Search Results

You are looking at 41 - 50 of 2,043 items for :

  • native plant x
  • Refine by Access: User-accessible Content x
Clear All
Full access

Carlos Efraín Reyes-González, José Pablo Torres-Morán, Blanca Catalina Ramírez-Hernández, Liberato Portillo, Enrique Pimienta-Barrios, and Martha Isabel Torres-Morán

use and energy savings in extreme climates ( McFarland, 2017 ; Timur and Karaca, 2013 ; van den Berg and van den Berg, 2015 ), but there is a need to increase the set of native plants with potential to be used in green vertical structures and

Open access

Orville C. Baldos, Aleta Corpuz, and Lindsey Watanabe

species possess a compact growing habit and have interesting leaf and stem coloration, research of the ornamental potential of these native species has been limited. Currently, Peperomia blanda is the only native Hawaiian species that is commercially

Open access

Lyn A. Gettys and Michael A. Schnelle

plants. It is becoming increasingly clear that some native plants have the ability to grow aggressively, outcompete other native species, and form dense monocultures, resulting in the same problems associated with invasions by introduced plants. The

Free access

Anthony P. Keinath

; Robert et al., 2005 ). Although each mycologist assigned the fungus to a different genus, they coined the same species name “bryoniae” following the convention that the specific epithet of the fungus should be taken from the generic name of the plant host

Free access

Jerry A. Payne

Free access

Kwang-Chool Ko

Fifty nine morphological characters and isozyme band patterns of glutamate oxaloacetate transminase, peroxidase, glucose phosphate isomerase from fully expanded leaves were used for taxonomic study on 51 taxa consisted of Korean native and principal cultivars of the genus Pyrus. Taxonomic relationships were analyzed by complete cluster analysis method based on Euclidean taxonomic distance of IBM PC SPSS/PC+(ver. 3.0). Among the 39 qualitative morphological characters, a great deal of variations among 51 taxa were observed in immature fruit shape, skin lusterness, hair density on pedicel, anther color, shape of leaf apex and base, hair density on leaf surface, and leaf margin. Considerable variations were found in most tested quantitative characters except in the number of petals and styles. More reliable taxonomic results could be obtained by comparing morphological characters rather than examining isozyme band patterns. Even though there were considerable differences depending upon the methods of investigation, classification of the genus Pyrus by using isozyme band patterns was proved to be a good tool for rapid taxonomic studies.

Free access

Alison M. Fox, Doria R. Gordon, and Randall K. Stocker

vasive Plants Working Group are much appreciated. This research was supported by a grant from the Florida Nurserymen and Growers Association, and the Florida Agricultural Experiment Station, approved for publication as Journal Series No. R-08546.

Free access

J.C. Vlahos and P. Ververidis

Lupinus albus ssp. graecus, L. Fabaceae (Boiss. and Spruner) Franco and P.Silva, is being studied at the TEI of Heraklion since 1998 as a new plant with potential use in floriculture and ornamental horticulture. The plant has been recorded botanically; however, little is known about its physiology and genetic profile. Lupinus albus ssp. is a herbaceous annual plant 10 to 20 cm tall, growing at roadsides, field margins, vineyards, and olive groves up to 700 m altitude. The leaves are 5 to 11 cm wide, palmate shaped in alternate orientation, with five to nine leaflets 10 to 18 mm wide, all arising from the same point. The flowers are borne in terminal or lateral spike-like racemes 10 to 20 cm long. Florets are 15 mm long, dark blue occasionally with a white patch, stamens forming a tube. Pods are 60 to 70 mm long,with four to six black-spotted seeds. In the present work, seed germination studies were conducted combining chilling pretreatments with physical scarification (scratching). Mature seeds chilled at 5 °C for 6 weeks germinated readily (83%) when scarified with sand paper. Furthermore, we tested the effects of several plant growth regulators (chlorocholine chloride, paclobutrazol, maleic hydrazide and Ethrel 48) on young plants of Lupinus in order to obtain compact pot plants with more flowering racemes. Paclobutrazol at 5 and 10 mg/L achieved the best retardation effect, but did not affect flowering. In another trial with different potting media,the commercial potting soil proved the most suitable for growing lupins satisfactorily. It is concluded that Lupinus albus spp. graecus L. need further investigation in order to establish the best cultural conditions for its growth and development. Furthermore, due to its high genetic variability, selection and genetic improvement is required for optimal results.

Full access

Philip J. Kauth and Hector E. Pérez

.52 billion ( Hodges, 2011 ). With support from the federal government, state agencies, and private organizations, the use of native plants has been a growing segment in the horticulture industry ( Executive Order 13112, 1999 ; National Wildlife Federation

Free access

Lenore J. Nash and William R. Graves

Responses of five bottomland tree taxa to drought and flooding were studied to identify those adapted to urban environments. During one experiment, containerized `Franksred' red maple [Acer rubrum L. `Franksred' (trademark = Red Sunset)], sweetbay magnolia (Magnolia virginiana L.), black tupelo (Nyssa sylvatica Marsh.), bald cypress [Taxodium distichum (L.) Rich.], and pawpaw [Asimina triloba (L.) Dunal.] were treated with various irrigation regimes for up to 118 days. Net assimilation rate (NAR) and relative growth rate (RGR) were reduced more by flooding than by drought for plants of all taxa, except pawpaw, which showed similar NAR and RGR during flooding and drought. Only sweetbay magnolia and bald cypress maintained positive NAR and RGR during flooding, and sweetbay magnolia was the only taxon that did not produce significantly less leaf surface area, shoot dry mass, and root dry mass during flooding and drought. Apparent morphological mechanisms of stress resistance included an increase in specific mass of leaves (mg·cm-2) during drought for red maple and bald cypress and a 385% increase in the root: shoot mass ratio for droughted plants of pawpaw. Leaf water relations of drought- and flood-stressed `Franksred' red maple and sweetbay magnolia were determined in a second experiment. Predawn and mid-day leaf water potential (ψ) decreased with decreasing root-zone matric potential for both taxa, and transpiration rate was reduced by drought and flooding. Pressure-volume analysis showed that leaves of `Franksred' red maple responded to drought by shifting symplastic water to the apoplast. Leaves of drought-stressed sweetbay magnolia adjusted osmotically by reducing osmotic potential (ψπ) at full turgor by 0.26 MPa. Our results suggest that sweetbay magnolia and bald cypress will perform well at urban planting sites where episodes of drought and flooding regularly occur.