are described for one side only.

Egg (Figure 11)

Length ca. 1.13 mm, width ca. 0.57 mm, oval, smooth, shiny, whitish-yellow.

Mature larva (L₃) (Figures 1, 12)

Length ca. 2.78 mm, width ca. 1.24 mm. Body massive and strongly curved, whitish-yellow, with short setae.

Figure 1. 

Mature larva (L₃), lateral view.

Head (Figures 2, 9, 10): Yellow-brown, oval, with clear frontal suture completely extended to mandibular joint. Epicranium: length ca. 0.72 mm, width ca. 0.56 mm. Endocarina (enc) long, extended to 2/3 the length of the frons. One pair of ocelli (oc). Antennae (at) with conical sensorium and 2 small spinose sensilla (Fig. 10). Clypeus with 1 pair of short setae (cls1). Frons with 5 pairs of setae (fs) – fs2 and fs5 longer, fs1, fs3 and fs4 much shorter, at the apex of the endocarina, fs2-4 near the epistoma, fs5 close to the antennae (Fig. 2). Epicranium with 2 pairs of lateral setae (les) – les1 short, les2 long, more than 3 times longer than les1.; 5 pairs of dorsal setae (des) – des1 very long, des2 and des5 a bit shorter and des3 and des4 much shorter; 4 pairs of minute posterior setae (pes) (in line with des2); 1 sensillum between epicranial suture and pes and another sensillum laterally to des1 and close to des2.

Figure 2. 

Epicranium (L₃), dorsal view: les lateral epicranial setae fs frontal s. des dorsal s. pes posterior epicranial s. cls clypeus s. at antenna oc ocellus enc endocarina, es endocarina suture.

Mouthparts (Figures 3–5, 9): Dorsal side of labrum with 3 pairs of setae (lrms1-3) – lrms1 and 2 long, lrms3 nearly half the length of lrms2. Epipharynx with 7 pairs of setae (3 ams, 3 als, 1 mes) and rather short labral rods (lmr) (Fig. 3a, b). Mandibles massive, dark brown, with 2 mandibular setae (mds1, 2) and 2 sensilla (Fig. 4). Maxillae: palpifer with 2 long setae (pfs1, 2) – pfs2 longer than pfs1, 1 longer stipital seta (stps1) and 2 very short sensilla. Maxillary palpus with 2 segments. Basal segment with digitiform sensorium and 3 very short setae, distal segment cylindrical with 1 short sensilla and 10 conical papillae. Lacinia with 8 robust setae arranged like a comb (dms) (Fig. 5, 9). Labium: premental sclerite (pmsc) Y-shaped. Mentum-submentum complex with 2 pairs of postmental setae (pms1, 3) and 3 pairs of prelabial setae (prms1-3) – prms1 short, prms2 and 3 very short. Additionally, submentum with 3 pairs of sensilla. Labial palpi (lbp) 1-segmented, raised, with numerous papillae (Fig. 5).

Figure 3. 

Labrum and epipharynx (L₃) (a dorsal b ventral view): a lrms labral setae b mes median s. ams anteromedial s. als anterolateral s. lmr labral rods.

Figure 4. 

Mandible (L₃), left: mds dorsal malae setae.

Figure 5. 

Maxillae and labium (L₃): dms dorsal maxillary setae pfs palpiferal s. stps stipal s. prms prelabium s. pms postlabium s. pmsc premental sclerite lbp labial palpus.

Thorax. Pronotal shield unsclerotized, meso- and metanotum each with 2 folds: pro- and postdorsum. Thoracic spiracle intersegmental, in membrane between pro- and mesothorax, bicameral. Prothorax with 7 setae: pronotum with 5, epipleurum indistinct, with 1 seta, sternum with 1 seta. Meso- and metathorax with 12 setae: prodorsum with 1 seta, postdorsum with 5 setae, epipleurum (clearly visible) with 4 clear setae, pleurum and sternum with 1 seta. Pedal area with two long setae for all segments (Fig. 1).

Abdomen. Tergites I-VII with 2 folds, prodorsum with 1 seta on the ridge, postdorsum with 6 setae – 5 dorsally located and 1 seta surrounded by a circle of sparse tubercles. Tergites VIII-IX without folds (single), VIII with 4 setae and XI with 3 setae, reduced. Segments I-VII with unicameral spiracles, others without spiracles. Pleura and sterna I-VIII with 1 short seta, sterna IX with 1 short seta (Fig. 1).

Pupa (Figures 6–8, 13)

Figure 6. 

Pupa, lateral view: as apical s., sls sublateral s., pls posterolateral s. vs vertical s. rs rostral s. fes femoral s. pc urogomphi.

Figure 7. 

Pupa, ventral view: as apical s. sls sublateral s. vs vertical setae rs rostral s. fes femoral s. pc urogomphi.

Figure 8. 

Pupa, dorsal view: as apical s. sls sublateral s. pls posterolateral s. fes femoral s. pc urogomphi.

Figures 9–14. 

9 Maxillary palpus (dms – dorsal robust setae) 10 ocellus (oc) and antenna (at) 11 egg 12 L₃ during construction of the pupal chamber 13 pupa 14 urogomphi (pc).

Body length: ca. 2.67 mm, width ca. 0.94 mm. Colour whitish-grey.

Head (ventral view). Rostrum reaching ventrite V, with 1 distinct seta (rs) at mid-length, in front of the antennal insertion. Antennae relatively long, club with conical papillae. Antennae sub-parallel to protibia. Frons with 1 pair of setae (vs), about as long as rostral setae, situated at the level of the hind margin of the eyes (Figs 6, 7). Pronotum length greater than width, with 5 pairs of setae (as1, as2, sls, pls1, pls2) (Figs 6–8). Setae as1and as2 long and located at the apical margin. Setae sls a bit shorter, located at the external margin in the middle of the edge. Setae pls1and pls2 as long as sls, and located close to the back margin. Mesonotum short and metanotum two times longer than mesonotum. Mesonotum with clearly visible scutellar shield, metanotum with 3 pairs of short setae, medially located. All femora with 1 long, thin seta (fes1-3) located apically (Figs 6–8). Abdomen. Abdominal tergites I-III with 7 pairs of setae arranged in two rows – 2 closer to the upper edge of the segment, nearly at the external margin, 5 closer to the base. Tergites IV-VI with 5 pairs of setae arranged in two rows – 1 closer to the upper edge of the segment, nearly at the external margin, 4 closer to the base. Tergite VII with 3 pairs of setae arranged in one row, VIII with one pair. Segment IX without setae. Urogomphi (pseudocerci) (pc) on abdominal segment IX, laterally parted, crescent-shaped, narrow. Segment X reduced (Figs 6–8, 14). Spiracles on abdominal segments I-VI functional, well visible, positioned longitudinally on pleura (Fig. 6). Gonotheca visibly divided in female, single in male.

This is the first description of the immature stages of a species of the genus Squamapion. The features described were compared with those described by Scherf (1964) for the genus Apion Herbst, 1797 sensu lato, by Marvaldi (2003) for Apioninae, by Łętowski (1991) for Stenopterapion Bokor, 1923, Omphalapion Schilsky, 1906 and Hemitrichapion Voss, 1959, by Gosik et al. (2010) for Diplapion Reitter, 1916, by Wang et al. (2013) for Pseudaspidapion Wanat, 1990 and by Alonso-Zarazaga and Wanat (2014) for Apioninae Schoenherr, 1823.

The morphology of the egg does not differ substantially from the typical characteristics of the eggs of apionid beetles. The localization of eggs on the plant and the duration of this stage are also similar to those of other apionid beetles with the same lifestyle.

In general the body of larval S. elongatum does not deviate from representatives of the subfamily Apioninae described by Alonso-Zarazaga and Wanat (2014). It is very similar to that of larvae of species living inside common sainfoin described by Łętowski (1991) or Diplapion confluens (Kirby, 1808) living in the roots of Anthemis tinctoria L. (Gosik et al. 2010). The larvae of S. elongatum have a typical number of spiracles for Apionidae, as described in Emden (1938), Scherf (1964) and Łętowski (1991), the absence of spiracles on abdominal segment VIII being an important apomorphic character defining the group (as Apioninae in Marvaldi 2003). Larvae of different stages differ from one another in some characteristics, mainly changes in the distribution pattern of the setae. However, no change in the colour of the larvae was observed during growth, unless caused by internal parasitic infection. The differences in the chaetotaxy of the larval body are shown using L₃ of Squamapion elongatum, Diplapion confluens and Pseudaspidapion botanicum as examples (Table 2).

The characteristics of the pupae of this weevil species do not differ from other representatives of Apionidae, except for the presence of a mesofemoral seta, also found in Diplapion but not in Pseudaspidapion, and the lack of a pair of setae on the 8th abdominal tergite, in contrast to one pair of setae in Pseudaspidapion and two in Diplapion. Relatively long urogomphi flared to the sides were present, as in Pseudaspidapion and Diplapion (Gosik et al. 2010; Wang et al. 2013).

The laboratory work confirmed that the food and breeding plant for this species is meadow sage (Salvia pratensis). The preimaginal development of S. elongatum occurs in the nodes and internodes of the stems, as well as in the basal part of the root.