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Figure 4 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 4 Mesabolivar clade aOtavaloalisei (Brazil) bMesabolivarmaraba (Brazil) cLitoporus sp. n. "Br16-153" (Brazil) dMesabolivarcyaneotaeniatus (Brazil) eMesabolivarkathrinae (Brazil) fMesabolivarsaci (Brazil).
Figure 6 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 6 Smeringopinae aHoplopholcus sp. n. "Mar66" (Turkey) bStygopholcusabsoloni? (Bosnia and Herzegovina) cCrossopriza sp. n. "Om11" (Oman) dSmeringopuspallidus (Philippines) eSmeringopinapulchra (Ghana) fSmeringopinaankasa (Ghana).
Figure 3 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 3 'Basal' Modisiminae a Gen. n., sp. n. "Br16-50" (Brazil) bPrisculaandinensis? (Venezuela) c Gen. n., sp. n. "Br16-196" (Brazil) dTupigea sp. n. "Br14-47" (Brazil) ePisaboasilvae (Brazil) fPsilochorusimitatus (USA) gModisimusincertus (Cuba).
Figure 12 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 12 PholcusaP.creticus (Crete) bP.camba (Sulawesi) cP.mulu (Sarawak) dP.baka (Gabon) eP. sp. n. "SL43" (Sri Lanka).
Figure 9 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 9 Pholcinae 'group 2' (Zatavua and relatives, Metagonia), and Quamtana (marked: non-South African species). Photos aMetagoniataruma (Brazil) bMetagonia sp. n. "Br07-1" (Brazil) cMetagoniabifida? (Brazil) dQuamtana sp. n. (cf. mabusai) (Germany).
Figure 11 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 11 Micropholcus-Leptopholcus clade aMicropholcus sp. n. "Br15-152" (Brazil) bCanticussepaku (East Kalimantan) cMicromerysbaiteta (West Papua) dLeptopholcusborneensis (Singapore).
Figure 2 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 2 Ninetinae and ArteminaeaArtema sp. n. "Om14" (Oman) b Gen. n. (Ninetinae) sp. n. "Om6" (Oman) cChisosadiluta (USA) d Gen. n. (Arteminae) sp. n. "Ind82" (Sulawesi).
Figure 1 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 1 Backbone of the pholcid tree shown in Figs 2–12, derived from IQ-TREE analysis of the complete dataset.
Figure 5 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 5 Venezuelan clade + Aymaria + CarapoiaaMecolaesthusyawaperi (Brazil) bAymaria sp. n. "Br16-188" (Brazil) cCarapoiarubra (Brazil) dCarapoiakaxinawa (Brazil) eCarapoiapulchra (Brazil) fCarapoiaagilis (Brazil).
Figure 7 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 7 Pholcinae 'group 1' (Spermophora and relatives) a Gen. n., sp. n. "Ind206" (Halmahera); b' Spermophora sp. n. "Ind27" (Sumatra) cAetanabaganihan (Philippines) dSpermophorasenoculata (Turkey) eSavarnatessellata (Thailand) fWanniyalaagrabopath (Sri Lanka).
Figure 10 from: Huber BA, Eberle J, Dimitrov D (2018) The phylogeny of pholcid spiders: a critical evaluation of relationships suggested by molecular data (Araneae, Pholcidae). ZooKeys 789: 51-101. https://doi.org/10.3897/zookeys.789.22781
Figure 10 Calapnita-Panjange clade aKintaqasatun (Malaysia) bMerahanarathiwat (Thailand) cCalapnitavermiformis (Philippines) dApokayanakapit (Sarawak) eUthina sp. n. "Ind121" (Indonesia) fPanjangecasaroro (Philippines).
Figure 6 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956
Figure 6 Habit of Blitumasiaticum showing the senescing leaf rosette. Photographer: Igor Pospelov (Russia, Krasnoyarsk prov., Taymyr, Khatanga, August 2014).
Figure 7 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956
Figure 7 Shoot of Micromonolepispusilla showing the characteristic fleshy leaves. Photographer: Steve Matson (USA, California, Mono County, Long Valley, 2007).
Figure 5 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956
Figure 5 Cross-section of the seed of Neomonolepisspathulata. Abbreviations: T – testa, TE – tegmen, PE – perisperm, ST – stalactites in the outer walls of the testa cells.
Figure 4 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956
Figure 4 Cross-section of the seed of Blitumantarcticum. Abbreviations: T – testa, TE- tegmen, PE – perisperm.
Figure 1 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956
Figure 1 Best tree from the BEAST analysis of the ITS Chenopodioideae dataset. Bayesian posterior probabilities are given above the branches, jackknife values (left) and bootstrap percentages of the maximum likelihood analyses (right) are given below branches.
Figure 2 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956
Figure 2 Best tree from the BEAST analysis of the combined trnL-trnF + rbcL + atpB-rbcLChenopodioideae dataset. Bayesian posterior probabilities are given above the branches, jackknife values (left) and bootstrap percentages of the maximum likelihood analyses (right) are given below branches.
Figure 8 from: Sukhorukov AP, Nilova MV, Krinitsina AA, Zaika MA, Erst AS, Shepherd KA (2018) Molecular phylogenetic data and seed coat anatomy resolve the generic position of some critical Chenopodioideae (Chenopodiaceae – Amaranthaceae) with reduced perianth segments. PhytoKeys 109: 103-128. https://doi.org/10.3897/phytokeys.109.28956
Figure 8 SEM detail of the inflorescence of Neomonolepisspathulata. Abbreviations: B – bract (stained in green), FF – female flowers (orange), MF –male flower (perianth stained in blue, stamen in yellow), S – stem.
Figures 20-23 from: Chen K, Liu Q, Jin J, Zhang D (2019) Revision of the genus Emphylica Turner, 1913 based on morphology and molecular data (Lepidoptera, Crambidae, Pyraustinae). ZooKeys 836: 113-133. https://doi.org/10.3897/zookeys.836.32796
Figures 20-23 Female genitalia of Emphylica spp., ventral views 20E.diaphana, Chongqing (genitalia slide no. SYSU0969) 21E.crassihamata, Hunan (genitalia slide no. SYSU0957) 22E.cruoralis, Tibet (genitalia slide no. ZDD12100) 23E.xanthocrossa, Queensland (genitalia slide no. ANIC18162). Scale bar: 1.0 mm.
Figures 12-15 from: Chen K, Liu Q, Jin J, Zhang D (2019) Revision of the genus Emphylica Turner, 1913 based on morphology and molecular data (Lepidoptera, Crambidae, Pyraustinae). ZooKeys 836: 113-133. https://doi.org/10.3897/zookeys.836.32796
Figures 12-15 Adults of Emphylica spp. 12E.diaphana, male (Hexi, Fujian) 13E.crassihamata, holotype, male (Shixing, Guangdong) 14E.cruoralis, male (Khasis, India) 15E.xanthocrossa, female (Hidden Valley, Western Australia). Scale bar: 5.0 mm.
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