Samples of D. pennellii var. chilensis were collected in Socoroma (18˚16'38''S, 69˚35'28''W) in the highlands of the Andes mountains at 3200 m asl. D. pennellii var. chilensis were growing in a slope with a northern exposure, 125 km northeast of Arica city and 3 km from Socoroma, in the north of Chile (Figure 1). A total of 10 entire plants of D. pennellii var. chilensis showing rust, symptoms, and signs on the leaflets were collected in April and June 2017. Each sample was identified, labeled, and taken to the Plant Pathology Laboratory at Universidad de Tarapacá, where morphological and molecular studies were conducted. Besides, ten plant samples were desiccated at room temperature (20˚C - 22˚C) and kept in a herbarium.

Morphometric studies were conducted on water mount urediniospores and teliospores collected from rust sori developed on leaflet samples of D. pennellii var. chilensis.

The identification included studies of wall thickness, ornamentation, color, size, and shape of the 30 urediniopores and 30 teliospores. The characteristics of the teliospore pedicels and the number and position of the germinative pores and spore size were determined. An aqueous solution of chloral hydrate 450 g/L was used to facilitate seeing the germinal pores of the teliospores [7]. For the observation of morphological details of the spores, the Bruzesse and Hassan dye [8] was used. The preparations were sealed with nail polish, labeled, and stored at room temperature until used. Measurements and digital photographs were made with the aid of an Olympus BX51 microscope and the Q Capture-Pro version 6 Software (Surrey, BC, Canada).

For scanning electron microscope (SEM) EVO LS 10 (Carl Zeiss, Bonn, Germany) observations, where sections of leaflets of (0.2 cm²) with telia were obtained. The specimens were mounted on aluminum sample holders with double-contact carbon adhesives and analyzed in a low vacuum and in variable pressure mode, where the chamber pressure was 150 Pa (under vacuum) and in the column 2 × 10⁻⁵ Torr (high vacuum). The working distance used (WD) varied depending on the type of sample, and what was needed to observe, the acceleration voltage used was 15 KV and a tilt (tilt) from 0˚ to 90˚, while the images were taken with a resolution of 3024 × 2304 pixels at a scanning speed of 12 minutes with 54 seconds.

The specimens were deposited in the mycological collection of Universidad de Concepción Herbarium (CONC-F 1894).

Due to rust cannot be grown in culture media, teliospores were used for molecular analysis, which was removed and collected from telia on leaves with a sterile scalpel. DNA from three independent infected plants was extracted using EZNA® Insect DNA Kit (Omega Bio-Tek Inc, Norcross, GA, USA) according to the manufacturer’s instructions. Subsequently, the D1/D2 domain of the large subunit ribosomal DNA 28S (LSU rDNA) was amplified using primers LR6 (5’-CGCCAGTTCTGCTTACC-3’) and Rust2inv (5’-GATGAAGAACACAGTGAAA-3’) [9]. Polymerase chain reactions of LSU rDNA were conducted in an Amplitronyx®6 thermal cycler (Nyx-Technik, San Diego, California, USA) using a final volume of 20 μl. Each reaction contained 1 μl of DNA extract, 5 pmoles of each primer, 2.5 mM of each dNTP, 2 mM MgCl₂, 1X PCR buffer (KCl), 1 unit of Taq DNA polymerase (Thermo Scientific, Waltham, MA, USA), and sterile distilled water. Cycling conditions were: 5 min at 94˚C; 35 cycles of 1 min at 94˚C; 1 min at 55˚C; 1 min at 72˚C and a final elongation step of 2 min at 72˚C. PCR blank reaction control without template DNA was always incorporated. The PCR products were visualized on 1.0% agarose gel and stained with GelRed (Biotium Inc., Hayward, CA, USA). The amplified PCR products were purified and sequenced by Macrogen (Macrogen, Geumcheon-gu, South Korea). The nucleotide sequences were visualized and edited using the 4 Peaks software (http://nucleobytes.com). A BLASTn analysis was used to compare the DNA sequence obtained of the rust fungus isolates from Socoroma with rDNA D1/D2 data sequences available in GenBank (http://www.ncbi.nlm.nih.gov/).

Phylogenetic reconstruction was performed using the maximum likelihood algorithm, using Molecular Evolutionary Genetics Analysis (MEGA version 6.0) software [10], and the robustness of the branches was assessed by bootstrap analysis [11] of 1000 replicates. The sequence of Encyclometra sp. (KY781819) was used as an outgroup.

Uropyxis daleae (Dietel & Holw.) Magnus var. nova socoromensis.

Holotype. Dalea pennelli (Mac Bride) Mac Bride var. chilensis Barneby, Socoroma, Arica and Parinacota, Chile, Sep. 2017, leg. G. Sepúlveda 101 ColMic-UTA 183. The specimen was deposited as a dried specimen in the the mycological collection of Universidad de Concepción Herbarium (CONC-F 1894).

Etymology. From the Andean village of Socoroma, in reference to the collection site (Figure 1).

Uredinial stage with amphiphigenous subepidermal uredinia with inconspicuous rupture of the epidermis, reddish to tan-brown, pulverulent, solitary or in small groups, round to oblong. Paraphyses not observed. Ellipsoid to obovoid urediniospores, hyaline to pale yellow, of 22 - 28 × 20 - 23 µm, finely echinulate wall of 2 - 2.5 µm of thickness, golden brown with 5 to 8 scattered germinative pores (Table 1).

Telia were anfigenous, subepidermal in origin, with inconspicuous epidermal rupture, dark brown to black, predominantly hypophyllous, frequently coming from uredinium, pulvinate, paraphyses were absent-Teliopores were bicellular, ellipsoid to oblong, 32 - 50 × 25 - 30 µm. Uniform laminate wall, with scattered warts, 2.5 µm thick and hyaline, two germinating pores per cell; fragile pedicel, 30 - 35 µm long, hygroscopic at the point of union with the spore, up to 23 μm wide, hyaline in color. Spermogonia (pycnial) and aecia were absent.

Fresh leaves of Dalea pennelli (Mac Bride) Mac Bride var. chilensis Barneby, Socoroma, Arica and Parinacota, Chile. 2017, Province of Parinacota, Socoroma, S lat. 18˚16'38'', W 69˚35'28'', 3200 m asl. Leg. et det. W. Huanca-Mamani & G. Sepúlveda, (CONC-F 1894).

Spermogonia (pycnia) and aecia were not detected. Sori containing teliospores, hypophyllous subepidermic, erumpents, small, dark brown, 1 - 2.1 × 1 - 1.8 mm, powdery, non-paraphysated (Figure 2). Teliospores elipsoides to oblong 32 - 50 × 25 - 30 µm, echinulated, dark brown, two germinative pores per

¹Based on Baxter’s description (1959) [12].

cell, walls of uniform thickness 1.3 - 3.3 mm, the majority 2.5 mm thick, pedicellated, hyaline pedicels, campanulated lateral wall of 14.3 - 10 mm of thickness, the majority of 12.5 mm thicks (Figure 3).

To confirm the morphological identification, a PCR fragments of LSU rDNA of isolates from Socoroma were successfully amplified and sequenced, obtaining fragments of LSU of 1446, 1456 and 1443 bp, which were deposited in the GenBank (Accession number MG969964, MN337264 and MN337263, respectively). A BLAST search showed 91.20% similarity of the isolates Socoroma with Uropyxis daleae (KY798364) and 87.85%, 87.78%, and 87.76% with Puccinia ocimi, P. unciniarum, and P. caricis, respectively (KY764149, KX985746, and KX798380). The phylogenetic analysis using sequences of the LSU rDNA grouped the isolates Socoroma in a different cluster from other rust fungi, and it was phylogenetically close to the reference isolate of U. daleae (KY798364) (Figure 4).