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Article

New Genera and Species of the Family Throscidae (Coleoptera: Elateroidea) in Mid-Cretaceous Burmese Amber

1
State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology and Center for Excellence in Life and Paleoenvironment, Chinese Academy of Sciences, Nanjing 210008, China
2
School of Life Sciences, Peking University, Beijing 100871, China
3
School of Earth Sciences, University of Bristol, Life Sciences Building, Tyndall Avenue, Bristol BS8 1TQ, UK
*
Author to whom correspondence should be addressed.
Insects 2021, 12(1), 63; https://doi.org/10.3390/insects12010063
Submission received: 26 November 2020 / Revised: 9 January 2021 / Accepted: 9 January 2021 / Published: 12 January 2021

Abstract

:

Simple Summary

Throscidae is a relatively small lineage in the beetle superfamily Elateroidea. The Mesozoic fossil records of this family are sparse. Here we describe three new throscid species found in mid-Cretaceous Burmese amber, all represented by well-preserved specimens. These newly discovered species suggest that Throscidae had a high diversity in the Cretaceous.

Abstract

Captopus depressicepsgen. et sp. nov., Electrothroscus yanpingaegen. et sp. nov. and Pseudopactopus robustus gen. et sp. nov. are reported from the mid-Cretaceous Burmese amber. These new findings greatly extend the Mesozoic diversity of Throscidae, which implies a high degree of morphological disparity for this family in the Cretaceous.

1. Introduction

The family Throscidae is one of the relatively small lineages of elateroids, with five extant genera and about 150 extant species [1]. Throscids are characterized by their unusual antennal grooves running by the notosternal suture and extending posteriolaterad along the hind margins of hypomera, which could also be a possible apomorphy of this family [2,3]. Historically, Throscidae also included genera such as Drapetes Dejean and Lissomus Dalman (e.g., [4,5,6]), which were later moved into Elateridae, as supported by both morphological and molecular studies [7,8,9]. Throscidae appears to be closely related to the elateroid families Eucnemidae and Cerophytidae, but the relationship among them is far from being settled. Analytical phylogenetic studies have suggested Throscidae to be the sister group of Lissominae + Thylacosterninae [10], Eucnemidae [11], Cerophytidae [9], or Eucnemidae + Cerophytidae [8,12], or an independent lineage [9].
Most fossils of Throscidae were discovered in amber deposits, including Lebanese amber [2] and Burmese amber [3,13] of the Cretaceous, and Oise amber [14] and Baltic amber [3,15] of the Oligocene to Eocene. Despite the great diversity of fossil insects preserved in the mid-Cretaceous Burmese amber [16,17], only two throscid species has been reported in this material to date [3,13]. Here, we report another three members of Throscidae from Burmese amber, which greatly enrich our knowledge on the early diversity of this family.

2. Materials and Methods

The Burmese amber specimens studied here are derived from amber mines near Noije Bum Village (26°20′ N, 96°36′ E), Hukawng Valley, Kachin State, northern Myanmar. The specimens are deposited in the Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences (NIGP), Nanjing, China. The amber piece was trimmed with a small table saw, ground with emery papers of different grit sizes, and finally polished with polishing powder. Photographs under incident light were taken with a Discovery V20 stereo microscope (Zeiss, Jena, Germany). Widefield fluorescence images were captured with the Zeiss Axio Imager 2 light microscope combined with a fluorescence imaging system. Confocal images were obtained with a Zeiss LSM710 confocal laser scanning microscope. Images under incident light or widefield fluorescence were automatically stacked in Helicon Focus 7.0.2 or Zerene Stacker 1.04. Confocal images were automatically stacked and colour-coded in ZEN 2011 or ZEN 2.3 (Blue Edition), or manually stacked in Adobe Photoshop CC. In the multicoloured images, the colours were coded based on z-depth. Images were further processed in Adobe Photoshop CC to enhance contrast. This published work and the nomenclatural acts have been registered in ZooBank, the official registry of Zoological Nomenclature. The LSID for this publication is urn:lsid:zoobank.org:pub:4797AF94-8912-4DCA-B375-A7D25F16B2A6.

3. Systematic Palaeontology

Order Coleoptera Linnaeus, 1758
Suborder Polyphaga Emery, 1886
Superfamily Elateroidea Leach, 1815
Family Throscidae Laporte, 1840
 
Diagnosis. Antennae 11-segmented, with a distinct club; antennomere 1 attached to antennomere 2 apically. Prothoracic antennal grooves running along the notosternal suture and extending posterolaterally along the hind margins of the hypomera. Prosternal process apically acute, fitting into mesoventral cavity. Metacoxal plates medially extending posteriorly. Abdomen with five connate ventrites.
 
GenusCaptopus Li & Cai gen. nov.
 
LSID. urn:lsid:zoobank.org:act:CB5975DC-1566-406B-88C1-B70512D32B40
Type species.Captopus depressicepssp. nov.
Etymology. The generic name is an anagram of “Pactopus”, another genus in Throscidae. The name is masculine in gender.
Diagnosis. Frons without carina, but with a deep cavity on both sides. Eyes large. Lateral pronotal ridge incomplete. Prosternum with subparallel prosternal carinae. Metaventrite with well-developed mesotarsal grooves. Abdomen with metatarsal grooves extending beyond the posterior margin of the third ventrite.
Remarks. The new genus Captopus is similar to the extant genus Pactopus Horn and the extinct genus Tyrannothroscus Muona in having both well-developed mesotarsal and metatarsal grooves. Captopus shows some crucial differences from other known extant or extinct species in Pactopus. For example, the metatarsal grooves of Pactopus do not extend beyond the posterior edge of ventrite 3, while in Captopus, the metatarsal grooves extend well beyond ventrite 3 and reach the middle of ventrite 4. More importantly, there is a deep cavity on both sides of frons in Captopus, formed by the expansion of the groove around the ridge bordering antennal insertion. This feature is unique among all known extant and extinct throscids. Captopus differs from Tyrannothroscus additionally in having no supraocular ridges, and lateral pronotal ridge incomplete.
 
Captopus depressiceps Li & Cai sp. nov. (Figure 1, Figure 2 and Figure 3).
 
LSID. urn:lsid:zoobank.org:act:4D81D22F-D7B1-4BD3-B4AB-03B594624094
Etymology. The specific name is derived from the Latin “depressus”, sunken, and “caput”, head, referring to the deep cavities on its head.
Material. Holotype, NIGP173915, an exceptionally well-preserved specimen.
Locality and horizon. Amber mine located near Noije Bum Village, Tanai Township, Myitkyina District, Kachin State, Myanmar; unnamed horizon, mid-Cretaceous, Upper Albian to Lower Cenomanian [18,19].
Diagnosis. As for the genus.
Description. Body elongate, length 2.5 mm, width 0.9 mm.
Head (Figure 3A) transverse; frons without median carina, but with a deep cavity on both sides formed by the expansion of the sulcus around the ridge semi-encircling antennal insertion. Eyes large, moderately emarginate, finely facetted, without interfacetal setae. Antennae with 11 antennomeres; antennomere 1 (scape) large, longer than wide, attached to antennomere 2 apically; antennomere 2 subrectangular, shorter and narrower than scape; antennomere 3 thinner than antennomere 2; terminal three antennomeres enlarged, forming a club.
Pronotal disc about 1.6 times as wide as long along the middle; sides not sinuate, converging anteriorly; posterior angles strongly acute and produced posteriorly; posterior edge bisinuate, with an additional slight emargination in the middle fitting against scutellum; lateral pronotal ridge incomplete. Scutellum polygonal. Elytra widest behind the base, about 2.1 times as long as wide combined; elytral surface with punctate striae (Figure 3C).
Prosternum subtrapezoidal; prosternal carinae almost parallel; prosternal process apically acute, fitting into mesoventral cavity. Metaventrite without discrimen; mesotarsal grooves well-developed (Figure 3B). Mesocoxae round; metacoxal plates medially extending posteriorly. Tarsal formula 5-5-5; pretarsal claws simple.
Abdomen with five connate ventrites; ventrite 5 twice as long as ventrite 4; metatarsal grooves well-developed, arcuate, reaching the middle of ventrite 4.
 
GenusElectrothroscus Li & Cai gen. nov.
 
LSID. urn:lsid:zoobank.org:act:8A15D241-02F9-4A9C-8144-94944D2E51DD
Type species.Electrothroscus yanpingaesp. nov.
Etymology. The generic name is derived from the Greek noun “elektron”, amber, and the generic name Throscus Latreille, a junior synonym of Trixagus Kugelann. The name is masculine in gender.
Diagnosis. Frons without modifications. Eyes large. Prosternum with subparallel prosternal carinae. Metaventrite without mesotarsal grooves. Abdomen without metatarsal grooves.
Remarks. In Throscidae, only Pseudothroscus Muona is known to lack median head carina and both tarsal grooves [3]. Pseudothroscus is also characterized by its nonparallel prosternal carinae [13]. However, the prosternal carinae of Electrothroscus are subparallel, which is similar to most Throscidae.
 
Electrothroscus yanpingae Li & Cai sp. nov. (Figure 4, Figure 5 and Figure 6).
 
LSID. urn:lsid:zoobank.org:act:76502D09-035D-4F20-9A0A-CA568096CF45
Etymology. The specific name is after Prof. Yan-Ping Guo (Beijing Normal University), an evolutionary botanist.
Material. Holotype, NIGP173916, a well-preserved specimen with elytra partially polished away.
Locality and horizon. Amber mine located near Noije Bum Village, Tanai Township, Myitkyina District, Kachin State, Myanmar; unnamed horizon, mid-Cretaceous, Upper Albian to Lower Cenomanian [18,19].
Diagnosis. As for the genus.
Description. Body elongate, length 2.3 mm, width 0.8 mm.
Head transverse (Figure 6A); frons without median carina or other modifications. Eyes large, slightly emarginate, finely facetted, without interfacetal setae. Antennae not properly visible; antennomere 1 attached to antennomere 2 apically; terminal three(?) antennomeres enlarged, forming a club.
Pronotal disc about 1.6 times as wide as long along the middle; sides not sinuate, converging anteriorly; posterior angles strongly acute and produced posteriorly; posterior edge bisinuate. Elytra widest behind the base, about 2.2 times as long as wide combined.
Prosternum subtrapezoidal; prosternal carinae almost parallel; prosternal process slightly narrowed in middle, apically acute, fitting into mesoventral cavity. Metaventrite without discrimen; mesotarsal grooves absent (Figure 6B). Mesocoxae round; metacoxal plates medially extending posteriorly. Tarsal formula 5-5-5; pretarsal claws simple.
Abdomen with five connate ventrites; ventrite 5 twice as long as ventrite 4; metatarsal grooves or impressions absent (Figure 6C).
 
GenusPseudopactopus Li & Cai gen. nov.
 
LSID. urn:lsid:zoobank.org:act:8CA0EA80-040B-4924-AF10-F9D0F6453D1C
Type species.Pseudopactopus robustussp. nov.
Etymology. The generic name is derived from the Greek “pseudes”, false, and the generic name Pactopus LeConte. The name is masculine in gender.
Diagnosis. Body wide (length/width ratio ~2.1). Frons without modifications. Eyes large. Lateral pronotal ridge incomplete. Prosternum with subparallel prosternal carinae. Protibiae simple. Metaventrite with well-developed mesotarsal grooves. Abdomen with metatarsal grooves reaching or almost reaching the posterior margin of the third ventrite.
Remarks. The new genus Pseudopactopus possesses well-developed mesotarsal and metatarsal grooves, which, together with its unmodified head, link the new genus with Pactopus. However, the protibiae of Pseudopactopus are simple (Figure 8b), while protibiae are enlarged apically and with tarsal grooves in Pactopus (Figure 12 in [3]). Such simple protibiae are known previously only in Pseudothroscus, Tyrannothroscus, Potergosoma Kovalev & Kirejtshuk, Rhomboaspis Kovalev & Kirejtshuk, and Trixagosoma Li et al. [20].
Additional characters also differentiate Pseudopactopus from Pactopus. The body shape of Pseudopactopus robustus is broader than all other known extant and extinct Pactopus species. The type specimens of Pactopus burmensis Muona and Pactopus americanus Wickham have a length/width ratio of about 2.4–2.5, and Pactopus horni LeConte, Pactopus fasolti Muona and Pactopus fafneri Muona are even much narrower [3]. By contrast, the width of Pseudopactopus robustus almost reaches half of its length. The sides of pronotal disc are more or less sinuate in P. horni [21], and also possibly sinuate in P. americanus (Plate VI, Figure 10 in [22]), whereas Pseudopactopus does not have such sinuate sides of pronotal disc. Similar to P. horni and P. americanus, the metatarsal grooves of Pseudopactopus reaches the posterior margin of the third ventrite. However, in P. fasolti and P. fafneri, the metatarsal grooves do not even reach the posterior half of the third ventrite (Figures 13 and 15 in [15]).
 
Pseudopactopus robustus Li & Cai sp. nov. (Figure 7, Figure 8, Figure 9 and Figure 10).
 
LSID. urn:lsid:zoobank.org:act:500CA10A-2F6E-459B-8109-68238492ED8F
Etymology. The species is named for its robust appearance.
Material. Holotype, NIGP173917, a well-preserved specimen. Paratype, NIGP173918, a well-preserved specimen with body moderately distorted.
Locality and horizon. Amber mine located near Noije Bum Village, Tanai Township, Myitkyina District, Kachin State, Myanmar; unnamed horizon, mid-Cretaceous, Upper Albian to Lower Cenomanian [18,19].
Diagnosis. As for the genus.
Description. Body broad, covered with short hairs. Holotype length 2.9 mm, width 1.4 mm.
Head (Figure 10A) transverse; frons without median carina or other modifications. Eyes large, slightly emarginate, finely facetted, without interfacetal setae. Antennae (Figure 10C) with 11 antennomeres; antennomere 1 large, longer than wide, attached to antennomere 2 apically; antennomere 2 subquadrate, shorter and narrower than scape; antennomere 3 longer and thinner than antennomere 2; terminal three antennomeres enlarged, forming a club.
Pronotal disc about 2.2 times as wide as long along the middle; sides not sinuate, converging anteriorly; posterior angles strongly acute and produced posteriorly; posterior edge bisinuate, with an additional slight emargination in the middle fitting against scutellum; lateral pronotal carinae incomplete (Figure 10C). Scutellum subpentagonal, rounded. Elytra widest behind the base, about 1.6 times as long as wide combined; elytral surface with small to medium-sized punctures on the striae.
Prosternum subtrapezoidal; prosternal carinae almost parallel; prosternal process slightly narrowed in middle, apically acute, fitting into mesoventral cavity. Protibiae simple. Metaventrite without discrimen; mesotarsal grooves well-developed (Figure 10B). Mesocoxae round; metacoxal plates medially extending posteriorly. Tarsal formula 5-5-5; pretarsal claws simple.
Abdomen with five connate ventrites; ventrite 5 twice as long as ventrite 4; metatarsal grooves well-developed, merely extending to the hind margin of ventrite 3.

4. Discussion

The three throscid species presented in this paper, together with two previous reported species, show a high degree of morphological variation of Throscidae in Burmese amber. Specialized throscids have also been reported in Lower Cretaceous Lebanese amber [2]. Compared to their extant relatives, these Mesozoic throscids seem to be morphologically more diverse. There are only four known extant genera in Throscidae, while six genera have been established based on Cretaceous fossils. An identification key to genera in Throscidae is updated in light of the new specimens discovered from Burmese amber (Appendix A). Many interesting features found in Mesozoic throscids have hitherto been unknown in Recent Throscidae (e.g., deep cavities on head in Captopus gen. nov., small and very narrow eyes in Potergosoma, nonparallel prosternal carinae in Potergosoma and Trixagosoma). The divergence between Throscidae and the group of Eucnemidae + Cerophytidae has been dated to Middle Jurassic, approximately 165 Ma [12]. Therefore it is reasonable to expect that Throscidae might have already been highly diversified in late Mesozoic. We hope further findings on Mesozoic throscid fossils could help us understand the early diversification of this family.
Despite the wide distribution of the family, throscids are poorly studied and their taxonomy is not well resolved. Though the monophyly of Throscidae has been supported by recent molecular phylogenetic analyses [9,23], no molecular-based analysis has focused on the inter-generic relationships within Throscidae. A morphology-based phylogenetic analysis of both extant and extinct throscids was performed by Muona [3]. Although two of three equally shortest trees he obtained from the parsimony analysis showed Aulonothroscus as non-monophyletic, he concluded it was reasonable to opt for the tree supporting a monophyletic Aulonothroscus. However, later Li et al. [13] performed an analysis under implied weights with a slightly modified dataset, in which Aulonothroscus appeared to be paraphyletic in the majority-rule consensus tree.
The generic assignment of some species by Muona [3] was also dubious. For example, a throscid from Eocene Baltic amber, Trixagus parvulus Muona, was assigned to genus Trixagus. However, the most important diagnostic feature for Trixagus, the vestigial tarsal grooves, is not visible on the specimen: the position for possible tarsal groove is concealed by its femur. The club-forming antennomeres in T. parvulus seems to be rather symmetrical and moniliform (Figure 16 in [3]), whereas in Trixagus they should be asymmetrically expanded and serratiform. Besides, we need to be cautious when evaluating the systematic position of insects in preserved in amber, especially when the specimen is not well-preserved. A failure in identifying a certain structure in an amber specimen does not necessarily mean that it is absent [24]. Various decomposition and distortion processes may lead to the misinterpretation of morphological characters. Further better preserved fossils could be helpful for clarifying the accurate position of these species.

5. Conclusions

Our discovery of Captopus depressiceps gen. et sp. nov., Electrothroscus yanpingae gen. et sp. nov. and Pseudopactopus robustus gen. et sp. nov. in the mid-Cretaceous Burmese amber greatly extends the Mesozoic diversity of Throscidae. These newly discovered species imply a high degree of morphological disparity for this family in the Cretaceous. Further phylogenetic analysis with incorporation of both molecular data and fossil taxa would be helpful for elucidating the early evolutionary history of Throscidae.

Author Contributions

Conceptualization, C.-Y.C. and Y.-D.L.; methodology, Y.-D.L. and C.-Y.C.; investigation, Y.-D.L. and C.-Y.C.; resources, C.-Y.C. and D.-Y.H.; data curation, Y.-D.L.; writing—original draft preparation, Y.-D.L. and C.-Y.C.; writing—review and editing, Y.-D.L. and C.-Y.C.; visualization, Y.-D.L.; project administration, C.-Y.C.; funding acquisition, C.-Y.C. and D.-Y.H. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB26000000 and XDB18000000), the National Natural Science Foundation of China (42072022, 41688103), and the Second Tibetan Plateau Scientific Expedition and Research project (2019QZKK0706).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The original series of confocal slices are available on Zenodo repository (doi:10.5281/zenodo.3994927).

Acknowledgments

We are grateful to Yan-Chen Zhao for arranging a loan of an unpublished throscid specimen, Gary Griswold for providing photos of some extant throscids, and Yan Fang for technical help in confocal imaging. We thank Jyrki Muona and two anonymous reviewers for the helpful comments.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A. Key to Genera of Throscidae (Modified from Muona, 2019)

1. Metathorax and abdomen without tarsal grooves; body elongate2
1′. At least metathorax with tarsal grooves5
2. Head without median carina3
2′. Head with median carina4
3. Prosternum with nonparallel prosternal carinaePseudothroscus Muona
3′. Prosternum with subparallel prosternal carinaeElectrothroscus gen. nov.
4. Antennae with 4 enlarged apical antennomeresJaira Muona
4′. Antennae with 3 enlarged apical antennomeresPotergosoma Kovalev & Kirejtshuk
5. Abdomen with tarsal grooves6
5′. Abdomen at most with slight impressions for tarsi11
6. Head with median carina7
6′. Head without median carina8
7. Metaventrite simplePotergus Bonvouloir
7′. Metaventrite medially widely keeled, anteriorly deeply bifidRhomboaspis Kovalev & Kirejtshuk
8. Supraocular ridges strong, well developedTyrannothroscus Muona
8′. Supraocular ridges not present9
9. Frons with a pair of deep cavitiesCaptopus gen. nov.
9′. Frons simple10
10. Protibiae apically enlarged, with tarsal groovesPactopus LeConte
10′. Protibiae simplePseudopactopus gen. nov.
11. Prosternum with nonparallel prosternal carinaeTrixagosoma Li et al.
11′. Prosternum with subparallel prosternal carinae12
12. Metaventrite with vestigial tarsal grooves; median lobe longer than parameresTriagus Kugelann
12′. Metaventrite with deep, long tarsal grooves; median lobe shorter than parameresAulonothroscus Horn

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Figure 1. General habitus of Captopus depressiceps gen. et sp. nov., holotype, NIGP173915, under incident light. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
Figure 1. General habitus of Captopus depressiceps gen. et sp. nov., holotype, NIGP173915, under incident light. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
Insects 12 00063 g001
Figure 2. General habitus of Captopus depressiceps gen. et sp. nov., holotype, NIGP173915, under widefield fluorescence. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
Figure 2. General habitus of Captopus depressiceps gen. et sp. nov., holotype, NIGP173915, under widefield fluorescence. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
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Figure 3. Details of Captopus depressiceps gen. et sp. nov., holotype, NIGP173915, under confocal microscopy, with depth colour coding in (B,C). (A) Head and prothorax, ventral view, showing the deep cavity on frons (arrowhead). (B) Hind legs and abdomen, ventral view, showing the metatarsal groove (arrowhead). (C) Apex of elytra, dorsal view. Abbreviations: an, antenna; el, elytron; ey, compound eye; mtc, metacoxa; mtf, metafemur; mtv, metaventrite; pf, profemur; ps, prosternum; v2–3, ventrites 2–3. Scale bars: 200 μm.
Figure 3. Details of Captopus depressiceps gen. et sp. nov., holotype, NIGP173915, under confocal microscopy, with depth colour coding in (B,C). (A) Head and prothorax, ventral view, showing the deep cavity on frons (arrowhead). (B) Hind legs and abdomen, ventral view, showing the metatarsal groove (arrowhead). (C) Apex of elytra, dorsal view. Abbreviations: an, antenna; el, elytron; ey, compound eye; mtc, metacoxa; mtf, metafemur; mtv, metaventrite; pf, profemur; ps, prosternum; v2–3, ventrites 2–3. Scale bars: 200 μm.
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Figure 4. General habitus of Electrothroscus yanpingae gen. et sp. nov., holotype, NIGP173916, under incident light. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
Figure 4. General habitus of Electrothroscus yanpingae gen. et sp. nov., holotype, NIGP173916, under incident light. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
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Figure 5. General habitus of Electrothroscus yanpingae gen. et sp. nov., holotype, NIGP173916, under widefield fluorescence. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
Figure 5. General habitus of Electrothroscus yanpingae gen. et sp. nov., holotype, NIGP173916, under widefield fluorescence. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
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Figure 6. Details of Electrothroscus yanpingae gen. et sp. nov., holotype, NIGP173916, under confocal microscopy, with depth colour coding. (A) Head and prothorax, ventral view. (B) Middle legs and metaventrite, ventral view. (C) Hind legs and abdomen, ventral view. Abbreviations: ey, compound eye; msf, mesofemur; msts, mesotarsus; msv, mesoventrite; mtc, metacoxa; mtts, metatarsus; mtv, metaventrite; ps, prosternum. Scale bars: 200 μm.
Figure 6. Details of Electrothroscus yanpingae gen. et sp. nov., holotype, NIGP173916, under confocal microscopy, with depth colour coding. (A) Head and prothorax, ventral view. (B) Middle legs and metaventrite, ventral view. (C) Hind legs and abdomen, ventral view. Abbreviations: ey, compound eye; msf, mesofemur; msts, mesotarsus; msv, mesoventrite; mtc, metacoxa; mtts, metatarsus; mtv, metaventrite; ps, prosternum. Scale bars: 200 μm.
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Figure 7. General habitus of Pseudopactopus robustus gen. et sp. nov., holotype, NIGP173917, under incident light. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
Figure 7. General habitus of Pseudopactopus robustus gen. et sp. nov., holotype, NIGP173917, under incident light. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
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Figure 8. General habitus of Pseudopactopus robustus gen. et sp. nov., holotype, NIGP173917, under widefield fluorescence. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
Figure 8. General habitus of Pseudopactopus robustus gen. et sp. nov., holotype, NIGP173917, under widefield fluorescence. (A) Dorsal view. (B) Ventral view. Scale bars: 500 μm.
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Figure 9. General habitus of Pseudopactopus robustus gen. et sp. nov., paratype, NIGP173918 (A) Dorsal view, under incident light. (B) Ventral view, under incident light. (C) Ventral view, under widefield fluorescence. Scale bars: 500 μm.
Figure 9. General habitus of Pseudopactopus robustus gen. et sp. nov., paratype, NIGP173918 (A) Dorsal view, under incident light. (B) Ventral view, under incident light. (C) Ventral view, under widefield fluorescence. Scale bars: 500 μm.
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Figure 10. Details of Pseudopactopus robustus gen. et sp. nov., under confocal microscopy. (A,B) Holotype, NIGP173917, with depth colour coding. (A) Head and prothorax, ventral view, showing the prothoracic antennal groove (arrowhead). (B) Middle leg and metaventrite, ventral view, showing the mesotarsal groove (arrowhead). (C) Paratype, NIGP173918, head and prothorax, ventral view, showing the incomplete lateral pronotal carinae (arrowhead). Abbreviations: an1, antennomere 1; ey, compound eye; hy, hypomeron; msc, mesocoxa; msf, mesofemur; mtv, metaventrite; pf, profemur; ps, prosternum. Scale bars: 200 μm.
Figure 10. Details of Pseudopactopus robustus gen. et sp. nov., under confocal microscopy. (A,B) Holotype, NIGP173917, with depth colour coding. (A) Head and prothorax, ventral view, showing the prothoracic antennal groove (arrowhead). (B) Middle leg and metaventrite, ventral view, showing the mesotarsal groove (arrowhead). (C) Paratype, NIGP173918, head and prothorax, ventral view, showing the incomplete lateral pronotal carinae (arrowhead). Abbreviations: an1, antennomere 1; ey, compound eye; hy, hypomeron; msc, mesocoxa; msf, mesofemur; mtv, metaventrite; pf, profemur; ps, prosternum. Scale bars: 200 μm.
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Li, Y.-D.; Huang, D.-Y.; Cai, C.-Y. New Genera and Species of the Family Throscidae (Coleoptera: Elateroidea) in Mid-Cretaceous Burmese Amber. Insects 2021, 12, 63. https://doi.org/10.3390/insects12010063

AMA Style

Li Y-D, Huang D-Y, Cai C-Y. New Genera and Species of the Family Throscidae (Coleoptera: Elateroidea) in Mid-Cretaceous Burmese Amber. Insects. 2021; 12(1):63. https://doi.org/10.3390/insects12010063

Chicago/Turabian Style

Li, Yan-Da, Di-Ying Huang, and Chen-Yang Cai. 2021. "New Genera and Species of the Family Throscidae (Coleoptera: Elateroidea) in Mid-Cretaceous Burmese Amber" Insects 12, no. 1: 63. https://doi.org/10.3390/insects12010063

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