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zenodo28/100

Figure 106 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 106 Fruits and seeds in the Adenanthera clade AAdenanthera pavonina L. dehisced fruits with exposed persistent red seeds BAmblygonocarpus andongensis (Welw. ex Oliv.) Exell & Torre Indehiscent four-angled fruits (Catarino 2067) CPseudoprosopis fischeri Harms young fruit (Bingham 8055) DXylia xylocarpa var. kerrii (Craib & Hutch.) I.C.Nielsen young dolabriform pod ETetrapleura tetraptera (Schumach. & Thonn.) Taub. immature winged, indehiscent pod (Harris 9659) FPentaclethra macrophylla Benth. pod and recalcitrant seeds G, HCalpocalyx ngouniensis Pellegr. woody valves from dehisced pod (Texier 695). Photo credits A Shelbyfarmer B L Catarino C MG Bingham D B Peroth E DJ Harris 9659 F CJ Porto, Fundación Tierra Ibérica G H N Texier.

opencc-by-4.0Apr 2024View details →
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Figure 99 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 99 Habit, bark and foliage of ErythrophleeaeAErythrophleum fordii Oliv. at Hùng Temple, Vietnam B bark of Erythrophleum couminga Baill. in Madagascar CPachyelasma tessmannii (Harms) Harms in Congolian rainforest D, E, HErythrophleum chlorostachys Baill. D rugous bark E tree in northern Australian savannas H foliage FErythrophleum lasianthum Corbishley foliage GErythrophleum suaveolens (Guill. & Perr.) Brenan foliage and terminal inflorescences, Ntumbachusi falls, Zambia. Photo credits A Hungda (https://tropical.theferns.info/image.php?id=Erythrophleum+fordii) B Solofo Eric Rakotoarisoa, iNaturalist (https://www.inaturalist.org/photos/42581094) C Bart Wursten (https://www.flickr.com/photos/zimbart/8212743587/in/photolist-dvJsxn-dvJnwi) D, E, H G Mahajan (https://alchetron.com/Erythrophleum-chlorostachys) F JMK (https://wikiwand.com/en/Erythrophleum_lasianthum) G MG Bingham (https://malawiflora.com/speciesdata/image-display.php?species_id=126540&image_id=8).

opencc-by-4.0Apr 2024View details →
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Figure 1 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 1 ACaesalpinioideae genus richness across floristic realms (according to Liu et al. 2023). The numbers within the circles represent the total number of genera in each realm. The numbers on the lines represent the number of genera shared between two realms (> 10 genera) B Number of Casalpinioideae genera in the floristic subrealms (sensu Liu et al. 2023). The numbers associated with the two polygons indicate the number of genera restricted to the two major blocks of tropical and subtropical areas in the New World and the Old World (maps modified from Liu et al. 2023, CC BY 4.0).

opencc-by-4.0Apr 2024View details →
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Figure 95 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 95 Flower, fruit and vegetative characters of tribe CampsiandreaeA foliage and fruits, Campsiandra comosa Benth., Brazil B compound inflorescence, Campsiandra angustifolia Spruce ex Benth., Peru C fruit and seed, Campsiandra laurifolia Benth., cultivated Rio de Janeiro Botanic Gardens, Brazil D inflorescence and foliage, Campsiandra sp., Amazonas, Brazil E–IDinizia jueirana facao G.P. Lewis & G.S. Siqueira, Reserva Natural Vale, Espírito Santo, Brazil E foliage and fruits F trunk and crown of mature tree G inflorescences H mature fruits (hand for scale) I rough bark of trunk. Photo credits A D Cardoso B T Pennington D M Falção E, G, I D Folli C, F, H GP Lewis.

opencc-by-4.0Apr 2024View details →
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Figure 104 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 104 Habit and growth form in the Adenanthera clade AXylia xylocarpa var. kerrii (Craib & Hutch.) I.C. Nielsen scaly bark BXylia torreana Brenan canopy CPentaclethra macroloba (Willd.) Kuntze trunk showing buttresses DTetrapleura tetraptera (Schumach. & Thonn.) Taub. canopy (Harris 9659) EAmblygonocarpus andongensis (Welw. ex Oliv.) Exell & Torre pale grey, scaly bark (Catarino 2067) FPseudoprosopis gilletii (De Wild.) Villiers liana with leaves and lignified tendrils (Texier 1558) GAdenanthera pavonina L. thin scaly bark H habit IAmblygonocarpus andongensis (Welw. ex Oliv.) Exell & Torre growing in savanna (Coates Palgrave M806). Photo credits A Dechaphaetkrathok B F du Randt C D DeMelo D DJ Harris E L Catarino F N Texier G, H Shelbyfarmer I M Coates Palgrave.

opencc-by-4.0Apr 2024View details →
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Figure 101 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 101 Tribe Erythrophleeae inflorescences, fruits and seeds A–D Spicate racemes of species of Erythrophleum with small flowers, erect sepals and petals and hairy stamen filaments AE. suaveolens (Guill. & Perr.) Brenan with a visiting fly BE. chlorostachys (F. Muell.) Baill. (Ironwood) C, DE. lasianthum Corbishley E–I Fruits and seeds E dehisced fruits of Erythrophleum suaveolensF, G ripe fruits of Erythrophleum lasianthumH, I dispersed fruits of Pachyelasma tessmannii (Harms) Harms on the forest floor, showing the flat valves and raised margins. Photo credits: A AlkalIn (https://commons.wikimedia.org/wiki/File:Flowers_of_Erythrophleum_suaveolens.jpg) B T Harley (https://territorynativeplants.com.au/erythrophleum-chlorostachys-ironwood) C, D SAplants E Oliver Haumann, iNaturalist (https://www.inaturalist.org/photos/60428121) F, G JMK (https://commons.wikimedia.org/wiki/File:Erythrophleum_lasianthum,_loof_en_peule,_Manie_van_der_Schijff_BT,_a.jpg) H B Wursten (https://flickr.com/photos/zimbart/8212726705) I T Stévart (https://tropicos.org/ImageDownload.aspx?imageid=100336252).

opencc-by-4.0Apr 2024View details →
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Figure 93 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 93 Distribution of Burkea based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data.

opencc-by-4.0Apr 2024View details →
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Figure 94 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 94 Generic membership and phylogenetic position of tribe Campsiandreae. For description of phylogeny and support values, see Fig. 6 caption (page 63).

opencc-by-4.0Apr 2024View details →
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Figure 103 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 103 Generic relationships in the Adenanthera clade (tribe Mimoseae). For description of phylogeny and support values, see Fig. 6 caption (page 63).

opencc-by-4.0Apr 2024View details →
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Figure 100 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 100 Distribution of Erythrophleum based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data.

opencc-by-4.0Apr 2024View details →
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Figure 97 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 97 Distribution of Dinizia based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data.

opencc-by-4.0Apr 2024View details →
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Figure 96 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 96 Distribution of Campsiandra based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data.

opencc-by-4.0Apr 2024View details →
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Figure 98 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 98 Generic membership and phylogenetic position of tribe Erythrophleeae. For description of phylogeny and support values, see Fig. 6 caption (page 63).

opencc-by-4.0Apr 2024View details →
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Figure 102 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 102 Distribution of Pachyelasma based on quality-controlled digitised herbarium records. See Suppl. material 1 for the source of occurrence data.

opencc-by-4.0Apr 2024View details →
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FIGURE 7 in First comprehensive study on distribution frequency and incidence of seed-borne pathogens from cereal and legume crops in Sri Lanka

FIGURE 7. Uprooted seedlings of a Arachis hypogea b Vigna radiata and c Vigna sinensis.

opennotspecifiedJan 2022View details →
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Supplementary material 1 from: Warrington S, Ellis AG, Keet J-H, Le Roux JJ (2022) How does familiarity in rhizobial interactions impact the performance of invasive and native legumes? NeoBiota 72: 129-156. https://doi.org/10.3897/neobiota.72.79620

Supplementary materials

opencc-zeroMar 2022View details →
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Legume-Rhizobium symbiosis phenotypes

<p>We coded 771 articles published between January 1, 2009 and September 30, 2020 based on presence of relevant legume or rhizobium phenotypes. We were broadly interested in articles that quantified rhizobia and identified other relevant legume phenotypes. We used Web of Science through Chapman University to search for articles related to the legume-rhizobium symbiosis. After filtering articles for relevance, we identified 25 phenotypes present at least once in a single article, and we indicated which articles report data on that phenotype.</p>

opencc-zeroApr 2022View details →
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FIGURE 3 in Rediscovery of Bauhinia conceptionis (Leguminosae: Cercidoideae), a rare and endemic species of Colombian legume from Chocó - Colombia, after eighty years

FIGURE 3. Map of Quibdó showing the area where Bauhinia conceptionis was rediscovered.

opennotspecifiedJun 2022View details →
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Data from: Multiple polyploidy events in the early radiation of nodulating and non-nodulating legumes

Unresolved questions about evolution of the large and diverse legume family include the timing of polyploidy (whole-genome duplication; WGDs) relative to the origin of the major lineages within the Fabaceae and to the origin of symbiotic nitrogen fixation. Previous work has established that a WGD affects most lineages in the Papilionoideae and occurred some time after the divergence of the papilionoid and mimosoid clades, but the exact timing has been unknown. The history of WGD has also not been established for legume lineages outside the Papilionoideae. We investigated the presence and timing of WGDs in the legumes by querying thousands of phylogenetic trees constructed from transcriptome and genome data from 20 diverse legumes and 17 outgroup species. The timing of duplications in the gene trees indicates that the papilionoid WGD occurred in the common ancestor of all papilionoids. The earliest diverging lineages of the Papilionoideae include both nodulating taxa such as the genistoids (e.g. lupin), dalbergioids (e.g. peanut), phaseoloids (e.g. beans), and galegoids (= Hologalegina, e.g. clovers), and clades with non-nodulating taxa including Xanthocercis and Cladrastis (evaluated in this study). We also found evidence for several independent WGDs near the base of other major legume lineages, including the Mimosoid-Cassiinae-Caesalpinieae (MCC), Detarieae, and Cercideae clades. Nodulation is found in the MCC and papilionoid clades, both of which experienced ancestral WGDs. However, there are numerous non-nodulating lineages in both clades, making it unclear whether the phylogenetic distribution of nodulation is due to independent gains or a single origin followed by multiple losses.

opencc-zeroDec 2013View details →
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Innovafrica-Sorghum-Legume trials lindi

<p>Ensuring food security in small-scale farming requires improvement of productivity of food crops to ensure access of food in local communities. the objective of the sorghum-legume demonstration trial was to demonstrate the performance of proven Sustainable Agricultural Intensification (SAI) practices in terms of yield, soil quality and labour efficiency. A farmers-led field trails were conducted in Nachunyu and Mmumbu villages in Lindi district, Tanzania. The SAI technologies validated include:  i) Treatment 1: Conventional tillage – farmers practice, consisting of hand hoe cultivation, residue were removed, no herbicides applied (hand hoe weeding) and continuous sorghum  ii) Treatment 2: Conservation tillage dibble stick, retention of crop residues but no herbicide use (traditional weeding), and cropping system of continuous sorghum, applied fertilizers and no burning of residues; iii) Treatment 3: Conservation tillage using dibble stick, retention of crop residues, applied herbicide immediately after planting , but continuous sorghum, applied fertilizer (NPS) and no burning of residues; iv) Treatment 4: Conservation agriculture with legume-sorghum rotation, tillage dibble stick, retention of crop residues, apply herbicide roundup soon after planting followed by traditional hand hoe weeding when needed after crop germination, apply fertilizers (NPS), started with sorghum in  season one (1) 2017/18. Soil samples were collected before the trials and after the trials. Data collected includes grain yields and residue biomass. </p>

opencc-zeroDec 2021View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

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behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record