Insecta, Linnaeus, 1758

Kolibáč, Jiří, Bocakova, Milada, Liebherr, James K., Ramage, Thiboult & Porch, Nick, 2021, Extinct and extant Pacific Trogossitidae and the evolution of Cleroidea (Coleoptera) after the Late Triassic biotic crisis, Zoological Journal of the Linnean Society 191 : -

publication ID

C1BDE9AB-5360-48B1-8689-E16F497A417A

publication LSID

lsid:zoobank.org:pub:C1BDE9AB-5360-48B1-8689-E16F497A417A

persistent identifier

https://treatment.plazi.org/id/F047DF66-FFE4-FFD4-8732-FF1BFA93FA35

treatment provided by

Felipe

scientific name

Insecta
status

 

( Insecta View in CoL View at ENA : Coleoptera ) from the Burmese amber. Annales

Zoologici 67: 549–554.

Zhang C, Stadler T, Klopfstein S, Heath TA, Ronquist F. 2016. Total-evidence dating under the fossilized birth–death process. Systematic Biology 65: 228–249.

Zhang S-Q, Che L-H, Li Y, Liang D, Pang H, Ślipiński A, Zhang P. 2018. Evolutionary history of Coleoptera revealed by extensive sampling of genes and species. Nature Communications 9: 205.

Zimmerman EC. 1948. Introduction. Insects of Hawaii 1: 1–222.

Zimmerman EC, Perrault GH. 1989. Aglycyderidae of the Society Islands (Coleoptera: Curuclionidae). Bishop Museum Occasional Papers 29: 151–173.

SUPPORTING INFORMATION Additional Supporting Information may be found in the online version of this article at the publisher's web-site.

Table S2. Morphological matrix.

Table S3. GeneBank accession numbers. Newly generated sequences designated with an asterisk.

Fig. S1. Strict clock Cleroidea tree displayed substantial differences, particularly in basal relationships of former trogossitid subfamilies.

Fig. S2. Phylogeny of the Cleroidea based on Bayesian node-dating analysis from the four-gene dataset with the mean of the exponential root age prior set to 221.5 Mya. Monophyly constraints are marked by black ovals, numbers inside ovals refer to node age constraints by fossil priors ( Table 1). Blue bars indicate 95% HPD intervals for estimated node ages. Position of Tenebroides tahiti denoted with an arrow.

Fig. S3. A, B, two most parsimonious trees computed from morphological analysis by TNT (L = 29, Ci = 62, Ri = 73).

Fig. S4. Measurements of Parallelodera species ( Tenebroides luteicornis , T. fairmairei and T. quadraticollis ).

Fig. S5. Measurements of Parallelodera species ( Tenebroides parallelus and Tenebroides sp. : specimen from Colombia).

Fig. S6. Measurements of Tenebroides tahiti . Extant specimens (females J and K) from Fig. 8, Tahiti, Society Islands.

Fig. S7. Measurements of Tenebroides tahiti . Subfossil fragments from Mo’orea, Society Islands.

Fig. S8. Measurements of Tenebroides atiu . Subfossil fragments from Atiu, Cook Islands.

Fig. S9. Measurements of Tenebroides moorea . Subfossil fragments from Mo’orea, Society Islands.

Fig. S10. Measurements of Tenebroides rimatara . Subfossil fragments from Rimatara, Austral Islands.

Fig. S11. Measurements of Tenebroides mihiura . Subfossil fragments from Tubuai, Austral Islands.

Fig. S12. Measurements of Tenebroides tubuai . Subfossil fragments from Tubuai, Austral Islands.

Fig. S13. Measurements of Tenebroides raivavae . Subfossil fragments from Raivavae, Austral Islands.

Kingdom

Animalia

Phylum

Arthropoda

Class

Insecta

Darwin Core Archive (for parent article) View in SIBiLS Plain XML RDF