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Supplementary material 1 from: Zuo Z-Y, Lu J-M, Li C-F, Li D-Z (2024) Dryopteris jinpingensis, a critically endangered diploid new species of Dryopteridaceae from Yunnan, China. PhytoKeys 239: 195-204. https://doi.org/10.3897/phytokeys.239.118655
The voucher information and GenBank accession numbers of complete plastid genome used in this study
Supplementary material 2 from: Zuo Z-Y, Lu J-M, Li C-F, Li D-Z (2024) Dryopteris jinpingensis, a critically endangered diploid new species of Dryopteridaceae from Yunnan, China. PhytoKeys 239: 195-204. https://doi.org/10.3897/phytokeys.239.118655
The voucher information and GenBank accession numbers of nuclear marker AK1 used in this study
Figure 5 from: Zuo Z-Y, Lu J-M, Li C-F, Li D-Z (2024) Dryopteris jinpingensis, a critically endangered diploid new species of Dryopteridaceae from Yunnan, China. PhytoKeys 239: 195-204. https://doi.org/10.3897/phytokeys.239.118655
Figure 5 Maximum likelihood phylograms of Dryopteris sect. Diclisodon based on nine plastid regions (A) and nuclear gene AK1 (B). ML ultrafast bootstrap support values (UFBS) and the posterior probabilities of Bayesian inference (BIPP) are indicated near nodes (UFBS/BIPP). The stars (*) indicate UFBS=100% or BIPP=1.00, the minus (-) indicate UFBS<50% or BIPP<0.50. The name of the new species is in bold.
Figure 4 from: Zuo Z-Y, Lu J-M, Li C-F, Li D-Z (2024) Dryopteris jinpingensis, a critically endangered diploid new species of Dryopteridaceae from Yunnan, China. PhytoKeys 239: 195-204. https://doi.org/10.3897/phytokeys.239.118655
Figure 4 Spores and prothallus of Dryopteris jinpingensisA 64 spores in one sporangium B cultured prothallus on 1/2 Murashige and Skoog plant cell culture medium (MS) C prothallus.
Figure 3 from: Zuo Z-Y, Lu J-M, Li C-F, Li D-Z (2024) Dryopteris jinpingensis, a critically endangered diploid new species of Dryopteridaceae from Yunnan, China. PhytoKeys 239: 195-204. https://doi.org/10.3897/phytokeys.239.118655
Figure 3 Morphological comparison of Dryopteris jinpingensis (A, C, E) and D. gaoligongensis (B, D, F) A, B rhizome and stipe base C, D lamina E, F pinna stalks of basiscopic pinnules.
Figure 2 from: Zuo Z-Y, Lu J-M, Li C-F, Li D-Z (2024) Dryopteris jinpingensis, a critically endangered diploid new species of Dryopteridaceae from Yunnan, China. PhytoKeys 239: 195-204. https://doi.org/10.3897/phytokeys.239.118655
Figure 2 Illustration of Dryopteris jinpingensis Z.Y. Zuo, Jin Mei Lu & D.Z. Li A plant B sori on ultimate pinnules C glandular hairs on the abaxial surface of pinnules D indusia E young plant F scales of stipe (Drawn by Yi-Fan Li, based on Z.Y. Zuo 5378).
Figure 1 from: Zuo Z-Y, Lu J-M, Li C-F, Li D-Z (2024) Dryopteris jinpingensis, a critically endangered diploid new species of Dryopteridaceae from Yunnan, China. PhytoKeys 239: 195-204. https://doi.org/10.3897/phytokeys.239.118655
Figure 1 Photos of Dryopteris jinpingensis (Z.Y. Zuo 5378) A habitat B plant C proximal part of the lamina D sori on ultimate pinnules E glandular hairs on the abaxial surface of pinnules F young plant G rhizome H portion of stipe base, showing adnate scale I scales of stipe.
Figure 195 from: Bruneau A, Queiroz LP, Ringelberg JJ, Borges LM, Bortoluzzi RLC, Brown GK, Cardoso DBOS, Clark RP, Conceição AS, Cota MMT, Demeulenaere E, Duno de Stefano R, Ebinger JE, Ferm J, Fonseca-Cortés A, Gagnon E, Grether R, Guerra E, Haston E, Herendeen PS, Hernández HM, Hopkins HCF, Huamantupa-Chuquimaco I, Hughes CE, Ickert-Bond SM, Iganci J, Koenen EJM, Lewis GP, Lima HC, Lima AG, Luckow M, Marazzi B, Maslin BR, Morales M, Morim MP, Murphy DJ, O'Donnell SA, Oliveira FG, Oliveira ACS, Rando JG, Ribeiro PG, Ribeiro CL, Santos FS, Seigler DS, Silva GS, Simon MF, Soares MVB, Terra V (2024) Advances in Legume Systematics 14. Classification of Caesalpinioideae. Part 2: Higher-level classification. PhytoKeys 240: 1-552. https://doi.org/10.3897/phytokeys.240.101716
Figure 195 Distribution of Mariosousa based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data.
Figure 1 from: Gueidan C, Li L (2022) A long-read amplicon approach to scaling up the metabarcoding of lichen herbarium specimens. MycoKeys 86: 195-212. https://doi.org/10.3897/mycokeys.86.77431
Figure 1 Examples of lichen herbarium specimens used for this study AParmotrema perlatum, specimen J.A. Elix 43686 (CANB790817) BEndocarpon pusillum, specimen H. Streiman 45100 (CBG9011273) CBuellia albula, specimen J.A. Elix 45138 (CANB810791) DCatillaria sp., specimen J.A Elix 37142 (CANB872684). Scale bar: 1 cm. Photos C. Gueidan.
Figure 2 from: Gueidan C, Li L (2022) A long-read amplicon approach to scaling up the metabarcoding of lichen herbarium specimens. MycoKeys 86: 195-212. https://doi.org/10.3897/mycokeys.86.77431
Figure 2 Sequencing success for different morphological groups of taxa included in this study. Specimens were grouped into three main morphological categories: 1Buellia, Catillaria and other crustose saxicolous taxa 2Endocarpon and other squamulose terricolous taxa 3 the foliose corticolous genus Parmotrema. In the graph, stalked columns show successful samples (sequence generated for the target species) in dark grey and unsuccessful samples (no sequence generated or generated sequences not from the target species) in light grey. The total number of samples (N) is indicated below each corresponding column.
Figure 3 from: Gueidan C, Li L (2022) A long-read amplicon approach to scaling up the metabarcoding of lichen herbarium specimens. MycoKeys 86: 195-212. https://doi.org/10.3897/mycokeys.86.77431
Figure 3 Sequencing success for different ages of specimens included in this study. Specimens were grouped in five categories: 1966–1980, 1981–1990, 1991–2000, 2001–2010, 2011–2020. In the graph, stalked columns show successful samples (sequence generated for the target species) in dark grey and unsuccessful samples (no sequence generated or generated sequences not from the target species) in light grey. The total number of samples (N) is indicated below each corresponding column.
Figs 195–202. Maghreba gen. nov., live specimens. 195. M in Revisions of Holocnemus and Crossopriza: the spotted-leg clade of Smeringopinae (Araneae, Pholcidae)
Figs 195–202. Maghreba gen. nov., live specimens. 195. M. saghro gen. et sp. nov., male from Morocco, between Irherm and Tiferki. 196–198. M. stifadma gen. et sp. nov., male and female from Morocco, Setti-Fatma. 199–202. M. nkob gen. et sp. nov., male and female from Morocco, E of Nkob.
Figure 2 from: Satria D, Sofyanti E, Wulandari P, Fajarini, Pakpahan SD, Limbong SA (2022) Antibacterial activity of Medan Butterfly pea (Clitoria ternatea L.) corolla extract against Streptococcus mutans ATCC®25175™ and Staphylococcus aureus ATCC®6538™. Pharmacia 69(1): 195-202. https://doi.org/10.3897/pharmacia.69.e77076
Figure 2 Minimum inhibitory zones and biofilm activity of BPCE against S. mutans and S. aureus at different concentrations. Each colour represents the millimetre and percentage from different concentrations of BPCE (mg/mL) in each bacteria.
Figure 4 from: Satria D, Sofyanti E, Wulandari P, Fajarini, Pakpahan SD, Limbong SA (2022) Antibacterial activity of Medan Butterfly pea (Clitoria ternatea L.) corolla extract against Streptococcus mutans ATCC®25175™ and Staphylococcus aureus ATCC®6538™. Pharmacia 69(1): 195-202. https://doi.org/10.3897/pharmacia.69.e77076
Figure 4 The effect of BPCE on calcium and potassium ions leakage from S. mutans and S. aureus at different concentrations. Each colour represents the absorbance from different concentrations of BPCE (mg/mL) in each bacteria.
Figure 3 from: Satria D, Sofyanti E, Wulandari P, Fajarini, Pakpahan SD, Limbong SA (2022) Antibacterial activity of Medan Butterfly pea (Clitoria ternatea L.) corolla extract against Streptococcus mutans ATCC®25175™ and Staphylococcus aureus ATCC®6538™. Pharmacia 69(1): 195-202. https://doi.org/10.3897/pharmacia.69.e77076
Figure 3 The effect of BPCE on membrane intracellular (DNA and protein) leakage from S. mutans and S. aureus at different concentrations. Each colour represents the absorbance from different concentrations of BPCE (mg/mL) in each bacteria.
Figure 195 from: Fernandez-Triana J, Shaw MR, Boudreault C, Beaudin M, Broad GR (2020) Annotated and illustrated world checklist of Microgastrinae parasitoid wasps (Hymenoptera, Braconidae). ZooKeys 920: 1-1089. https://doi.org/10.3897/zookeys.920.39128
Figure 195 Promicrogaster fabriciocambroneroi female DHJPAR0012588 A Habitus, lateral B Head, frontal C Fore wing and hind wing D Metasoma, dorsal E Mesosoma, dorsal.
FIGURES 195–200 in Revision of the genus Charippus Thorell, 1895, with descriptions of eight new species (Araneae, Salticidae, Euophryini)
FIGURES 195–200. Living female of Charippus yinae Wang & Li, 2020 (© Weihang Wang).
Supplementary material 1 from: Wei Z (2022) The complete mitochondrial genomes of five Agrilinae (Coleoptera, Buprestidae) species and phylogenetic implications. ZooKeys 1092: 195-212. https://doi.org/10.3897/zookeys.1092.80993
Figures S1–S7
Supplementary material 1 from: Niu Z-Y, Cai Z-Y, Liao C-L, Xia N-H (2022) Chimonobambusa sangzhiensis (Poaceae, Bambusoideae), a new combination supported by morphological and molecular evidence. PhytoKeys 195: 127-141. https://doi.org/10.3897/phytokeys.195.83004
Table S1
Supplementary material 2 from: Niu Z-Y, Cai Z-Y, Liao C-L, Xia N-H (2022) Chimonobambusa sangzhiensis (Poaceae, Bambusoideae), a new combination supported by morphological and molecular evidence. PhytoKeys 195: 127-141. https://doi.org/10.3897/phytokeys.195.83004
Chimonobambusa sangzhiensis nrDNA
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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