|
Non-social hymenopteran species for which sl-CSD has been proposed to be the sex determining mechanism. Confidence codes indicate the levels of evidence: 1 = post hoc explanations for exceptionally high male biased sex ratios in cultures or field surveys, 2 = on the basis of the verification of male diploidy through cytological (chromosome number), morphological (size, weight, density of wing microchaetae), genetical (microsatellites) or electrophoretical (allozymes) methods, 3 = on the basis of the sex ratios in inbreeding experiments in accordance with predictions under CSD, 4 = the joint combination of level 2 and 3, and 5 = linkage mapping of the sex locus and/or its molecular characterization |
||
| Species |
Confidence code |
Reference |
|
|
||
| Sub-order Symphyta |
||
| Family Tenthredinideae |
||
| Athalia rosae |
4 |
[117] |
| Family Diprionidae |
||
| Neodiprion nigroscutum |
4 |
[118] |
| Neodiprion pinetum |
2 |
Wallace pers. comm. in [7] |
| Sub-order Apocrita Infra-order Parasitica |
||
| Family Braconidae |
||
| Aphidius rhoplosiphi |
3 |
[119] |
| Bracon brevicornis |
4 |
[120] |
| Bracon hebetor |
4 |
[121] |
| Bracon serinopae |
4 |
[122] |
| Cotesia rubecula |
2 |
Steiner pers. comm. in [7] |
| Cotesia glomerata |
3 |
[20] |
| Microplitis croceiceps |
4 |
[123] |
| Family Ichneumonidae |
||
| Bathyplectes curculionis |
2 |
[124] |
| Diadegma armillata |
4 |
[32] |
| Diadegma chrysostictos |
4 |
[125] |
| Diadegma eucerophaga |
4 |
[32] |
| Diadegma fabriciane |
4 |
[32] |
| Diadegma fenestralis |
4 |
[32] |
| Diadegma insulare |
4 |
[32] |
| Diadegma pulchellus |
4 |
[32] |
| Diadegma semiclausum |
4 |
[126] |
| Diadromus pulchellus |
4 |
[34,127] |
| Heteropelma scaposum |
1 |
[128] |
| Venturia canescens |
3 |
[62] |
| Sub-order Apocrita Infra-order Aculeata |
||
| Family Vespidae |
||
| Ancistrocerus antilope |
2 |
[58] |
| Euodynerus foraminatus |
4 |
[56,57] |
van Wilgenburg et al. Frontiers in Zoology 2006 3:1 doi:10.1186/1742-9994-3-1 |
||