Types of species of Apionidae (Coleoptera) described by Carl Peter Thunberg (1743-1828) with description of a new genus.

The type specimens of species of Apionidae described by Carl Peter Thunberg are reviewed and lecto- and paralectotypes are designated for Apion craccae Thunberg, 1813, Apion limbatum Thunberg, 1813, Apion punctigerum Thunberg, 1815 and Apion astragali Thunberg, 1815. A new genus Thunbergapion (type species Apion limbatum Thunberg, 1813) is described, figured and placed in the tribe Aplemonini Kissinger, 1968. The new combination Thunbergapion limbatum (Thunberg, 1813) is proposed. A key to the known South African genera of the tribe is given. The following new synonymies are established: Oxystoma craccae (Linnaeus, 1767) = Apion craccae Thunberg, 1813 syn. n., Ischnopterapion (Ischnopterapion) loti (Kirby, 1808) = Apion punctigerum Thunberg, 1815, syn. n., and Pseudoprotapion astragali (Paykull, 1800) = Apion astragali Thunberg, 1815, syn. n.

Introduction

Carl Peter Thunberg (*1743, †1828) was a Swedish botanist and entomologist and disciple of Carolus Linnaeus. He stayed in South Africa from 16 April 1772 to 2 March 1775, when he sailed to Batavia. During his stay in the Cape Colony of the Dutch East India Company (now South Africa) he undertook several short excursions and three long trips beyond the hinterland to collect animals and plants. He visited the colony again during his return journey to Europe, from 27 April to 15 May 1778 (Forbes 1986; Muller and Rookmaaker 1992).

As a result of his trips, Thunberg (1813) presented a list of hitherto known weevil species from the Cape of Good Hope area. He added short diagnoses and references to those previously described. The genera and species treated are summarised in Table 1. None of the new species have been treated in later regional or worldwide catalogues, although they were included in Sherborn’s Index Animalium. The new species were:

Table 1.

Genera and number of species treated in Thunberg (1813), and new species described therein. Names as given originally.

Genus	Total species	New species
Cordyle	2	0
Lixus	4	0
Rhynchaenus	12	0
Apion	2	2
Curculio	32	10
Brachycerus	32	0
Platyrynchos	1	0
Attelabus	4	0
Rhinomacer	1	0

(p. 382)

(p. 382)

(p. 384)

(p. 388) (non Gmelin, 1790, nec Paykull, 1792)

(p. 389) (non Olivier, 1790)

(p. 390)

(p. 390) (non Linnaeus, 1758, nec Herbst, 1795, nec Weber, 1801)

(p. 390) (non Fabricius, 1775, nec Goeze, 1777, nec Paykull, 1792)

(p. 391) (non Drury, 1782, nec Geoffroy, 1785, nec Rossi, 1790, nec Paykull, 1792, nec Olivier, 1807)

(p. 391)

(p. 392)

(p. 393).

The descriptions of these species are insufficient to allow their proper placement to genus. Those described under will be treated below, after studying their type specimens. Those described under may merit a separate study, although it appears from the descriptions that probably the first four and the last two may belong to the Cyclominae (Cyclomini, Hipporhinini). As can be seen from the list above, five of these available names are potentially valid but five are permanently invalid because of primary homonymy.

Thunberg (1815) published another revision of the genera and species of weevils known to him (including Bruchinae), giving descriptions for all of the genera (new were , , and ), enumerating the species belonging to each genus and describing, apparently as new, 29 species. Of these, three were new species attributed to the genus , namely , and . Contrary to the species included in his previous article, these have usually been included in the catalogues of Coleoptera and are well known, at least by name. A summary of the genera and species treated is included in Table 2.

Table 2.

Genera and number of species treated in Thunberg (1815), and new species described therein. Names as given originally.

Genus	Total species	New species
Cordyle	12	3
Ramphus	12	1
Lixus	13	2
Rynchaenus	116	8
Rynchites	12	3
Apion	12	3
Brentus	4	0
Curculio	99	4
Cossonus	2	0
Hyselinus	14	0
Antribus	5	0
Amblycerus	8	3
Platyrhynchus	2	1
Temnocerus	2	0
Brachycerus	29	0
Chyphus	1	0
Attelabus	3	1
Bruchus	12	0
Rhinomacer	2	0

Material and methods

Type specimens of Thunberg’s collection were received from the Zoological Museum of Uppsala University (Sweden). The specimens were studied under a binocular Leica Wild MZ8 microscope and photographed with an Olympus C7070WZ camera mounted on the same microscope or on a photographic frame Kaiser RA1. Microscope slides were studied and photographed with the same camera mounted on a Leitz Diaplan microscope, and some details were drawn by using a drawing tube. Extended focus images were generated using the software CombineZP. The programs Adobe Illustrator CS5.0 and Adobe Photoshop CS5.0 were used for image postproduction and mounting.

Dissection methods and nomenclature of genitalia follow Alonso-Zarazaga (1990). Genitalia and terminalia have been placed in a drop of DMHF on an acetate card accompanying the specimen for long term conservation (Steedman 1958; Bameul 1990).

Labels are described as they were copied by the curators, since they were retained in the drawers. These labels are red and read “Uppsala Univ. Zool. Mus. / Thunbergsaml. nr. # / Genus species / ## TYP.” In the treatment for each species, only the data represented by the marks # and ## are given. Specimens designated as lectotypes are labelled as such, with white labels bordered and printed in red: (PARA)LECTOTYPUS / Genus / species / Thunberg, 181(3-5) / Alonso-Zarazaga des. 2013. Each specimen was also provided with white identification labels printed in black.

Taxonomy

Thunberg, 1813: 382

http://species-id.net/wiki/Apion_craccae

Original description.

A. craccae: nigrum opacum, elytris striatis. *.

Magnitudine pulicis, globosum, nigrum, opacum, omnino simile A. craccae, europaeo.

Material studied.

I have received four specimens from the collection Thunberg: 539, Mus.Thunb. Pierced midway with a long thin pin without head, abdomen glued to a white card below.

1188, Cap. Pierced low with a short thick pin with head.

1189, Sv. Pierced midway with a long thin pin with head. The abbreviation “Sv.” stands for “Svecia” [= Sweden].

15075, no data. Pierced midway with a long thin pin with head.

The specimen with the number 1188 has a further label reading “Cap” and is here designated as lectotype and labelled accordingly. Although the specimens with the numbers 539, 1189 and 15075 are pinned in a similar manner, they cannot be considered as syntypes as their label data do not conform with the original locality, Cape Province, as it can be inferred from the title of the article. However, all four specimens belong to the same species, the European (Linnaeus, 1767). Thunberg, 1813 is thus a new synonym of the name of Linnaeus’ species. It is almost certain that the locality on the lectotype is a mistake.

Thunberg, 1813: 382

http://species-id.net/wiki/Apion_limbatum

Figs 1–2 , 6 –11

Figures 1–5.

Type specimens in Thunberg’s collection 1 Thunberg, 1813, lectotype male, dorsal view 2 Thunberg, 1813, lectotype male, lateral view 3 Thunberg, 1815, lectotype male, dorsolateral view 4 Thunberg, 1815, lectotype, dorsolateral view 5 Thunberg, 1815, syntype, dorsal view.

Figures 6–8.

(Thunberg, 1813) 6 Abdominal sternites, ventral view 7 Male pygidium, dorsal view 8 Male ninth sternite (spiculum gastrale). Scale: 100 µm.

Figures 9–11.

(Thunberg, 1813) 9 Penis, dorsal view, inner sac armature figured outside 10 Penis, lateral view 11 Tegmen, dorsal view. Scale: 100 µm.

A. limbatum: cinereo-fuscum, elytrorum sutura basi margineque externo albidis.

Magnitudo minoris pediculi; totum glabrum, cinereo-coerulescens.

Elytra striata sutura basi margineque externo albo.

Pedes inermes.

One male specimen, glued to a pin 20.4 mm long and 0.59 mm in diameter with the following data: 1293, Cap. The original Thunberg labels, which I have not seen, read: “Apion” (genus label) and “limbatum. Cap.” (species label). It is here designated as the lectotype of this species. The specimen is severely damaged, the abdomen is broken and separated from the body and the elytra are open, but fortunately all legs and antennae are entire. I have been able to recover the abdomen and prepare the remainder of the ventrites, terminalia and genitalia in a drop of DMHF (water- or ethanol-soluble resin) on an acetate card. Study of the specimen showed it to be a member of an hitherto undescribed genus, which is described below.

Thunberg, 1815: 118

Fig. 5

Note.

This species is represented by a single pinned specimen belonging, as usually accepted, to the genus . I refrain from redescribing it here, since a revision of is in preparation by my good colleague and friend Dr. Marek Wanat (Wrocław, Poland).

Thunberg, 1815: 118

http://species-id.net/wiki/Apion_punctigerum

Fig. 4

A. punctigerum: niger, elytris nigris, striatis.

Habitat in Smolandia Sveciae.

Magnitudine pediculi totus opacus, niger.

Elytra gibba, striata, atra.

I have received three specimens, as follows: one divided into three parts and glued onto a square white card, this on a short thin pin with head, with data: 543a, Mus. Thunb.; one headless, worn, pinned high on a long thin pin with head, with data: 543b, Mus. Thunb.; and a third glued to a rectangular label, this on a short thick pin with head, with data: 1191, Smol. The first specimen is a female of (Marsham, 1802), the second a female of either (Gyllenhal, 1813) or (Kirby, 1808), and the third is an etiolated (probably female) specimen of (Kirby, 1808). The first two are coloured brightly, with the elytra more or less metallic, and do not fit Thunberg’s description. The third fits Thunberg’s description, although the body colour has become brownish, and is labelled with the type locality, Smolandia (= Småland, Sweden). I hereby designate this specimen as the lectotype of Thunberg, 1815, and its name becomes a new synonym of that of .

Thunberg, 1815: 118

http://species-id.net/wiki/Apion_astragali

Fig. 3

A. Astragali: caerulescens nitidus, elytris striatis.

Habitat in Vestrogothia Sveciae.

Totus supra nitens, caerulescens; subtus magis niger magnitudine pediculi.

Elytra gibba, striata.

I have received three specimens with red type labels as above, carrying the numbers 1206, 1289 and 1290. Only specimen nr. 1289 has an additional label reading “Vestrog.”. This specimen, pinned high on a long pin with head, is PageBreaka female (Paykull, 1800) and is here designated as lectotype. This allows establishment of the following new synonymy: (Paykull, 1800) = Thunberg, 1815. Specimen 1206 is a male of the same species and is designated as paralectotype. However, specimen 1290 does not fit the original description and is not considered to represent a syntype, not being bright bluish as the others but dull bronze-black. It is a female of (Marsham, 1802). Thunberg’s original species label of this specimen carries a question mark and the letter β, in contrast with the other two, which carry the letter α.

Alonso-Zarazaga gen. n.

urn:lsid:zoobank.org:act:EAAA82B8-0D85-462D-8659-E2F4A1D2FA47

http://species-id.net/wiki/Thunbergapion

Figs 1–2 , 6 –11

Type species.

Thunberg, 1813. Gender neuter.

Description.

With the characters of tribe Aplemonini Kissinger, 1968, as detailed by Alonso-Zarazaga (1990: 88).

Integument. Colour black, elytra with a faint leaden-bluish glint.

Vestiture subsquamose, scales elliptical to lanceolate, in one ordered row on each interstria, sometimes row disordered in the middle of some interstriae. Pronotal vestiture centripetal.

Rostrum 1.28 × as long as pronotum, sparsely squamose in basal third, almost glabrous in apical two thirds, in dorsal view sides slightly convergent to mesorostrum, tubiform from mesorostrum to apex, 5.2 × as long as wide at apex, mesorostrum not dilated, punctures dense and large at base, becoming progressively less dense and smaller towards apex, integument scarcely microreticulate, bright; in side view straight at basal half, weakly deflexed and curved in apical half. Scrobes weakly sulciform.

Head short, separated from occiput by a dorsal transversal depression, forehead little narrower than rostral apex, with two irregular lines of scale-bearing punctures near inner margin of eyes and a central oblong-elliptical, moderately deep fovea. Eyes slightly oblong, moderately convex. Temples very short, ca. ¼ length of eye.

Antennae inserted at basal 0.33 of rostrum. Scapes moderately long, 1.33 × as long as mesorostral width. Clubs elongate, fusiform, 2.6 × as long as wide, sutures visible.

Pronotum moderately transverse, 0.90 × as long as wide, maximum width near middle, weakly narrowed towards base, more strongly so towards apex. Basal flange absent. Prescutellar fovea obsolete, reduced to a very weak oblong depression near base, not longer than a puncture. Base straight.

Scutellum small, subtriangular, glabrous, impunctate.

Elytra oval-elongate, ca. 1.6 × as long as wide (a more precise measure impossible due to the condition of the specimen), widest at middle, humeral calli moderately developed. Striae at apex joining 1+2+9, 3+4, 5+6, 7+8, 2nd not extended outwards, at base 1st shortened before scutellum. No specialized setae.

Ventral areas. Mesocoxae tangent. Median apophysis of mesoventrite triangular, short, median apophysis of metaventrite rather narrow and elongate, tuberculiform. Anterior metasternal rim fine. Abdomen (Fig. 6) strongly and densely punctate, punctures moderately deep, scales not condensed, finer than on disc of metaventrite. First abdominal ventrite ca. 1.8 × as long as 2nd, this as long as 5th. Suture I marked. Fifth ventrite subtruncate at apex.

Pygidium (Fig. 7) of apionine type, with apical flange weakly and widely notched medially.

Legs. Tibiae unarmed. Tarsi robust, 1st protarsomere 1.11 × as long as wide, 2nd transverse, 0.73 × as long as wide, 0.8 × as long as 1st, 3rd 0.69 × as long as wide, deeply bilobed, onychium 3.24 × as long as wide, surpassing lobes of 3rd tarsomere by 0.54 × its own length. No tarsomere ventrally spined. Claws weakly incrassate at base, not toothed.

Genitalia and terminalia: Tegmen (Fig. 11) with parameroid lobes shorter than dorsal portion of ring, apically subtriangular, with short apical membranous microsetose area, basal sclerotized area with some irregularly arranged short macrochaetae and sensilla. Fenestrae separated, curved. Prostegium fused to free ring, with a deep triangular notch and one basal tooth on each side, the teeth with a small inner prominence. Linea arquata obsolete. Free ring and manubrium flattened. Penis (Figs 9–10) weakly compressed, apex of pedon prominent as a trapezoidal truncate plate in dorsal view, in side view gently curved with the apex weakly recurved. Internal sac with apical spicules uniform, ca. 10 µm long, rather condensed in a subtriangular patch, medially with two pieces apparently formed by conglomerate teeth, ca. 80 µm long, and basally with some sparse minute spicules and asperities. Spiculum gastrale (Fig. 8) Y-shaped, slightly asymmetrically curved, manubrium ca. 2.5 × as long as arms.

This description is based only on the male sex, the female is presently unknown.

Material examined.

The lectotype male of Thunberg, 1813, as mentioned above.

Etymology.

This genus is named after Carl Peter Thunberg, the illustrious Swedish naturalist and almost certainly the collector of the type species, during his travels in present-day South Africa.

(Thunberg, 1813) comb. n.

http://species-id.net/wiki/Thunbergapion_limbatum

Description of lectotype.

Measurements (in µm): Body length (not including head and rostrum): 1834. Rostrum: length: 628; width (apical): 120, (mesorostral): 126. Distance from antennal insertions to base: 209. Forehead: width: 107. Eyes: length: 168. Scapes: length: 168; maximum width: 26. Desmomeres 1–7 (length × width): 52 × 26, 31 × 21, 31 × 21, 31 × 21, 31 × 21, 21 × 21, 21 × 21. Clubs (length × width): 178 × 68. Pronotum: length: 492; width (apical): 429, (maximal): 544, (basal): 492. Elytra: length: 1342; joint width (at humeri): 650, (maximal): 900 (last two gross estimations due to open elytra).

Vestiture of upperside consisting of short, lanceolate to elliptical white scales, ca. 30 ×10 µm on pronotum, sparse, not or hardly surpassing margins of punctures, those on elytral interstriae similar, usually touching one another in the row, rarely overlapping, forming duplicate irregular rows in some parts along the interstriae, those of striae smaller, about half the size of the interstrial ones, not touching; elytral scales condensed on the basal third of scutellar interstriae and on basal two thirds of the costal interstriae; ventral scales finer and longer (ca. 50 ×7 µm), condensed on mesoventrite and mesopleural sclerites and on sides of metaventrite and metanepisternum, except the strikingly bare anterolateral angles of metaventrite, sparser on metasternal disc.

Antennae dark piceous brown, shortly setose. Funicles subcylindrical, rather compact.

Pronotum with large superficial punctures ca. 30 µm in diameter, separated by ca. 10 µm, integument weakly microreticulate, shining.

Elytra with striae about half as wide as interstriae.

Wings. Macropterous.

Legs robust, profemora 2.34 × as long as wide, protibiae straight, widening towards apex, 5.35 × as long as wide.

Discussion

The new genus PageBreak belongs to the tribe Aplemonini Kissinger, 1968 by the presence of a male pygidium of the normal apionine type, the abdominal ventrites similarly punctate, the manubrium of the spiculum gastrale much longer than the arms, the absence of a specialized seta on the middle of the 7th interstriae, the deeply notched prostegium with one tooth on each side, fused to the free ring, the elytral striae 1, 2 and 9 not more impressed at apex than on disc, and the tangent mesocoxae. The simple claws and the almost straight rostrum are also common features in this tribe.

Peculiar characters of this genus are the squamose vestiture, condensed on the sutural and marginal interstriae and on the meso- and metapleurites, the long, almost straight rostrum, the fusiform antennal clubs and the two strongly dentate median pieces of the internal sac.

This genus seems to include also at least two other undescribed species from the same area (Marek Wanat, pers. comm.) and may constitute and endemic element.

Using the key to the genera of the Palaearctic region (Alonso-Zarazaga 1990, p. 88 and ff.), which includes all the know genera of Aplemonini except the Mexican Kissinger, 1991, doubtfully a member (Alonso-Zarazaga and Wanat in press), agrees with the characters of couplet 3 and runs to either Wagner, 1930 or Wagner, 1930. It differs from both these genera by the squamose vestiture (piliform in the others), the longer rostrum (shorter than pronotum in the others), the narrower forehead compared with the rostral apex (much wider than apex in the others), the scapes longer than the mesorostral width (0.5–0.7 × as long in the others), the longer, fusiform clubs (ca. 1.9 × as long as wide and oboval in the others), the male pygidium with rim margin weakly notched (angulate in the others), the obsolete linea arquata of tegmen (well marked in the others) and the two medial toothed structures of the internal sac (only small teeth, spicules or asperities in the others).

additionally differs from by its shorter, plumper form (elongate in ), the moderately shiny integument (matt in ), the punctate prorostrum (smooth and shining in ) and the transverse pronotum (oblong in ); the tegmen in both genera is very similar in general and the penis shows a prominent apical knob in .

From additionally differs by its longer 2nd abdominal ventrite (very short in ), the transverse 2nd tarsomere (isodiametric in ) and the shorter manubrium (ca. 7 × as long as arms in ); the apex of the penis is slightly recurved in both genera, but its general shape is rather cylindrical and elongate in . also shares with the condensed vestiture in some ventral areas.

Because of its elongate rostrum, shows some similarity also to , a Mediterranean endemite and probably a relict. The genital structures are very similar in both genera, except for the presence in of long macrochaetae on the parameroid lobes of the tegmen and a well marked linea arquata. In addition, the temones of the penis are very short in this genus (less than half the length of the pedon), which is not the case in .

The species of and are stenophagous on species of the plant genus L. (Hypericaceae), and it is possible that also lives on plants of this genus (there are six species in the Cape Province).

In South Africa, three genera of the tribe Aplemonini are present: Schoenherr, 1847, Wagner, 1907 and gen. n. These genera can be distinguished using the following simple key:

1	Claws toothed. Elytra strongly convex behind middle, anteriorly concave in side view. Host: Zizyphus spp. (Rhamnaceae)	Aplemonus
–	Claws simple or slightly incrassate at base. Elytra uniformly and weakly convex in side view	2
2	Antennal clubs oboval. Metasternal apophysis shortly triangular. Antennal scapes at most as long as mesorostral width. Vestiture piliform. Host: Emex spp. (Polygonaceae)	Perapion
–	Antennal clubs fusiform. Metasternal apophysis narrow and elongate, tuberculiform. Antennal scapes 1.33 × as long as mesorostral width. Vestiture squamose. Host unknown	Thunbergapion