Otiorhynchus
publication ID |
https://doi.org/ 10.11646/zootaxa.4108.1.1 |
publication LSID |
lsid:zoobank.org:pub:B802F2B1-944E-4B84-A856-8091E60D88FC |
DOI |
https://doi.org/10.5281/zenodo.6062734 |
persistent identifier |
https://treatment.plazi.org/id/03EB857D-FFEF-AD13-0592-FADA42DB1086 |
treatment provided by |
Plazi |
scientific name |
Otiorhynchus |
status |
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Otiorhynchus View in CoL (s. str.) armadillo (Rossi, 1792)
Material examined: 28 larvae ( Figs. 210 View FIGURES 203 – 210 , 231 View FIGURES 226 – 231 ). Larvae were obtained from permanent breeding in the climate chamber of the JKI, Braunschweig, continued until today and started in 2010 with first instar larvae from Thorsten Ufer, Ellerhoop. On 12.07.2010, 0 9.08.2010 and 12.09.2010 first instar larvae from adults collected in Mühlacker (on 17.06.2010) were placed mainly in flowerpots with Euonymus fortunei cultivar ‘Emerald ‘n Gold’ ( Fig. 221 View FIGURES 220 – 225 ), and also with a cultivar of Bergenia cordifolia and with Primula veris L. Since June 2011 only different cultivars of Euonymus fortunei were used. In flowerpots with first instar larvae from 12.09.2010 the first teneral adult specimen was seen on 0 3.01.2011. The following larvae were used for the description: JKI, Braunschweig, breeding with Primula veris , 16.11.2010, 1 ex.; JKI, permanent breeding with Euonymus fortunei , 21.09.2011, 10 ex.; dto., 28.10.2011, 1 ex.; dto., 0 5.01.2012, 6 ex.; dto., 10.01.2013, 5 ex.; Ellerhoop, breeding by Thorsten Ufer with Euonymus fortunei flowerpots, received on 0 3.01.2011, 5 ex., from plants used for efficacy tests of entomopathogenous nematodes.
Remarks about breeding and development. The life-cycle of this species was studied for the first time by Del Bene & Parrini (1986), but together with Otiorhynchus sulcatus , as preimaginal instars could not be distinguished. This paper contains a long list of ornamental plants from 25 families on which O. armadillo was found, exclusively woody plants including some conifers. According to Del Bene & Parrini (1986) eggs from both species were deposited from June to September, larvae were present from August during the whole winter until April, then pupation occurred from April to end of May, followed by the presence of adults from May to September. Our results for O. armadillo are not completely in accordance with these life-cycle data. There were also overwintering adults already in April, e.g. on Thuja and other bushes. Pupae were found from end of April until end of July and newly hatched adults from mid-May or June until September, which may indicate pupation at least until August. Usually recently emerged adults of O. armadillo were found up 2 to 3 weeks later than the last teneral adults of O. sulcatus (Sprick 2012, in Sprick & Stüben 2012). Apparently, the life-cycle of O. armadillo is very similar to that of O. sulcatus , but should be studied at further sites to complete and validate the data.
Description ( Figs. 56–66 View FIGURES 56 – 61 View FIGURES 62 – 66 ).
Coloration. Head light yellow; all thoracic and abdominal segments milk-white, cuticle smooth.
Body elongated ( Fig. 56 View FIGURES 56 – 61 ). Chaetotaxy. Setae different in length, relatively long, filiform, light yellowish. Thorax. Prothorax with 4 long and 4 medium long to short prns; and 2 ps, different in length. Mesothorax with 1 medium long prs; 4 pds (ordered: 2 short and 2 long); 1 long as; 1 long eps; and 1 long ps. Chaetotaxy of meso- and metathorax similar. Each pedal area of thoracic segments well isolated, with 4 pda, different in length. Each thoracic segment with 1 short eus ( Fig. 57 View FIGURES 56 – 61 ). Abdomen. Abdominal segments I–VIII with 1 short prs; 5 pds (ordered: 2 short, 1 long, 1 short and 1 long); 1 long sps [abd. seg. VIII without sps]; 2 long eps; 1 long and 1 minute ps [abd. seg. VIII with only 1 long ps]; 1 long lsts; and 2 eus ( Figs. 58, 60, 61 View FIGURES 56 – 61 ). Abdominal segment IX with 4 ds, different in length; 1 very long ps; and 2 sts, equal in length ( Figs. 59–61 View FIGURES 56 – 61 ). Lateral lobes of abdominal segment X without seta.
Head subglobose, slightly narrowed bilaterally ( Fig. 62 View FIGURES 62 – 66 ). Head capsule with 4 des, des 1 and des 2 placed on central part of epicranium, des 3 located on frontal suture, des 5 located anterolaterally; 2 fs, fs 4 placed anteromedially, fs 5 located near to antenna; 2 les and 1 ves; all setae relatively long with the exception of fs 4, which is distinctly shorter than the others. Stemmata (2 pairs) very small, feebly visible. Antennal segment membranous, bearing 1 conical sensorium and 2–3 filiform sensilla. Clypeus 2.8 times as wide as long with 1 very short cls, placed posterolaterally ( Fig. 63 View FIGURES 62 – 66 ). Labrum about 2 times as wide as long with 3 straight lms of different length, placed medially or mediolaterally; lms 2 distinctly longer than other setae, only lms2 exceeding the outline of the labrum; the anterior margin of labrum almost rounded ( Fig. 63 View FIGURES 62 – 66 ). Epipharynx with 3 finger-like als, different in length; 3 ams, different in length, one very small ams similar to mes, but the position is more to ams; and 2 very short mes (see comments about ams and mes in Material and Methods); labral rods (lr) elongated, strong convergent ( Fig. 64 View FIGURES 62 – 66 ). Mandible ( Fig. 65 View FIGURES 62 – 66 ) feebly bifid, teeth almost of equal height; with 2 mds, different in length; internal edge with a triangular tooth. Maxilla ( Fig. 66 View FIGURES 62 – 66 ) with 1 very long stps and 2 very long pfs, placed ventrolaterally; 1 very short mbs, situated ventrally. Mala with 5 dms, different in length and 4 straight vms, different in length. Maxillary palpi with two palpomeres; basal palpomere larger than distal; basal palpomere with 1 mxps; distal palpomere with a group of 5 conical, cuticular processes apically; each palpomere with a sensillum. Praelabium heart-shaped ( Fig. 66 View FIGURES 62 – 66 ), with 2 very short ligs and 1 very long prms. Labial palpi with two palpomeres, relatively elongated; both palpomeres almost equal in length; praemental sclerite well visible. Postlabium with 3 pms, different in length; pms 2 very long, 3 times as long as pms 1 and pms 3 ( Fig. 66 View FIGURES 62 – 66 ).
Differential diagnosis. See “Key to larvae of selected Otiorhynchus species” and Tables 1, 2.
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Entiminae |