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Figure 5 from: Meerow AW, Cano A (2019) Taxonomic novelties in Amaryllidaceae from the Department of Ancash, Peru, and a new combination in Clinanthus. PhytoKeys 131: 115-126. https://doi.org/10.3897/phytokeys.131.36160

Figure 5 Ismene parviflora. Drawing by Klei Sousa. A Habit B whole flower C whole flower cut open to show staminal corona and ovule number.

Figure 1 from: Meerow AW, Cano A (2019) Taxonomic novelties in Amaryllidaceae from the Department of Ancash, Peru, and a new combination in Clinanthus. PhytoKeys 131: 115-126. https://doi.org/10.3897/phytokeys.131.36160

Figure 1 A–CClinanthus inflatus. Photos by anonymous source, used with permission. A Inflorescence in habitat B bouquet of cut inflorescences C habit in nature D–FIsmene parviflora, photos by Asunción Cano D–E flowers F habit in cultivation.

Figure 2 from: Liu H-M, Shen J-Y, Liang Z-L, Peng F, Wang W-Z, Yang Z-W, Wang S, Parris B, Schneider H (2019) Two out of one: revising the diversity of the epiphytic fern genus Scleroglossum (Polypodiaceae, Grammitidoideae) in southern China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 115-133. https://doi.org/10.3897/phytokeys.130.33979

Figure 2 Reconstruction of the phylogenetic relationships of Scleroglossum species occurring in China including all accessions available in GenBank (October 2018). Newly generated accessions are printed in bold: HaiAcc = Hainan Accessions, two sequences obtained from individual A and B; YunAcc = Yunnan Accessions; VieAcc1 and VieAcc2 = two accessions obtained from the herbaria collections at KUN representing two independent collections (see Suppl. material 1: Table S1). The areas of origin are given for Scleroglossum GenBank accessions. The presented consensus phylogram is based on a Bayesian inference of Phylogeny including 690 accessions represented by rbcL sequences. Clades composed by non-Scleroglossum accessions were pruned. Two stars mark clades with a posterior confidence of p = 1.00 whereas one star marks clade with a posterior confidence p ≥ 0.95 and < 1.00. p.p. = pro parts to indicate the polyphyly of S. sulcatum.

Figure 3 from: Liu H-M, Shen J-Y, Liang Z-L, Peng F, Wang W-Z, Yang Z-W, Wang S, Parris B, Schneider H (2019) Two out of one: revising the diversity of the epiphytic fern genus Scleroglossum (Polypodiaceae, Grammitidoideae) in southern China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 115-133. https://doi.org/10.3897/phytokeys.130.33979

Figure 3 Similarity clustering of the Chinese provinces that are home to at least one grammitid ferns. The clustering analysis was carried out using Jaccard distances and the NJ-tree building algorithm. The underlying scoring (Table 1) was carried out as absence (0) and presence (1).

Figure 1 from: Liu H-M, Shen J-Y, Liang Z-L, Peng F, Wang W-Z, Yang Z-W, Wang S, Parris B, Schneider H (2019) Two out of one: revising the diversity of the epiphytic fern genus Scleroglossum (Polypodiaceae, Grammitidoideae) in southern China. In: Cai J, Yu W-B, Zhang T, Li D-Z (Eds) Revealing of the plant diversity in China's biodiversity hotspots. PhytoKeys 130: 115-133. https://doi.org/10.3897/phytokeys.130.33979

Figure 1 The grammitid genus Scleroglossum in China. A–EScleroglossum pusillum in Yunnan (YunAcc) and F–HScleroglossum sulcatum in Hainan (HaiAcc). A habitat of S. pusillum occurrences in Yunnan B germinated green spore recovered from opened mature sporangia of S. pusillum. The remains of the spore wall are visible at the lower part of the larger of the two cells that both contain mature chloroplasts. The smaller cell is the first daughter cell formed by the first cell division C habit of S. pusillumD close up of the dorsal surface of the simple leaves showing the location of the submarginal sori and the occurrences of brown branched hairs of S. pusillumE close up of the sorus structure showing the placement at the submargin of the leaves in S. pusillum. F habit of S. sulcatumG close up of the dorsal surface of the simple leaves showing the location of the not submarginal sori and the occurrences of brown branched hairs of S. sulcatumH close up of the sorus structure showing the placement of the sori in dorsal grooves and a distinct lamina margin in S. sulcatum. Scale bars: 0.02 mm (B); 1 mm (E, H).

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Supplementary material 1 from: Rokni S, Wursten B, Darbyshire I (2019) Synsepalum chimanimani (Sapotaceae), a new species endemic to the southern foothills of the Chimanimani Mountains of Mozambique and Zimbabwe, with notes on the botanical importance of this area. PhytoKeys 133: 115-132. https://doi.org/10.3897/phytokeys.133.38694

: Data type: species data

Figure 3 from: Rokni S, Wursten B, Darbyshire I (2019) Synsepalum chimanimani (Sapotaceae), a new species endemic to the southern foothills of the Chimanimani Mountains of Mozambique and Zimbabwe, with notes on the botanical importance of this area. PhytoKeys 133: 115-132. https://doi.org/10.3897/phytokeys.133.38694

Figure 3 Geographical distribution map of S. chimanimani, S. kaessneri, and S. muelleri. Circles – S. chimanimani; triangles – S. muelleri; stars – S. kaessneri.

Figure 1 from: Rokni S, Wursten B, Darbyshire I (2019) Synsepalum chimanimani (Sapotaceae), a new species endemic to the southern foothills of the Chimanimani Mountains of Mozambique and Zimbabwe, with notes on the botanical importance of this area. PhytoKeys 133: 115-132. https://doi.org/10.3897/phytokeys.133.38694

Figure 1 Synsepalum chimanimani (A-K) and Synsepalum kaessneri (L) A habit B stem apex with apical buds/young leaves and petioles showing indumentum C medifixed hairs on stem D abaxial leaf surface showing sparse medifixed hairs on midrib E leaf showing (faint) secondary veins F flower cluster showing bud, open flower and partially opened flower G flower, side view (hydrated) H corolla after removal of two petals and stamens (hydrated) I stamen and staminodes in situ on petal, inner face bases of neighbouring petals shown J side view of stamen and petal (staminodes omitted) K immature fruit (from photograph) L leaf (abaxial) of Synsepalum kaessneri.A, D-K drawn from B.T. Wursten BW897 (BR0000020700003) B, C from Timberlake et al. 6197 (K001291035) L drawn from Magogo & Glover 280 (K). Scale bars: 1mm (Single bar); 2 mm and 5 mm (graduated single bar); 1 cm (double bar); 5 cm (graduated double bar). Drawn by Andrew Brown, November 2018.

Figure 2 from: Rokni S, Wursten B, Darbyshire I (2019) Synsepalum chimanimani (Sapotaceae), a new species endemic to the southern foothills of the Chimanimani Mountains of Mozambique and Zimbabwe, with notes on the botanical importance of this area. PhytoKeys 133: 115-132. https://doi.org/10.3897/phytokeys.133.38694

Figure 2 Synsepalum chimanimaniA habit and leaves B, C flowering stems D flowers E immature fruit (Photographs by Bart Wursten).

Figure 4 from: Zhu XX, Zheng HL, Wang J, Gao YQ, Ma JS (2019) Taxonomic studies on the genus Isotrema (Aristolochiaceae) from China: I. I. cangshanense, a new species from Yunnan. PhytoKeys 134: 115-124. https://doi.org/10.3897/phytokeys.134.37243

Figure 4 A–CIsotrema cangshanense X.X.Zhu, H.L.Zheng & J.S.Ma, sp. nov. A leaves B flower (lateral view) C longitudinal section of flower (showing the inside structure) D–FIsotrema utriforme (S. M. Hwang) X. X. Zhu, S. Liao & J. S. Ma D leaves E flower (lateral view) F longitudinal section of flower (showing the inside structure) G–II. forrestianum (J. S. Ma) X. X. Zhu, S. Liao & J. S. Ma G leaves H flower (lateral view) I longitudinal section of flower (showing the inside structure) J–LI. obliquum (S. M. Hwang) X. X. Zhu, S. Liao & J. S. Ma J leaves K flower (lateral view) L longitudinal section of flower (showing the inside structure). A–C, G–I Photographed by Xinxin Zhu D–F photographed by Lei Cai; J–L photographed by Yuan Wang.

Figure 3 from: Zhu XX, Zheng HL, Wang J, Gao YQ, Ma JS (2019) Taxonomic studies on the genus Isotrema (Aristolochiaceae) from China: I. I. cangshanense, a new species from Yunnan. PhytoKeys 134: 115-124. https://doi.org/10.3897/phytokeys.134.37243

Figure 3 Holotype of Isotrema cangshanense X. X.Zhu, H.L.Zheng & J.S.Ma, sp. nov. (CSH-0164770).

Figure 1 from: Zhu XX, Zheng HL, Wang J, Gao YQ, Ma JS (2019) Taxonomic studies on the genus Isotrema (Aristolochiaceae) from China: I. I. cangshanense, a new species from Yunnan. PhytoKeys 134: 115-124. https://doi.org/10.3897/phytokeys.134.37243

Figure 1 Isotrema cangshanense X.X.Zhu, H.L.Zheng & J.S.Ma, sp. nov. A habit B flower (lateral view) C flower (front view) D opened flower (showing the inner structure) E anthers and gynostemium F the dehiscent capsule G seed. Illustration by Shizhen Qiao.

Figure 2 from: Zhu XX, Zheng HL, Wang J, Gao YQ, Ma JS (2019) Taxonomic studies on the genus Isotrema (Aristolochiaceae) from China: I. I. cangshanense, a new species from Yunnan. PhytoKeys 134: 115-124. https://doi.org/10.3897/phytokeys.134.37243

Figure 2 Isotrema cangshanense X.X.Zhu, H.L.Zheng & J.S.Ma, sp. nov. A habit B leaves C flower bud D inflorescence E flower (front view) F flowers (lateral view) G anthers and gynostemium H the dehiscent capsule I seeds. Photographed by Xinxin Zhu.

Figure 5 from: Lyons J, Piller KR, Artigas-Azas JM, Dominguez-Dominguez O, Gesundheit P, Köck M, Medina-Nava M, Mercado-Silva N, García AR, Findley KM (2019) Distribution and current conservation status of the Mexican Goodeidae (Actinopterygii, Cyprinodontiformes). ZooKeys 885: 115-158. https://doi.org/10.3897/zookeys.885.38152

Figure 5 Pie chart of the conservation status of Mexican goodeid evolutionarily significant units (ESUs).

Figure 2 from: Lyons J, Piller KR, Artigas-Azas JM, Dominguez-Dominguez O, Gesundheit P, Köck M, Medina-Nava M, Mercado-Silva N, García AR, Findley KM (2019) Distribution and current conservation status of the Mexican Goodeidae (Actinopterygii, Cyprinodontiformes). ZooKeys 885: 115-158. https://doi.org/10.3897/zookeys.885.38152

Figure 2 Photos of four representative types of goodeid habitats A Lake Chapala, near Ajijic, Jalisco, 6 January 2005. The largest natural lake in Mexico and historically the home of at least six species of goodeids. Currently, only Chapalichthys encaustus (see Figure 1), Goodea atripinnis, and Zoogoneticus purhepechus remain B 27 de Noviembre Springs, Durango, 11 January 2008, home of Characodon species C Molino Viejo Reservoir, Jalisco, 17 January 2008, home of Xenotoca melanosomaD Cuzalapa River, Jalisco, 11 January 2006, home of Ilyodon furcidens and Xenotaenia resolanae (see Figure 1).

Figure 1 from: Lyons J, Piller KR, Artigas-Azas JM, Dominguez-Dominguez O, Gesundheit P, Köck M, Medina-Nava M, Mercado-Silva N, García AR, Findley KM (2019) Distribution and current conservation status of the Mexican Goodeidae (Actinopterygii, Cyprinodontiformes). ZooKeys 885: 115-158. https://doi.org/10.3897/zookeys.885.38152

Figure 1 Photos of eight representative goodeid fishes. All photos taken by John Lyons of freshly preserved, wild-caught, adult, male specimens. AAllotoca goslinei, Potrero Grande Stream, Jalisco, 8 January 2004 BAlloophorus robustus, Opopeo Lake, Michoacán, 9 January 2011 CAmeca splendens, Almoloya Springs, Jalisco, 17 January 2008 DChapalichthys encaustus, Lake Chapala near Ajijic, Jalisco, 6 January 2005 EGoodea atripinnis, Tierra Quemada Stream, San Luis Potosí, 15 January 2011 FSkiffia lermae, Zacapu Lake, Michoacán, 11 January 2005 GXenotaenia resolanae, Cuzalapa River, Jalisco, 10 January 2006 HXenotoca doadrioi, San Marcos Stream, Jalisco, 9 January 2005.

Figure 3 from: Lyons J, Piller KR, Artigas-Azas JM, Dominguez-Dominguez O, Gesundheit P, Köck M, Medina-Nava M, Mercado-Silva N, García AR, Findley KM (2019) Distribution and current conservation status of the Mexican Goodeidae (Actinopterygii, Cyprinodontiformes). ZooKeys 885: 115-158. https://doi.org/10.3897/zookeys.885.38152

Figure 3 General distribution of goodeid fishes in Mexico, with the location of major river basins and lakes shown. Shaded areas indicate the range of most goodeid species (blue) and the disjunct range of Characodon (brown).A Mezquital River basin B Grande Santiago River Basin CAmeca River basin D Purificación and Marabasco River basins E Armería River basin F Coahuayana River basin G Balsas River Basin H Lake Chapala I Lerma River Basin J Lake Cuitzeo/Grande de Morelia River basin (endorheic) K Lake Pátzcuaro and Lake Zirahuén basins (endorheic) L Lake Atotonilco, Lake San Marcos, Lake Sayula, and Lake Zapotlán basins (endorheic) M Lake Magdalena basin (endorheic) N Valley of Mexico/ Mexico City (endorheic) O Pánuco River basin P Valley of Parras,(endorheic), Characodon garmani collection site Q Tunal River drainage (part of Mezquital River basin), home of Characodon species.

Figure 11 from: Lyons J, Piller KR, Artigas-Azas JM, Dominguez-Dominguez O, Gesundheit P, Köck M, Medina-Nava M, Mercado-Silva N, García AR, Findley KM (2019) Distribution and current conservation status of the Mexican Goodeidae (Actinopterygii, Cyprinodontiformes). ZooKeys 885: 115-158. https://doi.org/10.3897/zookeys.885.38152

Figure 11 Distribution of Characodon species. The single record far to the east represents C. garmani and the remainder of points represent C. audax and C. lateralis.

Figure 115 from: Carolina Arias-Penna D, Whitfield JB, Janzen DH, Hallwachs W, Dyer LA, Smith MA, Hebert PD.N, Fernández-Triana JL (2019) A species-level taxonomic review and host associations of Glyptapanteles (Hymenoptera, Braconidae, Microgastrinae) with an emphasis on 136 new reared species from Costa Rica and Ecuador. ZooKeys 890: 1-685. https://doi.org/10.3897/zookeys.890.35786

Figure 115 Glyptapanteles jaquioconnorae sp. nov. female EC-2997 YY-A025 A Habitus B, D Head B Frontal view D Dorsal view C Head, pronotum, propleuron, lateral view ET1–3, dorsal view F Mesonotum, dorsal view G Scutellum, metanotum, propodeum, dorsal view H, J Metasoma H Dorsal view J Lateral view I Mesosoma, lateral view K, L Wings K Fore L Hind.