Next Article in Journal
Isorhamnetin Influences the Viability, Superoxide Production and Interleukin-8 Biosynthesis of Human Colorectal Adenocarcinoma HT-29 Cells In Vitro
Next Article in Special Issue
First Record of the Family Malachiidae (Coleoptera: Cleroidea) from Mid-Cretaceous Burmese Amber with a Description of Burmalachius acroantennatus Gen. et Spec. Nov.
Previous Article in Journal
Ultrasound Landmarks in the Approach to the Common Peroneal Nerve in a Sheep Model—Application in Peripheral Nerve Regeneration
Previous Article in Special Issue
First Fossil Record of Trichomanes sensu lato (Hymenophyllaceae) from the Mid-Cretaceous Kachin Amber, Myanmar
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Life
Volume 13
Issue 9
10.3390/life13091920
life-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

First Record of the Genus Cartorhynchites Voss, 1958 (Coleoptera: Rhynchitidae) from Eocene Baltic Amber with a List of Fossil Tooth-Nosed Snout Weevils

by
Andrei A. Legalov
1,2,3,
Andris Bukejs
4,*,
Anarina Vanaga
4 and
Vitalii I. Alekseev
5,6
1
Institute of Systematics and Ecology of Animals, Siberian Branch, Russian Academy of Sciences, 630091 Novosibirsk, Russia
2
Department of Ecology, Biochemistry and Biotechnology, Altai State University, 656049 Barnaul, Russia
3
Department of Forestry and Landscape Construction, Tomsk State University, 634050 Tomsk, Russia
4
Institute of Life Sciences and Technologies, Daugavpils University, Vienıbas 13, 5401 Daugavpils, Latvia
5
Kaliningrad Regional Amber Museum, Marshal Vasilevskii Square 1, 236016 Kaliningrad, Russia
6
Immanuel Kant Baltic Federal University, Nevskogo Str. 14, 236016 Kaliningrad, Russia
*
Author to whom correspondence should be addressed.
Life 2023, 13(9), 1920; https://doi.org/10.3390/life13091920
Submission received: 21 August 2023 / Revised: 9 September 2023 / Accepted: 12 September 2023 / Published: 15 September 2023
(This article belongs to the Special Issue Recent Research on Palaeontology)
Browse Figures
Versions Notes

Abstract

:
A new species of the genus Cartorhynchites (Rhynchitini, Rhynchitina) is described from Baltic amber. Cartorhynchites groehni Legalov, Bukejs et Alekseev sp. n. differs from C. struvei Zherikhin, 1992 from the Miocene of Germany in its smaller body size (2.6 mm), strongly convex eyes, narrower pronotum and wide elytra, and dark brown legs. A new species is studied and illustrated in detail using X-ray micro-computed tomography (μCT). It is the earliest fossil record of subtribe Rhynchitina. A list of fossil Rhynchitidae was compiled. A key to species of Rhynchitidae in Baltic amber was given. Fossil finds of the family Rhynchitidae were discussed. The assumption was made that the Recent distribution range of the genus Cartorhynchites is within the range of its host plant of the genus Symplocos. Probably, a new Eocene species developed on Symplocos kowalewskii, and the Oligocene C. struvei was associated with Symplocos myosotis (Unger).

1. Introduction

Curculionid beetles are a diverse group, numerous in fossil and modern ecosystems. This group includes approximately 62,000 described species [1] and is characterized by a complex taxonomic structure. There is no consensus on how many families this superfamily comprises [1,2,3,4,5,6,7,8,9,10]. Curculionoidea is represented by 131 extinct species in Baltic amber (e.g., [9,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34]).
The family Rhynchitidae, often considered part of the family Attelabidae, was also found in Eocene amber [9,16,25,27,28,31,32,33,34]. Adults are characterized by mandibles externally dentate with which they gnaw plants’ vegetative or generative organs for the development of their larvae; some groups roll packets of leaves [35,36,37]. Previously, all tooth-nosed snout weevils found in Baltic amber belonged only to primitive groups such as the extinct tribe Sayrevilleini, the modern tribe Auletini, and the subtribes Temnocerina and Perrhynchitina from Rhynchitini [33]. Representatives of advanced groups (Deporaini, Byctiscini, and Rhynchitina of Rhynchitini) have not been described from Baltic amber.
This article describes a new extinct species of the genus Cartorhynchites Voss, 1938. A three-dimensional model reconstructed from μCT data was used to assist in the description of the new species. This is not only the first record of a representative of the subtribe Rhynchitina in Baltic amber but also the earliest find of this group in the fossil record. A list of fossil tooth-nosed snout weevils and a key to Rhynchitidae from Baltic amber are compiled.

2. Materials and Methods

The paleontological material examined is deposited in the collection of Carsten Gröhn (Glinde, Germany) [CCGG], separately deposited in the Center of Natural History (Centrum für Naturkunde–CeNak; formerly the Geological-Paleontological Institute and Museum–das Geologisch-Paläontologische Museum) [GPIH] of the University of Hamburg, Germany. The amber piece was polished manually with emery papers of different grit sizes, allowing improved views of the included specimen. The amber piece was not subjected to any supplementary fixation.
The X-ray micro-CT (μCT) observations of specimen “5098” [GPIH] were conducted at the Daugavpils University, Daugavpils, Latvia, using Zeiss Xradia 510 Versa system. Scans were performed with a polychromatic X-ray beam at energy of 40 kV and power of 3W. The sample–detector distance was set to 38 mm, and source to sample distance was 46 mm. Tomographic slices were generated from 2401 rotation steps through a 360-degree rotation, using a 4× objective, and exposure time during each projection was set to 12 s. Acquired images were binned (2 × 2 × 2), giving a voxel size of 3.69 μm. Prior to each full scan, a 20 min warm-up scan was conducted with identical stitch parameters but with reduced rotational steps (201 steps) and exposure times set to 2 s. Images were imported into Dragonfly PRO (ver. 2022.2) software platform for interactive segmentation, data alignment and stitching, 3D visualization, and producing videos of scan data (Supplementary Materials Videos S1–S3).
The photographs of the specimen were taken using a Canon 90D camera with a macro lens (Canon MPE-65 mm). Extended depth of field at high magnifications was achieved by combining multiple images from a range of focal planes using Helicon Focus v. 6.0.18 software, and the resulting images were edited to create figures using Adobe Photoshop CS5.
Specimen observations were made using a Nikon SMZ 745T stereomicroscope. Measurements of the holotype were made using the 3D reconstruction dataset within Dragonfly PRO.
We used previous reports from the literature [37,38,39,40,41,42,43,44,45,46,47,48] and collection data from the Institute of Systematics and Ecology of Animals, Siberian Branch, Russian Academy of Sciences (Novosibirsk, Russia), the Natural History Museum (London, UK), Hungarian Natural History Museum (Budapest, Hungary), Institut Royal des Sciences Naturelles de Belgique (Brussels, Belgium), National Museum of Natural History (Prague, Czech Republic), Zoological Institute of Russian Academy of Sciences (St. Petersburg, Russia), and Museum für Naturkunde der Humboldt-Universität (Berlin, Germany) to show the Recent distributions and localities of fossil forms of the genus Cartorhynchites.
Fossil Rhynchitidae have been described and recorded from 11 localities:
New Jersey amber—United States: Central New Jersey, near the town of Sayreville, South Amboy Fire Clay, Raritan Formation; Upper Cretaceous, Turonian, 93.9–89.8 ± 0.3 Ma;
Orapa—Botswana: Central Botswana, Orapa diamond mine; Upper Cretaceous, Turonian, 91 Ma;
Menat—France: Puy-de-Dome, Middle-Upper Paleocene, Selandian-Thanetian, 61.0–59.0 Ma;
Green River—United States: Colorado, 3–4 km west of railway crossing of Green River, Green River Formation; Lower Eocene, Ypresian, 50.6–48 Ma;
Baltic amber—Russia: Kaliningrad Oblast, Baltic Sea coast and Primorsky amber quarry 2 km east of Yantarny village, Prussian Formation, Middle–Late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma;
Florissant—United States: Colorado, Rocky Mountains, near Pike’s Peak, Florissant Formation; Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma.
Rott—Germany: Nordrhein-Westfalen, Siebengebirge, near Bonn, Rott Formation; Uppermost Oligocene, Upper Chattian, 24.0–23.0 Ma;
Enspel—Germany: Rheinland-Pfalz, Westerwald, Bad Marienberg; Upper Oligocene, Upper Chattian, 24.79–24.56 Ma;
Dominican amber—Dominican Republic: mines in the Cordillera Septentrional, Lower Miocene, Burdigalian, 20–16 Ma;
Mexican amber—Mexico: Yukatan, Chiapas; Sinojovel Formation; Lower Miocene, Burdigalian, 20–16 Ma;
Öhningen (=Oeningen)—Germany: Baden-Württemberg, near Constance Lake (=Bodensee); Upper Freshwater Molasse Formation; Upper Miocene, Langhian-Tortonian (Sarmatian), 15–11.1 Ma;
Binagady—Azerbaijan: Binagady District, 7 km northwest of Baku, 0.5 km southeast of Binagady, Binagady tar pits; Quaternary, Middle Pleistocene; Odintsovo (=Korshov, =Lublinian) interglaciation, 0.190 Ma.
The morphological terminology used in this paper follows Lawrence et al. [49].
The systematics of studied taxa is based on the works of A. Legalov [9,10,37].
Nomenclatural acts introduced in the present work are registered in ZooBank (www.zoobank.org accessed on 8 September 2023) under LSID urn:lsid:zoobank.org:pub:C7B2216C-C3A9-44D7-ADCC-E9EB2847708F.

3. Results

Systematics
Superfamily Curculionoidea Latreille, 1802
Family Rhynchitidae Gistel, 1848
Subfamily Rhynchitinae Gistel, 1848
Supertribe Rhynchititae Gistel, 1848
Tribe Rhynchitini Gistel, 1848
Subtribe Rhynchitina Gistel, 1848
Genus Cartorhynchites Voss, 1938
Subgenus Hyperinvolvulus Legalov, 2003
Type species: Cartorhynchites angusticlavus Legalov, 2003
Cartorhynchites (Hyperinvolvulus) groehni Legalov, Bukejs et Alekseev sp. n. (Figure 1, Figure 2 and Figure 3), (Supplementary Materials Videos S1–S3)
LSID: urn:lsid:zoobank.org:act:3D343D7E-2575-4245-9234-67E90B8E0242.
Type stratum. Baltic amber; Middle–Late Eocene [50,51,52,53,54].
Type locality. Yantarny village (formerly Palmnicken), Kaliningrad Region, Russia.
Derivation of name. The specific epithet is a patronym and is dedicated to Carsten Gröhn (Glinde, Germany), an enthusiast and specialist in Baltic amber.
Diagnosis. The new species differs from C. struvei Zherikhin, 1992 from the Miocene of Germany in its smaller body sizes (2.6 mm), strongly convex eyes, narrower pronotum and wide elytra, and dark brown legs. It is distinguished From other Baltic amber Rhynchitini by its elytra lacking scutellar striole and its rostrum being shorter than its pronotum.
Description. Measurements: body length (without rostrum) about 2.56 mm, body maximum width 1.47 mm; rostrum length 0.62 mm; head length 0.43 mm and head width (across eyes) 0.63 mm; pronotum length 0.72 mm and pronotum maximum width 0.75 mm; and elytra length 1.89 mm and elytra maximum combined width 1.47 mm.
Body convex, dark brown (as preserved). Pubescence: head, pronotum, and elytra with rather dense and long, semierect to erect setae; ventral side of body and legs with shorter, recumbent to semierect setae.
The head has a flat forehead, convex vertex, and large temples about as long as one eye length. Rostrum is quite thick, rather short, 0.86× as long as pronotum, almost straight in lateral view, widest apically, about 2.0× as long as wide basally, 1.8× as long as wide medially, 1.4× as long as wide apically, and is covered with very fine and sparse punctures. The compound eyes are large, subhemispherical, and strongly convex, with a vertical diameter of about 0.88× the horizontal diameter. The mandibles are externally dentate. The maxillary palpi apparently have four palpomeres.
The Antennae have 11 antennomeres, not geniculate, with a distinct three-antennomered club; they are rather long, about 1.36× as long as the rostrum, reaching the middle of the pronotum, inserted laterally in basal one-third of rostral length. The scape is cylindrical, 1.5× as long as it is wide; antennomere 2 is subcylindrical, equal in size as the scape, and 1.3× as wide as antennomere 3; antennomeres 3–4 are conical, elongate, 2.2× as long as they are wide, and equal in size; antennomere 5–8 are conical, subequal in width, 1.2–1.4× as long as they are wide, and slightly shorter than antennomere 4; the antennal club (antennomeres 9–11) is about 0.7× as long as the flagellum (antennomeres 2–8); antennomere 9 is suboval, about 1.3× as long as it is wide, slightly dilated apically, and about 1.5× as wide as antennomere 8; antennomere 10 is suboval, slightly dilated apically, about 1.2× as long as it is wide, and slightly wider than antennomere 9; and antennomere 11 is ovoid, 1.6× as long as it is wide. The relative length ratios of antennomeres 1–11 are equal to 12:12:13:13:10:10:10:10:16:16:23.
The pronotum is nearly bell-shaped, widest in the middle, slightly narrowed posteriad and greatly narrowed anteriad, nearly as long as it is maximum wide, and moderately densely covered with small punctations; its disc is slightly convex, lateral margins are widely rounded medially and oblique anteriorly and posteriorly, posterior margin is convex, and anterior margin is convex from the dorsal view.
The scutellum is nearly pentagonal and is about 0.8× as long as its maximum width.
The Elytra are widely oval, convex, elongate, widest in the middle and 1.3× as long as they are wide combined, 1.5× as long as they are wide combined at the anterior margin, 1.4× as long as they are wide combined in the posterior one-quarter, and 2.6× as long as the pronotum length; the elytral base is emarginated and distinctly wider than the posterior pronotal margin; setae spots are absent; the humeral callus is distinct and prominent; and each elytron is widely rounded separately. The elytral punctations are rather coarse and dense, apparently forming 10 regular rows; the distance between punctures in rows is smaller than the diameter of the punctures; punctures do not merge and do not form pits; and scutellary strioles are absent. Stria 9 is shortened and connected with stria 10 near the metacoxal cavity; interstriae are convex, and the distance between rows is about 1.0× the diameter of the punctures; the apices of the elytra are separately rounded. The elytral epipleuron is wide; it is widest at the humeri and gradually narrows posteriad.
The pre- and postcoxal parts of the prosternum are short. The precoxal part is about 0.05× as long as the procoxal cavity length. The postcoxal part is 0.2× as long as the procoxal cavity length and about 3.7× as long as the precoxal part. The metaventrite with disc convex is about 0.8× as long as the metacoxal cavity length. The metepisternum is about 7.0× as long as wide in the middle. The abdomen is convex and covered with small punctations, with five visible ventrites. Ventrites 1 and 2 are fused, and the suture between ventrites 1 and 2 is indistinct; the sutures between ventrites 2 and 5 are complete and almost straight; ventrite 1 is slightly longer than the metaxocal cavity length; ventrite 5 has a widely rounded apical margin; and the relative length ratios of ventrites 1–5 equal to 6.2:6.8:4.7:3.5:3 (medially). The propygidium is concealed by the elytra. The pygidium is exposed.
The legs are long and slender. The procoxae are conical, contiguous, and located in the middle of the prosternum; the mesocoxae are widely oval, transverse, about 1.3× as wide as they are long, and separated by 0.25× the width of the mesocoxa; the metacoxae are suboval, transverse, and reach the metepisternum. The femora clavate is slightly flattened, covered with fine, sparse punctations, and about 3.0× as long as it is maximum wide. The tibiae are cylindrical, straight, about 6.1× as long as they are maximum wide, nearly as long as the femora, and have sparse and fine punctures. They are not serrated on the inner margin and have a fringe of spinulae apically, without uncus and mucro. The tarsi are long but shorter than the tibiae; the metatarsus is about 0.6× as long as the metatibia. Tarsomere 1 is subconical, slightly dilated apically, and elongate; tarsomere 2 is trapezoidal, nearly as long as it is wide; tarsomere 3 is deeply bilobed, as long as it is wide; tarsomere 4 (apical tarsomere) is subcylindrical, elongate, and slightly curved; metatarsomere 1 is about 1.9× as long as it is maximum wide, slightly shorter than tarsomere 4, 1.9× as long as tarsomere 2, and about 0.4× as long as tarsomeres 2–4 combined; metatarsomere 2 is about 1.2× as long as it is maximum wide; metatarsomere 3 is as long as it is maximum wide; metatarsomere 4 is about 2.6× as long as it is maximum wide; and the relative length ratios of metatarsomeres 1–4 are subequal to 15:8:10:18. The Tarsal claws are free, apparently have teeth basally, and are slightly divergent.
Material examined. Holotype: collection number “5098” [GPIH], “8700” [CCGG] (ex. coll. Jonas Damzen JDC-10503); adult, female. A complete beetle is included in a transparent, yellow amber piece with dimensions of 24 × 15 mm and a maximum thickness of 5 mm and is preserved without supplementary fixation. The right part of the specimen is completely obscured by milky amber. Syninclusions: two larvae of mites (Araci), a few stellate Fagaceae trichomes, and numerous small gas vesicles. The sex of the examined specimen was determined based on micro-CT results. There is no sclerotized aedeagus-like structure present inside the abdomen, and therefore, the specimen appears to be female.
Remarks. The specimen under consideration possesses the combination of characters corresponding to the family Rhynchitidae: antennae that are not geniculate, a distinct epipleuron, maxillary palpi with four palpomeres, ventrites 1 and 2 being fused, tarsomere 1 not being extended, claws that are free at the base, and tibiae that are not serrated on the inner margin. This fossil specimen can be classified into the subfamily Rhynchitinae based on slightly divergent tarsal claws. Externally dentate mandibles suggest placement in the supertribe Rhynchititae. The new species belongs to the tribe Rhynchitini based on contiguous procoxal cavities, separately rounded apices of the elytra, a propygidium concealed by the elytra, metacoxa reaching the metepisternum, convex eyes, and striate elytra. Elytra lacking scutellar strioles suggest placement in the subtribe Rhynchitina. The new species belongs to the genus Cartorhynchites based on a quite thick rostrum that is shorter than the pronotum, a quite short antennal club that is shorter than the flagellum, setae spots on the elytra being absent, punctures in the elytral striae that do not merge and do not form pits, and the eyes being strongly protruding. The dark body covered with long semierect to erect setae suggests placement in the subgenus Hyperinvolvulus.
Key to species of Rhynchitidae in Baltic amber
1. Tarsal claws strongly divergent and lacking teeth ([10] (Figure 62)) (Baltocar, Sayrevilleinae) ..…………………………………..……………………..………………..……………….2
– Tarsal claws are slightly divergent ([10] (Figure 61)) and as is the rule with teeth, if lacking teeth, then the rostrum is longer than the pronotum (Rhynchitinae)…………......7
2. Rostrum shorter or subequal to pronotum. Elytra with irregular punctations ([9] (pl. 7, Figure 1)) ……..…………………………………………………………………………….……..3
– Rostrum longer or subequal to pronotum. Elytra with punctations forming regular rows ([9] (pl. 7, Figure 2)) ……….………………………………………………………………4
3. Rostrum slightly curved ([9] (pl. 7, Figure 1)), subequal to pronotum. Body covered with dense………..………………………………………..…………………..………B. convexus
– Rostrum distinctly curved ([25] (Figure 55)), shorter than pronotum. Body without distinct pubescence …………………………………………………………………….B. subnudus
4. Pronotum coarsely punctate. Setae widened………………………………….B. succinicus
– Pronotum transversely irregularly rugose. Setae narrow……………………..…………..5
5. Pronotum with slightly rounded lateral sides ([25] (Figure 28)), about 1.1× as long as wide. Tarsomere 1 is about 0.6× as long as tarsomeres 2–5 combined ….……………. ……………………………………………………………………………………...B. hoffeinsorum
– Pronotum with subparallel lateral sides ([25] (Figure 21)), 1.4× as long as it is wide. Tarsomere 1 is about 0.4× as long as tarsomeres 2–5 combined …………………………….6
6. Rostrum long ([25] (Figure 16)), 18.0× as long as it is wide medially. Tarsomere 1 is slightly longer than tarsomere 5 and 1.2× as long as tarsomere 2. Elytra 1.2× as long as their maximum combined width. Body longer (2.9 mm).…………………………..B. groehni
– Rostrum shorter ([27] (Figure 1)), 6.8× as long as it is wide medially. Tarsomere 1 is shorter than tarsomere 5 and 1.4× as long as tarsomere 2. Elytra 1.5× as long as their maximum combined width. Body shorter (2.4 mm)…….………………..……….B. sontagae
7. Rounded apex of elytra when both together. (Auletini).…………...……………………..8
– Apices of elytra separately rounded (Rhynchitini).……………………………………… 11
8. Tarsal claws lacking teeth (Electrauletes, Auletini)………………………………...E. unicus
– Tarsal claws with teeth…………………………………………..…………………………….9
9. Rostrum very long ([27] (Figure 3)), 10.5× as long as wide at middle Tibiae lacking costate dorsal margin (Pseudomesauletes, Pseudomesauletina) ….…….………....P. lobanovi
– Rostrum 4.6-7.3× as long as wide at middle ([28] (pl. 6, Figure 4); [32] (Figure 1)). Tibiae with costate dorsal margin (Pseudauletina) …………………………………………………10
10. Body covered with dense protruding setae. Rostrum dorsally flattened, 7.3× as long as wide at middle (Pseudauletes)………….….………………………………………...…P. balticus
– Body almost glabrous. Rostrum dorsally not flattened, 4.6× as long as wide at middle (Eoropseudauletes)……………….………………………………………………...…..E. plucinskii
11. Elytra lacking scutellar striole. Rostrum shorter than pronotum (Figure 2) (Cartorhynchites, Rhynchitina)…………………………….……….………………..C. groehni sp. n.
– Elytra with scutellar striole. Rostrum longer than pronotum…..…………….…………..12
12. Body black, without bronze luster. Rostrum 2.7× as long as pronotum, about 14× as long as wide at middle ([30] (Figure 1)) (Eocenorhynchites, Temnocerina) …….………………………………………………………………………………………... E. vossi
– Body black, with bronze luster. Rostrum 1.1× as long as pronotum, about 5× as long as wide at middle ([31] (Figures 17 and 18)) (Succinorhynchites, Perrhynchitina) .…….... ………………………………………………………………………………………….….S. alberti
List of fossil Rhynchitidae
Subfamily Sayrevilleinae Legalov, 2003
Tribe Sanyrevilleini Legalov, 2003
Genus Orapauletes Legalov, 2009
O. cretaceus Legalov, 2009 [55]–Orapa, Botswana, Turonian, 91 Ma
Genus Sanyrevilleus Gratshev et Zherikhin, 2000
S. grimaldii Gratshev et Zherikhin, 2000 [56]–New Jersey amber, USA, Raritan Formation, Turonian, 93.9–89.8 ± 0.3 Ma
Genus Baltocar Kuschel, 1992
B. convexus Legalov, 2015 [9]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
B. groehni Riedel, 2012 [25]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
B. hoffeinsorum Riedel, 2012 [25]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
B. sontagae Bukejs et Legalov, 2021 [27]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
B. subnudus Riedel, 2012 [25]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
B. succinicus Voss, 1953 [16]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
Tribe Vossicartini Legalov, 2003
Genus Germanocartus Legalov, 2007
G. heydeni (Schlechtendal, 1894) [57]–Rott, Germany, Rott Formation, Upper Chattian, 24.0–23.0 Ma
Subfamily Rhynchitinae Gistel, 1848
Supertribe Rhynchititae Gistel, 1848
Tribe Auletini Desbrochers des Loges, 1908
Subtribe Auletina Desbrochers, 1908
Genus Electrauletes Legalov, 2015
E. unicus Legalov, 2015 [9]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
Subtribe Pseudomesauletina Legalov, 2003
Genus Pseudomesauletes Legalov, 2001
P. culex (Scudder, 1893) [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. ibis (Wickham, 1912) [59]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. lobanovi Bukejs et Legalov, 2021 [27]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
P. obliquus (Wickham, 1913) [60]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. striaticeps (Wickham, 1911) [61]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus Rhynchitobius Sharp, 1889
Rh. tanyrhinus Poinar et Legalov, 2015 [62]–Dominican amber, Dominican Republic, Lower Miocene, Burdigalian, 20–16 Ma
Rh. xuthocolus Poinar et Legalov, 2015 [62]–Dominican amber, Dominican Republic, Lower Miocene, Burdigalian, 20–16 Ma
Subtribe Pseudauletina Voss, 1933
Genus Pseudauletes Voss, 1922
Subgenus Eopseudauletes Legalov, 2007
P. (E.) balticus Legalov, 2022 [32]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
Genus Eoropseudauletes Kania et Legalov, 2019
E. plucinskii Kania et Legalov, 2019 [28]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
Subtribe incertae sedis
Genus Teretrum Scudder, 1893
“T.” quiescitum Scudder, 1893 [58]–Green River, USA, Green River Formation, Lower Eocene, Ypresian, 50.6–48 Ma
T. primulum Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus Docirhynchus Scudder, 1893
D. terebrans Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus incertae sedis
“Trypanorhynchus” depratus Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
“Paltorhynchus” rectirostris Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
“Trypanorhynchus” sedatus Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus Paleauletobius Legalov, 2007
P. silenus (Heer, 1847) [63]–Öhningen, Germany, Upper Freshwater Molasse Formation, Upper Miocene, Langhian-Tortonian, 15–11.1 Ma
Tribe Rhynchitini Gistel, 1848
=Isotheinae Scudder, 1893
Subtribe Temnocerina Legalov, 203
Genus Eocenorhynchites Legalov, 2012
E. vossi Legalov, 2012 [30]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
Subtribe Perrhynchitina Legalov, 2003
Genus Succinorhynchites Legalov, 2013
S. alberti Legalov, 2013 [31]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
Genus Tatianaerhynchites Legalov, 2002
T. goergesi (Zherikhin, 1992) [48]–Rott, Germany, Rott Formation, Upper Chattian, 24.0–23.0 Ma
Subtribe Rhynchitina Gistel, 1848
Genus Cartorhynchites Voss, 1938
C. struvei Zherikhin, 1992 [48]–Rott, Germany, Rott Formation, Upper Chattian, 24.0–23.0 Ma
C. groehni sp. n. [present paper]–Baltic amber, Russia, Prussian Formation, Middle–late Eocene, Bartonian–Priabonian, 41.3–33.9 Ma
Genus Opacoinvolvulus Legalov, 2003
O. rottensis (Zherikhin, 1992) [48]–Rott, Germany, Rott Formation, Upper Chattian, 24.0–23.0 Ma
O. zherichini Legalov, 2003 [48]–Rott, Germany, Rott Formation, Upper Chattian, 24.0–23.0 Ma
Genus Epirhynchites Voss, 1969
Subgenus Tshernyshevinius Legalov, 2003
E. (T.) auratus (Scopoli, 1763)–Binagady, Azerbaijan, Middle Pleistocene; Odintsovo interglaciation, 0.190 Ma
=Rhynchites martynovi Ter-Minassian, 1947 [64]
Subtribe incertae sedis
Genus Isothea Scudder, 1893
I. alleni Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus Trypanorhynchus Scudder, 1893
T. corruptivus Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus Prodeporaus Legalov, 2003
=Paleauletes Legalov, 2003
P. curiosum Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. exanimale Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. exilis (Wickham, 1913) [60]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. minutissimus (Wickham, 1913) [60]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. smithii (Scudder, 1893) [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus Prodeporaides Legalov, 2003
“P.” laminarum (Wickham, 1916) [65]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
“P.” subterraneus (Scudder, 1893) [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
“P.” vulcan (Wickham, 1916) [65]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
P. wymani (Scudder, 1893) [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus incertae sedis
“Masteutes” saxifer Scudder, 1893 [58]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
“Rhynchites” hageni Heyden et Heyden, 1866 [66]–Rott, Germany, Rott Formation, Upper Chattian, 24.0–23.0 Ma
“Rhysosternum” punctatolineatum Piton, 1940 [67]–Menat, Middle-Upper Paleocene, Selandian-Thanetian, 61.0–59.0 Ma
Tribe Eugnamptini Voss, 1930
Genus Eugnamptidea Wickham, 1912
“E.” florissantensis (Wickham, 1913) [60]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
E. robusta Wickham, 1916 [65]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
E. tertiaria Wickham, 1912 [68]–Florissant, USA, Florissant Formation, Uppermost Eocene, Priabonian, 34.07 ± 0.10 Ma
Genus Eugnamptus Schoenherr, 1839
E. proterus Poinar et Brown, 2007 [69]–Mexican amber, Mexico, Sinojovel Formation, Lower Miocene, Burdigalian, 20–16 Ma

4. Discussion

The oldest Rhynchitidae, which belong to the subfamily Sanyrevilleinae, were found in the Turonian age in the USA and Botswana [25,55,56]. A representative of the tribe Rhynchitini, “Rhysosternum” punctatolineatum, was described from the Paleocene in France [34,67]. A specimen, probably in Auletini, was recorded from the early Eocene in Green River [34,58]. In total, 13 tooth-nosed snout weevils have been described from Baltic amber. Nearly half of the species [9,16,25,27] are of the genus Baltocar (Sayrevilleinae). Rhynchitinae are represented by seven species from the subtribes Auletina [9], Pseudomesauletina [27], Pseudauletina [28,32] of the tribe Auletini, and Temnocerina [30], Perrhynchitina [31], and Rhynchitina [given here]. The rhynchitid fauna of the terminal Eocene of Florissant is quite diverse, but the type material needs to be re-examined to clarify the systematic position of the taxa. It includes the first record of the earliest tribe, Eugnamptini [60,65,68]. Representatives of the tribes Auletini and Rhynchitini are also known from the Florissant [9,34,58,60,65].
The Oligocene tooth-nosed snout weevils were found in two Lagerstätten of Germany. An undetermined species of the tribe Rhynchitidae is illustrated in the book “Fossil Insects: an introduction to palaeoentomology” on p. 60, Figure 48 [70] from Enspel. Six species of the tribes Vossicartini (Sayrevilleinae) and Rhynchitini (Rhynchitinae) were described from the upper Chattian of Rott [9,34,48,57,66]. Four species belong to the extant genera Tatianaerhynchites, Cartorhynchites, and Opacoinvolvulus. Representatives of the tribe Auletini and Eugnamptini are found in Dominican [62] and Mexican amber [69] and also in the upper Miocene of Germany [63].
Quaternary Rhynchitidae are very rare. Rhynchites martynovi was described as a new species by Ter-Minassian [64] from the Odintsovo (=Korshov, =Lublinian) interglaciation (Middle Pleistocene, MIS-7). However, it was synonymized with the common extant species Epirhynchites auratus of Azerbaijan fauna [9].
The genus Cartorhynchites includes more than 30 extant and 2 extinct species [37,48,71]. Modern forms are distributed in the Oriental and Australian regions (Figure 4). Records of the genus for the south of the Russian Far East [47] are doubtful. Fossil species are known from late Eocene Baltic amber (represented by the newly described species) and the uppermost Oligocene of Germany [48]. This is an additional example confirming the links between the late Eocene fauna of Europe and the Oriental fauna as well as the previously recorded [29,33] Metrioxenini (Belidae), Rhadinocybini, and Notapionini (Brentidae, Apioninae), Conapium Motschulsky, 1866 (Brentidae, Apioninae, Piezotrachelini), Aedemonini (Curculionidae: Molytinae), and Stromboscerini (Curculionidae, Dryopththorinae). The presence of the genus Cartorhynchites in the late Oligocene suggests that the elements of modern Oriental fauna survived during the Eocene–Oligocene extinction event in Europe and possibly lived until the Pleistocene cooling. Although the genus Cartorhynchites was not found in the European Miocene and later, the genus Phialodes Roelofs, 1874, actually distributed in East Asia [37], is represented in the Miocene (Öhningen) of Germany [31,72]. A representative of the Oriental group Hoplapoderina (Attelabidae), Phymatapoderus flavimanus (Motschulsky, 1860), lived in Belarus during the warm period of the Pleistocene [73].
Species of the genus Cartorhynchites develop on different representatives of the genus Symplocos Jacq. (S. microcalyx Hayata, S. coreana (H. Lév.) Ohwi) from the family Symplocaceae [35,74]. The present-day distribution of the genus Cartorhynchites is completely situated within the range of Symplocaceae (Figure 4). Symplocos kowalewskii (Casp.) Sadowski et Hofmann has recently been reported in Baltic amber [75]. This extinct plant could be a suitable host plant for Cartorhynchites groehni sp. n. described in the current paper. Symplocos myosotis (Unger) Weyland was known from Rott (Oligocene) [76], and possibly Cartorhynchites struvei was associated with this plant.
Studies of the fossil Coleoptera fauna in Baltic amber have been particularly intensive in the last decade. An especially large amount of material has been processed, or sufficient study progress has been made for such beetle groups as, for example, the predatory Cantharidae [77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113] and Coccinellidae [114,115,116,117,118], as well as the herbivorous Cerambycidae [119,120,121,122,123,124,125,126,127,128,129]. New descriptions of species and genera have significantly added to the picture of the fossil beetle assemblage in the Fennosarmatian landmass during the Late Eocene and made adjustments to the conclusions about the paleoecosystems of amber forests. The recent active work on the inventory of the Baltic amber flora [50,51,75,130,131,132,133,134,135] provides a very useful tool for understanding the possible trophic habits of phytophagous beetles and for the reconstruction of possible “host plant–phytophagous beetle” associations in the Paleogene. The family Rhynchitidae is a small part of the Eocene Baltic amber assemblage, consisting of 13 species within 8 genera, but the ongoing study of tooth-nosed snout weevils is a promising addition to the understanding of the interactions between plant-feeders and vegetation as well as the late Eocene stage of insect–plant co-evolution.

5. Conclusions

A new extinct species of the evolutionarily advanced subtribe Rhynchitina was found in Baltic amber. Perhaps it developed on a species of Symplocos from the family Symplocaceae, e.g., S. kowalewskii, also known in Baltic amber. The discovery of a representative of the genus Cartorhynchites confirms the links between modern Oriental fauna and the fauna of the late Eocene of Europe.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/life13091920/s1.

Author Contributions

Conceptualization, A.A.L. and A.B.; writing—original draft preparation, review and editing, A.A.L., A.B. and V.I.A.; visualization, A.V. and A.B.; project administration, A.A.L. and A.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The specimen is deposited in the Center of Natural History (Centrum für Naturkunde–CeNak; formerly the Geological-Paleontological Institute and Museum–das Geologisch-Paläontologische Museum) [GPIH] of the University of Hamburg, Germany.

Acknowledgments

We are sincerely grateful to Carsten Gröhn (Glinde, Germany) for the loan of interesting material, to Aleksej and Jonas Damzen (Vilnius, Lithuania) for photographic preparation and assistance during our amber research, and to Darren A. Pollock (Eastern New Mexico University, Portales, NM, USA) for a native English speaker proofreading of our manuscript. We thank the two anonymous reviewers for their helpful comments and efforts to improve our manuscript.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Oberprieler, R.G.; Marvaldi, A.E.; Anderson, R.S. Weevils, weevils, weevils everywhere. Zootaxa 2007, 1668, 491–520. [Google Scholar] [CrossRef]
  2. Thompson, R.T. Observations on the morphology and classification of weevils (Coleoptera, Curculionoidea) with a key to major groups. J. Nat. Hist. 1992, 26, 835–891. [Google Scholar] [CrossRef]
  3. Kuschel, G. A phylogenetic classification of Curculionoidea to families and subfamilies. Mem. Entomol. Soc. Wash. 1995, 14, 5–33. [Google Scholar]
  4. Shin, A.; Clarke, D.J.; Lemmon, A.R.; Lemmon, E.M.; Aitken, A.L.; Haddad, S.; Farrell, B.D.; Marvaldi, A.E.; Oberprieler, R.G.; McKenna, D.D. Phylogenomic data yield new and robust insights into the phylogeny and evolution of weevils. Mol. Biol. Evol. 2017, 35, 823–836. [Google Scholar] [CrossRef] [PubMed]
  5. Cai, C.; Tihelka, E.; Giacomelli, M.; Lawrence, J.F.; Ślipiński, A.; Kundrata, R.; Yamamoto, S.; Thayer, M.K.; Newton, A.F.; Leschen, R.A.B.; et al. Integrated phylogenomics and fossil data illuminate the evolution of beetles. R. Soc. Open Sci. 2022, 9, 211771. [Google Scholar] [CrossRef] [PubMed]
  6. Zherikhin, V.V.; Egorov, A.B. Weevils (Coleoptera, Curculionidae) from Russian Far East; Institute Biology Soil Science: Vladivostok, Russia, 1991. [Google Scholar]
  7. Morimoto, K.; Kojima, H. Systematic position of the tribe Phylloplatypodini, with remarks on the definitions of the families Scolytidae, Platypodidae, Dryophthoridae and Curculionidae (Coleoptera: Curculionoidea). Esakia 2004, 44, 153–168. [Google Scholar] [CrossRef] [PubMed]
  8. Gratshev, V.G.; Legalov, A.A. The Mesozoic stage of evolution of the family Nemonychidae (Coleoptera, Curculionoidea). Paleontol. J. 2014, 48, 851–944. [Google Scholar] [CrossRef]
  9. Legalov, A.A. Fossil Mesozoic and Cenozoic weevils (Coleoptera, Obrienioidea, Curculionoidea). Paleontol. J. 2015, 49, 1442–1513. [Google Scholar] [CrossRef]
  10. Legalov, A.A. Annotated key to weevils of the world. Part 1. Families Nemonychidae, Anthribidae, Belidae, Ithyceridae, Rhynchitidae, Brachyceridae and Brentidae. Ukr. J. Ecol. 2018, 8, 780–831. [Google Scholar] [CrossRef]
  11. Motschulsky, V. Voyages. Lettres de M. de Motschulsky a M. Ménétriés, 4. Étud. Entomol. 1857, 5, 21–38. [Google Scholar]
  12. Wagner, H. Ein neues Apion aus dem baltischen Bernstein (Coleoptera, Curculionidae). Dtsch. Entomol. Z. 1924, 1924, 134–136. [Google Scholar]
  13. Hustache, A. Un curculionide de l’ambre de la Baltique. Bull. Mens. Soc. Lin. Lyon 1942, 11, 108–109. [Google Scholar] [CrossRef]
  14. Schedl, K. Die Borkenkäfer des baltischen Bernsteins. Zentralb. Ges. Entomol. 1947, 2, 12–45. [Google Scholar]
  15. Ulke, T. A new genus and species of Curculionidae (Coleoptera) in Baltic amber. Not. Nat. 1947, 19, 1–5. [Google Scholar]
  16. Voss, E. Einige Rhynchophoren der Bernsteinfauna (Col.). Mitt. Geol. Paläontol. Inst. Hambg. 1953, 22, 119–140. [Google Scholar]
  17. Zherikhin, V.V. On weevils (Insecta, Coleoptera) from the Baltic amber. Tr. Paleontol. Inst. Akad. Nauk SSSR 1971, 130, 197–209. [Google Scholar]
  18. Voss, E. Einige Rüsselkäfer der Tertiärzeit aus baltischen Bernstein (Coleoptera, Curculionidea). Steenstupia 1972, 2, 167–181. [Google Scholar]
  19. Wanat, M.; Borovec, L. New genus of weevil (Coleoptera, Curculionidae) from Baltic amber. Pol. Pismo Entomol. 1986, 56, 243–247. [Google Scholar]
  20. Kuska, A. Three new species of beetles (Coleoptera: Cantharidae, Anobiidae, Curculionidae) from the Baltic amber. Ann. Up. Sil. Mus. Bytom Entomol. 1992, 3, 107–113. [Google Scholar]
  21. Kuska, A. New beetle species (Coleoptera, Cantharidae, Curculionidae) from the Baltic amber. Prace Muz. Ziemi. 1996, 44, 13–23. [Google Scholar]
  22. Gratshev, V.G.; Zherikhin, V.V. A new anthribid genus from the Baltic amber (Insecta: Coleoptera: Anthribidae). Mitt. Geol. Paläontol. Inst. Hambg. 1995, 78, 149–157. [Google Scholar]
  23. Rheinheimer, J. Neue fossile Rüsselkäfer (Coleoptera: Curculionidae) aus dem Eozän des Baltischen Bernsteins und der Grube Messel bei Darmstadt. Staatl. Mus. Nat. 2007, 365, 1–24. [Google Scholar]
  24. Riedel, A. A new tribe, genus and species of Nemonychidae from Baltic amber (Coleoptera: Curculionoidea: Nemonychidae: Cimberidinae). Insect Syst. Evol. 2010, 41, 29–38. [Google Scholar] [CrossRef]
  25. Riedel, A.; dos Santos Rolo, T.; Cecilia, A.; van de Kamp, T. Sayrevilleinae Legalov, a newly recognised subfamily of fossil weevils (Coleoptera, Curculionoidea, Attelabidae) and the use of synchrotron microtomography to examine inclusions in amber. Zool. J. Linn. Soc. 2012, 165, 773–794. [Google Scholar] [CrossRef]
  26. Yunakov, N.N.; Kirejtshuk, A.G. New genus and species of broad-nosed weevils from Baltic amber and notes on fossils of the subfamily Entiminae (Coleoptera, Curculionidae). ZooKeys 2011, 160, 73–96. [Google Scholar] [CrossRef] [PubMed]
  27. Bukejs, A.; Legalov, A.A. Two new species of the family Rhynchitidae (Coleoptera: Curculionoidea) from Eocene Baltic amber, with key to species and assumed trophic relationships. Foss. Rec. 2021, 24, 117–127. [Google Scholar] [CrossRef]
  28. Kania, J.; Legalov, A.A. A new genus of tooth-nosed snout weevils (Coleoptera: Rhynchitidae) in Baltic amber. Paleontol. J. 2019, 53, 58–62. [Google Scholar] [CrossRef]
  29. Legalov, A.A. A new weevil genus of the tribe Metrioxenini (Coleoptera: Belidae) in Eocene Baltic amber. Hist. Biol. 2012, 24, 213–217. [Google Scholar] [CrossRef]
  30. Legalov, A.A. New Curculionoid beetles (Coleoptera: Curculionoidea) from the Baltic amber. Paleontol. J. 2012, 46, 262–272. [Google Scholar] [CrossRef]
  31. Legalov, A.A. New and little known weevils (Coleoptera: Curculionoidea) from the Paleogene and Neogene. Hist. Biol. 2013, 25, 59–80. [Google Scholar] [CrossRef]
  32. Legalov, A.A. A new species of the genus Pseudauletes Voss (Coleoptera: Rhynchitidae) from Baltic amber. Paleontol. J. 2022, 56, 559–563. [Google Scholar] [CrossRef]
  33. Legalov, A.A. A review of the Curculionoidea (Coleoptera) from European Eocene ambers. Geosciences 2020, 10, 16. [Google Scholar] [CrossRef]
  34. Legalov, A.A. Fossil history of Curculionoidea (Coleoptera) from the Paleogene. Geosciences 2020, 10, 358. [Google Scholar] [CrossRef]
  35. Sawada, Y. A systematic study of the family Rhynchitidae of Japan (Coleoptera, Curculionoidea). Hum. Nat. 1993, 2, 1–93. [Google Scholar]
  36. Zuppa, A.; Osella, G.; Biondi, S. Parental care in Attelabidae (Coleoptera, Curculionoidea). Ethol. Ecol. Evol. 1994, 3, 113–118. [Google Scholar] [CrossRef]
  37. Legalov, A.A. Leaf-Rolling Weevils (Coleoptera: Rhynchitidae, Attelabidae) of the World Fauna; Agro-Siberia: Novosibirsk, Russia, 2007. [Google Scholar]
  38. Pascoe, F.P. Descriptions of some new Asiatic species of Rhynchites. Ann. Mag. Nat. Hist. 1875, 16, 391–395. [Google Scholar] [CrossRef]
  39. Sharp, D. The rhynchophorous Coleoptera of Japan. Part I. Attelabidae and Rhynchitidae. Trans. Entomol. Soc. Lond. 1889, 1, 41–75. [Google Scholar]
  40. Voss, E. Entomologia Malayana Bakeri: Einige unbeschrebene Rhynchitinen (Coleoptera, Curculionidae) (25. Beitrag zur Kenntnis der Curculioniden). Philipp. J. Sci. 1932, 49, 555–563. [Google Scholar]
  41. Voss, E. Ein Beitrag zur Kenntnis der Attelabiden Javas (57. Beitrag zur Kenntnis der Curculioniden). Tijdschr. Voor Entomol. 1935, 78, 95–125. [Google Scholar]
  42. Voss, E. Monographie der Rhynchitinen Tribus Rhynchitini. V. 2. Teil der Monographie der Rhynchitinae-Pterocolinae. (45. Beitrag zur Kenntnis der Curculioniden). Koleopterol. Rundsch. 1938, 24, 129–171. [Google Scholar]
  43. Voss, E. Über Rüsselkäfer der indomalayischen Subregion, vorwiegend von Java (Col., Curc.) (82. Beitrag zur Kenntnis der Curculioniden). Tijdschr. Entomol. 1940, 83, 17–93. [Google Scholar]
  44. Voss, E. Ein Beitrag zur Kenntnis der Curculioniden im Grenzgebiet der orientalischen zur Paläarktischen Region (Coleoptera, Curculionidae). Die von J. Klapperich und Tschung Sen in der Provinz Fukien gesammelten Rüsselkäfer (132. Beitrag zur Kenntnis der Curculioniden). Decheniana 1958, 5, 1–139. [Google Scholar]
  45. Voss, E. Monographie der Rhynchitinen-Tribus Rhynchitini. 2. Gattungsgruppe: Rhynchitina (Coleoptera-Curculionidae). V.2. Teil der Monographie der Rhynchitinae-Pterocolinae). (195. Beitrag zur Kenntnis der Curculioniden). Entomol. Arb. Mus. Frey 1969, 20, 117–375. [Google Scholar]
  46. Voss, E. Coleoptera of the Loo-Choo Archipelago (III). 24. Families Attelabidae and Curculionidae. Uber Attelabiden und Curculioniden von den japanischen Inseln) (208. Beitrag zur Kenntnis der Curculioniden). Mem. Fac. Educ. Kagawa Univ. 1971, 2, 43–55. [Google Scholar]
  47. Egorov, A.B. Fam. Rhynchitidae–rinchitidy. In A Key to Insects of the Russian Far East; Ler, P.A., Ed.; Dal’nauka: Vladivostok, Russia, 1996; Volume 3, pp. 199–215. [Google Scholar]
  48. Zherichin, V.V. Tertiary weevils (Insecta, Coleoptera: Curculionoidea), identified from the collections of the Senckenberg Museum. Senckenberg. Lethaea 1992, 72, 169–178. [Google Scholar]
  49. Lawrence, J.F.; Beutel, R.G.; Leschen, R.A.B.; Slipinsky, S.A. Chapter 2. Glossary of morphological terms. In Handbook of Zoology. Arthropoda: Insecta. Coleoptera, Beetles. Volume 2: Morphology and Systematics (Elateroidea, Bostrichiformia, Cucujiformia Partim); Kristensen, N.P., Beutel, R.G., Eds.; Walter de Gruyter: Berlin, Germany; New York, NY, USA, 2010; pp. 9–20. [Google Scholar]
  50. Sadowski, E.-M.; Seyfullah, L.J.; Schmidt, A.R.; Kunzmann, L. Conifers of the ‘Baltic amber forest’ and their palaeoecological significance. Stapfia 2017, 106, 1–73. [Google Scholar]
  51. Sadowski, E.-M.; Schmidt, A.R.; Denk, T. Staminate inflorescences with in situ pollen from Eocene Baltic amber reveal high diversity in Fagaceae (oak family). Willdenowia 2020, 50, 405–517. [Google Scholar] [CrossRef]
  52. Seyfullah, L.J.; Beimforde, C.; Dal Corso, J.; Perrichot, V.; Rikkinen, J.; Schmidt, A.R. Production and preservation of resins-past and present. Biol. Rev. 2018, 93, 1684–1714. [Google Scholar] [CrossRef]
  53. Bukejs, A.; Alekseev, V.I.; Pollock, D.A. Waidelotinae, a new subfamily of Pyrochroidae (Coleoptera: Tenebrionoidea) from Baltic amber of the Sambian peninsula and the interpretation of Sambian amber stratigraphy, age and location. Zootaxa 2019, 4664, 261–273. [Google Scholar] [CrossRef]
  54. Kasiński, J.R.; Kramarska, R.; Słodkowska, B.; Sivkov, V.; Piwocki, M. Paleocene and Eocene deposits on the eastern margin of the Gulf of Gdańsk (Yantarny P-1 bore hole, Kaliningrad region, Russia). Geol. Q. 2020, 64, 29–53. [Google Scholar]
  55. Legalov, A.A. Contribution to the knowledge of the Mesozoic Curculionoidea (Coleoptera). Amur. Zool. Zh. 2009, 1, 283–295. [Google Scholar] [CrossRef]
  56. Gratshev, V.G.; Zherikhin, V.V. The weevils from the Late Cretaceous New Jersey amber (Coleoptera, Curculionoidea). In Studies on Fossils in Amber, with Particular Reference to the Cretaceous of New Jersey; Backhuys Publ.: Leiden, The Netherlands, 2000; pp. 241–254. [Google Scholar]
  57. Schlechtendal, D.H.R. Beiträge zur Kenntnis Fossiler Insekten aus dem Braunkohlengebirge von Rott am Siebengebirge. Abh. Naturforsch. Gesellsch. Halle 1894, 20. [Google Scholar]
  58. Scudder, S.H. Tertiary rhynchophorus Coleoptera of the United States. Monogr. US Geol. Surv. Tert. 1893, 21, 1–206. [Google Scholar]
  59. Wickham, H.F. A report on some recent of fossil Coleoptera from the Miocene Shales of Florissant. Bull. Lab. Nat. Hist. State Univ. Iowa 1912, 6, 3–38. [Google Scholar]
  60. Wickham, H.F. Fossil Coleoptera from the Wilson Ranch near Florissant, Colorado. Bull. Lab. Nat. Hist. State Univ. Iowa 1913, 6, 3–29. [Google Scholar]
  61. Wickham, H.F. Fossil Coleoptera from Florissant, with descriptions of several new species. Bull. Am. Mus. Nat. Hist. 1911, 30, 53–69. [Google Scholar]
  62. Poinar, G.; Legalov, A.A. Two new species of the genus Rhynchitobius Sharp, 1889 (Coleoptera: Rhynchitidae) in Dominican amber. Ann. Soc. Entomol. France (NS) 2015, 51, 70–77. [Google Scholar] [CrossRef]
  63. Heer, O. Die Insektenfauna der Tertiargebilde von Oeningen und von Radoboj in Croatien. Erste Theil. Käfer. Neue Denksch. Allgem. Schweizer. Gesellsch. Gesam. Naturwiss. Leipzig 1847, 8, 1–230. [Google Scholar]
  64. Ter-Minassian, M.E. New fossil species of the genus Rhynchites Schneid. (Coleoptera, Attelabidae) from the Binagady Beds. Dokl. Akad. Nauk Arm. SSR 1947, 7, 227–229. [Google Scholar]
  65. Wickham, H.F. New fossil Coleoptera from the Florissant beds. Bull. Lab. Nat. Hist. State Univ. Iowa 1916, 7, 3–20. [Google Scholar]
  66. Heyden, C.; Heyden, L. Käfer und Polypen aus der Braunkohle des Siebengebirges. Palaeontographica 1866, 15, 131–156. [Google Scholar]
  67. Piton, L. Paléontologie du Gisement Éocène de Menat (Puy-de-Dôme) (Flore et Faune); Imprim. Paul Vallier: Clermont-Ferrand, France, 1940. [Google Scholar]
  68. Wickham, H.F. On some fossil Rhynchophorus Coleoptera from Florissant Colorado. Bull. Am. Mus. Nat. Hist. 1912, 31, 41–55. [Google Scholar]
  69. Poinar, G.O.; Brown, A.E. Eugnamptus proterus sp. n. (Coleoptera: Curculionoidea: Rhynchitidae), a tooth nosed snout beetle in Mexican amber. Proc. Entomol. Soc. Wash. 2007, 109, 880–885. [Google Scholar]
  70. Penney, D.; Jepson, J.E. Fossil Insects: An Introduction to Palaeoentomology; Siri Scientific Press: Manchester, UK, 2014; pp. 1–223. [Google Scholar]
  71. Legalov, A.A. New species of the family Rhynchitidae (Coleoptera) from Asia and Africa. Stud. Rep. Distr. Mus. Prague-East. Taxonom. Ser. 2011, 7, 333–342. [Google Scholar]
  72. Heer, O. Die Urwelt der Schweiz; F. Schulthess Verlag: Zürich, Switzerland, 1865. [Google Scholar]
  73. Nazarov, V.I. New species of the entomofauna of the Mikulin Interglacial in Belarus. In Novyye i Maloizvestnyye Vidy Zhivotnykh i Rasteniy Belorussii; Nauka i Tekhnika: Minsk, Belarus, 1986; pp. 167–171. [Google Scholar]
  74. Sawada, Y. Oviposition behavior of two rhynchitid weevils (Coleoptera, Curculionoidea). Hum. Nat. 1994, 1, 57–61. [Google Scholar]
  75. Sadowski, E.M.; Hofmann, C.C. The largest amber-preserved flower revisited. Sci. Rep. 2023, 13, 17. [Google Scholar] [CrossRef]
  76. Weyland, H. Beiträge zur Kenntnis der Rheinischen Tertiärflora III. Palaeontographica 1938, 83, 123–171. [Google Scholar]
  77. Fanti, F. Malthodes michalskii: A new species of Cantharidae from Baltic amber (Coleoptera). G. It. Ent. 2017, 14, 685–690. [Google Scholar]
  78. Fanti, F. New fossil Cantharidae genus and species from Baltic amber (Insecta Coleoptera). G. It. Ent. 2017, 14, 709–714. [Google Scholar]
  79. Fanti, F. Malthodes meriae sp. nov.: A new fossil Malthodes Kiesenwetter, 1852 from the Eocene Baltic forests (Coleoptera: Cantharidae). Stud. Rep. Taxon. Ser. 2018, 14, 243–248. [Google Scholar]
  80. Fanti, F. New fossil Malthodes Kiesenwetter, 1852 of the subgenus Libertimalthodes Kupryjanowicz & Fanti, 2019 from Baltic amber (Coleoptera: Cantharidae). Palaeodiversity 2019, 12, 65–68. [Google Scholar]
  81. Fanti, F. Two new fossil soldier beetles from the Baltic amber (Coleoptera: Cantharidae). Stud. Rep. Taxon. Ser. 2020, 16, 13–19. [Google Scholar]
  82. Fanti, F. Two new Malthodes and a new Podistra from Eocene Baltic amber (Coleoptera, Cantharidae). Balt. J. Coleopterol. 2021, 21, 1–9. [Google Scholar]
  83. Fanti, F. A new genus of Cantharidae from Eocene Baltic amber found in Poland, with phoretic mites. Balt. J. Coleopterol. 2021, 21, 105–110. [Google Scholar]
  84. Fanti, F. Taxonomical notes on some fossil soldier beetles (Cantharidae). Balt. J. Coleopterol. 2022, 22, 319–325. [Google Scholar]
  85. Fanti, F. A new fossil of Mantimalthinus (Coleoptera: Cantharidae) sheds light on its tribal attribution. Stud. Rep. Taxon. Ser. 2022, 18, 281–286. [Google Scholar]
  86. Fanti, F.; Castiglione, E. Description of a new genus and species of Cantharidae from Eocene Baltic amber (Insecta, Coleoptera). Palaeodiversity 2017, 10, 123–127. [Google Scholar] [CrossRef]
  87. Fanti, F.; Damgaard, A.L. Fossil soldier beetles from Baltic amber of the Anders Damgaard amber collection (Coleoptera Cantharidae). Balt. J. Coleopterol. 2018, 18, 1–32. [Google Scholar]
  88. Fanti, F.; Damgaard, A.L. New soldier beetles (Cantharidae) from Baltic, Burmese and Dominican ambers of the Anders Damgaard amber collection. Balt. J. Coleopterol. 2019, 19, 101–125. [Google Scholar]
  89. Fanti, F.; Damgaard, A.L. Fossil soldier beetles of the Anders Damgaard amber collection. Fourth update. Balt. J. Coleopterol. 2020, 20, 125–139. [Google Scholar]
  90. Fanti, F.; Kupryjanowicz, J. A new soldier beetle from Eocene Baltic amber. Acta Palaeontol. Pol. 2017, 62, 785–788. [Google Scholar] [CrossRef]
  91. Fanti, F.; Kupryjanowicz, J. Discovery of a new fossil soldier beetle in Eocene Baltic amber, with the establishment of the new tribe Cacomorphocerini. Ann. Paléontol. 2018, 104, 149–153. [Google Scholar] [CrossRef]
  92. Fanti, F.; Michalski, A.R. An unusual fossil Malthodes with long elytra (Insecta Coleoptera Cantharidae). G. It. Ent. 2018, 15, 127–132. [Google Scholar]
  93. Fanti, F.; Pankowski, M.J. A new fossil soldier beetle (Coleoptera, Cantharidae, Silinae) from Eocene Baltic amber. Zootaxa 2018, 4370, 189–193. [Google Scholar] [CrossRef] [PubMed]
  94. Fanti, F.; Pankowski, M.K. Three new species of soldier beetles from Baltic amber (Coleoptera, Cantharidae). Zootaxa 2018, 4455, 513–524. [Google Scholar] [CrossRef] [PubMed]
  95. Fanti, F.; Pankowski, M.K. A new soldier beetle of the extinct tribe Cacomorphocerini Fanti & Kupryjanowicz, 2018. Zootaxa 2019, 4651, 589–595. [Google Scholar]
  96. Fanti, F.; Pankowski, M.G. A new Eocene soldier beetle (Cantharidae) of the genus †Cacomorphocerus Schaufuss, 1892 from Baltic amber. Zootaxa 2020, 4869, 437–443. [Google Scholar] [CrossRef]
  97. Fanti, F.; Pankowski, M.G. Two new species of Cantharis Linnaeus, 1758 from Baltic amber. Zootaxa 2020, 4878, 401–411. [Google Scholar] [CrossRef]
  98. Fanti, F.; Pankowski, M.G. A new fossil Silis Charpentier, 1825 from Baltic amber (Cantharidae, Silinae, Silini). Zootaxa 2022, 5195, 087–091. [Google Scholar] [CrossRef]
  99. Fanti, F.; Sontag, E. A new fossil soldier beetle (Coleoptera: Cantharidae: Malthininae) from Baltic amber. Zootaxa 2019, 4629, 583–588. [Google Scholar] [CrossRef]
  100. Fanti, F.; Vitali, F. Key to fossil Malthininae, with description of two new species in Baltic amber (Coleoptera Cantharidae). Balt. J. Coleopterol. 2017, 17, 19–27. [Google Scholar]
  101. Fanti, F.; Vitali, F. A new species of the enigmatic genus Kuskaella Fanti & Kupryjanowicz, 2017 (Coleoptera, Cantharidae) from Baltic amber. Balt. J. Coleopterol. 2020, 20, 1–6. [Google Scholar]
  102. Kazantsev, S.V. New taxa of Baltic amber soldier beetles (Insecta: Coleoptera: Cantharidae) with synonymic and taxonomic notes. Russ. Entomol. J. 2013, 22, 283–293. [Google Scholar]
  103. Kazantsev, S.V. New Baltic amber soldier beetles (Coleoptera, Cantharidae, Cantharinae). Euroasian Entomol. J. 2018, 17, 146–152. [Google Scholar] [CrossRef]
  104. Kazantsev, S.V. New Baltic amber soldier beetles (Insecta: Coleoptera: Cantharidae) with some taxonomic notes. Palaeoentomology 2020, 3, 260–268. [Google Scholar] [CrossRef]
  105. Kazantsev, S.V. New species of Baltic amber soldier beetles (Insecta: Coleoptera: Cantharidae). Russ. Entomol. J. 2021, 30, 153–158. [Google Scholar] [CrossRef]
  106. Kupryjanowicz, J.; Fanti, F. New subgenus and three new species of soldier beetles from the Eocene of Baltic amber. Palaeontol. Electron. 2019, 22, 1–14. [Google Scholar] [CrossRef] [PubMed]
  107. Pankowski, M.G.; Fanti, F. Two new fossil species of soldier beetles (Coleoptera, Cantharidae, Malthininae) from Baltic amber. Zootaxa 2022, 5165, 548–556. [Google Scholar] [CrossRef]
  108. Pankowski, M.G.; Fanti, F. Six new species of fossil soldier beetles (Coleoptera: Cantharidae) from Eocene Baltic amber. Palaeoentomology 2023, 6, 300–312. [Google Scholar] [CrossRef]
  109. Parisi, F.; Fanti, F. A new fossil Malthodes Kiesenwetter, 1852 from the Eocene Baltic amber (Coleoptera Cantharidae). Zootaxa 2019, 4652, 189–195. [Google Scholar] [CrossRef]
  110. Parisi, F.; Fanti, F. A new fossil species of the extinct tribe Mimoplatycini Kazantsev, 2013 (Coleoptera Cantharidae). Ann. Paléontol. 2019, 105, 119–122. [Google Scholar] [CrossRef]
  111. Parisi, F.; Fanti, F. On the first Silis Charpentier, 1825 from Baltic amber (Coleoptera, Cantharidae). Foss. Rec. 2019, 22, 119–123. [Google Scholar] [CrossRef]
  112. Parisi, F.; Fanti, F. Baltic amber: A new Cacomorphocerus Schaufuss, 1892 with two specimens preserved in a single piece, and four new Malthodes Kiesenwetter, 1852. Zootaxa 2020, 4778, 546–560. [Google Scholar] [CrossRef] [PubMed]
  113. Wentzel, D.; Bonino, E.; Fanti, F. A new Cacomorphocerus Schaufuss, 1892 (Cantharidae) from Baltic amber. Balt. J. Coleopterol. 2022, 22, 313–318. [Google Scholar]
  114. Szawaryn, K.; Szwedo, J. Have ladybird beetles and whiteflies coexisted for at least 40 Mya? PalZ 2018, 92, 593–603. [Google Scholar] [CrossRef]
  115. Szawaryn, K. Unexpected diversity of whitefly predators in Eocene Baltic amber-new fossil Serangium species (Coleoptera: Coccinellidae). Zootaxa 2019, 4571, 270–276. [Google Scholar] [CrossRef]
  116. Szawaryn, K. The first fossil Microweiseini (Coleoptera: Coccinellidae) from the Eocene of Europe and its significance for the reconstruction of the evolution of ladybird beetles. Zool. J. Linn. Soc. 2021, 193, 1294–1309. [Google Scholar] [CrossRef]
  117. Szawaryn, K.; Tomaszewska, W. New and known extinct species of Rhyzobius Stephens, 1829 shed light on the phylogeny and biogeography of the genus and the tribe Coccidulini (Coleoptera: Coccinellidae). J. Syst. Palaeontol. 2020, 18, 1445–1461. [Google Scholar] [CrossRef]
  118. Szawaryn, K.; Tomaszewska, W. The first fossil sticholotidini ladybird beetle (Coleoptera, Coccinellidae) reveals a transition zone through northern Europe during the Eocene. Pap. Palaeontol. 2020, 6, 651–659. [Google Scholar] [CrossRef]
  119. Vitali, F. Six new fossil cerambycids included in Baltic and Saxon amber (Coleoptera Cerambycidae). Entomapeiron (PS) 2011, 4, 1–34. [Google Scholar]
  120. Vitali, F. New fossil cerambycids (Coleoptera: Cerambycidae) from Baltic amber belonging to the collection Hoffeins. Balt. J. Coleopterol. 2014, 14, 103–112. [Google Scholar]
  121. Vitali, F. Mesalocerus tetropoides n. gen., n. sp. from Baltic amber: The first fossil member of the tribe Anisarthrini Mamaev & Danilevsky, 1973 (Coleoptera, Cerambycidae). Cah. Mage. NS 2015, 18, 69–73. [Google Scholar]
  122. Vitali, F. Obrium damgaardi sp. n. (Coleoptera: Cerambycidae), the first fossil species of the genus Obrium Dejean from the Baltic amber. Balt. J. Coleopterol. 2015, 15, 165–170. [Google Scholar]
  123. Vitali, F. Eurapatophysis groehni n. gen. and n. sp. (Coleoptera: Cerambycidae) from Baltic amber: The first fossil member of the tribe Apatophyseini Lacordaire, 1869. Balt. J. Coleopterol. 2016, 16, 117–122. [Google Scholar]
  124. Vitali, F. Two new fossil species of Tillomorphites Vitali (Coleoptera: Cerambycidae) and remarks on the morphological evolution, mimicry, biogeography and phylogeny of the tribe Tillomorphini. Balt. J. Coleopterol. 2017, 17, 147–160. [Google Scholar]
  125. Vitali, F. Procleomenes gouverneuri sp. n. (Coleoptera: Cerambycidae) from Baltic amber: The first fossil member of the tribe Sestyrini Lacordaire, 1869. Balt. J. Coleopterol. 2018, 18, 33–38. [Google Scholar]
  126. Vitali, F. Paratimia succinicola sp. n. (Coleoptera: Cerambycidae) from Baltic amber, with palaeogeographical remarks on the tribe Atimiini LaConte, 1873. Balt. J. Coleopterol. 2020, 20, 53–60. [Google Scholar]
  127. Vitali, F. Eurocrossotus alekseevi gen. n., sp. n. (Coleoptera: Cerambycidae) from Baltic amber, the first fossil member of the tribe Crossotini Thomson, 1864. Balt. J. Coleopterol. 2021, 21, 221–228. [Google Scholar]
  128. Vitali, F. Two new Pogonocherus species (Coleoptera: Cerambycidae) from Baltic amber. Balt. J. Coleopterol. 2022, 22, 103–110. [Google Scholar]
  129. Vitali, F.; Daamgard, A.L. Dicentrus mehli sp. n. (Coleoptera: Cerambycidae) implies close trophic association between Opsimini and Calocedrus, dating back the Baltic amber to the Early Oligocene. Balt. J. Coleopterol. 2016, 16, 37–43. [Google Scholar]
  130. Alekseev, P.I. The revision of gymnosperm species from Eocene Baltic amber. Bot. Zh. 2018, 103, 229–245. [Google Scholar]
  131. Alekseev, P.I.; Gnilovskaja, A.A. The diversity of Pinaceae pollen cones from Baltic amber (Late Eocene). Palaeobotany 2016, 7, 47–55. [Google Scholar] [CrossRef]
  132. Ignatov, M.S.; Abakarova, A.S.; Alekseev, P.I.; Kučera, J. Cynodontium eocenicum, a new moss from the Baltic amber. Arctoa 2016, 25, 236–240. [Google Scholar]
  133. Tarasevich, V.F.; Alekseev, P.I. Inclusions of angiosperm pollen in the Baltic amber (Late Eocene). Bot. Zh. 2017, 102, 206–213. [Google Scholar]
  134. Sadowski, E.-M.; Seyfullah, L.J.; Regalado, L.; Skadell, L.E.; Gehler, A.; Gröhn, C.; Hoffeins, C.; Hoffeins, H.W.; Neumann, C.; Schneider, H.; et al. How diverse were ferns in the Baltic amber forest? J. Syst. Evol. 2019, 4, 305–328. [Google Scholar] [CrossRef]
  135. Sadowski, E.-M.; Schmidt, A.R.; Kuzmann, L. The hyperdiverse conifer flora of the Baltic amber forest. Palaeontogr. Abt. B Palaeophytologie 2022, 304, 1–148. [Google Scholar] [CrossRef]
Life 13 01920 g001
Figure 1. Photomicrograph of Cartorhynchites (Hyperinvolvulus) groehni sp. n., holotype, No. 5098 [GPIH], habitus in lateral view. Scale bar represents 1.0 mm.
Figure 1. Photomicrograph of Cartorhynchites (Hyperinvolvulus) groehni sp. n., holotype, No. 5098 [GPIH], habitus in lateral view. Scale bar represents 1.0 mm.
Life 13 01920 g001
Life 13 01920 g002
Figure 2. X-ray μCT renderings of Cartorhynchites (Hyperinvolvulus) groehni sp. n., holotype, No. 5098 [GPIH], habitus. (A) dorsal view; (B) ventral view; (C) idem, with legs and antennae removed; (D) frontal view; (E) left lateral view; (F) right lateral view. Scale bar represents 1.0 mm.
Figure 2. X-ray μCT renderings of Cartorhynchites (Hyperinvolvulus) groehni sp. n., holotype, No. 5098 [GPIH], habitus. (A) dorsal view; (B) ventral view; (C) idem, with legs and antennae removed; (D) frontal view; (E) left lateral view; (F) right lateral view. Scale bar represents 1.0 mm.
Life 13 01920 g002
Life 13 01920 g003
Figure 3. X-ray μCT renderings of Cartorhynchites (Hyperinvolvulus) groehni sp. n., holotype, No. 5098 [GPIH], right antenna in different views. Scale bar represents 0.1 mm.
Figure 3. X-ray μCT renderings of Cartorhynchites (Hyperinvolvulus) groehni sp. n., holotype, No. 5098 [GPIH], right antenna in different views. Scale bar represents 0.1 mm.
Life 13 01920 g003
Life 13 01920 g004
Figure 4. Distribution of the species of the genus Cartorhynchites and genus Symplocos: recent members of Cartorhynchites—green shaded area; recent distribution of Symplocos—red line; blue circle—Eocene record of Cartorhynchites; and brown circle—Oligocene record of Cartorhynchites.
Figure 4. Distribution of the species of the genus Cartorhynchites and genus Symplocos: recent members of Cartorhynchites—green shaded area; recent distribution of Symplocos—red line; blue circle—Eocene record of Cartorhynchites; and brown circle—Oligocene record of Cartorhynchites.
Life 13 01920 g004
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Legalov, A.A.; Bukejs, A.; Vanaga, A.; Alekseev, V.I. First Record of the Genus Cartorhynchites Voss, 1958 (Coleoptera: Rhynchitidae) from Eocene Baltic Amber with a List of Fossil Tooth-Nosed Snout Weevils. Life 2023, 13, 1920. https://doi.org/10.3390/life13091920

AMA Style

Legalov AA, Bukejs A, Vanaga A, Alekseev VI. First Record of the Genus Cartorhynchites Voss, 1958 (Coleoptera: Rhynchitidae) from Eocene Baltic Amber with a List of Fossil Tooth-Nosed Snout Weevils. Life. 2023; 13(9):1920. https://doi.org/10.3390/life13091920

Chicago/Turabian Style

Legalov, Andrei A., Andris Bukejs, Anarina Vanaga, and Vitalii I. Alekseev. 2023. "First Record of the Genus Cartorhynchites Voss, 1958 (Coleoptera: Rhynchitidae) from Eocene Baltic Amber with a List of Fossil Tooth-Nosed Snout Weevils" Life 13, no. 9: 1920. https://doi.org/10.3390/life13091920

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop