Some effects of Ceratocystis ulmi on the phloem and vascular cambium of Ulmus americana

1972 ◽  
Vol 50 (5) ◽  
pp. 1009-1011 ◽  
Author(s):  
Jerry D. Davis ◽  
Roy Saigo ◽  
Ray F. Evert
Keyword(s):  
Vascular Cambium ◽  
Secondary Phloem ◽  
Ulmus Americana ◽  
American Elm ◽  
Fusiform Initials ◽  
Sieve Plates

Preliminary studies of naturally infected American elm trees show that abnormalities occur in the vascular cambium and the secondary phloem. Abnormalities include deposition of callose on sieve plates, septation of fusiform initials, lack of fiber differentiation, and accumulation of lipoidal substances in the vascular cambium. The sequence of these abnormalities and their importance in the death of the tree are yet to be determined.

Lateral sieve-area pores in woody dicotyledons

1971 ◽  
Vol 49 (8) ◽  
pp. 1509-1515 ◽  
Author(s):  
R. F. Evert ◽  
B. P. Deshpande ◽  
S. E. Eichhorn
Keyword(s):  
Electron Microscopy ◽  
Osmium Tetroxide ◽  
Populus Deltoides ◽  
Robinia Pseudoacacia ◽  
Quercus Alba ◽  
Secondary Phloem ◽  
Salix Nigra ◽  
Ulmus Americana ◽  
P Protein ◽  
Sieve Plates

The secondary phloem of seven species of woody dicotyledons (Populus deltoides, Quercus alba, Rhus glabra, Robinia pseudoacacia, Salix nigra, Tilia americana, and Ulmus americana) was fixed in glutaraldehyde and in formaldehyde–glutaraldehyde and postfixed in osmium tetroxide for electron microscopy. The pores of the lateral sieve areas are essentially similar in structure to those of the sieve plates, with the exception that many of the lateral sieve-area pores contain median nodules at maturity. In addition, some pore groups in Rhus, Robinia, and Tilia are associated with median cavities, median enlargements arising through the union of two or more median nodules, similar to those associated with the sieve areas of conifers. The lateral sieve-area pores are lined by the plasmalemma and variable amounts of callose and contain P-protein. It has been concluded that the P-protein normally is loosely arranged in the pores.

Anatomy of the Secondary Phloem in Winteraceae

IAWA Journal ◽  
1984 ◽  
Vol 5 (1) ◽  
pp. 13-43 ◽  
Author(s):  
Katherine Esau ◽  
Vernon I. Cheadle
Keyword(s):  
Protein Body ◽  
Sieve Element ◽  
Secondary Phloem ◽  
Phloem Parenchyma ◽  
The Family ◽  
Companion Cells ◽  
Parenchyma Cells ◽  
Evolutionary Level ◽  
Fusiform Initials ◽  
Sieve Plates

The secondary phloem of nine species in five genera of Winteraceae was examined with regard to features that could serve for taxonomic and phylogenetic evaluation of the family. The species examined were as follows: Bubbia pauciflora, B. semecarpoides, Drimys lanceolata, D. winteri, Exospermum stipitatum, Pseudo wintera axillaris, Zygogynum baillonii, Z. bicolor, and Z. vinkii. The nine species showed the following common characteristics: 1) origin from nonstoried vascular cambium with long fusiform initials; 2) ray system consisting of high multiseriate and high uniseriate rays; 3) occurrence of secondary partitioning in the differentiating phloem so that the sieve elements are much shorter than the tracheids; 4) lack of sharp differentiation between lateral sieve areas and those of the sieve plates; 5) predominance of compound sieve plates; 6) short companion cells, often single in a given sieve element; 7) phloem parenchyma cells in strands; 8) lack of specialised fibres (bast fibres) in the secondary phloem; 9) presence of nondispersing protein body in the sieve element protoplast. Features numbered 1, 2, 4-6 are considered to be indications of low evolutionary level. The significance of the other three features (3, 7-9) requires further evaluation. Among these three is the secondary partitioning the occurrence of which seems to imply that in some taxa the well known sequence of evolutionary shortening of cambial initials and their derivatives may be accelerated on the phloem side.

Developmental Changes in the Wood of Bocconia Vulcanica Donn. Smith

IAWA Journal ◽  
1983 ◽  
Vol 4 (2-3) ◽  
pp. 131-140 ◽  
Author(s):  
Billy G. Cumbie
Keyword(s):  
Developmental Changes ◽  
Vascular Cambium ◽  
Secondary Phloem ◽  
Growth Rings ◽  
Axial Parenchyma ◽  
Primary Xylem ◽  
Thin Walls ◽  
Wood Fibres ◽  
Fusiform Initials ◽  
Square Cells

Developmental changes in the xylem were studied in a stem of Bocconia vulcanica Donn. Smith with a xylem radius of 3.0–4.5 cm. Growth rings are absent. The vascular cambium is nonstoried with fusiform initials averaging 282 µm long. The specialised vessel members are short, with oblique to transverse end walls, simple perforations, and alternate intervascular pitting. Vessels are relatively uniform in diameter and arrangement throughout the wood. Fibres have moderately thin walls and do not increase in length from the primary xylem to the cambium. Axial parenchyma is paratracheal, scanty to vasicentric. Rays are exclusively multiseriate, tall, and heterocellular with a predominance of erect and square cells. Sheath cells occur along the sides. There are no fibres in the secondary phloem and a periderm is not present. The xylem and bark are similar in many respects to that formed in some groups of dicotyledons that are basically herbaceous with evolution toward woodiness.

The Microscopy of Compatibility and Incompatibility in Ulmus

1985 ◽  
Vol 43 ◽  
pp. 504-505
Author(s):  
B. L. Redmond ◽  
Christopher F. Bob
Keyword(s):  
Dutch Elm Disease ◽  
Economic Losses ◽  
Hybrid Progeny ◽  
Ulmus Pumila ◽  
Ulmus Americana ◽  
American Elm ◽  
Asian Species ◽  
Ulmus Parvifolia ◽  
Initial Appearance ◽  
Chinese Elm

The American Elm (Ulmus americana L.) has been plagued by Dutch Elm Disease (DED), a lethal disease caused by the fungus Ceratocystis ulmi (Buisman) c. Moreau. Since its initial appearance in North America around 1930, DED has wrought inexorable devastation on the American elm population, triggering both environmental and economic losses. In response to the havoc caused by the disease, many attempts have been made to hybridize U. americana with a few ornamentally less desirable, though highly DED resistant, Asian species (mainly the Siberian elm, Ulmus pumila L., and the Chinese elm Ulmus parvifolia Jacq.). The goal is to develop, through breeding efforts, hybrid progeny that display the ornamentally desirable characteristics of U. americana with the disease resistance of the Asian species. Unfortunately, however, all attempts to hybridize U. americana have been prevented by incompatibility. Only through a firm understanding of both compatibility and incompatibility will it be possible to circumvent the incompatibility and hence achieve hybridization.

Phi Thickenings in Fossil Seed Plants from Antarctica

IAWA Journal ◽  
1987 ◽  
Vol 8 (3) ◽  
pp. 191-201 ◽  
Author(s):  
Michael A. Millay ◽  
Thomas N. Taylor ◽  
Edith L. Taylor
Keyword(s):  
Middle Triassic ◽  
Cell Layer ◽  
Vascular Cambium ◽  
Secondary Development ◽  
Water Regulation ◽  
Secondary Phloem ◽  
Primary Xylem ◽  
Sieve Cells ◽  
Ray Parenchyma ◽  
Cell Layers

Primary anatomy and secondary development is described for two root types from the Fremouw Peak locality (Transantarctic Mts, Antarctica) of early to middle Triassic age. Roots of Antarcticycas have a bilayered cortex with thick surface cuticle, diarch xylem, and a clearIy defined endodermis surrounded by a single cell layer possessing phi thickenings. Secondary development begins with phellern and phelloderm production from the out er primary phloem position, and is followed bya bifacial vascular cambium next to the primary xylem that pro duces sieve cells and ray parenchyma to the outside. Young roots of Antarcticoxylon are similar to those of Antarcticycas, but may possess 2-3 cell layers with phi thickenings. Secondary development from a bifacial vascular cambium produces alternating bands of sieve cells and phloem parenchyma cells in the secondary phloem and wood with uniseriate rays and scattered axial parenchyma. The presence of phi thickenings and an epidermal cutieie in both roots suggests environmental stress related to water regulation. The occurrence of phi thickenings in the roots of some conifers, angiosperms, a fossil cycad and a probable seed fern suggests this character is of ecological rather than phylogenetic significance.

Development of Included Phloem in the Stem of Combretum Nigricans (Combretaceae)

IAWA Journal ◽  
1995 ◽  
Vol 16 (2) ◽  
pp. 151-158 ◽  
Author(s):  
R. W. den Outer ◽  
W. L. H. van Veenendaal
Keyword(s):  
Secondary Xylem ◽  
Vascular Cambium ◽  
Secondary Phloem ◽  
Xylem Parenchyma ◽  
Long Period ◽  
Short Period ◽  
Outer Border

The development of diffuse included phloem strands in Combretum nigricans sterns is described, During a short period of time, a small phloem strand is cut off locally in an inward direction by an otherwise normal bidirectional vascular cambium. This contrasts with previous descriptions and interpretations because these strands are not formed after redifferentiation of secondary xylem parenchyma. A complementary cambium formed at the inner border of the young strand somewhat enlarges the strand and, during a relatively long period, produces secondary phloem outwards. Finally this complementary cambium stops functioning as a cambium and merges with the secondary phloem it has produced. Radial rows of cells are present within the included phloem strands which continue into the later-formed secondary xylem; rays transverse the strands. Crushing of the phloem takes place near the outer border of the strand, forming cap-like tissues of disorganized cells.

Anatomy of Pilostyles hamiltonii C. A. Gardner (Rafflesiaceae) in stems of Daviesia

1982 ◽  
Vol 30 (1) ◽  
pp. 1 ◽  
Author(s):  
B Dell ◽  
J Kuo ◽  
AH Burbidge
Keyword(s):  
Vegetative Growth ◽  
Host Cells ◽  
Vascular Cambium ◽  
Flower Initiation ◽  
Nutrient Requirements ◽  
Secondary Phloem ◽  
Undifferentiated Cells ◽  
Host Parasite

In Daviesia stems the vegetative body of Pilostyles hamiltonii occurs as thin strands of undifferentiated cells within the secondary phloem of the host. Parasite cells have prominent nuclei, extended plasmalemma, and lack chloroplasts and amyloplasts. Plasmodesmata are abundant between parasite and host cells. Early vegetative growth of the parasite appears to depend on host phloem tissues for its nutrient requirements. At flower initiation Pilostyles taps the host xylem by producing pegs of tissue across the vascular cambium of the host.

Vertical migration of rays leads to the development of a double-storied phenotype in the cambium of Aesculus turbinata

Botany ◽  
2008 ◽  
Vol 86 (1) ◽  
pp. 36-44 ◽  
Author(s):  
Elżbieta Myśkow ◽  
Beata Zagórska-Marek
Keyword(s):  
Vertical Migration ◽  
Hippophae Rhamnoides ◽  
Vascular Cambium ◽  
Common Descent ◽  
Hippophaë Rhamnoides ◽  
Fusiform Initials ◽  
Hippophae Rhamnoïdes L ◽  
Ray Cell ◽  
Ray Initials

In the vascular cambium of Aesculus turbinata (Blume) the double-storied structure develops slowly. Initially, the arrangement of primary rays is nonstoried. New secondary rays are initiated during cambial expansion. Rays grow by addition of new initials at both ray margins and then split by the intrusive elongation of adjacent fusiform cells. The repetitive splits give rise to groups of several rays of common descent. Initially, the secondary rays are also nonstoried. Later, they become organized into horizontal tiers. This results from the vertical migration of ray initials in the vascular cambium. Controlled polar additions and eliminations of ray-cell initials at the opposite margins of the ray continue until it reaches the appropriate position within the storey of fusiform initials. We postulate that there are at least two mechanisms for the formation and maintenance of ray tiers in cambium. They are unrelated to cell inclination changes, which as described earlier, are known to sometimes induce a double-storied phenotype. The first of these mechanisms, involves initiation of secondary rays exactly within the storeys of fusiform initials, as in Hippophaë rhamnoides L. The second mechanism, present in A. turbinata, is based on the dynamic, controlled migration of rays.

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