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70 results for “L. bicolor”
Sorghum bicolor (L.) Moench (BR0000012615384)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000005698028)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000011615651)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000012354511)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000014444913)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000011616191)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000011614968)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000012354610)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000012389469)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000011615293)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000014444999)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Sorghum bicolor (L.) Moench (BR0000024508445)
Belgium Herbarium image of <a href="https://www.plantentuinmeise.be">Meise Botanic Garden</a>.
Pera bicolor (Klotzsch) Müll. Arg. from Colombia collected by L. Ramos, E. Álvarez, J. Cabezas, J. Rodriguez & C. Ibañez #65
<p><strong>File Name</strong>: <span>TOLI-24030-RAN-01-8-Y-65.jpg</span></p> <p><strong>CÓDIGO FOTO</strong>: <span>TOLI-24030-RAN-01-8-Y-65-</span></p> <p><strong>Fotografía</strong>: <span>SI</span></p> <p><strong>Nº TOLI</strong>: <span>TOLI-24030</span></p> <p><strong>PARCELA</strong>: <span>RAN-01</span></p> <p><strong>CÓDIGO</strong>: <span>8-Y-65</span></p> <p><strong>Nº COLECTA</strong>: <span>65</span></p> <p><strong>NUEVOS COLECTORES</strong>: <span>Laura Isabel Ramos</span></p> <p><strong>COLECTORES</strong>: <span>L. Ramos, E. Álvarez, J. Cabezas, J. Rodriguez & C. Ibañez</span></p> <p><strong>Nº MUESTRAS MONTADAS</strong>: <span>1</span></p> <p><strong>Homologación</strong>: <span>Homologado</span></p> <p><strong>Nueva fecha del evento </strong>: <span>20/12/2018.</span></p> <p><strong>Fecha del evento</strong>: <span>27/11/2018.</span></p> <p><strong>Proyecto </strong>: <span>Recursos Botánicos Disponibles en Línea (BRAVO) para la flora Colombiana</span></p> <p><strong>Hábitat</strong>: <span>Bosque húmedo tropical (bh-T)</span></p> <p><strong>Continente</strong>: <span>SA</span></p> <p><strong>Pais</strong>: <span>Colombia</span></p> <p><strong>Estado/Provincia</strong>: <span>Meta</span></p> <p><strong>Municipio</strong>: <span>Puerto López</span></p> <p><strong>Centro poblado / Cabecera municipal</strong>: <span>La Serranía</span></p> <p><strong>Localidad</strong>: <span>Reserva Natural El Amparo</span></p> <p><strong>Elevación minima en metros</strong>: <span>200</span></p> <p><strong>Elevación maxima en metros</strong>: <span>250</span></p> <p><strong>Latitud</strong>: <span>4.020</span></p> <p><strong>Longitud original</strong>: <span>-72.600</span></p> <p><strong>datum geodésico</strong>: <span>WGS 84</span></p> <p><strong>Latitud decimal</strong>: <span>4.020</span></p> <p><strong>Longitud decimal</strong>: <span>-72.600</span></p> <p><strong>Identificado por</strong>: <span>Federico Fabriani</span></p> <p><strong>Fecha de identificación</strong>: <span>24/01/2019.</span></p> <p><strong>Familia antigua</strong>: <span>Euphorbiaceae</span></p> <p><strong>Especie antigua</strong>: <span>Pera arborea Kunth</span></p> <p><strong>Nombre cientifico</strong>: <span>Pera bicolor (Klotzsch) Müll. Arg. </span></p> <p><strong>Reino</strong>: <span>Plantae</span></p> <p><strong>Filo</strong>: <span>Magnoliophyta</span></p> <p><strong>Clase</strong>: <span>Equisetopsida</span></p> <p><strong>Orden</strong>: <span>Malpighiales</span></p> <p><strong>Familia nueva</strong>: <span>Peraceae</span></p> <p><strong>Género nuevo</strong>: <span>Pera</span></p> <p><strong>especie nueva</strong>: <span>bicolor</span></p> <p><strong>Autoría del nombre científico</strong>: <span>(Klotzsch) Müll. Arg. </span></p> <p><strong></strong>: <span>Euphorbiaceae</span></p> <p><strong>genero herbario</strong>: <span>Pera</span></p> <p><strong>especie herbario</strong>: <span>bicolor</span></p> <p><strong>Especie de herbario para TNRS</strong>: <span>Pera bicolor</span></p> <p><strong>Especie corregida herbario y desde TNRS</strong>: <span>Pera bicolor</span></p> <p><strong>Familia corregida desde TNRS</strong>: <span>Euphorbiaceae</span></p> <p><strong></strong>: <span>3114</span></p>
Protein sequences of LbNoxA, LbNoxB and LbNoxR in L. bicolor and other different species
<p>Ectomycorrhizal symbiosis, which involves mutually beneficial interactions between soil fungi and tree roots, is essential for promoting tree growth. To establish this symbiotic relationship, fungal symbionts must initiate and sustain mutualistic interactions with host plants while avoiding host defence responses. In recent years, the ectomycorrhizal association between the ectomycorrhizal basidiomycete<em> L. bicolor </em>and its host<em> Populus tremula × alba</em>,<em> </em>has been used to elucidate the molecular mechanisms that drive the development of ectomycorrhizal symbiosis. The gene repertoire of<em> L. bicolor</em> contained three <em>Nox</em> genes: <em>LbNoxA</em> (JGI ID Lacbi2|399780), <em>LbNoxB</em> (JGI ID Lacbi2|173015), and <em>LbNoxR</em> (JGI ID Lacbi2|383559). LbNoxA, protein sequence (JGI database + |gene numbers): Clapu1|8615, Sclsc1|12632, Morcra1|822478, Ophsi1|5059, PhlFC14_2|1813626, Pleery1|1506038, Armbor1|1922489, Trave1|68345, Dicsqu463_1|970488, Polbr1|1451927, Ganluc1|486672, Musmu1|NP_031833.3, Lacbi2|399780, LacbiH82_1|443856, Lacbi81306_1|757325, Lacbi55996_1|1021277, LacbiH53_1|522216, LacbiN203_1|820777, LacbiS238N_1|410357, LacbiS238O_1|87145, LacbiCham3_1|66106, LacbiH70_1|500846, Lacbi59489_1|1094392, LacbiH82×H70_1|455396, Lacbi9312_2|1966069, LacbiDR170_1|936588, LacbiD101_1|770957, Lacam2|675282. LbNoxB, protein sequence: Clapu1|2069, Sclsc1|4716, Morcra1|717130, Ophsi1|1953, PhlFC14_2|1930601, Pleery1|1513566, Armbor1|1788315, Trave1|154726, Dicsqu463_1|1002687, Polbr1|1407584, Ganluc1|380884, Musmu1|NP_031833.3, Lacbi2|173015, LacbiH82_1|402315, Lacbi81306_1|388494, Lacbi55996_1|1012552, LacbiN203_1|692258, LacbiS238N_1|466368, LacbiCham3_1|119176, LacbiS238O_1|142990, LacbiH70_1|481432, Lacbi59489_1|1017543, LacbiH82×H70_1|424508, Lacbi9312_2|2376025, LacbiDR170_1|961381, LacbiD101_1|744494, Lacam2|673882, LacbiH53_1|399281. LbNoxR, protein sequence: Clapu1|5169, Sclsc1|101, Morcra1|909770, Ophsi1|2065, PhlFC14_2|1902619, Pleery1|1379754, Armbor1|1887170, Trave1|31426, Dicsqu463_1|961540, Polbr1|1449735, Ganluc1|555878, Musmu1|NP_035007.1, Lacbi2|383559, LacbiH82_1|404736, Lacbi81306_1|796955, Lacbi55996_1|396143, LacbiH53_1|580999, LacbiN203_1|781452, LacbiS238N_1|524632, LacbiS238O_1|142040, LacbiCham3_1|116334, LacbiH70_1|479311, Lacbi59489_1|951497, LacbiDR170_1|1040569, Lacbi9312_2|2114762, Lacam2|671404, LacbiD101_1|660911, LacbiH82×H70_1|470284.</p>
Protein sequences of LbNoxA, LbNoxB and LbNoxR in L. bicolor and other different species
Open the record for dataset details and reuse information.
FIGURE. Pollen of Hylaeaicum and Aechmea aculeatosepala. A. H. eleutheropetalum (Leme 4491). B. H. eleutheropetalum var. bicolor (SEL 86-44). C. H. aff. myrmecophilum (Leme 3487). D. H. myrmecophilum (Leme 2555). E. H. levianum (Leme 2777). F. H. margaretae (Leme 2748). G. H. aff. myrmecophilum (Leme 2553). H. H. margaretae (Leme 2331). I. H. wurdackii (Leme 2567). J. H pendulum (Leme 1979). K. H. tarapotoense (Leme 1977). L. Aechmea aculeatosepala (Leme 3235). Bars = 10 µm. in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence
FIGURE. Pollen of Hylaeaicum and Aechmea aculeatosepala. A. H. eleutheropetalum (Leme 4491). B. H. eleutheropetalum var. bicolor (SEL 86-44). C. H. aff. myrmecophilum (Leme 3487). D. H. myrmecophilum (Leme 2555). E. H. levianum (Leme 2777). F. H. margaretae (Leme 2748). G. H. aff. myrmecophilum (Leme 2553). H. H. margaretae (Leme 2331). I. H. wurdackii (Leme 2567). J. H pendulum (Leme 1979). K. H. tarapotoense (Leme 1977). L. Aechmea aculeatosepala (Leme 3235). Bars = 10 µm.
FIGURE. Conduplicate-erect (CE), conduplicate-patent (CP), conduplicate-spiral (CS), and simple-dilated (SD) stigma types of different genera in Bromelioideae. A. Aechmea (Pseudaechmea) filicaulis (CP, Leme 2268). B. Aechmea subg. Podaechmea: A. lueddemanniana (CS, Leme 001). C. Aechmea subg. Pothuava s.l: A. pectinata (CS, Leme 231). D. Aechmea subg. Platyaechmea s.l.: A. smithiorum (CS, Leme 1709). E. Aechmea subg. Chevaliera s.l.: A. tayoensis (CS, Leme 3240). F. Ananas nanus (CS, Leme 9381). G. Araeococcus flagellifolius (SD, Leme 9696); H. Billbergia subg. Billbergia: B. amoena var. robertiana (CS, Leme 246). I. Billbergia subg. Helicodea: B. porteana (CS, Leme 9584). J. Bromelia auriculata (CE, Leme 8108). K. Fernseea bocainensis (CS, Leme 1422); L. Hohenbergia catingae (CS, Leme 2330). M. Neoglaziovia variegata (CS, Leme 9153). N. Greigia stenolepis (CS, Leme 9738). O. Portea grandiflora (CS, Leme 4011). P. Pseudananas sagenarius (CS, Leme 5556). Q. Quesnelia arvensis (CS, Leme 2695). R. Wittmackia bicolor (CS, Leme 4228). S. Wittmackia (Wittmackiopsis) penduliflora (CS, Leme 3832). T. Wittmackia silvana (CS, Leme 7060). Bars = 1 mm. in Re-evaluation of the Amazonian Hylaeaicum (Bromeliaceae: Bromelioideae) based on neglected morphological traits and molecular evidence
FIGURE. Conduplicate-erect (CE), conduplicate-patent (CP), conduplicate-spiral (CS), and simple-dilated (SD) stigma types of different genera in Bromelioideae. A. Aechmea (Pseudaechmea) filicaulis (CP, Leme 2268). B. Aechmea subg. Podaechmea: A. lueddemanniana (CS, Leme 001). C. Aechmea subg. Pothuava s.l: A. pectinata (CS, Leme 231). D. Aechmea subg. Platyaechmea s.l.: A. smithiorum (CS, Leme 1709). E. Aechmea subg. Chevaliera s.l.: A. tayoensis (CS, Leme 3240). F. Ananas nanus (CS, Leme 9381). G. Araeococcus flagellifolius (SD, Leme 9696); H. Billbergia subg. Billbergia: B. amoena var. robertiana (CS, Leme 246). I. Billbergia subg. Helicodea: B. porteana (CS, Leme 9584). J. Bromelia auriculata (CE, Leme 8108). K. Fernseea bocainensis (CS, Leme 1422); L. Hohenbergia catingae (CS, Leme 2330). M. Neoglaziovia variegata (CS, Leme 9153). N. Greigia stenolepis (CS, Leme 9738). O. Portea grandiflora (CS, Leme 4011). P. Pseudananas sagenarius (CS, Leme 5556). Q. Quesnelia arvensis (CS, Leme 2695). R. Wittmackia bicolor (CS, Leme 4228). S. Wittmackia (Wittmackiopsis) penduliflora (CS, Leme 3832). T. Wittmackia silvana (CS, Leme 7060). Bars = 1 mm.
Data from: Surveying the spatial distribution of feral sorghum (Sorghum bicolor L.) and its sympatry with johnsongrass (S. halepense) in South Texas
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Data from: Accelerating seed germination and seedling development of Sorghum (Sorghum bicolor L. Moench) through hydro-priming
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Data from: Seed priming and Zaï pit practice improve field performance of sorghum (Sorghum bicolor L. Moench) in the Sahelian zone of Mali
Poor seed germination caused by a variety of seed, soil and environmental factors lead to suboptimal seedling stand and ultimately yield suffers a serious setback. A number of priming techniques have been found to be effective in increasing germination and seedling growth and development. This includes techniques such as on-farm hydro-priming (seed soaking in well water) and osmo-priming (seed soaking in low osmotic solutions of Potassium silicate). Also, Zaï practice, a cropping system concentrating runoff water and manure in pits, may be a simple solution in addition to seed priming techniques for crop establishment under early drought and heat prone areas and for increased productivity of poor soils. This study aims to evaluate the combined effect of priming and cultural practices (ridge and zaï pits) on three sorghum varieties in the Sahelian zone of Mali. Data were collected during two growing seasons in 2014 and 2015. Monitored parameters were assessed by comparing the impact of priming with untreated sorghum seeds (the control) cultivated on ridges and zaï pits with or without compost. We also compared the effect of hydro-priming in water from well to osmo-priming using K2SiO3 performance. Hence, each of the 3 sorghum variety seeds were subjected to 3 different priming, sowed on ridges and zaï treatments. Variety banidoka and CSM63E recorded the maximum GP (54.0%) which was significantly higher than saba-tienda GP (48%). The priming treatments were not statistically different for germination but showed slight improvement in GP for primed (54%) compared to unprimed (48%). Germination percentages were significantly higher in zaï pits practice without (55%) and with compost (55%) compared to ridges (48%). Grain yield varied significantly among sorghum varieties (p<0. 04) and cultural practices (p<0. 01). There was no significant difference among priming treatments for grain yield. However, variety banidoka produced the highest grain yield (961 kg ha-1) followed by CSM63E (874 kg ha-1) and lastly saba-tienda (671 kg ha-1) with banidoka showing statistically different yield compared to saba-tienda. Zaï pits practice with compost obtained the highest GY (1131 kg ha-1), which was statistically different from the GY of zaï pits practice without compost (695 kg ha-1) and ridge practice (742 kg ha-1). Zaï pits practice without compost did not statistically differ from ridge practice. The findings showed that seed priming in addition to zaï pits practice improves seed germination and seedling development of sorghum probably by accelerating imbibition and providing continuous moisture during the germination phase. Combining seed priming and zai pit practice with compost appears a simple practice that will improve crop establishment and grain yield in the Sahelian zone of West Africa.
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