THE UNIVERSITY OF ILLINOIS LIBRARY AGRICULTURAL LIBRARY BULLETIN No. 220 BLACK SPOT OF ONION SETS BY FEANK LINCOLN STEVENS AND ESTHER YOUNG TRUE TIRBANA, ILLINOIS, MAY, 19] 9 CONTENTS OF BULLETIN No. 220 PAGE INTRODUCTION 507 THE DISEASE 507 The Three Types 508 THE CAUSAL FUNGUS 509 Culture Studies 509 The Subicle 510 The Tubercle 510 THE PERITHECIUM 511 CORRELATION WITH EARLIER MORPHOLOGICAL WORK 529 TAXONOMIC POSITION OF THE ASCIGEROUS STAGE 529 SUGGESTIONS REGARDING CONTROL 531 BIBLIOGRAPHY . . 532 BLACK SPOT OF ONION SETS VOLUTELLA CIRCINANS AND ITS PERITHECIAL FORM, CLEISTOTHECOPSIS CIRCINANS BY FRANK LINCOLN STEVENS, PROFESSOR OF PLANT PATHOLOGY, UNIVER- SITY OF ILLINOIS, AND ESTHER YOUNG TRUE, RESEARCH ASSISTANT, IN COOPERATION WITH THE DEPARTMENT OF HORTICULTURE INTRODUCTION Serious losses of onions during storage, particularly of onion sets, led to the present study. Loss in storage, especially of the white varieties, is very high. It is estimated that in the Chicago district alone, for the 1917 season, there was a loss of approximately 150,000 bushels of sets valued at about $300,000. In the present study onions and onion sets were examined cither directly in the markets and stores or by sample lots which were sup- plied by large holders. Results of such examinations showed the presence of several fungi apparently as the cause of loss in storage, as follows: "Vermicularia," Sclerotium, Botrytis (several species),, Fusarium, Aspergillus, Bacillus, and a few apparently saprophytic forms. The so-called " Vermicularia" was present in 60 to 80 per- cent of the white onion sets examined, and Sclerotium in 2 to 7 percent. The other fungi appeared in a lesser quantity. It is to the fungus found most generally present that chief attention has been given in the studies reported in this bulletin. THE DISEASE This disease is easily recognized by both macroscopic and mi- croscopic observation. As a disease it was first described under the name " V ermicularia, circinans" by Berkeley in Gardener's Chronicle in 1851. ia It has later been referred to by Clinton, 2 Cooke, 3 Hal- sled, 4 Massee, 5 Selby, Stevens, 7 Stevens and Hall, 8 Stoneman, 9 Thaxter, 10 Tubeuf and Smith, 11 Voglino, 12 and a few others. It has been reported under many common names, such as anthracnose, rot, smudge, surface rot of the bulb, mold, vermiculariose, black spot, and neck rot. The records of the Plant Disease Survey, U. S. De- partment of Agriculture, show its distribution in the following states : Connecticut, Indiana, Louisiana, Maryland, Massachusetts, Minnesota, New York, Ohio, Pennsylvania, Texas, and Wisconsin. "Superior figures are used thruout this bulletin to indicate the literature cita- tions given in the bibliography, page 532. 507 508 BULLETIN No. 220 [May, THE THREE TYPES The disease assumes three distinctly different aspects, which are here described separately as Types A, B, and C. Type A. This type of the disease is the most common and the most striking in appearance. It is the one that is usually regarded as typical and the one commonly described and figured as the onion disease due to " Vermicularia. " Upon the dry outer scale of the bulb it presents an approximately circular spot, usually about the size of a dime or a quarter. The hue is prevailingly black, owing to much black mycelium within the tissues, and numerous black knots of mycelium are seen, often grouped in a series of concentric circles, as shown in Fig. 1 (1). (See also Massee, 5 Fig. 130, and Thaxter, 10 Fig. 44.) Variations from this typical concentric arrangement are met. In some instances the prevailing direction of the mycelium is at right angles to the main veins, resulting in transverse black bands (see cover illustration). In other instances neither the concentric nor the banded 'arrangement predominates but the spots consist of irregularly arranged minute specks, as illustrated in Fig. 1(2). In still other instances the area involved in the spot is entirely black and the minute component black specks are lost to view, as in Fig. 1 (3, 4). (See also Clinton, 2 Plate 20, .Fig. a). Another view of the condition shown in Fig. 1 (1) and in the cover illustration is shown in Fig. 2 (1). In many of these spots there is a pronounced tendency for the fungus to follow the course of the veins, as may be seen in Fig. 2 (2). All of the varying forms of Type A occur on the outermost scales of the bulb, as in Fig. 2 (3), and in all cases on scales which are perfectly dry. Type B. This type, like Type A, occurs on the dry outer scales but it is usually limited to the upper part of the bulb, as illustrated in Fig. 3(1); at least it always starts at the top of the bulb and progresses toward the base. This type may assume any of the vari- ations mentioned under Type A. Several views are shown in Figs. 4 and 5. The essentially distinguishing character of this type is that the invasion of the fungus starts at the top of the bulb, usually stop- ping with the drying of the scale before the equatorial region is reached. It is probable that Type B results from infection thru the wounds caused in removing the "top." Type C. This type is manifest in those scales of the bulb which are still succulent and juicy or which remained so for considerable time after the invasion by the fungus. As shown in Fig. 3 (2), the spots may lie directly under and originate from spots of Type A, but on account of their very different appearance and character this type is described separately. Fig. 3 (3) shows Type A; Fig. 3 1919] BLACK SPOT OP ONION SETS 509 (4) shows the same bulb as Fig. 3 (3) but with the outer scale re- moved, showing Type C below. In Type C the fungus, owing to the fact that it lives and develops for a longer time within the juicy tis- sue, attains developmental stages not shown in the more limited life period in the outer scales. The chief manifestation of this develop- ment is in the formation of tubercles, or warty growths. These are usually located at the centers of the infected areas, whether the spot is small, 2 to 3 mm., or larger, .5 to 1 cm. In the| older, larger spots, secondary or tertiary series of tubercles may occur, often in roughly concentric arrangement. The tubercles are frequently 1 or even 2 mm. in diameter and rise fully 1 mm. above the surrounding scale. The distinguishing character of this type is the presence of these tubercles and the fact that the disease often remains progressive, tho of course scales with the tubercular development may later dry and thus inhibit further progress. That these three types of disease are due to the same fungus is fully borne out by the study of the culture characters, by the micro- scopic studies detailed below, and by the fact that the types to an extent merge one into the other. THE CAUSAL FUNGUS The mycelium is rather coarse, 3.6 to 10.8 ^ wide, branches fre- quently and irregularly, and is cut by septa at irregular intervals, usually about 12 to 16 ^ apart. It is crooked, intercellular, and intracellular, or even superficial (Figs. 8, 9, 10). When young it is hyaline, later turning quite dark. The fungus shows a strong tendency to develop mats of parallel hyphae, as illustrated in Fig. 7 (3). It is these that are largely responsible for the banded appear- ance, shown in the figure on the front cover. It is also characteris- tic of the mycelium to produce branches, the terminal cells of which turn dark and swell, producing an effect much like that of the so- called appressoria of the germinating anthracnose spores. Inter- calary cells also often darken and swell, as do frequently whole series of cells. CULTURE STUDIES Studies of the fungus in agar showed general agreement with the facts stated above. The methods used in isolating the fungus were: direct planting on plates of small pieces of infected onion tissue; dilution plating of spores in agar; and direct planting of spores which had previously germinated. For most of the studies an onion-broth agar was used. When white onions were used in the agar, the growth of fungus was abundant ; when yellow and red onions were used, the growth was slight and not many sporing bodies developed. In Petri-dish 510 BULLETIN No. 220 [May, cultures the fungus produced a light-colored mycelium near the up- per surface of the medium and under some conditions an aerial mycelium. Contrasting the structure with that found on the onion in nature, the cells of the mycelium were much more elongated and very seldom was there an appearance of oil drops in them. More- over, on agar there were very few of the dark, swollen end cells so characteristic of the fungus under natural conditions. As the col- ony became older, the aerial mycelium gradually shriveled and the colony assumed a gray or grayish-brown color with numerous small protuberances on the surface. These are the sporodochia, acervulus- like structures on subicles of interwoven hyphae. They were not confined to the upper surface alone but often developed below the surface of the agar. Many of the sporodochia were seen to have a pedicel, or neck, arising from the subicle. As the fungus grew older, it often colored the medium a dark brown. A portion of an agar plate showing a colony is shown in Fig. 15, The small black dots seen are the sporodochia. THE SUBICLE As the fungus ages, the mycelium in numerous points develops subicles, which are at first one cell thick. Various stages are shown in Figs. 6 (1, 2, 3), 7 (3), and 12 (1). The subicle may attain dimensions of 224 to 784 p by 336 to 1,344 /x. Often setae appear upon it, varying in number from one to many, as shown in Figs. 6 (1, 3) and 7 (3). Fig. 12 (1) shows one of these setigerous subicles in section. The setae are 125 to 240 fi long, about 4 p. wide at the base, acute at the apex, and very dark in color. THE TUBERCLE "When the fungus grows for a sufficient time in the still juicy scale, numerous host cells as well as intercellular spaces become filled and largely distended with mycelium, as shown in Fig. 8 (1, 2, 3). This results in greatly increasing the thickness of the host at these points, producing distinctly swollen spots (Figs. 9 and 10). The subicles, present superficially over these regions, increase in thickness by division of the cells in a direction tangential to the sur- face of the onion, resulting in distinct rounded protuberances, or tubercles. Several stages in the development of these structures arc shown in Fig. 11 (1, 2, 3, 4). The Sporodocliium. This is seen to consist of a pseudoparenchy- matous inner tissue covered by a continuous surface layer. It may or may not bear setae in the early stages of development. The young sporodochium eventually ruptures its covering membrane. Occa- sionally the surface is overgrown by loose mycelial masses, as shown in Fig. 12 (2). 19 19] BLACK SPOT OF ONION SETS 511 When sufficient growth time allows, especially when one of the deeper scales of the onion is affected, the sporodochium increases largely in diameter, reaching even more than 2 mm., and becomes nearly flat-topped or corrugated, as shown in Figs. 13 (2), 14, and 16. In all cases the conidiophores are borne upon a raised superficial base which constitutes the sporodochium (see Figs. 13 (1, 2), 14, and 16), in contradistinction to the innate form of the acervulus, which has no such base. The tubercular swelling, due to the massing of mycelium below and in the epidermis, partakes of sporodochial char- acter also, and while this subepidermal part may not be regarded as constituting a true sporodochium, it serves to emphasize the tendency of the fungus to produce such structures. Conidiophores. Soon after rupturing the covering membrane, the sporodochium develops on its surface numerous parallel coni- diophores of palisade arrangement, as shown in Figs. 12 (3) and 13 (1, 2, 3). Interspersed with the conidiophores are few or many setae. The conidiophores are 24 to 48 /x long, 2.4 p. thick, straight, simple, hyaline, few-septate, obtuse, and bear the conidia acro- genously. Conidia. The conidia are falcate, acute at each end, continuous, hyaline, 19.2 to 26.4 /x by 3.6 to 7.2 /x. In germination they become one-septate and send out germ tubes from one or both cells, from either the side or the tip of the spore. Appressoria similar to those produced by Gloeosporium are also found in abundance. THE PERITHECIUM Onion sets which were heavily infected with the fungus under discussion were placed in sand in the greenhouse. Upon examination of certain of these sets after about thirty days, black bodies were seen on the outer scales. Some of these were imbedded for micro- tome sectioning; others were examined direct. These structures, the perithecia, are irregularly globular, dark brown to black, and from 89.6 to 313.6 p. in extreme dimensions. The surface is characteristically reticulated, as seen in Fig. 17 (1), and there are often numerous short hairs growing from the surface cells. The perithecia are borne either in or on the host tissue. Or- ganically connected with the perithecia is the typical mycelium of the Volutella, a point that is especially clear in the study of young perithecia. Fig. 17 (3). There is no ostiole. Microtome sections show the perithecia in early stages to resemble sclerotia in general structure, i. e., the whole structure is pseudoparenchymatous, the cells of the outer layer being darker and thicker-walled than those of the. interior. This point is illustrated in Fig. 17 (1 and 4). In a later stage an ascogeiums region is differentiated. This assumes the 512 BULLETIN No. 220 form of numerous filiform hyphae of nearly parallel direction aris- ing from the basal portion of the perithecium, as shown in Fig. 18 (2) . Perithecia of this age when crushed release this ascogonium en masse. In still older perithecia the central part is filled with asci, lying in close contact and without paraphyses, as seen in Fig. 18 (3). In still later stages the asci disappear and the ascospores lie free in the perithecial cavity. Figs. 18 (4) and 19. In Fig. 17 (4) is shown a perithecium in a very early stage of development ; general views of ascigerous perithecia are shown in Figs. 18 (3, 4) and 19. The asci are here seen to arise approximately from a region which may be designated as basal, i. e., not in Plectascinaceous fashion. The asci are about 72 to 96 p, by 19.2 to 24 /x and are evanescent, disappear- ing early. The spores are dark, obtuse at each end, 24 to 36 /x by 9.6 to 14.4 p., muriform, usually with 4 to 7 /* transverse and 1 to 2 /x longi- tudinal septa, as seen in the optical section shown in Fig. 17 (2). Two variant spores were found (in situ in microtome section), each with one septum, Fig. 17 (2). These would be regarded as immature except for the fact that they were of mature color. It is probable that the spores do really show this extreme variation in septation and that the septa may increase greatly in number even after ma- turity of the spores. The evidence that these perithecia belong to the Volutella may be summarized as follows: (1) they occurred on sets badly infected with the Volutella; (2) no other fungi or other types of mycelium were seen to be connected with them; (3) when studied in various stages of development, the typical Volutella mycelium, which offers definite characters for recognition, was seen in organic connection with them, as illustrated in Fig. 18 (1) ; (4) the outgrowths from the perithecia are like those of the Volutella. FIG. 1. VOLUTELLA, TYPE A: (1) SHOWING CONCENTRIC ARRANGEMENT OF FUNGUS KNOTS; (2) BLACK SPECKS IRREGULARLY ARRANGED THRU THE SPOTS; (3) DIFFUSE, NEARLY STRUCTURELESS, BLACK BLOTCHES; (4) SAME AS (3) 513 FlG. 2. VOLUTELLA, TYPE A: (1) OTHER VIEWS OF PORTIONS SHOWN IN FlG. 1 (1) AND IN THE COVER ILLUSTRATION; (2) ILLUSTRATING A TENDENCY OP THE FUNGUS TO FOLLOW A VEIN; (3) A PORTION OF THE DRY OUTER SCALE HAS BEEN REMOVED SHOWING THE FLESHY SCALE BELOW To BE CLEAN AND HEALTHY 514 FIG. 3. VOLUTELLA: (1) TYPE B. THE SPOT is LIMITED TO THE TOP OF THE BULB; (2) TYPE C. SPOT IN A LIVING SCALE BELOW A SPOT SUCH AS SHOWN IN FIG. 1 (1); (3) SHOWING CHARACTERISTIC TYPE A, ALSO TYPE C BENEATH; (4) TYPE C. SAME AS (3) BUT WITH THE OUTER SCALE REMOVED 515 FlG. 4. VOLUTELLA, TYPE B. SHOWING VARIATIONS IN THE TYPE FIG. 5. VOLUTELLA, CHARACTERISTIC TYPE B 516 FIG. 6. (1) A SUBICLE BEARING SEVERAL SETAE, H.P. ; (2) SUBICLE SIMILAK BUT WITHOUT SETAE, H.P. ; (3) SUBICLE IN VERY YOUNG STAGE BEARING ONE SETA, H.P. 517 FIG. 7. (1) PHOTOGRAPH OF TUBERCLES WITH SETAE AS SEEN IN SIDE VIEW; (2) A VIEW OP SETOSE TUBERCLE FROM ABOVE; (3) SHOWING MATS OF PARALLEL HYPHAE DEVELOPED IN EARLY STAGES, ALSO SUBICLES OF COMPARATIVELY LARGE SIZE, SOME WITH SETAE 518 FIG. 8. (1) SUPERFICIAL MYCELIUM ON A DRIED SCALE, H.P. ; (2, 3) INTERNAL MYCELIUM IN A DRIED SCALE, H.P. 519 FIG. 9. SHOWING A SUPERFICIAL SUBICLE OVER A VEIN, H.P. FIG. 10. DRIED SCALE, VOLUTELLA, TYPE A. A SECTION SHOWING THAT THE FUNGUS Is EPIDERMAL AS WELL AS SUBEPIDERMAL AND SUBCUTICULAR. SHOWING ALSO THE EELATION OF THE FUNGUS TO THE VEIN, H.P. 520 FIG. 11. (1, 2, 3, 4) EARLY STAGES IN THE DEVELOPMENT OF THE TUBERCLE, H.P. 521 FIG. 12. (1) A SETIGEROUS SUBICLE IN SECTION, H.P. ; (2) VIEW TO SHOW THE THICKENING OF THE ONION SCALE BY THE FUNGUS, THE DEPOSITION OF MASSES OF FUNGUS MYCELIUM, AND THE RELATION TO THE SPORODOCHIUM!, L.P. ; (3) A SMALL SPORODOCHIUM WITH SETAE AND CONIDIOPHORES ON A DRIED ONION SCALE, H.P. 522 FIG. 13. A TUBERCLE WHICH HAS EUPTURED AT THE TOP PREPARATORY TO BECOMING CONIDIIFEROUS AND SETIGEROUS, H.P. ; (2, 3) MEDIAN SECTION THRU A SETIGEROUS, CONIDIIFEROUS SPORODOCHIUM. A DETAIL OF SETAE, CONIDIOPHORES, AND CONIDIA, H.P. 523 y FIG. 14. A LARGE SETIGEROUS, CONIDIIFEROUS SPORODOCHIUM IN MEDIAN SECTION, L.P. " FIG. 15. PHOTOGRAPH OF A PORTION OF AN AGAR COLONY X10 524 FIG. 16. MEDIAN SECTION THRU AN OLD, LARGE SPORODOCHIUM. A LOW- POWER DRAWING SHOWING SHAPE AND KELATION TO THE SUBSTRATUM; THE POR- TIONS A AND B ENLARGED TO SHOW CELLULAR STRUCTURE, H.P. 525 FIG. 17. (1) A PERITHECIUM IN TANGENTIAL SECTION SHOWING SURFACE CELLS, ALSO CELLS JUST BELOW THE SURFACE, H.P.; (2) ASCOSPORES, H.P.; (3) A VERY YOUNG PERITHECIUM, H.P. ; (4) A VERY YOUNG STAGE IN THE DEVELOPMENT OF A PERITHECIUM, MEDIAN SECTION SHOWING ATTACHMENT TO A BASAL STRUC- TURE, H.P. 526 527 FIG. 19. MATURE PERITHECIUM IN MEDIAN SECTION. SPORES FREE, H.P. 528 1919} BLACK SPOT OF ONION SETS 529 CORRELATION WITH EARLIER MORPHOLOGICAL WORK Thaxter in 1889 gave the first American account of this fungus, placing it in the genus "Vermicularia" because he believed it to be identical with a fungus described as "Vermicidaria circinans" by Berkeley in Gardener's Chronicle, in 1851, tho Thaxter clearly was not satisfied that the fungus was really of pycnidial nature. The structure which Thaxter figures as " perithecium " in Fig. 45 10 is clearly identical in character with that shown in the accompanying Fig. 7(1), and from neither Thaxter 's figure, this figure, nor the slides made in these studies is there any reason for regarding it as a pycni- dium. There is at no time in its growth a covered conidial cavity, nor in fact a conidial cavity of any kind. The structure is a tubercle with a differentiated cortical outer layer. This outer layer ruptures and the tubercle develops as a sporodochium. * These facts exclude the fungus from the Sph'aeropsidales and from Vermicularia and place it in the Tuberculariaceae under Volutella. Bertha Stoneman, 9 in 1898, made the following statement re- garding this fungus: ' ' There is not, however, a perithecium developed and altho the fungus has been placed among the Sphaeropsideae, the character of the pustule shows a close resemblance to those species of Colletotrichum in which an abundant basal stroma is developed, while the marginal setae and the elevated basidia, as well as the characters in artificial cultures, intimately associate the fungus with the genus Volutella. ' ' The authors fully concur in this view so far as the conidial stage is concerned. That the fungus under artificial culture may develop acervuli rather than sporodochia has led Voglino, 12 followed by Walker," to class it as Colletotrichum. In the minds of the present writers this course is not justified, since under its natural conditions the fungus produces a well-marked sporodochium. TAXONOMIC POSITION OF THE ASCIGEROUS STAGE The classification of the ascomycete presents certain difficulties. It has the general appearance of a Pleospora so far as the character of the ascus and the fully developed mature spores go, but the peri- thecium is distinctly unlike a Pleospora in that it has no ostiole, it is usually hairy, and in general structure it is like an ascigerous cav- ity developed by a sclerotium rather than the usual perithecium. "Walker, J. C. Abstract of paper presented at the annual meeting of the American Phytopathological Society, New York City, Dec., 1916, Phytopath. Vol. 7, No. 1. 1917. 530 BULLETIN No. 220 [May, The variation in spore septation is also noteworthy and does not accord well with a Pleospora. In general, the perithecium and the mycelium agree well with the Perisporiaceae, and in that family with the genus Cleistotheca, a genus with only one representative and that recorded as a sapro- phyte. Comparison of the material obtained in these studies with the excellent figure of Zukal 13 gives many points in common. The differences are chiefly in spore septation, which is irregular in the present species ; in the arrangement of the asci ; and in the conidial stages, Cleistotheca possessing a Stachybotryos while this species has a Volutella as the conidial stage. Were it not for the difference in conidial forms the authors would place their fungus in the genus Cleistotheca. However, since the conidial forms are so different, there is proposed for the perithecial fungus a new genus: Cleistothecopsis gen. nov. Characters Uke Cleistotheca except that its eonidial stage is a Volutella. Type Cleistothecopsis circinans. Perithecia superficial, irregularly globular, dark brown to black, no ostiole, surface reticulate, often with numerous short hairs extending out from surface cells, entirely pseudoparenchymatous, outer layer of darker thick-walled cells, 89.6 to 313.6 /*. Asci clavate, basal, evanescent, 8-spored, approximately 72 to 96 /x by 19.2 to 24 p.. Paraphyses present but evanescent. Ascospores muriform, dark, obtuse at each end, usually with 4 to 7 transverse and 1 to 2 longitudinal septa, 24 to 36 ju, by 9.6 to 14.4 /*. Its conidial form is the following: Volutella circinans comb. nov. Vermicularia circinans Berk. Sporodochia scattered or often in concentric circles usually in the centers of infected areas, numerous, black, subepidermal, erum- pent, becoming covered with loose mycelium, 1 to 2 mm. in diameter, 1 mm. in elevation. Mycelium hyaline, becoming dark, rather coarse, 3.6 to 10.8 ^ wide, branching irregularly, and with characteristic darkening of end cells where mycelium is superficial. Setae one to many, scattered thruout, dark brown to black, 125 to 240 /i long, 4 /x wide at base tapering to apex. Conidiophores straight, simple, hyaline, few-septate, obtuse, 24 to 48 by 2.4 /*, bearing conidia acrogenously. Conidia falcate, acute at each end, continuous, hyaline, 19.2 to 26.4 fji by 3.6 to 7.2 /*. 1919} BLACK SPOT OP ONION SETS 531 SUGGESTIONS REGARDING CONTROL This Volutella reaches its maximum conidial development when it grows for a considerable time on succulent onions, as for ex- ample on an inner scale, or rarely on an outer scale if conditions are such that this remains succulent. When drying of the host tissue occurs soon after infection, normal conidial development is precluded. Thus it happens that infection of the outer scale, which in a comparatively short time dries to papery thinness, leads in most cases merely to the production of mycelium forming dark blotches, of subicles bearing few to many setae, of sterile tubercles, and of sporodochia; but rarely is there sufficient time and succu- lence for the production of conidiiferous sporodochia in any abun- dance. These conditions obtain in what has been here designated as Types A and B, and account for the difference between these types and Type C. Infection can pass readily from an outer scale to an inner scale and Type A can thus give rise to Type C, tho Type B does not often do so. The presence of atmospheric moisture, including in that term the moisture in the air between the scales, retards drying of the in- fected scale, thereby lengthening the growth period of the fungus and increasing the damage done. That the progress of the fungus within a still succulent scale may be stopped by atmospheric drying is shown in some examples of Type B (see Fig. 5). Here the ad- vance of the fungus has been checked, as is indicated by the line of demarcation between dried and succulent tissue, by simply plac- ing the onion in dry air. From these observations it is obvious that moisture favors the rot, which is indeed a common observation of practical growers. It allows the fungus to develop longer in the outer scale, perhaps to make some spores there, and surely to infect the lower scales, mak- ing many spores and developing a genuine rot. Dry air, on the other hand, hastens the drying and maturing of the outer scale, per- haps entirely prevents spore formation, and imprisons the fungus, even preventing it from proceeding to the inner scales. It is therefore advisable to dry onion sets as rapidly and thoroly as possible immediately after they are harvested. The usual method of curing in shallow slatted crates stacked in the field has been found inadequate when the weather is moist. Artificial drying of the sets in rooms properly equipped for the purpose appears to be the most promising method for checking the progress of this dis- ease and reducing the loss from rot. The desirability of properly curing the onions to prevent loss from this disease was mentioned 532 BULLETIN No. 220 by Thaxter in 1889, by Halsted in 1890, by Clinton in 1903, by Stevens and Hall in 1910, and by Walker (see footnote p. 529). Thus, the recommendation that the sets be dried rapidly and thoroly is not a new one ; nevertheless it is worthy of careful consideration by growers who have been meeting with losses on account of the disease in question. BIBLIOGRAPHY 1. BERKELEY. Gard. Chron., 595. 1851. 2. CLINTON, G. P. Conn. Agr. Exp. Sta. Rpt. 27, 333, Plate 20, Fig. a. 1903. 3. COOKE, M. C. Handbook of British Fungi, 439. 1871. 4. HALSTED, B. D. N. J. Agr. Exp. Sta. Rpt. 11, 354. 1890. 5. MASSEE, G. E. Diseases of Cultivated Plants, 417, Fig. 130. 1910. 6. SELBY, A. D. Ohio Agr. Exp. Sta. Bui. 214, 413, Fig. 64. 1910. 7. STEVENS, F. L. Fungi Which Cause Plant Disease, 497. 1913. 8. STEVENS AND HALL. Diseases of Economic Plants, 252. 1910. 9. STONEMAN, BERTHA. Bot. Gaz., 26, 69. 1898. 10. THAXTER, R. Conn. Agr. Exp. Sta. Rpt. 13, 163. 1889. 11. TUBEUF AND SMITH. Diseases of Plants, 470. 1897. 12. VOGLINO, P. Annali della R. Academia d 'Agricolture di Torino, 49, 197. 1907. 13. ZUKAL, H. Mykologische Mittheilungen. Oesterr. Bot. Zeit., 43, 160-66. 1893. Also in Engler and Prantl. Die Naturlichen Pflanzenfamilien, 1, Part 1, 335. UNIVERSITY OF ILLINOIS-URBANA