Next Article in Journal
Anatomy of the Nervous System in Chelifer cancroides (Arachnida: Pseudoscorpiones) with a Distinct Sensory Pathway Associated with the Pedipalps
Next Article in Special Issue
Peering into the Darkness: DNA Barcoding Reveals Surprisingly High Diversity of Unknown Species of Diptera (Insecta) in Germany
Previous Article in Journal
Conversion of Mixtures of Soybean Curd Residue and Kitchen Waste by Black Soldier Fly Larvae (Hermetia illucens L.)
Previous Article in Special Issue
Just a Fragment of Undescribed Diversity: Twenty New Oriental and Palearctic Species of Sciaroidea (Diptera), including DNA Sequence Data and Two New Fossil Genera
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Extant Genus in the Mesozoic: Paleoplatyura Meunier (Diptera: Keroplatidae) Found in the Cretaceous Amber of Myanmar †

1
Department of Biology and Ecology, Faculty of Science, University of Ostrava, Chittussiho 10, 710 00 Ostrava, Czech Republic
2
Institute of Systematics and Evolution of Animals Polish Academy of Sciences, 31-016 Kraków, Poland
*
Author to whom correspondence should be addressed.
Publications: urn:lsid:zoobank.org:pub: 90A627F2-9ECB-4ACE-81FC-9AC006D90656. Nomenclatural Acts: urn:lsid:zoobank.org:act:6BAC66C5-2B32-4C4D-8AD9-FA6729F8E6EC; urn:lsid:zoobank.org:act:35C369DE-C8EC-4561-96C3-75C03E3D8E06; urn:lsid:zoobank.org:act:E0E4BF32-60A9-4C69-86C4-390591FB6B30.
Insects 2022, 13(1), 24; https://doi.org/10.3390/insects13010024
Submission received: 20 November 2021 / Revised: 9 December 2021 / Accepted: 22 December 2021 / Published: 24 December 2021
(This article belongs to the Special Issue Diptera Diversity in Space and Time)

Abstract

:

Simple Summary

Burmese amber is very rich in perfectly preserved insects. Consequently, it is an invaluable source of information for taxonomic and evolutionary studies. Moreover, it forms a unique connection between the Jurassic and Cretaceousfaunas and documents the first representatives of modern genera. In this paper, a primitive genus of Keroplatidae, Paleoplatyura Meunier, 1899, is recorded from Burmese amber for the first time. This represents a rather rare case of the presence of an extant insect genus in the Mesozoic. Three new species of Paleoplatyura are described, indicating that this genus was relatively diverse already in the Cretaceous.

Abstract

Three new species of Paleoplatyura Meunier, 1899, i.e., Paleoplatyura agnieszkae sp. nov., P. miae sp. nov., and P. magnifica sp. nov., are described and figured. The concept of the genus is briefly discussed, and its systematic position is clarified. A key to fossil species is provided. The genus Paleoplatyura is described from the Eocene Baltic amber. It is concluded that, in Baltic amber, this group is represented only by the type species, and the identity of the other two species is problematic. No additional specimens have been found so far in this amber. Therefore, the presence of as many as three new species in Burmese amber, certainly belonging to Paleoplatyura, is a confirmation of its occurrence already in the Mesozoic.

1. Introduction

The fossil record of the family Keroplatidae (Diptera: Bibionomorpha) is still relatively scarce, especially from the Mesozoic, with only several taxa formally described [1,2]. This family currently comprises six extant subfamilies, Arachnocampinae Matile, 1981 [3], Keroplatinae Rondani, 1856 [4], Lygistorrhininae Edwards, 1925 [5], Macrocerinae Rondani, 1856 [4], Platyurinae Loew, 1850 [6], Sciarokeroplatinae Papp and Ševčík, 2005 [7], and one fossil subfamily, Adamacrocerinae Ševčík, Krzemiński and Skibińska, 2020 [2], from the mid-Cretaceous Burmese amber. Unfortunately, the limited number of clear morphological criteria defining some of the subfamilies of Keroplatidae, as well as the absence of a unique synapomorphy of the family [1,2] and the still widely discussed phylogenetic relationships within Sciaroidea [8], make it difficult to classify new fossil taxa of Keroplatidae to particular subfamilies. A typical example represents the genus Paleoplatyura Meunier, 1899 [9]. This genus has traditionally been considered to belong to the subfamily Keroplatinae, in the tribe Orfeliini Matile, 1990 [10] (e.g., Matile [10]); although, some authors (e.g., Shaw [11]) pointed out that Paleoplatyura shows the most plesiomorphic wing venation among fungus gnats (Sciaroidea) and can be considered as a “living fossil” [12]. Mantič et al. [1] reinstated and redefined a separate subfamily Platyurinae Loew, 1850 [6], for the Palearctic species Platyura marginata Meigen, 1803 [13], and the Nearctic Platyura pectoralis Coquillett, 1895 [14], and Paleoplatyura melanderi Fisher, 1941 [15] (the latter species not considered by them as true Paleoplatyura), while Paleoplatyura johnsoni Johannsen, 1910 [16], was classified as Keroplatidae incertae sedis, in a well-supported clade of various genera more or less related to Macrocerinae.
The genus Paleoplatyura currently formally includes three extant species, i.e., P. aldrichii Johannsen, 1909 [17]; P. johnsoni Johannsen, 1910 [16], and P. melanderi Fisher, 1941 [15], and three described fossil species, i.e., P. macrocera (Loew, 1850 [6]), P. loewi Meunier, 1922 [18], and P. (?) eocenica Cockerell, 1921 [19]. However, the placement of P. aldrichii, P. melanderi, P. loewi and P. eocenica in the genus Paleoplatyura is questionable and most probably wrong. The holotype of P. aldrichii is probably lost [20], and the original description by Johannsen [17] is very short, without any figure provided, only Johannsen [16] mentioned that “this species differs in several important structural characters from P. johnsoni” (he explicitly specifies only the subcostal cross-vein absent and cubital vein not reaching wing margin), indicating that P. aldrichii probably does not belong to true Paleoplatyura. Concerning P. melanderi, Mantič et al. [1] did not consider this species as true Paleoplatyura, because of R2+3 ending in R1 and its considerable molecular distance from P. johnsoni. Additionally, P. loewi does not belong to Paleoplatyura, because this species lacks the transverse r-m vein characteristic for this genus and possesses the more apomorphic r-m fusion, typical of most keroplatids. This can be seen exactly in the drawing of the wing given in the work of Meunier [18], p. 3, Figure 1., where the vein M1+2 merges at some distance with the vein Rs. The identity of P. eocenica is most obscure, because nothing important can be inferred from the original description and it is even unclear if the species belongs to Keroplatidae. Cockerell [19] himself was not sure whether this species belongs to the genus Paleoplatyura, providing a question mark after the genus name in the original description.
In this paper, we aim to clarify the taxonomic concept of the genus Paleoplatyura and describe three new Cretaceous species of this remarkable keroplatid genus.

2. Materials and Methods

Specimens were examined using a Nikon (Minato, Japan) SMZ25 stereomicroscope, equipped with a Nikon DS-Ri2 digital camera. Photomicrographs are focus stacks captured using this system and processed using NIS-Elements Imaging Software (Minato, Japan). Line drawings were produced by tracing photographs. The terminology follows Ševčík et al. [21], where the homology and wing vein nomenclature in Bibionomorpha are briefly explained. The holotypes are deposited in the collection of the Institute of Systematic and Evolution of Animals Polish Academy of Sciences (ISEA PAS) and paratypes in the National Museum, Prague, Czech Republic (NMPC). The specimens described here come from the Hukawng Valley in Kachin State, northern Myanmar. Burmese amber was dated by Cruickshank and Ko [22] to the middle–late Albian, based on insect inclusions and a specimen of the ammonite, but Grimaldi et al. [23] estimated the age of this resin to the Turonian– Cenomanian, based on arthropod inclusions. Shi et al. [24], based on U-Pb dating of zircons from the volcaniclastic matrix of the amber, estimated the age of Burmese amber at 98.79 ± 0.62 Ma (earliest Cenomanian).
This published work and the nomenclatural acts it contains have been registered in ZooBank, the online registration system for the ICZN. The LSID for this publication is: urn:lsid:zoobank.org:pub:90A627F2-9ECB-4ACE-81FC-9AC006D90656.

3. Results

3.1. Systematics Palaeontology

Order Diptera Linnaeus, 1758 [25].
Infraorder Bibionomorpha Hennig, 1948 [26].
Superfamily Sciaroidea Billberg, 1820 [27].
Family Keroplatidae Rondani, 1856 [4].
Genus Paleoplatyura Meunier, 1899 [9].
Type species: Mycetobia macrocera Loew, 1850 = Paleoplatyura macrocera (Loew, 1850) [9].
The genus includes one extant Holarctic species, P. johnsoni, and four fossil species, i.e., P. macrocera; P. miae sp. nov., P. magnifica sp. nov., P. agnieszkae sp. nov.
Diagnosis: Cross-vein r-m present; basal part of Mb clearly visible; cross-vein m-cu situated in between M1+2 and Cu; R2+3 oblique and ending in C, anal vein strong and reaching wing margin; gonostylus narrow and apically bifurcated.

3.2. Description of Amber Materials

Paleoplatyura macrocera(Loew, 1850).
Mycetobia macrocera Loew, 1850—Baltic amber (about 42 MA).
Amended diagnosis: Antennae reach almost 2/3 of the wing length, probably 16 segmented; wing 2.5× longer than wide; Sc vein ends distinctly before Rb forks into Rs and R1; R4+5 almost 3× longer than Rs and almost equal in length to R2+3+4+5; cross-vein r-m short; M1 almost 4× longer than M1+2; m-cu distinctly beyond fork of Mb.
Remarks: P. macrocera is the type species of the genus Paleoplatyura. It was described on the basis of a single female inclusion in the Baltic amber. Unfortunately, the study is made more difficult by the missing holotype and the fact that despite the analysis of numerous specimens classified to Sciaroidea in various Baltic amber collections, no specimen belonging to this species was found. Therefore, the concept of the genus is based on the figure provided in the work of Meunier (1899, Figure 9 [9]).
Paleoplatyura agnieszkae sp. nov.
urn:lsid:zoobank.org:act:6BAC66C5-2B32-4C4D-8AD9-FA6729F8E6EC
Diagnosis: Sc ends just beyond Rb bifurcation into R1 and Rs; R4+5 more than 3× longer than Rs and about 2× longer than R2+3+4; M1 2.5× longer than M1+2; gonostylus slightly longer than gonocoxites, strongly forked at end, the upper arm of bifurcation much shorter than the lower one; gonocoxite much expanded in basal part.
Etymology: The specific name, honours dr hab. Agnieszka Soszyńska-Maj, a well-known paleoentomologist, specializing in fossil Diptera and Mecoptera.
Material examined: Holotype (male), No. MP/4288, Burmese amber; deposited in the collection of ISEA PAS.
Description: Wing length 1.6 mm, width 0.6 mm (Figure 1A). Head: Antennae with 16 segments; scapus wide and barrel-shaped; pedicel oval; flagellomeres almost 1.5× longer than its width, and the last segment almost 3× longer than its width; palpi short (Figure 4A). Wing almost 3× longer than its width; Sc ends just beyond fork of Rb into R1 and Rs; R1 ends opposite half the length of R2+3, near tip of R2+3; R2+3 distinctly waved at mid-length; R4+5 more than 3× longer than Rs and 2× longer than R2+3+4; r-m short, equals ⅕ of length of Rs, located in ⅓ length of M1+2; Mb present, distinctly visible; M1 about 2.5× longer than M1+2; m-cu just beyond fork of Mb, located between M3+4 and Cu; Cu slightly arched; pseudovein (ps) clearly visible; A1 visible only in basal part (Figure 3A). Legs: foreleg with a single spur almost 3.5 times the width of tibia; hind and middle leg with two spurs of unequal length (Figure 4D). Hypopygium; Gonocoxite broad, greatly expanded in basal part (length about: 0.12 mm); gonostylus slightly longer than gonocoxites (length about: 0.14), strongly forked at end, the upper arm of bifurcation much shorter than the lower one (Figure 2A and Figure 5A).
Paleoplatyura miae sp. nov.
urn:lsid:zoobank.org:pub:90A627F2-9ECB-4ACE-81FC-9AC006D90656
Diagnosis: Sc ends distinctly beyond Rb bifurcation at R1 and Rs; R4+5 3× longer than Rs and almost 2× longer than R2+3+4; M1 about 4.5× longer than M1+2; gonostylus almost equal in length to gonocoxites, strongly bifurcated at end, the upper arm of bifurcation almost 2× longer than lower one.
Etymology: The specific epithet is given after name of the granddaughter, Mia, of one of the authors (WK).
Material examined: Holotype (male), No. MP/4075, Burmese amber; deposited in the collection of the ISEA PAS.
Description: Wing length 2.9, width 1.2 (Figure 1B). Head. Antennae with 16 segments; scapus tubular; pedicel short and oval; flagellomeres increasing in length and the last segment nearly 5× longer than its width; palpi short (Figure 4B). Thorax: Wing about 2.7 times longer than its width; Sc ends beyond fork of Rb into R1 and Rs; approximately opposite ⅓ of length of Rs; R1 ends opposite half the length of R2+3, near tip of R2+3; R2+3 nearly straight; R4+5 more than 3× longer than Rs and almost 2× longer than R2+3+4; r-m short, equals ⅙ of length of Rs, located distinctively before middle of length of M1+2; Mb present, clearly visible; M1 more than 4× longer than M1+2; m-cu just beyond fork of Mb, located between M3+4 and Cu; Cu at end strongly waved; pseudovein (ps) clearly visible; A1 with apical half strongly bent to wing margin (Figure 3B). Legs: foreleg and midleg with single spur that are nearly 3.5 times the width of tibia; hind leg with two spurs of unequal length (Figure 4E). Hypopygium: Gonocoxites long and narrow (length about: 0.28 mm); gonostylus almost equal in length to gonocoxites (length about: 0.27 mm), forked at end, the upper arm of bifurcation almost 2× longer than the lower (Figure 2B and Figure 5B,C).
Paleoplatyura magnifica sp. nov.
LSID urn:lsid:zoobank.org:act: E0E4BF32-60A9-4C69-86C4-390591FB6B30
Diagnosis: Wing length: 3.8 mm. Sc ends far beyond Rb bifurcation to R1 and Rs; R4+5 more than 3× longer than Rs and about 2× longer than R2+3+4; M1 3× longer than M1+2; gonostylus almost equal in length to gonocoxite, at end bifurcated, processes of equal length, strongly sclerotized; gonocoxite broad and much expanded in basal part.
Etymology: The specific epithet is given to emphasize the large size of the specimen (from the Latin magnifico/feminine magnifica/, meaning magnificent or gorgeous).
Material examined: Holotype (male), No. MP/4076—Burmese amber; deposited in the collection of the ISEA PAS.
Description: Wing length 3.8 mm, width 1.8 mm (Figure 1C). Head: antennae with 16 segments; scapus tubular; pedicel short and oval; flagellomeres nearly 2× longer than their width; palpi relatively long, segments of nearly the same length (Figure 4C). Wing about 2⅓× longer than its width; Sc ends far beyond fork of Rb into R1 and Rs, opposite ⅔ of length of Rs; R1 ends opposite half the length of R2+3, near the tip of R2+3; R2+3 distinctly waved at basal part; R4+5 more than 3× longer than Rs and about 2× longer than R2+3+4; r-m short, equals ⅛ of length of Rs, located close to middle of length of M1+2; Mb present, clearly visible; M1 3× longer than M1+2; m-cu more than its own length beyond fork of Mb, situated between M3+4 and Cu; Cu at end strongly bent; pseudovein (ps) clearly visible; A1 slightly wavy at the middle of its length (Figure 3C). Legs: front leg with a single spur, middle and hind leg with two spurs of nearly the same length and nearly 3× longer than the width of tibia (Figure 4F). Hypopygium: Gonocoxite broad and greatly expanded in the basal part; gonostylus almost equal in length to gonocoxite, forked at the end, processes of equal length, strongly sclerotized (Figure 2C and Figure 5D).

3.3. Key to Fossil Species of Paleoplatyura

1. Sc ends before Rb forks into R1 and and Rs …………… P. macrocera (Loew, 1850)
  - Sc ends after Rb forks into R1 and and Rs ………………………………… 2
2. Pattern of tibial spurs 1:1:2 ………………………………………… P. miae sp. nov.
  - Pattern of tibial spurs 1:2:2 ……………………………………… ………… 3
3. Costa produced to less than ¼ of the distance between tips of R4+5 and M1; tibial spurs of same length; apical processes strongly sclerotized ………… P. magnifica sp. nov.
  - Costa produced to about ¼ of the distance between tips of R4+5 and M1; tibial spurs of different length; gonostylus narrow throughout its length; apical processes not sclerotized ……………………………………………………… P. agnieszkae sp. nov.

4. Discussion

The type species of the genus Paleoplatyura, P. macrocera, from Baltic amber, differs from all congeners in Burmese amber by the short vein Sc, which ends clearly before the bifurcation of Rb into R1 and Rs. Surprisingly, the Burmese amber species of Paleoplatyura are thus more similar in this respect to the extant species P. johnsoni than to the Baltic amber type species. However, the relative length of Sc also differs among various species of Macrocera Meigen, 1803 [13], and similar variation is known in some genera of Mycetophilidae, so that this character appears as species-specific rather than of fundamental phylogenetic importance. We thus prefer to maintain the concept of Paleoplatyura as defined in this paper; which means including intrageneric variation of the length of Sc, considering the well-known fact that higher taxonomic categories, like genus or subfamily, are usually more or less subjective, and their concept (breadth) may differ, even within one family. The subjective concept of genera, with different breadth defined by various authors, may also be a key to the understanding why Mesozoic genera, such as Paleoplatyura, are (seemingly) present in both the Tertiary and extant fauna.
The presence of extant genera in the Mesozoic fauna is a remarkable phenomenon itself. Recent studies of Burmese amber inclusions increasingly indicate the origin of modern genera as early as in the Cretaceous. Examples of extant insect genera found in the Mesozoic are well documented, though not common. Grimaldi and Cumming [28] stated that Apalocnemis canadambris Grimaldi and Cumming [28] (family Empididae), was the only species out of 49 species studied within their paper on Cretaceous ambers Brachycera belonging to an extant genus. In Diptera, several other similar cases are known from Burmese amber, e.g., Antocha lapra Podenas and Poinar [29], and Helius lebanensis Kania, Krzemiński and Azar [30], from the family Limoniidae, or Nemopalpus quadrispiculatus Stebner et al. [31], and Phlebotomus vetus Stebner et al. [31], from the family Psychodidae. In some cases, a recent genus serves only as a “wastebasket taxon”, to tentatively place a problematic species in a described genus, as is the case of some genera of Mycetophilidae in Cretaceous ambers [32]. A similar situation is reported in [33], e.g., for the click-beetle genus Elater Linnaeus [25]. Some taxa of Diptera appeared even earlier, e.g., the genus Protanyderus Handlirsch, 1909 (family Tanyderidae), in the Upper Jurassic of Mongolia [34].
The extant species Paleoplatyura johnsoni, which unambiguously belongs to Paleoplatyura, was described from North America, and recently found also in Europe (southern Italy, see [12]). It is a large species (wing length is 8 mm), significantly larger than the fossil congeners, with the wings strongly marked, and relatively short antennae, only slightly longer than the head and thorax together. Surprisingly, there are no new specimens of Paleoplatyura available from Baltic amber. In contrast, several specimens from this genus, belonging to the three species described in this paper, have been found in Burmese amber. A major problem in the study of fossil Keroplatidae, is the loss of most of the holotypes of previously described species, especially from Baltic amber, and the lack of a recent, comprehensive morphological study of Keroplatidae belonging to the tribe Orfeliini. Additionally, the concept of the tribes Keroplatini and Orfeliini appears as outdated in the light of modern molecular studies [1].
A similar wing venation and structure of the male terminalia as in Paleoplatyura are found in the genus Asynaphleba Matile, 1974 [35], containing a single South African extant species, which differs from Paleoplatyura only by the absence of the vein Mb and by shorter anal vein, not reaching the wing margin. Thus, it seems that the presence of both Mb and the cross-vein r-m are good diagnostic characters for the genus Paleoplatyura. Taking into consideration only a distinct vein Mb, as a clear plesiomorphic character state, it is not unique to Paleoplatyura within keroplatids, but it is present also in several genera of Macrocerinae, including the species-rich genus Macrocera, and also in the South African genus Schizocyttara Matile, 1974 [35], which was shown to be closely related to Paleoplatyura johnsoni by Mantič et al. [1], although it lacks cross-vein r-m. Both Mb and cross-vein r-m are well developed also in the genus Arachnocampa Edwards, 1924 [36], from the most plesiomorphic keroplatid subfamily Arachnocampinae, which, however, differs from Paleoplatyura in some other characters, such as the absence of R2+3 and different proportion of wing veins.

5. Conclusions

Genus Paleoplatyura represents one of the most ancient and plesiomorphic genera of Keroplatidae, with the most complete wing venation representing a ground plan within the family (together with genus Arachnocampa). This group possesses also the most plesiomorphic structure of male terminalia, which appears to be simple with long and apically forked gonostyli. Molecular data indicate a close relationship of Paleoplatyura with Macrocerinae [1]; additionally, if we compare the wing of Paleoplatyura with that of Macrocera, we can see many similarities, confirming the evolutionary trend to the reduction of radio-medial cross-vein to the so-called radio-medial fusion, typical of most keroplatids, together with prolongation of the antennae in Macrocera and elimination of some wing veins in Lygistorrhininae. The basal part of medial vein is still retained in most Macrocerinae, while it is absent in almost all species of the more apomorphic subfamilies of Keroplatinae and Lygistorrhininae. The overall structure of male terminalia is also very similar in Paleoplatyura and most Macrocerinae.

Author Contributions

Conceptualization, J.Š., K.S. and W.K.; methodology, J.Š., K.S. and W.K.; validation, J.Š., K.S. and W.K.; investigation, J.Š., K.S. and W.K.; resources, J.Š., K.S. and W.K.; writing—original draft preparation, J.Š., K.S. and W.K.; writing—review and editing, J.Š., K.S. and W.K.; visualization, K.S.; supervision, J.Š., K.S. and W.K.; project administration, J.Š., K.S. and W.K.; funding acquisition, J.Š., K.S. and W.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by a grant from National Science Centre of Poland No. UMO-2016/23/B/NZ8/00936.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We are very grateful to Peter Chandler (Melksham, UK) and Olavi Kurina (Tartu, Estonia) whose suggestions helped to improve this manuscript. Thanks to four anonymous reviewers for their valuable comments and suggestions on this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Mantič, M.; Sikora, T.; Burdíková, N.; Blagoderov, V.; Kjærandsen, J.; Kurina, O.; Ševčík, J. Hidden in Plain Sight: Comprehensive Molecular Phylogeny of Keroplatidae and Lygistorrhinidae (Diptera) Reveals Parallel Evolution and Leads to a Revised Family Classification. Insects 2020, 11, 348. [Google Scholar] [CrossRef]
  2. Ševčík, J.; Krzemiński, W.; Skibińska, K. Intriguing and Beautiful: Adamacrocera adami gen. et sp. nov. from the Upper Cretaceous Amber of Myanmar Represents a New Subfamily of Keroplatidae (Diptera: Bibionomorpha). Insects 2020, 11, 552. [Google Scholar] [CrossRef]
  3. Matile, L. Description d’un Keroplatidae du crétacé moyen et données morphologiques et taxonomiques sur les Mycetophiloidea (Diptera). Ann. Soc. Entomol. Fr. 1981, 17, 99–123. (In French) [Google Scholar]
  4. Rondani, C. Dipterologiae Italicae Prodromus. In Volume: I. Genera Italica Ordinis Dipterorum Ordinatim Disposita et Distincta et in Familias et Stirpes Aggregata; Stocchi, A., Ed.; Alexandri Stoschi: Parmae, Italy, 1856; Volume 1, pp. 1–226. [Google Scholar] [CrossRef]
  5. Edwards, F. British Fungus-Gnats (Diptera, Mycetophilidae). With A Revised Generic Classification of the Family. Trans. R. Entomol. Soc. Lond. 1925, 73, 505–670. [Google Scholar] [CrossRef]
  6. Loew, H. Ueber den Bernstein und die Bernsteinfauna. Programm der Könglichen Realschule zu Meseritz; Lorentz, F.W., Ed.; Springer: Meseritz, Poland, 1850; pp. 1–44. (In German) [Google Scholar]
  7. Papp, L.; Ševčík, J. Sciarokeroplatinae, a new subfamily of Keroplatidae (Diptera). Acta Zool. Acad. Sci. Hung. 2005, 51, 113–123. [Google Scholar]
  8. Ševčík, J.; Kaspřák, D.; Mantič, M.; Fitzgerald, S.; Ševčíková, T.; Tóthová, A.; Jaschhof, M. Molecular phylogeny of the megadiverse insect infraorder Bibionomorpha sensu lato (Diptera). PeerJ 2016, 4, e2563. [Google Scholar] [CrossRef] [Green Version]
  9. Meunier, F. Revision des diptères fossiles types de Loew conservés au Musée Provincial de Koenigsberg. Misc. Entomol. 1899, 7, 161–165, 169–182. [Google Scholar]
  10. Matile, L. Recherches sur la systématique et lʹévolution des Keroplatidae: Diptera, Mycetophiloidea. Mém. Mus. Natl. Hist. Nat. Sér. A Zool. 1990, 148, 1–682. (In French) [Google Scholar]
  11. Shaw, F.R. The external anatomy of Palaeoplatyura johnsoni Joh. (Diptera—Mycetophilidae). Trans. Am. Entomol. Soc. 1952, 78, 21–31. [Google Scholar]
  12. Mantič, M.; Ševčík, J. Macrocera rohaceki sp. nov. and other interesting records of Keroplatidae (Diptera) from southern and central Europe, with DNA sequence data. Acta Entomol. Mus. Nat. Pragae 2017, 57, 751–764. [Google Scholar] [CrossRef] [Green Version]
  13. Meigen, J.W. Versuch einer neuen Gattung Eintheilung der europäischen zweiflügligen Insekten. Mag. Insektenkunde 1803, 2, 259–281. (In German) [Google Scholar]
  14. Coquillett, D.W. New North American Mycetophilidae. Can. Entomol. 1895, 27, 199–200. [Google Scholar] [CrossRef] [Green Version]
  15. Fisher, E.G. Distributional notes and keys to American Ditomyiinae, Diadocidiinae and Ceroplatinae with descriptions of new species (Diptera: Mycetophilidae). Trans. Am. Entomol. Soc. 1941, 67, 275–301. [Google Scholar]
  16. Johannsen, O.A. The Mycetophilidae of North America. Part II. In Bulletin of the Maine Agricultural Experiment Station; Springer: Orono, ME, USA, 1910; Volume 180, pp. 125–192. [Google Scholar]
  17. Johannsen, O.A. Diptera, fam. Mycetophilidae. In Genera Insectorum; Witsman, P., Ed.; Bartschii: Bruxelles, Belgium, 1909; Volume 93, pp. 1–141. [Google Scholar]
  18. Meunier, F.A. Nouvelle contribution a la monographie des “Mycetophilidae” (Ceroplatinae, Mycetophilinae et Sciophilinae) de l’ambre de la Baltique. Rev. Sci. Bourbon. Cent. Fr. 1922, 114–120. [Google Scholar]
  19. Cockerell, T.D.A. Fossil arthropods in the British Museum—VI. Oligocene insects from Gurnet Bay, Isle of Wight. Ann. Mag. Nat. Hist. 1921, 7, 453–480. [Google Scholar] [CrossRef]
  20. Evenhuis, N. Catalog of The Keroplatidae of The World (Insecta: Diptera); Bishop Museum Press: Honolulu, HI, USA, 2006. [Google Scholar]
  21. Ševčík, J.; Skartveit, J.; Krzemiński, W.; Skibińska, K. A Peculiar New Genus of Bibionomorpha (Diptera) with Brachycera-Like Modification of Antennae from Mid-Cretaceous Amber of Myanmar. Insects 2021, 12, 364. [Google Scholar] [CrossRef] [PubMed]
  22. Cruickshank, R.D.; Ko, K. Geology of an amber locality in the Hukawng Valley, northern Myanmar. J. Asian Earth Sci. 2003, 21, 441–445. [Google Scholar] [CrossRef]
  23. Grimaldi, D.A.; Engel, M.S.; Nascimbene, P.C. Fossiliferous Cretaceous amber from Myanmar (Burma): Its rediscovery, biotic diversity, and paleontological significance. Am. Mus. Novit. 2002, 3361, 1–71. [Google Scholar] [CrossRef] [Green Version]
  24. Shi, G.; Grimaldi, D.A.; Ge, H.; Wang, J.; Yang, M.; Lei, W.; Li, Q.; Li, X. Age constraint on Myanmar amber based on U-Pb dating of zircons. Cretac. Res. 2012, 37, 155–163. [Google Scholar] [CrossRef]
  25. Linnaeus, C. Systema Naturae per Regna tria Naturae: Secundum Classes, Ordines, Genera, Species, cum Characteribus, Differentiis, Synonymis, Locis; Laurentius Salvius, Holmiae: Stockholm, Sweden, 1758; Volume 1, p. 824, (In Latin). [Google Scholar] [CrossRef] [Green Version]
  26. Hennig, W. Die Larvenformen der Dipteren: Eine Übersicht über die Bisher Bekannten Jungendstadien Derzweiflügeligen Insekten; Akademie Verlag: Berlin, Germany, 1948. [Google Scholar]
  27. Billberg, G.J. Enumeratio insectorum in Museo/Gust. Joh. Billberg.; Smithsonian Institution: Stockholm, Sweden, 1820; p. 138. [Google Scholar]
  28. Grimaldi, D.; Cumming, J. Brachyceran Diptera in Cretaceous ambers and Mesozoic diversification of the Eremoneura. Bull. Am. Mus. Nat. Hist. 1999, 239, 1–124. [Google Scholar]
  29. Podenas, S.; Poinar, G.O., Jr. New crane flies (Diptera: Limoniidae) from Burmese amber. Proc. Ent. Soc. Wash. 2009, 111, 470–492. [Google Scholar] [CrossRef]
  30. Kania, I.; Krzemiński, W.; Azar, D. The oldest representative of Helius Lepeletier & Servile 1828 (Diptera: Limoniidae) from Lebanese amber (Early Cretaceous). Insect Syst. Evol. 2013, 44, 231–238. [Google Scholar]
  31. Stebner, F.; Solórzano Kraemer, M.M.; Ibáñez-Bernal, S.; Wagner, R. Moth flies and sand flies (Diptera: Psychodidae) in Cretaceous Burmese amber. PeerJ 2015, 3, e1254. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Blagoderov, V.; Grimaldi, D. Fossil Sciaroidea (Diptera) in Cretaceous Ambers, Exclusive of Cecidomyiidae, Sciaridae, and Keroplatidae. Am. Mus. Novit. 2004, 2004, 1–76. [Google Scholar] [CrossRef]
  33. Kundrata, R.; Packova, G.; Prosvirov, A.S.; Hoffmannova, J. The Fossil Record of Elateridae (Coleoptera: Elateroidea): Described Species, Current Problems and Future Prospects. Insects 2021, 12, 286. [Google Scholar] [CrossRef] [PubMed]
  34. Kalugina, N.S. Psychomorphan Diptera from the Jurassic of Mongolia Altai (Diptera: Tanyderidae, Eoptychopteridae). Paleontol. J. 1992, 26, 110–113. [Google Scholar]
  35. Matile, L. Diptera: Mycetophilidae Keroplatinae. S. Afr. Anim. Life 1974, 15, 511–532. [Google Scholar]
  36. Edwards, F.W. XIV—A note on the ‘New Zealand glow-worm’ (Diptera: Mycetophilidae). Ann. Mag. Nat. Hist. 1924, 14, 175–179. [Google Scholar] [CrossRef]
Figure 1. Habitus photographs of Paleoplatyura agnieszkae sp. nov. ((A) holotype), P. miae sp. nov. ((B) holotype), and P. magnifica sp. nov. ((C) holotype). Scale bar = 1 mm.
Figure 1. Habitus photographs of Paleoplatyura agnieszkae sp. nov. ((A) holotype), P. miae sp. nov. ((B) holotype), and P. magnifica sp. nov. ((C) holotype). Scale bar = 1 mm.
Insects 13 00024 g001
Figure 2. Male genitalia of Paleoplatyura agnieszkae sp. nov. (A), P. miae sp. nov. (B), and P. magnifica sp. nov. (C). Scale bar = 0.1 mm.
Figure 2. Male genitalia of Paleoplatyura agnieszkae sp. nov. (A), P. miae sp. nov. (B), and P. magnifica sp. nov. (C). Scale bar = 0.1 mm.
Insects 13 00024 g002
Figure 3. Wing of Paleoplatyura agnieszkae sp. nov. (A), P. miae sp. nov. (B), and P. magnifica sp. nov. (C). Scale bar = 0.5 mm.
Figure 3. Wing of Paleoplatyura agnieszkae sp. nov. (A), P. miae sp. nov. (B), and P. magnifica sp. nov. (C). Scale bar = 0.5 mm.
Insects 13 00024 g003
Figure 4. Paleoplatyura agnieszkae sp. nov., antenna (A) and middle leg (D); P. miae sp. nov., antenna (B); hind and middle leg (E); P. magnifica sp. nov., antenna (C), hind, middle, and foreleg (F). Scale bar = 1 mm.
Figure 4. Paleoplatyura agnieszkae sp. nov., antenna (A) and middle leg (D); P. miae sp. nov., antenna (B); hind and middle leg (E); P. magnifica sp. nov., antenna (C), hind, middle, and foreleg (F). Scale bar = 1 mm.
Insects 13 00024 g004
Figure 5. Male terminalia of Paleoplatyura agnieszkae sp. nov. (A), P. miae sp. nov. ((B) dorsal, (C) ventral), and P. magnifica sp. nov. (D). Scale bar = 0.1 mm.
Figure 5. Male terminalia of Paleoplatyura agnieszkae sp. nov. (A), P. miae sp. nov. ((B) dorsal, (C) ventral), and P. magnifica sp. nov. (D). Scale bar = 0.1 mm.
Insects 13 00024 g005
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Ševčík, J.; Krzemiński, W.; Skibińska, K. Extant Genus in the Mesozoic: Paleoplatyura Meunier (Diptera: Keroplatidae) Found in the Cretaceous Amber of Myanmar. Insects 2022, 13, 24. https://doi.org/10.3390/insects13010024

AMA Style

Ševčík J, Krzemiński W, Skibińska K. Extant Genus in the Mesozoic: Paleoplatyura Meunier (Diptera: Keroplatidae) Found in the Cretaceous Amber of Myanmar. Insects. 2022; 13(1):24. https://doi.org/10.3390/insects13010024

Chicago/Turabian Style

Ševčík, Jan, Wiesław Krzemiński, and Kornelia Skibińska. 2022. "Extant Genus in the Mesozoic: Paleoplatyura Meunier (Diptera: Keroplatidae) Found in the Cretaceous Amber of Myanmar" Insects 13, no. 1: 24. https://doi.org/10.3390/insects13010024

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