162,350 research outputs found
Solanum catilliflorum G. J. Anderson, Martine, Prohens & Nuez 2006, sp. nov.
No full textSolanum catilliflorum G. J. Anderson, Martine, Prohens & Nuez, sp. nov. TYPE: U.S.A. Connecticut: cultivated at Univ. Conn. Ecol. & Evol. Biol. Conservatory, Storrs, 19 Nov. 2004, C. T. Martine 949 (holotype, CONN; isotypes, MO, MOL, NY, US, VAL) [Peru, Abancay: near Abancay, rubbish heap in wet terrain, 19 Mar. 2001, seed collection, J. Prohens & F. Nuez 80]. Figure 1E–H. Habitus reptans; folia et foliola parva; folia in foliola pleraque 3 divisa; sine pugiotis pilis glandulosis; flores parvuli; stylus brevis, extendens vix ultra columnam staminalem; fertile secum; fructus parvi. Viney or trailing shrub; branches to 1 m long; internodes 15–60 mm; stem woody or thick-herbaceous, moderately strigose when young, older branches commonly rooting at nodes. Leaves with mostly 3 (rarely 1) leaflets, 32–58 mm long, with petiole 7–14 mm long; leaflets lanceolate to elliptic, base obtuse, apex acute or acuminate, not sticky, with moderately dense strigose vestiture of 2-celled bayonet hairs intermixed with short square gland hairs on both surfaces; bayonet hairs about 0.5 mm in length; short square gland hairs about 0.07 mm in length; gland-tipped finger hairs not present; terminal leaflet somewhat larger than the first pair of lateral leaflets, 23–36 × 14–22 mm, the petiolule 2–5 mm long; first pair of lateral leaflets 8–18 × 5–11 mm, short-petiolulate; pseudostipules present. Inflorescence an indeterminate pseudoterminal cymose raceme with 1 axis and 5(to 8) hermaphrodite flowers; pedicels 5–8 mm long, basally articulate, with dense strigose vestiture of 2-celled bayonet hairs intermixed with short square gland hairs. Corolla white, rotate, moderately reflexed, lobes 7–9 mm long, sinuses 4.0– 6.5 mm long, the lobe:sinus ratio about 1.35:1, glabrous adaxially, sparsely strigose to hispid abaxially; calyx green, acute to acuminate, ca. 1/2 length of corolla lobes, strigose vestiture moderate to heavy; anthers pale yellow, 2.8–3.4 mm long, apices rounded, 2.8–3.4 mm long, glabrous adaxially and abaxially, filaments 0.7–1.1 mm long, fused for less than 1/4 length, with scattered stiff hairs at midpoint; style 4.7–6.1 mm long, sparingly to moderately strigose over lower half, stigma slightly capitate, exceeding staminal column by 1.6–2.4 mm. Fruits globose, the mature fruits pale green or yellowish green with darker green or purple-black stripes, with darker maculae on the lighter areas, 13–18 × 12–18 mm, round in cross section, smooth, apex rounded, locules 2; soluble solids concentration 5%–8%; seeds 100 to 175 per fruit; fruits falling from plant when ripe. Pollen grains per anther ca. 39,800, pollen:ovule ratio ca. 2170:1 (Table 1); plants self-compatible; n = 12 (Martine 949, CONN). Habitat and distribution. Collections of this new species have been made at elevations near 2100 m on open, wet terrain in Peru. The ripened fruits of Solanum catilliflorum are eaten by locals. Near Auquibamba, Abancay, the species is known as pipino (Prohens, pers. obs.). This new taxon is distinguished from morphologically similar species in Solanum sect. Basarthrum ser. Caripensia by its scrambling habit, small flowers (smallest in the Caripense complex), and short styles extending only slightly beyond the staminal column, similar to the other self-compatible species in section Basarthrum. However, these styles extend farther beyond the staminal column than any other selfcompatible species in the series. Plants of this species are not only self-compatible, but autogamous, as demonstrated by greenhouse observations (G. Anderson, pers. obs.). The other self-compatible species in section Basarthrum are the domesticated pepino (S. muricatum), two herbaceous annuals (S. canense Rydberg, S. suaveolens Kunth & Bouché), and one woody perennial (S. trachycarpum) limited to lowelevation xeric sites in Ecuador. Solanum catilliflorum is easy to distinguish from S. trachycarpum based on the small flowers, compound leaves (vs. simple), and scrambling habit (vs. erect). Likewise, S. catilliflorum lacks the gland-tipped finger hairs present in the majority of the species in series Caripensia. Etymology. The epithet reflects the small flowers of this species, the Latin catillus being a small plate or dish. Conservation status. Estimated IUCN rank: VU. Rare and known from a limited number of localities. Total wild population still unknown. Paratypes. U.S.A. Connecticut: cultivated at Univ. Conn. Ecol. & Evol. Biol. Conservatory, Storrs, 18 July 2005, C. T. Martine & M. R. Opel 1084 (CONN) [Peru, Abancay/ Apurimac, road cut near Auquibamba, 18 Mar. 2001, seed collection, J. Prohens & F. Nuez 71]; 18 July 2005, C. T. Martine & M. R. Opel 1085 (CONN) [Peru: Auquibamba, 18 Mar. 2001, seed collection, J. Prohens & F. Nuez 74]; 18 July 2005, C. T. Martine & M. R. Opel 1086 (CONN) [Peru, Abancay, 19 Mar. 2001, seed collection, J. Prohens & F. Nuez 82].Published as part of Anderson, G. J., Martine, C. T., Prohens, J. & Nuez, F., 2006, Solanum Perlongistylum and S. Catilliflorum, New Endemic Peruvian Species of Solanum, Section Basarthrum, Are Close Relatives of the Domesticated Pepino, S. Muricatum, pp. 161-167 in Novon: A Journal for Botanical Nomenclature 16 (2) on pages 164-165, DOI: 10.3417/1055-3177(2006)16[161:spascn]2.0.co;2, http://zenodo.org/record/632765
Solanum catilliflorum G. J. Anderson, Martine, Prohens & Nuez 2006, sp. nov.
No full textSolanum catilliflorum G. J. Anderson, Martine, Prohens & Nuez, sp. nov. TYPE: U.S.A. Connecticut: cultivated at Univ. Conn. Ecol. & Evol. Biol. Conservatory, Storrs, 19 Nov. 2004, C. T. Martine 949 (holotype, CONN; isotypes, MO, MOL, NY, US, VAL) [Peru, Abancay: near Abancay, rubbish heap in wet terrain, 19 Mar. 2001, seed collection, J. Prohens & F. Nuez 80]. Figure 1E–H. Habitus reptans; folia et foliola parva; folia in foliola pleraque 3 divisa; sine pugiotis pilis glandulosis; flores parvuli; stylus brevis, extendens vix ultra columnam staminalem; fertile secum; fructus parvi. Viney or trailing shrub; branches to 1 m long; internodes 15–60 mm; stem woody or thick-herbaceous, moderately strigose when young, older branches commonly rooting at nodes. Leaves with mostly 3 (rarely 1) leaflets, 32–58 mm long, with petiole 7–14 mm long; leaflets lanceolate to elliptic, base obtuse, apex acute or acuminate, not sticky, with moderately dense strigose vestiture of 2-celled bayonet hairs intermixed with short square gland hairs on both surfaces; bayonet hairs about 0.5 mm in length; short square gland hairs about 0.07 mm in length; gland-tipped finger hairs not present; terminal leaflet somewhat larger than the first pair of lateral leaflets, 23–36 × 14–22 mm, the petiolule 2–5 mm long; first pair of lateral leaflets 8–18 × 5–11 mm, short-petiolulate; pseudostipules present. Inflorescence an indeterminate pseudoterminal cymose raceme with 1 axis and 5(to 8) hermaphrodite flowers; pedicels 5–8 mm long, basally articulate, with dense strigose vestiture of 2-celled bayonet hairs intermixed with short square gland hairs. Corolla white, rotate, moderately reflexed, lobes 7–9 mm long, sinuses 4.0– 6.5 mm long, the lobe:sinus ratio about 1.35:1, glabrous adaxially, sparsely strigose to hispid abaxially; calyx green, acute to acuminate, ca. 1/2 length of corolla lobes, strigose vestiture moderate to heavy; anthers pale yellow, 2.8–3.4 mm long, apices rounded, 2.8–3.4 mm long, glabrous adaxially and abaxially, filaments 0.7–1.1 mm long, fused for less than 1/4 length, with scattered stiff hairs at midpoint; style 4.7–6.1 mm long, sparingly to moderately strigose over lower half, stigma slightly capitate, exceeding staminal column by 1.6–2.4 mm. Fruits globose, the mature fruits pale green or yellowish green with darker green or purple-black stripes, with darker maculae on the lighter areas, 13–18 × 12–18 mm, round in cross section, smooth, apex rounded, locules 2; soluble solids concentration 5%–8%; seeds 100 to 175 per fruit; fruits falling from plant when ripe. Pollen grains per anther ca. 39,800, pollen:ovule ratio ca. 2170:1 (Table 1); plants self-compatible; n = 12 (Martine 949, CONN). Habitat and distribution. Collections of this new species have been made at elevations near 2100 m on open, wet terrain in Peru. The ripened fruits of Solanum catilliflorum are eaten by locals. Near Auquibamba, Abancay, the species is known as pipino (Prohens, pers. obs.). This new taxon is distinguished from morphologically similar species in Solanum sect. Basarthrum ser. Caripensia by its scrambling habit, small flowers (smallest in the Caripense complex), and short styles extending only slightly beyond the staminal column, similar to the other self-compatible species in section Basarthrum. However, these styles extend farther beyond the staminal column than any other selfcompatible species in the series. Plants of this species are not only self-compatible, but autogamous, as demonstrated by greenhouse observations (G. Anderson, pers. obs.). The other self-compatible species in section Basarthrum are the domesticated pepino (S. muricatum), two herbaceous annuals (S. canense Rydberg, S. suaveolens Kunth & Bouché), and one woody perennial (S. trachycarpum) limited to lowelevation xeric sites in Ecuador. Solanum catilliflorum is easy to distinguish from S. trachycarpum based on the small flowers, compound leaves (vs. simple), and scrambling habit (vs. erect). Likewise, S. catilliflorum lacks the gland-tipped finger hairs present in the majority of the species in series Caripensia. Etymology. The epithet reflects the small flowers of this species, the Latin catillus being a small plate or dish. Conservation status. Estimated IUCN rank: VU. Rare and known from a limited number of localities. Total wild population still unknown. Paratypes. U.S.A. Connecticut: cultivated at Univ. Conn. Ecol. & Evol. Biol. Conservatory, Storrs, 18 July 2005, C. T. Martine & M. R. Opel 1084 (CONN) [Peru, Abancay/ Apurimac, road cut near Auquibamba, 18 Mar. 2001, seed collection, J. Prohens & F. Nuez 71]; 18 July 2005, C. T. Martine & M. R. Opel 1085 (CONN) [Peru: Auquibamba, 18 Mar. 2001, seed collection, J. Prohens & F. Nuez 74]; 18 July 2005, C. T. Martine & M. R. Opel 1086 (CONN) [Peru, Abancay, 19 Mar. 2001, seed collection, J. Prohens & F. Nuez 82].Published as part of Anderson, G. J., Martine, C. T., Prohens, J. & Nuez, F., 2006, Solanum Perlongistylum and S. Catilliflorum, New Endemic Peruvian Species of Solanum, Section Basarthrum, Are Close Relatives of the Domesticated Pepino, S. Muricatum, pp. 161-167 in Novon: A Journal for Botanical Nomenclature 16 (2) on pages 164-165, DOI: 10.3417/1055-3177(2006)16[161:spascn]2.0.co;2, http://zenodo.org/record/632765
Fruit shape and colour variation in cultivars of the common eggplant, <i>Solanum melongena</i>. Photograph taken by J. Prohens.
No full text<p>Fruit shape and colour variation in cultivars of the common eggplant, <i>Solanum melongena</i>. Photograph taken by J. Prohens.</p
Plant breeding: a success story to be continued thanks to the advances in genomics
No full textThis work has been funded by the Ministerio de Ciencia y Tecnología (AGL2009-07257), Generalitat Valenciana (ACOMP/2011/032), and Universitat Politècnica de València (PAID-05-10-2318)Prohens Tomás, J. (2011). Plant breeding: a success story to be continued thanks to the advances in genomics. Frontiers in Plant Science. 2(51):1-3. https://doi.org/10.3389/fpls.2011.00051S1325
[Report to Chief J. E. Curry, by an unknown author #1]
No full textReport to Chief J. E. Curry, by an unknown author. The report contains a list of officers who gave depositions to the United States Attorney
[Report to Chief J. E. Curry, by an unknown author #2]
No full textReport to Chief J. E. Curry, by an unknown author. The report contains a list of officers who gave depositions to the United States Attorney
`Puzol': A Facultatively Parthenocarpic Hybrid of Pepino (Solanum muricatum)
No full textProhens Tomás, J.; Leiva Brondo, M.; Rodríguez Burruezo, A.; Nuez Viñals, F. (2002). `Puzol': A Facultatively Parthenocarpic Hybrid of Pepino (Solanum muricatum). HortScience. 37(2):418-419. https://riunet.upv.es/handle/10251/78988S41841937
Root seedling morphology diversity in Capsicum spp
No full textPeláez Andérica, E.; Rodríguez Burruezo, A.; Prohens Tomás, J.; Fita, A. (2011). Root seedling morphology diversity in Capsicum spp. Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca : Horticulture. 68(1):535-536. https://riunet.upv.es/handle/10251/62876S53553668
Evaluation of androgenic competence through anther culture in common eggplant and related species
No full textAnther culture is a convenient technique to obtain androgenic haploid and doubled haploid (DH) plants. In common eggplant (Solanum melongena), this technique has been used to develop DH pure lines for producing uniform F1 hybrid seed of some commercial varieties. However, a comprehensive study of the variation of this useful trait among different materials of common eggplant and related species is still lacking. In this work, we studied the androgenic response of 12 accessions of common eggplant and related materials from the primary (eggplant complex) and secondary genepools. We cultured anthers of all the accessions under the same experimental conditions, and studied their competence to produce calli, embryos and plants, as well as the quality and origin of the embryos produced. In our conditions, anthers of 11 out of the 12 accessions produced somatic calli, whereas only 5 also produced microspore-derived embryos, with variable results in terms of embryo quality and of frequency of embryo induction and plant germination. Embryos of responding accessions were initially haploid, and reached the DH status, verified with SSR markers, after a defined period of culture. In addition to other aspects common to many androgenesis-responsive species, our results allowed us to extract conclusions particular to common eggplant and relatives, including the difficulty for finding sources of androgenic competence out of S. melongena, the reduced impact of calli in the production of non-DH individuals, and the need to avoid the occurrence of severe anatomical and functional problems in the apex of most embryos, which seriously reduces their germinative success. © 2011 Springer Science+Business Media B.V.We acknowledge Drs. Begona Renau and Antonio Serrano, and Mrs Nuria Palacios for their excellent technical work, as well as the staff of the COMAV greenhouses for their valuable help. Thanks are also due to Dr. Santiago Vilanova for providing us with the SSRs used in this work. This work was supported by grants from Spanish MICINN AGL2006-06678 and AGL2010-17895 to JMSS, and AGL2009-07257 to JP.Salas Aragon, P.; Prohens Tomás, J.; Seguí-Simarro, JM. (2011). Evaluation of androgenic competence through anther culture in common eggplant and related species. Euphytica. 182(2):261-274. doi:10.1007/s10681-011-0490-2S2612741822Alpsoy HC, Seniz V (2007) Researches on the in vitro androgenesis and obtaining haploid plants in some eggplant genotypes. Acta Hortic 729:137–141Barchi L, Lanteri S, Portis E, Stagel A, Vale G, Toppino L, Rotino GL (2010) Segregation distortion and linkage analysis in eggplant (Solanum melongena L.). 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