Bulb Development in Onion (Allium cepa L.) III. Effects of the Size of Adjacent Plants, Shading by Neutral and Leaf Filters, Irrigation and Nitrogen Regime and the Relationship between the Red: Far-red Spectral Ratio in the Canopy and Leaf Area Index

Field experiments were done to investigate why onion crops witha high leaf area index (LAI) initiate bulb scales and maturesooner than those with a low LAI. When small plants were growneither mixed with large plants or in pure stands, those in themixed stands initiated bulb scales earlier than those in purestands. The timing of bulb development therefore depended onthe size of neighbouring plants and the LAI of the stand andwas not simply determined by the size or age of individual plants.Shading plots with neutral filters which caused no spectralchanges slightly accelerated bulb development compared to unshadedplots but shading by a canopy of climbing pea and bean leaveshad a larger effect. Lack of irrigation advanced bulb maturitybut in the highly irrigated treatments plots of high plant densitystill initiated bulb scales and matured before those of lowdensity. Quantitative relationships between the change in R : FR andeither LAI or total radiation interception were determined foronion leaf canopies. It is suggested that the decrease in thered to far-red spectral ratio (R : FR) as LAI increases maybe the cause of the earlier bulb scale initiation and maturitythat occurs as LAI increases. Onion, Allium cepa (L.), spacing, competition, leaf area index, red: far red, irrigation, nitrogen, shading, bulbing     

SHORT COMMUNICATION Factors Affecting Protoplast Culture ofCucumis melo'Green Delica'

Hypocotyls, cotyledons and etiolated half-expanded leaves ofCucumismelo‘Green Delica’ were used as explants for protoplastisolation and culture. Protoplasts isolated from cotyledonsand etiolated half-expanded leaves cultured in Durand, Potrykusand Donn (DPD) medium supplemented with 0.9 µMbenzylaminopurine(BAP), 3.6 µM2,4-dichlorophenoxyacetic acid (2,4-D) and1% sucrose, using the agarose bead culture method, were ableto form cell walls and subsequently go through cell division.Pretreatment of half-expanded leaf explants in the dark for14 d provided the best material for protoplast isolation andcell division. Approximately one third of protoplasts from etiolatedhalf-expanded leaves formed microcolonies. For hypocotyl protoplasts,none of the treatments used were suitable to induce cell division.There was no significant difference between sucrose, glucose,and sucrose plus glucose, in culture media on the plating efficiencyof leaf protoplasts ofC. melo‘Green Delica’; however,bigger colonies were formed in media supplemented with 1% sucrose.No shoot or whole plant regeneration was achieved. However,the methods reported here provide further information onC. meloprotoplastculture.Copyright 1998 Annals of Botany Company Cucumis melo,protoplast culture, 2,4-D, BAP, yeast extract, casein hydrolysate.