Bark Tissue (bark + tissue)

Distribution by Scientific Domains
Distribution within Life Sciences


Selected Abstracts


The effect of periderm formation in the cortex of Pinus thunbergii on early invasion by the pinewood nematode

FOREST PATHOLOGY, Issue 3 2000
Y. Ichihara
Summary The distribution of cortical resin canals and periderm formation in the cortex of Pinus thunbergii was studied in relation to early invasion of the pinewood nematode, Bursaphelenchus xylophilus. Nematode invasion was restricted in stem cuttings of P. thunbergii in which periderm closed cortical resin canals. Early invasion of the nematodes was also restricted in stem cuttings where wound periderm had formed in response to prior nematode inoculation. It was concluded that early invasion of pinewood nematodes in living bark tissue is restricted by periderm in mature stems and by wound periderm that had formed as the result of previous nematode infection. [source]


Impact of Elevated PCO2 on Mass Flow of Reduced Nitrogen in Trees,

JOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 12 2006
Xi-Ping Liu
Abstract To analyze the effects of elevated carbon dioxide concentration (PCO2) on the mass flow of reduced nitrogen (N) in the phloem and xylem of trees, juvenile beech (Fagus sylvatica L.) and spruce (Picea abies (L.) Karst.) were grown in phytotrons and exposed to ambient and elevated PCO2 (plus 687.5 mg/m3 CO2) for three growing seasons. Elevated PCO2 significantly decreased the mass flow of N from the shoot to roots of beech by significantly reducing the concentration of soluble amino compounds in the phloem, even if the area of conductive phloem of cross-sectional bark tissue was significantly increased, because of less callus deposition in the sieve elements. In spruce, the downward mass flow of reduced N also tended to be decreased, similar to that in beech. Resembling findings in the phloem, N mass flow from roots to shoot in both tree species was significantly diminished owing to significantly reduced concentrations of amino compounds in the xylem and a lower transpiration rate. Therefore, the mass flow of reduced N between shoots and roots of trees was mainly governed by the concentrations of soluble amino compounds in the phloem and xylem in relation to the loading of reduced N in both long-distance transport pathways. (Managing editor: Ya-Qin Han) [source]


Detection and Identification of Brenneria nigrifluens, the Causal Agent of the Shallow Bark Canker of Walnut by, PCR Amplification

JOURNAL OF PHYTOPATHOLOGY, Issue 7-8 2008
S. Loreti
Abstract A 1 kb DNA band from strains of Brenneria nigrifluens, as shown by amplification of their genomic DNA by polymerase chain reaction (PCR) using minisatellite primer designed on the minisatellite sequence of the M13 phage, was isolated, cloned and sequenced. Specific oligonucleotides (F1,C3) were selected into this 1 kb DNA sequence and used in a PCR assay to detect and identify strains of B. nigrifluens. Several strains of B. nigrifluens were assessed with F1,C3 primers producing a specific band of approximately 250 bp pairs in length. This target was successfully amplified from purified genomic DNA, from bacterial culture and directly from infected walnut bark tissue. No amplification was obtained when the PCR assay was performed on other plant-pathogenic species from the following genera Brenneria, Erwinia, Agrobacterium, Pseudomonas, Ralstonia, Pectobacterium, Xanthomonas and from walnut-associated bacteria, indicating the specificity of these primers. The PCR assay with the primers described here provides a rapid, specific and sensitive diagnostic method for B. nigrifluens and a useful tool for epidemiological studies. [source]


Phomopsis alnea, the cause of dieback of black alder in Italy

PLANT PATHOLOGY, Issue 6 2002
S. Moricca
Black alder (Alnus glutinosa) occurs naturally on moist soils and along streams and rivers throughout most of its range. Groves of this species in north-central Italy were recently found to be attacked by the mitosporic coelomycete Phomopsis alnea, which causes perennial stem cankers and dieback. The fungi Melanconium apiocarpium and a Hymenopsis sp. were also frequently found on necrotic alder tissue, occasionally invading the living bark. All these fungi were tested for pathogenicity in two seasonal inoculation trials on seedlings of black alder, Italian alder (Alnus cordata) and green alder (Alnus viridis) that were either normally watered or water-stressed. Phomopsis alnea actively colonized the seedlings and reproduced the symptoms observed in the field. The other fungi behaved as weak parasites, only occasionally spreading to apparently healthy bark tissue. It appears that these fungi are saprobes, commonly colonizing bark and twigs already killed by P. alnea. Symptoms caused by P. alnea in the field were exacerbated on dry sites and by seasonal drought stress. On artificially inoculated and water-stressed seedlings, both the incidence and severity of P. alnea also increased, causing extensive mortality. The data provide evidence for the belief that P. alnea becomes a factor in the dieback of natural black alder woodlands when trees are first impaired by wounding agents and then subjected to unusual extended drought. [source]


Targeted gene analysis in Ulmus americana and U. pumila tissues

FOREST PATHOLOGY, Issue 2 2008
C. Nasmith
Summary Steady-state gene expression was compared between Dutch elm disease (DED)-susceptible Ulmus americana and DED-resistant U. pumila callus, leaf midrib, root and inner bark tissues. Stress-related cDNAs including phenylalanine ammonia-lyase (PAL), chitinase (CHT) and polygalacturonase-inhibiting protein (PGIP) were isolated and compared following RT-PCR of elm tissues. Complete CHT and partial PAL and PGIP cDNA transcripts were identified, each displaying sequence variation between elm species. These transcripts were Dig-labelled and subsequently used for northern analyses of the elm tissues. Midrib and root tissue displayed highest steady-state gene expression compared with inner bark and callus tissues. A modified nucleic acid isolation technique was necessary for downstream RNA analyses. Lithium chloride and polyvinylpyrrolidone were critical for efficient removal of polysaccharides and phenolics associated with some of the elm tissues. Steady-state gene expression is discussed in relation to the tissues investigated. The use of tissues other than in vitro callus culture more closely represents the tissues associated with the elm's vascular response to DED. [source]


Vegetative Storage Protein with Trypsin Inhibitor Activity Occurs in Sapindus mukorassi, a Sapindaceae Deciduous Tree

JOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 4 2009
Shi-Biao Liu
Abstract A vegetative storage protein (VSP) with trypsin inhibitor activity in a deciduous tree, Sapindus mukorassi, was characterized by means of sodium dodecyl sulfate-polyacrylamide gel electrophoresis, Western-blot, immuno-histochemical localization, light- and electro-microscopy, together with analysis of proteinase inhibitor activity of the purified VSP in vitro. There were two proteins with molecular masses of about 23 and 27 kDa in a relatively high content in the bark tissues of terminal branches of S. mukorassi in leafless periods. The proteins decreased markedly during young shoot development, indicating their role in seasonal nitrogen storage. Immuno-histochemical localization with the polyclonal antibodies raised against the 23 kDa protein demonstrated that the 23 kDa protein was the major component of protein inclusions in protein-storing cells. The protein inclusions were identified by protein-specific staining and should correspond to the electron-dense materials in different forms in the vacuoles of phloem parenchyma cells and phloem ray parenchyma cells under an electron microscope. So, the 23 kDa protein was a typical VSP in S. mukorassi. The 23 and 27 kDa proteins shared no immuno-relatedness, whereas the 23 kDa protein was immuno-related with the 22 kDa VSP in lychee and possessed trypsin inhibitor activity. The 23 kDa protein may confer dual functions: nitrogen storage and defense. [source]