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opennotspecifiedJan 2019View details →

FIGURE 2 in Grebennikovius, a new genus to accommodate Epactoides basilewskyi (Balthasar, 1960) (Coleoptera: Scarabaeidae: Deltochilini)

FIGURE 2. Aedeagus in dorsal (A), right lateral (B) and left lateral (C, D) view. A–C, Grebennikovius basilewskyi (Balthasar, 1960) new combination; D, Epactoides humberti (Paulian, 1975). Scale bar = 0.5 mm.

opennotspecifiedJun 2019View details →

TEXT-FIGURE 2. Precisions on some dorsal internal terms used for the thecideoid brachiopods (Ospreyella mayottensis sp. nov., MNHN-IB-2017-179). Abbreviations: ibl, interbrachial lobe, i.e. the lobes occurring between the main arms of the lopho- phore in Ospreyella in particular; ibr, intrabrachial ridge, i.e. the ridges immediately within the main arms of the lophophore and which define the brachial lobes; lg, lophophore groove, i.e. the groove that accommodates the main arms of the lophophore; pbr, peribrachial ridge, i.e. the ridge that encloses the outer margins of the main arms of the lophophore. in Recent thecideide brachiopods from a submarine cave in the Department of Mayotte (France), northern Mozambique Channel

TEXT-FIGURE 2. Precisions on some dorsal internal terms used for the thecideoid brachiopods (Ospreyella mayottensis sp. nov., MNHN-IB-2017-179). Abbreviations: ibl, interbrachial lobe, i.e. the lobes occurring between the main arms of the lopho- phore in Ospreyella in particular; ibr, intrabrachial ridge, i.e. the ridges immediately within the main arms of the lophophore and which define the brachial lobes; lg, lophophore groove, i.e. the groove that accommodates the main arms of the lophophore; pbr, peribrachial ridge, i.e. the ridge that encloses the outer margins of the main arms of the lophophore.

Fig. 8 in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 8. Distribution of Platycesta depressa, form with bicolored elytra and with only apex of terminal ventrite yellow or brown.

Fig. 10 in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 10. Distribution of Platycesta depressa, form with entirely black elytra and with entirely pale terminal ventrite.

Fig. 9 in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 9. Distribution of Platycesta depressa, form with bicolored elytra and with majority of terminal ventrite yellow or brown.

Fig. 7 in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 7. Distribution of Platycesta depressa, form with bicolored elytra and entirely black terminal ventrite.

Fig. 5. Platycesta depressa, male. A in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 5. Platycesta depressa, male. A) Median lobe of aedeagus, dorsal view, B) Median lobe of aedeagus, lateral view, C) Median lobe of aedeagus, distal portion, D) Spiculum, E) Last visible tergite, F) Last (internal) tergite, G) Abdominal ventrites.

Fig. 3. Platycesta depressa. A in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 3. Platycesta depressa. A) Female, antenna, B) Female, distal abdominal ventrites, C) Male, distal abdominal ventrites.

Fig. 2. Platycesta depressa. A in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 2. Platycesta depressa. A) Form with entirely pale elytra, dorsal view, B) Form with entirely pale elytra, ventral view, C) Form with bicolored elytra, dorsal view, D) Anterior view, E) Epipleuron.

Fig. 4. Platycesta depressa, female. A in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 4. Platycesta depressa, female. A) Reproductive organs, B) Spermatheca, C) Vaginal palpi, D) Last visible tergite, E) Tignum, F) Abdominal ventrites, G) Last (internal) tergite.

Fig. 1. Platycesta depressa, form with entirely black elytra. A in A New Genus to Accommodate Central and South American Beetles with Broadly Explanate Elytra, Formerly Assigned to Monocesta Clark and Coelomera Chevrolat (Coleoptera: Chrysomelidae: Galerucinae: Galerucini)

Fig. 1. Platycesta depressa, form with entirely black elytra. A) Dorsal view, B) Lateral view, C) Ventral view, D) Pronotum.

opennotspecifiedSep 2015View details →

FIGURE 2 in Continuous variation supports accommodating Lilium habaense and L. xanthellum within L. stewartianum (Liliaceae)

FIGURE 2. Continuous variation within one population of Lilium xanthellum or of my inclusive L. stewartianum in Xiangcheng, Sichuan.—A. Four individuals exhibiting differences in the amount of tepal spots and in filament length.—B, C. the ridges at the base of the tepal show different prominence of projections at early (B) and late (C) stages.—D, E. Two flowers showing variation in the amount of spots on tepals.

opennotspecifiedSep 2015View details →

FIGURE 1 in Continuous variation supports accommodating Lilium habaense and L. xanthellum within L. stewartianum (Liliaceae)

FIGURE 1. An illustration of features traditionally used to delimit Lilium habaense, L. stewartianum, and L. xanthellum.

opennotspecifiedSep 2016View details →

FIGURE 3 in Accommodating Nomocharis in Lilium (Liliaceae)

FIGURE 3. Field pictures of Lilium apertum in western Yunnan: a–c, population from Zhongdian, Yunnan showed spot variation; c–e, population of Fugong, Yunnan showed variations in tepal color; f–h, habits of L. apertum under different habitats; i–j, anatomical pictures showed two types of L. apertum from Zhongdian and Fugong, as well as a comparison of outer and inner tepals.

opennotspecifiedSep 2016View details →

FIGURE 1 in Accommodating Nomocharis in Lilium (Liliaceae)

FIGURE 1. Field pictures of western China Lilium (formerlly Nomocharis): a–c, L. basilissum; d–f, L. farreri; g–i, L. gongshanense; j–l, L. meleagrinum.

FIGURE 4 in Two new Pseudohalonectria species on beech cupules (Fagus sylvatica) and a new genus to accommodate P. suthepensis

FIGURE 4. Pseudohalonectria hampshirensis (MFLU 16-1086, holotype) a, b. Appearance of ascomata on host substrate. c, d. Longitudinal section through ascoma. e. Close up of the base of neck f. Close up of the peridium. g. Paraphyses. h, i. Immature and mature asci. j. Ascus in Melzer's reagent. k–n. Ascospores. o. Germinating ascospore. p, q. Cultures on MEA. Bars: b, c = 200 μm, d–f = 100 μm, g–j = 50 μm, k–n = 20 μm.

FIGURE 2 in Two new Pseudohalonectria species on beech cupules (Fagus sylvatica) and a new genus to accommodate P. suthepensis

FIGURE 2. Phylogram generated from maximum likelihood analysis based on combined LSU and SSU sequence data of the genus Pseudohalonectria. Maximum likelihood bootstrap support values greater than 50% and Bayesian posterior probabilities (PP) above 95% are shown near the nodes. The new isolates are in blue and ex-type sequences in bold. The tree is rooted with Ophioceras dolichostomum and Ceratosphaerella castillenses.

FIGURE 3 in Two new Pseudohalonectria species on beech cupules (Fagus sylvatica) and a new genus to accommodate P. suthepensis

FIGURE 3. Pseudohalonectria fagicola (MFLU 16-1085, holotype) a, b. Appearance of ascomata on host substrate. c. Longitudinal section through ascoma. d, e. Close up of the ostiole with periphyses. f. Peridium in surface view. g. Peridium. h. Paraphyses. i–k. Immature and mature asci. l. Ascus in Melzer's reagent. m. Ascospores. n. Germinating ascospore. o, p. Cultures on MEA. Bars: b = 500 μm, c = 200 μm, d, e = 50 μm, f = 20 μm, g = 50 μm, h–k = 20 μm; l = 10 μm, m, n = 20 μm.

FIGURE 1 in Two new Pseudohalonectria species on beech cupules (Fagus sylvatica) and a new genus to accommodate P. suthepensis

FIGURE 1. Phylogram generated from maximum likelihood analysis based on combined LSU, SSU and TEF1 sequence data. Maximum likelihood bootstrap support values greater than 50% and Bayesian posterior probabilities (PP) above 95% are shown near the nodes. The new isolates are in blue and ex-type sequences in bold. The tree is rooted with Ophiostoma piliferum.