?Transfer cells? Plant cells with wall ingrowths, specialized in relation to short distance transport of solutes?Their occurrence, structure, and development

PROTOPLASMA ◽  
1969 ◽  
Vol 68 (1-2) ◽  
pp. 107-133 ◽  
Author(s):  
B. E. S. Gunning ◽  
J. S. Pate
1970 ◽  
Vol 23 (3) ◽  
pp. 709 ◽  
Author(s):  
TP O'brien ◽  
S Zee ◽  
JG Swift

Wooding and Northcote (1965), Gunning, Pate, and Briarty (1968), Gunning and Pate (1969), and Pate and Gunning (1969) have drawn attention recently to the presence of cells with wall ingrowths in a number of sites in plants at which one might expect short-distance transport of considerable quantities of solutes. Gunning and Pate (1969) suggested that these cells be called "transfer cells" and surveyed their distribution in the leaves of a large sample of Angiosperms. These cells have not been found in the leaves of any grasses, and they have been demonstrated in the Gramineae only in the embryo sac of maize (Diboll 1968). In this paper, transfer cells are illustrated in the vascular tissue at the coleoptilar node in wheat, and the possible functions of these cells at this site are discussed.


Animals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 177 ◽  
Author(s):  
Gizella Aboagye ◽  
Stefania Dall’Olio ◽  
Francesco Tassone ◽  
Martina Zappaterra ◽  
Salvatore Carpino ◽  
...  

Despite the increasing interest in the welfare of animals during transport, very little is known on the response of local pig breeds to the transport procedures. This study aims to compare the effect of short journey on behaviour, blood parameters, and meat quality traits in 51 Apulo-Calabrese and 52 crossbreed [Duroc × (Landrace × Large White)] pigs. All the animals were blood sampled five days before delivery (basal condition) and at exsanguination for the analysis of creatine kinase, cortisol, glucose, lactate, albumin, albumin/globulin, total protein, urea, creatinine, aspartate aminotransferase (AST), alanine aminotransferase, alkaline phosphate, sodium, and potassium. Post mortem pH, color, drip loss, cooking loss, and Warner-Bratzler shear force were measured at different times in longissimus thoracis samples. Univariate and multivariate analyses showed that glucose, albumin/globulin, urea, and AST at exsanguination were influenced by the genetic type. Apulo-Calabrese showed the highest increase in blood values of lactate, creatinine, sodium and potassium after the short distance transport. Behavioural occurrences were similar in both genetic types during unloading and lairage. Small differences were observed for meat quality although significantly higher a* and lower L* were found in Apulo-Calabrese pigs, showing meat with a deeper red colour than crossbreeds.


1986 ◽  
Vol 64 (1) ◽  
pp. 177-192 ◽  
Author(s):  
H. B. Massicotte ◽  
R. L. Peterson ◽  
C. A. Ackerley ◽  
Y. Piché

Alnus crispa (Ait.) Pursh seedlings were grown in plastic pouches and inoculated with Frankia to induce nodules and subsequently with Alpova diplophloeus (Zeller & Dodge) Trappe & Smith to form ectomycorrhizae. The earliest events in ectomycorrhiza formation involved contact of the root surface by hyphae, hyphal proliferation to form a thin mantle, and further hyphal growth to form a thick mantle. Structural changes in the host, the mycosymbiont, and the fungus–epidermis interface were described at various stages in the ontogeny of ectomycorrhizae. Fungal hyphae in contact with epidermal cells in the regions of intercellular penetration and paraepidermal Hartig net developed numerous rough endoplastic reticulum cisternae. In more proximal regions of the mycorrhiza, these gradually became fewer in number and smooth. A complicated labyrinthine wall branching system also developed in the fungus in these regions. Concurrently, epidermal cells formed wall ingrowths in regions adjacent to Hartig net hyphae. There was a gradient in the formation of these epidermal transfer cells as the mycorrhiza developed, and an additional deposition of secondary cell wall over the wall ingrowths occurred as transfer cells senesced. Nonmycorrhizal control roots did not develop epidermal wall ingrowths. Electron-dense material, which was also autofluorescent, was deposited in the outer tangential walls of the exodermis contiguous to the paraepidermal Hartig net.


2010 ◽  
Vol 1 (2) ◽  
pp. 15 ◽  
Author(s):  
Yankun Zheng ◽  
Zhong Wang

Endosperm transfer cells mainly occur in the epithelial layer of the endosperm and transport the nutrient unloaded by the maternal vascular tissue. They have wall ingrowths that can facilitate solute transportation. Here we report our further investigation of endosperm transfer cells in sorghum (Sorghum bicolor L. Moench). We observed endosperm transfer cells, embryo, and endosperm with different kinds of microscopes. Our experimental results showed that the distribution and configuration of endosperm transfer cells were fit for solute transportation, and they had a tight relationship with the embryo and endosperm.


2018 ◽  
Vol 6 ◽  
Author(s):  
Jana S. Segmehl ◽  
Alessandro Lauria ◽  
Tobias Keplinger ◽  
John K. Berg ◽  
Ingo Burgert

PROTOPLASMA ◽  
2012 ◽  
Vol 250 (2) ◽  
pp. 495-503 ◽  
Author(s):  
Paulo Monjardino ◽  
Sara Rocha ◽  
Ana C. Tavares ◽  
Rui Fernandes ◽  
Paula Sampaio ◽  
...  

1975 ◽  
Vol 53 (5) ◽  
pp. 432-438 ◽  
Author(s):  
Edward C. Yeung ◽  
R. L. Peterson

A number of cytological changes occur in rhizome transfer cells with age, the most striking being the appearance of microbodies each with a crystalline nucleoid and the presence of unusual plastids. Plastids in older transfer cells develop one or more electron-translucent regions and lack a defined thylakoid system. The number and size of vacuoles increases until ultimately one large vacuole is formed in old transfer cells. Accompanying these cytological changes in the cytoplasm the wall ingrowths change from being highly involuted and reaching a considerable distance into the cytoplasm of the cell to becoming thicker and less numerous, and finally form a rather uniformly thickened wall layer. The orientation of microfibrils in the thickened cell wall, resulting from the joining of the original wall projections adjacent to the tracheary elements, is random, while the wall thickenings away from the tracheary elements have more orderly arrangements of cellulose microfibrils.


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