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Mycol. Res. 108 (7): 846–848 (July 2004). f The British Mycological Society 846 DOI: 10.1017/S0953756204000681 Printed in the United Kingdom. Aecidium kalanchoe sp. nov., a new rust on Kalanchoe blossfeldiana (Crassulaceae) José R. HERNÁDEZ1*, M. Catherine AIME1 and Brad NEWBRY2 1 USDA/ARS, Systematic Botany and Mycology Laboratory, 10300 Baltimore Avenue, Beltsville, MD 20705-2350, USA. Idaho State Department of Agriculture, Plant Industry Division, 434 Shoshone Street West, Twin Falls, ID 83301, USA. E-mail : jose@nt.ars-grin.gov 2 Received 13 February 2004; accepted 26 May 2004. A rust fungus found on cultivars of Kalanchoe blossfeldiana (Crassulaceae) is described as a new species, Aecidium kalanchoe sp. nov., and compared to the other described rusts on members of the Crassulaceae. Only one other rust is known to parasitize Kalanchoe spp. A DNA sequence of A. kalanchoe suggests that the teleomorph is related to Puccinia. INTRODUCTION Plants of Kalanchoe blossfeldiana (Crassulaceae ; syn. Kalanchoe globulifera var. coccinea) growing in a greenhouse in Idaho were found to be parasitized by a rust fungus. Kalanchoe blossfeldiana, ‘Christmas kalanchoe’, is native to Madagascar. It is grown extensively in the USA and Europe as a prized perennial that has succulent leaves and bears yellow, orange, red, pink and purple flowers. Plants of K. blossfeldiana are often propagated in greenhouses in Costa Rica and are imported as small plants usually in spring for sale and distribution throughout North America. Although a number of diseases are known on K. blossfeldiana and other cultivated species of Kalanchoe (Daughtrey et al. 1995), only one rust fungus, Aecidium umbilici Trott. 1901, has previously been described on this plant genus. The rust on plants from Idaho is unlike A. umbilici nor does it fit the description of any of the sixteen other species of Uredinales previously reported on Crassulaceae, thus it is described as a new species. TAXONOMY Aecidium kalanchoe J. R. Hern., sp. nov. (Figs 1–6) Spermogonia subepidermalia, typus 4, pertinentes, badia punctia facientes, circumcincta aeciis. Aecia amphigenia, ad 0.2 mm lata, ad 1.2 mm longa, cylindrica, laceratescentes, lutea. Cellula peridialia 21.5–33r14–24 mm, parietibus 2.5–3 mm, hyalinis. Aeciosporae catenulatae, sphaeroideae, * Corresponding author. ovoideae-obovoideae, 19–27r16.5–22 mm, minute verrucosae. Uredinia et telia incognita. Typus: USA : Idaho: Twin Falls County, Buhl, on living leaves of Kalanchoe blossfeldiana cv. ‘Colbuco ’, 7 May 2003, E. K. Vavricka (BPI 843633 – holotypus). [DNA sequence of the nLSUrDNA deposited in GenBank, accession no. AY463163.] Spermogonia subepidermal, type 4, appearing as chestnut-brown dots, surrounded by aecia. Aecia in chlorotic, circular lesions that measure 1–1.5 cm diam, forming concentric circles around spermogonia, amphigenous, to 0.2 mm wide and 1.2 mm long, cylindrical, becoming lacerate, yellowish orange. Peridial cells 21.5–33r14–24 mm, walls 2.5–3 mm thick, hyaline, polyhedral or shield-shaped, outer surface densely and minutely verrucose, inner surface striate verrucose. Aeciospores catenulate, sphaeroid, ovoid to obovoid, 19–27r16.5–22 mm, minutely verrucose, contents yellowish, wall 1–2 mm thick, hyaline. Uredinia and telia unknown. Specimens of Aecidium umbilici examined : Portugal : São Fiel, on Umbilicus erectus, April 1903, C. Torrend (BPI 153538) ; São Fiel near Castello Branco, on U. rupestris, April 1901, C. Zimmermann (BPI 153539). DISCUSSION About 20 plants of Kalanchoe blossfeldiana growing in a greenhouse in Idaho were infected with Aecidium kalanchoe. Infected plants gradually shed the affected leaves. Although several cultivars of this species were growing together, only two (cvs ‘Sofie ’ and ‘Colbuco ’) J. R. Hernández, M. C. Aime and B. Newbry 847 Figs 1–6. Aecidium kalanchoe on Kalanchoe blossfeldiana. Fig. 1. Chlorotic leaf spot with concentrically arranged aecia. Fig. 2. Cylindric aecia. Fig. 3. Densely and minutely verrucose outer surface of peridial cells. Fig. 4. Striate verrucose inner surface of peridial cells. Fig. 5. Aeciospores. Fig. 6. Spermogonium. Bars: Fig. 1=25 mm ; Fig. 2=1 mm ; Figs 3–5=20 mm; and Fig. 6=30 mm. were infected. All of the plants of Kalanchoe had been propagated in Costa Rica prior to being relocated to Idaho. The only other rust reported on a species of Kalanchoe is Aecidium umbilici, known from K. marmorata (Canonaco 1936). A. umbilici was originally described on Umbilicus erectus (Crassulaceae), a plant native to Europe and the eastern Mediterranean. A. kalanchoe differs from A. umbilici in the size and shape of both the aecia and aeciospores. Based on the specimens examined, aecia of A. umbilici are short, less than 0.5 mm tall, while those of A. kalanchoe are cylindrical, and to Aecidium kalanchoe sp. nov. on Kalanchoe 1.2 mm tall. Aeciospores of A. umbilici are ovoid to elongate, 18–25 (–34)r20–23 mm with cell walls 2–2.5 mm thick, while those of A. kalanchoe are sphaeroid, ovoid to obovoid, 19–27r16.5–22 mm, with cell walls 1–2 mm thick. A. umbilici is known from Africa, Italy, Portugal and Norway (Farr et al. 2003). In addition to A. umbilici, several other rust fungi that produce aecia are known on hosts in the Crassulaceae. Puccinia australis Koern 1873 (Cummins 1971) that produces its aecial stage (A. erectum) on Sedum is characterized by polyhedric aeciospores that are smaller (18–20r16–18 mm) than those of A. kalanchoe. Puccinia longissima Schroet. 1879 (syn. Aecidium sedi) systemically infects species of Sedum and Rhodiola (Cummins 1971) and has larger aeciospores, (22)– 24–27 (–31)r(18–) 21–24 (–26) mm, with thicker cell walls (2–3 mm thick). P. sedi-triseti Dupias 1971 (Dupias 1971) on Sedum produces aecia that are caulicolous or distributed on the leaves. The aeciospores of P. sedi-triseti (21–28r18–22 mm) are similar in size to those of A. kalanchoe, however, they have ten germ pores while none were observed in aeciospores of A. kalanchoe. A. sedi-aizoontis Tranzschel 1910 on Sedum (Saccardo 1925) also has aeciospores with conspicuous germ pores and a thick cell wall up to 5 mm. Uromyces sedi Gäum. 1954 (Gäumann 1954) and Caeoma sedi Azbukina 1970 (Azbukina 1970) produce Caeoma-like aecia, whereas in A. kalanchoe the aecia are aecidioid. A number of other rust fungi have been observed on Crassulaceae but have no known aecial stage. Puccinia umbilici Guépin ex Duby 1830 (Hiratsuka et al. 1992) is commonly reported on various genera of the Crassulaceae including Cotyledon, Sedum and Umbilicus in Europe, Japan, and the USA (Farr et al. 2003). P. benkei Kusano 1904 is known on Sedum (Crassulaceae) in Japan (Hiratsuka et al. 1992). P. umbilicicola Gjaerum & Bahcecioglu 2003 was described from U. erectus in Turkey (Bahcecioglu & Gjaerum 2003). Aecia also are not described for P. echeveri Linder 1938 (Linder 1938) on Echeveria, P. exanthematica McOwan 1892 on Crassula (Doidge 1927), P. rydbergii Garrett 1914 on Sedum (Arthur 1934), Puccinia sedi Körn. 1884 on Sedum (Pantidou 1969) and Uredo tillaeae McAlp. 1906 (McAlpine 1906) on Tillaea. The rust species Endophyllum sempervivi (Alb. & Schwein.) de Bary 1863 (Arthur 1934) and E. sempervivi var. aecidioides Maire 1900 (Maire 1900), both known on species of Sempervivum (Crassulaceae), and E. sedi (DC.) Lév. 1825 on Sedum spp. (Saccardo 1888), produce spermogonia and aecidioid telia with onecelled, catenulate teliospores. Although the telia and teliospores of those species of Endophyllum are similar to the aecia and aeciospores of A. kalanchoe, the teliospores of those taxa are larger than the aeciospores of A. kalanchoe and have a thick (3–4 mm), pigmented cell wall. 848 A nucleotide BLAST analysis (http://www.ncbi.nlm. nih.gov/BLAST) and preliminary phylogenetic analyses (Aime, data not shown) of the nuclear ribosomal large subunit (nLSU) DNA sequences place A. kalanchoe in the Pucciniaceae, and suggest that the teleomorph is most likely allied to Puccinia. ACKNOWLEDGEMENTS Many thanks are extended to Elizabeth Vavricka (Idaho Department of Agriculture, Boise) for sending the infected material. We gratefully acknowledge Christian Feuillet for the Latin description, and Amy Y. Rossman for many improvements to the text and other useful comments and suggestions. REFERENCES Arthur, J. C. (1934) Manual of Rusts in United States and Canada. Purdue Research Foundation, Lafayette, Indiana. Azbukina, Z. M. (1970) O sistematicheskom polozhenii i geneticheskikh rodov triby Phakopsoreae Arth. emend. Azb. Novosti sistematiki nizshikh rastenii 7: 208–232. Bahcecioglu, Z. & Gjaerum, H. B. (2003) New and rare rust fungi (Uredinales) from Anatolia (Turkey). Mycotaxon 85: 165–173. Canonaco, A. (1936) Contributo alla Flora Micologica dell ‘Africa Orientale Italiana. I. Micromiceti dell’ Eritrea. Bollettino di Studi ed Informazione del Reale Giardino Coloniele di Palermo 14 : 1–21. Cummins, G. B. (1971) The Rust Fungi of Cereals, Grasses and Bamboos. Springer-Verlag, New York. Daughtrey, M. L., Wick, R. L. & Peterson, J. L. (1995) Compendium of Flowering Potted Plant Diseases. American Phytopathological Society Press, St Paul, MN. Doidge, E. M. (1927) A preliminary study of the South African rust fungi. Bothalia 2: 1–227. Dupias, G. (1971) Contribution à l’étude biologique et morphologique des rouilles brunes. Bulletin de la Sociéte´ Mycologique de France 87 : 307–317. Farr, D. F., Rossman, A. Y., Palm, M. E. & McCray, E. B. (2003) Fungal Databases. Systematic Botany and Mycology Laboratory, ARS-USDA, Beltsville, MD. http://nt.ars-grin.gov/fungaldatabases. Gäumann, E. (1954) Uromyces sedi n. sp. Revue de Mycologie 19: 250–254. Hiratsuka, N., Sato, S., Katsuya, K., Kakishima, M., Hiratsuka, Y., Kaneko, S., Ono, Y., Sato, T., Harada, Y., Hiratsuka, T. & Nakayama, K. (1992) The Rust Flora of Japan. Tsukuba Shuppankai, Takezono, Ibaraki. Linder, D. H. (1938) New California fungi. Mycologia 30 : 664–671. Maire, M. R. (1900) Quelques Urédinées et Ustilaginées nouvelles ou peu connues. Bulletin de la Sociéte´ Mycologique de France 16: 65–72. McAlpine, D. (1906) The Rusts of Australia: their structure, nature and classification. Department of Agriculture, Victoria. Pantidou, M. E. (1969) Fungi of Greece III. Species of Puccinia. Annales de l’Institut Phytopathologique Benaki 9: 33–45. Saccardo, P. A. (1888) Sylloge Fungorum. Vol. 7. P.A. Saccardo, Padova. Saccardo, P. A. (1925) Sylloge Fungorum. Vol. 23. P.A. Saccardo, Padova. Corresponding Editor: R. W. S. Weber