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39 results for “Capparis”
Herbarium specimen image of Capparis sclerophylla Iltis & Cornejo, part of the collection of Botanic Garden and Botanical Museum Berlin
Part of a training dataset of scanned herbarium specimens. The data paper and a summary landing page will be published on Zenodo as it gets published.<br><br>Content of this deposition:<br><br>- A JSON-LD datafile listing the label data associated with this herbarium specimen. The Darwin and Dublin Core data standards are used for most values.<br>- A JPEG image file of the scanned herbarium sheet.<br>- A lossless TIFF image from which the JPEG image has been derived.
FIG. 2 in Studies on the genus Capparis L. (Capparaceae) in Lao PDR. V: A new species from limestones of the Luang Prabang Province
FIG. 2. — Capparis lianosa Fici & Souvannakhoummane, sp. nov.: A, vegetative branch; B, leaf base with stipular thorn; C, flower; D, dissected flower showing sepals, petals, gynophore and ovary. (All from the holotype). Drawn by S. Fici. Scale bars: A, 1 cm; B, 4 mm; C, D, 3 mm.
Data from: Mechanism of cryptovivipary in wild caper bush (Capparis sepiaria L.) Capparaceae
<p>Cryptovivipary is the process in which seeds germinate inside the fruit but the seedling or plumule comes out when the fruit detaches from the mother plant. This dataset highlights the details of the mechanism of cryptovivipary in wild caper bush. In addition, an updated classification of viviparous plants is provided to better describe and understand this trait.</p>
Data from: Mechanism of cryptovivipary in wild caper bush (Capparis sepiaria L.) Capparaceae
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FIGURE 5 in A taxonomic revision of the Capparis spinosa group (Capparaceae) from eastern Africa to Oceania
FIGURE 5. Holotype of Capparis himalayensis (E) (reproduced with permission from the Royal Botanic Garden Edinburgh).
FIGURE 2. Capparis spinosa subsp. cordifolia. A. Flower. B. Ripe fruit. C in A taxonomic revision of the Capparis spinosa group (Capparaceae) from eastern Africa to Oceania
FIGURE 2. Capparis spinosa subsp. cordifolia. A. Flower. B. Ripe fruit. C. Plant in natural habitat (Hawaii). (Photos A, C by G. Carr, B by M. LeGrande).
FIGURE 1. Capparis spinosa subsp. cartilaginea. A. Flower. B. Opening flower showing the deeply saccate posterior sepal. C in A taxonomic revision of the Capparis spinosa group (Capparaceae) from eastern Africa to Oceania
FIGURE 1. Capparis spinosa subsp. cartilaginea. A. Flower. B. Opening flower showing the deeply saccate posterior sepal. C. Plant in natural habitat (Sinai). (Photo A by S. Cambria, B by F. M. Raimondo).
FIGURE 4. Capparis spinosa subsp. nummularia. A. Fertile branch. B. Fruit. C in A taxonomic revision of the Capparis spinosa group (Capparaceae) from eastern Africa to Oceania
FIGURE 4. Capparis spinosa subsp. nummularia. A. Fertile branch. B. Fruit. C. Plant in natural habitat (Northern Territory).
FIGURE 1. Capparis parvifolia. A. Flowering branch. B. Flower. C. Ovary. D in A new species of Capparis (Capparaceae) from ultramafic substrata in New Caledonia
FIGURE 1. Capparis parvifolia. A. Flowering branch. B. Flower. C. Ovary. D. Fruit (A, B, C from MacKee 16170; D from MacKee 33063). Drawn by Silvio Fici.
FIGURE 7 in Plastome data provide insights into intra and interspecific diversity and ndh gene loss in Capparis (Capparaceae)
FIGURE 7. MultiPip analysis showing overall sequence similarity of plastid genomes based on complete plastome alignment using Capparis spinosa var. spinosa as a reference sequence. Levels of sequence similarity are indicated by red (75±100%), green (50±75%), and white (<50%). Arrows indicate gene losses.
FIGURE 6 in Plastome data provide insights into intra and interspecific diversity and ndh gene loss in Capparis (Capparaceae)
FIGURE 6. Nucleotide diversity and hotspot regions in genus Capparis. The X-axis represents the nucleotide position and Y-axis represents nucleotide diversity (Pi). 6a. Interspecific variation among four taxa of Capparis. 6b. Intraspecific variation among two varieties of Capparis spinosa viz. var. spinosa and var. herbacea.
FIGURE 2 in Plastome data provide insights into intra and interspecific diversity and ndh gene loss in Capparis (Capparaceae)
FIGURE 2. Plastome maps of Capparis spinosa var. spinosa and Capparis spinosa var. herbacea. Genes shown outside the circles are transcribed clockwise and those inside are transcribed anticlockwise. Genes belonging to different functional groups are in various colours. The dashed area in inner circles indicates the GC content of plastome. ORF – Open reading frame. Asterisks indicate genes containing introns.
FIGURE 5 in Plastome data provide insights into intra and interspecific diversity and ndh gene loss in Capparis (Capparaceae)
FIGURE 5. Comparison of SSRs in four Capparis taxa viz. C. spinosa var. herbacea, var. spinosa, C. versicolor and C. urophylla. 5a. Types of SSRs; 5b. Size of SSRs; 5c. Number of SSR repeats in LSC, SSC and IRs. Numbers above each bar represents the number of repeats.
FIGURE 4 in Plastome data provide insights into intra and interspecific diversity and ndh gene loss in Capparis (Capparaceae)
FIGURE 4. Codon usage of four taxa of Capparis viz. Capparis spinosa var. spinosa, var. herbacea, C. versicolor and C. urophylla. Xaxis: Amino acid, Y- axis: codon usage in percentage. * indicates stop codon.
FIGURE 1 in Plastome data provide insights into intra and interspecific diversity and ndh gene loss in Capparis (Capparaceae)
FIGURE 1. Map depicting distribution and altitudinal ranges of seven varieties of Capparis spinosa. (as per Jacobs 1965, Fici 2014, and POWO 2019).
FIGURE 3 in Plastome data provide insights into intra and interspecific diversity and ndh gene loss in Capparis (Capparaceae)
FIGURE 3. Comparison of LSC, SSC and IR borders of Capparaceae with members of Cleomaceae (Tarenaya hassleriana) and Brassicaceae (Aethionema arabicum). Numbers in boxes indicate total length of the particular region; numbers below the arrows show base pair shift or overlapping regions. Gene and IR lengths are not to scale.
Combined sequence matrix for: Molecular phylogenetic tools reveal the phytogeographic history of the genus Capparis L. and suggest its reclassification
<p><em><span>Capparis</span></em><span> L. is the largest genus of the family Capparaceae, represented by 142 species in the tropics and subtropics of the Old World. Despite being one of the medicinally and economically important genera with its unique distribution pattern, the evolutionary history of <em>Capparis</em> remained unexplored. Moreover, the phylogenetic relationships, origin, dispersal, and character evolution of the genus were poorly understood. With the objectives to (i) test the congruence between the molecular and morphological datasets, (ii) validate Jacobs' hypothesis on the origin, dispersal, and speciation pattern of <em>Capparis</em> using new fossil data, and (iii) understand the possible evolutionary role of some key morphological characters, we sampled across the five speciation centres of <em>Capparis</em>. The results derived from three plastidial markers (<em>matK</em>, <em>trnL</em>-<em>F</em> and <em>rbcL</em>) revealed incongruence with the morphological datasets and suggested a new sectional classification in <em>Capparis</em>. Divergence dating analysis revealed that Capparaceae originated in Africa at 47.25 MYA and <em>Capparis</em> in Peninsular India at about 29.32 MYA. <em>Capparis</em> followed multiple forward and backward dispersal, supporting the "into and out of India" hypothesis. These dispersal events were consistent with the various land bridges present during the Eocene to Miocene in different parts of the old world. The only long-distance dispersal event was observed in the case of the new world Capparaceae, corroborating the earlier findings. Our results suggest West Asia to the North African region as another centre of speciation for <em>Capparis</em> and present a robust age estimate for the genus. The character state reconstruction of <em>Capparis</em> revealed a unique evolutionary adaptation due to exposure to various climatic conditions and the acquisition of suitable pollination strategies. We hypothesize that the gynophore length, calyx shape, and blotches on petals contribute substantially to the pollination success. </span></p>
Combined sequence matrix for: Molecular phylogenetic tools reveal the phytogeographic history of the genus Capparis L. and suggest its reclassification
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FIG. 3 in Studies on the genus Capparis L. (Capparaceae) in Lao PDR. V: A new species from limestones of the Luang Prabang Province
FIG. 3. — Capparis lianosa Fici & Souvannakhoummane, sp. nov.: A, habitat; B, view of the vegetation in the type locality; C, base of stem bearing knobs with thorns; D, vegetative branch; E, base of young leaf with stipular thorn; F, leaf; G, flower. Photos by S. Fici.
Fig. 3 in Capparis macrantha sp. nov. (Capparaceae, Brassicales), a new shrub species from a deciduous forest of the Nam Kading National Protected Area (central Lao PDR)
Fig. 3. Known distribution of Capparis macrantha Souvannakhoummane, Fici & Lanorsavanh sp. nov. (red circle).
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