Regulation of Leaf Form in Centaurea solstitialis L. II. The Developmental Potentialities of Excised Leaf Primordia in Sterile Culture

1970 ◽  
Vol 131 (1) ◽  
pp. 39-49 ◽  
Author(s):  
Lewis J. Feldman ◽  
Elizabeth G. Cutter
1986 ◽  
Vol 64 (11) ◽  
pp. 2645-2649 ◽  
Author(s):  
E. K. Merrill

Green ash (Fraxinus pennsylvanica var. subintegerrima) seedlings are heteroblastic; during development they produce two types of leaves, simple and compound. When grown under controlled conditions, the sequence of leaf types is predictable. Simple leaves are always at the first four nodes; compound leaves are always at node 8 and above. Nodes 5 through 7 have progressively fewer simple leaves and more compound leaves. Leaf growth on seedlings meets the preconditions of the plastochron index and leaf plastochron index. These indices, as well as the length of single expanding leaves, can be used to predict lengths of leaf primordia at nodes 4 and 8 so that early, simple and compound leaf development can be compared in further studies of green ash.


1967 ◽  
Vol 45 (11) ◽  
pp. 2109-2113 ◽  
Author(s):  
Charles Carroll Kuehnert

In the fern Osmunda cinnamomea, leaf primorida may be excised and grown in sterile culture before or subsequent to their irreversible determination as leaves. It has been demonstrated that P3 primordia (third-oldest primordia) are not irreversibly determined as leaves at the time of excision for they exhibit a tendency to develop as shoots rather than leaves when cultured aseptically. When grown singly they become shoots 75.0% of the time; when grown in physiological contact as paired units they exhibit a tendency to become shoots at approximately the same level. The hypothesis that the active site of leaf determination is through the direct or indirect control of the shoot apical meristem is questioned and an alternative hypothesis is proposed which suggests that a morphogenetic factor is formed in older primordia which will diffuse to younger primordia to influence younger primordia to develop as leaves rather than shoots. The latter hypothesis is supported by experiments in which P3 primordia grown in physiological contact (as pairs) with P10 or P12 primordia produce more than twice as many leaves as unpaired or paired P3 primordia.


1969 ◽  
Vol 47 (1) ◽  
pp. 69-72 ◽  
Author(s):  
Charles Carroll Kuehnert

Undetermined P3 leaf primordia of the fern Osmunda cinnamomea were excised and grown in sterile culture, as pairs, with P12 or P13 primordia, primordia already irreversibly determined as leaves. Undetermined P3 primordia of a pair (P3 with P3 or P3 with P12) separated by an impervious barrier membrane (mica sheets) exhibit a tendency to develop as shoots rather than leaves. When the barrier membrane was a Millipore Filter, P3's growing with other P3's also exhibited the tendency to develop as shoots. By contrast, undetermined P3 primordia of a pair (P3 with P13) separated by a Millipore Filter barrier membrane exhibit the tendency to develop as leaves. These results would suggest that cell-to-cell contact is not a necessary adjunct to transmission of a leafness morphogen, and they present still further evidence in favor of a hypothesis that determination of a leaf primordium as a leaf may be under the control of more than one control center, and that one such control center is associated with certain of the older leaf primordia of a sibling series.


1969 ◽  
Vol 47 (1) ◽  
pp. 59-63 ◽  
Author(s):  
Charles Carroll Kuehnert

In the fern Osmunda cinnamomea, leaf primordia may be excised and grown in sterile culture before or after their irreversible determination as leaves. It has been demonstrated that P3 primordia (third most recently formed primordia) are not irreversibly determined as leaves at the time of excision for they exhibit a tendency to develop as whole shoots (approximately 67.0% of the time) whether grown singly, or as pairs grown in physiological contact. Results from the present investigation support the hypothesis that a morphogenetic factor(s) is found in older primorida which is transmitted to younger primordia to influence the latter to develop as leaves rather than shoots, for P3's grown in physiological contact (as pairs) with P10, P12, or P13 primordia are expressed as leaves at a level approximately twofold or greater than P3's grown singly (controls). Results from the present investigation do not support the hypothesis that increased bulk of tissue, and therefore increased capacity for nutrient productivity by older and larger primordia, is responsible for imposition of leafness on undetermined P3 primordia, for P14 primordia grown in physiological contact with P3 primordia (as pairs) are observed to increase the percentage of P3's expressing leafness at a level only slightly greater than P3's grown singly, and slightly less than when P3's are grown in physiological contact with other P3's as pairs. The slight enhancement in leafness exhibited by undetermined P3's grown as pairs with other P3's, or with P14's has been shown to be non-significant at the 5% level (P < 0.05) by the standard t test and Kramer's (1956) modification of Duncan's (1955) new multiple range test.


Author(s):  
Glenn M. Cohen ◽  
Radharaman Ray

Retinal,cell aggregates develop in culture in a pattern similar to the in ovo retina, forming neurites first and then synapses. In the present study, we continuously exposed chick retinal cell aggregates to a high concentration (1 mM) of carbamylcholine (carbachol), an acetylcholine (ACh) analog that resists hydrolysis by acetylcholinesterase (AChE). This situation is similar to organophosphorus anticholinesterase poisoning in which the ACh level is elevated at synaptic junctions due to inhibition of AChE, Our objective was to determine whether continuous carbachol exposure either damaged cholino- ceptive neurites, cell bodies, and synaptic elements of the aggregates or influenced (hastened or retarded) their development.The retinal tissue was isolated aseptically from 11 day embryonic White Leghorn chicks and then enzymatically (trypsin) and mechanically (trituration) dissociated into single cells. After washing the cells by repeated suspension and low (about 200 x G) centrifugation twice, aggregate cell cultures (about l0 cells/culture) were initiated in 1.5 ml medium (BME, GIBCO) in 35 mm sterile culture dishes and maintained as experimental (containing 10-3 M carbachol) and control specimens.


2020 ◽  
Vol 13 (3-4) ◽  
pp. 267-275
Author(s):  
Pablo I. Becerra ◽  
Lohengrin Cavieres ◽  
Ramiro O. Bustamante

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