Anatomy of the Legume Nodule Cortex: Species Survey of Suberisation and Intercellular Glycoprotein

1996 ◽  
Vol 23 (2) ◽  
pp. 211 ◽  
Author(s):  
SM Brown ◽  
KB Walsh

Nodules of 29 species from 23 legume genera were examined for suberisation and glycoprotein deposits. Extensive suberisation of the nodule outer cortex to form a peridem was considered a primitive feature, common to non-legume and caesalpinioid nodules. The periderm was less extensive in nodules of Mimosoideae and Papilionoideae. Vascular bundles within the nodule were always surrounded by a vascular endodermis, defined by the presence of suberin on radial walls. Suberisation of the tangential walls of this endodermis was considered to be a primitive feature (present in all species examined of Caesalpinioideae and Mimosoideae, and in 10 out of 21 Papilionoideae) which may limit solute import to and export from the nodule. Glycoprotein was observed in the apoplast of the cortex in the three papilionoid species examined, but was absent in the caesalpinioid species examined. The common endodermis was recognised as an advanced feature, present only in certain species of the subfamily Papilionoideae (5 of 7, and 11 of 15 species of indeterminate and determinate nodule growth respectively). A membrane impermeant dye (lucifer yellow-CH), supplied in the rhizosphere under a mild vacuum, was observed to infiltrate through the cortex and into the infected zone in caesalpinioid nodules, and as far as the inner cortex in mimosoid and papilionoid nodules. Thus the common endodermis does not serve as an apoplastic barrier, and is unlikely to serve as a significant oxygen 'diffusion barrier'.


In the fourth of this series of Memoirs (‘Phil. Trans.,' 1873, p. 377, et seq .) I described a remarkable plant under the name of Dictyoxylon Oldhamium ; I also gave reasons for substituting the late Mr. Gourlie ’s generic name of Lyginodendron for that of Dictyoxylon . In the same Memoir (p. 403) I referred to some petioles, to which I proposed to assign the name of Edraxylon ; but later researches demonstrated the necessity for abandoning this as a generic term and substituting for it the more comprehensive one of Rachiopteris aspera . In my Memoir, Part VI. ('Phil. Trans.,' 1874, Plate 2, p. 679, et seq .), I described this proposed Edraxylon under the name of Rachiopteris aspera . Certain similar features exhibited by the above two plants led me to remark in Memoir IV., p. 403, after showing that the Rachiopteris aspera was obviously the petiole of a Fern, “I think it far from impossible that these may prove to belong to Dictyoxylon ( Lyginodendron ) Oldhamium ; but since I have not yet succeeded in correlating them with any certainty, 1 shall add no more respecting them at present.” Since 1873 1 have accumulated a vast amount of material illustrative of the structure and relations of these two plants, and am now in a position to demonstrate that they respectively represent the stem and petiole of the same organism which proves to be a Fern. I was long under the conviction that the remarkable exogenous development of the stems of many of the Carboniferous Cryptogams, which I have so continuously demonstrated to exist, and which is now so universally recognised by Palæontologists, had no existence amongst Ferns. I have now to show that this development did exist amongst Ferns as well as amongst the arborescent Lycopods and Calamites, in which it is so conspicuous. Fig. 1 (Plate 12) is part of a transverse section of a stem or branch of Lyginodendron Oldhamium , in which a represents the medulla; b , the exogenous xylem zone; c , the place of the inner cortex, wanting in this specimen; d , one of the pairs of vascular bundles, so characteristic of the, cortex of this plant; e , the outermost cortex, composed, in transverse sections, of radiating bands of sclerenchyma, g , alternating with parenchymatous areas, f . At k, k we find two bundles of tracheids, like those at d , forming the centre of the cortical structures of a petiole of Rachiopteris aspera , i, i , which petiole is organically united to the cortex e of the Lyginodendron . The two bundles k, k are assuming the oblique relative positions seen in the similar bundles of the free petiole of R. aspera , represented in fig. 2. Other sections in my cabinet, similar to fig. 1, demonstrate the same facts, viz., that the pairs of bundles, fig. 1, d , which form so characteristic a feature of transverse sections of the middle cortex of Lyginodendrom Oldhamium , pass outwards, through the outer cortex, to become the tracheæal bundles of the petioles of the plant, and which petioles I had previously designated Rachiopteris aspera . I may state that my friend Graf Solms-Laubach, who has obtained numerous specimens of the Lyginodendron associated with others of Rachiopteris aspera from a locality on the continent, agrees with me in the conclusion at which I have arrived respecting their unity. The more perfect specimens of the Lyginodendron obtained during the last seventeen years have thrown yet further light upon those figured in 1873. In the latter, as at fig. 1, c, no traces of the middle bark were preserved; but examples from Halifax, for which I am indebted to my friends Mr. Cash and Mr. Spencer, of Halifax, have supplied what was wanting. Fig. 3 is a transverse section in which this inner cortex, c , is shown to consist of a zone of extremely delicate, thin-walled parenchymatous cells, scattered throughout which are numerous gum-canals, l . Three of these canals are represented, enlarged 250 diameters, in figs. 4 and 5, embedded in the thin-walled cells, c, c , of the cortex.



1994 ◽  
Vol 21 (1) ◽  
pp. 49 ◽  
Author(s):  
SM Brown ◽  
KB Walsh

We describe the anatomy of the cortex of a range of legume nodules (43 species of 31 genera of 13 tribes, principally of the Papilionoideae). To our knowledge, the nodule anatomy of 19 of the genera examined (30 species) was previously unreported. All nodules have a layer(s) in the inner cortex with distorted radial walls ('boundary layer') and occlusions of the intercellular spaces within the middle cortex. The 'nodule endodermis' as defined by Frazer (1942) was difficult to identify unless modified by sclerification or tannin deposition. In other species, the outer cortex contains a well developed periderm, often with several layers of tannin-containing cells. When present, sclereids contain a living cytoplasm, and are interspersed with parenchyma cells to form a water-filled barrier c. 50 μm in width about the nodule. Nodule sclereids are apparent within 5 days of inoculation in Glycine max. Sclerification of the common endodermis did not significantly increase following growth at 50 or 80% rhizosphere pO2. We suggest that the intercellular space deposition, the common endodermal layer and the periderm layer will act as a fixed resistance to gas diffusion into the nodule, allowing for a fine control of a variable resistance (boundary) layer within the inner cortex.



1982 ◽  
Vol 30 (2) ◽  
pp. 189-191 ◽  
Author(s):  
R L Michaels

Lucifer Yellow CH may be injected into pancreatic islet cells and visualized in Epon sections of the embedded tissue both before and after plastic removal and immunocyto-chemical staining. The dye retains its fluorescence, clearly marking the injected cell and adjacent dye-coupled cells, but does not interfere with the indirect immunofluorescent staining patterns that are characteristic of the islet cells



2000 ◽  
Vol 279 (2) ◽  
pp. R629-R638 ◽  
Author(s):  
Kate M. Denton ◽  
Warwick P. Anderson ◽  
Raja Sinniah

The diversity of renal arteriole diameters in different cortical regions has important consequences for control of glomerular capillary pressure. We examined whether intrarenal angiotensin II (ANG II; 0.1, 1, or 5 ng · kg−1 · min−1) in anesthetized rabbits acts preferentially on pre- or postglomerular vessels using vascular casting. ANG II produced dose-related reductions in afferent and efferent diameters in the outer, mid, and inner cortex, without effecting arterial pressure. Afferent diameter decreased more than efferent in the outer and mid cortex ( P < 0.05) but by a similar extent in juxtamedullary nephrons ( P = 0.58). Calculated efferent resistance increased more than afferent, especially in the outer cortex (127 vs. 24 units; 5 ng · kg−1 · min−1 ANG II). ANG II produced significant dose-related increases in the distance between the arterioles at the entrance to the glomerular pole in all regions. Thus afferent diameter decreased more in response to ANG II, but efferent resistance rose more due to smaller resting luminal dimensions. The results also indicate that glomerular pole dimensions change in response to ANG II.



Blood ◽  
1989 ◽  
Vol 74 (2) ◽  
pp. 645-651 ◽  
Author(s):  
ST Koury ◽  
MJ Koury ◽  
MC Bondurant ◽  
J Caro ◽  
SE Graber

Abstract In situ hybridization was used to quantitate the cells that produce erythropoietin (EP) in the renal cortices of mice with varying severities of acute anemia and of mice recovering from severe, acute anemia. The number of EP-producing cells in the renal cortex increased in an exponential manner as hematocrit was decreased. Individual EP- producing cells had very similar densities of silver grains in autoradiograms regardless of whether they were from normal mice or from slightly, moderately or severely anemic animals. With increasingly severe anemia, total renal EP mRNA levels and serum EP concentrations showed increases that correlated with the number of renal EP-producing cells. These results indicate that as mice become more anemic, additional cells are recruited to produce EP rather than the cells already producing EP being stimulated to increase their individual production. In mildly and moderately anemic animals, small clusters of EP-producing cells were found in the inner cortex with large areas of cortex containing no EP-producing cells. In severely anemic mice, EP- producing cells were found throughout the inner cortex with only a very few found scattered in the outer cortex and outer medulla. The data indicate that only a subset of total renal interstitial cells produce EP. During recovery from severe, acute anemia, the numbers of EP- producing cells decreased exponentially as hematocrits rose and correlated with decreases in total renal EP mRNA and serum EP concentrations. These results suggest that following an acute blood loss and during the recovery from a blood loss, the capacity to deliver oxygen, as represented by hematocrit, is the major regulator of EP production.



2017 ◽  
Vol 26 (2) ◽  
pp. 9
Author(s):  
Darius Batulevičius ◽  
Gertrūda Skripkienė ◽  
Greta Graužinytė ◽  
Augustina Grigaitė ◽  
Valdas Skripka

This study was designed to compare the morphology of neurons in relation to their distance from the major nerve trunks in the heart of the frog Rana temporaria. Seventy-nine intracardiac neurons were labelled intracellularly with fluorescent markers Lucifer Yellow CH and Alexa Fluor 568. The neurons located on the extensions of the vagus nerve were considered as ganglionic, while neurons spread loosely at further distance from these extensions were considered as non-ganglionic. The mean area of the soma in ganglionic neurons was about 25% larger than in non-ganglionic neurons. Ganglionic neurons had a higher soma area/nucleus area ratio than non-ganglionic neurons. Although both the total number and the total length of dendrite-like processes was similar between the two groups, ganglionic neurons had significantly fewer dendrite-like processes from the soma (1.5±0.3 vs. 3.9±1.0; P<0.05) and shorter total length of these processes from the soma (63±18 μm vs. 178±51 μm; P<0.05). In conclusion, ganglionic and non-ganglionic frog intracardiac neurons exhibit substantial morphological differences. We hypothesize that these differences may indicate different projections or variations in the number of their preganglionic inputs.



2015 ◽  
Vol 55 (2) ◽  
pp. 149-181
Author(s):  
Agata Jarzynka ◽  
Grzegorz Pacyna

AbstractSphenopsid remains from Grojec clays (Grojec, Poręba, Mirów) collected and described by Raciborski in 1894 are re-examined for the first time and supplemented by Raciborski’s unpublished material housed at the Jagiellonian University (Institute of Botany) and by Stur’s preliminarily described material stored at the Geological Survey of Austria. Three species of Equisetum created by Raciborski (Equisetum renaulti, E. remotum, E. blandum) are now attributed to the common Jurassic species Equisetites lateralis, and the earlierundescribed Equisetites cf. columnaris is recognised. The occurrence of Neocalamites lehmannianus (originally described by Raciborski as Schizoneura hoerensis) has been confirmed from Grojec. The material that Raciborski referred to this species seems to be heterogeneous, and some specimens are now removed to the new proposed species Neocalamites grojecensis Jarzynka et Pacyna sp. nov. The new species is diagnosed by the following features: only a few prominent ribs present on shoot, leaf scars relatively large and ellipsoidal, numerous free leaves, vascular bundles alternate at node. Possibly the new species derives from Neocalamites lehmannianus or at least is closely related to it. Part of the poorly preserved remains can be determined only as Neocalamites sp. Another species created by Raciborski, Phyllotheca (?) leptoderma, is based on poorly preserved type specimens. Some of the unpublished specimens stored at the Jagiellonian University (Institute of Botany) correspond to Raciborski’s description, but considering the poor preservation of the original material and the not very realistic published illustrations of this species, they rather should be regarded as indeterminate cortical fragments of Neocalamites lehmannianus and/or badly preserved external cortical surfaces of the new species Neocalamites grojecensis. Phyllotheca (?) leptoderma should be considered a nomen dubium.



1983 ◽  
Vol 731 (2) ◽  
pp. 261-266 ◽  
Author(s):  
Charles L. Bowman ◽  
Henry Tedeschi




Sign in / Sign up

Export Citation Format

Share Document