Aronia melanocarpa, black chokeberry, is a deciduous shrub native to the Great Lakes Region and eastern North America. In August 2014, aronia plants with brown leaf spots (approximately 60% disease incidence) were sampled from an orchard in Hamyang, South Korea. Leaf symptoms included small, 1 to 5-mm-diameter, circular to irregularly shaped, brown spots surrounded by distinct dark, brownish-red haloes. Later, spots expanded and coalesced into irregularly shaped lesions. Leaves with severe infection dried and eventually dropped. To isolate fungal pathogens from infected leaves, diseased leaf tissues excised from the margin of lesions were surface-disinfested in 1% NaOCl for 30 s, rinsed three times with distilled sterilized water, then placed on water agar and cultured at 25°C for 4 days. Mycelial tips of developing fungal cultures were transferred to potato dextrose agar (PDA) for identification. Five Alternaria isolates were recovered from the infected plant samples. All fungal colonies were dark olive and produced loose, aerial hyphae on the surface of the colony. Conidia, which had 3 to 6 transverse septa, 1 to 2 longitudinal septa, and sometimes also a few oblique septa, were pale brown to golden brown, ellipsoid to ovoid, obclavate to obpyriform, and measured 12 to 38 × 7 to 16 μm (n = 50). On the basis of the morphological characteristics, the fungi were placed in the Alternaria alternata group (Woudenberg et al. 2013). A representative isolate was deposited in the Korean Agricultural Culture Collection under Accession No. KACC 47991. To confirm the identity of the fungus, the complete internal transcribed spacer (ITS) rDNA region and the large intron of translation elongation factor 1 alpha (EF-1α) of isolate KACC 47991 were amplified using ITS1/ITS4 and EF1-728F/EF1-986R primers, respectively (White et al. 1990; Deng et al. 2013). The DNA products were cloned into the pGEM-T Easy vector (Promega, Madison, WI) and the resulting plasmids were sequenced using universal primers. The ITS rDNA sequence of isolate KACC 47991 (GenBank Accession No. KT355705) was homologous and shared 100% identity with A. alternata strains HBxn2-1 from China and STE-U4349 from South Africa, causing ramie leaf spot (HQ645083) and citrus black rot (AF404664), respectively, while the EF-1α gene sequence (KT355704) was 99% identical to that of A. alternata isolate PhP2 from Italy (KP861903), causing heart rot of pomegranate (Faedda et al. 2015). Isolate KACC 47991 was used to conduct pathogenicity tests on detached aronia leaves. Ten leaves were rinsed with distilled sterilized water and inoculated by spraying with a conidial suspension of 2 × 106 conidia/ml until run-off. Ten negative control leaves were treated with sterilized distilled water. All leaves were kept in a moist chamber with >90% relative humidity at 25°C. After 15 days, leaf spot symptoms similar to those observed in the field developed on the inoculated leaves, whereas the control leaves remained asymptomatic. A. alternata was reisolated from the lesions of the inoculated plants to fulfill Koch’s postulates. The morphological features of fungi reisolated from inoculated plants were the same as those of the original isolates. To our knowledge, this is the first report of brown leaf spot caused by A. alternata on aronia in Korea. As the plants are imported, little is known about pathogens associated with aronia in Korea. The recent outbreak of brown leaf spot poses a potential threat to aronia production in Korea. © 2016, American Phytopathological Society. All rights reserved.