S M I T H S O N I A N C O N T R I B U T I O N S T O B O T A N Y N U M B E R 6 8 Morphological, Anatomical, and Taxonomic Studies in Anomochloa and Streptochaeta (Poaceae: Bambusoideae) Emmet J . Judziewicz and Thomas R. Soderstrom SMITHSONIAN INSTITUTION PRESS Washington, D.C. 1989 A B S T R A C T Judziewicz, Emmet J., and Thomas R. Soderstrom. Morphological, Anatomical, and Taxonomic Studies in Anomochloa and Streptochaeta (Poaceae: Bambusoideae). Smithsonian Contributions to Botany, number 68,52 pages, 24 figures, 1 table, 1989.-Although resembling the core group of the bambusoid grasses in many features of leaf anatomy, the Neotropical rainforest grass genera Anomochloa and Streptochaeta share characters that are unusual in the subfamily: lack of ligules, exceptionally long microhairs with an unusual morphology, a distinctive leaf blade midrib structure, and 5-nerved coleoptiles. Both genera also possess inflorescences that are difficult to interpret in conventional agrostological terms. Anomochloa is monotypic, and A. marantoidea, described in 1851 by Adolphe Brongniart from cultivated material of uncertain provenance, was rediscovered in 1976 in the wet forests of coastal Bahia, Brazil. The inflorescence terminates in a spikelet and bears along its rachis several scorpioid cyme-like partial inflorescences. Each axis of a partial inflorescence is subtended by a keeled bract and bears as its first appendages two tiny, unvascularized bracteoles attached at slightly different levels. The spikelets are composed of an axis that bears two bracts and terminates in a flower. The lower, chlorophyllous, deciduous spikelet bract is separated from the coriaceous, persistent, corniculate upper bract by a cylindrical, indurate internode. The flower consists of a low membrane surmounted by a dense ring of brown cilia (perigonate annulus) surrounding the andrecium of four stamens, and an ovary bearing a single hispid stigma. Other peculiarities of A. marantoidea include its hollow leaf sheaths and long, hollow, bipulvinate pseudopetioles and chromosome number of n = 18. The caryopsis and embryo are large, but their structure is typically bambusoid. Streptochaeta consists of three species and one subspecies (S. spicata subsp. ecuatoriana, newly described here) and conforms to the bambusoid core group in seedling morphology and leaf anatomy. Streptochaeta and Anomochloa are quite divergent but may be more closely related to each other than to any other grass. They share features that indicate affinities with the Olyreae. OFFICIAL PUBLICATION DATA is handstamped in a limited number of initial copies and is recorded in the Institution?s annual report, Smithsonian Year. SERIES COVER DESIGN: Leaf clearing from the katsura tree Cercidiphyllum japonicum Siebold & Zuccarini. Library of Congress Cataloging-in-Publication Data Judziewicz, Emmet J. Morphological, anatomical, and taxonomic studies in Anomochloa and Streptochaeta (Poaceae, Bambusoideae). (Smihsonian contributions to botany ; no. 68) Bibliography: p. Supt of Docs. no. SI 1.29:68 1. Anornochloa 2. Streptochaeta I. Soderstrorn, Thomas R. 11. Title. 111. Series. QKlS2747 no. 68 581 s [584?.9] 88-600187 [QK495.G74] Contents Page Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Materials and Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Acknowledgments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Anomochloa Brongniart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 History and Rediscovery. by T.R. Sodcrstrom . . . . . . . . . . . . . . . . . . . . . 2 1 . Anomochloa marantoidea Brongniart . . . . . . . . . . . . . . . . . . . . . . 5 Morphology-Anatomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 Culm and Leaf Sheath . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 Ligule and Pseudopetiole . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 Pulvini . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 Leaf-blade Anatomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 Inflorescence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Spikelet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 Fruit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Chromosomes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Discussion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Habit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Leaves . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Inflorescence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 Spikelet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 Fruit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 Reproductive Biology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 Streptochaeta Schradcr ex Nees von Esenbcck . . . . . . . . . . . . . . . . . . . . . 29 History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29 Key to the Species of Streptochaeta . . . . . . . . . . . . . . . . . . . . . . . . 29 1 . Streptochaeta sodiroana Hackel . . . . . . . . . . . . . . . . . . . . . . . . 30 2a . Streptochaeta spicata subsp . spicata Schrader ex Nees von Esenbeck . . . . 34 2b . Streptochaeta spicata subsp . ecuatoriana. new subspecies . . . . . . . . . . 39 3 . Streptochaeta angustijolia Soderstrom . . . . . . . . . . . . . . . . . . . . . 39 Morphology-Anatomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41 Culm. Leaf Sheath. and Pulvinus . . . . . . . . . . . . . . . . . . . . . . . . . . 41 Leaf-blade Anatomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41 Inflorescence and Pseudospikelets . . . . . . . . . . . . . . . . . . . . . . . . . 42 Fruit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43 Chromosomes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43 Habit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44 Leaves . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44 Inflorescence and Pseudospikelets . . . . . . . . . . . . . . . . . . . . . . . . . 44 Reproductive Biology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46 Interspecific Relationships . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46 Phylogenetic Position of Anomochloa and Streptochaeta . . . . . . . . . . . . . . . . 46 Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52 Taxonomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Taxonomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29 Discussion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . - 4 4 Fruit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45 Literature Cited . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49 111 Morphological, Anatomical, and Taxonomic Studies in Anomochloa and Streptochaeta (Poace ae : B ambus oideae) Emmet J . Judziewicz and Thomas R. Soderstrom Introduction The eight tribes of herbaceous bamboos have long interested the agrostologist concerned with tracing the evolution of the Poaceae. Although they appear to have their closest affinities with the woody bamboos (Bambuseae) of the Bambusoideae, the intertribal relationships of the herbaceous group have remained uncertain until recently because of a lack of suitable material for the study of such taxonomically critical characters as inflorescence, spikelet, lodicule, gynecium, fruit, and seedling morphology. Of the eight tribes the Olyreae, with about 20 genera and over 100 species, is native only to the New World and is dealt with in detail in the papers of Soderstrom and collaborators (Calder6n and Soderstrom, 1973, 1980). In leaf anatomy this tribe appears to be closest to the woody bamboos (Bambuseae) (Soderstrom and Ellis, 1987). It may also be related to the poorly known Buergersiochloeae, a monotypic tribe of northern New Guinea (Fijten, 1975). The other tribes of herbaceous bamboos are more isolated. For example, the Phareae, with inverted, obliquely veined leaves bearing distinctive fibrous epidermal bands, but lacking bicellular microhairs, is perhaps the most isolated tribe among the herbaceous bamboos. The Streptogyneae, with a unique seedling morphology for the subfamily (Soderstrom, 1981a), is nearly as isolated as the Phareae (Soderstrom et al., 1987). While the African Puelia (Puelieae) and Guaduella (Guadu- elleae) bear many-flowered spikelets of a typical graminoid type, more material, including caryopses and seedlings, is required to understand their affinities. Emmet J. Judziewicz, Department of Botany, University of Wisconsin, Madison, Wisconsin 53706. Thomas R. Soderstrom (deceased}, Department of Botany, National Museum of Natural History, Smithsonian Institution, Washington, D.C. 20560. The two remaining tribes, the monotypic Anomochloeae and Streptochaeteae, are the subject of this paper. Above all others these Neotropical forest herbs have intrigued agrostologists because their inflorescence and spikelet structures are so different from those of other grasses. They have been called the most primitive grasses, and until recently some workers have questioned whether they were truly graminaceous (Campbell, 1985). The present investigation was made possible because of the rediscovery of Anomochloa. Material gathered in 1976, 1978, 1982, 1983, and 1986 by various botanists is the basis of our studies of the inflorescence and spikelet structure and taxonomic affinities of Anomochloa marantoidea. T.R. Soder- mom wrote the section herein on the history and rediscovery of this taxon. For purposes of comparison we have also studied Strepto- chaeta. Inflorescences of both genera are unique within the grass family and the present study is intended to clarify the relationship of these peculiar bamboos. MATERIALS AND METHODS Herbarium specimens of Anomochloa and Streptochaeta were examined from the following herbaria (acronyms follow Holmgren et al., 1981): AAU, B, BM, BR, CANB, CAY, CEPEC, DUKE, F, G, IBGE, INPA, ISC, K, L, LE, M, MO, NA, NY, P, PDA, QCA, R, RB, S, SI, UC, US, W, and WIS. Observations of living plants of Streptochaeta were made by Soderstrom (Costa Rica, 1966; Brazil, 1972) and Judziewicz (Costa Rica, Panama, 1983), and of Anomochloa by Soder- strom (October 1983) and Judziewicz (February and March 1986). Some of these plants were preserved in FAA (90% ethanol, 5% acetic acid, 5 % formalin) and later transferred to 1 2 SMITHSONIAN COSTRIBUTIONS TO BOTASY 70% ethanol (see Appendix). The culms, leaves, and reproductive structures of voucher specimens were studied using a Wild M5 dissecting micro- scope. These structures were also studied by serial cross- sections at thicknesses of 8-13 pm using a rotary microtome. Before dehydration with dimethoxypropanol (DMP), infiltra- tion with tertiary butyl alcohol (TBA), and embedding in paraffin, leaves and spikelets were soaked for several days in hydrofluoric acid (HF) in order to remove silica. For the study of bicellular microhairs in Anomochloa marantoidea a preserved leaf was stained in Chlorazol Black E and areas with abundant microhairs were scraped with a razor blade. Formal descriptions of the leaf anatomy of Anomochloa and Strepto- chaeta follow the model of Soderstrom et al. (1987). Embryos of both genera were dissected out of the caryopses, rehydrated using Aerosol-OT, embedded in agar, then dehydrated and embedded in paraffin using the procedure described above. Sections were cut at widths of from 4-10 pm, and stained with Chlorazol Black E. Starch grains from caryopses were sectioned with a freezing microtome and then stained with 1,KI. Epidermal scrapes were prepared using the method of Tomlinson (1961). Photomicrographs were made using Zeiss microscopes with green filters and Kodak Panatomic X ASA 32 film. ACLYO WLEDGM ESTS We are grateful to Alice R. Tangerini and Gesina B. Threlkeld for preparing the illustrations, and to Stanley Yankowski for the anatomical preparations, all of the Smithsonian Institution (SI). Many people helped us in our field work and we are especially grateful to Dr. Luis A. M. da Silva (Centro de Pesquisas do Cacao, or CEPEC), Dmitri Sucre, Talmon S . dos Santos, and Gustavo Martinelli. We would like to thank especially Dr. Paulo de T. Alvim, director of the Cacao Research Center, CEPEC, in Itabuna, Bahia, Brazil, who on several occasions extended to C.E. CaldeOh and us the use of the facilities of the institute. In Paris the assistance given by Dra. Alicia Lourteig and M. Jolinon in locating Brongniart?s manuscripts and archival correspondence is acknowledged. In London the facilities of the Royal Horticultural Library, Vincent Square, were generously ex- tended, Dr. Leslie Garay of the orchid herbarium, Harvard University, offered helpful information. We also appreciate the advice and comments of Dr. Roger Ellis (Botanical Institute, Pretoria) and Dr. H. Trevor Clifford (University of Queensland) on certain aspects of the study. Victor E. Krantz (SI) produced the photographs for Figures 8 and part of 9. Judziewicz conducted part of the research that led to this paper while a predoctoral fellow at the Smithsonian Institution (September 1985-August 1986). His field work in Brazil was funded by the Smithsonian?s Neotropical Lowland Ecosystems Program and the E.K. and O.N. Allen Herbarium Fund of the Department of Botany, University of Wisconsin, Madison. We also thank the curators of the herbaria from which we borrowed specimens. Anomochloa Brongniart Anornochluu Brongniart, 1850:57 [nomen nudum]; 1851 :368. HISTORY A S D REDISCOVERY by T.R. Soderstrom When Adolphe Brongniart described Anomochloa (1850, 1851) he chose an apt name for this weird and remarkable, truly anomalous grass that reportedly had come from Brazil. One or more plants of the genus were in cultivation in the greenhouse of the Jardin dcs Plantes in Paris in the 1840s. When Brongniart, then director of the MusEum d?Histoire Naturelle, saw the plant he decided it was a grass and described it as Anomochloa marantoidea, because the clustered broad pseudopetiolate leaves gave i t the appearance of a genus of Marantaceae. A plant was later sent to Kew by Charles Decaisne, Professor of Culture at the Serres (greenhouses) du Jardin des Plantes and was cultivated there until at least 1866. Herbarium specimens made of the plants at Paris and Kew represented the only material available for study by later workers. The desire to rediscover this genus and have fresh material for further study was well expressed by Agnes Arbcr who made studies on herbarium material (1934:131-133): It will be recognised even from this brief description, that Anomochloa, if a member of the Gramineae, is a most erratic one. Its rediscovery is much to be desired; a complete study of its structure and development would be of deepest interest. Besides Arber, several other botanists studied the plant from dried specimens. Schuster (19O9:3&32) examined the spikelet of Anomochloa as part of his dissertation on the morphology of grass flowers. Page (1947) noted the presence of large mesophyll cells in the leaf, based on an external study of the single leaf in the collections at the U.S. National Herbarium. Metcalfe (1960:28-29) was the first to give a description of the leaf cross-section anatomy and epidermis, stating that ?this grass has obvious points in common with the bamboos.? My own early studies of herbaceous bamboos began during field work in Guyana in 1962 and Suriname in 1963 when I collected several genera of bambusoid grasses. This work led me to the literature on Anomochloa and a desire to relocate this grass in particular. Its rediscovery took many paths and I think the story interesting enough to relate here. Brongniart (1851), in his beautiful paper on the new genus, did not mention anything about the plant in cultivation and gave as its provenance only the name of Morel and the province of Bahia, Brazil. The earliest mounted specimen at Paris has two labels, one a handwritten note signed ?herb. Houllet, July 1890,? stating: ?This plant was given by Monsieur Morel who NUMBER 68 3 received it from Brazil from Monsieur Pinelle from Morro chemado, Province of Rio de Janeiro in 1842? [my translation from the French]. The other label, with a printed heading of the Paris Herbarium, has the following information [my translation]: ?Brazil. Bahia. Monsieur Porte, given by Mon- sieur Morel. Paris Botanical Garden, August 1848.? The U.S. National Herbarium has two herbarium collections, one with a piece of inflorescence from a sheet at Paris, the other with a floret from a sheet at Leiden (in turn from the Balansa Herbarium at Paris), in addition to a leaf from a cultivated specimen at Kew. Both of the US sheets have annotations by Agnes Chase who wrote ?Bahia $- Porto,? having misread ?Bahia E[on- sieur] Porto.? She added a note, ?Is ?Bahia? alleged locality for this ?bay,? meaning bay of Rio de Janeiro?? This was a logical conclusion since the word for bay in Portuguese is ?bahia.? Mrs. Chase, who collected for several months in Brazil in 1924 and 1925, was anxious to relocate this grass and thought that it grew around Rio de Janeiro where she spent several days. In the files of L.B. Smith (Smithsonian Institution) is a letter of 6 December 1927 to Dr. Smith (who was going to Brazil the following year) from Mrs. Chase, who wrote the following. The grass I most wanted in Brazil and failed to find was Anomochloa. It occurs to me that you may like to read the original manuscript of the paper I had to reduce to 50 percent for the Smithsonian Report, so I shall send it. Please return it when you have read it. In this manuscript you will see that this grass was described from ?the province of Bahia.? In the Paris Museum last May I found a note on the specimen in that herbarium which shows that ?bahia? (bay in Portuguese) referred to the bahia of Rio de Janeiro . . .. I can not find where M o m Chemado (if Chemado is a proper name) is . . . Anomochloa is a broad-leaved grass obviously of shaded places. So Prov. Rio de Janeiro is a far more likely place for it than and or semiarid Bahia. The many steps that led to the eventual rediscovery of Anomochloa actually started with my first trip to Brazil in 1964 when I accompanied Dr. Howard S . Irwin, Jr., on his expedition to the cerrados of the central part of the country. In BrasIlia I made the acquaintance of a young botanist, Romeu BelEm, who collected with us one day in a gallery forest near the city. There we found large clumps of a species of the herbaceous bamboo, Olyra, with beautifully purple-mottled culms (later described as 0. taquara Swallen). I showed BelEm how to make a collection of such a grass and encouraged him to look for these on his collecting trips. He was shortly to go to Bahia, where he was being sent by Dr. Joao Murca Pires, to start an herbarium at the CEPEC in Itabuna. The first collections in that now-rich herbarium are those of BelEm. His collections and those of others that followed are cited in a paper by Scott Mori and L.A. Silva (1979), the former of whom spent two years (1978-1980) collecting in the wet coastal forest region of Bahia and curating the CEPEC herbarium. Shortly after BelEm?s arrival in Itabuna we received a small package of bambusoid grasses, many unknown to me at the time and quite different from the others that I had so far studied. Among these was a collection that BelEm made with C.M. MagalhAes (no. 886) in 1965. I had provisionally dubbed that collection ?Raddiolyra? when I first saw it because it resembled both Raddia and Olyra but was certainly distinct from either of them. I later described this as a new genus, Sucrea (Soderstrom, 1981b). In June 1967 in a forest near Maracay, Venezuela, I noticed that insects were always to be found around the inflorescences of the bambusoid genus, Parianu. Since this association seemed to be common I made collections of the plants and the insects, which in this case turned out to be a new genus of Diptera (Cecidomyiidae), described by GagnE (1969). The possibility of insect pollination in these herbaceous bambusoid grasses that grew in the rainforest was intriguing and deserved further investigation. Upon my return from Venezuela I discussed my observations with an Argentine colleague, CleofE CalderOn, who was working in my laboratory at the time. We decided to pursue the problem and made plans for her to visit a number of localities in Central and South America where she would collect bambusoid grasses and make observations on the insects that visited the inflorescences. Thus in late 1967 Calderon left for Panama and continued on eColombiaLand Brazil, making collections in each of these localities. Most of the insect observations were made in the forests around Belem, Para Brazil, and the results of this work were published in Soderstrom and Calderon (1971). However, the most interesting part of the trip, from the standpoint of new bamboo taxa, turned out to be Bahia, which was included in her itinerary because of the interesting collections that Romeu Belem had sent us. Calderon?s further collections from Bahia showed the region?s wet forest region, where Itabuna was located, to be rich indeed in bambusoid taxa. Up to this point we still had no idea where Anomochloa might be found. However, based on Brongniart?s statement (1851) and the other kinds of bambusoid grasses found by BelCm and Calder6n in Bahia, that locality was a good possibility. Mrs. Chase, who had discounted Bahia as a suitable habitat, felt it was too arid but she was referring to the part of the state where she had traveled, between Salvador and Juazeiro on the Rio Sao Francisco. She was not familiar with the narrow strip of tropical rainforest along the coast. With funds from the National Geographic Society and Smithsonian Institution, Caldeoh and I traveled to Brazil in 1972 to explore various parts of the eastern coastal forest with the purpose of finding Anomochloa, along with another bambusoid grass, Diandrolyra, known only from cultivation at Kew. At that time we felt that Anomochloa could be found either in Bahia or in the mountains around Rio de Janeiro. Thus Calderon returned for further exploration in Bahia, where she collected with R.S. Pinheiro and Talmon S . dos Santos. I returned to the states of Rio de Janeiro and Espirito Santo, collecting with Dimitri Sucre of the Jardim Botanic0 in Rio de Janeiro. These concurrent trips yielded a fine collection of bamboos, including two species of Diandrolyra, new genera, and many new species. But Anomochloa still eluded us. It was time now to see if information about those persons involved with the original collection might offer a clue as to 4 SMITHSONIAN COSTRIBUTIONS TO BOTASY where the plant was first collected. Who were Morel, Pinel, and Porte-names associated with Brongniart in the begin- ning? One of the original labels stated ?Bahia M. Porte? and ?Dn par [given by] M. Morel.? Since I had seen these names in species of orchids, a search through the horticultural literature of the time was undertaken by an assistant, Stephen Cahir (SI), during the summer of 1973. Some leads came about through this effort and that fall I spent a few weeks in London and Paris continuing the search. This involved literature reviews at the Royal Horticultural Society library in London, the archives at Kew herbarium, of old manuscripts at the Paris herbarium, and a visit to the records in the town archives of St. Mande where Morel had lived. Through all of this effort we were persuaded to return to Bahia, which we were now convinced was the home of Anomochloa. Charles Morel had lived in a suburb of Paris called St. Mande, which is now a part of the city itself. The town records show that he was born in Reims (Maxne) on 28 July 1793 and was listed as a proprietaire (property owner?). The horticultural literature speaks highly of this gentleman and his greenhouses with their large collection of rare orchids. Morel was active in horticultural societies and had several correspondents who sent him orchids from abroad. One of these correspondents was Monsieur Pinel, who sent material from Brazil. Morel must have received material of Anomochloa, which he gave to Brongniart for cultivation in the greenhouses of the Museum. Morel was the author of a book on orchid culture (1855), which he dedicated to his friend, Prof. Brongniart. On page 9 he speaks of Pinel from Rio and Porte of Bahia: ?This is the place to pay just tribute and give thanks to M. Pinel of Rio de Janeiro and to M. Porte of Bahia, for it is to their activity and their good taste that we owe the greater part of beautiful plants of these regions? [my translation from the French]. Monsieur (or Chevalier) Pinel, a merchant who resided in Bahia, appears in the literature with two spellings, Pinel and Pinelle. Pinel, whose first name I have not found, collected living plants, probably from the region of Rio de Janeiro and sent them to horticultural establishments in France and Belgium. Mulford Foster purportedly remarked that the bromeliad, Aechmea pineliana, was named possibly for Dr. Pinel, French consul in Rio de Janeiro at the time (1851), but I have not been able to confirm this. There are many plants named for Pinel and records of his sending material to Morel in Paris. The name of ?Morro chemado? appears more than once in Pinel collections, one of which is for an orchid with locality ?Station Sommite des Serra de Morro-queimado.? I collected on a Morro Queimado in Rio de Janeiro, which was within the boundaries of the Tijuca forest, but I do not know if this is the same locality. It is possible that Pinel lived in the area during the last century and that ?M. Pinel, Morro chemado? referred to the man and where he lived rather than a locality for Anomochloa (which he may not have collected). On the label of the type of the bromeliad, Aechmea (Echinostachys) pineliana Brongniart in the Houllet herbarium, which is part of the Paris herbarium, is a note: ?This plant has been sent to Mr. Morel by Mr. Pinel of Morro-chemado (near Rio de Janeiro) in 1846 and has been introduced into botanical culture by him [Morel?]? [translation from the French by E. Judziewicz]. This again suggests that the plant was sent by Pinel of Morro-chemado. Marius Porte, whose name appears on one of the Paris labels as having sent a plant to Pinel, was a businessman in Bahia. Like Pinel he must have been interested in exotic plants for horticulture such as orchids. Only because of its great beauty and possibility for horticulture would Pinel have collected a grass such as Anomochloa and he most likely would have mistaken it for a member of the Marantaceae. I was hoping that Porte, in his correspondence in the Paris Museum archives, would have described some of his collecting localities. But I found only three letters, all from Manila to Prof. Brongniart in 1860, and remarking on the orchids of the Philippines where he had moved. Porte is said to have died shortly after arrival due to the results of a long and tedious journey to the Philippines from Brazil. Adolphe Brongniart was Professor of Botany at the Paris Museum and at one time its director. He was an expert in many fields, including botany and paleobotany. His paper on Anomochloa is superb and his analysis and illustration of the original plant outstanding. At the Paris Herbarium, M. Jolinon led me to boxes of old manuscripts where I came upon the original handwritten manuscript of Brongniart on Anomochloa. He included sketches of his dissections (which were not published) and the spikelet he had studied was still attached to the paper in an envelope. In 1975 Calderon and I again were granted funds from the National Geographic Society to return to Brazil and intensify our field efforts in Bahia. We spent January through March in the eastern coastal forests of the state, headquartered at CEPEC in Itabuna. We each made several separate trips of about two weeks each to different areas, and we returned to Itabuna for a few days in between each trip to prepare the herbarium specimens. Our efforts were finally rewarded with the rediscovery of Anomochloa on 21 April 1976. Calderon was traveling along a small road with Sr. Talmon S . dos Santos near the city of Una, Bahia. Cleo felt a peculiar-or psychic, as she put it-urge to stop near a particular wooded area. Not far into the woods, which bordered a cultivated area of cacao on somewhat rocky slopes, they came upon a colony of the grass. Further observations of the colony were made by Victoria Hollowell (University of South Carolina) in 1982 and by myself in 1983. In 1986, another colony was found by dos Santos and Judziewicz who had gone to Brazil to make field observations for the present study. The rich forested areas in the Bahian municipality of Una, where Anomochloa is native, are rapidly disappearing, a common story today in the Neotropics. The only populations of Anomochloa with which we are familiar occur on rocky slopes adjacent to cacao plantations; these may survive as long as the plantations are not expanded. Any opening in the canopy NUMBER 68 5 with a concommitant increase in light intensity, however, could well cause these communities to succumb. A few plants are in cultivation at Rio de Janeiro and in the United States but they are not thriving and, like the plants of 19th century Paris greenhouses, they have never attained the robust size observed in the tall, densely shaded, and rocky rainforest in which they are native. Unless there are colonies still to be discovered we are probably facing the imminent demise of this unique grass. TAXONOMY 1. Anomochloa marantoidea Brongniart FIGURFS 1-4 Anomochloa maranfoidea Brongniart. 1851:368. pl. 23. [Type: Brazil, Bahia: ?e provincia Bahiensi Brasiliae accepit clar. Morel, Morro Queimado,? anno 1842, without collector [or collector Pmel?], cultivated in Pans, August 1848 (Holotype, P; photograph and fragment, US; isotype, P).] A. macrantoidea Brongniart in Pritzel, 1866:74 [error for A. marantoidea Brongniart.] DESCRIPTION.--PI~~~S cespitose, to 1 m tall in many- stemmed loose clumps, prop roots not present; rhizomes sympcdial, 0.5-5 cm long, to 7 mm in diameter, papery and weak. Culms weak, up to 0.5 m tall, all but the uppermost leaves borne at the base of the plant; bladeless sheaths below, preceding 5-10 fully developed leaves, the lowest with ovate leaf blades, several mm long, finely puberulent, these grading above into longer linear ones, the Uppermost bladeless sheath linear, up to 23 cm long; leaves with reduced, transitional blades not present. Leaves 4-7 per culm, all clustered at the base of the culm except frequently for the uppermost one; the bases of the sheaths strongly two-ranked and divergent, the blades held at different heights above the ground; leaf sheaths erect, yellowish green, hollow, striate, open, 15-30 cm long and up to 1 cm wide (folded width), semicircular in cross-section, the margins extended into prominent membranous wings up to 5 mm wide near the base of sheath, these narrowing abruptly to a width of 1-2 mm near the apex, with one margin prolonged into a rounded, glabrous auricle 1-3 mm long; summit of sheath without lateral appendages and oral setae; inner ligule a dense, emarginate fringe of clear cilia 1-2 mm long, not membranous; outer ligule absent; pseudopetioles strongly divergent from summit of sheath, (5)13-18(23) cm long, hollow, grooved adaxially, bipulvinate, the lower pulvinus up to 3 mm long, the upper pulvinus up to 5 mm long, both pulvini solid, turgid, dark-colored, and covered with clear, appressed hairs up to 1.5 mm long, especially on the adaxial surface; expanded portion of blade (18)2540 cm long, (4)6-10 cm wide, narrowly lanceolate to most commonly oblong- lanceolate, the margins parallel in the lower half of the blade, then gradually tapering to the apex in the upper portion; lamina thin, papery, glabrous above, scaberulous below, the venation almost strictly parallel, with nearly all of the nerves meeting at the base; base truncate to slightly subcordate with the slightly auriculate portions on each side of the upper pulvinus slightly upturned; midrib raised on both surfaces, prominent and with slightly overhanging margins adaxially (0.8-1.2 mm wide near the base of the blade), low dome-shaped and not as prominent abaxially (where 0.4-0.5 mm wide); blade margins glabrous, or scaberulous near apex; primary lateral veins 4-6 on each side of the midrib; tertiary lateral veins spaced 0.8-1 mm apart, prominent only on the lower (abaxial) surface, transverse veinlets present, also prominent only abaxially: a vein intermediate in size between the primary and tertiary lateral veins often present midway between each pair of primary lateral veins: uppermost leaf of culm frequently small, with a slightly inflated leaf sheath about 10 cm long, a short pseudopetiole, and the expanded portion of the lamina ovate, 10-15 cm long. Inflorescence borne on a subglabrous peduncle 5-7 cm long, terminal (but often inconspicuous because of the overtopping leaf blades on the same shoot), spike-like, often curved when developing but straight at maturity, laterally compressed and bilaterally symmetrical, 7-14 cm long, 1.3-2.5 cm wide (or up to 5 cm wide when bracts subtending partial inflorescences (main branches) fully spread at maturity), terminating in a fully developed spikelet; rachis zigzag, puberulent (especially below the nodes), alternately bearing 4-7 partial inflorescences, the lowest partial inflorescence often separated from the upper ones by an exposed portion of the rachis up to 5 cm long; general bracts subtending each partial inflorescence 4.5-9 cm long, folded width 0.7-1 cm, lanceolate, attenuate, rounded on the back but somewhat carinate near apex, prominently many-nerved and cross-veined, green, the general bract subtending the lowermost partial inflorescence always appressed- ascending and frequently bearing a small blade up to 5 cm long, the general bracts subtending the upper partial inflores- cences always strongly overlapping, bladeless, gradually smaller and becoming divergent from the rachis with age. Partial injlorescences bearing up to 5 spikelets in a secund arrangement along a greatly twisted axis: main axis of partial inflorescence erect, terminating in a spikelet borne on a thickened and slightly obconic pedicel 7-15 mm long and 2-3 mm wide; main axis bearing near its base on the adaxial side 2 linear, membranous, nerveless, apically brown-ciliate, and unequal bracteoles, the smaller member linear, delicate, not keeled, up to 5 mm long, the larger attached slightly higher on the branch, typically lanceolate, strongly keeled, up to 10 mm long; main axis bearing above the bracteole pair on the side opposite the rachis a membranous to scarious, elliptic or ovate bract 7.5-15 mm long with a strong, often ciliate midnerve and several faint lateral nerves, often ciliate at the apex; this bract subtending a lateral branch, the latter continuous with the pedicel of the second spikelet, 5-13 mm long, often slightly exceeding the pedicel of the first spikelet, and bearing a rudimentary or fully developed spikelet in robust inflorescences; branching of partial inflorescences reiterating in a scorpioid cyme-like manner to produce up to 3 fully 6 SMITHSONIAN CONTRIBUTIOSS TO BOTANY FIGURE 1.-Field photographs of Streprochaeta and Anomochloa: a , fruiting clump of S. spicata subsp. spicafa on Barro Colorado Island, Panama (note tangled, pendent masses of pseudospikelets); b, Habit of A. marantoidea, Bahia, Brazil (site of collection of Calderdn ef al. 2381), showing leaf blades borne at different heights and in different orientations due to varying lengths of the leaf sheaths and pseudopetioles. Photographs by Judziewicz NUMBER 68 7 FIGURE 2.-Field photographs of Strepfochaefa and Anomochloa: a, upper leaves and inflorescence of S. sodiroana, La Selva, Costa Rica. A . marantoidea, Bahia, Brazil (site of collection of Calderdn ef al. 2381): b, inflorescence during late phase of flowering, showing exserted stamens (note the varying lengths of the leaf pseudopetioles and the cupped bases of the expanded portion of the leaf blades); c, inflorescence during early phase of flowering, showing solitary stigmas exserted from the comiculate upper spikelet bracts; d, inflorescence as it appears among the foliage as viewed from the "back" side (a few stigmas visible). Photographs by Judziewicz. 8 SMITHSONIAN COSTRIBUTIONS TO BOTASY developed spikelets and 2 progressively smaller rudimentary spikelets, each successive lateral branch subtended by an ovate, keeled, scarious bract whose midrib nests with those of successive lower and higher subtending bracts, and the axis of each branch oriented so that the smaller (lower) member of the 2 bracteoles of a given branch is positioned directly behind (abaxial to) the keel of the bract subtending the branch of the next highest order. Spikelets terminal, I-flowered, bisexual, deciduous from pedicels at maturity, consisting of a deciduous lower bract separated by a cylindrical internode from a persistent upper bract that encloses the floret. Lower spikelet bract 10-15 mm long, broadly lanceolate, rounded on the back below, somewhat carinate near the tip, green, 10-17-nerved, conspicuously cross-veined, the apex with hyaline, ciliate margins, at length deciduous, separated from the upper spikelet bract by an indurate, whitish, slightly obconic intern0d.e 3-4 mm long and 2.5-3.5 mm in diameter, this glabrous or with scattered cilia above, at length deciduous from lower spikelet bract and summit of pedicel along with the persistent upper spikelet bract and its enclosed caryopsis. Upper spikelet bract on the opposite side of the cylindrical internode of the lower spikelet bract, consisting of an ovoid body surmounted by a linear horn-like appendage (cornicu- lum): body of upper bract 9-13 mm long, coriaceous at maturity, whitish, densely pubescent with prickles and clear hairs about 1 mm long, the margins meeting and strongly overlapping and locking with one another (except near the summit at anthesis), the venation inconspicuous externally, consisting of 4-6 irregularly spaced principal nerves (including a midnerve only slightly more conspicuous than the main lateral nerves) and 5-8 minor nerves, the former not visible on the outer surface of the body but visible as ridges on the interior surface; corniculum 13-18 mm long, -1-2 mm wide (often slightly wider near the summit), firmly membranous, finely pubescent, slightly grooved, slightly curved and protruding from the lower spikelet bract, at length deciduous. Perigonate annulus closely surrounding base of andrecium, consisting of a continuous fringe of brown cilia 0.5-2 mm tall borne on the summit of a low membranous ring. Andrecium of 4 stamens (occasionally the rudiment of a 5th present), these extruded from between the upper margins of the body of the upper spikelet bract at anthesis: filaments free, to 2 cm long, 2 mm wide, succulent, white, the anthers 3-5 mm long, white, elliptic-sagittate, attached to the filaments in such a way that the connective surrounds the summit of the filament without fusing to it ?or 0.4-0.7 mm; thecae introrse, facing the center of the andrecial circle. Gynecium with ovary stout, ellipsoid, 3-4 mm long and 1-2 mm wide, oblong-pyramidal, obliquely tipped, glabrous: style and stigma 1, the latter papillose, white, exiting through the open tip of the corniculum and extending up to 1 cm beyond it, lax. Caryopsis oblong-rectangular, laterally compressed, up to -10 mm long, 2.5 mm wide, and 4 mm deep (in profile), glabrous, the summit of the style persistent as a short, folded, oblique beak: hilum inconspicuous, a shallow groove extend- ing nearly the full length of the grain; pericarp thin, yellowish brown: endosperm mealy; embryo oblique-basal, large, up to 2.7 mm tall and 1.8 mm wide. DISTRIBUTION.-Known only from wet, lowland tropical forests in the Municipio of Una, Bahia, Brazil. ADDITIONAL SPECIMENS SEEN.-(Because of the rarity of this species, the specimen labels are quoted in their entirety to avoid any future confusion.) BRAZIL. Specimens from the type plant (or descendents) were cultivated as late as 1866 (K!, fragment US ex L, W!). Municipio de Una: Primary forest on steep (45") rocky slope bordering cacao plantation, altitude 180-200 m, old inflorescences, 21 Apr 1976, C.E. Calderdn, TS . dos Santos, and L.B. de Oliveira 2381 (CEPEC, IBGE, K, LE, RB, US 13 sheets], WE) , 11 Jul 1978, old inflorescences, TS. dos Santos and L.A. Mattos da Silva 3236 (CEPEC, K, MO), 20 Jan 1982, sterile, only a few plants in old fruit, V.C. Hollowell, T S . dos Santos and A.M. de Carvalho 3000 (CEPEC, F, ISC, R, SI, UC, US, W), 3001 (B, P), 3002 (INPA), 3003 (SP), 3004 (G), 18 Oct 1983, in all stages of flowering and fruiting, T S . dos Santos, G. Martinelli, and TR. Soderstrom 3880 (CANB, CEPEC, NY, RB, US), 21 Feb 1986, all sterile, E.J. Judziewicz and TS . dos Santos s.n. (US), 12 Mar 1986, most plants sterile, E.J. Judziewicz and T S . dos Santos s.n. (US); Municipio de Una, disturbed primary forest on 30" rocky slopes, altitude 160-180 m; 21 Feb 1986, all sterile, T S . dos Santos and E.J. Judziewicz 4111 (CEPEC), 12 Mar 1986, all sterile, TS. dos Santos and E.J. Judziewicz 4266 (CEPEC, US; living plants cultivated at CEPEC and US). VOUCHER SPECIMENS FOR ANATOMICAL STUDIES .-Brazil: Calderon, dos Santos, and Oliveira 2381 (US) (leaves); dos Santos, Martinelli, and Soderstrom 3880 (US) (leaves, inflorescence, spikelets, starch grains, embryos). DIscUssIox.-The two localities at which Anomochloa marantoidea grows are humid, tall forests on the steep, rocky (with granite boulders), lowermost slopes of the low mountains west of Una. At each site the area throughout which the plants grow consists of only a hectare or two, and only about 90 individual plants were counted at any one station. Individuals growing in treefall gaps, partial shade, or forest edges are much smaller than those growing in dense shade. Visits to the extant sites from January through April (1976, 1982, 1986) have revealed plants with mostly old infructescences and only a few in flower. The October 1983 visit by Talmon dos Santos et al. revealed the 1976 colony in all stages of flowering and fruiting, but dos Santos (pers. comm., 1986) indicates that the plants usually bloom during the height of the local rainy season during June and July. Anomochloa marantoidea is the only species in its genus and tribe. Because of its rarity (and because the species is not well established in cultivation) we are not citing here the exact collection localities of the two known populations: this information is available in the files of the McClure Bamboo Library, Department of Botany, National Museum of Natural NUMBER 68 9 History, Smithsonian Institution. Unfortunately most other potentially suitable sites for the species in the Una region have been destroyed in recent years through increased planting of cacao. Because only about 30 herbarium sheets exist we urge that anyone visiting the sites refrain from making further gatherings. FIGURE 3.-Anomochloa marantoidea: a, habit, showing leaf blades borne on leaf sheaths and pseudopetioles of varying lengths (X 0.22); b, inflorescence terminating culm with uppermost subtending leaf, the lowest leaves removed (X 0.22); c, upper portion of pseudopetiole and base of leaf blade showing upper pulvinus, adaxial view (X 1.72); d, upper portion of pseudopetiole and base of leaf blade showing upper pulvinus, abaxial view (X 1.72); e , inner (adaxial) view andf, side view of summit of sheath and lower portion of pseudopetiole showing lower pulvinus and ciliate inner ligule (x 1.72); g, portion of leaf blade, abaxial surface showing transverse veinlets (x 1.72). (a and g based on Cafderon et a f . 2381, b-fon dos Sanfos ef a f . 3880, both from Brazil.) Illustration by Alice R. Tangerini. 10 n 0 P SMITHSONIAN CONTRIBUTIONS TO BOTANY NUMBER 68 11 FIGURE 4 (lef).-Details of partial inflorescences and spikelets of Anomochloa marantoidea: a, portion of inflorescence showing the lowest and next to lowest partial inflorescences (note reduced leaf blade on bract subtending lowest partial inflorescence) (x 1.59). Base of partial inflorescence, the bract subtending the partial inflorescence removed (x 3.18): b, ventral view; c, dorsal view, showing keeled, nested bracts that subtend each successive branch. d-J Variation in bract that subtends each lateral branch (x 3.18); g, basal portion of primary axis, showing pair of small, lower (left) and large, upper (right) bracteoles at base (subtending bract between bracteoles and axis removed) (x 3.18); h, variation in the small bracteole found as the first appendage on each successive lateral branch (X 6.36); i, variation in the large bracteole found as the second appendage of each successive lateral branch (X 6.36); j , spikelet showing deciduous lower bract and pedicelled upper bract (the comiculum fallen from the latter) (x 3.18). Caryopsis (x 4.77): k, side view, showing oblique beak; 1, ventral view. showing linear hilum; m, dorsal view. n, Portion of spikelet (upper bract partially dissected away) showing ovary surrounded by perigonate annulus and with anomalous bract found in one spikelet (stamens removed) (x 6.36), o, lower spikelet bract, adaxial view (X 3.18); p, spikelet, side view showing comiculate upper bract embraced by lower bract (note exserted stigma) (X 3.18); q, longitudinal section of spikelet (lower bract removed), with thickened internode supporting upper bract, perigonate annulus, stamens, and gynecium (x 3.18); r, anther, adaxial view (X 6.36); s, anther, abaxial view (x 6.36); t , spikelet (lower bract removed) at male flowering stage, showing the stamens emerging from between the margins of the summit of the body of the upper bract (x 3.18). (Based on dos Santos et al. 3880, Brazil.) Illustration by Alice R. Tangerini. FIGURE 5.-Transverse sections of sheaths and pseudopetiolar regions of leaves of Anomochloa and Streptochaeta. A. marantoidea (Calderdn et al. 2381): a, leaf sheath showing prominently winged margins and hollow body; b, lower pulvinus, showing smaller sheath margin wings and ciliate inner ligule (arrow); c, upper pulvinus as it expands into the blade, showing complex vasculature (adaxial epidermis on right). d , Pulvinus of S. spicala subsp. spicata (Calderdn 2046, Brazil), showing complex vasculature and pubescent adaxial surface below. Scale bar: a = 400 pm; b-d = 250 pm. 12 SMITHSONIAN CONTRIBUTIOSS TO BOTANY FIGURE 6.--Leaf epidermides of Anomochloa marantoidea: a,b, adaxial epidermis, showing buUiform cells, crescentic silica/cork cell pairs, and isolated vertical-crenate silica cells; c, abaxial epidermis (note scattered prickles and bicellular microhairs; basal cell only intact); d, bicellular microhairs from abaxial epidermis (note constricted basal cell, arrow). Abbreviations: bm = bicellular microhair, co = costal silica cell; is = intercostal isolated silica cell; ip = intercostal paired silica cell; pr = prickle. Scale bar: a,c = 100 l m ; b = 25 p; d = 30 pm. (Based on Calderon et al. 2381, Brazil.) MORPHOLOGY- ANATOMY Culm and Leaf Sheath The culm of Anomochloa marantoidea is solid. The leaf sheaths are hollow with a large lacuna and prominent winged margins (Figure 5a), which embrace successive leaf sheath bodies. The marginal wings have about five vascular bundles and are often inrolled in a scroll-like fashion, The adaxial side of the leaf sheath is thicker and has several superposed tiers of small vascular bundles. Toward the summit of the sheath its marginal wings narrow and approach each other, and the summit of the sheath and lower pulvinus are nearly elliptical (Figure %).The sheath becomes solid in the area of the lower pulvinus for a few millimeters, but the vascular bundles still consist of a circle of approximately 10 to 12 large bundles with a roughly alternating circle of small vascular bundles just interior to them. Continuing acropetally through the lower pulvinus, these smaller vascular bundles and some of the larger ones contribute to a complex plexus in the center of the sheath. Ligule and Pseudopetiole No external ligule is present; the internal ligule is present as a fringe of ciliate hairs. At the summit of the lower pulvinus the pseudopetiole begins; again there is a lacuna in its center, but not so large as in the leaf sheath. The body of the pseudopetiole is V-shaped in cross-section. Pulvini In cross-section the upper pulvinus is slightly V-shaped, with the trough of the V on the adaxial surface. The ground NUMBER 68 13 tissue consists of large parenchyma cells. The epidermis is sparsely papillate and pubescent. The main vascularization consists of a V-shape arch of bundles near the abaxial epidermis. These bundles are connected, or nearly so, to that epidermis by sclerenchyma caps. Subjacent to the adaxial surface are 5 to 8 sclerenchymatous areas that lack vascular bundles. The area between the adaxial epidermis and the main arch of vascular bundles consists of parenchyma cells in which are embedded about 10 small vascular bundles in a complex pattern. At its base the pulvinus encloses a large block of sclerenchyma buried a few cells beneath the adaxial epidermis (Figure 5c). Farther up, this block of cells approaches the epidermis and is contiguous with a broad, shallow, scler- enchyma plate covering the top of the adaxial midrib (Figure 7 4 . Toward the base of the lamina the adaxial midrib appears abruptly and soon takes on its characteristic square or anvil shape. Leaf-blade Anatomy TRANSVERSE CTION (Figure 7d-g).-Outline: blade flat, expanded (except near cup-like base), the epidermides nearly straight, the margins rounded to slightly acute. Midrib outline: distinctive, projecting both adaxially and abaxially; adaxial projection in lower 2/3 of the blade anvil- or keystone-shaped, narrowed at the base and with a broad, flat, top with margins that slightly overhang the lamina (this keel reduced to merely an inverted U-shape in the uppermost l/3 of the lamina); abaxial projection less prominent, low dome-shaped. Midrib vascula- lure: complex in well-developed blades, with at least two tiers of vascular bundles; one large, median, first-order bundle with a lysigenous cavity and a pair of metaxylem vessels always present subjacent to the abaxial epidermis, this not flanked by any smaller bundles; several third-order vascular bundles present in adaxial half of the midrib, characteristically in a crude T- or Y-shaped pattern, with the base of the Y or T in about the center of the midrib. Midrib sclerenchyma: in two plates, one on the adaxial keel, relatively shallow (5-8 cells wide), and unconnected to any of the subjacent minor vascular bundles; the other on the abaxial keel deeper (-8-12 cells wide), more well developed, and partially surrounding the median vascular bundle, with the sclerenchyma continuous with the bundle sheath. Vascular bundle arrangement in the lamina: all bundles closer to the abaxial than adaxial epidermis. Primary vascular bundles: ovate in outline; double sheath present, the outer sheath of large, thin-walled, inflated cells with few plastids, complete on the adaxial side and often with a small extension to the adaxial sclerenchyma cap, but interrupted on the abaxial side, where interrupted by the sclerenchyma of the abaxial bundle cap; inner sheath of two complete rows of narrow, achlorophyllous, thick-walled cells; lysigenous cavity and two metaxylem vessels present; adaxial sclerenchyma cap squarish or inverted triangular, 10-17-celled, abaxial sclerenchyma cap narrow, horizontal, about 15-20- celled. Third-order vascular bundles: somewhat rectangular in outline; double sheath present, similar to that of the first-order vascular bundles, but adaxial outer bundle sheath extension never developed and abaxial sclerenchymatous interruption of the outer sheath only one cell wide; inner bundle sheath one or two cell-layers thick; adaxial sclerenchyma cap small, usually inverted-triangular, consisting of (2-) 5-1 2 cells, the abaxial cap of 8-14 cells. Intercostal sclerenchyma: absent. Mesophyll: chlorenchyma not radiate, consisting of one layer of cells immediately subjacent to each epidermis on either side of inflated fusoid cells, each one cell-layer thick, and separated by inflated fusoid cells; adaxial chlorenchyma rectangular, horizontal, the cells with several moderately developed arms projecting inward towards the fusoid cells; abaxial chlorenchyma cells less conspicuous than adaxial layer, narrowly rectangular and lacking any projections; fusoid cells well developed, rectangular, adjacent fusoid cells separated by a well-developed chlorenchymatous column 1-3 cells wide. ABAXIAL EPIDERMIS (Figure Bc,d).-Costal and intercostal zones well differentiated. Intercostal long cells: homogeneous, rectangular (length:width, 4-6: l), with strongly sinuous walls; in well-developed cells the sinuations themselves undulating. Stomata: in 1-3 short, interrupted rows along each side of the costal zones, each short row staggered so that it continues where the last row terminated; subsidiary cells low dome- shaped to slightly triangular; stomates separated by 1(-3) long cells. Bulliform cells: absent. Papillae: absent. Prickle hairs: fairly common in intercostal zones; base greatly inflated, tip small, narrow, sharp; usually paired with a cork cell. Macrohairs: absent. Microhairs: scattered throughout intercos- tal zone between the stornatal regions; apparently bicellular; basal cell 40-50 pm long, cylindrical, relatively thick-walled, with an apparent constriction near the base; apical cell narrowly ellipsoid, 45-65 pm long, tapering to a blunt tip, thin-walled and easily deflated; total length of microhair 90-1 15 pm. Short cells: abundant, typically in pairs (silicalcork), these alternating with the long cells; cork cells crescent- or kidney-shaped, embracing a similarly shaped but slightly smaller silica cell; occasionally, solitary short cells (apparently cork cells) alternating with the long cells in the stomatal region. Costal cells: in rows of 2 4 , consisting of modified, long-rectangular (length:width, -10: 1) long cells separated by short to long (2-8 individual cells) rows of squarish silica cells; cork cells rare or absent. ADAXIAL EPIDERMIS (Figure &).-Basically similar to the abaxial epidermis. Bulliform cells: in 3 or 4 rows, covering about l/4 of the intercostal zones, well developed and distinct from typical long cells, square to rectangular (length:width, 1-3:1), with moderately sinuous walls; not alternating with any other cell type. Intercostal long cells: rectangular (1ength:width 34:1), strongly sinuous, alternating with short cell pairs. Papillae: absent. Prickles: not seen. Macrohairs: absent. Microhairs: extremely rare, only one seen. Short cells: similar to those of abaxial epidermis. Silica cells: occasional to fairly common in intercostal zones, interpolated between adjacent 14 SMITIISOSIAN COSTRIBUTIONS TO BOTANY FIGURE 7.-Transverse sections of leaf blades of Streptochaeta sodirwna ( a x ) and Anomochloa marantoidea (d-g) (in all cases the adaxial epidermis faces upwards): S. sodirwna (Soderstrom 1205): a, characteristic midrib with its complex vasculature; b, detail of fusoid cell and primary vascular bundle in the lamina: c, detail of lamina showing minor vascular bundle, fusoid cells, and primary vascular bundle. A. marantoidea (Calderon et al. 2381, Brazil): d , section of lamina showing minor vascular bundle, fusoid cells, and primary vascular bundle; e,g, midrib section from a robust leaf, showing characteristic shape and complex vasculature;f, section of lamina including midrib, cut from a small leaf. Scale bar: a,c-e = 100 p; b = 50 p;f= 200; g = 250 pm. long cells in the same row, and protruding above and below subsidiary cells generally more triangular than those of abaxial that row halfway into the rows of long cells above and below epidermis. Costal cells: similar to those of the abaxial it; consisting of a vertical, elliptic cell enclosing a crenate silica epidermis, but silica cells tending to be rounder. body. Stomata: occasional near veins, in short irregular rows; .\'UMBER 68 15 Inflorescence In the above description .of the inflorescence and spikelets of Anomochloa marantoidea we have chosen not to give any formal morphological interpretations of the components of the partial inflorescences, spikelet bracts, and perigonate annulus at this point. We do wish to elaborate on the complex patterns of branching and bract disposition in the inflorescence, features that do not lend themselves well to a formal taxonomic description (Figures 4, 8, 9, 15). The structure of the partial inflorescence in the following robust individual is typical of all other individual partial inflorescences examined in the species. The rachis of the inflorescence always terminates in a fully developed spikelet (Figure 15), which is not associated with any rudimentary spikelets or prolongation of the rachis. Below the terminal spikelet are a series of 4-7 alternating lanceolate, chlorophyllous, foliaceous bracts spaced along the rachis. The lowest of these bracts, which, unlike the upper ones, often bears a reduced, pseudopetiolate leaf blade (Figure 4a), is frequently separated from the second lowest by an exposed portion of the rachis several centimeters long. Each of these prominent subtending bracts, which we shall refer to as "general bracts" (after the designation "bractks generales" of Brongniart), subtends a partial inflorescence bearing from 1 to 3 fully developed and 1 or 2 rudimentary spikelets (Figure 4a). Figure 4 illustrates a partial inflorescence taken from a robust inflorescence. The general bract subtends the primary axis of the lateral branch, which terminates in a fully developed spikelet. Near the base of the primary axis, on the side nearest the rachis, is usually borne a pair of delicate unequal bracteoles, with the smaller bracteole borne on a slightly lower level (Figure 4g) than the larger bracteole. The bracteoles are separated by about 120" with respect to the center of the axis that bears them. The lower bracteole of this pair is narrowly linear (Figure 4h) while the other is broadly lanceolate and strongly keeled (Figure 44. Both bracteoles lack any vascularization and are hyaline and covered, especially in the upper portion, with brown cilia. Slightly above them on the primary axis of the branching system is a bract (Figure 4d-f) that subtends a secondary axis. The smaller of the two bracteoles just discussed is positioned near the keel of this bract (Figure 4c), which is ovate, hyaline, and has a well-developed midrib containing a vascular bundle. Its keel is positioned at right angles with respect to a line drawn from the center of the rachis through the center of the successive axes of the lateral inflorescence. As in the primary axis, the secondary axis subtended by the bract terminates in a fully developed spikelet and bears a pair of delicate, unequal bracteoles from near its base on the side facing the rachis. The smaller member is borne on a slightly lower level than the larger. Again, the members of the bracteole pair are separated by about 120" and tipped with a fringe of brown cilia. Above these bracteoles on the secondary axis is situated an ovate, keeled bract subtending the tertiary axis of the partial inflorescence. Like the preceding branch-subtending bract, this subtending bract is rotated about 90" with respect to a line connecting the rachis and successive lateral branches. Because of this its keel appears to be nested within the keel of the preceding branch-subtending bract (Figure 4c). In the specimen examined (dos Santos et al. 3880) the tertiary axis emanating from the axil of this subtending bract also terminates in a fully developed spikelet, bears near its base a pair of unequal bracteoles with the smaller bracteole arising on a slightly lower level, and above these bracteoles bears a keeled bract (whose keel nests with the keels of the bracts subtending the secondary and tertiary axes) that subtends a fourth-degree axis. The fourth-degree axis of the partial inflorescence terminates in a small spikelet containing a rudimentary gynecium and four stamens and bears a pair of tiny unequal bracteoles attached at nearly the same level near its base, and above these bracteoles a small keeled bract that subtends an axis bearing two tiny bracteoles as its first appendages and terminating in a tiny, rudimentary fifth spikelet. Each axis in the branching system terminates in a spikelet and bears near its base on the adaxial side a pair of delicate bracteoles. The smaller member of the pair is borne on a slightly lower level and is positioned near the keel of the bract subtending the next axis of the branching system (Figure 4). The larger bracteole is lanceolate, keeled, and is separated from the smaller bracteole by about 120" with respect to the axis that bears it. The bracteole pair members are tipped with a fringe of brown cilia and lack any vascular bundles. The bracts actually subtending each successive lateral axis of the branching system are much larger than the bracteoles and are ovate, scarious, and keeled (Figure 4d-f. In a robust partial inflorescence the keels of successive subtending bracts are nested at an angle of 90" with respect to a line drawn from the center of the rachis through the centers of successive lateral axes. The bracteole pair members of successive axes are also nested to the extent that all large bracteole pair members are aligned on one side of the partial inflorescence (Figure 46) while all small bracteoles are aligned on nearly the opposite side of the partial inflorescence. The smaller member of the bracteole pair arises slightly lower on the axis than the larger member, and the pair members are always completely separate from each other, even at their bases. The inflorescence of Anomochloa marantoidea, then, is qped with a spikelet and bears on its axis alternating partial inflorescences, each of these subtended by a prominent general bract that gives the inflorescence its marantaceous aspect. The inflorescence is laterally compressed and has a quite different appearance depending on which side is viewed. From one side all that is seen are the overlapping general bracts subtending each partial inflorescence (Figure 36). But viewed from the opposite side many features are observed (Figure 26,c): the general bracts subtending each successive partial inflorescence are visible but so are the upper portions of one or two of the spikelets in each partial inflorescence. Typically the upper 16 SMITHSONIAN COSTRIBUTIONS TO BOTANY FIGURE 8.-Acropetal serial transverse sections through a partial inflorescence of Anomochloa marantoidea: a, rachis (above) and pedicel of first spikelet (below) enclosed by the ?general bract? (B); b, emergence of pedicel of second spikelet (below); c, pedicel of second spikelet completely free from pedicel of first spikelet; d, beginning of emergence of pedicel of third spikelet. Abbreviations: B = bracts subtending successive branches of the partial inflorescence; b(1,2) = first or second bracteoles on each successive lateral branch; P(l-3) = successive lateral branches, terminating in a spikelet pedicel; R = rachis. (Based on dos Santos et al . 3880, Brazil). Scale bar: 500 pm for all sections. NUMBER 68 17 FIGURE 9.-Acropetal serial transverse sections through a partial inflorescence of Anomochloa muranfoidea: a, pedicels of first three spikelets with pedicel of rudimentary fourth spikelet emerging; b, rudimentary third spikelet; c, detail of o; d, detail of 6, showing rudimentary third spikelet with three rudimentary stamens surrounding the rudimentary gynecium. Abbreviations: B = bracts subtending successive branches of the partial inflorescence; b( 1,2) = first or second bracteoles on each successive lateral branch; gy = gynecium; LSB = lower spikelet bract; P(1-4) = successive lateral branches terminating in a spikelet pedicel; st = stamen; USB = upper spikelet bract. (Based on dos Snnfos ef al. 3880, Brazil.) Scale bar: a,b = 500 pm; c,d = 150 p. 18 SbliTIISONIAN COKTRIBUTIONS TO BOTANY portion of the bodics and the cornicula of the upper spikelet bracts are visible, as wcll as the thc upper portion of the lower spikelct bracts that sheath the upper bract (Figure 4a). In robust partial inflorcsccnccs the cornicula of the upper spikelet bracts of the second and third spikelets are also visible. In any case the cornicula of the upper spikelet bracts have a characteristic curvature, arching towards the partial inflorescences on the opposite side of the rachis. The stigmas are exserted through thcse cornicula (Figure 4q,t), face the same direction as that to which the cornicula point, and are held close to the inflorescence. Thus at anthcsis (see following discussion; Figure 2c) the stigmas are conspicuous against the green background of the general bracts and lower spikelet bracts. In contrast the stamcns, whcn cxtrudcd from bctwccn the margins of the body of the upper spikclct bract, arc held almost horiLontAly away from the body of the inflorcsccnce at a distance of a 1 or 2 cm (Figurc 2b). Spikelet LOWER SI?IKELBT BRACT.-This appendage bears a strong resemblance to the general bracts that subtend each partial inflorescence. It is chlorophyllous and strongly nerved, with many transverse veinlcts. This bract does not possess fusoid cclls as would a typical lamina, nor does it possess the laminated structure typical of the upper bract (sce ?Upper Spikclct Bract?). THICKENED 1NTErLYoDn.-The internal anatomy of this structure is difficult to interpret bccausc the cclls were highly distorted in preparation. In clcarcd spikclcts and longitudinal sections (Figure 12b) a complcx florct stele or vascular plexus is found in the uppermost */s of the internode. The cpidcrmis of the internodc is smooth or may bear scattered brown or clear cilia. UPPER SPIKELET BRACT.-Thc upper bract is complex, and for convcnicnce it may be divided into two parts: the lower, ellipsoid body and an apical, deciduous horn or corniculum. The abaxial epidermis of the body is covered with a dense, fine indumentum of clear, l-celled ciliate macrohairs, inter- mixed with prickles and roundcd, silicified papillae (Figure 10a-c). Subjacent to this is a similar layer of undifferentiated parenchyma cells. Just bclow this are transverscly elongated cells (length:width, -10: 1) with moderately thickened walls; this stratum is 6-8 cells thick. In some sections single transverse vcinlets, consisting of only a single xylcm vcsscl, arc apparcnt. This transverse stratum givcs the organ a distinctive ?laminated? appearance, especially well displayed in paradcrmal sections (Figure 124. This laminated slructure continues for a millimeter or more into the summit of the thickened internode below the bract. Subjacent (adaxial) to the transversely elongated layer are the vascular bundles and 4-7 layers of roundish, thin-walled, vertically elongated paren- chyma cells, these subjacent to the adaxial epidcrmis. There are 5 or 6 principal vascular bundles in the upper bracts of the spikelets examined, each containing well-developed metaxy- lcm vessels and a protoxylem lacuna, and associated with a slight rib on the adaxial surface of the bract. The median vascular bundle is slightly more prominent than the others. Alternating with these major bundles are from 8-12 minor bundles, these located close to the adaxial boundary of the transverse cell layer. Many of these minor bundles consist of but a single xylem vessel. One, occasionally 2, or rarely 3 minor bundles are situated between successive major bundles. The bract margins overlap strongly so that one margin retains a spiral- or sickle-like aspect and curls over and interlocks with the other, which resembles the head of a hammer (Figure 1 la). This tight interlocking is maintained throughout the lower two-thirds of thc b rx t , but bccomcs looser in the upper portion of the body. The corniculum of the uppcr bract is covered externally with the same type of ciliate, transparent macrohairs that cover the body; internally the corniculum is 5-8-nerved. PERIGONATE ~ N U L V S (Figures lOa-c, lla-b, 12c).-The basal membranous part of this circular structure is only a few cells high and wide, and is appressed to the base of the filaments. The ring is complete; in acropetal serial cross- sections of the spikelet it is not evident which side of the ring appears first; it appears to arise, along with the andrecium and gynecium, from the summit of the cylindrical internode separating the lower and upper spikelet bracts. No vascular bundles were detected entering or even approaching the perigonate ring. The dense fringe of hairs surmounting the ring consists of tapcring, brown (less commonly transparent), thin-walled, apparcntly l-cellcd cilia. These hairs vary in lcngth from 0.5-2 mm. Whcn cross-sectioned, thcse hairs often appear to break up into, or release, round brown globules. The hairs appear to be identical in structure to the cilia found in the ligular and pulvinar areas of the leaf and also on the surface of the upper spikelet bract. AYDRECICM.-h cross-sections made just below the bases of the filaments (Figures 10, l l ) , we found two large gaps on either side of the vascular bundle leading into the posterior stamen opposite the single, anterior stigma bundle (Le., on the side of the upper spikelet bract in which the margins overlap; Figure 10a). Several unusual structures were found in some spikelets: in one andrecium the base of the filament of the anterior stamen had a distinct lateral appendage (Figure 1 lb) that appeared to represent the rudiment of a fifth stamen; this rudiment was less than 50 pin long and bore no anther. In another spikelet the gap betwccn the anterior and one of the posterior lateral stamens was occupied by a hyaline, unvascularized linear (U-shaped in cross-section) appendage 5 mm long with strongly brown-ciliate margins (Figure 4n). The connective of the anthers completely encircles but does not fuse with the summit of the filaments for a short distance (0.4-0.7 mm) near the base of the anthers (Figures l l d , 12a). In cross-sections through their lower and middle portions, the anthers have an introrse aspect because their thecae are rotated forward slightly NUMBER 68 19 FIGURE 10.-Transverse sections of spikelet of Anomochlua and pseudospikelet of Streptochela. A . marantoidea (lower spikelet bract not sectioned) (dos Santus et al. 3880., Brazil): a, near base, showing flower still partially attachcd to base of uppcr spikelct bract, and perigonate annulus and filaments starting to separate from the ovary; b, detail of spikelet showing perigonate annulus, three posterior filaments, and portion of ovary; c, detail of spikelet showing laminated anatomy of upper spikelet bract (right), with perigonate annulus and part of ovary (left). d, Pseudospikelet of S. spicata subsp. spicata (Soderstrum and Cafderon 1861, Brazil), showing overlapping bracts X through XI1 surrounding the flower; flower composed of six stamens surrounding an ovary with three stigmatic vascular bundles (arrows); note attachment of ovule on right side of ovary. Abbreviations: B = pseudospikelet bracts X-XII; gy = gynecium; per = perigonate annulus; st = stamen; svt = stigmatic vascular trace; usb = upper spikclet bract. Scale bar: a = 300 pm; b-d = 100 pn. 20 SMITHSONIAN CONTRIBUTIOKS TO BOTANY FIGURE 1 1.-Transverse sections of spikelet of Anomochloa marantoidea: a , characteristic interlocking margins of the upper splkelet bract; b, rudimentary 5th stamen located between anterior stamen (upper) and one of the posterior lateral stamens (lower); c, detail of ovary showing absence of posterior lateral stigmatic vascular traces; anterior stamen at top, posterior at lower left; d, detail of stamen showing filament unfused to connective and the pollen sacs rotated towards the adaxial side of the stamen (upper right in this section); note also the laminated structure of the upper spikelet bract (lower). Abbreviations: en = connective; fi = filament; gy = gynecium; ovt = ovular (posterior) vascular trace; ow = ovule; per = perigonate annulus; rs = rudimentary stamen; s t = stamen; svt = stigmatic (anterior) vascular trace; usb = upper spikelet bract.(Based on dos Sanros et al. 3880, Brazil.) Scale bar: 100 pm for all sections. NUMBER 68 21 FIGURE 12.--longitudmal sections of spikelet of Anomochloa muruntoidea: u, laminated structure of upper spikelct bract (left) and filament attachcd to anther (right); b, detail of gynecium (note the vascular plexus at summit of internode below); c, detail of upper spikelet bract, perigonate annulus, and filament; d, oblique paradermal section of upper splkclet bract showing laminated structure. Abbreviations: an = anther, fi =filament; gy = gynccium; ii = inncr integument; nu = nucellus; oi = outer integument; ovt = ovular vascular trace; per = pcrigonate annulus; pl = vascular plexus at base of flower, re = internode between lower and upper spikelet bracts; svt = stigmatic vascular trace; usb = upper spikelet bract. (All based on doJ Suntos ef ~ l . 3880, Brazil.) Scale bar: u-c = 100 pm; d = 25 p. 22 SMITHSONIANCONTRIBUTIONS TO BOTANY and face the center of the andrccial circle (Figure 116). In the upper portion of the anther, however, the thecae have a more lateral arrangement on both sides of the connective. GYNEC1UM.-Cross-sections of the gynecium revealed the presence of two vascular bundles, one located on the posterior side (i.e., on that side at which the ovule is attached) of the ovary and leading into the ovule (ovular strand) and one located on the anterior side of the ovary and leading into the style (Figures 10a, l lb,c). Longitudinal sections of the ovary revealed the presence of two integuments surrounding the megasporangium (Figure 12b), which is attached to the ovary wall near the apex of the ovular cavity. The style with its single vascular bundle tapers apically into a single papillose stigma. Fruit CARYOPS1S.-The caryopsis, which is tightly invested by the uppcr spikelet bract at maturity, is elongate-prismatic with a slightly oblique beak and a shallow, inconspicuous linear hilum. The embryo is oblique-basal and is hidden by the papery, light brown pcricarp. STARCH GRAINS.-The endosperm of the mature caryopsis is mealy, and the starch grains are highly compound. Approximately 50-100 ellipsoidal grains occur in each cell and each grain ranges in size from 10-20 pm in diameter. Each grain is composed of 20-50 sharply angular granules and the granules range in size from 2.5-4.5 prn in diameter. EMBRYO.-In median sagittal scction (Figure 13c,d) the embryo exhibits a massive scutellum, an epiblast, and a fairly inconspicuous cldt bctween the lowcr part of the scutcllum and thc colcorhiza. Due to the promincnce of the scutellum and the relative inconspicuousness of the colcoptile and coleorhiza this cleft appears not basal but is situated about l/3 of the way up the abaxial side of the embryo. The coleoptilar-coleorhizal axis is rotated about 60? from the vertical, and no internode (mesocotyl) is prcscnt between the divergence of the vascular traces to the scutellar and coleoptilar nodes. In acropetal series of transverse sections through the embryo (Figure 14) near the base of the coleoptile 5 nerves are evident, 2 being submarginal, 2 submedian, and 1 median. The median nerve is soon lost distally, appearing to merge with one of the submcdial ncrves. Scctions madc ncarer the middle of the coleoptile reveal the structure of the first embryonic leaf; it is 3-ncrvcd, has margins that mcct but do not ovcrlap, and cncloscs a small sccond crnbryonic lcaf, In scctions madc still furthcr up the colcoptile, a distinct cleft begins to appear on the sidc of the colcoptile opposite the scutellum. This cleft broadcns until a distinct, oblique slit is observcd in the colcoptilc near its summit (Figure 14a, arrow). It is difficult to intcrpret the free margins of the coleoptile as either mceting without overlapping or as actually overlapping. Until near its apex, all four rcmaining nerves are still apparent in cross- sections of the coleoptile. CHROMOSOMES The only count was made by Juan H. Hunziker (pers. comm.), who found n = 18, based on the following collection: dos Santos, Martinelli, and Soderstrom 3880. DISCUSSION Habit In the dense shade of the forest Anomochloa marantoidea is a robust, clumped plant reaching up to a meter in height (Figure lb). In cultivation or in treefall gaps individuals are much smaller; Brongniart (1851) used the adjective ?humile? in his original description of greenhouse material. Plants of Anomochloa prcsent an unusual aspect in that the heights and orientations of successive leaf blades are regulated by several adaptations involving the leaf sheaths, pseudopetioles, and possibly the pulvini, and not by their disposition at the successive nodes of an elongated culm as in most grasses. The leaf sheaths have a nearly vertical orientation, but diverging from their summits by 45? or more are long pseudopetioles of varying lengths, with those of the upper leaves much longer than those of the lower. The variable lengths of the leaf sheaths and pseudopetioles may ensure that the blades are held at differing heights above the soil. The leaf sheaths are unusual in that they are consistently hollow. The base of the expanded portion of the lamina is slightly cordate and cupped upwards (Figures 2b, 3), a trait Anomochloa shares with other large-leaved umbrophilic herbaceous bamboos, such as the Bahian endcmic Sucrea monophylla (Bambusoideae: Olyreae) and the African Puelia schumanniana (Bambusoideae: Puelieae), as well as the broad-leaved Ichnanthus grandifolius (Panicoi- deae: Paniceae). Although Brongniart (1851) described the leaf blades as subarticulating we found no evidence that they are deciduous. The hollow leaf sheaths and pseudopetioles of Anomochloa may be unique in the family. Diurnal sleep movements of the leaf blades of the type observed in certain olyroid herbaceous bamboos (Arberella, Cryptochloa, Lithachne, Raddia; cf. Soderstrom, 1980) have not been seen in Anomochloa. However, in mature plants the blades have quite different orientations on the same shoot: some are held horizontally, while others are distinctly descending or ascending, and the blades of successive leaves are not placed in a strictly opposite orientation with respect to one another. It may be that the pulvini, although not involved in diurnal movcmcnts of the blades, help determine the mature orientation of the lamina. Bipulvinate pseudopetioles, although not common in the Poaceae, are known from large-leaved species of the centothecoid genus Zeugites. Leaves Two features are prominent in a transverse section of a leaf blade (Figure 7) of Anomochloa marantoidea. First, the fusoid NUMBER 68 23 FIGURE 13.-Median sagittal sections, embryos of Streptochaeta and Anomochloa: a , S. spicata subsp. spicata (Soderstrom and Sucre 1896, Brazil), showing poorly developed cleft between scutellum and coleorhiza (arrow); b, S. sodiroana (Calderon 2096, Panama), showing overlapping margins of coleoptile (arrow); c , A , marantoidea (dos Sanfos el al. 3880, Brazil), showing massive scutellum; d , detail of c showing abaxial position of cleft between coleorhiza and scutellum (arrow). Abbreviations: cp = coleoptile; cr = coleorhiza; ep = epiblast; If = first embryonic leaf; ra = radicle; sc = scutellum; vt = vascular trace. Scale bar: a,b,d = 100 pm; c = 25 pm. 24 SMITHSOXIAN CONTRIBUTIONS TO BOTANY FIGURE 14.-Transverse sections through plumule of embryo of Anomochloa marantoidea (dos Santos et a/. 3880, Brazil) (a through d proceeding in a downward (basipetal) direction with respect to the embryonic axis): u, unfused, obliquely meeting margins of coleoptile (arrow); b,c, margins of first embryonic leaf; d , entrance of vascular trace from scutellum, which becomes the midnerve of the coleoptile. Abbreviations: cp = c oleoptile; ep = epiblast; If = first embryonic leaf. Scale bar: 100 pn in all sections. NUMBER 68 25 cells are large, occupying about one-half of the volume of the lamina (Figure 7e). And secondly, the midrib posscsscs two projecting keels. The adaxial keel is more prominent and has a strongly flattened top with edges that overhang the base slightly. The abaxial keel is low, dome-shaped and is associated with the median vascular bundlc, which lics just bclow thc epidermis. Small blades have mcrcly a dome-like adaxial keel, no abaxial kecl, and a simple vasculature with but a single median vascular bundle lying close to the abaxial epidermis (Figure 7j). The vascular bundles of the leaf blades of Anomochloa have typically bambusoid sheaths, with an outer sheath of large, thin-walled cells with few plastids, and an inner sheath of one or two layers of small, thick-walled, fibrous cells. Arm cells are not well developed in the mesophyll subjacent to the adaxial epidermis, and bulliform cells on the adaxial epidermis are only moderately well developed. The epidcrmides of Anomochloa exhibit typically bam- busoid sinuous long cells. Leaf epidermal papillae, common in most bambusoids, are lacking in Anomochloa. The silica-cork cell pairs arc unusual in that both mcmbcrs arc vertically crcsccnt-shaped with the larger cork cell embracing the much smaller silica cell. The costal silica cells contain silica bodies that vary from round to squarish to slightly cross- shaped. A third type of silica cell is found on the adaxial epidermis, present as large, solitary, vertically elliptical cells enclosing olyroid crenate silica bodies. The microhairs of A. marantoidea are found almost exclusively on the abaxial epidermis and are large, some attaining 115 pm in length (Figure 6b). Metcalfe (1960:28) first reported their presence and noted that it was difficult to find examples in which the distal cell had not collapsed and, thus, many of the hairs appeared to be unicellular. Renvoize (1985), using the same material as ours (Calderon et al. 2381), reported and illustrated anomalous short bicellular microhairs in which the distal cell was globose, not long and pointcd as we found them in undamaged hairs. Wc have bccn unable to find this hair type in our preparations. The basal cell (40-50 pm long) is cylindrical but has an apparent constriction or invagination approximately one-third of he way up from the base; that part of the cell below the constriction is conical in shape and might be mistaken for a separate cell. The delicate upper cell of the microhair (45-65 pm long) is narrowly ellipsoidal and tapers to a slightly pointed apex. It is rare in the bamboos for the upper cell to be distinctly longer than the lower one (Metcalfe, 1960, fig. 16). This character is frequent in the panicoid grasses, which, however, have much smaller microhairs. Inflorescence The principal difficulty in interpretation of the inflorescence of Anomochloa is the highly contorted and bracteate nature of the partial inflorescences. If we take as a generalized ancestor the typical graminaceous branching pattern, we should expect to find a bract subtending each successive branch of the inflorescence; and secondly, a bikeeled bract (prophyllum) would be the first appendage borne on each lateral branch. In grasses with complex branching systems, such as many bamboos, this organ can be a useful ?marker? in interpreting branching pattcrns. Instead of bicarinate bracts as the first appendage of each successive lateral branch, Anomochloa has a pair of tiny bracteoles. Brongniart, as revealed in his unpublished notes in the Paris Herbarium on the inflorescence of Anomochloa, did note the presence of these bracteoles, but he did not figure them in his published schematic diagram of a partial inflorescence (1851). Doell (1871:24) also detected the bracteoles (?squamulae?) and he suggested that they result from the separation of a single organ. He correctly placed them about 120? apart between the areas of contact of the rachis and axis of the primary lateral branch. He also noted that they appear to be the result of the splitting of a single organ by the compression of the rachis against this lateral branch. He suggested that the two organs might be the result of a prophyllum that had been split by the pressure of the two axes just mcntioncd. Doc11 did not, however, observe the smaller bracteole pairs that were almost certainly present in the higher orders of branching in his partial inflorescence. While the position and consistent morphology of these bracteole pairs does suggest the possibility that they are the remnants of a prophyllum that has split into two portions, it should be noted that the bracteoles are never in actual contact, even at their bases, and that in dissections and in acropetal serial sections they appear to arise at different levels on the lateral branch. Also, split prophylls are not known from any other grass. The interpretation of the partial inflorescence of Anornochloa depends on how one interprets the nature of these bracteole pair members, which are the first appendages of each successive branch of the partial inflorescence. Since the smaller member of each bracteole pair arises slightly below the upper member, the formcr appcndage is best interpreted as a prophyll and the upper bracteole as the second appendage on the lateral branch, that is, simply an empty bract lacking a bud in its axil. The third appendage on the axis is the prominent keeled bract that subtends the next lateral branch. If this interpretation is correct, then in formal morphological terms each partial inflorescence could be labeled a scorpioid cyme (Figure 15). This was the interpretation of Brongniart (1851) although he did not give a detailed explanation for his designation. Spikelet Perhaps the best way to understand the structure of the spikelet ofAnomochloa is to begin examination at the apex of the branch bearing the flower and to proceed downward along this axis. For the purposes of the following discussion we will assume that the primitive grass had 6 stamens (arranged in alternating whorls of 3) and a 3-styled ovary with the vascular 26 SMITHSONIAN CONTRIBUTIONS TO BOTANY FIGURE 15.4chematic of the inflorescence of Anomochloa marantoidea showing partial inflorescences (PI) (only those on right side fully diagrammed) alternating on a rachis that terminates in a spikelet. Solid dots rcpresent fully developed spikelets, open dots represent rudimentary spikelets. Abbreviations: B = bracts subtending lateral branches; b( 1.2) = first or second bracteole of a lateral branch. bundles leading to the stigmas placed altcrnatc to the thrce stamens of the inncr whorl. Howcvcr, it is by no mcans ccrtain that this supposition is correct. There is evidcnce, for example, that in grasses the stamens do not arise in whorls of 3, and that the lodicules do not all arise from a single whorl (see Clifford, 1987, for a review of this subject). Lacking developing inflorescences of Anomochloa for study we will draw our conclusions using conventional assumptions on the interpretation of the parts of the grass flower. GYNEC1UM.-Our observation that the ovary of Anomochloa marantoidea retains but a single anterior stigmatic vascular bundle is in accordance with the observation of Arbcr (1929) but not that of Schuster (1909), who figured three stigmatic bundles in the gynccium. The latcral posterior pair of stigmatic bundles present, for example, in species of Streptochaeta (Figure 106) is not present in Anomochloa. ANDREC1UM.-The flowcrs of Anomochloa muruntoidea consistcntly bcar four stamens. Bascd on comparison with other Bambusoideae we assume that the primitive state in the subfamily is six and that two have been lost. This idca was first suggcsted by Brongniart (1851), who stated that the stamens are arranged in a homogeneous cycle such that it is impossible to determine which pair had been lost. The schematic figure of Schuster (1909, fig. 22) of a spikelet cross-section shows two gaps in the andrecial ring that might pertain to the lost stamen pair. His figure is otherwise misleading, however, in that thrce stigma bundles are figurcd and the position of the interlocking margins of the upper spikelet bract with respect to the andrecium and gynecium is incorrect. In transverse sections madc just below the bascs of the filaments (Figure 10a), we found two large gaps on either side of the vascular bundle leading into the postcrior stamcn oppositc thc single stigma bundle. If it is assumed that the ancestor of Anomochloa indeed had six stamens and three stigmas, and that the three stamens of the inner whorl were placed alternately with the three stigmatic bundles of the ovary (of which only the anterior remains), then it seems reasonable to conclude that these two gaps in the andrecium correspond to positions of the lateral anterior pair of stamens from the inner whorl, which have been lost. Arber (1929) arrived at this same hypothesis by a different line of reasoning. Based on her studies of the flowers of woody bamboos she noted that the inner whorl of stamcns was more liable to reduction than the outer whorl and that the posterior stamen of the inner whorl was less liable to reduction than the anterior latcral pair. Although not observing gaps in the andrecium base of Anomochloa she did note that the posterior stamen was slightly smaller than the other thrce and thus might correspond to a stamcn of the inncr whorl, in which casc the 6 PI PI 4 2 PI U 1 PI NUMBER 68 two lateral anterior members of the whorl have been lost. An additional fact in support of the hypothesis that it is the anterior lateral pair of stamens that have been lost is the observation that in several sections of one spikelet the base of the filament of the anterior (outer whorl) stamen had a distinct lateral appendage (Figure l lb) that may represent the rudiment of a fifth stamen (one of the anterior lateral pair of the inner whorl). In the specimen examined this rudiment is less than 50 pm long and bears no anther. Arber (1929) also pointed out that the stamens of Anomochloa rescmblc those of no othcr grass in that the bases of the anthers completely encircle but do not fuse with the filament for a short distance near the base of the former. We also found this to be the case (Figure 116). In cross-sections through their middle portions the anthers have an introrse aspect because their thecae are rotated forward slightly and face the center of the andrecial circle. In the upper portion of the anther, however, the thecae have a more lateral arrangement on both sides of the connective. PERIGONATE A?ULLJs.-completely surrounding and closely appressed to the base of the stamen ring is a low membrane bearing at its summit a dense fringe of brown cilia. Brongniart (185 1) called this circular structure simply a ?discus annulus? and, although he offered no formal interpretation of it, he did note that lodicules (?squamulae?) are lacking in Anornochloa, thus implying that the ring could not represent a highly modified set of lodicules. Hooker (1862), Doell (1871), Schuster (1909), and Pilger (1954) all appear to agree with this interpretation although Doell (1871:24) does add in his description of the feature the query ?perigonio?? [perianth]. Arber (1929) offered two suggestions as to the nature of the ring: it could indced represent a reduced and fused ring of lodiculcs (the ?ciliate perigon? of her figure 52) or that i t could represent a greatly reduced lemma. The latter interpretation was suggested to Arber by the condition in the pooid genus Lygeum in which lemmas from adjacent florets are fused into a tubc whose summit bears a dense fringe of hairs. Hubbard (1934:219) apparently was influenced by Arber?s first intcrpre- tation as he describes the ring as ?lodicules?.? We shall call this structure the perigonate annulus, a term that is dcscriptive of its morphology and position in the spikelet but that lacks the interpretive implications of ?pcrigon.? Bccausc thc annulus does have a membranous portion it might reprcsent a ring of reduced, fused lodicules as hinted by Doell. Grasses (e.g., Melica) are known that have partially to totally fused lodicules. These lodiculcs, however, retain discrete sets of vascular bundles indicating the individual nature of these organs. Because the pcrigonate annulus of Anomochloa is a homogene- ous ring and does not have any vascular bundles entering it or even lcading to it, the structure is of little use in interpreting the nature of the upper spikelct bract that surrounds it. We are unable to find convincing evidcnce that it is either a reduced lemma, palca, ring of lodicules, or outgrowth of thc base of the andrecium. UPPER SPIKBLBT BRACT.4utside of the pcrigonate annu- lus, and enclosing it and the floret, is the upper spikelet bract. 21 Its tightly interlocked margins (Figure l l a ) meet on the side of the flower (with respect to the position of the attachment of the ovule to the wall of the ovary) that would correspond to the position of a palea in a conventional grass spikelet, and indeed Brongniart interpreted it as a palea. However its laminated structure, deciduous apical appendage, many nerves, and lack of an associated prolongation of the rachilla is not characteristic of a palea. THICKENED INTERNODE.-BelOW the upper bract is a thickened, barrel-like indurate internode that separates the lower from the upper spikelet bracts. LOWER SPIKELET BRACT.-The base of the thickened internode bears the lower spikelet bract, a many-nerved, tessellate structure that is placed alternate to the upper bract and alternate to the bract that subtends the branch that terminates in the flower. Brongniart (185 1) mainly based his interpretation of the Anomochloa spikelet on the terminal position of the flower and the position of the upper spikelet bract with respect to the stamens. He pointed out that despite the fact that the upper spikelet bract lacked two keels, paleas were known in the oryzoid grasses (e.g., Oryza) that were 3-nerved and lacked well-defined bicarinate keels. Given this ?marker,? the lower bract, he argued, must represent a lemma. The oryzoid grasses often have reduced or absent glumes. But teratological evidcnce suggests that the so-called palea of Oryza is actually a lemma and that the true paleas in the spikelet have been lost (Nune z, 1968:95). Schuster (1909, fig. 23) was impressed with the peculiar hammer-and-sickle fit of the upper bract margins of Anomochloa, and turning, like Brongniart, to Oryza, he noted (1909:32) that the lemmas in that genus have at least superficially similar interlocking margins; in his interpretation, then, the lower bract represented a glume. Unfortunately Schuster?s (1909, fig. 22) schematic drawing of a cross-section of a spikelet Anomochloa is misleading on several counts. First, as already noted he figures three vascular bundles in the gynecium; and secondly, his floret is rotated 180? with respect to its true orientation within the upper spikelet bract, so that the missing stamen pair would appear to be the lateral posterior pair of the outer whorl. Still, his hypothesis that the upper bract rcprcscnts a lcmma is a reasonable one. One fact lending support to this idea is that the female lemmas of all genera of the Phareae, another tribe of herbaceous bamboos, possess a ?laminated? internal structure quite similar to that found in the upper bract of Anomochloa (figured by Schuster (1909, fig. 23) but first noted by Arber (1934, fig. 52); see Figures l ld , 12a,b-d). Although it is difficult to imagine that this striking feature was independently derived in the two groups, it may be noted that in the pharoids the transversely elongated cell layer is subjacent to the adaxial epidermis, while in Anomochloa the similar cell layer is subjacent to the abaxial epidermis. We have also observed a laminated structure in the culm-leaf sheaths of some woody bamboos. Arber (1929, fig. 52) labeled the lower and upper spikelet bracts and the perigonate annulus in her drawing of a 28 SMITHSONIAN CONTRIBUTIONS TO BOTANY cross-section of an Anomochloa spikelet as the flowering glume (Icmma), palea, and ciliate pcrigon, respectively. Yet she was also impressed by the similarity of the perigonate annulus of Anomochloa to the reduced, hairy lemma found in the anomalous genus Lygeum. Although not claiming that the two groups were particularly closely related, Arber suggested that if the reduction of the grass lemma could definitcly proceed so far in Lygeum, it was not impossible for it to have proceeded farthcr yet in Anomochloa. Clayton and Renvoize (1986:58) apparcntly find this suggestion attractive as well. None of the three extant hypothcses has an overwhclming weight of evidcnce bchind it. The suggcstion of Schustcr (1909:32) that the two spikclct bracts be intcrpretcd as just bracts appears to be the most reasonable at this point. Developmental studies of abundant material of initiating and developing inflorescences of Anomochloa will be required to elucidate furthcr the problem of how to interpret the spikelet structures morc satisfactorily. For now we must tentatively interpret the spikclet bracts as two lateral appendages on an axis that terminates in the flower. The terminal position of the flower on the branch indicates that, as in Stipa (Clifford, 1987), the uppcrmost spikelet bract cannot always be correctly designated as a palea. Fruit The caryopsis of Anomochloa maranloidea is remarkable for its large size (Figurc 4k-m). Although many woody bamboos have larger caryopscs, among the herbaceous bamboos only the fruits of Olyra caudata approach those of Anomochloa in volume. The three available caryopses that we cxamincd were roughly cylindrical in shape and tightly invested by the upper spikelet bract at maturity. The oblique-basal embryo, although relatively small (as is typical for bambusoid grasses) when compared with the size of the caryopsis, is in absolute terms the largest known for any herbaceous bamboo. The embryo has a Reeder (1957) formula F+PF (Figures 13c,d, 14): there is no internode between the divergence of the coleoptilar and scutellar traces (F, a pooid [festucoid] feature); an epiblast is present (+, a pooid feature); therc is a cleft bctween the lowcr part of the scutellum and the coleorhiza (P, a panicoid feature), and the margins of the embryonic first leaf meet but do not overlap (F, pooid). Thus, except for the non-overlapping embryonic lcaf margins, Anomochloa has a typically bambusoid embryo formula (Reeder, 1962). Other bambusoid grasses are known that have a formula of F+PF, that is, with non-overlapping first leaf margins, for example Pharus mezii and P. lappulaceus (see Judziewicz, 1987) and the woody bamboo Alvimia (Soderstrom and Londono, 1988). Reproductive Biology Depending on whether or not the stigmas or stamens are visible the aspect of the inflorescence of Anomochloa marantoidea is quite different. The following preliminary description of anthesis is based on observations of two small flowering plants followed daily in Bahia, Brazil, for several weeks in February and March 1986. The entire flowering episode took approximately two weeks in these plants, which bloomed out of season and exhibited small inflorescences with only one functional spikelet in each partial inflorescence. The stigmas appear before the stamens, and in both plants the terminal spikelet (the only spikelet not borne in a partial inflorescence) was the first to exsert its stigma through the corniculum of its upper spikelet bract. A day or two later the stigmas of the spikelet of the lowest partial inflorescence (PI, in Figure 15) were exsertcd. A few days later those of the spikelets of the subapical partial inflorescences appeared in acropetal sequence (P12-P16). Several days after the last stigmas had been exserted, that is, about a week after the appearance of the first stigma, the stamens began to be extruded from between the margins of the upper part of the body of the upper spikelet bracts. The terminal spikelet extruded its stamens first. On the next day, the spikelet of the lowermost partial inflorescence extruded its stamens, and male flowering then proceeded upward, with the spikelet of the subapical partial inflorescence the last to extrude its stamens. Based on our field observations Anomochloa is protogynous, as noted by Brongniart ( M I ) , whose figure of an inflorescence ?au commencement de la floraison? shows all of its stigmas exserted but no stamens visible. This type of flowering pattern is frequent in the herbaceous bamboos. Several species of Pharus (Judziewicz, pers. obs.) and Leptaspis (collectors? notes), Streptochaeta sodiroana (Judziewicz, pers. obs.) and S. spicata (Soderstrom, pers. obs.) all exhibit this pattern. This pattern was also observed by Soderstrom in the woody bamboo, Dendrocalamus membranaceus (Soderstrom 2660, US) in plants cultivated in India. What is the dispersal mechanism for the caryopsis of Anomochloa marantoidea? Unlike the Phareae, Streptochae- teae, and Streptogyneae, the spikelets and inflorescences of Anomochloa show no adaptations for external animal dispersal (Ridley, 1930:598ff; Van Der Pijl, 1982:78ff), a dispersal strategy that may have enabled these tribes to survive as widespread taxa to the present day (Soderstrom and Calderon, 1974; Soderstrom, 1981a). The diaspore of Anomochloa consists of the thickened, cylindrical internode between the lower and upper spikelet bracts, above which is attached the persistent, indurate upper spikelet bract, this enclosing the large caryopsis (Figure 4j). Davidse (1987) has shown that the superficially similar internodes between the glumes and floret of the olyroid Cryptochloa (all species) and Olyra (some species) are elaisomes that at maturity contain oils that attract foraging ants. Davidse notes that although similar-appearing thickened internodes in the olyroids Arberella and Lithachne produce no oils, Anomochloa should be investigated for this feature. Unfortunately, all of the mature spikelets available for this study were preserved in FAA, which destroys oils. Our sections of the central part of the internode showed either poor cell preservation or lack of cellular structure. NUMBER 68 29 Streptochaeta Schrader ex Nees von Esenbeck Streptochela Schrader ex Nees von Esenbeck, 1829536. HISTORY Streptochaeta is widely distributed in Neotropical forests and thus material has long been available for its study. The papers of Nees von Esenbeck (1829,1835,1836), Doell (1877), Clakovskfy(1889), Hackel (1890), Arber (1929), Page (1951), Dobrotvorskaya (1962), and Sodersuom (1981a) all represent contributions to the understanding of the inflorescence of this grass, long thought to be the most primitive genus in the family. The embryo of Streptochaeta has also been the subjcct of studies by Yakovlev (1950) and Reeder (1953); starch grains by Yakovlev (1950) and Tateoka (1962); and leaf anatomy by Page (1947), Metcalfe (1960), and Renvoize (1985). Because the genus shares certain features of the microhair, leaf midrib, starch grain, and embryo structure with AnomochIoa we are presenting here a formal study of its leaf anatomy and taxonomy. TAXONOMY DIAGNOSIS.-Perennial forest grasses. Culms hollow, erect, branched or not above; lowermost leaves consisting of bladeless sheaths; prophylls many-nerved, not bicarinate. Leaves lacking both inner and outer ligules, but with lateral appendages and oral setae present at the summit of the sheath; pseudopetiole short, terminating in a stout, appresscd-hispid, dark-colored pulvinus at the base of the expanded portion of the blade; lamina usually broad, the midrib raised on both surfaces (more prominently so above), the secondary lateral veins and transverse veinlets prominent below (abaxially) only, both surfaces glabrous or rarely the abaxial surface hirtellous; venation pattern slightly oblique, at least one primary lateral vein joining the midrib a few centimeters above the base of the lamina; uppermost leaf (or two) below the inflorescence a bladeless sheath(s) surrounding the developing inflorescence. Inflorescence a terminal spike or contracted raceme of spirally arranged, appressed pseudospikelets, these borne on short cupulate pedicels; peduncle absent to well developed; occa- sionally a second inflorescence produced from a bud in the axil of the uppermost leaf. Pseudospikelets lacking glumes, lemmas, paleas, and lodicules, terete, falling entire, composed of 11 or 12 spirally arranged bracts on 4 different axes; first 5 bracts short, membranous, greenish stramineous, irregularly truncate, lobed, or dentate at the summit, strongly several- nerved, bracts 1-111 facing the rachis of the inflorescence and smaller than bracts IV and V; bract VI separated from bracts I-V by a curved, glabrous internode; bract VI large, indurate, slightly saccate-based (gymnostegial flap), obscurely many- nerved, bearing a long terminal awn, this straight in the lower portion, strongly coiled in the upper part and at maturity becoming entangled with the awns of other pseudospikelets, all pseudospikelets in the inflorescence frequently shed as a unit; bracts VII and VIII similar, appearing to be placed opposite bract VI, sometimes fused at the base, triangular- lanceolate, indurate, their summits spreading away from each other; bract IX usually present only as a minute flange of tissue above and opposite the attachment of bracts VII and VIII; bracts X-XI1 subequal, coriaceous, lanceolate, unawned, strongly nerved, forming a trimerous whorl around the floret, but with overlapping margins. Andrecium: Stamens 6 , exserted from the pseudospikelet but not pendent, the filaments attached to the anthers a short distance above their bases, the filaments free to fused into a stamen tube; ovary glabrous. Gynecium: Stigmas 3, hispid; fruit a linear-lanceolate caryopsis, the hilum linear (or broadening in center of caryopsis), extending only about 2/3 of the length of the grain; embryo small, basal, lacking an epiblast. Key to the Species of Streptochaeta 1. Pseudospikelets (42)70-100 per inflorescence; leaf blades large, 17-30 cm long, 5-9.5 cm wide [moist to more commonly wet forests, Mexico to Panama; Venezuela (rare); Pacific Ecuador; Amazonian Peru (rare)] . . . . . . . . . . 1. S. sodiroana 1. Pseudospikelets 5-19 per inflorescence; leaf blades various, in the common species usually less than 17 cm long and 5 cm wide. 2. Leaf blades 5-18 mm wide, hirtellous below; pseudospikelet bracts X-XI1 12-14.5 mm long [rare endemic of Espirito Santo, Brazil] . 3. S. angustifolia 2. Lcafblades 30-73 mm wide, glabrous or rarely hirtellous below; pseudospikelet bracts X-XI1 16-23(30) mm long. . . . . . . . . . . . . . . . .2 . S . spicata 3. Pseudospikelets 5-1 1 per inflorescence; leaf blades 11-16(20) cm long, 3-5(6) cm wide; widespread; Mexico and Trinidad to Paraguay and Rio Grande do Sul, Brazil . . . . . . . . . . . . . 2a. S. spicata subsp. spicata 3. Pseudospikelets 13-19 per inflorescence; leaf blades 19-29 cm long, 4.8-7.3 cm wide; endemic to Pacific Ecuador. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2b. S . spicata subsp. ecuatoriana, new subspecies 30 SMITHSONIAN CONTRIBUTIONS TO BOTANY 1. Streptochaeta sodiroana Hackel FIGURE^ 16, 17 Streplocheta sodiroam Hackel, 1890:111. [Type: Ecuador. Pichincha: T a n Mguel, in silv. trop. flumen Peripa," anno 1883, L. Sodiro 911 [or 9 l l ? ] (Holotype, W; isotypes, W (2 sheets), fragment at US.] Los Angeles, Molina et al. 17684 (BM, F, MO, NY); between Upala and San Antonio de Upala, Pohl and Gabel 13563 (F, MO); El Fo/sforo, 3 km N of Upala, Pohl and Gabel 13707 0; 12.6 km N Of Bijagua by road, Pohl and Pinette 13231 (F, MO, NY). GUANACASTE: Frontera Norte, anno 1910, Brenes sen. 0. HEREDIA: Finca La Selva, 3 km S of Puerto Viejo, Hammel 8056 (DUKE), 8429 (DUKE). LIMoN: Rio aI , 10305 (F, MO); Finca neobroma, Rio Hondo, near Rio, cimarrones viejo, caldordn 2108 ( U S ) ; Bandeco Farm #3, km E of ~1 carmen, bnt 2435 (F, MO); base of ceno Tortugero, Pohi and Lucas 13046 0; Laguna Alova [sic, for Jalaba], 55 km of Main, pohl and ,rucas 13048 0; La Columbiana farm, Standley 36809 (US); Collines de Sikubeta, Talamanca, Tonduz 9201 (BR, US). PUNTARENAS: hills above DESCRIPT1oN*--plants cespitose in Of a few culms, Camam (Ria Sand Box), Bribri, 9O37'N, 82049'W, Burger et mature culms sometimes becoming decumbent and rooting at the lower nodes. Culms 50-100 cm tall, unbranched above the base, frequently stout, 3-9 mm in diameter, glabrous, with a small cen@al lumen; lower nodes exposed, short-hispid. Leaves: Leaf sheaths glabrous below, the margins fringed near Summit with papillose Cilia; sheath auricles absent Or uncommonly Present and UP to 5 mm long; lateral appendages do, near inconspicuous, rarely to 3 mm long, if present fringcd with oral setae 1-2.5 mm long; pseudopetiole 4-lO(13) mm long, terminating in a stout pulvinus; pulvinus dark, turgid, covered with fine appressed hairs; expanded portion of blade oval to less commonly lanceolate, 17-30 cm long, 5-9.5 cm wide, glabrous or with the margins fringed with a few cilia at the base; secondary lateral veins and transverse veinlets conspicu- ous below, 1" nerves 6-8 on each side of the midrib, 3" lateral veins spaced 0.6-0.9 mm apart; well-developed blades 3-6 per culm. Inflorescence 17-27 cm long, 0.9-1.3 cm wide, erect at first but becoming pendent with age, its base included in the uppermost bladeless sheath or exserted on a peduncle up to 20 cm long; rachis finely papillose to appressed-pubescent, with a conspicuous tuft of cilia up to 4 mm long on the pedicel of each pseudospikelet. Pseudospikelets (42)70-100, crowded; bracts I-V 2-4.5 mm long; body of bract VI 12-18 mm long, 9-13-nervcd, the terminal awn 4-9 cm long, scabrous; bracts VII-VIII 8-12 mm long; bracts X-XII10-17 mm long; anthers yellow, -5 mm long, the filaments apparently not fused; caryopsis 9-12 mm long, 1.5-2 mm wide, the hilum a narrow groove in the lower third of the grain, terminating in a broad, shallow depression in the central third; embryo 1-1.2 mm long. DIsTRIBUTION.--OcCurring from sea level to 250 meters (occasionally to 830 meters) in the shaded understory of moist to more commonly wet lowland rainforests of Central America (Caribbean slope from Chiapas, Mexico, and southern Belize south to the canal area of Panama; Pacific slope from near Quepos, Costa Rica, south to Darien, Panama), Venezuela (Caribbean slope south of Lake Maracaibo), Pacific slope of Ecuador (common); Amazonian Peru (rare); not known from Colombia (Figure 18). At La Selva, Costa Rica, it is most often found at the base of slopes near small sucams. ADDITIONAL SPECIMENS SEEN.-BELIZE. Tolcdo, Peck 652 (K, NY); Tcmash River, Schipp S-961 (US). COSTA RICA. ALAJUELA: 1 mi (1.6 km) s Of RiO Penas Blancas bridge of CR-142, Hammel et al. 14052 (MO); 4 km W of Muclle San Carlos, lO"28' N, 84"30'W, Liesner 14111 (MO); 2 km N of Santa Rosa, 10"38'N, 84"31'W, Liesner et al. 1501 7 (MO, WIS); 1 km W of Jabillos, 10?23'N, 84"33'W, Liesner et al. 15162 (MO, WIS); Llanura de San Carlos, near . . , Palmar Norte, trail to Buenos Aires, Allen 5913 (BM, F, US), Croat 35131 (MO), Schubert 1161 (US); 1 km SE of Rio Claro along NE side of Carretera Interamericana, 8"39'N, 83"04'W, Burger and Matta 4818 (F, NY); 5 km W of Rincon de Osa, Burger and Liesner 7214 (F, MO, NY); Finca El Eden, km 183, Route 2, near Santa Marta, Gomez 22950 (MO); Rincon airstrip, Kennedy 1929 (MO); 2 miles (3.2 km) W of Golfito, Lathrop 5581 ( S , US); Osa forest camp, Lathrop 5585 (US); Rincon de Osa, Liesner 1783 (MO), Pohl and Davidse 10749 0; Sirena, 8"29", 83"36W, Liesner 2941 (MO); 2 km S of Hatillo, 9 Oct 1968, Pohl and Davidse (F); 5 km W of Palmar Norte on road to Puerto Cortez, Pohl and Davidse 11584 (F, K); 3 km NE of Quepos, Pohl and Davidse 11691 0; valley of Rio Terraba, S of crossing of Rio Ceibo and Carretera Interamericana, Pohl and Davidse 11 773 (F); between Golfo Dulce and Rio Terraba, Skutch 5291 (F, US); -10 km S of Palmar Sur on the Carretera Interamericana, Finca 18, Soderstrom and Calderon 1205 (US, WIS); Playa Blanca, Golfo Dulce, Valerio 425 (BR, F). ECUADOR. Without locality, Lehmann 4400 ( U S fragment ex K). ESMERALDAS: km 170-175, via Santo Domingo- Quininde, Acosta-Solis 13644 (F); Rosa Zarate, Quininde, Asplund 16302 (B, G, NY, S ) ; E of Rio Blanco and S of Quininde, Fagerlind and Wibom 2553 (S); via Esmeraldas- Tanaty-Cuchilla de Timbre, Jaramillo 57 (AAU, QCA); Rio Cayapas, Kvist s.n. (AAU); Coronel C. Concha, -30 km S of Esmeraldas, Maas et a]. 2925 (K, MO). LOS RiOS: Rio Palenque Biological Station, km 56 highway Quevedo-Santo Domingo, Croat 38964 (MO), Dodson 5021 (US), Gentry 9866 (MO), b j tnan t and Molau s.n., F1. Ecuador 15752 (AAU); Hacienda Ana Maria, Canton Vinces, Mexia 6648 (BM, US); Hacienda Monica, 12 km E of San Carlos, Sparre 19388 ( S ) . PICHINCHA: 20 km W of Santo Domingo de 10s Colorados, Cazalet and Pennington 5109 (NY, US); 37 km S of Santo Domingo de 10s Colorados, Pennington 49 S.D. (K, NY); Rancho Brahman, -10 km NW of Santo Domingo do 10s Colorados on road to Esmeraldas, Sparre 15208 (S). GUATEMALA. IZABAL: h s Amates, Deam 97 (F, MO, NY, W). P E E N : between Finca Yalpamech along Rii San Diego and San Diego on Rio Cancun, Steyermark 45355 (F); between NUMBER 68 31 FIGURE 16.-Sirepfochaefa sodiroana: (I, habit, showing pseudospikelets disarticulating from rachis (x 0.29); b, junction of leaf shealh wilh blade, showing prominent pulvinus (x 1.42); c, portion of rachis (x 2.29); d, pseudospikelet (X 2.29). (a,c,d based on Schubert 1161, Costa Rica (US), b based on Siandley 54180, Honduras (US). Illustration by Gesina B. Threlkeld. 32 SMITHSONIAN CONTRIBUTIONS TO BOTANY h 0 9 FIGURE 17.-S~repfochuefa sodiroanu, showing detail of the pseudospikelet: a,b, two views of the complex of bracts I-V from the base of the pseudospikelet (X 5.75); c-g, bracts I-V (x 5.75); h,i, two views of a pseudospikelet (bracts I-V removed) (X 2.88); j , bract VI, showing gymnostegiurn near base (x 2.88); k, bracts VII-VIII; 1-n, bracts X-XII, which envelop the flower (x 2.88); 0, flower in early stage of anthesis, showing six stamens and gynecium wilh three stigmas (X 2.88); p , pistil surrounded by delicate stamina1 tube, late stage of anthesis (X 2.88); q, caryopsis, ventral face showing hilum terminating in a broad, central depression (X 2.40); r, caryopsis, dorsal face showing persistent beak and small, basal embryo (x 2.40). (a, b. h-j, 1-n, q, r based on Schuberf 1161, Costa Rica (US); c-g, k, 0, p based on Sfandley 54180, Honduras (US).) Illustration by Gesina B. Threlkeld. NUMBER 68 33 Finca Yalpamech and Chinaja, Steyermark 45425 (F, K). NICARAGUA. ZELAYA: region Of Braggman?s Bluff, Engles- HONDURAS. ATLANTIDA: Lancetilla Botanical Garden, S of Tela; rainforest on way to Tela water supply dam, Pohl and Gabel 13813 (F, ISC), Sfandley 52876 (F, US), 53139 (F, U S ) , 54180 (F, US), 55416 (F, US); Puerto Sierra, Lippmann?s plantation, Rio Esperanza, Wilson 548 (NY). ing 184-8 (F); Cerro Waylawas, 13?38-39?N, 84?48-49113 Pipoly 4193 (MO); montanas de Esquipulas y Aleman, drenaje Rio Aleman, Shank and Molina 4829 0; drenajes de 10s Rios Punta Gorda, Alemain, y Zapote, Shank and Molina 4974 0; trail Cerro Saslaya to San Jose del Hormiguero, between Cano PICUKE 18.-Distribution of Slreptochaeta sodiroana. 34 SMITHSONIANCONTRIBUTIONS TO BOTANY Majagua and Cano Sucio, approximately 13"45'N, 85"00'W, Stevens 6852 (ISC); along Rio Waspuk, -1 km upstream from confluence of Rio Pis Pis, 14"15'N, 84"36W, Stevens 13084 (MO); -1.5 km NE of La Esperanza de Las Quebradas, 13"38'N, 85"02'W, Stevens 19341 (MO). PANAMA. BOCAS DEL TORO: Filo Almirante, trail to Risco Abajo, 3 km SW of Almirante, Nee and Hansen 14104 (F, MO, WIS). CANAL AREA: Barro Colorado Island, Aviles 23-B (MO), Busey and Croat 246 (MO), Calderon 2096 ( U S ) , Croat (F, MO), 12930 (MO), 13226 (MO), Foster 1764 0, Judziewicz 4435 (MO, WIS), Kenoyer 103 ( U S ) , Maron et al. 6824 (NY, US), Shattuck 755 (F, MO), Standley 31374 ( U S ) , 4I084 ( U S ) ; Juan Mina, Salvador Hill, Bartlett and Lasser 16790 (MO); Pipeline Road, 9"15'N, 79"45W, Hamilton et al. 3242 (MO); headwaters of Rio Chinilla, above Nuevo Leon Mamn 6896 (US). CHIRIQUI: road from Puerto Armuelles to San Bartolo Limite, 7 km W of Puerto Armuelles, Croat 35066 (MO); Rabo de Puerco, 8 km W of Puerto Armuelles, Liesner 26 (MO); Cerro de la Plata, near San Felix, Pittier 5164 ( U S ) . c o c L E : Cerro Moreno between Molejon and Coclecito, 8"46'44"N, 80"31'54"W, Davidse and Hamilton 23707 (MO); road fom La Pintada to Coclecito, 8"45'N, 8Oo30'W, Hamilton and Davidse 2871 (MO). COLON: Rio Escandaloso, near abandoned manganese mine, Hamme12666 (MO). DARIEN: Rio Aruza, Bristan 1364 (US?), upper Rio Tuquesa, le Clezio 45 (MO); Rioo San JoeC, Duke and Bristan 415 (MO); Cerro S a p , Hammel 1217 (MO); 2-3 mi (34 .8 km) SE of Pijibasal on Rio Paraseneco, -9-10 mi (14.5-16 km) S of El Real, Hartman 12056 (MO); Rio Pirre, trail up river from house of Bartolo, Kennedy 2900 (MO, US). PANAMA: 3 km from Caiiitas towards Bayano Dam, Calderon and Dressler 2153 ( U S ) ; Serrania de Maje, trail between headwaters Rio Ipeti Grande and Charco Rico, So53'N, 78"32'W, Churchill and de Nevers 4408 (MO); 4-5 hours walk upriver from Torti Arriba, Folsom et af . 6836 (MO); 9 km N of Margarita on road to Madrono, Hamme16036 (MO); Serranias de Maje, ridges S of Choc6ovillage of Ipeti, So47'N, 78"27'W, Knapp and Sytsma 2366 (MO); ChimAn, Lewis et al. 3252 (MO). PERU. LORETO: Prov. Nauta, Rio Samiria, puesto vigilancia Santa Elena, 115 m, Encarnacion 25321 (USM, not seen; fragment and photocopy, WIS). VENEZUELA. M R E I D A : El Vigia-Panamericana-Cniio Ama- rillo, 100-200 m, selva pluvial, abundante en cierta zona del bosque, Bernardi 1891 (NY, US). VOUCHER SPECIMENS FOR ANATOMICAL STUDIES.- costa Rica: Calderon 2108 ( U S ) (starch grains, embryos), Liesner, Judziewicz, and Garcia 15162 (MO) (starch grains, embryos), Soderstrom and Calderon 1205 (US) (leaves, starch grains, embryos). Ecuador: Mexia 6648 (US) (starch grains, embryos). Panama: Calderon 2096 ( U S ) (starch grains, embryos). DIscUssIoN.-Srreptochaeta sodiroana flowers principally during the dry season, from December through March. Lars P. Kvist (AAU, pers. comm.) indicates that both the Cayapas 5313 (F, MO), 6325 (MO), 7092 (F, MO), 7380-A (MO), 8816 and Colorado tribes of Pacific Ecuador use the immature inflorescences to remove facial hair, a process he has witnessed several times. 2a. Streptochaeta spicata subsp. spicata Schrader ex Nees von Esenbeck FIGURE 19,20 Sfrep fochefu spicufu Schrader ex Nees von Esenbeck, 1829537. [Type: Brazil. Bahia: "Im urwald an der Estrada de Minas [illegible] Capitain Fdisbeno" [Fazenda of Felisberto Caldeira Brant, Marques de Barbacena, near Ilheus], anno 1816, Prince Muximilkn A.F. de Neuwied s.n. [or 120?] (Holotype, B, fragment US; isotype, BR).] f ep ide i l em luncifoliwn Trinius, 1830:93. [Type: Brazil, no collector or exact locality given.] D E S C R I P ~ O N . - P ~ ~ ~ ~ ~ cespitose in clumps of a few culms, sometimes becoming decumbent and rooting at the nodes. Culms 35-105 cm tall, 2-4 mm in diameter, unbranched above the base or rather frequently rebranched 1-3 times in scorpioid fashion, successive branches borne on one side of the plant, each branch bearing a terminal inflorescence; lower nodes exposed, glabrous to finely appressed-hispid. Leaves when fully developed (3)5-7(10) per culm, the leaf sheaths 4-6(7) cm long, glabrous except sometimes puberulent on the back and ciliate on the margins near the summit; sheath auricles absent to frequently prominent, up to 9 mm long; lateral appendages usually inconspicuous, up to 2 mm long, fringed with oral setae 1-2.5 mm long; pseudopetiole 2-7 mm long, the terminal pulvinus dark, turgid, pubescent; expanded portion of blades elliptic-lanceolate, less commonly oval or narrowly lanceolate, 11-16(20) cm long, 3-5(6) cm wide, shiny, dark green, and glabrous above, glabrous or (rarely) hirtellous below, especially near the apex, the margins smooth to scabrous, the 1' lateral veins 4-6 on each side of the midrib, the 3" lateral veins spaced 0.45-0.65 mm apart, the transverse veinlets inconspicuous on both surfaces. Inflorescence 9-16 cm long, included in uppermost bladeless sheath or exserted on a peduncle up to 16 cm long; rachis pubescent with rusty-colored, curling cilia, especially on the pseudospikelet pedicels near the summit. Pseudospikelets 5-1 1, separated by internodes 10-23 mm long, borne on pedicels 0.9-1.3 mm long; bracts I-V up to 3-6 mm long; body of bract VI 17-28 mm long, 7-13-nerved, the terminal awn 3-9 cm long, glabrous to slightly scabrous; bracts VII-VIII 11-15 mm long; bracts X-XII14-23(30) mm long; stamens in 2 groups of 3 each, the filaments of each group apparently fused for a short distance at the base; caryopsis 12-16 mm long, 1.5-2 mm wide, lanceolate, tapering to apex, the ovary persistent at the summit as a small, glabrous beak, the hilum a narrow groove extending through the lower two-thirds of the grain; embryo 1-1.2 mm long. DISTRIBUTION.-Moist or wet forests below 500 meters (occasionally to 1000 meters), often in old treefall gaps or on steep rocky slopes, from Veracruz, Mexico, and Trinidad to NUMBER 68 35 FIGURE 19.Streptochaeia spicata subsp. spicaia: a, habit, showing disarticulated pseudospikelets pendent by awns from the apex of the rachis (note lateral branch of culm terminating in a second inflorescence) (x 0.26); b, base of plant showing stout sympodial rhizomes (x 0.52); c, summit of leaf sheath and base of blade showing prominent sheath auricle tipped oral setae (X 1.57); d, view of opposite side of summit of leaf sheath and base of blade showing smaller sheath auricle and turgid pulvinus (X 1.57). (a based on Bailey and BaiIey 723, Brazil (US); b, d based on Chase 11011, Brazil (US); c based on Garnier4459, Nicaragua (US).) Illustration by Cesina B. Threlkeld. 36 SMITHSONIAN CONTRIBUTIONS TO BOTANY the Pacific slope of Ecuador (rare), Amazonian Peru (rare), BOLIVIA. SANTA CRUZ: Estancia La Dolorida, 500 m, Paraguay, and Rio Grande do Sul, Brazil; scattered throughout 16"15'S, 62"15W, Killeen 1968 (ISC). its range; most common in Atlantic and southern Brazil (Figure ADDITIONAL SPECIMENS SEEN.-BRAZIL. Without locality, 21). Riedel s.n. (G, P). BAHIA: km 5 , rodovia Lages-Ubaitaba, P ~ f 4 d 0 FIGURE 2 0 . S f r e p f o c h e f a spicala subsp. spicata, showing details of pseudospikelet: a, portion of rachis showing pseudospikelet pedicel covered with hooked hairs (x 2.35); b, pseudospikelet, showing long awn on bract VI (X 2.35); c-g, series of bracts I-V at the base of a pseudospikelet, showing their variable venation and shape (X 2.35); h, views of base of bract VI, showing the gymnostegial area and the internode between bract V and bract VI (X 2.35); i, bracts VII and VIII (x 2.35); j-l, bracts X-XI1 (x 2.35); m, andrecium showing short, elongating stamen tube (x 2.35); n, gynecium (x 2.35); o, caryopsis, ventral view, showing linear hilum (x 2.35); p, caryopsis, dorsal view showing persistent style and small, basal, embryo (x 2.35). (All based on Bailey and Bailey 723, Brazil (US).) Illustration by Gesina B. Threlkeld. NUMBER 68 37 approximately 14'1 8'33"S, 39' 19'30"W, Calderon 2041 (US); km 5 camino hacia Santa Cruz Cabralia, approximately 16'15'06"S, 39'00'18'W, Calderon 2046 (US); Ferradas, Fazenda Aberta Grande, 14 km SW of Itabuna, approximately 14'51'S,39"20'W, Calderon and Pinheiro 2162 (US); Reserva Biologica Pau Brasil, 16 km W of Porto Seguro, approximately 16'23'S, 39'11W, Calderon and Pinheiro 2193 (US); 6 km E of Ubaira City, Rio JequiriCA, approximately 13'163, 39'37'W, Calderon and Pinheiro 2246 (US); rodovia BA-265, trecho Caatiba-Barra do Choca, 6 km W de Caatiba, Mori and dos Santos 11577 (MO, NY, US); CEPEC, Municipio Ilheus, dos Santos 3419 (RB); Fazenda Uruguayana, 8 km S of Santa I I I 1000 km I I i Cruz de Vitoria, Soderstrom et al. 2118 ( U S ) ; Reserva Gregorio Bondar, experimental station of CEPEC, Municipio Belmonte, Soderstrom et al. 2139 ( U S ) . CEARA: Serra de Baturite, Ule 8991 (G, K). ESPIRITO SANTO: Canto Grande, Reserva Florestal de Linhares, 19'24'S, 4Oo04W, Soderstrom and Sucre 1881 ( U S ) , 1896 (US), Zulouga et al. 2437 ( U S ) ; Flecheira, Municipio Atilio Vivacqua, Soderstrom and Sucre 1911 ( U S ) ; road from Cachoeiro de Itapemirin to Itabira, 20'51' S , 41"05W, Soderstrom and Sucre 1963 (RB, US). MAT0 GROSS0 DO SUL: vicinity of Dourados, Chase 11011 (F, MO, RB, US), Swallen 9403 ( U S ) . PARA: range of hills -20 km W of Rendencao, near Corrego Sila Joga and Troncamento FIGURE 21.-Distribution of Sfrepfochaeta spicata subsp. spicata (dots) and S. s. subsp. ecuutoriana (asterisks). Inset shows distribution of Slreptochaeta angustijolia (triangle) and Anomochloa marantoidea (circled star). SMITHSONIAFV CONTRIBUTIONS TO BOTANY 38 Santa Teresa, approximately 8"03'S, 50" IO'W, Plowrnan et al. 8646 (MO, NY, US). PARANA: Rio Ivai, Municipio Terra BOa, Hatschbach 15727 (F, MO); 7 km E of Londrina, Swallen 8743 (US); Rio Vermelho, 18 km NE de Bela Vista, Tessmann 3830 (us). RIO DE JANEIRO: Mun. Macaee, Lagoa Comprida, Araujo 4984 (K); Corcovado range, Bailey and Bailey 723 (US), Glaziou 13327 (BM, K, P, W), Hoehne 17226 (NY, US); Camino dos Macacos, Jardim Botahica to Alto Boa Vista, Chase 8430 (F, MO, NY, US, W); Rio Comprido, Rio de Janeiro, Glaziou 5438 (US fragment), 5439 (P, W), 5449 (S), 17925 (K, W); Palmeiras, Hemmendorff 303 (S); Parque Estadual de Desengano, Fazenda Agulha do Imbe, 21'56'S, 41'52'W, Plowman and de Lima 12929 ( F ) ; Morro Novo Mundo, Soderstrom and Calderon 1861 (B, US); Reserva de Tinguai, Municipio Nova Iguacu, Soderstrom 2632 (US). NO GRANDE DO SUL: estrada BR-101, Colonia Sao Pedro, Municipio Torres, Valls 1095 (US); Tres Cachociras, 6 km from ocean, 29'27'S, 49'56'W, Soderstrom et al. 1989 (US). RONo~NIA: Igara-pe, Miolo, affl. do Gy-Parana, Kuhlmann 1834 (US). RORAIMA: Coohia Fernando Costa, iio Mucajai, Black and Magalha'es 51-12891 (K, P, US). SANTA CATARINA: Blumenau, anno 1887, Miiller s.n. (MO, RB), Schwacke 5749 (RB), Ule 980 (P); Municipio Icra, km 376 da BR-101, no trecho de Tubaraio a Criciuma, Valls et al. 2736 (US). saao PAULO: 1 km W Rio Sao Mateus, Municipio ParaguaCU Paulista, 22'32'S, 5Oo48W, Clayton 4581 (K); beira de mata de Planalto, Municipio Adamantina, Taroda s.n. (F). COLOMBIA. META: RIo GUejar, -10 km below junction with RIo Zanza, N end of Cordillera Macarena, Smith and Idrobo 1530 (US). COSTA RICA. GUANACASTE: Hacienda Guachipelin, ParqUe Nacional Volcan Rincon de la Vieja, Pohl and Davidse 11672 (K); 1 km W of hcadquartcrs, Santa Rosa National Park, Pohl and Erickson 12631 (ISC), Janzen 12213 (MO), Judziewicz 4279 (F, WIS). ECUADOR. LOS Rios: Hacienda Clementina on Rio Pita, Asplund 5562 (S, US). Montana del Mico, trail between Dartmouth and Morales, towards Lago Izabal, Steyermark 39029 (F, US); N slope of ridge N of Quirigua, Weatherwax 105 (US). PETEBN: Ceiba Molina 15864 (F, NY). HONDURAS. OLANcHO: Rio Talgua, near the Escuela Granja Demonstrativa de Catacamas, Molina 8328 (US); along Hwy. 3, 12 km SW of Dulce Nombre de Culmi, Pohl and Davidse 12447 (ISC). MEXICO. CHIAPAS: near junction of Rio Pcrhs and Rio Jatate at San Quintin, near Laguna Miramar, Sohns 1725 (US). OAXACA: Cerro de Nacimiento, E of Cosolapa, 17-20 km NE of Campo Experimental de Hule, Sanfos 2438 (US). VER- ACRUZ: Atoyac, Dull 125a (B); Cordova, Finck s.n., Feb 1893 (K, NY); 7 km E of Sarabia, San Juan Guichicobi, Vazquez 1399 (BM, MO, WIS); Ejido de Manzanares, 1-4 km NW of Campo Experimental de Hule, Santos 2301 (US). NICARAGUA. Without locality, Garnier 4459 (US). ZELAYA: GUATEMALA. IZABAL: El Estor, Confreras 11538-A (LL); between Waspam and Ulwas, Pohl and Davidse 12296 (ISC); Miguel Bikan, -52 km SE of Waspam, Pohl and Davidse 12311 (F, ISC); crossing of Rio Lekus on road to Puerto Cabezas, Pohl and Davidse 12319 (F, ISC). PANAMA. CANAL AREA: Barro Colorado Island, Calderon 2095 (US), Caldero'n and Dressler 2145 ( U S ) , Croat 4243 (F, MO, NY), 11832 (MO), Foster 2038 (F), 2316 0, Knight s.n. (WIS), Shattuck 724 (F, MO); hills N of Frijoles, Standley 27489 (BM, MO, US). CHIRIQIf: Cerro de la Plata, near San Felix, Pittier 5164'/z (US). DARIEN: trail between Pinogana and Yavisa, Allen 245 (MO, US); Rio Chico, 1 hour by boat from Yaviza at junction of Rio Chucunaque (MO, US), Duke and Bristan 451 (MO); trail from Pucuro to Cerro Mali, Quebrada Pobre to La Laguna, Gentry and Mori 13549 (MO, NY); Rio Chico, 10 km upstream from Narazeth, 8'20'N, 77'25'W, flahn 113 (MO); 0.5-2.5 mi (0 .84 km) NE of Manene, Hartman 121 73 (MO); trail from Canglon-Yaviza road to Rio Chucunaque, 7.7 mi (12 km) E of Canglon, 8'20'N, 77'50'W, Knapp and Mallet 3962 (MO); junction Rio Canglon and Rio Chucunaque, 15 km N of Yaviza, Mori 374 (WIS). PANAAA: -2 mi (3 km) up Rio La Maestra, Kennedy 1186 (US); Chiman, 3-4 mi (4.8-6.4 km) up Rio Pasiga, Kennedy 1209 (MO, US), Lewis et al. 3237 (MO); edge of mangrove swamp S of Ft. Kobbe and Ft. Howard, E of Rio Venado, 8'54'N, 79'35'W, Knapp 1893 (MO). PARAGUAY. Plaine de Pirayu-bi, Balansa 179-A (G, also fragment US); Cordillera de Peribebuy, fhret de Naranjo, Balansa 4373 (BM, G, K, P), Hassler 131 7 (G); Puerto Bertoni, Bertoni 5825 (W); Prov. Amambay, Parque Nacional Cerro Coro, Soloman et al. 6869 (MO). PERU. AMAZONAS: Prov. Bagua, Quebrada Mirana (above km 277 of Maranon Road), valley of Rio Marano6n above Cascadas de Mayasi, Wurdack 1895 (F, NY, US). TRINIDAD. Caparo forests, Broadway 4929 (US). VENEZUELA. ANZOATEGUI: Cerro La Danta, bordering tributary of Rio Leon, NE of Bergantin, Steyermark 61087 (F, US). APURE: Selva de Cutufi, 7'09-1 I'N, 7I056-58W, Davidse and Gonzalez 21723 (MO, NY, US). BARINAS: SW of Barinitas, Bunting 2265 (MO). ZULIA: cuenca del Embalse Burro Negro (Pueblo Viejo), sector between Quiros-El Pensado and the foot of Cerro Socopo, -10 km E of Churuguarita, Bunting 9448 (MO); Cerro Las Manantiales, E of Rio Guasare, 12 km W of Corpozulia Campamento Carichuano, 1 l0O1'N, 72'20'W, Steyermark et al. 123241 (MO, NY, US). Calderon 2046 (US) (leaves), Chase 8430 ( U S ) (starch grains, embryos), Soderstrom and Calderon 1861 ( U S ) (spikelet), Soderstrom and Sucre 1896 ( U S ) (starch grains, embryos). Panama: Allen 245 (MO) (embryos), Calderon and Dressler 2145 (US) (culm, leaves). DrsCUSSION.-~af blade number, size, and shape are variable in Streptochaeta spicata. While most populations have lanceolate blades, those from near Rio de Janeiro, Brazil and near Lake Maracaibo in Venezuela have ovate blades, VOUCHER SPECIMENS FOR ANATOMICAL STUDIES.- Brazil: NUMBER 68 39 which are, however, no longer than those of most populations of the species. Bahian populations of S. spicata also exhibit vegetative variability: some individuals have only 3 fully developed ovate blades per culm, while others possess up to 10 narrowly lanceolate blades, and some narrow-leaved populations (Mori and Santos 11577; Soderstrom et al. 2118) have abaxial surfaces bearing an indumentum of scattered pilose hairs with distinctive swollen bases, a feature that is otherwise well developed only in S. angustifalia (Figure 24c,6). However, these unusual specimens of S. spicata have overall blade surface areas that are much closer to that of characteristic specimens of S. spicata subsp. spicata (Figure 22) and their pseudospikelets are not as small as those of S. angustifolia. In Central America S. spicata subsp. spicata exhibits a flowering peak during November and December, and possibly also July and August. Nearly all Atlantic Brazil collections have been made during the period from February through April. 2b. Streptochaeta spicata subsp. ecuatoriana, new subspecies TYPE SPECIMEN.-Ecuador, Los Rios: Jauneche forest, Canton Vinces, km 70 on road from Quevedo to Palenque, N of Mocachi on Estero Penafiel, 100 m, 23 Mar 1980, C.H. Dodson and A.H. Gentry 9832 (Holotype, MO). DESCRIPTION.-Differt a Streptochaeta spicata subspecies spicata laminae longiore (19-29 cm) latioreque (4.8-7.3 cm), inflorescentia longiore (18-30 cm), et spiculis 13-19. Plants apparently cespitose. Culms 70-100 cm tall, appar- ently unbranched above the base, 3-5 mm in diameter, the lower nodes exposed. Leaves 4-6 per culm, the leaf sheaths glabrous except along margins near the summit; sheath auricles inconspicuous, to 1.5 mm long; lateral appendages inconspicu- ous, to 1 mm long; oral setac 1-2 mm long; pseudopetiole 2-10 mm long, the expanded portion of the blade 19-29 cm long, 4.8-7.3 cm wide, glabrous except occasionally for a few scattered hairs on the lower surface near the margins, the 3" lateral veins and transverse veinlets not particularly conspicu- ous on eithcr surface. Inflorescence 18-30 cm long, -0.8 cm wide, exsertcd on a peduncle 1-14 cm long; rachis pubescent. Pseudospikelets 13-19, not crowded; bracts I-V up to 4-7 mm long; body of bract VI 20-25 mm long, 12-nerved, the awn -6 cm long; bracts VII-VIII 12-15 mm long; bracts X-XI1 17-22 mm long; stamens not seen; immature caryopsis 8 mm long, linear-lanceolate. DISTRIBUTION.-Endemic to moist, lowland forests on the Pacific slope of Ecuador (Figure 21). PARATYPES.-ECUADOR. GUAYAS: between Las Americas and Palme, 28 Scp 1952, Fagerlind and Wibom 374 (MO, S); Rio Daulc bclow Pichincha, Hacienda Santa Barbarita, 18-26 Apr 1959, Hurling 4798 (S). Los RIOS: Jauneche forest [topotypes], 15 Aug 1978, Dodson et al. 7067 (MO, US), 1 Apr 1980, Dodson and Gentry 10126 (MO), 20 Feb 1982, Dodson and Gentry 12706 (MO), 14 Jan 1981, Gentry el al. 30709 (MO). MAIVABI: El Recreo, 22 Aug 1893, Eggers 14863 CF, M, US). dor: Dodson et al. 7067 ( U S ) (leaves). COMMENTS.-FOW of the five populations of S. spicata known from Ecuador are robust plants with blades twice as large (as measured in surface area) and with twice as many pseudospikelets than is average for subspecies spicata (Figure 22). We have chosen to recognize these plants as the new subspecies S. spicata subsp. ecuatoriana. The single specimen of subspecies ecuatoriana examined anatomically had ex- tremely long bicellular microhairs on the leaf blades. The herbaceous bamboo flora of western Ecuador is impoverished by the apparent absence of common olyroid genera such as Pariana, Arberella, and Piresia, but non-olyroid tribes are well represented by Pharus (5 species, including a new endemic) and Streptochaeta. VOUCHER SPECIMENS FOR ANATOMICAL STUDIES.- ECU- 3. Streptochaeta angustifolia Soderstrom Streptochaefa angustifoliu Soderstrom, 1981a:30. [Type: Brazil. Espirito Santo: Municipio Cachoeiro de Itapemirim. 10 km from Cachoeiro toward Alegre, 2Oo47'S, 41'09W, low forest dominated by Rutaceae with open understory, soil sandy clay, about 35 plants seen growing in several rhizomatous clumps, in fruit, 26 Apr 1972, TR. Soderstrom and D. Sucre 1969 (Holotype, RB; isotypes, CEPEC, F, INPA, K, LE, MO, NY, P, US).] DESCRIPTION.-P~~~~S cespitose from a knotty, short- rhizomatous base, but also spreading by decumbent and rooting culms to form large clones. Culms 40-70 cm tall, hollow, glabrous except pubescent in a line below the nodes; nodes finely appressed-pubescent; unbranched or sparingly branched above, 2-2.5 mm in diameter. Leaves 4-8, evenly distributed on culms or in some sterile shoots the internodes shortened near the summit, forming a crowded fascicle of leaves with strongly overlapping sheaths; leaf sheaths glabrous except for ciliate margins in upper portion; sheath auricles, lateral appendages, and oral setae inconspicuous; pseudopetiole poorly differentiated from expanded portion of blade; blades narrowly lanceolate, 12-15 cm long, 1.3-1.7(2) cm wide, scaberulous on the upper surface, hirtellous or less commonly glabrous on the lower, the margins smooth at the base, scabrous near the apex; primary nerves 3 or 4 on each side of midrib; 3" lateral veins spaced about 0.4 mm apart; transverse veinlets inconspicuous on both surfaces. Inflorescence 8-1 1 cm long, borne on a subglabrous peduncle 10-13 cm long, the rachis flocculose. Pseudospikelets 6-9, not crowded, borne on ciliate-uncinate pedicels about 0.7 mm long; bracts I-V up to 3 mm long; bract VI 10-14 mm long, 12-nerved, with an awn 3-5 cm long, scabrous; bracts VII-VIII 8.5-10.5 mm long, 8-or 9-nerved; bracts X-XI1 12-14.5 mm long, 12-15-nerved; filaments fused, forming a delicate tube surrounding the gynecium, the anthers yellow, 5.4 mm long, the free part of the filaments above -2 mm long; ovary fusiform, -4 mm long, the style to 3 mm long; stigmas -5 mm long. DISTRIBUTION.-Known only from a single moist lowland 40 SMITHSONIANCONTRIBUTIONS TO BOTANY forest (-90 meters elevation) in Espirito Santo, Brazil (Figure 21). ADDITIONAL SPECIMENS SEEN.-BRAZIL. BAHIA: Plants from type population cultivated at Sucre property, Vargem Grande, Jacarepagua, Rio de Janciro, 15 Mar 1986, Judziewicz VOUCHER SPECIMENS FOR ANATOMICAL STUDIES.- Brazil: Soderstrom and Sucre 1969 ( U S ) (leaves). DISCUSSION.-S~~ comments under Streptochueta spicata subsp. spicata. As noted by Soderstrom (1981a, fig. 6h) the filaments of this species are fused into a delicate stamen tube, s.n. (WIS). a feature also present in the herbaceous bamboos Froesiochloa 20 18 16 14 12 10 8 6 4 3 * * * * A A A A A 0 0 0 0 0 0 0 : 0 0 n f A 1 .o 1.5 2.0 2.4 Leaf Blade Area FIGURE 22.-Plot of pseudospikelet number versus leaf-blade size for MO and US collections of Sfrepfochaeta spicala subsp. spicata (solid circles); S. s. subsp. ecuaforinna (triangles), and S. angurfifolia (stars). The index for leaf-blade size (area) was computed by taking the logarithm of the product of leaf-blade length times width (both measured in centimeters). NUMBER 68 41 (Olyreae), Puelia spp. (Puelieae), and Buergersiochloa (Buer- gersiochloeae), as well as in several genera of woody bamboos such as Gigantochloa (Soderstrom, 198 la). As is evident to anyone flying from Salvador to Rio de Janeiro, the forests of the Brazilian state of Espirito Santo, except for a few small reserves, have been destroyed. The olyroid herbaceous bamboo Sucrea sampaiana (two collcc- tions, 1924 and 1929), which grew here, is probably extinct, and it is likely that Streptochaeta angustifolia, collected only in a tiny remnant forest patch in 1972, is by now also extinct in the wild. However, the species has survived for 14 years in cultivation near Rio de Janeiro due to the care of Sr. Dimitri Sucre, who recently donated a plant from his thriving population to the Smithsonian Institution greenhouse in Washington, D.C., where it bloomed in August 1986. MORPHOLOGY-ANATOMY Culm, Leaf Sheath, and Pulvinus The culms of all species of Streprochaeta are hollow, with the lumen ranging from about l/3 to over of Lhc diamcter of the culm. In a culm sectioned for this study (S. sodiroana, Soderstrom 1205) a circle of 42 alternating large and small vascular bundles, partially embedded in sclerenchyma, was noted subjacent to the epidermis and separated from it by a few rows of parenchyma. Interior to this ring was a ground tissue of parenchyma cells that extended all the way to the central lacunae, within which were embcdded numerous scattered vascular bundles. The parenchyma cells were largest in the region midway between the epidermis and the lacunae, with the cells immediately adjacent to the lacunae noticeably smaller and with slightly thicker walls. The leaf shcaths of Streptochaeta species are solid and crescent-shape in cross-scction and do not have membranous, winged margins. In acropetal serial sections of S. sodiroana and S. spicata subsp. spicata the shape changcs from concave to triangular, as the pulvinar area is approached, with the adaxial side slightly concave and the corners of the triangle rounded (Figure 54. The epidermis has abundant rounded, silicified papillae and long, ciliate macrohairs, the latter particularly abundant on the adaxial epidermis. The main vascular bundles are disposed in a V-shape arc of about 20 bundles situated closer to the abaxial epidermis than to the center of the pulvinus; the peripheral bundles each have an irregular sclcrenchymatous cap proceeding to the adaxial epidermis. Several arcs of minor vascular bundles are also present: an arc of about five tiny bundles is present abaxial to the main arc; an irregular arc of about ten small bundles is present subjacent to the adaxial epidermis; and there is an isolated medium-size vascular bundle present in nearly the exact centcr of the pulvinus, bctwccn thc main arc and the adaxial arc of small bundles. Leaf-blade Anatomy TRANSVERSE CTION (Figure 7a-c).-Outline: blade flat, the epidermides straight or with only slight undulations on the abaxial surface, with the blade thickest near the vascular bundles and thinnest near the bulliform cells. Midrib outline: distinctive, projecting both adaxially and abaxially; adaxial projection anvil- or keystone-like, slightly narrowed at the base and with a broad, flat top and overhanging corners; abaxial projection low-domed or low-rectangular. Midrib vasculature: complex, with several tiers of vascular bundles; one large median bundle always present subjacent to the abaxial epidermis, this flanked or not with minor bundles, and one to several vascular bundles usually present subjacent to the abaxial epidermis. Midrib sclerenchyma: a broad, shallow plate always present on the adaxial keel but unconnected to vascular bundles; a deeper, irregular plate present on the abaxial keel and often with minor bundles wholly embedded in it and the median bundle barely or not embedded in it. Lacunae: apparently present near the abaxial surface in the ground parenchyma in at least one species. Vascular bundle arrange- ment in the lamina: bundles of the first and third orders present, noticeably closer to the abaxial surface. Vascular bundle description: first-order bundles ovate; lysigenous cavity present; third-order vascular bundles small. Vascular bundle sheaths of primary bundles: double sheath present; outer sheath of large, thin-walled cells containing few plastids; usually incomplete both above and below because of interruptions by the sclerenchyma caps, no bundle sheath extensions present; inner sheath of two rows of small, achlorophyllous cells with uniformly thickened walls, complete. Vascular bundle sheaths of third-order bundles: double sheath present, the outer sheath of thin-walled cells, interrupted abaxially but usually not adaxially by sclerenchyma caps. Sclerenchyma: present as strands or caps above and below each vascular bundle; adaxial cap few-celled, abaxial cap larger, of cells with thicker walls; intercostal sclerenchyma not present. Mesophyll: chlorenchyma not radiate, consisting of two layers of cells located immediately subjacent to the adaxial epidermis and one layer subjacent to the abaxial epidermis, these two layers separated by fusoid cells; chlorenchyma cells vertically rectangular in basic outline, lacking arm-like extensions but lobed in most directions with much intercellular air space; fusoid cells well developed; uniseriate columns of chlorenchyma connecting adaxial and abaxial chlorenchyma layers and separating adjacent fusoid cells. ABAXIAL EPIDERMIS (Figure 23).-Costal and intercostal zones well differentiated. Intercostal long cells: variable; strongly sinuous and rectangular to long, straight-walled, and fiber-like. Stomata: typically in rows flanking the veins; subsidiary cells low dome-shape or subhexagonal, separated by one to several thin-walled interstomatal cells. Bulliform cells: absent. Papillae: absent. Prickle hairs: typically absent. Microhairs: long, slcndcr, 2-cellcd, typically found in the intercostal regions; basal cell curving, often silicified, distinctly 42 SMITHSONIAN CONTRIBUTIONS TO BOTANY shorter than the pointed distal cell and with an apparent constriction about one-third of the way up from the base. Macrohairs: absent or present, if present commonest along the margins of the row of bulliform cells and borne on a prominent inflated base. Silica cells: uncommon intercostally, if present saddle-shape and projecting above and below the row in which developed; common costally, these solitary, paired with cork cells, or in short rows, and tending to be more square in outline and less saddle-shape. Costal cells in several rows, consisting of elongate, slightly sinuous long cells altcrnating with solitary or short rows of silica and cork cells. ADAXIAL EPIDERMIS (Figure 24).-Basically similar to the abaxial epidermis. Bulliform cells: well developed in center of intercostal zone; walls sinuous. Intercostal long cells: consis- tently sinuous, never strongly tapering. Stomata: uncommon or absent. Papillae: absent. Prickle hairs: often present in intercostal and/or costal regions; consisting of a prominent, inflated base and a relatively slender, short prickle. Microhairs: present, commonest near margins of the zone of bulliform cells. Macrohairs: absent. Silica cells: common, and larger than those on the adaxial surface; those in costal regions tending to be square rather than saddle-shape. Costal cells: similar to those of the abaxial epidermis. Inflorescence and Pseudospikelets The inflorescence, treated in detail most recently by Soderstrom (1981a), is spicate and consists of few to numerous (in S. sodiroana) short-pedicelled pseudospikelets arranged spirally along the rachis. Each pseudospikelet consists of 12, or more commonly 11, bracts arranged spirally on a curving axis. The bracts I-V are small, scale-like, and irregular in shape, while the upper bracts (except the ninth, which is only rarely present) are larger and elongate. Bract VI bears a long, FIGURE 23.-Abaxial epidermides of Sfrepfochaefa species: a , S. sodiroana, showing elongate mid-intercostal long cells; b, S. spicata subsp. spicafa, showing shorter mid-intercostal long cells with more sinuous walls; c,d, S. angustifolia, showing (c) prominent mid-intercostal cilia and (4 bicellular microhairs. (a based on Soderstrom 1205, Costa Rica; b based on Soderstrom and Calderon 1861, Brazil; c, d based on Soderstrom and Sucre 1969, Brazil.) Scale bar: a = 60 p: b = 70 p; c = 80 pm; d = 20 p. NUMBER 68 43 tendrilous awn, and the seventh and eighth bracts are inserted nearly side-by-side and have slightly recurved apices. Bract IX is only rarely present. Bracts X-XI1 are of nearly identical morphology and tightly invest the flower, which consists of six stamens (often delicately fused into a tube, at least near the base), and a gynecium with 3 hispid stigmas. Fruit STARCH GRAINS.-The endosperms of Streptochaeta sodi- roana and S. spicata subsp. spicata are charactcrized by elliptical, highly compound grains, with 15-30 grains occur- ring in each endosperm cell. Each grain is 10-25(50) pm in diameter and is composed of 50-300 strongly angular granules that are approximately 2-4 pm in diameter. EMBRYO.-Sections of the embryos of several specimens of S. sodiroana and S. spicata subsp. spicata (Figure 13a,b) show that in median sagittal sections no mesocotyledonar internode is present between the scutellar and coleoptilar nodes of the vascular bundle 0, no trace of an epiblast is present (-), a small, shallow cleft is present between the lower part of the scutellum and the coleorhiza (P), and the embryonic leaf margins appear to overlap (P), giving a formula of F - PP (in the formula of Reeder, 1957). At least the margins of the coleoptile are not fused in the upper portions and there is a hint that they overlap. Five nerves were noted in the basal portion of the coleoptile and three in the first embryonic leaf. CHROMOSOMES There have been three gametic chromosome counts for two species of Streptochaeta: Pohl and Davidse (1971) and FIGURE 24.--Leaf epidermides of Streplocheta species: a,b, adaxial view of S. sodiroana showing (a) bulliform cells (below) and (b) structure of costal and isolated intercostal silica cells; c, adaxial view of S. angustifofia showing poorly differentiated bulliform cells; d , abaxial, S. spicata subsp. spicata, showing bicellular microhairs (arrows). (a, b based on Soderstrom 1205, Costa Rica; c based on Soderstrom and Sucre 1969, Brazil; d based on Soderstrom and Calderon 1861, Brazil.) Scale bar: a = 100 pm; b,d = 40 p; c = 120 pm. 44 SMITHSONIAN CONTRIBUTIOKS TO BOTANY Hunziker et al. (1982) studied S. sodiroana, and Valencia (1962) studied S. spicata subsp. spicata. All report that n = 11 with perfect pairing of bivalents. DISCUSSION Habit Species of Streptochaeta are forest understory herbs to 1 meter tall. The plants are generally cespitose (Figure la) but apparently it is possible for a culm to become lodged in the soil, develop adventitious roots at the nodes, and spread vegetatively. Unlike Anomochloa, the culms of Streptochaeta are promincnt and leafy and thc lcaf phyllotaxy rcprcscnts a 2/5 or 3/s spiral of a type rare in grasscs (Page, 1951). In all taxa except S. sodiroana the upper portion of the culms may rebranch in a secund manner with each branch terminating in an inflorescence. Prominent prophylls are present as the first appendage of each lateral branch in such cases, but these organs are many-nerved, not bicarinate as are the prophylls of most grasses. The last leaf or two preceding the inflorescence is invariably a sheath lacking a blade. The leaf sheaths of the plants are open. Neither an internal nor external ligule is found at the summit of the sheath, but lateral appendages of a type described for other bamboos by Tran Van Nam (1972) and minute oral setae are present, as is a prominent, turgid, hairy pulvinus. Cross-sections of the pulvinus reveal a complex vascular structure roughly similar to that of the upper pulvinus of Anomochloa. The blades of Streptochaeta are promincntly tessellate and have a basically parallcl venation. However, the venation is oblique to the extent that vcins converge into the midrib for a distance of several centimeters above the base of the lamina. Leaves Cross-sections of the leaf bladcs of Streptochaera reveal prominent fusoid cells and a distinctive midrib morphology, first noted by Metcalfe (1960:488), in which the adaxial keel is flat-topped and prominent while the abaxial keel is dome-shape. The midrib retains its peculiar morphology and complex vasculature to near the apex of the blade. The devclopment of the fusoid cells in S. spicata was studied by Page (1947). The epidermides of Streptochaeta (Figures 23, 24) bear several resemblances to the bambusoid core group. The long cells are clongate with straight walls (S. sodiroana) to rectangular with sinuous walls, depending on the epidermis and species. Bulliform cells are well developed on the adaxial epidermis but epidermal papillae are totally lacking. Intercostal silica-cork cell pairs, characteristic of most bambusoid grasses, are absent in Streptochaeta. Streptochaeta has silica cells of a single type, vertical saddle-shape, although those silica cells found in the costal zones are smaller than the prominent isolated ones found in the intercostal zones. By contrast, Anomochloa has three types of silica cells (costal; intercostal associated with cork cells; and isolated intercostal), all with different morphologies. The microhairs of Streptochaeta are 2-celled and vary in length from 75-150 pm. The apical cell is about half again as long as the basal cell and is narrowly elliptic to linear, with a somewhat pointed apex (Figures 23d, 246). The microhairs of the examined specimen of S. spicata subsp. ecuatoriana were remarkable for their very large size (120-150 pm), and in fact were half again as long as those of the other three species as noted both in our study and the survey of Metcalfe (1960:487). Based on a review of the grasses treated by Metcalfe (1960) and Tateoka et al. (1959), as well as our own studies, it appears that the bicellular microhairs of S. spicata subsp. ecuatoriana are the longest of any grass. The herbaceous bamboo Guaduella has microhairs approaching 250 pm in length (Metcalfe, 1960:487; personal observation) but these hairs are multicellular, not bicellular. Tateoka and Takagi (1967) found that the microhairs on the epidermis of the ?lodicules? (spikelet bracts X-XII) of S. spicata have an apical cell much shorter than the basal cell. The three species of Streptochaeta differ in the abaxial leaf blade epidermides (Table 1). Leaves of S. sodiroana possess elongate, nearly straight-walled, tapering mid-intercostal long cells (Figure 23a) reminiscent of those of Streptogyna species (Soderstrom et al., 1987) and these are set off sharply from the interstomatal long cells, which are rectangular with strongly sinuous walls. In S. spicata there is barely any differentiation of the mid-intercostal long cells and interstomatal cells; both are rectangular with sinuous walls (Figure 23b). The abaxial intercostal region of Streptochaeta angustifolia (Figure 23c) is differentiated into a central zone of rectangular, sinuous-walled long cells (these interspersed with ciliate macrohairs) flanked by two zones of elongate, slightly tapering long cells, and a zone of interstomatal cells that are elongate-rectangular with moderately sinuous walls. Cilia with broad inflated bases are common in the mid-intercostal regions of S. angustijolia, as are prickles. Both of these features, however, are rare or absent in S. spicata and are never seen in S. sodiroana. The abaxial epidermis of S. sodiroana exhibits occasional large, isolated silica cells enclosing ellipsoid- crenate silica bodies, a feature not observed in the abaxial intercostal zones of the other three species. Sfreptochaeta sodiroana has more rows of stomates flanking the veins than the other taxa. The adaxial epidermis exhibits less interspecific differentia- tion, but the stomates appear to be randomly scattered in S. sodiroana but only occur in zones flanking the veins in S. spicata. Also, both epidermides of S. sodiroana lack prickles, a feature that has been observed in at least one epidermis in the other three taxa. Inflorescence and Pseudospikelets The inflorescences and pseudospikelets of Streptochaeta have been the objects of detailed studies, the most recent of NUMBER 68 45 TABLE l.-Comparison of leaf epidermal anatomy of Streptochaeta species. S. suicata Character S. sodiroana ssp. ecuatoriana ssp. spicata S. angustifolia LOWER ( A B ~ L ) EPIDERMIS: Intercostal long cells Elongate; walls not sinuous Elongate-rectangular, walls sinuous Rectangular, walls strongly sinuous Elongate-rectangular walls moderately sinuous Rows of stomates flanking each side of vein Interstomatal long cells B icellular microhairs (length in pm) 7-9 2 2 4 2 o r 3 Very sinuous Moderately sinuous Moderately sinuous Not sinuous Present only in stomata1 regions (75-90) Present in all intercostal regions (1 20-150) Present in all intercostal regions (85-1 05) Present in all intercostal regions (90-1 15) Macrohairs Absent Absent Rarely present Present, mostly in center of intercostal mne Intercostal prickles Costal prickles and microhairs Vein spacing (mm) Costal short cells Absent Absent Common Common Absent Absent Absent Present 0.7-0.9 0.7-0.8 0.4-0.6 0.3-0.4 Solitary, paired, or in threes Solitary, paired, or in threes Solitary, paired, or mostly in short rows (3-8 cells) Solitary, paired. or mostly in short rows (3-8 cells) Intercostal silica cells Present Absent Absent Absent UPPER (ADAXIAL) EPIDERMIS: Stomates Scattered throughoi intercostal areas Uncommon, in rows flanking veins Uncommon, in rows flanking veins Moderately large, only very close to veins Edges of and among bulliform cells Rare Intercostal silica cells Very large, saddle-shaped, in intercostal areas Uncommon, near veins Uncommon, near veins Prickles Absent Absent Edges of (but not among) bulliform cells Bicellular microhairs Throughout intercostal zone, but not among bulliform cells Edges of m e of bulliform cells Edges of (rarely among) zone of bulliform cells Edges of mne of bulliform cells which have been Page (1951) and Soderstrom (1981a); both are recommended for their reviews of the many previous studies of this genus. Soderstrom interpreted the spikelet-like CARY0PSIS.-The hila in the caryopses of Streptochaeta diaspores as consisting of a series of ?bracts on different axes spicata subsp. spicata and S. sodiroana are quite different in of a highly modified pseudospikelet,? basing this view on morphology; in the former the hilum is strictly linear (Figure (among other features) the occasional presence of buds in the 200) while in the lattc there is an elliptical trough occupying axils of bracts I-V and the anomalous structure and the center of the ventral face (Figure 17q). This is interesting arrangement of the putative ?lodicules? (bracts X-XI I). in that hilum morphology is generally considered to be a Fruit 46 SMITHSONIAN CONTRIBUTIONS TO BOTANY conservative character even at the subfamilial level in the Poaceae. The Bambusoideae are usually considcrcd to be characterized by a strictly linear hilum (Calderbn and Soderstrom, 1980: 11). However, nonlinear hila somewhat resembling the type found in S. sodiroana are known from species of the olyroid genera Raddiella (Calderbn and Soderstrom, 1967, fig. 9a) and Diandrolyra (Soderstrom and Zuloaga, 1985, fig. lo). STARCH GRAINS.-The endosperm starch grains of Strepto- chaeta spicata were first studied by Yakovlev (1950, fig. 20), who illustrated them as strongly compound. Tateoka (1962) studied an unspecified species of Streptochaeta and reported that the grains were of his Type IV; that is, strictly compound with eight to numerous granules in each grain. He noted that this type is typical of festucoid, eragrostoid, and oryzoid grasses, and that the olyroid herbaceous bamboos show a similar type that differed in having only 3 to 10 granules per grain. Our findings of highly compound grains for both S. sodiroana and S. spicata confirm these studies. EMBRYO.-Yakovlev?s (1950, fig. 78) illustration of a longitudinal section of the embryo of Streptochaeta spicata shows a cleft between the scutellum and the coleorhiza, no mesocotyledonar internode, and no evident epiblast. The embryo of the same species was studied in detail by Reeder (1953), who reported that Streptochaeta was unique among grasses in possessing a coleoptile with unfused, overlapping margins and 5 nerves. He recorded the presence of a short midnerve but noted that it was not prominent and disappeared soon above the base. Reeder was also impressed by the unfused, overlapping margins of the coleoptile. Most bam- busoid grasses examined have coleoptiles with margins that are unfused for at least part of their length and some have the free portions of these margins overlapping (Ghopal and Ram, 1985; Usui, 1957; Philip and Haccius, 1976; de la Cruz, 1985; X. Londono (Instituto Vallecaucano de Investigaciones Cientificas, Cali, Colombia; pers. comm.) for a fleshy-fruited species of Guadua; sections by the present authors of most olyroid and pharoid genera). Later, in general surveys of grass embryos, Reeder (1962) reported a formula of F - PP for Streprochaera, that is, typically bambusoid except for the absence of an epiblast. No other bambusoid grasses are known that lack an epiblast, except possibly for some woody, fleshy-fruited Indian species (Ghopal and Ram, 1985). Our sections of the embryos of several specimens of S. sodiroana and S. spicata confirm the findings of Yakovlev (1950:195) and Reeder (1953). rachis and become intertwined with the bract VI awns of the other pseudospikelets in a tangled, oftcn pendent mass (Figures la, 16a, 19a) adapted for external animal dispersal (epi- zoochory; Ridley, 1930, Van der Pijl, 1982). In S. spicata the upper part of the rachis and the pedicels of the pseudopetioles are covered with hooked hairs (Figure 20a) that aid in securing the spikelets by the bract VI awns. The pseudospikelets then serve as diaspores that become entangled, often en masse, in the fur of mammals or in clothing; the Schipp collection of S. sodiroana from Belize bears the comment that the species is ?one of the worse grass pests we have in the colony.? The slightly recurved apices of bracts I-V, VII, and VIII may help to secure the pseudospikelet in the pelage of the disperser. Interspecific Relationships Streptochaeta sodiroana is quite distinct from the taxa of the S. spicata group. The depressed, trough-like area in the hilum of the caryopsis, the fiber-like mid-intercostal long cells on the abaxial leaf epidermis (Figure 23a), and the absence of foliar prickles may all be interpreted as specializations when S. sodiroana is compared with possible outgroups of the genus, such as Anomochloa or the Olyreae. Members of the S. spicata group also have some specializations: branched culms; the tendency of the andrecium to form a stamen tube; the presence of hooked hairs on the pedicels of the pseudospikelets and summit of the rachis; and the restriction of bicellular microhairs on the adaxial leaf epidermis to the areas immediately adjacent to the bulliform cells. The presence of these apomorphic characters may indicate that neither group is directly ancestral to the other. Phylogenetic Position of Anomochloa and Streptochaeta The affinities of Anomochloa marantoidea have long puzzled agrostologists. Brongniart (185 1) suggested that Anomochloa might be related to the Oryzeae, based on its resemblance to Oryza in its many-nerved (according to his interpretation) palea, possession of more than three stamens, and I-flowered, terminal spikelets without glumes. Lacking material for further studies later authors had to concur with this placement (Doell, 1871:24; Hackel, 1887:42; Baillon, 1893:297; Schuster, 1909:32), although Bentham (1883:1111) tentatively placed the genus, along with other herbaceous bamboos, in the Paniceae. Early and mid-twentieth century agrostologists emphasized the distinctiveness of Anomochloa. Hubbard (1934:219) erected the tribe Anomochloeae for the genus but did not allocate any of his tribes to subfamilies. Pilger (ex Potztal, 1957) placed it in its own subfamily, the Anomochlooideae. Exceptions to this trend of recognition at successively higher taxonomic levels were Stapf (1898) and Roshevits (1937: 199), who placed Anomochloa in the Phareae, along with several olyroid genera. The anatomical work of At maturity the pseudospikelets become detached from the Page (1947) and Metcalfe (1960:29) revealed that the Reproductive Biology Observations of Streptochaeta sodiroana at La Selva, Costa Rica, in February 1983 indicated that the pseudospikelets bloomed protogynously and in a basipetal sequence in the inflorescence. NUMBER 68 47 epidermal and cross-sectional leaf anatomy of Anomochloa, with its prominent fusoid cells, was similar to the bamboos. Later authors (Calderon and Soderstrom, 1980: 16; Watson et al., 1985:460; Clayton and Renvoize, 1986:57), therefore, have maintained the plant in its own tribe within the Bambusoideae. The highly bracteate nature of the inflorescence of Streptochaeta has long hinted at its affinities to the woody bamboos, as recognized by Nees von Esenbeck (1835), who placed the genus in a group that corresponds to the modern broad view of the Bambusoideae. Both Steudel(1855:339) and Doell (1877:217) agreed that the affinities of Streptochaeta were, if anything, to the bamboos. Most later 19th century authors, however, placed the genus in either the Oryzeae (Hackel, 1887:42; Baillon, 1893:296) or Paniceae (Kunth, 1833:164; Bentham, 1883:ll l l) . In the present century most agrostologists have placed the genus close to the bamboos. Hubbard (1934:205) placed Streptochaeta in its own tribe, the Streptochaeteae, near the Bambuseae, and Roshevits (1937: 157) included the tribe in his ?Series Bambusiformes? along with the Phareae and Bambuseae. Subsequent authors (Parodi, 1961; Soderstrom, 1981a: 17; Clayton and Renvoize, 1986:58) have recognized this grass as a monotypic tribe and included it in the Bambusoideae, although Butzin (1973: 121) established the Streptochaetoideae with the Streptochaeteae as its only tribe. Most evidence of relationships of Anomochloa and Strepto- chaeta to other herbaceous bamboos is of a negative nature, that is, two or more of the tribes often lack a feature found in the others. For example, the Anomochloeae, Streptochaeteae, Phareae, Streptogyneae, and Puelieae lack the prominent epidermal papillae and well-developed arm cells found in the B ambuseae, B uergersiochloeae, Olyreae, G uaduelleae, and many oryzoids; Anomochloa and Streprochaeta lack the membranous inner ligules found in all other bambusoids except for the African Puelia schumanniana, which is highly specialized. Because of the possibility of indcpcndcnt loss, however, the shared absence of a feature is not as strong an indication of relationship as the shared presence of a derived c harac ter. There are some characters that may indicate a distant relationship between Streptochaeta and Anomochloa and the olyroid bamboos. A single meiotic chromosome count has been made ?or Anomochloa marantoidea recently, and a gametic number of n = 18 has been observed (J.H. Hunziker and A. Wulff, pers. comm.). The chromosome number of n = 18 is uncommon but scattered in the grass h m i l y . Joinvillea (Joinvilleaceae), which has been suggested as closely related to the grasses (Dahlgren et al., 1985:425; Campbell and Kellogg, 1987), however, has an identical count (Newell, 1969). It is interesting to note that the only bambusoid grass known with a chromosome numbcr equaling half that of Anomochloa is the olyroid Diandrolyra bicolor ( n = 9; Dakcr, 1968). Thc basic number of Streptochaeta (n = 11) is quite common in the Olyreae. Bcsidcs its similar basic chromosome numbcr, Lhc seedling of S. spicata subsp. spicata is of the typical olyroidjbambusoid type, with a few bladcless or reduced-leafy sheaths preceding the first fully developed leaf, which bears a broad, horizontal lamina (Soderstrom, 1981a:24). The highly compound starch grains of both Anomochloa and Streptochaeta are common in the Oryzeae and in several olyroid genera, such as Maclurolyra (Calderbn and Soder- strom, 1973, fig. 140. Compound grains of this type are also found in Joinvillea (Joinvilleaceae; personal observation) and Restio (Restionaceae; Yakovlev, 1950, fig. 39), both putative relatives of the grasses. The isolated intercostal silica cells of Anomochloa enclose typical olyroid (vertical-crenate) silica bodies; silica-cork cell pairs are common throughout the intercostal zones, as in the many olyroids; the partial inflorescences recall those of many olyroid genera (cf. Calderon and Soderstrom, 1973, fig. 11); and the leaf venation is of the parallel type found in the olyroids. Streptochaeta bears less of a resemblance to the Olyreae in exhibiting a distinctly oblique type of leaf venation (at least in the lower quarter of the blade) never found in the olyroids but found in the African tribe Puelieae, and especially well developed in the Phareae. The leaves have vertical silica bodies of a saddle-shape type, rather than the crenate type found in the olyroids; the embryo of Streptochaeta lacks an epiblast, which is found in all olyroid genera examined. It is natural to begin the search for a sibling group of Anomochloa with Streptochaeta, because both genera are the only herbaceous bamboos that have inflorescences and spikelets (or the functional equivalents of spikelets) that are difficult to interpret in conventional agrostological terms. Further study, however, has made it clear that the inflores- cences and spikelets of the two genera have little in common. The spikelet-equivalent in Streptochaeta is a pseudospikelet composed of 12 spirally arranged bracts (Soderstrom, 1981a, fig. 8j), and the pseudospikelets are borne spirally in a spike-like arrangement. We have shown that in Anomochloa the 2-bracted spikelets, exccpt for the solitary terminal one, are borne in alternating scorpioid cyme-like partial inflorescences subtended by prominent general bracts. Anomochloa and Streptochaeta share features of leaf anatomy and fruit morphology that may qualify as shared- derived characters (synapomorphies). 1. A similar leaf midrib structure in which the keel projects both abaxially (as a small dome) and adaxially in a prominent ?anvil? or ?keystone? configuration. This distinctive morphol- ogy has not been found in any other bambusoid genus studied by us. Both genera also have a complex vasculature, Streptochaeta along the entire length of the blade, Anomochloa in at least the lower half. 2. Exceptionally large (75-150 pm long) bicellular mi- crohairs of a distinctive type, with the pointed apical cell averaging at least half again as long as the basal cell and with the basal cell having an apparent constriction about one-third of the way from the base (also a feature not seen in other bamboos). Most bambusoid grasses have microhairs ranging from 40-75 pm in length, with the unconslricted basal cell longer than the blunt apical cell (Metcalfe, 1960, fig. 16). 48 SMITHSONIANCONTRIBUTIONS TO BOTANY 3. Isolated, vertically elongated silica cells on the leaf epidermis. Isolated intercostal short cells that project above and below the file in which they are borne are typical of the Olyreae, but in that tribe they never project so prominently above and below the file in which they are situated as they do in Anomochloa and Streptochaeta. 4. Strongly compound starch grains of a type common in the Oryzeae but less common in the core group of the Bambusoideae. 5. Five-nerved coleoptiles with unfused margins in which the midnerve is soon lost distally, although recent anatomical studies of woody bamboos have revealed that several have many-nerved coleoptiles with at least partially unfused margins (Ghopal and Ram, 1985). These five features may constitute evidence for a relatively close relationship between Anomochloa and Streptochaeta. It must be emphasized, however, that in many ways besides inflorescence and spikelet structure the two genera are amply distinct from each other, including significant differences in chromosome number (n = 18 and n = 11, respectively), embryo structure (epiblast present in Anomochloa but absent in Streptochaeta), and leaf epidermal anatomy (typical silica cells crescent to roundish in Anomochloa, tall saddle-shape in Streptochaeta); the phenetic studies of Watson et al. (1985463) have led them to place Streptochaeta in their supertribe Bambusanae (with the woody bamboos and the several- flowered herbaceous bamboo tribes) and Anomochloa in their Oryzanae (with the single-flowered tribes of herbaceous bamboos). Based on their common possession of 1-flowered spikelets, symmetrical, predominantly adaxially projecting leaf midribs, herbaceous culms, and noncyclic flowering, Soder- strom and Ellis (1987) place the Anomochloeae and Strepto- chaeteae in their supertribe Olyrodae, along with the Olyreae and Buergersiochloeae. We still must examine the seedling of Anomochloa before coming to definite conclusions about its affinities. Despite its bizarre inflorescence, the leaf anatomy and embryo structure of Anomochloa marantoidea are not so different from that of the olyroid grasses. "he species is definitely a member of the grass family. Literature Cited Arber, A. 1929. 1934. Baillon, H. 1893. Studies in the Gramineae, VI: 1, Streptochaeta; 2, Anomochloa; 3, Ichnanthus. Annals of Botany (London), 43:35-53.7 figures. The Gramineae: A Study of Cereal, Bamboo, and Grass. 480 pages, 212 figures. Cambridge, England: The University Press. 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Kornarov Botanical Institute of the Academy of Sciences of the USSR, series 7 (Morphology and Anatomy of Plants)] 1:121-218, 91 figures. [Unpublished English translation for the Smithsonian Institution and the National Science Foundation, Washington, D.C., 1975, in the files of the Hitchcock and Chase Library, Department of Botany, Smithsonian Institution.] Usui, H. 1957. Valencia, J.I. 1962. Van der Pijl, L. 1982. 1985. Yakovlev, M.S. 1950. Index Olyreae Kunth, 1,22, 41, 46, 47, 48 Olyrodae Soderstrom and Ellis, 48 Oryza Linnaeus, 27, 46 Oryzanae Watson, Clifford, and Dallwitz, 48 Oryzeae Dumortier, 46,47,48 Aechmea pineliana Brongniart, 4 Alvimia Soderstrom and bndoiio, 28 Anomochloa Brongniart, 1,2,22-29,44,46 A. macranfoidea A. Brongniart ex Pritzel, 5 A. marantoidea Brongniart, 37,46,47,48 Anomochloeae C.E. Hubbard in Hutchinson, 46, 47, 48 Anomochlooideae Pilger ex Potnal, 46 Arberella Soderstrom and CalderQ, 22,28,39 Bambusanae Watson, Clifford, and Dallwitz, 48 Bambuseae Kunth, 1 ,47 Bambusoideae Nees von Esenbeck, 1 ,22,46,47,48 Buergersiochloa Pilger, 41 Buergersioch1oeaeS.T Blake, 1 ,41,47,48 Crypfochloa Swallen in Woodson and Schery, 22,28 Dendrocalamus Nees von Esenbeck, 28 D. membranaceus Munro, 28 Diandrolyra Stapf, 3,46 D. bicolor Stapf, 47 Froesiochloa G.A. Black, 40 Gigantochloa Kurz, 41 Guadua Kunth, 46 Guaduella Franchet, 1, 44 Guaduelleae Soderstrom and Ellis, 1, 47 Ichnanthus grandijolius Doell in Martius, 22 Joinvillea Gaudichaud, 47 Joinvilleaceae Tomlinson, 47 Lepideilema Trinius, 34 L. lancijoliwn Trinius, 34 Leptarpis R. Brown, 28 Lithache Palisot de Beauvois, 22,28 Lygewn befling ex Linnaeus, 27,28 Maclurolyra Calder6n and Soderstrom, 47 Melica Linnaeus, 27 Olyra Linnaeus, 3.28 0. caudata Trinius, 28 Q U.S. GOVERNMENT PRINTING OFFICE: 1989 - 20 2 -41 6/600 3 2 52