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Figure 2 from: Flinte V, Abejanella A, Daccordi M, Monteiro RF, Macedo MV (2017) Chrysomelinae species (Coleoptera, Chrysomelidae) and new biological data from Rio de Janeiro, Brazil. In: Chaboo CS, Schmitt M (Eds) Research on Chrysomelidae 7. ZooKeys 720: 5-22. https://doi.org/10.3897/zookeys.720.13963
Figure 2 - Seasonal distribution of Chrysomelinae. Number of Chrysomelinae species recorded on each month, obtained for 40 species from collections and fieldwork, in Serra dos Órgãos National Park, southeast Brazil.
Figure 1 from: Flinte V, Abejanella A, Daccordi M, Monteiro RF, Macedo MV (2017) Chrysomelinae species (Coleoptera, Chrysomelidae) and new biological data from Rio de Janeiro, Brazil. In: Chaboo CS, Schmitt M (Eds) Research on Chrysomelidae 7. ZooKeys 720: 5-22. https://doi.org/10.3897/zookeys.720.13963
Figure 1 - Chrysomelinae species in Rio de Janeiro. Some Chrysomelinae species occurring in Serra dos Órgãos National Park, State of Rio de Janeiro, Brazil. Calligrapha polyspila (A); Deuterocampta sedula adult (B1) and larva (B2); Elytrosphaera xanthopyga (C); Grammodesma rubroaenea adult (D1) and larva (D2); Platyphora axillaris adult (E1) and larva (E2); Platyphora bigata (F); Platyphora congener (G); Platyphora curticollis adult (H1), larval cannibalism (H2) and larval aggregation (H3); Platyphora dejeani adult (I1) and larva (I2) Calligrapha polyspila (Platyphora difficilis) (J); Platyphora fasciatomaculata adult (K1) and larva (K2); Platyphora fervida yellow-pronotum adult and larva (L1) and red-pronotum female ovipositing (L2); Platyphora flavovittata (M); Platyphora fraterna adult (N1) and larval aggregation (N2); Platyphora itatiayensis adult (O1) and larvae (O2); Platyphora jucunda adult (P1) and larval aggregation (P2); Platyphora langsdorfi adult (Q1) and larva (Q2); Platyphora pastica (R) Platyphora vidanoi (S); Platyphora zikani adult (T1) and young larvae (T2); Platyphora zonata (U); Stilodes thetis (V); Stilodes (Grammomades) impuncticollis adult (W1), eggs (W2) and larva (W3); Trichomela xantholoma (X); Zygogramma appendiculata polymorphic adults in copula (Y1), larvae feeding (Y2), larval cycloalexy (Y3), adult aggregation (Y4), egg mass (Y5), larva attacked by hemipteran nymph (Y6).
Figure 5 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 5 - Dendryphiella variabilis sp. nov. (ex-type CBS 584.96). A–E Colonies on A PDA B PCA C SNA D OA E MEA at 25 °C after 14 d F Exudates and conidiophores produced on OA G–K Conidiophores and conidia. Scale bars: 50 µm (G–H), 10 µm (I–K).
Figure 4 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 4 - Neodendryphiella tarraconensis sp. nov. (ex-type FMR 16234). A–E Colonies on A PDA B PCA C SNA D OA E MEA at 25 °C after 14 d F–K Conidiophores and conidia. Scale bars:10 µm (G–K).
Figure 1 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 1 - Maximum Likelihood (ML) tree constructed with the ITS and LSU sequences of 30 strains representatives of different taxa in the families Dictyosporiaceae and Pleosporaceae . The phylogenetic tree was rooted with Paradendryphiella arenaria and P. salina . Bootstrap support values for ML greater than 70% and Bayesian posterior probabilities greater than 0.95 are given near nodes, respectively. Names of species newly described here are indicated in bold. Branch lengths are proportional to distance. T Ex-type strain.
Figure 3 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 3 - Neodendryphiella michoacanensis sp. nov. (ex-type FMR 16098). A–E Colonies on A PDA B PCA C SNA D OA E MEA at 25 °C after 14 d F–J Conidiophores and conidia. Scale bars: 10 µm (G–J).
Figure 2 from: Iturrieta-González I, Gené J, Guarro J, Castañeda-Ruiz RF, García D (2018) Neodendryphiella, a novel genus of the Dictyosporiaceae (Pleosporales). MycoKeys 37: 19-38. https://doi.org/10.3897/mycokeys.37.27275
Figure 2 - Neodendryphiella mali sp. nov. (ex-type CBS 139.95). A–E Colonies on A PDA B PCA C SNA D OA E MEA at 25 °C after 14 d F–K Conidiophores and conidia. Scale bars: 10 µm (F–K).
Figure 9 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 9 PontederiaL.subg.Pontederia. A–C habit: A dense population of P.parviflora Alexander B population of P.ovalis Mart. ex Schult. & Schult.f. C habit of P.rotundifolia L.f. D–E petiolate leaves: D blade of P.rotundifoliaE blade of P.parvifloraF–H inflorescences: F inflorescence of P.cordata L., showing flowers with two yellow nectar guides in the posterior perianth lobes G inflorescence of P.parviflora, showing flowers with a sole yellow nectar guide in the posterior perianth lobes H inflorescence of P.rotudifolia, showing a lilac-flowered form I oblique view of a flower of P.ovalisJ–K fruits: J detail of the apex of the infructescence of P.ovalis, showing the anthocarp with sinuate ridges K detail of an achene of P.cordata, showing the toothed ridges. A by C. Willig & L. Nusbaumer B, I, J by M.O.O. Pellegrini C by L.O.A. Teixeira, D, H by R. Aguilar E by M.R. Engels F by Ashitaka-f Studio G by M.V. Lameiras and K by A. Haines.
Figure 6 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 6 Pontederiasubg.Monochoria (C.Presl) M.Pell. & C.N.Horn. A–B habit: A paludal habit of P.australasica (Ridl.) M.Pell. & C.N.Horn B paludal habit of P.cyanea (F.Muell.) M.Pell. & C.N.Horn C ligule of P.vaginalis Burm.f., showing the truncate apex D–E petiolate leaf-blades: D blade of P.cyanea, showing the lack of a posterior division E blade of P.vaginalis, showing the presence of a posterior division F–G inflorescences: F inflorescence of P.australasica, showing the developed main axis G inflorescence of P.plantaginea Roxb., showing the contracted main axis H front view of a flower of P.korsakowii (Regel & Maack) M.Pell. & C.N.Horn I–J inflorescences at post-anthesis: I erect inflorescence of P.hastata L. bearing flowers at post-anthesis J infructescence of P.hastata, showing the deflexed posture and the elongated pedicels K sections of immature capsules of P.vaginalis, showing developing seeds. A, F by M. Barritt B by R. Cumming C, E, K by P.B. Pelser & J.F. Barcelona D by A. & S. Pearson G by D. Valke H by Ashitaka-f Studio and I & J by Cerlin Ng.
Figure 3 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 3 Majority-rule tree recovered for the parsimony and Bayesian analysis of the combined morphological + plastid dataset. Yellow: Philydraceae. Orange: Haemodoraceae. Blue: Heterantheras.l. Pink: Pontederias.l.
Figure 2 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 2 Majority-rule tree recovered for the morphological and plastid datasets. Morphology: bootstrap support values are depicted over the branches, while Bremer Index support values are depicted under the branches. Plastid: posterior probability values are depicted over the branches. Yellow: Philydraceae. Orange: Haemodoraceae. Blue: Heterantheras.l. Pink: Pontederias.l.
Figure 1 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 1 Strict consensus tree (length=209 steps; CI=0.5913; RI=0.8618) recovered by the morphological dataset, showing the character state optimisations at each node of the cladogram, represented by circles. In each circle, the numbers above and below represent the character and character state numbers, respectively (as presented in Suppl. material 1).
Figure 8 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 8 Pontederiasubg.Eichhornia (Kunth) M.Pell. & C.N.Horn. A–B habit: A habit of P.heterosperma (Alexander) M.Pell. & C.N.Horn, showing the emerged petiolate leaves B habit of P.diversifolia (Vahl) M.Pell. & C.N.Horn, showing the floating petiolate leaves C–F inflorescence: C 2–3-flowered inflorescences of P.diversifolia, showing the flowers with a yellow nectar guide in the posterior perianth lobes D 1-flowered inflorescence of P.natans P.Beauv., showing the lack of a nectar guide E inflorescence of P.heterosperma, showing the lack of nectar guides in the posterior perianth lobes F morphological variation of inflorescences and perianth colour of P.azurea Sw G front view of a flower of P.azurea H front view of a flower of P.natans. A, B by O. Gaubert C by A.S. Castro D by P. Birnbaum E by H. Medeiros F by L.O.A. Teixeira G by M.O.O. Pellegrini and I by T.C. Buruwate.
Figure 5 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 5 Pontederiasubg.Cabanisia (Klotzsch ex Schltdl.) M.Pell. & C.N.Horn. A habit B–C inflorescence: B young inflorescence, showing the inflated leaf-sheath and flat basal bract with caudate apex C mature inflorescence showing the pedunculate cincinni with elongate internodes D detail of a cincinni, showing (from left to right) an immature floral bud, a pre-anthesis floral bud and a post-anthesis flower E front view of a flower F detail of an immature capsule, showing the ridged anthocarp. All photos of P.paniculata Spreng.; A by C. Willig & L. Nusbaumer, remaining photos by M.O.O. Pellegrini.
Figure 4 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 4 Heteranthera Ruiz & Pav. A–D habit: A emerged and flowering population of H.gardneri (Hook.f.) M.Pell. during the dry season B floating specimen of H.reniformis Ruiz & Pav. C emergent habit with floating and emerged leaves of H.rotundifolia (Kunth) Griseb. D habit of H.dubia (Jacq.) MacMill., showing the persistent sessile leaves E petiolate leaf of H.pumila M.Pell. & C.N.Horn, showing the lack of a pulvinus F Ligule and inflorescence of H.pumilaG–J flowers: G pseudanthium of H.gardneriHH.reniformisIH.rotundifoliaJH.zosterifolia Mart. A by A.P. Fontana B, H by C.N. Horn C, I by A. Popovkin D by S.R. Turner E, F by M.O.O. Pellegrini G by C.P. Bove and J by S.S. Oliveira.
Figure 7 from: Pellegrini MOO, Horn CN, Almeida RF (2018) Total evidence phylogeny of Pontederiaceae (Commelinales) sheds light on the necessity of its recircumscription and synopsis of Pontederia L. PhytoKeys 108: 25-83. https://doi.org/10.3897/phytokeys.108.27652
Figure 7 Pontederiasubg.Oshunae M.Pell. & C.N.Horn. A–B habit: A dense population of the pink-flowered form B detail of a population, showing the free-floating rosettes, stolons and inflated petioles C–D petiolate leaves: C blade D detail of a young leaf showing its blade enclosing the inflated petiole of the presiding leaf E–G inflorescence: E young inflorescence of a lilac-flowered form F inflorescence of a lilac-flowered form at anthesis G inflorescence of a pink-flowered form at anthesis H–J flowers: H oblique view of a lilac flower I detail of the nectar guide J detail of the androecium and gynoecium showing the glandular hairs. All photos of P.crassipes Mart.; A by C. Willig & L. Nusbaumer B by O. Gaubert C by K. Pritchard & S.A. Harris, D–F, H–I by R. Aguilar and G by M.O.O. Pellegrini.
Figure 7 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 7 Mcvaughiapiauhiensis. A seasonally dry forests from Serra das Confusões, Piauí, Brazil B abaxial surface of a leaf C detail of epipetiolar stipules D inflorescence E rehydrated flower showing the stamens (white arrows= reduced stamens) and styles. A by S.E. Martins B–E by R.F. Almeida.
Figure 3 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 3 Leaf morphoanatomy of Mcvaughia species. A patterns of leaf glands distribution on the abaxial leaf surface of M.bahianaB patterns of leaf glands distribution on the abaxial leaf surface of M.piauhiensisC patterns of leaf glands distribution on the abaxial leaf surface of M.sergipanaD transverse section of leaf base showing the basilaminar pair of stalked glands (white arrows) E basilaminar leaf gland with a stalk (black arrow) in M.piauhiensisF basilaminar gland in M.sergipana showing a sessile position (SE= anatomical arrangement with secretory epidermis, SP= vascularized secretory parenchyma) G–H laminar glands on the apex of cleared leaves of M.sergipana and M.bahiana respectively, note the apical tooth (G) I sessile laminar glands in M.sergipanaJ stalked laminar gland in M.piauhiensisK–L transverse sections of the leaf blade; mesophyll with uniserial palisade-like parenchyma and spongy parenchyma composed by several or few layers in M.sergipana and M.bahiana, respectively; note the idioblast with druse crystals at the mesophyll (white arrow) and the stomata distribution at the abaxial leaf surface (black arrow) M–N adaxial epidermis surface of M.piauhiensis and M.sergipana, showing scars of malpighiaceous trichomes O abaxial epidermis surface of trichomes abundance in M.bahianaP–Q outline of the anticlinal epidermal cell walls: straight in M.sergipana (P) and sinuous in M.bahiana (Q). Laminar scale bars: 1 cm (A–C), 100 μm (D, F–K, N–O), 150 μm (E), 50 μm (L–M, P–Q).
Figure 1 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 1 Wood anatomy of Mcvaughiasergipana. A–B transverse sections: Growth rings marked by radially narrow fibers (arrowheads) and a discontinuous line of axial parenchyma (in B); vessels are narrow and abundant, arranged in radial rows of 4 or more cells; some solitary vessels present; parenchyma rare, paratracheal scanty or at the growth ring limits; heartwood vessels in the bottom with content C radial section: Rays 2–3 cells wide, non-storied; prismatic crystals present in ray cells (arrows); parenchyma with 3 cells per strand (arrowhead) D ray heterocellular with procumbent, square and upright cells mixed throughout the ray. Scale bars: 150 μm (A), 100 μm (B–C), 60 μm (D).
Figure 11 from: Almeida RF, Guesdon IR, Pace MR, Meira RMS (2019) Taxonomic revision of Mcvaughia W.R.Anderson (Malpighiaceae): notes on vegetative and reproductive anatomy and the description of a new species. PhytoKeys 117: 45-72. https://doi.org/10.3897/phytokeys.117.32207
Figure 11 Distribution map of Mcvaughia: triangle – M.bahiana, circle – M.piauhiensis, and square – M.sergipana. Solid blue line in the center represents the São Francisco River today. Dotted blue line represents the past course of São Francisco River. Blue circle represents the São Francisco paleo lake. Light green – Atlantic Forest domain, dark green – Amazon Forest domain, orange – Cerrado domain, and yellow – Caatinga domain. AL – state of Alagoas, BA – state of Bahia, CE – state of Ceará, MA – state of Maranhão, PB – state of Paraíba, PE – state of Pernambuco, PI – state of Piauí, RN – state of Rio Grande do Norte, and SE – state of Sergipe.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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