Partial Reversal by Cytokinin and (2-Chloroethyl)-Trimethylammonium Chloride of Near-Ultraviolet Inhibited Growth and Morphogenesis in Callus Cultures

Callus cultures of Haplopappus gracilis, Nicotiana tabacum and Allium cepa var. proliferum were in varying degrees inhibited by blue to near-UV light obtained from fluorescent tubes. The inhibition was considerably reduced for Haplopappus cultures by 6-(3-methyl-2-buten-1-ylamino)-purine (2 iP) and (2-chloro-ethyl)-trimethylammonium chloride (CCC) in combination. Even separately these compounds stimulated growth in blue but not in white light. A high concentration of 2 iP reduced the inhibiting effects of near-UV on tobacco tissue cultures, and a synergism was observed between 2 iP and CCC in respect to shoot formation in blue light. Allium callus was not significantly affected by CCC. It was also observed that the concentration of indol-3-acetic acid (IAA) was more important for the growth of tobacco cultures in blue than in white light. It is believed that the light-inhibition of growth is partly due to a photoinactivation of IAA and that 2 iP and CCC might be active through processes controlling the levels of IAA and other growth hormones.     

YOU CAN USE MY NAME; YOU DON'T HAVE TO STEAL MY STORY – A CRITIQUE OF ANONYMITY IN INDIGENOUS STUDIES

Our claim in this paper is that not being identified as the data source might cause harm to a person or group. Therefore, in some cases the default of anonymisation should be replaced by a careful deliberation, together with research subjects, of how to handle the issues of identification and confidentiality. Our prime example in this article is community participatory research and similar endeavours on indigenous groups. The theme, content and aim of the research, and the question of how to handle property rights and ownership of research results, as well as who should be in charge of the research process, including the process of creating anonymity, should all be answered, before anonymity is accepted.     

Induction of Adventitious Buds on Buds of Norway Spruce (Picea abies) Grown in vitro

Resting vegetative buds of Norway spruce, Picea abies (L.) Karst., were induced to form adventitious bud primordia when cultured on medium -containing cytokinin. After transfer of the induced buds to medium lacking cytokinin, adventitious buds developed. The adventitious buds arose from meristems formed de novo in the needle primordia. No differences were found in the ability to form adventitious buds among buds collected from trees ranging from 5–50 years old.     

Induction of Adventitious Buds on Embryos of Norway Spruce Grown in vitro

Adventitious buds were induced when isolated embryos of Norway spruce (Picea abies L.) were cultured on a defined medium containing 2iP. Anatomically different bud primordia were formed at high and low cytoldnin concentrations. The highest percentage of embryos forming bud primordia was obtained after 4–5 weeks on 2iP medium. Buds developed after transfer of the induced embryos to medium without growth regulators. Many of the buds developed into elongated shoots. No root primordia were observed in any of the induced embryos.     

Pretreatment of Cell Suspensions as a Method to Increase the Protoplast Yield of Haplopappus gracilis

A low yield of free protoplasts was obtained when fast-growing cell suspensions of Haplopappus gracilis were treated with Driselase, an active mixture of cellulase and pectinase. If the cells in the suspension culture were pretreated by increased levels of auxin, reduced sugar concentration, addition of sulphur-containing amino acids, or by the reducing agent mercaptoethanol, protoplasts were released from a higher proportion of the cells. These pretreatments did not adversely effect division of the protoplasts.     

Evolution of fruit characters and dispersal modes in the tropical family Rubiaceae

We investigated the evolution of fruit characters, animals versus abiotic dispersal modes, life forms and geographical distribution, in the large, mostly tropical, family Rubiaceae. As a basis for our analysis we used a phylogenetic tree derived from chloroplast DNA variation. Fleshy fruits have evolved independently at least 12 times in the family. Most of these originations appear to have occurred during Eocene to Oligocene, i.e. the radiation period for some animal taxa (bird families, mammal orders) comprising most extant dispersers of Rubiaceae fruits. Changes of dispersal modes may be of more recent origin in a few cases, e.g. evolution of drupes in some lineages, and shifts from drupes to nuts. The distribution of fruit characters suggested that in several lineages animal-dispersed fruits, such as berries and drupes have remained largely unaltered since the time of origination. This is in contrast to the occurrence of winged seeds in capsules, and pterophylls, i.e. enlarged calyx lobes promoting wind dispersal of fruits, which apparently have shifted more frequently during evolution, indicating a difference in 'phylogenetic plasticity' between modes of animal and wind dispersal.
Animal dispersal was over-represented among genera dominated by shrubs, whereas abiotic dispersal was most prevalent among herbaceous genera. Drupes were over-represented in groups with transoceanic distributions, and on islands, indicating dispersal over long distances, probably by birds. In contrast, no evidence was found to support the view that animal dispersal in general enhances long distance dispersal. We also analysed geographical patterns on the tribal level but these were too complex to yield any resolved area cladograms due to the occurrence of many widespread taxa and area redundancy.