Mesomantispinae Makarkin 1996

Mesomantispinae Mesomantispinae is composed of six genera and nine described species, and two indeterminate species one of Archaeodrepanicus (Jepson et al., 2013) and one Mesomantispinae gen et sp. indet. (herein), the species are listed in Table 1, other undescribed Mesozoic Chinese Mesomantispinae...

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Main Authors: Jepson, James E., Khramov, Alexander V., Ohl, Michael
Format: Text
Language:unknown
Published: Zenodo 2018
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ren
Online Access:https://dx.doi.org/10.5281/zenodo.5986646
https://zenodo.org/record/5986646
id ftdatacite:10.5281/zenodo.5986646
record_format openpolar
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Neuroptera
Mantispidae
spellingShingle Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Neuroptera
Mantispidae
Jepson, James E.
Khramov, Alexander V.
Ohl, Michael
Mesomantispinae Makarkin 1996
topic_facet Biodiversity
Taxonomy
Animalia
Arthropoda
Insecta
Neuroptera
Mantispidae
description Mesomantispinae Mesomantispinae is composed of six genera and nine described species, and two indeterminate species one of Archaeodrepanicus (Jepson et al., 2013) and one Mesomantispinae gen et sp. indet. (herein), the species are listed in Table 1, other undescribed Mesozoic Chinese Mesomantispinae fossils have also been discovered (Makarkin et al. , 2012). The subfamily represents one of the earliest records of the family Mantispidae, first recorded in the Middle–Upper Jurassic of Daohugou, China. The only older known mantispid is from the Lower Jurassic of Germany, Liassochrysa stigmatica . To date mesomantispines have only been found in Asia (China, Kazakhstan, and Siberia). Another mantispid is also known in the Kazakhstan fauna, Promantispa similis Panfilov, 1980, which is thought to be sister group to Liassochrysa ( Wedmann & Makarkin, 2007; Liu et al. , 2015), both being placed within the extant subfamily Drepanicinae (Liu et al. , 2015). The first record of mantispids in Europe and then their absence until the Eocene, may represent a lack of fossil localities, or specimens not yet discovered, or only sparse distribution or diversification compared to the diverse fauna observed in Asia. The presence of raptorial forelegs on the mesomantispines suggest a predatory lifestyle, as observed in the extant mantispids. A major difference however is the absence of a large sub-basal spine on the fore femur, which is considered to be a plesiomorphic condition of Mantispidae. The adaptive significance of the large sub-basal spine is unclear, but it cannot be excluded that its presence facilitates capturing of prey, so in this respect members of the extant subfamilies of Mantispidae may have had an advantage over mesomantispines. Nothing is known about the larvae of mesomantispinae, therefore no interpretations about larval lifestyle can be made, such as whether they had a relationship with spiders, as observed in modern Mantispinae and some extinct taxa (Ohl, 2004). The genera of Mesomantispinae are mostly differentiated on their body morphology, for example the structure of their raptorial forelegs, which is quite variable, ranging from clubbed, oval, to slender. Variation is also observed with the length of the pronotum, which ranges from relatively short to elongate. The wing venation on the whole is similar between the genera, however, some venation characters can be used to group genera together. Examples of this are the crossveins within the CuP area, separating Mesomantispa from the other genera, and also the structure of CuP, whether it is pectinate ( Clavifemora , Sinomesomantispa , Archaeodrepanicus ) or non-pectinate ( Karataumantispa , Ovalofemora gen. nov. , Longicollum gen. nov. ). Below is a key of Mesomantispinae genera, updated from Jepson (2015) to include the newly described genera: 1. Crossveins between branches of CuP present; area posterior to CuA approximately half the width of the wing...................................................................................................... Mesomantispa - Crossveins between branches of CuP absent; area posterior to CuA less than half the width of the wing................. 2 2. Forewing CuP pectinate, prostrate setae on foretibia not hooked, foretibia and foretarsus combined longer than forefemur... 3 - Forewing CuP non-pectinate, prostrate setae on foretibia hooked, foretibia and foretarsus combined longer than forefemur...................................................................................................... 5 3. Forelegs greatly enlarged to give a club-like appearance (Jepson et al ., 2013: fig. 7); forewing colour pattern consists of spots........................................................................................... Clavifemora - Forelegs not club-like in appearance; no spots on forewings.................................................... 4 4. Wide fore femur (1.7 mm) and very small fore femoral spines (<0.1–0.16 mm long) (Jepson et al. , 2013: Fig. 6B); costal margin concave before mid-point of wing; costal space of forewing sharply narrowed towards apex; RP with 9 branches, simple for most of their length; forewing colour pattern consists of a distal distinct thick dark band (Jepson et al. , 2013: fig. 6A)......................................................................................... Sinomesomantispa - Fore femur more slender (0.9–1 mm) and relatively larger femoral spines (0.1–0.25 mm long); costal margin not concave before mid-point of wing; RP with 6 branches, some branches forked before mid-point of wing; forewing colour pattern consists of 3 stripes (Jepson et al. , 2013: fig 1A)................................................. Archaeodrepanicus 5. Length to width ratio of forefemur (at widest part) is less than 3, forefemur oval shaped, forecoxa, foretrochanter stout, all covered in setae........................................................................ Ovalofemora gen. nov. - Length to width ratio of forefemur (at widest part) is 3 or more, some setae........................................ 6 6. Forefemur and forecoxa slender, pronotum slightly elongate 1.1x longer than wide, MP deeply forked..... Karataumantispa - Forefemur widened at proximal end, with spines at distal apex, pronotum very elongate 2.8x longer than wide, MP simple most of length forking distally.......................................................... Longicollum gen. nov. : Published as part of Jepson, James E., Khramov, Alexander V. & Ohl, Michael, 2018, New Mesomantispinae (Insecta: Neuroptera: Mantispidae) from the Jurassic of Karatau, Kazakhstan, pp. 563-574 in Zootaxa 4402 (3) on pages 572-573, DOI: 10.11646/zootaxa.4402.3.9, http://zenodo.org/record/1209798 : {"references": ["Jepson, J. E., Heads, S. W., Makarkin, V. N. & Ren, D. (2013) New fossil Mantidflies (Insecta: Neuroptera: Mantispidae) from the Mesozoic of North-Eastern China. Palaeontology, 56, 603 - 613. https: // doi. org / 10.1111 / pala. 12005", "Makarkin, V. N., Yang, Q., Peng, Y. Y. & Ren, D. (2012) A comparative overview of the neuropteran assemblage of the Lower Cretaceous Yixian Formation (China), with description of a new genus of Psychopsidae (Insecta: Neuroptera). Cretaceous Research, 35, 57 - 68. https: // doi. org / 10.1016 / j. cretres. 2011.11.013", "Panfilov, D. V. (1980) New representatives of lacewings (Neuroptera) from the Jurassic of Karatau. In: Dolin, V. G., Panfilov, D. V., Ponomarenko, A. G. & Pritykina, L. N. (Eds.), Mesozoic Fossil Insects. Nauka Dumka, Kiev, pp. 82 - 111. [in Russian]", "Wedmann, S. & Makarkin, V. N. (2007) A new genus of Mantispidae (Insecta: Neuroptera) from the Eocene of Germany, with a review of the fossil record and palaeobiogeography of the family. Zoological Journal of the Linnean Society, 149, 701 - 716. https: // doi. org / 10.1111 / j. 1096 - 3642.2007.00273. x", "Liu, X., Winterton, S. L., Wu, C., Piper, R. & Ohl, M. (2015) A new genus of mantidflies discovered in the Oriental region, with a higher-level phylogeny of Mantispidae (Neuroptera) using DNA sequences and morphology. Systematic Entomology, 40, 183 - 206. http: // dx. doi. org / 10.1111 / syen. 12096", "Ohl, M. (2004) Annotated catalog of the Mantispidae of the world (Neuroptera). Contribution on Entomology, International, 5, 133 - 242.", "Jepson, J. E. (2015) A review of the current state of knowledge of fossil Mantispidae (Insecta: Neuroptera). Zootaxa, 3964, 419 - 432. https: // doi. org / 10.11646 / zootaxa. 3964.4.2"]}
format Text
author Jepson, James E.
Khramov, Alexander V.
Ohl, Michael
author_facet Jepson, James E.
Khramov, Alexander V.
Ohl, Michael
author_sort Jepson, James E.
title Mesomantispinae Makarkin 1996
title_short Mesomantispinae Makarkin 1996
title_full Mesomantispinae Makarkin 1996
title_fullStr Mesomantispinae Makarkin 1996
title_full_unstemmed Mesomantispinae Makarkin 1996
title_sort mesomantispinae makarkin 1996
publisher Zenodo
publishDate 2018
url https://dx.doi.org/10.5281/zenodo.5986646
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spelling ftdatacite:10.5281/zenodo.5986646 2023-05-15T18:50:59+02:00 Mesomantispinae Makarkin 1996 Jepson, James E. Khramov, Alexander V. Ohl, Michael 2018 https://dx.doi.org/10.5281/zenodo.5986646 https://zenodo.org/record/5986646 unknown Zenodo http://zenodo.org/record/1209798 http://publication.plazi.org/id/7D42FFE3FFBDFF93FFA1CA76DE0CFFE0 http://zoobank.org/DAE383C6-6EF3-46C9-9DBC-6ADE75F0728A https://zenodo.org/communities/biosyslit https://dx.doi.org/10.11646/zootaxa.4402.3.9 http://zenodo.org/record/1209798 http://publication.plazi.org/id/7D42FFE3FFBDFF93FFA1CA76DE0CFFE0 http://zoobank.org/DAE383C6-6EF3-46C9-9DBC-6ADE75F0728A https://dx.doi.org/10.5281/zenodo.5986645 https://zenodo.org/communities/biosyslit Open Access Creative Commons Zero v1.0 Universal https://creativecommons.org/publicdomain/zero/1.0/legalcode cc0-1.0 info:eu-repo/semantics/openAccess CC0 Biodiversity Taxonomy Animalia Arthropoda Insecta Neuroptera Mantispidae article-journal ScholarlyArticle Taxonomic treatment Text 2018 ftdatacite https://doi.org/10.5281/zenodo.5986646 https://doi.org/10.11646/zootaxa.4402.3.9 https://doi.org/10.5281/zenodo.5986645 2022-04-01T08:54:36Z Mesomantispinae Mesomantispinae is composed of six genera and nine described species, and two indeterminate species one of Archaeodrepanicus (Jepson et al., 2013) and one Mesomantispinae gen et sp. indet. (herein), the species are listed in Table 1, other undescribed Mesozoic Chinese Mesomantispinae fossils have also been discovered (Makarkin et al. , 2012). The subfamily represents one of the earliest records of the family Mantispidae, first recorded in the Middle–Upper Jurassic of Daohugou, China. The only older known mantispid is from the Lower Jurassic of Germany, Liassochrysa stigmatica . To date mesomantispines have only been found in Asia (China, Kazakhstan, and Siberia). Another mantispid is also known in the Kazakhstan fauna, Promantispa similis Panfilov, 1980, which is thought to be sister group to Liassochrysa ( Wedmann & Makarkin, 2007; Liu et al. , 2015), both being placed within the extant subfamily Drepanicinae (Liu et al. , 2015). The first record of mantispids in Europe and then their absence until the Eocene, may represent a lack of fossil localities, or specimens not yet discovered, or only sparse distribution or diversification compared to the diverse fauna observed in Asia. The presence of raptorial forelegs on the mesomantispines suggest a predatory lifestyle, as observed in the extant mantispids. A major difference however is the absence of a large sub-basal spine on the fore femur, which is considered to be a plesiomorphic condition of Mantispidae. The adaptive significance of the large sub-basal spine is unclear, but it cannot be excluded that its presence facilitates capturing of prey, so in this respect members of the extant subfamilies of Mantispidae may have had an advantage over mesomantispines. Nothing is known about the larvae of mesomantispinae, therefore no interpretations about larval lifestyle can be made, such as whether they had a relationship with spiders, as observed in modern Mantispinae and some extinct taxa (Ohl, 2004). The genera of Mesomantispinae are mostly differentiated on their body morphology, for example the structure of their raptorial forelegs, which is quite variable, ranging from clubbed, oval, to slender. Variation is also observed with the length of the pronotum, which ranges from relatively short to elongate. The wing venation on the whole is similar between the genera, however, some venation characters can be used to group genera together. Examples of this are the crossveins within the CuP area, separating Mesomantispa from the other genera, and also the structure of CuP, whether it is pectinate ( Clavifemora , Sinomesomantispa , Archaeodrepanicus ) or non-pectinate ( Karataumantispa , Ovalofemora gen. nov. , Longicollum gen. nov. ). Below is a key of Mesomantispinae genera, updated from Jepson (2015) to include the newly described genera: 1. Crossveins between branches of CuP present; area posterior to CuA approximately half the width of the wing...................................................................................................... Mesomantispa - Crossveins between branches of CuP absent; area posterior to CuA less than half the width of the wing................. 2 2. Forewing CuP pectinate, prostrate setae on foretibia not hooked, foretibia and foretarsus combined longer than forefemur... 3 - Forewing CuP non-pectinate, prostrate setae on foretibia hooked, foretibia and foretarsus combined longer than forefemur...................................................................................................... 5 3. Forelegs greatly enlarged to give a club-like appearance (Jepson et al ., 2013: fig. 7); forewing colour pattern consists of spots........................................................................................... Clavifemora - Forelegs not club-like in appearance; no spots on forewings.................................................... 4 4. Wide fore femur (1.7 mm) and very small fore femoral spines (<0.1–0.16 mm long) (Jepson et al. , 2013: Fig. 6B); costal margin concave before mid-point of wing; costal space of forewing sharply narrowed towards apex; RP with 9 branches, simple for most of their length; forewing colour pattern consists of a distal distinct thick dark band (Jepson et al. , 2013: fig. 6A)......................................................................................... Sinomesomantispa - Fore femur more slender (0.9–1 mm) and relatively larger femoral spines (0.1–0.25 mm long); costal margin not concave before mid-point of wing; RP with 6 branches, some branches forked before mid-point of wing; forewing colour pattern consists of 3 stripes (Jepson et al. , 2013: fig 1A)................................................. Archaeodrepanicus 5. Length to width ratio of forefemur (at widest part) is less than 3, forefemur oval shaped, forecoxa, foretrochanter stout, all covered in setae........................................................................ Ovalofemora gen. nov. - Length to width ratio of forefemur (at widest part) is 3 or more, some setae........................................ 6 6. Forefemur and forecoxa slender, pronotum slightly elongate 1.1x longer than wide, MP deeply forked..... Karataumantispa - Forefemur widened at proximal end, with spines at distal apex, pronotum very elongate 2.8x longer than wide, MP simple most of length forking distally.......................................................... Longicollum gen. nov. : Published as part of Jepson, James E., Khramov, Alexander V. & Ohl, Michael, 2018, New Mesomantispinae (Insecta: Neuroptera: Mantispidae) from the Jurassic of Karatau, Kazakhstan, pp. 563-574 in Zootaxa 4402 (3) on pages 572-573, DOI: 10.11646/zootaxa.4402.3.9, http://zenodo.org/record/1209798 : {"references": ["Jepson, J. E., Heads, S. W., Makarkin, V. N. & Ren, D. (2013) New fossil Mantidflies (Insecta: Neuroptera: Mantispidae) from the Mesozoic of North-Eastern China. Palaeontology, 56, 603 - 613. https: // doi. org / 10.1111 / pala. 12005", "Makarkin, V. N., Yang, Q., Peng, Y. Y. & Ren, D. (2012) A comparative overview of the neuropteran assemblage of the Lower Cretaceous Yixian Formation (China), with description of a new genus of Psychopsidae (Insecta: Neuroptera). Cretaceous Research, 35, 57 - 68. https: // doi. org / 10.1016 / j. cretres. 2011.11.013", "Panfilov, D. V. (1980) New representatives of lacewings (Neuroptera) from the Jurassic of Karatau. In: Dolin, V. G., Panfilov, D. V., Ponomarenko, A. G. & Pritykina, L. N. (Eds.), Mesozoic Fossil Insects. Nauka Dumka, Kiev, pp. 82 - 111. [in Russian]", "Wedmann, S. & Makarkin, V. N. (2007) A new genus of Mantispidae (Insecta: Neuroptera) from the Eocene of Germany, with a review of the fossil record and palaeobiogeography of the family. Zoological Journal of the Linnean Society, 149, 701 - 716. https: // doi. org / 10.1111 / j. 1096 - 3642.2007.00273. x", "Liu, X., Winterton, S. L., Wu, C., Piper, R. & Ohl, M. (2015) A new genus of mantidflies discovered in the Oriental region, with a higher-level phylogeny of Mantispidae (Neuroptera) using DNA sequences and morphology. Systematic Entomology, 40, 183 - 206. http: // dx. doi. org / 10.1111 / syen. 12096", "Ohl, M. (2004) Annotated catalog of the Mantispidae of the world (Neuroptera). Contribution on Entomology, International, 5, 133 - 242.", "Jepson, J. E. (2015) A review of the current state of knowledge of fossil Mantispidae (Insecta: Neuroptera). Zootaxa, 3964, 419 - 432. https: // doi. org / 10.11646 / zootaxa. 3964.4.2"]} Text ren Siberia DataCite Metadata Store (German National Library of Science and Technology) Pala ENVELOPE(40.637,40.637,64.896,64.896)