Table 3.
Orders | Common name | Parthenogens | Total species | Proportion | Species total reference |
---|---|---|---|---|---|
Astigmata | Mites | 3 | 5000 | 0.001 | (Norton et al. 1993) |
Coleoptera: Micromalthidae | Telephone‐pole beetle* | 1 | 1 | 1 | (Normark 2003) |
Coleoptera: Scolytinae | Bark beetles | 1 | 4500 | 0.000 | (Farrell et al. 2001) |
Hemiptera: Aleyrodoidae | Whiteflies | 4 | 1556 | 0.003 | (Martin and Mound 2007) |
Hemiptera: Margarodidae | Scale insects | 3 | 428 | 0.007 | (García Morales et al. 2016) |
Hemiptera: Diaspididae | Scale insects | 1 | 2378 | 0.000 | (García Morales et al. 2016) |
Hymenoptera | Ants, bees, sawflies and wasps | 586 | 150,000 | 0.004 | (Mayhew 2007) |
Mesostigmata | Predatory mites | 43 | 5000 | 0.009 | (Norton et al. 1993) |
Prostigmata | Mites | 6 | 14,000 | 0.000 | (Norton et al. 1993) |
Thysanoptera | Thrips | 91 | 5938 | 0.015 | (Mayhew 2007) |
Trombidiformes | Mites | 26 | 25,821 | 0.001 | (Zhang et al. 2011) |
In mites and Scolytinae, the exact origin(s) of haplodiploidy are not known, so the higher taxonomic level was chosen. *The telephone‐pole beetle, Micromalthus debilis, is the only extant species in this monotypic family, which is considered to have a haplodiploid origin, see Normark (2003).
Only taxa with at least one case of parthenogenesis described are shown.