SUMMARY 1. Symptoms of infection on resistant and susceptible varieties of tomato (Lycopersicum esculentum Mill.) are briefly indicated, together with a numerical method of recording the progress of infection. 2. The histology of infection on tomato varieties is described. Penetration is stomatal and no appressoria or other modifications are formed. The mycelium is intercellular and without haustoria, and develops normally only for so long as the host cells are alive. 3. By the use of a controlled environment chamber, the frequency of penetration is shown to be far greater at a humidity fluctuating from saturation to 85 % than at constant saturation. The suggestion is made that penetration is controlled, in part at least, by a hydrotropic stimulus. 4. The initial rate of spread of the mycelium within the host, immediately subsequent to penetration, is lower in the variety “Mainerop” than in “Giant Red” and is lower also in the basal region of the plant than in the middle. This behaviour runs parallel with the subsequent differences observed in the external symptoms of infection. 5. Normal stomatal penetration occurs over a wide range of immune and “inappropriate” hosts. 6. Symptoms of infection have been recorded only in the varieties of L. esculentum, in L. Humboldtii Dun., and in two strains received as L. racemigerum which, appear to be more closely related to the cultivated varieties than, to the true currant tomato. 7. Confusion occurs as to the correct nomenclature of the currant tomato. The name Lycopersicum pimpinellifolium Mill, is preferred. L. racemigerum Lange (=Solanum racemigerum) and L. racemiforme Lange are synonyms. 8. The extent and distribution of the mycelium in the currant tomato appears to be determined largely by the age and relative maturity of the leaf. The mycelium is intercellular and without haustoria, and can apparently remain alive in the leaf for a considerable period of time. No conidiophores are produced. No reaction of the host cells is observed except where, on account of structural considerations, host and parasite are brought into more immediate contact. Here, individual host cells are frequently necrotic. 9. On many other Solanaceae, including species of Solatium, Hyos‐cyamus, Nicotiana, Schizanthus, and other genera, the course of events is essentially similar to that observed on the currant tomato. 10. In other Solanaceae, and in plants belonging to the Scrophu‐lariaceae, Compositae, and Cucurbitaceae, an extensive mycelium is never developed, even under apparently favourable conditions.
Wid fits IZ .nd 13 and 3 Tezt-figurcs) Usrum HYPODYTES was recorded by Berkeley & Broome (1841, 1850) and occurs on Elymw mclloritu and Agropyrvm species. A knowledge of its life-history on these plants appeared desirable in view of the possibility of an extension in host range to nearly related cmpls, added emphasis being given to this viewpoint by the recent production of perennial Ttitic~m-Agropynrm hybrids. Elynru~ m& is widely planted to prevent coastal erosion, and no knowledge was available of the dect of the fungus on its suitability for this purpose. The virtual absence of seed production by infected plants is known. In America, U~~o hypou'ytm was desaibed by Fischer (1938) as an increasing menace to the cultivation of AgropvMn rrisiahrm (L.) Beauv. and other valuable forage grasses. The disease on EZymur was studied by Bornhiivd (1936), who gave a full summary of the literature. She described the process of spore germination and the growth and nuclear behaviour of the fungus on artificial media, but dealt less adequately with the symptoms and spread of the disease and the histology of infection : her inoculation experiments were inconclusive. SmMsANDEFFEC'Is External mwphology of &eased shootsWilson (1910) states " . . .in the diseased shoot, in place of the ear, the upper part of the stem, where the ear ought to be, is changed into a series of short nodes, covered for the most part by leaf sheaths without blades. The nodes become shorter and shorter as they ascend, and at the top there is a flattened, deformed structure composed of a number of scales which are placed in a manner recalling to some degree the arrangement of the glumes and paleae of the normal spikelets." Bomhiivd (1936), and most other writers with the exception of Magnus (1896), overlooked the homology between the diseased shoots and the normal inflorescences, which is apparent from this account, and regarded the former merely as sterile leafy shoots ("Blattscho~se"). Comparisons have been made of the average height and number of internodes of the two kinds of shoot and different results have been obtained by Merent workers. Bornhsvd (1936) tends to regard these discrepancies as indications of the existence of biological specialization within the Ustilago hypodytes group.In the neighbourhood of Aberdeen the healthy flowering shoots were fairly uniform in height in different localities, the average height from the last rooting node being 100 cm. (74-117 an.). The diseased shoots were more variable (40-166 cm.); in some localities they were considerably shorter than the healthy, in others, taller. Comparisons of the number of internodes of the diseased and healthy shoots are permissible only between corresponding NOW at the T a Reaauch Institute of Ceylon, St Coombs, Talawakelle, Ceylon.r 330 I T. E. T. BOND 331regions of the stem. The flowering stems have from four to six vegetative internodes exceeding 0.5 cm. in length and an average of twenty-three internodes in the inflorescence. The ears average about 22 cm. in length, which is abou...
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