Research Article |
Corresponding author: Christopher H. Dietrich ( chdietri@illinois.edu ) Academic editor: James Zahniser
© 2018 Christopher H. Dietrich, M. Jared Thomas.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Dietrich CH, Thomas MJ (2018) New eurymeline leafhoppers (Hemiptera, Cicadellidae, Eurymelinae) from Eocene Baltic amber with notes on other fossil Cicadellidae. ZooKeys 726: 131-143. https://doi.org/10.3897/zookeys.726.21976
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Two new extinct fossil cicadellid taxa from Eocene Baltic amber, representing the subfamily Eurymelinae (sensu lato), are described and illustrated, and their relationships to modern leafhoppers are discussed. Eoidiocerus emarginatus gen. and sp. n. is the oldest known representative of the tribe Idiocerini. The new genus resembles some modern Afrotropical and Indomalayan idiocerine genera but differs in having the gena relatively narrow. Archipedionis obscurus gen. and sp. n., is the first well-preserved fossil representative of Macropsini to be described in detail. Previous reports of this tribe from Baltic amber, while credible, included too little morphological information to assess their relationships. Additional comparative notes are provided for previously described fossil taxa belonging to Idiocerini and Macropsini from the Oligocene of Germany. The new combinations Oncopsis sepultus sepultus (Statz, 1950), comb. n. and Oncopsis sepultus austerus (Statz, 1950), comb. n. are proposed for taxa previously included in Bythoscopus Germar. The previously unplaced cicadellid fossil taxon Priscacutius denticulatus Poinar & Brown, 2018 from mid-Cretaceous Myanmar amber is newly placed in subfamily Signoretiinae, tribe Phlogisini, and represents the oldest known member of this subfamily, the only one known from the fossil record and only the second modern cicadellid subfamily confirmed by direct fossil evidence to have been present during the Cretaceous period.
Auchenorrhyncha , Idiocerini , Macropsini , morphology, Phlogisini , Signoretiinae
The fossil record of leafhoppers (Cicadellidae), a group of sap-sucking hemipteran insects comprising >20,000 described extant species worldwide, is poorly documented, with fewer than 100 confirmed fossil species having been formally described so far from the Cretaceous (
Recent molecular phylogenetic studies of leafhoppers have attempted to estimate the ages of various cicadellid lineages (
Six modern cicadellid subfamilies (Aphrodinae, Bathysmatophorinae, Eurymelinae, Megophthalminae, Mileewinae and Typhlocybinae) have their oldest representatives recorded from Eocene Baltic amber (
Judging from the numerous amber specimens offered for sale online over the past few years by dealers in Lithuania, Poland and elsewhere in Europe, most of the leafhoppers preserved in Baltic amber are nymphs, and many of these are difficult to place taxonomically and phylogenetically, given the still highly incomplete knowledge of the morphology of modern leafhopper nymphs (reviewed by
The new fossil taxa described herein include the oldest known representative of the leafhopper tribe Idiocerini and the first report of the tribe from fossil amber. Idiocerini, at present, are distributed worldwide with 105 genera and ~700 known extant species. Previous records of fossil Idiocerini consist of three rock fossils from the Oligocene of Germany (
Fossil specimens were obtained from amber dealers in Palanga, Lithuania. Morphological characters were assessed by examination of the specimens using an Olympus SZX-12 dissecting microscope. Specimens were prepared by grinding flat facets in strategic locations to obtain a clear field of view for detailed photomicrographs according to
The concept of Eurymelinae adopted here is narrower than that of
Eoidiocerus emarginatus sp. n.; by present designation and monotypy.
This genus differs from other described genera of Idiocerini in having the following combination of traits: head with fine arcuate striations above ocelli, ocelli situated above mid-height of eye, gena strongly emarginate below eye; hind femur macrosetal formula 2+1; female abdominal sternite VII strongly emarginate, exposing base of ovipositor; length of ovipositor more than half that of entire abdomen.
Head in dorsal view with crown slightly shorter medially than next to eyes; face slightly longer than width across eyes, texture shagreen, area of vertex above ocelli with inconspicuous, fine arcuate parallel striations; ocelli approximately equidistant between eyes and midline, situated above mid-height of eyes; lateral frontal suture nearly straight, extended from antennal pit to ocellus; antennal ledge carinate but only weakly produced over antennal base; antenna shorter than head width, arista attenuate, with conspicuous preapical seta extended mesad; gena strongly concave and narrow below eye, partly exposing small proepisternum; lorum convex, extended nearly to lateral margin of face; anteclypeus broadened near apex; rostrum extended slightly past middle coxae, distal segment somewhat expanded toward apex. Pronotum shagreen, with indistinct transverse rugae. Forewing elongate, appendix broad, extended to wing apex, bordering first and second apical cells; vein R with three branches extended to wing margin; crossvein s absent; with two r-m and three m-cu crossveins (two closed subapical cells); vein CuA reaching submarginal vein near midlength of appendix; claval veins distinct. Front femur with AM1 strongly reduced; intercalary row with several long, fine setae; tibia cylindrical, with conspicuous setae only at apex. Middle femur and tibia without macrosetae. Hind femur macrosetal formula 2+1; tibia strongly flattened, distance between dorsal setal rows much less than distance between dorsal and ventral rows, row AD with fewer macrosetae than PD, row AV macrosetae distributed along distal 3/4 of tibia, row PV with alternating short and long tapered setae through most of length, tarsomere I with dorsoapical pair of macrosetae well developed, without plantar setae, pecten with 2 platellae. Female pygofer and ovipositor narrow and elongate, occupying 3/4 total length of abdomen; sternite VII with deep median parabolic emargination, exposing base of ovipositor.
The genus name, a masculine noun, combines the Greek word eos (dawn) with Idiocerus, the name of the type genus of Idiocerini, referring to the status of the fossil as the oldest known representative of Idiocerini..
Placement of Eoidiocerus in Idiocerini is unequivocal and supported by the presence of several synapomorphic features diagnostic for that tribe, including: head broader than pronotum, crown short, ocelli on face distant from dorsal margin and well separated from eyes, lateral frontal sutures present and extended to ocelli; pronotum in dorsal view with anterior margin not extended anteriad of eyes; chaetotaxy of front and middle legs strongly reduced; forewing appendix broad and extended to wing apex. Eoidiocerus resembles several modern idiocerines in most external structural features. Its most distinctive diagnostic traits are the arcuate series of fine striations on the vertex above the ocelli, present in several modern genera (e.g., Idiocerus Lewis, 1834, Idioceroides Matsumura, 1912; see also
Previously reported fossil Idiocerini include Oligoidiocerus pronotumnalis Statz, 1950, Idiocerus goeckii Statz, 1950 and an additional unnamed “Idiocerus ?” species from the Oligocene of Germany (
Measurements (mm): body length including wings 4.8; head width across eyes 1.4; height of face (crown apex to anteclypeus apex) 1.5; forewing length 3.8; forewing maximum width (across approximately midlength) 1.1 mm; front tibia length 0.7; hind tibia length 1.7; hind tarsus length 0.7; ovipositor length (portion exposed posterad of sternite VII) 1.3. Hind tibia rows PD, AD and AV with 10, 9 and 11 macrosetae, respectively. Other structural features as described for genus. Body apparently uniformly pale brown, without discernible markings or pattern.
The species name refers to the emarginate gena.
Holotype female, Eocene Baltic amber (37–44 Ma), purchased by the first author from an amber dealer in Palanga, Lithuania. Deposited in the Paleontological Collection of the Illinois Natural History Survey (INHSP 10320).
The exoskeleton of the holotype is well preserved and intact except the femoro-tibial joints and adjacent parts of the left legs have been sheared off, apparently during initial processing of the amber piece, and are missing; most of the tibia and the entire tarsus of the left middle leg are also missing. Variable preservation of different parts of the integument give the impression that the holotype specimen has a pattern of dark markings but these appear to be artifacts.
Archipedionis obscurus sp. n.; by present designation and monotypy.
This genus differs from other Macropsini in having the following combination of traits: crown shorter medially than next to eye; face with epistomal suture visible; ocelli slightly mesad of antennal pits, coronal pits dorsolaterad of ocelli; lorum not fused to frontoclypeus or anteclypeus; rostrum extended beyond middle coxae. Pronotum angulately produced medially but extended only slightly anterad of eyes in dorsal view, irregularly rugose. Forewing outer anteapical cell open, veins without markings.
Head in dorsal view with crown shorter medially than next to eyes; face relatively broad and short, texture minutely and more or less evenly punctate, ocelli slightly closer to eyes than to midline; coronal pits present dorsolaterad of ocelli; epistomal suture visible; gena strongly concave and narrow below eye, exposing flaplike proepisternum; lorum convex, extended nearly to lateral margin of face, not fused to anteclypeus; anteclypeus parallel-sided with apex truncate; rostrum extended past middle coxae, slender. Pronotum shagreen, with irregular transverse rugae. Forewing elongate, appendix narrow, extended around wing apex; most of membrane opaquely sclerotized; veins somewhat obscure, without obvious markings; inner and middle anteapical cells closed, outer anteapical cell open (crossvein s absent); claval veins distinct. Visible portion of hind wing apex with two closed apical cells, anterior branch of R absent. Front femur and tibia without conspicuous setae. Middle femur and tibia without macrosetae. Hind femur macrosetal formula 2+1; tibia strongly flattened, distance between dorsal setal rows much less than distance between dorsal and ventral rows, row AD with 8 preapical macrosetae (PD not visible in fossil), row AV macrosetae extended most of length of tibia, row PV with numerous close-set slender setae subequal in length, tarsomere I with dorsoapical pair of macrosetae well developed, with two rows of plantar setae, pecten with 2 platellae. Female pygofer relatively short, occupying < half total length of abdomen; sternite VII angulately emarginate, covering base of ovipositor.
The genus name, a masculine noun, combines the prefix archi- derived from the Greek archaeos, meaning old, with Pedionis, the name of a modern macropsine genus with similar forewing venation.
This genus has forewing venation resembling that of the modern genus Pedionis Hamilton, 1980, i.e., with the s crossvein delimiting an outer anteapical cell absent, but differs in having the structure of the head more plesiomorphic, resembling Zelopsis Evans, 1966. Specifically, the face has the epistomal suture visible and arcuate and the anteclypeus is well delimited laterally and basally by sutures. The pronotum is not strongly produced anteromedially, although it still extended slightly anterad of the eyes medially, and the transverse rugae are only slightly arched anterad medially. Unfortunately, because only one female specimen is known, it is not known whether the structure of the lower part of the face is sexually dimorphic in Archipedionis, as is usual among modern macropsines. The elongate rostrum of this genus is apparently unusual in the modern macropsine fauna and has been reported only in Galboa Distant, 1909 (Seychelles Islands) and Paragalboa Yang, Dietrich & Zhang, 2016 (Madagascar), but also occurs in some species of Pedionis.
Three previously described fossil species from Baltic amber have been included in Macropsini: Bythoscopus homousius Germar & Berendt, 1856, B. punctatus Bervoets, 1910, and Pediopsis minuta Bervoets, 1910 (
Length including forewing 4.6 mm. head width across eyes 1.6; pronotum width: 1.3; height of face (crown apex to anteclypeus apex, approximate) 1.0; forewing length 3.4; forewing maximum width (across approximately midlength) 1.2 mm; front tibia length 0.7; hind tibia length 1.7; hind tarsus length 0.7; ovipositor length (portion exposed posterad of sternite VII) 0.9. Hind tibia rows AD, AV and PV with 8, 8 and >17 macrosetae, respectively (PD not visible and PV only partly visible in holotype). Other structural features as described for genus. Dorsal coloration uniformly black except pale distal third of forewing (possibly an artifact of preservation), legs testaceous except for black macrosetal sockets on hind tibia. Female sternite VII only slightly longer than sternite VII, posterior margin shallowly obtusely emarginate.
The species name, obscurus, refers to the dark overall coloration.
Holotype female, Eocene Baltic amber (37–44 Ma), purchased by the first author from an amber dealer in Palanga, Lithuania. Deposited in the Paleontological Collection of the Illinois Natural History Survey (INHSP 10321).
The holotype is well preserved and intact with the right side of the body well visible in dorsal view but the left side largely obscured by a fracture in the amber extended along the midline. In ventral view, much of the head and parts of the legs are obscured by fractures and a milky veil also obscures parts of the legs and abdomen.
A–E Eoidiocerus emarginatus: A head, anteroventral view B head, pronotum and mesonotum, slight anterodorsal view C forewing D prothoracic femur and tibia, anterior view E hind femur, tibia and tarsus, anterior view F–J Archipedionis obscurus F head, pronotum and mesonotum, slight anterodorsal view G head, ventral view H forewing I visible part of hind wing J hind femur, tibia and tarsomere, anterior view.
This recently described fossil taxon from mid-Cretaceous Myanmar (Burmese) amber (~99 Ma) was originally considered unplaced to subfamily (
We are grateful to Dr. S. W. Heads for advice and for the use of his equipment to prepare and photograph the fossils included in this study. We also thank M. D. Webb and two anonymous referees whose constructive criticism led to substantial improvements of the manuscript. This work was funded in part by a grant from the National Science Foundation (DEB-1239788).