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51 results for “Inflata”
Lobelia inflata (Campanulaceae) - inflorescence - unspecified
Image of Lobelia inflata (Campanulaceae) - inflorescence - unspecified
Lobelia inflata (Campanulaceae) - whole plant - in flower - general view
Image of Lobelia inflata (Campanulaceae) - whole plant - in flower - general view
Lobelia inflata (Campanulaceae) - leaf - basal or on lower stem
Image of Lobelia inflata (Campanulaceae) - leaf - basal or on lower stem
Lobelia inflata (Campanulaceae) - inflorescence - lateral view of flower
Image of Lobelia inflata (Campanulaceae) - inflorescence - lateral view of flower
Lobelia inflata (Campanulaceae) - inflorescence - whole - unspecified
Image of Lobelia inflata (Campanulaceae) - inflorescence - whole - unspecified
Lobelia inflata (Campanulaceae) - leaf - on upper stem
Image of Lobelia inflata (Campanulaceae) - leaf - on upper stem
FIGURE 3. Ascocoryne inflata. A, B. Apothecia. C in Ascomycetes from the relic forest of Oreomunnea mexicana, Oaxaca, Mexico
FIGURE 3. Ascocoryne inflata. A, B. Apothecia. C. Globose cells of ectal excipulum. D. Paraphysis. E. Ascospores.
FIGURE 111. Daviesia inflata. A. Flowering branchlet. B. Inflorescence. C. Pod, lateral view. D. Pod viewed from distal end. A from Ashby 2375 in A monograph of Daviesia (Mirbelieae, Faboideae, Fabaceae)
FIGURE 111. Daviesia inflata. A. Flowering branchlet. B. Inflorescence. C. Pod, lateral view. D. Pod viewed from distal end. A from Ashby 2375; B from Crisp 6092; C, D from Crisp 5354. Drawn by B-J. Osborne.
Data from: Microsatellite evidence for obligate autogamy, but abundant genetic variation in the herbaceous monocarp Lobelia inflata (Campanulaceae)
Although high levels of self-fertilization (>85%) are not uncommon in nature, organisms reproducing entirely through selfing are extremely rare. Predominant selfers are expected to have low genetic diversity because genetic variation is distributed among rather than within lineages, and is readily lost through genetic drift. We examined genetic diversity at 22 microsatellite loci in 105 individuals from a population of the semelparous herb Lobelia inflata L., and found (1) no evidence of heterozygosity through outcrossing, yet (2) high rates of genetic polymorphism (2-4 alleles per locus). Furthermore, this genetic variation among lineages was associated with phenotypic traits (e.g. flower colour, size at first flower). Coupled with previous work characterizing the fitness consequences of reproductive timing, our results suggest that temporal genotype-by-environment interaction may maintain genetic variation and, because genetic variation occurs only among lineages, this simple system offers a unique opportunity for future tests of this mechanism.
FIGURE 3. Peniophora inflata—a in Type study of Peniophora inflata (Agaricomycetes), and the introduction of the term "subicystidium"
FIGURE 3. Peniophora inflata—a) basidiospores, b) 3 basidioles and two basidia, c) generative subhymenial hyphae forming basidioles (on the right immature hymenial cells with projecting lamprocystidium) d) hymenial and subhymenial lamprocystidia, e) subicystidia; line-drawing from the type of Peniophora inflata (in KOH)—coll. Murrill 4 (FH); for a scale bar = 5 µm, for b-e scale bar = 10 µm.
FIGURE 2 in Type study of Peniophora inflata (Agaricomycetes), and the introduction of the term "subicystidium"
FIGURE 2. Peniophora inflata section through basidioma; line-drawing from the holotype (in KOH)—coll. Murrill 4 (FH), scale bar = 10 µm.
FIGURE 1 in Type study of Peniophora inflata (Agaricomycetes), and the introduction of the term "subicystidium"
FIGURE 1. The type of Peniophora inflata—a) the best preserved fragments of basidioma with substrate, scale bar = 1 cm, b) original herbarium envelope annotated by Burt, c) content of herbarium envelope in plastic bag with best retained fragments, d) description of species from envelope made by Burt's hand, e) Burt's slide, f) Liberta's slide.
FIGURES 1248–1256. 1248, 1252. Mallinella okinawaensis. 1249. M. sadamotoi, holotype. 1250, 1253. M. fulvipes, type. 1251. M. inflata, type. 1254–1255. M. hoosi, type. 1156. M in Systematics and biogeography of the spider genus Mallinella Strand, 1906, with descriptions of new species and new genera from Southeast Asia (Araneae, Zodariidae) 3369
FIGURES 1248–1256. 1248, 1252. Mallinella okinawaensis. 1249. M. sadamotoi, holotype. 1250, 1253. M. fulvipes, type. 1251. M. inflata, type. 1254–1255. M. hoosi, type. 1156. M. langping, type. Illustrations courtesy of Dr. H. Ono.
Figure 1 in Multilocus phylogeny and historical biogeography of the Crematogaster inflata-group (Hymenoptera: Formicidae) in South-East Asia
Figure 1. The Crematogaster inflata-group examined in this study and their natural distributions (modified from Hosoishi & Ogata, 2009). Inset, specimen photographs in profile view. Scale bar represents 0.5 mm.
Figure 4. A in Multilocus phylogeny and historical biogeography of the Crematogaster inflata-group (Hymenoptera: Formicidae) in South-East Asia
Figure 4. A, historical biogeography of the Crematogaster inflata-group based on BEAST2 and BioGeoBEARS analyses using the dispersal multiplier [Scheme (ii)] and two time slices. Blue horizontal bars depict the 95% highest posterior probability (HPD). Node labels N1–N11 correspond with denotations in Table 2. Biogeographical analysis employed a DEC model, with eight regions. The left-bottom map represents the Indo-Australian Archipelago delimited into eight areas. Colours of squares correspond to the coloured area on the map. Coloured squares indicate the most likely ancestral area recovered at each node. The present distribution of each species is given by coloured squares. B–D, palaeogeographic maps were redrawn and modified from Hall (2013): B, 15 Mya. C, 10 Mya. D, 5 Mya.
Figure 7 in Multilocus phylogeny and historical biogeography of the Crematogaster inflata-group (Hymenoptera: Formicidae) in South-East Asia
Figure 7. Characters of the Crematogaster inflata-group. A, mesosoma in profile view (C. difformis). B, mesosoma in profile view (C. mucronata). C, mesosoma in profile view (C. Ʋacca). D, arrow indicates comma-shaped metapleural gland opening in dorsolateral view (C. subcircularis).
Figure 6 in Multilocus phylogeny and historical biogeography of the Crematogaster inflata-group (Hymenoptera: Formicidae) in South-East Asia
Figure 6. Characters of the Crematogaser inflata-group. A, four-segmented antennal club (ii) (C. seaeardi). B, threesegmented antennal club (ii) (C. mucronata). C, swollen propodeum (iii) and circular-shaped metapleural gland opening (iv) (C. inflata). D, posterolateral denticles on the mesonotum (iii) and slit-shaped metapleural gland opening (iv) (C. modiglianii). E, oval petiole (v) and globular postpetiole (vi) in dorsal view (C. modiglianii). F, elliptical petiole (v) and globular postpetiole (vi) in dorsal view (C. seaeardi). G, subquadrate petiole (v) and globular postpetiole (vi) in dorsal view (C. mucronata).
Data from: The continuum between semelparity and iteroparity: plastic expression of parity in response to season length manipulation in Lobelia inflata.
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Data from: Microsatellite evidence for obligate autogamy, but abundant genetic variation in the herbaceous monocarp Lobelia inflata (Campanulaceae)
Open the record for dataset details and reuse information.
Рис. 4. Синтипы Arca inflata Reeve, 1844 (A, B и C, D – наруЖный и внутренний виды двух раЗных створок), МуЗей естественной истории, Лондон, рег. номер 1969167. in On the fauna of bivalve mollusks of Hong Kong (South China Sea)
Рис. 4. Синтипы Arca inflata Reeve, 1844 (A, B и C, D – наруЖный и внутренний виды двух раЗных створок), МуЗей естественной истории, Лондон, рег. номер 1969167.
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