The Permeability of the Guard Cell Plasma Membrane and Tonoplast

Uptake experiments and efflux compartmental analysis of planthormones, osmotica and toxins using ‘isolated’ guardcells of Valerianella locusta and guard cell protoplasts (GCP)of Vicia faba were performed in order to study the permeabilityproperties of guard cell plasma membrane and tonoplast. Theplasma membrane of guard cells exhibits a higher permeabilitythan plasma membranes of mesophyll cells for most solutes investigated.The permeability coefficients (P_s calculated for the guard cellplasma membranes are also significantly higher than the P_s valuesfor the guard cell tonoplast. This applies also for protonatedABA. We suppose that the high permeability for ABAH could bepart of the target cell properties. A Collander analysis demonstratesa linear correlation between P_s, values and the ratio K_r/M_r^1,5for both plasma membrane (r = 0.87) and for the tonoplast (r=0.93). Because of deviations from the observed correlations,the permeation of some solutes (ABA, GA, IAA through the tonoplast;methylamine through the plasma membrane) seems to be facilitatedby an additional transport mechanism. The Collander analysisof the plasma membrane of GCP shows very similar results tothe analysis of the plasma membrane of ‘isolated’guard cells, indicating that isolation of protoplasts does notalter the permeability of the guard cell plasma membrane. Key words: Permeability coefficient, guard cells, plasma membrane, tonoplast     

Differential Stimulation of PEP-carboxylation in Guard Cells and Mesophyll Cells by Ammonium or Fusicoccin

Dark CO₂-fixation in guard cells of Vicia faba was much moresensitive to ammonium than in mesophyll cells. Addition of ammonium(5.0 mol m^–3; pH₀ 7.6) caused up to a 7-fold increasein dark CO₂-fixation rates in guard cell protoplasts (GCP),whereas in leaf slices, mesophyll cells, and mesophyll protoplaststhe increase was only about 1.4-fold. In both cell or tissuetypes, total CO₂-fixation rates were higher in the light (2–12-foldhigher in GCP and 28-fold in mesophyll); these rates were onlyslightly changed by ammonium treatment. However, separationof ¹⁴C-labelled products after fixation of CO₂ in the lightby GCP revealed a large ammonium-induced shift in carbon flowfrom starch and sugars to typical products of C₄-metabolism(mainly malate and aspartate). In contrast, in mesophyll cellsamino acid and malate labelling was only moderately increasedby ammonium at the expense of sucrose. The data suggest thatin vivo ammonium might facilitate stomatal opening and/or delaystomatal closing through an increased production of organicacids. Key words: PEP-carboxylation, guard cell protoplasts, ammonium, fusicoccin     

Comparative cytogenetic analysis of four species of <Emphasis Type="Italic">Dendropsophus</Emphasis> (Hylinae) from the Brazilian Atlantic forest

We conducted a cytogenetic study of four hyline frog species (Dendropsophus elegans, D. microps, D. minutus and D. werneri) from southern Brazil. All species had 2n = 30 chromosomes, with interspecific and intraspecific variation in the numbers of metacentric, submetacentric, subtelocentric and telocentric chromosomes. C-banding and fluorochrome staining revealed conservative GC-rich heterochromatin localized in the pericentromeric regions of all species. The location of the nucleolus organizer regions, as confirmed by fluorescent in situ hybridization, differed between species. Telomeric probes detected sites that were restricted to the terminal regions of all chromosomes and no interstitial or centromeric signals were observed. Our study corroborates the generic synapomorphy of 2n = 30 chromosomes for Dendropsophus and adds data that may become useful for future taxonomic revisions and a broader understanding of chromosomal evolution among hylids.     

Investigations on the Retroactive Influence of Latent Visual Learning on Previously Formed Memory Traces in Fish1

Experiments with crucians (Carassius carassius L.) and goldfish (Carassius auratus L.) have shown that a consolidated memory trace of a simple visual pattern became disturbed by later seeing series of similar patterns (unrewarded), that is to say by latent learning. In a test in which the experimental group (es) had to choose between the originally learnt and the similar pattern, it did not prefer the former, whereas the control group (cs), which had only seen white walls of the aquarium, still preferred the originally learnt pattern. The same happened when es learnt a similar pattern by reward after the memory of the original pattern had been consolidated. In another set of experiments the negative influence of post-exposure could be demonstrated in facilitation of later learning the postexposed pattern as positive versus the originally learnt pattern, now negative. When es had seen a dissimilar wall-paper pattern then the memory of the primarily learnt pattern was not disturbed. A tentative explanation is based on the notion that two similar engrams have part of the neuronal network in common.     

Phyllanthus section Choretropsis (Euphorbiaceae) in Brazil

Section Choretropsis genus Phyllanthus (Euphorbiaceae) is formed by plants whose branches are modified into phylloclades. Despite the suitable characteristics of phylloclades within the Phyllanthus genus, the systematics of these species are poorly understood. Morphological data are presented here to allow future revision of this taxonomic group. The section is represented by nine species distributed in South America, eight of them endemic to Brazil. Our taxonomic studies distinguish the species and propose the synonymization of nine varieties of P. klotzschianus and two varieties of P. flagelliformis based on vegetative and reproductive characters. The diversity of branching and the morphology of phylloclades are discussed.  © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 150 , 131–164.     

Phylloclade anatomy in Phyllanthus section Choretropsis (Phyllanthaceae)

The phylloclade anatomy of nine Brazilian species of the genus Phyllanthus section Choretropsis was studied, and its systematic significance was analysed. The arrangement of epidermal cells varied according to the species, with the guard cells of the stomatal apparatus distributed randomly or with the longitudinal axis parallel to the branch. In both branch types, the stomata were distributed on the phylloclade surface, except in P. gladiatus which showed hypostomatic branches. In most of the species, phylloclades developed a vascular system surrounded by clusters of fibres and cortical parenchyma, which could differentiate into palisade‐like tissue and ground tissue like a true leaf blade. The distribution of the vascular system followed the cylindrical or flattened diameter shape of the branch. In subsection Choretropsis, the cylindrical branches of P. choretroides, contrary to other species, developed a second ring formed by clusters of fibres surrounded by large parenchymal cells. In subsection Applanata, the palisade‐like cells of P. flagelliformis phylloclades acquired an isodiametric shape. The highest level of specialization was observed in P. gladiatus, which developed phylloclades with a dorsiventral structure, a main vein, and small sets of lateral vascular bundles like a typical leaf blade. The tissue arrangement of different species showed a gradual pattern, which was correlated with the different branch morphology and plant architecture. Despite the transitional pattern, it was suggested that some of the phylloclades had an independent origin and convergent evolution in the Choretropsis section. The anatomy of different branch types was shown to be useful, either in isolation or in association with other morphological characters, to delimit the species and to further understand their relationships and phylogeny. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 157 , 91–102.     

Small GTP-binding Proteins Associated with Secretory Vesicles of Paramecium

GTP-binding proteins act as molecular switches in a variety of membrane-associated processes, including secretion. One group of GTP-binding proteins, 20–30 kDa, is related to the product of the ras proto-oncogene. In Saccharomyces cerevisiae, ras -like GTP-binding proteins regulate vesicular traffic in secretion. The ciliate protist Paramecium tetraurelia contains secretory vesicles (trichocysts) whose protein contents are released by regulated exocytosis. Using [α-³²P]GTP and an on-blot assay for GTP-binding, we detected at least seven GTP-binding proteins of low molecular mass (22–31 kDa) in extracts of Paramecium tetraurelia. Subcellular fractions contained characteristic subsets of these seven; cilia were enriched for the smallest (22 kDa). The pattern of GTP-binding proteins was altered in two mutants defective in the formation or discharge of trichocysts. Trichocysts isolated with their surrounding membranes intact contained two minor GTP-binding proteins (23.5 and 29 kDa) and one major GTP-binding protein (23 kDa) that were absent from demembranated trichocysts. This differential localization of GTP-binding proteins suggests functional specialization of specific GTP-binding proteins in ciliary motility and exocytosis.