Action of growing degree days on the morphogenesis and physiological responses of calla lily

The calla lily (Zantedeschia aethiopica) is an ornamental plant with growing acceptance in the market place that shows thermal constraints during planting. This study aimed to analyse its biological cycle in growing degree days (GDD) to determine the best time for planting and production of flower stalks. Rhizomes were planted in pots during all four seasons, and the pots were kept in a greenhouse. Growth analysis and gas exchange measurements were performed every 30 days. Rhizomes planted in the fall and summer showed greater shoot growth, a larger root system and increased production of flower stalks, and they remained in the vegetative phase longer before the onset of flowering, attaining a lower GDD value. Rhizomes planted in winter and spring matured early, which resulted in a higher GDD value and a decrease or lack of flower stalk production during this period. Calla lily rhizomes planted in the fall and summer showed higher water-use efficiency, light-use efficiency and net photosynthesis. It is possible to characterise the stages of development according to gas exchange. The calla lily must be cultivated with an irradiance of 250–400 µmol m^?2 s^?1 in a temperature range of 25–28 °C during the initial growth phase (up to 1,000 GDD). Thereafter, the temperature range should be reduced to between 13 and 15 °C until 3,500 GDD are reached, which was found to enable increased flower stalk production.     

New approaches for shoot production and establishment of in vitro root cultures of Cleome rosea Vahl.

Alternative methods for in vitro shoot culture of Cleome rosea, a Brazilian herbaceous species with ornamental value and medicinal potential, were evaluated. A protocol for rapid in vitro multiplication of roots, a valuable source of medicinal compounds, was also developed. Stem explants were cultured in liquid media (continuous immersion and paper bridge), while root explants were cultivated in continuous immersion and on solidified media. The highest numbers of shoots, 20 ± 4.6 shoots/explant, were obtained from stem explants incubated in a continuous immersion system in a liquid medium supplemented with 2.2 μM BA. Root explants cultivated in liquid media produced only hyperhydrous adventitious shoots. However, these explants generated 5.8 ± 0.8 shoots/explant by indirect organogenesis when cultivated on solidified medium supplemented with 2.2 μM BA. In addition, root multiplication was achieved in liquid medium in the presence of α-naphthaleneacetic acid. Adventitious shoots developed on newly formed roots when inoculated on solidified medium supplemented with 2.2 μM BA. Shoot microcuttings developed roots when transferred onto solidified MS medium without growth regulators. Rooted microcuttings were efficiently acclimatized when transferred ex vitro.     

Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy.

OBJECTIVE--To examine the significance of fetal nuchal translucency at 10-14 weeks'' gestation in the prediction of abnormal fetal karyotype. DESIGN--Prospective screening study. SETTING--The Harris Birthright Research Centre for Fetal Medicine, King''s College Hospital, London. SUBJECTS--827 fetuses undergoing first trimester karyotyping by amniocentesis or chorionic villus sampling. MAIN OUTCOME MEASURE--Incidence of chromosomal defects. RESULTS--The incidence of chromosomal defects was 3% (28 of 827 cases). In the 51 (6%) fetuses with nuchal translucency 3-8 mm thick the incidence of chromosomal defects was 35% (18 cases). In contrast, only 10 of the remaining 776 (1%) fetuses were chromosomally abnormal. CONCLUSION--Fetal nuchal translucency > or = 3 mm is a useful first trimester marker for fetal chromosomal abnormalities.     

Electroporation of intact embryonic leaflets of peanut: Gene transfer and stimulation of regeneration capacity

Summary Direct gene transfer into peanut intact embryonic leaflets was performed through electroporation. In transient β-glucuronidase expression assays, maximal expression was obtained by using pulses of 625 V cm⁻¹ in EPRm (modified electroporation) buffer supplemented with 75 μM NaCl. Kanamycin-resistant plants were obtained, and the presence of the nptII gene was demonstrated by PCR analysis. The positive effect of electroporation on the efficiency of in vitro regeneration was demonstrated. Explants submitted to field strengths between 500 and 625 V cm⁻¹ displayed a significantly increased number of shoots and originated faster growing calluses relative to control explants. Whereas in control explants callus formation occurred only at the petiolule, electroporated leaflets developed additional organogenic calluses on the foliar lamina. These authors have contributed equally to this work.