Stenophlebiidae

Last updated

Stenophlebiidae
Temporal range: 160–Cenomanian  Ma
Stenophlebia latreillei coll Koschny 0004.jpg
Stenophlebia latreillei, Upper Jurassic, Solnhofen Plattenkalk, in private collection
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Odonata
Infraorder: Stenophlebioptera
Superfamily: Stenophlebioidea
Family: Stenophlebiidae
Needham, 1903
Type genus
Stenophlebia
Hagen, 1866
Genera
Synonyms

The Stenophlebiidae is an extinct family of medium-sized to large fossil odonates from the Upper Jurassic and Cretaceous period that belongs to the damsel-dragonfly grade ("anisozygopteres") within the stem group of Anisoptera. They are characterized by their long and slender wings, and the transverse shape of the discoidal triangles in their wing venation.

Contents

Description

Adult

Body

Cratostenophlebia schwickert, Lower Cretaceous, Brazil, head of male holotype Cratostenophlebia schwickert male holotype WDC 136 head.jpg
Cratostenophlebia schwickert, Lower Cretaceous, Brazil, head of male holotype

The head is similar to that of Recent Gomphidae with two large and globular compound eyes that are distinctly separated. The three ocelli are arranged in a triangle on the globular vertex. The mandibles are strong. The legs have short and strong spines. [1]

Wings and wing venation

Stenophlebia amphitrite, Upper Jurassic, Solnhofen Plattenkalk, drawing of wing venation and terminalia Stenophlebia amphitrite coll. Kuempel 4D drawing Bechly.gif
Stenophlebia amphitrite, Upper Jurassic, Solnhofen Plattenkalk, drawing of wing venation and terminalia

The largest species Stenophlebia amphitrite reached a wingspan of about 17.3 centimetres (6.8 in), while the smallest species Hispanostenophlebia barremiana reached only a wingspan of about 7.7 centimetres (3.0 in). [2]

Stenophlebiidae are distinguished by the following set of eight derived wing characters (synapomorphies):
(1) a long not zigzagged secondary longitudinal convex vein in the postdiscoidal area, parallel to MP, the base of this vein being just distal of the discoidal triangle; (2) Cr long or very long, covering more than one or two cells between RA and RP; (3) pterostigma shifted basally; (4) pterostigma very long; (5) hindwing subdiscoidal space transverse and crossed by two veins or more; (6) the four wings elongate and more or less falcate; (7) forewing discoidal triangle long transverse; (8) numerous and well defined straight intercalary secondary longitudinal veins reaching posterior wing margin. [3]

Furthermore they share the following four synapomorphies with Prostenophlebiidae in the superfamily Stenophlebioidea:
(1) a long and not zigzagged (or slightly zigzagged) secondary longitudinal convex vein in postdiscoidal area, parallel to MP, the base of this vein being about two or three cells or just distal of discoidal triangle; (2) a long and not zigzagged concave Mspl; (3) oblique vein "O" absent; (4) wings elongate. [3]

And they share these four synapomorphies with Prostenophlebiidae and Liassostenophlebiidae in the suborder Stenophlebioptera:
(1) nodal crossvein Cr very oblique, i.e. angle Cr-RA > 140°; (2) subnodus Sn very oblique, with or without cross-veins reaching it; (3) CuAa with a broad area between the two most distal posterior branches; (4) presence of straight supplementary longitudinal veins in the areas between IR2 and MP near posterior wing margin. [3]

Sexual dimorphism

Cratostenophlebia schwickert, Lower Cretaceous, Brazil, cerci of male holotype Cratostenophlebia schwickert male holotype WDC 136 terminalia.jpg
Cratostenophlebia schwickert, Lower Cretaceous, Brazil, cerci of male holotype
Cratostenophlebia schwickerti, Lower Cretaceous, Brazil, ovipositor of female allotype specimen Cratostenophlebia female allotype ovipositor.jpg
Cratostenophlebia schwickerti, Lower Cretaceous, Brazil, ovipositor of female allotype specimen

Males are distinguished by a weak anal angle of the hindwing base and in some species of Upper Jurassic Stenophlebia by a club-like dilation of the terminal part of the abdomen. The male secondary genitalia are unknown, but probably were of the anisopterid type. The male terminalia of the abdomen are of the anisopterid type, thus composed of a pair of dorsal claspers (cerci) and an unpaired ventral process (epiproct). [1]

Nel et al. (1993) stated that the female ovipositor is reduced, while Bechly (2007, 2010) could demonstrate that at least the female of the stenophlebiid genus Cratostenophlebia had a distinct endophytic ovipositor. [4]

Larva

Fossil larvae of this extinct family have not been formally described yet, but Bechly (2007) suggested that the Nothomacromia larvae from the Lower Cretaceous Crato Formation of Brazil may be the larvae of Cratostenophlebia. [5]

Classification

The family group taxon was established by Needham (1903) as subfamily Stenophlebinae (sic) of the extinct damsel-dragonfly family Heterophlebiidae. It was emended and elevated to family rank Stenophlebiidae by Handlirsch (1906). [3] Stenophlebia Hagen, 1866 is the type genus of this family.

The species Sinostenophlebia zhanjiakouensis was originally assigned to the family Stenophlebiidae; however, the position and status of this species is very uncertain due to the poor preservation and insufficient original description. Zheng et al. (2016) transferred this species to the family Aeschnidiidae, and considered the genus Sinostenophlebia to be a likely junior synonym of the genus Leptaeschnidium . [6]

Bechly (2005) could show that the very small species "Stenophlebia" casta from the Upper Jurassic Solnhofen Plattenkalk of Germany is not related to Stenophlebiidae. It is now classified as Parastenophlebia casta in a separate family Parastenophlebiidae that belongs to the extinct damsel-dragonfly suborder Heterophlebioptera. [7]

Stenophlebia amphitrite, Upper Jurassic, Solnhofen Plattenkalk, in private collection Stenophlebia amphitrite coll Kuempel.jpg
Stenophlebia amphitrite, Upper Jurassic, Solnhofen Plattenkalk, in private collection
Cratostenophlebia schwickerti, Lower Cretaceous, Brazil, male holotype Cratostenophlebia schwickerti male holotype WDC 136.jpg
Cratostenophlebia schwickerti, Lower Cretaceous, Brazil, male holotype
Cratostenophlebia schwickerti, Lower Cretaceous, Brazil, female allotype Cratostenophlebia schwickerti female allotype WDC 137.jpg
Cratostenophlebia schwickerti, Lower Cretaceous, Brazil, female allotype

The family contains 9 described genera with a total of 18 species: [2]

Phylogeny

The set of shared derived characters listed in the description section above demonstrate that Stenophlebiidae is clearly a monophyletic group (clade). [3]

Before the advent of cladistic classification Stenophebiidae was classified within the odonate suborder Anisozyoptera, which was later recognized to be a paraphyletic grade. In modern classifications the taxon Anisozygoptera is therefore either abandoned or restricted to the Recent relict family Epiophlebiidae. [1]
Bechly (1996) established a new suborder Stenophlebioptera for Stenophlebiidae and its closest relatives. Stenophlebioptera is closer related to Anisoptera than Epiophlebiidae. [14]

The extinct family Prostenophlebiidae is the sister group of Stenophlebiidae within the superfamily Stenophlebioidea. Stenophlebioidea is the sister group of Liassostenophlebiidae within the suborder Stenophlebioptera. [3]

Nel et al. (1993) suggested that Recent Epiophlebiidae is the sister group of Stenophlebiidae within a superfamily Epiophlebioidea, [1] and Bechly (1996) suggested that extinct Gondvanogomphidae is the sister group of Stenophlebiidae within Stenophlebioptera. [14] However, these hypotheses have been refuted by Fleck et al. (2003). [3]

The phylogenetic position of Stenophlebiidae according to Bechly (1996, 2007) and Fleck et al. (2003, 2004):

Odonatoptera

Biology

Next to nothing is known about the ecology and behavior of Stenophlebiidae, but it probably was quite similar to Recent odonates. The shape of the wings suggests that they were slow flyers that fed on smaller flying insects. The females probably inserted their eggs into plants in or close to the water.

Geographical and geological distribution

The fossil record of this family ranges from Upper Jurassic of Germany (Solnhofen Plattenkalk, Nusplingen limestones [9] ) and Kazakhstan (Karabastau Svita) to the Lower Cretaceous of Brazil (Crato Formation), Mongolia (Bon Tsagaan), Spain (Las Hoyas), and England (Durlston Formation) to the Upper Cretaceous (Cenomanian) of France [12] and Myanmar. [10]

History

Larger revisions of this family have been provided by Nel et al. (1993) and Fleck et al. (2003). [1] [3]

Earliest finds

The first stenophlebiid fossil was described as "Agrion" latreillei by Germar (1839) from the Upper Jurassic Solnhofen Plattenkalk of Germany. [2]

Notable specimens

Beside the important type specimens there are also several exceptionally well preserved fossils that contribute to our knowledge of the morphology of Stenophlebiidae. [2] These include specimens of Stenophlebia amphitrite and Stenophlebia latreillei in several private fossil collections.

Related Research Articles

<span class="mw-page-title-main">Solnhofen Limestone</span> Geological formation preserving rare fossils in Germany

The Solnhofen Limestone or Solnhofen Plattenkalk, formally known as the Altmühltal Formation, is a Jurassic Konservat-Lagerstätte that preserves a rare assemblage of fossilized organisms, including highly detailed imprints of soft bodied organisms such as sea jellies. The most familiar fossils of the Solnhofen Plattenkalk include the early feathered theropod dinosaur Archaeopteryx preserved in such detail that they are among the most famous and most beautiful fossils in the world. The Solnhofen beds lie in the German state of Bavaria (Bayern), halfway between Nuremberg (Nürnberg) and Munich (München) and were originally quarried as a source of lithographic limestone. The Jura Museum situated in Eichstätt, Germany has an extensive exhibit of Jurassic fossils from the quarries of Solnhofen and surroundings, including marine reptiles, pterosaurs, and one specimen of the early bird Archaeopteryx.

<span class="mw-page-title-main">Weald Clay</span> Geological formation in England

Weald Clay or the Weald Clay Formation is a Lower Cretaceous sedimentary rock unit underlying areas of South East England, between the North and South Downs, in an area called the Weald Basin. It is the uppermost unit of the Wealden Group of rocks within the Weald Basin, and the upper portion of the unit is equivalent in age to the exposed portion of the Wessex Formation on the Isle of Wight. It predominantly consists of thinly bedded mudstone. The un-weathered form is blue/grey, and the yellow/orange is the weathered form, it is used in brickmaking.

<span class="mw-page-title-main">Meganisoptera</span> Extinct order of dragonfly-like animals

Meganisoptera is an extinct order of large dragonfly-like insects, informally known as griffenflies or (incorrectly) as giant dragonflies. The order was formerly named Protodonata, the "proto-Odonata", for their similar appearance and supposed relation to modern Odonata. They range in Palaeozoic times. Though most were only slightly larger than modern dragonflies, the order includes the largest known insect species, such as the late Carboniferous Meganeura monyi and the even larger early Permian Meganeuropsis permiana, with wingspans of up to 71 centimetres (28 in).

<i>Stenophlebia</i> Extinct genus of dragonflies

Stenophlebia is an extinct genus of dragon-damselfly from late Jurassic and early Cretaceous period.

<span class="mw-page-title-main">Cordulegastroidea</span> Superfamily of dragonflies

Cordulegastroidea is a superfamily of dragonflies that contains three families.

<span class="mw-page-title-main">Libelluloidea</span> Superfamily of dragonflies

Libelluloidea is a superfamily of dragonflies.

<span class="mw-page-title-main">Hemiphlebiidae</span> Family of damselflies

Hemiphlebiidae is a family of damselflies. It contains only one extant species, the ancient greenling, native to Southern Australia and Tasmania. The fossil record of the group extends back to the Late Jurassic, making them the oldest known crown group damselflies.

<span class="mw-page-title-main">Palaeontinidae</span> Extinct family of true bugs

Palaeontinidae, commonly known as giant cicadas, is an extinct family of cicadomorphs. They existed from the Late Triassic to the Early Cretaceous. The family contains around 30 to 40 genera and around a hundred species. They are thought to have had a similar ecology to modern cicadas as feeders on plant xylem fluids. Despite being described as "giant cicadas"(with the wingspan of some species exceeding 15 centimetres ), they are not particularly closely related to true cicadas.

<span class="mw-page-title-main">Mesoraphidiidae</span> Extinct family of insects

Mesoraphidiidae is an extinct family of snakeflies in the suborder Raphidiomorpha. The family lived from the Late Jurassic through the Late Cretaceous and is known from twenty-five genera. Mesoraphidiids have been found as both compression fossils and as inclusions in amber. The family was first proposed in 1925 by the Russian paleoentomologist Andrey Vasilyevich Martynov based on Upper Jurassic fossils recovered in Kazakhstan. The family was expanded in 2002 by the synonymizing of several other proposed snakefly families. The family was divided into three subfamilies and one tribe in a 2011 paper, further clarifying the relationships of the included genera.

<span class="mw-page-title-main">Tarsophlebiidae</span> Extinct family of flying insects

The Tarsophlebiidae is an extinct family of medium-sized fossil odonates from the Upper Jurassic and Lower Cretaceous period of Eurasia. They are either the most basal member of the damsel-dragonfly grade ("anisozygopteres") within the stem group of Anisoptera, or the sister group of all Recent odonates. They are characterized by the basally open discoidal cell in both pairs of wings, very long legs, paddle-shaped male cerci, and a hypertrophied ovipositor in females.

<i>Chresmoda</i> Extinct insect genus

Chresmoda is an extinct genus of insects within the family Chresmodidae.

<span class="mw-page-title-main">Chresmodidae</span> Extinct family of insects

Chresmodidae is an extinct family of Mesozoic insects within the superorder Polyneoptera.

Rafaelnymphes is an extinct genus of lacewing in the family Nymphidae known from a fossil found in South America. The genus contains a single species, Rafaelnymphes cratoensis.

<i>Eichstaettisaurus</i> Genus of lizard from the Late Jurassic and Early Cretaceous periods

Eichstaettisaurus is a genus of lizards from the Late Jurassic and Early Cretaceous of Germany, Spain, and Italy. With a flattened head, forward-oriented and partially symmetrical feet, and tall claws, Eichstaettisaurus bore many adaptations to a climbing lifestyle approaching those of geckoes. The type species, E. schroederi, is among the oldest and most complete members of the Squamata, being known by one specimen originating from the Tithonian-aged Solnhofen Limestone of Germany. A second species, E. gouldi, was described from another skeleton found in the Matese Mountains of Italy. Despite being very similar to E. schroederi, it lived much later, during the Albian stage. Fossils of both species show exceptional preservation due to deposition in low-oxygen marine environments.

2018 in paleoentomology is a list of new fossil insect taxa that were described during the year 2018, as well as other significant discoveries and events related to paleoentomology that were scheduled to occur during the year.

<span class="mw-page-title-main">Steleopteridae</span> Extinct family of insects

Steleopteridae is a family of extinct winged damselflies whose fossils have been found in modern Germany, Great Britain and Kazakhstan, and which lived at the end of the Jurassic and the beginning of the Cretaceous.

<i>Steleopteron</i> Extinct genus of damselflies

Steleopteon is a genus of extinct winged damselflies whose fossils have been found in modern Germany, and Great Britain, and which lived at the end of the Jurassic and the beginning of the Cretaceous.

2017 in paleoentomology is a list of new fossil insect taxa that were described during the year 2017, as well as other significant discoveries and events related to paleoentomology that were scheduled to occur during the year.

<span class="mw-page-title-main">Coccolepididae</span> Extinct family of ray-finned fishes

Coccolepididae is an extinct family of ray-finned fish, known from the Early Jurassic to Early Cretaceous, most of which were originally referred to the type genus Coccolepis. They had a widespread distribution, being found in North and South America, Australia, Asia and Europe. They are mostly known from freshwater environments, though several species have been found in marine environments. They are morphologically conservative, and have poorly ossified endo and exoskeletons, which usually results in poor preservation. This makes it difficult to distinguish species. They are generally small fish, with the largest known specimens reaching a length of 210 mm. Historically, they have been classified as members of “Palaeonisciformes”, a paraphyletic grouping of non-neopterygian fish, due to their plesiomorphic conservative morphology closely resembling those of many other groups of primitive fish. Some recent authors have suggested that they may belong to the order Chondrostei as relatives of the Acipenseriformes.

<span class="mw-page-title-main">Aeschnidiidae</span> Extinct family of dragonflies

Aeschnidiidae is an extinct family of Anisopteran dragonfly. Aeschnidiids were widespread and could be found on nearly every continent on Earth. They were most diverse during the Early Cretaceous before completely disappearing at the end of the Maastrichtian. Many members of this family were large dragonflies, with wing lengths ranging from 35 to 45 mm.

References

  1. 1 2 3 4 5 6 Nel A, Martinez-Delclos X, Paicheler JC, Henrotay M (1993). "Les "Anisozygoptera" fossiles. Phylogénie et classification (Odonata)". Martinia. numéro hors série 3: 1–311.
  2. 1 2 3 4 Paleobiology Database entry for Stenophlebiidae
  3. 1 2 3 4 5 6 7 8 9 10 11 12 Fleck G, Bechly G, Martinez-Delclos X, Jarzembowski E, Coram R, Nel A (2003). "Phylogeny and classification of the Stenophlebioptera (Odonata: Epiproctophora)" (PDF). Annales de la Société Entomologique de France. 39 (1): 55–93. doi: 10.1080/00379271.2003.10697363 . S2CID   85417279.
  4. Bechly G (2010). "Additions to the fossil dragonfly fauna from the Lower Cretaceous Crato Formation of Brazil (Insecta: Odonata)" (PDF). Palaeodiversity. 3 (Supplement): 11–77.
  5. 1 2 3 Bechly G (2007). "Chapter 11.5: Odonata: damselflies and dragonflies" (PDF). In Martill DM, Bechly G, Loveridge RF (eds.). The Crato Fossil Beds of Brazil: Window into an Ancient World. Cambridge, UK: Cambridge University Press. pp. 184–222. ISBN   978-0-521-85867-0.
  6. 1 2 Daran Zheng; He Wang; Edmund A. Jarzembowski; Bo Wang; Su-Chin Chang; Haichun Zhang (2016). "New data on Early Cretaceous odonatans (Stenophlebiidae, Aeschnidiidae) from northern China". Cretaceous Research. 67: 59–65. Bibcode:2016CrRes..67...59Z. doi:10.1016/j.cretres.2016.07.005.
  7. Bechly G (2005). "A re-description of "Stenophlebia" casta (Insecta: Odonata: Parastenophlebiidae n. fam) from the Upper Jurassic Solnhofen Limestone in Germany" (PDF). Stuttgarter Beiträge zur Naturkunde, Serie B (Geologie und Paläontologie). 359: 1–12.
  8. Daran Zheng; André Nel; Bo Wang; Edmund A. Jarzembowski; Su-Chin Chang; Haichun Zhang (2016). "The first Early Cretaceous damsel–dragonfly (Odonata: Stenophlebiidae: Stenophlebia) from western Liaoning, China". Cretaceous Research. 61: 124–128. Bibcode:2016CrRes..61..124Z. doi:10.1016/j.cretres.2016.01.003.
  9. 1 2 Bechly G, Dietl G, Schweigert G (2003). "A new species of Stenophlebia (Insecta: Odonata: Stenophlebiidae) from the Nusplingen Lithographic Limestone (Upper Jurassic, SW Germany)" (PDF). Stuttgarter Beiträge zur Naturkunde, Serie B (Geologie und Paläontologie). 338 (Supplement): 1–10.
  10. 1 2 3 Diying Huang; Yanzhe Fu; André Nel (2019). "The first amber stenophlebiid damsel-dragonfly (Odonata, Epiproctophora, Stenophlebiidae) from mid-Cretaceous amber of northern Myanmar" (PDF). Cretaceous Research. 94: 40–44. Bibcode:2019CrRes..94...40H. doi:10.1016/j.cretres.2018.10.008. S2CID   135305970.
  11. Daran Zheng; Haichun Zhang; Bo Wang; Su-Chin Chang (2018). "A new species of damsel-dragonfly (Odonata: Stenophlebiidae: Cretastenophlebia) from the Lower Cretaceous of the Jiuquan Basin, northwestern China". Earth and Environmental Science Transactions of the Royal Society of Edinburgh. 107 (2–3): 185–189. doi:10.1017/S1755691017000093. S2CID   134456677.
  12. 1 2 André Nel; Günther Fleck; Géraldine Garcia; Bernard Gomez; Patrice Ferchaud; Xavier Valentin (2015). "New dragonflies from the lower Cenomanian of France enlighten the timing of the odonatan turnover at the Early – Late Cretaceous boundary". Cretaceous Research. 52, Part A: 108–117. Bibcode:2015CrRes..52..108N. doi:10.1016/j.cretres.2014.08.005.
  13. André Nel; Diying Huang (2015). "A new genus and species of damsel-dragonfly (Odonata: Stenophlebiidae) from the Lower Cretaceous of Inner Mongolia, China". Cretaceous Research. 56: 421–425. Bibcode:2015CrRes..56..421N. doi:10.1016/j.cretres.2015.06.008.
  14. 1 2 Bechly G (10 August 2007). "Phylogenetic Systematics of "Anisozygopteres"". Phylogenetic Systematics of Odonata. SMNS. Retrieved 19 August 2012.

Further reading