HANLIN, RICHARD T. (Georgia Experiment Station, Experiment.) Studies in the genus Necwria. II. Morphology of N. gliocladioides. Amer. Jour. Bot. 48(10): 900-908. Illus. 1961.-Swollen tips of vegetative hyphae develop into multicellular archicarps from which multinucleate ascogonia forrn. From basal cells of each archicarp arise hyphae which grow up into a prosenchymatous, true perithecial wall; around this wall is formed a thin pseudoparenchymatous stroma of compacted hyphae. The ascogonia give rise to ascogenous cells from which croziers and asci form directly. At the same time, an apical meristem forms cells that grow downward into the centrum. These are pseudoparaphyses. Asci grow up among the pseudoparaphyses, which deliquesce as the ascocarp matures. The ascus tip contains a thick ring with a pore and lateral thickening of the ascus wall. Ascospores are forcibly ejected. The chromosome number is 4. This species conforms to the Nectria Developmental Type of Luttrell. THE TAXONOMIC position of those Pyrenomycetes having brightly colored, fleshy ascocarps has been variouslv interpreted by different workers. Some (Lindau, 1897; Gaumann, 1926; Bessey, 1950; Miller, 1949; Luttrell, 1951) have placed them in a separate order, the Hypocreales, while others (Miller, 1928; Clements and Shear, 1931; Gaumann, 1952; Von Arx and Muller, 1954; Munk, 1957), not considering color and texture sufficient basis for separation, included them in the Sphaeriales in one or more families. In recent years, developmental data have become increasingly important in taxonomic arrangements. In 1951, Luttrell proposed a system based on types of development of the ascocarp. He recognized 8 different developmental patterns, 1 of which, the Nectria Developmental Type, served as the basis for the order Hypocreales. The extent of this developmental type among hypocreaceous fungi can be determined only by detailed studies of the different species. The few studies which have been carried out are mostly incomplete and, therefore, of little value in determining the position of these fungi in a taxonomic system based on developmental morphology. The genus Nectria is a good example of this. Of the 4 species studied previously (N. ribis Tode ex Rab. [Vincens, 1917]; N. galligena Bres. 1 Received for publication May 10, 1961. Paper No. 1121, Department of Botany, University of Michigan; and Paper No. 397, Journal Series, Georgia Experiment Station. This research was supported in part by National Science Foundation Grant G-10727. Portion of a dissertation submitted to the faculty of The University of Michigan in partial fulfillment of the requirements for the degree of Doctor of Philosophy. I am grateful to Dr. L. E. Wehmeyer for his guidance during this study and for reviewing the manuscript. [Cayley, 1921]; N. ipomoeae Halst. [Cook, 1923]; N. flava Bon. [Gilles, 1947]), only the work on N. flava approaches the detail necessary for modern taxonomic work. The present study was conducted to determine the position of N. gliocladioides Smalley & Hansen on the basis of its development. MATERIALS AND METHODS-Nectria gliocladioides was originally isolated from decaying bulbs of Lilium auratum Lindl. (Smalley and Hansen, 1957). The material used in this study was derived from a culture obtained from Dr. E. B. Smalley. Cultures were grown on complete mineral-medium agar plates containing 2% glucose under continuous fluorescent ("Daylight") light at 25 C. Suitable material was cut up into blocks approximately 5 mm2, then killed and fixed in Allen-Bouin Solution, Type II (Sass, 1951). Dehydration was carried out bv means of the tertiary butyl alcohol (TBA) method (Sass, 1951). Embedding was done in Fisher Tissuemat (mp 54-56 C). Sections were cut at a thickness of from 8 to 10 u, the ribbons were floated on a 3% solution of formaldehyde in distilled water, and affixed to the slides with Haupt's Adhesive (Johansen, 1940). A number of stains were tried but the majority gave poor results. The method finally selected was a modification of that used by Robinow (1957). Sections were stained with the Feulgen technique (Johansen, 1940), then counterstained in 0.5% acetocarmine (45% acetic acid). Optimum time for both hydrolysis and counterstaining was 3 min. A longer time intensified the stain too much, obscuring detail. Studies of asci were made with fresh material. Squash mounts were made in 1 % acetoorcein (60% acetic acid) or 1% acetocarmine Fig. 1-13. All magnifications X 1700 unless otherwise stated.-Fig. 1. Typical Gliocladium conidiophore.-Fig. 2. Typical Verticillium conidiophore. X 850.-Fig. 3-4. Conidiophores intermediate in structure. X 850.-Fig. 5, left to right. Stages in conidial development, from branch to mature conidium. X 3000.-Fig. 6. Two mature conidia.-Fig. 7. Two conidia germinating after 6 hr in distilled water.-Fig. 8. Three mature ascospores, 2 with germ tubes after 6 hr.Fig. 9. Germinating conidium after 10 hr.-Fig. 10-12. Germinating ascospores after 14 hr.-Fig. 13. Tip of mature ascus showing wall thickening and apical ring with pore. X 3000.