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156 results for “Camellia”

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zenodo28/100

Figure 2 from: Nguyễn D-H, Lương V-D, Lê T-H, Trần Q-T, Đỗ N-Đ, Lý N-S (2020) Camellia puhoatensis (Sect. Archecamellia – Theaceae), a new species from Vietnam. PhytoKeys 153: 1-11. https://doi.org/10.3897/phytokeys.153.49388

Figure 2 Camellia puhoatensis. A young shoot B terminal buds C solitary bud and axillary flower (side view) D flower and pollinated flower (side view) E close-up of flower (front view) F immature fruit G a part of branch showing leaves abaxial and opening flower H leaves adaxially I bracteoles J sepals K petals L androecium with stamens M gynoecium (with sepals and styles). Photos by Ngoc-Dai Do, the colour plate prepared by Ngoc-Sam Ly.

opencc-by-4.0Jul 2020View details →
zenodo28/100

Figure 1 from: Nguyễn D-H, Lương V-D, Lê T-H, Trần Q-T, Đỗ N-Đ, Lý N-S (2020) Camellia puhoatensis (Sect. Archecamellia – Theaceae), a new species from Vietnam. PhytoKeys 153: 1-11. https://doi.org/10.3897/phytokeys.153.49388

Figure 1 Camellia puhoatensis. A Leaf, adaxial view B venation detail of leaf (abaxial surface) C flower (lateral view) D flower (top view) E bracteoles (inner surfaces shown) F sepals (adaxial surfaces) G petals (adaxial surfaces) H androecium (one part) I stamen J gynoecium (with sepals and petals). Drawn from the holotype by Van-Dung Luong.

opencc-by-4.0Jul 2020View details →
dryad28/100

Data from: Worldwide core collections of tea (Camellia sinensis) based on SSR markers

Tea (Camellia sinensis (L.) O. Kuntze) is the world's most popular beverage crop. However, to date, no core collection has been selected from worldwide germplasm resources on the basis of genotype data. In this study, we analyzed 788 tea germplasm accessions using 23 simple sequence repeat (SSR) markers. Our population structure analysis divided the germplasms into a Japanese group and an exotic group. The latter could be divided into var. sinensis and var. assamica. The genetic diversity was higher in germplasms from China, Taiwan, India, and Sri Lanka than in those from other countries, and low in germplasms from Japan. Using the number of SSR alleles as a measure of genetic diversity, we developed a core collection consisting of 192 accessions and three subcore collections with 96, 48, and 24 accessions. Although the results might be affected by marker-selection bias, the core 192 collection adequately covered the range of variation of the 788 accessions in floral morphology, and the chemical composition of first-flush leaves. These collections will be powerful tools for breeding and genetic research in tea.

opencc-zeroDec 2013View details →
zenodo28/100

Figure 5 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 5 Diaporthe sojae (HNZZ022) A Culture on PNAB ascomata C–E asci and ascospores. Scale bars: 500 μm (B); 10 μm (C–E).

opencc-by-4.0Oct 2021View details →
zenodo28/100

Figure 4 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 4 Diaporthe hunanensis (HNZZ023) A Culture on PDAB conidiomata C conidiogenous cells D alpha conidia. Scale bars: 500 μm (B); 10 μm (C–D).

opencc-by-4.0Oct 2021View details →
zenodo28/100

Figure 3 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 3 Diaporthe hubeiensis (HNZZ019) A Culture on PDAB conidiomata C conidiogenous cells D alpha conidia. Scale bars: 500 μm (B); 10 μm (C–D).

opencc-by-4.0Oct 2021View details →
zenodo28/100

Figure 2 from: Yang Q, Tang J, Zhou GY (2021) Characterization of Diaporthe species on Camellia oleifera in Hunan Province, with descriptions of two new species. MycoKeys 84: 15-33. https://doi.org/10.3897/mycokeys.84.71701

Figure 2 Diaporthe camelliae-oleiferae (HNZZ027) A Culture on PDAB conidiomata C conidiogenous cells D–F alpha and beta conidia. Scale bars: 200 μm (B); 10 μm (C–D); 20 μm (E, F).

opencc-by-4.0Oct 2021View details →
zenodo28/100

Figure 3 from: Lin M, Ye Q-L, Zhang Z-J, Liao W-B, Fan Q (2024) Camellia zijinica (Theaceae), a new species endemic to Danxia landscape from Guangdong Province, China. PhytoKeys 237: 245-255. https://doi.org/10.3897/phytokeys.237.114768

Figure 3 Camellia zijinica sp. nov. A habit B, C flowering branch D leaf shape E flower in front view F flower in back view G pistil and ovary H flowering branch, showing the stamens I flowering branch, showing the bracteoles and sepals J fruits, showing young to ripe (a-c) K bracteoles, sepals and petals. Photographed by Zhi-Ming Zhong, Qiang Fan and Min Lin.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 2 from: Lin M, Ye Q-L, Zhang Z-J, Liao W-B, Fan Q (2024) Camellia zijinica (Theaceae), a new species endemic to Danxia landscape from Guangdong Province, China. PhytoKeys 237: 245-255. https://doi.org/10.3897/phytokeys.237.114768

Figure 2 Camellia zijinica sp. nov. A flowering and fruiting branch B flower in front view C fully ripe fruit, tending to split D young fruit in longitudinal section E seeds in obverse and reverse sides F bracteoles and sepals G petals H stamens (incomplete) I ovary in transverse section J pistil in longitudinal section. Illustrated by Yun-Xiao Liu.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 1 from: Lin M, Ye Q-L, Zhang Z-J, Liao W-B, Fan Q (2024) Camellia zijinica (Theaceae), a new species endemic to Danxia landscape from Guangdong Province, China. PhytoKeys 237: 245-255. https://doi.org/10.3897/phytokeys.237.114768

Figure 1 Maximum likelihood phylogenetic tree of C. zijinica and other 46 related species based on chloroplast genomes. Above the nodes of the tree, maximum likelihood ultrafast bootstrap support values were shown. The new species and C. microphylla were highlighted in bold. The red circles marked on the tree nodes indicated differences between the maximum likelihood and Bayesian inference. "CAI" and "CAII" refer to the two clades within CladeA.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure A1 from: Lin M, Ye Q-L, Zhang Z-J, Liao W-B, Fan Q (2024) Camellia zijinica (Theaceae), a new species endemic to Danxia landscape from Guangdong Province, China. PhytoKeys 237: 245-255. https://doi.org/10.3897/phytokeys.237.114768

Figure A1 Bayesian inference phylogenetic tree of C. zijinica and other 46 related species based on chloroplast genomes. Above the nodes of the tree, Bayesian posterior probabilities support values were shown. The new species and C. microphylla were highlighted in bold. The red circles marked on the tree nodes indicate differences between the maximum likelihood and Bayesian inference. "CAI" and "CAII" refer to the two clades within CladeA.

opencc-by-4.0Jan 2024View details →
zenodo28/100

Figure 3 from: Liu HY, Luo D, Huang HL, Yang Q (2024) Two new species of Diaporthe (Diaporthaceae, Diaporthales) associated with Camellia oleifera leaf spot disease in Hainan Province, China. MycoKeys 102: 225-243. https://doi.org/10.3897/mycokeys.102.113412

Figure 3 Diaporthe pseudofoliicola (HNCM045) A culture on PDAB, C conidiomata D conidiogenous cells E alpha and beta conidia. Scale bars: 200 μm (B, C), 10 μm (D), 20 μm (E).

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 2 from: Liu HY, Luo D, Huang HL, Yang Q (2024) Two new species of Diaporthe (Diaporthaceae, Diaporthales) associated with Camellia oleifera leaf spot disease in Hainan Province, China. MycoKeys 102: 225-243. https://doi.org/10.3897/mycokeys.102.113412

Figure 2 Diaporthe hainanensis (HNCM049) A culture on PNAB, C conidiomata D conidiogenous cells E alpha conidia F beta conidia. Scale bars: 500 μm (B, C); 10 μm (C, F), 20 μm (E).

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 1 from: Liu HY, Luo D, Huang HL, Yang Q (2024) Two new species of Diaporthe (Diaporthaceae, Diaporthales) associated with Camellia oleifera leaf spot disease in Hainan Province, China. MycoKeys 102: 225-243. https://doi.org/10.3897/mycokeys.102.113412

Figure 1 Phylogram of Diaporthe resulting from a Maximum Likelihood analysis, based on combined ITS, cal, his3, tef1 and tub2. Numbers above the branches indicate ML bootstraps (left, ML BS ≥ 50%) and Bayesian Posterior Probabilities (right, BPP ≥ 0.9). The tree is rooted with Diaporthella corylina. Isolates in the current study are in blue. "-" indicates ML BS < 50% or BI PP < 0.9.

opencc-by-4.0Feb 2024View details →
zenodo28/100

Figure 1 from: Zhao D (2024) Taxonomic revision of Camellia (Theaceae) in Thailand. PhytoKeys 239: 29-57. https://doi.org/10.3897/phytokeys.239.113878

Figure 1 Camellia caudataA canopy of a tree B branch C flower D petals and androecia E a dissected flower F gynoecium and pedicel. Scale bars: 5 cm (B); 1 cm (C, E); 5 mm (F). The minimum graduation of the ruler in D indicates 1 mm.

opencc-by-4.0Mar 2024View details →
zenodo28/100

Figure 3 from: Zhao D (2024) Taxonomic revision of Camellia (Theaceae) in Thailand. PhytoKeys 239: 29-57. https://doi.org/10.3897/phytokeys.239.113878

Figure 3 Camellia connataA habit B branchlets C a branch with an immature fruit D, E flowers F a dissected flower without corolla G a fruit and seeds. Scale bars: 5 cm (B); 2 cm (C); 5 mm (D, F); 1 cm (E). The minimum graduation of the ruler in G indicates 1 mm.

opencc-by-4.0Mar 2024View details →
zenodo28/100

Figure 6 from: Zhao D (2024) Taxonomic revision of Camellia (Theaceae) in Thailand. PhytoKeys 239: 29-57. https://doi.org/10.3897/phytokeys.239.113878

Figure 6 Camellia kissi var. confusaA habitat B branchlets with flowers, flower buds and caducous fruits C, D branchlet with flower E a pedicel and gynoecium. Scale bars: 2 cm (D); 1 cm (E). The minimum graduation of the rulers in B, C represents 1 mm.

opencc-by-4.0Mar 2024View details →
zenodo28/100

Figure 7 from: Zhao D (2024) Taxonomic revision of Camellia (Theaceae) in Thailand. PhytoKeys 239: 29-57. https://doi.org/10.3897/phytokeys.239.113878

Figure 7 Dry specimens of Camellia laotica, Wongprasert s.n. at BKF A specimen sheet B branchlet with flower buds C a flower bud D a flower E, F flower fragments showing sepals and gynoecia. Scale bars: 5 mm (C, D); 3 mm (E, F). The minimum graduation of the rulers in A, B represents 1 mm.

opencc-by-4.0Mar 2024View details →
zenodo28/100

Figure 2 from: Zhao D (2024) Taxonomic revision of Camellia (Theaceae) in Thailand. PhytoKeys 239: 29-57. https://doi.org/10.3897/phytokeys.239.113878

Figure 2 Distribution of Camellia taxa in Thailand: C. caudata (Pink square), C. connata (Purple star), C. furfuracea (Pink plus), C. kissi (Blue dot), C. kissi var. confusa (Brown diamond), C. laotica (Red star), C. sinensis var. assamica (Green triangle), C. suddeeana (Red dot) and C. taliensis (Blue plus).

opencc-by-4.0Mar 2024View details →
zenodo28/100

Figure 5 from: Zhao D (2024) Taxonomic revision of Camellia (Theaceae) in Thailand. PhytoKeys 239: 29-57. https://doi.org/10.3897/phytokeys.239.113878

Figure 5 Camellia kissiA habitat B, C branches with flowers D a dissected flower E a mature fruit with a single seed. Scale bars: 5 cm (B); 1 cm (D, E). The minimum graduation of the ruler in C represents 1 mm.

opencc-by-4.0Mar 2024View details →

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