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M.G. Volkovitsh. Presentation: Larval morphology of the jewel beetles of the subfamily Polycestinae...


М.Г. Волкович



Mark G. Volkovitsh. 2019.
Larval morphology of the jewel beetles of the subfamily Polycestinae and its significance for the taxonomy and phylogeny (Coleoptera: Buprestidae).
Oral Presentation on: Immature Beetles Meeting 2019. October 3-4, Prague, Czech Republic.



Презентация в файле PDF: volkovitsh_ibm-2019_presentation.pdf

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Presentation text (to slides)


Slide 1. 
Larval morphology of the jewel beetles of the subfamily Polycestinae and its significance for the taxonomy 
and phylogeny (Coleoptera: Buprestidae)
Mark G. Volkovitsh

Slide 2. Buprestoidea and Polycestinae: Taxonomic compositions and species numbers
Buprestidae is one of the largest coleopteran families counting 
about 15,300 species. 
Subfamily Polycestinae, which considered rather primitive, takes the 
4th place in the family being significantly inferior to Agrilinae, 
Buprestinae and Chrysochroinae. 
It includes about 1300 species belonging to 13 tribes and 82 genera, 
among them 35 genera are monotypic and only 11 genera comprise more 
than 20 species, with 3 genera counting above 100 species; 
more than half of polycestine species belong to Acmaeoderini. 
Polycestine larvae demonstrate almost the entire spectrum of morpho-ecological 
and functional adaptations and evolutionary trends inherent in Buprestidae.

Slide 3. Current state of knowledge of polycestine larvae
The larvae of about 100 (8%) species from 24 (29.6%) genera and 11 tribes of 
Polycestinae have been described so far; the larvae of Perucolini and Bulini 
are still unknown; larvae of Acmaeoderini are best studied, while the larvae 
of other groups are known only for individual or very few species. 
The only larval key to buprestid higher taxa including Polycestinae was 
published by Cobos (1986). Larval characters of supraspecific taxa were 
analyzed by Volkovitsh & Hawkeswood (1999) and Volkovitsh & Bily (2015).

Slide 4. Host plants of known polycestine larvae
The vast majority of polycestine larvae develop on angiosperms.
Associations of prospherioidtaxa Xyroscelidini, Prospheriniand Buliniwith 
such ancient relicsas Zamiaceaefrom Cycadophyta, Araucariacea and 
Podocarpaceae are most intriguing. Contrary to other Polyctesini,the species 
of Chrysophana group associated with gymnosperms. It is noteworthy that 
a number of polycestinespecies feeds on the plants characteristic ofmangrove 
communities. Feeding of Thryncopygini on Nolinaceae and leaf-mining 
Paratrachys on Ficusare regarded as most specialized.

Slide 5. Morpho-ecological types of buprestid larvae
General structure of buprestid larvae is determined by their habitats - 
either soil dwelling (schizopoid and julodoidmorpho-ecological types) or inside 
plant tissues (buprestoid, agriloid, and trachyoid types).

Slide 6. Morpho-ecological types of polycestine larvae
Polycestine larvae are predominantly buprestoid while the larvae of 
leaf-mining Paratrachysbelong to trachyoid type.Depending on the habitats 
(subcortical, xylophagous, grassy stem borers, etc.) and the hardness 
of the food substrate,several morpho-ecological subtypes distinguished 
within the buprestoid type. Leaf-miner trachyoid type occurs only in
Polycestinae and Agrilinae.

Slide 7. Diagnostic characters of Polycestinae larvae
Polycestine larvae can be recognized by a complex of characters,
of which a single pronotal groove (occurring also in Gabellinae and 
Agrilinae) and presence of additional lobe on stipes (except prospherioid 
genera) are most important. From Galbellinae they differ mainly by mouthpart 
structure, from Agrilinae - by presence of proventriculus, buprestoid spiracles 
and mouthparts.

Slide 8. Phyletic lineages of Polycestinae
Three phyletic lineages are established within Polycestinae: prospherioid, 
polycestioid, and acmaeoderioid.

Slide 9. Fragment of phylogenetic tree for Polycestinae, Julodinae,
Schizopodidae, outgroups based on molecular phylogenetic study
The distinguishing ofpolycestioid and acmaeoderioid lineages is supported 
by molecular studies which in turn do not support the separation of 
prospherioid lineage from polycestioid one. The most strange thing is 
a position of Haplostethini as a sister group of Julodinaewhich according 
to the authors determines their rank of distinct subfamily.

Slide 10. Prospherioid lineage
Separation of presumably most primitive Gondwanianprospherioid lineageis 
supported only by absence of additional lobe on larval stipes (plesiomorphy).
As seen on the phylogenetic tree, Xyroscelidini is sister to 
Thrincopygini + Chrysophana clade (though without a nodal support), 
while Astraeus is located in the base of polycestioid clade.

Slide 11. Polycestioid lineage: Thryncopigini, Chrysophana-gr., Polyctesini
Larval characters in part support the affinity of Thrincopygini and Polyctesini, 
while Chrysophana differs from all other genera of Polyctesini not only 
in larval morphology but also in host plants (Gymnosperms) and together 
with Beerelus deserves the separation in distinct tribe.

Slide 12. Polycestioid lineage: Polycestini, Tyndarini
Unique larval synapomorphies were found in all studied genera of Polycestini 
(paired sclerotized ring-shaped structures on the thoracic and 1st abdominal 
segment, multiple campaniformsensilla on mouth parts) and Tyndarini (expanded 
metathorax). 

Slide 13. Acmaeoderioid lineage: Ptosimini, Paratracheini
Most primitive states are found in Ptosimini: Ptosima still retains microsetal 
areas on prementum, lackingin Sponsor. Larval characters and feeding habits 
conflict with a placement of Sponsor in Paratracheini, in the same time they 
support close relationship of Paratrachys with Ptosimini.In spite of extreme 
specialization resulting from leaf-minning habit, the larvae of Paratrachys 
retain many buprestoidstates such as proventriculus, spiracles, 
and mouthparts which never occur in the mining larvae of Tracheini (Agrilinae).

Slide 14. Acmaeoderioid lineage: Acmaeoderini, Haplostethini
Larvae of Acmaeoderina demonstrate the most advanced states of many characters,
such as complete reduction of microsetal areas on labrum, prementum and 
integuments.
Taxonomic position and relationship of Haplostethiniare still enigmatic. 
Despite of the results of molecular study,the larval morphology of Mastogenius 
is very similar to that of Polycestini and acmaeoderioid taxa what give 
grounds to treat Haplostethini as a member of Acmaeoderioid lineage or 
as belonging to a separate lineage within Polycestinae.

Slide 15. Conclusions
This study demonstrates a great importance of larval morphology for taxonomy 
and phylogenetics not only Polycestinae but entire Buprestoidea.

Slide 16. Acknowledgements

Slide 17. Thanks for your time!