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Research Article
On a new genus of dwarf tarantulas (Araneae: Mygalomorphae: Theraphosidae) endemic from Peru: evidence from morphology and molecular phylogeny, with description of three new species
expand article infoOscar M. Quispe-Colca, Nelson E. Ferretti§|, Juan C. Chaparro, José A. Ochoa#, Rick C. West¤
‡ Universidad Nacional de San Agustín de Arequipa, Museo de Historia Natural (MUSA), Arequipa, Peru
§ Grupo de Investigaciones Aracnológicas del Sur (GIAS), Centro de Recursos Naturales Renovables de la Zona Semiárida (CERZOS-UNS, CONICET), Buenos Aires, Argentina
| Departamento de Biología, Bioquímica y Farmacia, Universidad Nacional del Sur, Buenos Aires, Argentina
¶ Museo de Biodiversidad del Perú, Cusco, Peru
# Facultad de Ciencias Biológicas, Universidad Nacional de San Antonio Abad del Cusco, Cusco, Peru
¤ Unaffiliated, Sooke, Canada
Open Access

Abstract

Recent field campaigns conducted in Peru along with the examination of museum specimens allowed us to identify small tarantulas that do not fit with any known Theraphosidae genera. Morphology and additional molecular evidence from the mitochondrial gene COI led us to propose Kiskalla gen. nov. from southern Peru, at Puno region. Three new species of Kiskalla gen. nov. (K. ignacioi sp. nov., K. yeisoni sp. nov. and K. zukuapasanka sp. nov.) are herein described, diagnosed and illustrated. Kiskalla gen. nov. differs from the known Theraphosinae genera in the presence of lateral stripes on the abdomen and a small dorsal arrowhead-shaped patch of type III urticating setae, presence of a large number of spines on all legs, short and stout setae on the dorsal metatarsi encircling the filiform trichobothria, an apical crown of long spines on the metatarsi of all legs in both sexes and scopula of tarsi IV slightly developed, restricted to the margins due to the presence of long ventral setae. Males and females show genitalic features that resemble those of Hapalotremus Simon, 1903, but differ by the development of copulatory bulb keels and the aspect of the spermathecae. We also present data on the natural history and distribution of the species.

Keywords

Andes, Araneae, Kiskalla, Puno, South America, southern Peru, Taxonomy

1. Introduction

Peru is recognized as a megadiverse country, harboring an exceptional number of endemic animal and plant species, likely driven by its complex topography (MINAM 2019). Despite being considered one of the world’s biodiversity hotspots, significant knowledge gaps remain, particularly in the context of accelerating biodiversity loss and habitat modification that now affect even well preserved environments (Perry et al. 2016). In recent years, efforts to document and understand Peru’s immense biological diversity, especially in mygalomorph spiders, have resulted in the description of numerous new species and recently even in several new genera, e.g. Antikuna Kaderka, Ferretti, West, Lüddecke & Hüsser, 2021, Anqasha Sherwood & Gabriel, 2022, Bistriopelma Kaderka, 2015, Chinchaysuyu Ferretti, Chaparro, Ochoa & West, 2023, Ewok Peñaherrera-R., Sherwood, Gabriel, León-E., Rollard, Leguin, Brescovit & Lucas, 2025, Murphyarachne Sherwood & Gabriel, 2022 and Urupelma Kaderka, Lüddecke, Řezáč, Řezáčová & Hüsser, 2023 (Kaderka 2015; Ferretti et al. 2016, 2018, 2023, 2025; Fukushima and Bertani 2017; Nicoletta et al. 2020; Quispe-Colca and Kaderka 2020; Kaderka 2023; Kaderka et al. 2021, 2023; Quispe-Colca and Ferretti 2021; Sherwood et al. 2021a, b; Sherwood and Gabriel 2022a, b, 2024; Gabriel et al. 2023; Ríos-Tamayo et al. 2023; Millenpeier et al. 2023; Kaderka and Quispe-Colca 2025; Signorotto et al. 2025).

The family Theraphosidae Thorell, 1869 represents the most species-rich group of mygalomorph spiders, currently comprising 1,193 species in 187 genera (World Spider Catalog 2026), and includes the largest tarantulas known worldwide. During the examination of theraphosids from high-altitude regions of Peru including specimens deposited in the collections of the Museo de Biodiversidad de Perú (Cusco, Peru) and the Museo de Historia Natural de la Universidad Nacional de San Agustín de Arequipa (Arequipa, Peru), as well as individuals collected during field expeditions in April 2022 and October 2023 in the department of Puno, we identified small-sized specimens resembling the genus Hapalotremus in several genitalic features (e.g. the palpal bulb and tibial apophysis in males, and spermathecae in females). However, beyond these similarities, the specimens display a distinctive combination of morphological traits that clearly separates them from other theraphosids: an abdominal pattern with an arrowhead-shaped patch of urticating setae; thick setae surrounding the booklung openings; short and stout setae on the dorsal metatarsi encircling the filiform trichobothria; and an apical crown of long spines on the metatarsi of all legs in both sexes. In addition, tarsi IV lack scopulae or, if present, they are poorly developed and interrupted by a broad band of setae.

A detailed morphological analysis, combined with a molecular phylogenetic reconstruction that includes representatives of the high-Andean genera Antikuna Kaderka et al., 2021, Bistriopelma Kaderka, 2015, Cyriocosmus Simon, 1903, Hapalotremus Simon, 1903, Thrixopelma Schmidt, 1994 and Urupelma Kaderka et al., 2023 together with the new specimens, supports the recognition of a new genus. Here, we describe and illustrate three new species of this genus, and provide diagnostic features, natural history data, and a distribution map.

2. Material and methods

2.1. Abbreviations

Legs and palp: Cy = cymbium; Mt = metatarsus; Ti = tibia. Eye sizes and interdistances: AME = anterior median eyes; ALE = anterior lateral eyes; OQ = ocular quadrangle (including lateral eyes); PME = posterior median eyes; PLE = posterior lateral eyes. Spination: d = dorsal; p = prolateral; r = retrolateral; v = ventral. Tibial apophysis: PB = prolateral branch; RB = retrolateral branch. Male palpal bulb: A = apical keel; SA = subapical keel; PI = prolateral inferior keel; PS = prolateral superior keel; R = retrolateral keel; TP = tegular projection. Cheliceral teeth pattern: v = small teeth; V = large teeth. PLS = posterior lateral spinnerets, PMS = posterior median spinnerets. Measures: m a.s.l. = meters above sea level.

2.2. Specimens and morphology

The material examined is deposited in the arachnid Collection of the Museo de Historia Natural de la Universidad Nacional de San Agustín de Arequipa, Arequipa, Peru (MUSA, Evaristo López Tejada curator) and in the Museo de Biodiversidad del Perú, Cusco, Peru (MUBI, José Antonio Ochoa curator). Specimens were examined using AmScope SM-1TSW2-L6W-M, ZEISS Stemi 305, ZEISS Stereo Discovery.V20 and Leica S APO stereomicroscopes. Digital images were taken with a Canon PowerShot SX530 HS digital camera, MShot and Zeiss Axiocam 820 color cameras coupled to the stereomicroscopes.

All measurements are given in millimeters and were obtained using a digital caliper with a precision of 0.01 mm and taken from photos using ImageJ software (National Institutes of Health, Bethesda, Maryland, USA). The total body length includes the carapace and abdomen, excluding chelicerae and spinnerets. Legs and palpal segments measurements were taken dorsally. Eye measurements were taken at the widest spans of each lens, AME in dorsal view, and ALE, PLE and PME in dorsolateral view. The extent of tarsal and metatarsal scopulae on ventral side of both leg podomeres was expressed as proportion of the total podomere length, measured from the apical end. Leg spination was described following Bertani (2001) and Kaderka (2015): Each leg podomere was divided into four views (ventral, prolateral, retrolateral and dorsal) and each view described separately for basal, central and apical sections. For example, “metatarsus I v 1-0-3” indicates one spine in basal section and three spines in apical section of the ventral quadrant. If the bases of all three apical spines are located distally, their position is specified as “apical” in brackets. Unequal numbers of spines on the right and left sides of the same leg segment are indicated in parentheses. Abdominal urticating setae were removed by forceps, preserved in alcohol and examined with ZEISS Primo Star and Leica microscopes. Terminology of urticating setae follow Cooke et al. (1972). For proper examination, female genitalia were detached from the abdomen. Terminology of the male palpal bulb follows Bertani (2000), with the exception of the tegular protuberance (TP), which is described following Kaderka et al. (2023) using four states: absent, weakly developed, developed, or well-developed.

2.3. Molecular procedures

Live specimens were euthanized by injection of lidocaine at the sternal margin of the sternum and subsequently preserved in absolute ethanol at –80°C. This procedure was performed in the facilities of MUBI (Cusco, Peru). Tissues samples were obtained from two specimens representing two different localities (Table 1). It was not possible to obtain DNA samples from K. yeisoni sp. nov. due to the inappropriate preservation of the specimen according to molecular protocols. Additional specimens of the genera Bistriopelma and Hapalotremus were sequenced for inclusion in the phylogenetic analysis. Furthermore, GenBank sequences from representatives of the Peruvian genera Antikuna, Cyriocosmus, Urupelma and Thrixopelma were incorporated (Table 1). Muscle tissue was extracted from legs III and IV. Total genomic DNA was isolated following a specific protocol developed at GENETyC (CERZOS-CONICET, UNS), Bahía Blanca, Argentina. We targeted the mitochondrial cytochrome c oxidase subunit I (COI) barcode region. The COI fragment was amplified using the universal primers LCO-1490 (5’-GGTCAACAAATCATAAAGATATTGG-3’) and HCO-2198 (5’-TAAACTTCAGGGTGACCAAAAAATCA-3’) (Folmer et al. 1994). Polymerase chain reaction (PCR) amplification were conducted under the following conditions: initial denaturation at 94°C for 9 min, 34 cycles of 94°C for 45 s; 48°C for 45 s; 72°C for 60 s; followed by a final extension at 72°C for 6 min. PCR products were purified and sequenced by Macrogen (Seoul, Korea). Chromatograms were edited, and sequences managed in Geneious R11 (https://www.geneious.com).

Table 1.

Samples of Kiskalla gen. nov. used in molecular analyses, with DNA voucher numbers, collection localities, and GenBank accession numbers for CO1.

Species Code Locality/bibliography GenBank
Kiskalla ignacioi sp. nov. GIAS_20 Huiquisa, Puno, Peru
Kiskalla zukuapasanka sp. nov. GIAS_24 Abra Sallaco, Puno, Peru
Bistriopelma sp. GIAS_61 La Raya, Cusco, Peru
Hapalotremus major GIAS_41 Sacsayhuaman, Cusco, Peru
Hapalotremus major GIAS_58 Sacsayhuaman, Cusco, Peru
Hapalotremus vilcanota GIAS_33 Cordillera Vilcanota, Peru
Hapalotremus carabaya GIAS_38 Tambopampa, Canchis, Cusco, Peru
Antikuna cimrmani Kaderka et al. (2023) OR178610
Antikuna majuski Kaderka et al. (2023) OR178637
Thrixopelma ockerti Kaderka et al. (2023) OR178629
Bistriopelma matuskai Kaderka et al. (2023) OR178612
Bistriopelma sp. Kaderka et al. (2023) OR178614
Urupelma sanctimariae Kaderka et al. (2023) OR178633
Urupelma machiguenga Kaderka et al. (2023) OR178631
Urupelma johannae Kaderka et al. (2023) OR178627
Urupelma awanqay Kaderka et al. (2023) OR178630
Cyriocosmus itayensis Kaderka et al. (2023) OR178619
Cyriocosmus peruvianus Kaderka et al. (2023) OR178621
Cyriocosmus aueri Kaderka et al. (2023) OR178616
Cyriocosmus elegans Kaderka et al. (2023) OR178618
Cyriocosmus leetzi Kaderka et al. (2023) OR178620
Cyriocosmus bicolor Kaderka et al. (2023) OR178617

2.4. Molecular phylogenetic analyses

Sequence alignments of the COI fragments were generated with MAFFT v7.017 (Katoh et al. 2002) implemented as a plug-in Geneious R11, using default parameters. The resulting matrices were subjected to Maximum likelihood (ML) and Bayesian inference (BI) phylogenetic analyses. ML analyses were conducted in IQ-TREE v.1.6.8 (Nguyen et al. 2015). We used IQ-TREE to first select the best-fit partitioning scheme and corresponding evolutionary models of the matrix through ModelFinder (Kalyaanamoorthy et al. 2017), and then inferred the best tree and estimate clade support with 1000 ultrafast bootstrap replicates (Hoang et al. 2018). Finally, we conducted a BI analysis using the program MrBayes v.3.2.3 (Ronquist et al. 2012). We first assessed the best partition scheme and corresponding evolutionary using the program PartitionFinder v.2.1.1 (Lanfear et al. 2017) and three subsets defined a priori (each codon position separately for COI). Two independent Markov chain Monte Carlo (MCMC) runs of 10 million generations with four each, starting from random trees and sampling every 1000 generations. The first 25% of sample trees were discarded as burn-in. Convergence among BI runs was evaluated in TRACER v.1.7 (Rambaut et al. 2018). All trees were visualized in TreeGraph2 (Stöver and Müller 2010) and final figures were prepared using CorelDRAW.

2.5. Geographic coordinates and distribution map

The distribution map of the new genus was prepared using QGIS (version 3.16). To reduce risk associated with illegal pet trade and wildlife trafficking activities prohibited under peruvian law, GPS coordinates of the collection sites were not provided.

3. Results

3.1. Molecular phylogeny

The phylogenetic analyses recovered the tribes Grammostolini and Hapalopini as monophyletic, both with high support values (Fig. 1). Within Hapalopini, a clade including Thrixopelma and Antikuna was recovered as sister to a larger clade comprising four other Peruvian genera. Within this latter clade, representatives of Urupelma formed a well-supported monophyletic group, recovered as sister to the genera Kiskalla gen. nov., Hapalotremus and Cyriocosmus, although with lower support values (Fig. 1). The clade uniting these three genera ((Kiskalla gen. nov., Hapalotremus), Cyriocosmus)) was strongly supported under both phylogenetic inference methods: it further indicated a close relationship between Kiskalla gen. nov. and Hapalotremus, together forming the sister group of Cyriocosmus (Fig. 1). Hapalotremus was recovered as monophyletic, sister to Kiskalla gen. nov., with both sampled representatives of H. major (the type species of the genus) clustering together. Similarly, the six species of Cyriocosmus represented by sequences obtained from GenBank formed a clade with high support under both phylogenetic inference methods (Fig. 1).

Figure 1. 

Summary tree from results obtained under ML and BI phylogenetic inferences showing support in relevant nodes. Taxa in blue represent the new species treated in this work.

3.2. Taxonomy

Order Araneae Clerck, 1757

Infraorder Mygalomorphae Pocock, 1892

Family Theraphosidae Thorell, 1869

Subfamily Theraphosinae Thorell, 1869

Kiskalla gen. nov.

Figures 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15; Tables 25

Etymology.

Kiskalla is an adjective in Quechua language that means “spiny” and refers to the large number of spines on all legs, particularly in males. The genus gender is feminine.

Type species.

Kiskalla ignacioi sp. nov.

Diagnosis.

The new genus differs from all remaining Theraphosinae genera by the following combination of characters: the presence of lateral abdominal stripes (Figs 2F, 4C, 9), a small dorsal arrowhead-shaped patch of type III urticating setae (Figs 8C, 9D, 10B, 12G), presence of short, stout setae on the dorsal metatarsi encircling the filiform trichobothria (Fig. 4H), an apical crown of long spines on ventral metatarsi of all legs in both sexes (Figs 4G, 10G) and tarsi IV with slightly-developed scopula restricted to the margins due to the presence of long ventral setae (Fig. 4G). In addition, males and females share a general similarity in the shape of the palpal bulb and spermathecae with those of Hapalotremus. However, males are readily distinguished by the presence of a very large and serrated SA keel on the palpal bulb, combined with a well-developed PI keel on embolus and a barely perceptible PS keel (Figs 3A–D, 7), a projection on the retrolateral face of the cymbium (Fig. 6A), tibiae of legs I about 1:3 longer (Fig. 5A), and a tibial apophysis not arising from a large common base (Fig. 5). Females are distinguished from Hapalotremus by having a single dome-shaped receptacle lacking both apical and basal lateral projections (Figs 8E, 10H, 12F, 13H).

Figure 2. 

Kiskalla ignacioi sp. nov., AD holotype male (MUSA-AR 317). A Carapace, dorsal view; B sternum, ventral view; C labium and maxillae, ventral view (green arrow indicates setae); D abdomen, dorsal view; E habitat at type locality in Corani, Carabaya, Puno; F holotype male in natural habitat, habitus. Scale bars = 1 mm. Photos: O. Quispe-Colca.

Figure 3. 

Kiskalla ignacioi sp. nov., holotype male (MUSA-AR 317). A Palpal bulb in prolateral view.; B palpal bulb in retrolateral view; C palpal bulb in ventral view; D palpal bulb in dorsal view; E tibial apophysis in ventral view. PB = prolateral branch, PI = prolateral inferior keel, RB = retrolateral branch, SA = subapical keel, TP = tegular projection. Scale bars = 1 mm. Photos: O. Quispe-Colca.

Figure 4. 

Kiskalla ignacioi sp. nov., paratype male (MUBI 313). A Carapace, dorsal view; B abdomen, dorsal view; C abdomen, lateral view; D sternum, ventral view; E labium and maxillae, ventral view; F eyes, dorsal view; G tarsus of leg IV, ventral view (green arrow indicates the crown of ventral spines); H metatarsus of leg IV, dorsal view (green arrow indicates the short setae around the trichobothria). Scale bars = 1 mm. Photos: N. Ferretti.

Figure 5. 

Kiskalla ignacioi sp. nov., paratype male (MUBI 313), tibial apophysis. A Retrolateral view; B ventral view; C prolateral view. Mt = metatarsus, PB = prolateral branch, RB = retrolateral branch, Ti = tibia. Scale bar = 1 mm. Photos: N. Ferretti.

Figure 6. 

Kiskalla ignacioi sp. nov., paratype male (MUBI 313), palp. A Retrolateral view; B prolateral view; Cy = cymbium, Ti = tibia. Scale bar = 1 mm. Photos: N. Ferretti.

Figure 7. 

Kiskalla ignacioi sp. nov., paratype male (MUBI 313), right palpal bulb. A Prolateral view; B retrolateral view; C dorsal view; D ventral view. Abbreviations: A = apical keel, PI = prolateral inferior keel, PS = prolateral superior keel, SA = subapical keel, TP = tegular protuberance. Scale bar = 1 mm. Photos: N. Ferretti.

Figure 8. 

Kiskalla ignacioi sp. nov., paratype female (MUSA-AR 318). A Carapace, dorsal view; B sternum, ventral view; C abdomen, dorsal view; D labium and maxillae, ventral view; E spermathecae, dorsal view. Scale bars = 1 mm. Photos: O. Quispe-Colca.

Figure 9. 

Kiskalla ignacioi sp. nov., paratype females (MUBI 313, 314), habitus. A dorsal view; B dorsolateral view; C recently molted female, dorsolateral view; D posterodorsal view. Scale bars = 1 cm. Photos: J.C. Chaparro.

Figure 10. 

Kiskalla ignacioi sp. nov., paratype female (MUBI 314). A Carapace, dorsal view; B abdomen, dorsal view; C sternum, ventral view; D abdomen, ventral view; E labium and maxillae, ventral view; F eyes, dorsal view; G tarsus IV, ventral view (green arrow indicates the crown of ventral spines); H spermathecae, dorsal view. Scale bars = 1 mm. Photos: N. Ferretti.

Affinities.

Kiskalla shares with other Peruvian Theraphosidae inhabiting high montane regions the presence of only type III urticating setae, as in Anqasha Sherwood and Gabriel, 2022; Antikuna; Bistriopelma; Chinchaysuyu Ferretti et al., 2023; and Hapalotremus. Females of Kiskalla differ from all the above genera (except Hapalotremus) by the presence of a single spermathecal receptacle. Kiskalla further differs from Anqasha by the general morphology of the male palpal bulb: the embolus of Kiskalla lacks the R keel, which is present and well-developed in Anqasha (Sherwood and Gabriel 2022a; Kaderka 2023). Males of Kiskalla also differ from those of Antikuna by possessing a well-developed, serrated SA keel and only a slightly-developed PS keel, whereas Antikuna species show a small SA keel and a well-developed PS keel (Kaderka et al. 2021). Kiskalla is easily distinguished from Bistriopelma by having a single dorsal patch of urticating setae on the abdomen instead of the two patches characteristic of Bistriopelma and by the morphology of male palpal bulb (Kaderka 2015). In addition, Kiskalla differs from Chinchaysuyu in the morphology of the male palpal bulb, which in Kiskalla bears PS and PI keels, whereas Chinchaysuyu shows a multiple rolateral accessory keels extending across the tegulum, along with the presence of an R keel (Ferretti et al. 2023; Kaderka 2024). Males of Kiskalla are further distinguished from those of Hapalotremus by the presence of a cymbial retrolateral projection, a well-developed serrated SA keel, and a weakly-developed PS keel on the prolateral face of embolus but highly distinct in ventral view; females differ by lacking apical and lateral projections on the spermathecae, which are variable developed in Hapalotremus (Ferretti et al. 2025). Finally, Kiskalla differs from some representatives of Thrixopelma that bear only type III urticating setae, by the non-spatulate embolus of the male palpal bulb, the PI keel lacking crests, and the absence of an R keel on the embolus (Sherwood et al. 2021).

General description.

Kiskalla comprises small-sized brown to grey tarantulas, with total body length ranging from 11.8 to 19.1 mm (excluding chelicerae and spinnerets). Carapace oval, uniformly colored; caput highly elevated in Kiskalla zukuapasanka sp. nov. Ocular tubercle oval, slightly to high elevated, wider than long, bearing eight eyes, anterior eye row slightly procurved to procurved, posterior row recurved in dorsal view. Clypeus narrow. Fovea transverse, deep and wide, procurved. Chelicerae lacking rastellum and stridulatory bristles; promargin with 10–12 teeth. Labium wider than long, with 4–24 cuspules restricted to the anterior third. Maxillae with 66–170 cuspules on the basal half of the ventral side. Ventral surface of maxillae with apical half to nearly the entire surface covered by short spiniform setae. Sternum rounded with long soft setae on margins, three pairs of oval sigillae. Abdomen with lateral black stripes along the margins (more conspicuous in Kiskalla ignacioi sp. nov.) and with a single dorsal arrowhead-shaped patch of type III urticating setae. Legs very spinose; tarsi IV lacking scopulae or with scopulae poorly developed and restricted to the margins by long setae. Leg formula: I>IV>II>III in males, IV>I>II>III in females. Femur III incrassate in males. Palpal bulb of males with globose tegulum and a tegular projection, embolus wide, retrolaterally curved with four keels: A, PI, PS and SA serrated. Spermathecae of females consists in a single subquadrate dome-shaped receptacle with large granules.

Species included.

Kiskalla ignacioi sp. nov., K. yeisoni sp. nov. and K. zukuapasanka sp. nov.

Kiskalla ignacioi sp. nov.

Figures 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 16; Tables 2, 3

Type material.

Holotype: PERU • 1♂; Puno, Carabaya, Corani; 4360 m a.s.l.; 19.IV.2022; Y. A. Calizaya Melo col.; MUSA-AR 317. Paratypes: PERU • 1♀; same locality and data as holotype; MUSA-AR 318 • 1♂; Puno, Carabaya, Corani, close to Chacomiza community; 4570 m a.s.l.; 18.I.2024; A. Quiroz col.; MUBI 313 • 2♀♀; same data as preceding male; MUBI 314.

Additional material examined.

PERU • 1♀; Puno, Carabaya, Juro Juro, road to Ollachea; 4115 m a.s.l.; 24.XI.2019; Chaparro and Richards cols.; MUBI 104 • 1♀; Puno, Huiquisa; 30.IX.2023; N. Ferretti, R. West and J. Chaparro cols.; MUBI 229.

Etymology.

This species is named in honor and in loving memory of Ignacio Enrique Quispe-Escobedo, father of Oscar M. Quispe-Colca, with whom Oscar spoke a lot about the discovery of this species.

Diagnosis.

Kiskalla ignacioi sp. nov. differs from K. yeisoni sp. nov. and K. zukuapasanka sp. nov. by its distinctive coloration: carapace, legs and palps blackish-brown with whitish pubescence; abdomen dorsally black with short lateral bands contrasting with a whitish ventral surface (Figs 2D, 2F, 4C, 9B). Females of K. ignacioi sp. nov. also differ from congeners by the shape of the spermathecae, which consists in a single sub-quadrate seminal receptacle (Figs 8E, 10H).

Description – male.

Male holotype (MUSA-AR 317). Total length: 11.8. Carapace: length 5.77, width 5.45. Chelicerae with 11–12 teeth on promargin; cheliceral teeth pattern from the basal end: right side: V-V-V-VVVVVV-V-v, left side: V-V-V-vvVVVV-V-V-v. Anterior eye row slightly procurved, posterior recurved (Fig. 2A). Eye sizes and interdistances: AME 0.21, ALE 0.24, PME 0.18, PLE 0.27, AMEAME 0.12, AMEALE 0.06, PMEPME 0.39, PMEPLE 0.07, ALEPLE 0.16, AMEPME 0.09, OQ length 0.43, width 0.63. Ocular tubercle oval and slightly elevated, length 0.62, width 1.01, clypeus narrow, length 0.22. Fovea transverse, deep, procurved, width 0.78 (Fig. 2A). Labium length 0.61, width 1.26, anterior third with 6 cuspules (Fig. 2B, C), maxillae right/left with 91/97 cuspules, ventral maxillae covered with short spiniform setae located on apical half (Fig. 2C). Sternum: length 3.12, width 2.05, with three pairs of oval sigillae (Fig. 2B). Abdomen: length 6.04, width 4.24. PLS three-segmented, length 1.93, basal segment 0.69, middle segment 0.41, apical segment 0.83, all digitiform. PMS (one segment), length 0.34. Abdomen with type III urticating setae located in a medial dorsal arrowhead-shaped patch (Fig. 2D), length 1.77, width 0.83. Leg pattern: I>IV>II>III (Table 1) with incrassate femora III. — Scopulae: All tarsi fully scopulated, tarsi I–II with scopula divided by one row of short setae, tarsi III–IV with scopula slightly developed, restricted to margins. Metatarsi I 1/3 scopulated, metatarsi II 1/3 scopulated, metatarsi III 1/6 scopulated and metatarsi IV without scopula. — Spination: Femora I–IV and femora of palps 0. Patellae I–IV and patellae of palps 0. Tibiae I v (1-2)-2-2 (apical), p 0-1-1, r 1-(1-0)-1; II right v 2-2-3 (apical), p 1-0-1, r 1-1-1; III v 2-3-2 (apical), p 0-1-1, r 1-1-0; IV v (0-1)-2-2 (apical), r 0-1-(0-1) and tibiae of palps left 0. Metatarsi I v 2-(1-0)-2 (apical), p 1-1-0, r (0-1)-1-0; II right v 3-2-4 (apical), p 1-1-1, r 0-1-0; III v 3-(3-2)-6 (5-6 apical), p 1-1-1, r (1-0)-1-2; IV v (2-3)-3-(5-6) (5 apical), p 0-(0-1)-1, r 1-2-1. Tarsi I–IV and tarsi of palps 0. Metatarsi of legs I–IV with short and strong dorsal spines interspersed with the trichobothria and a crown of apical ventral spines. — Tibial apophysis with two unequal branches, retrolateral branch longer than prolateral (Fig. 3E). Prolateral branch with a single inner spine of similar length and retrolateral branch with one apical short spine and two basal spines retrolaterally positioned (Fig. 3E). Metatarsus I slightly curved. Flexion of metatarsus I retrolateral to the tibial apophysis. — Cymbium with lobes unequal in sizes and a with retrolateral triangular projection; retrolateral lobe distinctly larger than the prolateral. Palpal bulb with developed tegular projection; embolus thick, relatively short, curved retrolaterally. PS keel weakly-developed, nearly imperceptible; PI keel well-developed with a crest above the embolus tip, SA well developed, apically pointed and serrated, A keel present, small (Fig. 3A–D).— Coloration (in life). Carapace blackish-brown with dense whitish pubescence and long whitish setae on margins, chelicerae dorsally covered with whitish setae (Fig. 2F). Legs and palps blackish-brown; femora with faint whitish pubescence; patellae, tibiae, metatarsi and tarsi with whitish pubescence (Fig. 2F). Femora of legs and palps with three parallel longitudinal stripes (two dorsal, one retrolateral); patellae I–II and palps with two nearly equal parallel longitudinal stripes; patellae III–IV with two unequal diagonal stripes; tibiae and palpal tibiae with two parallel longitudinal stripes; one longitudinal stripe reaching close to the third part of the metatarsi I–II. Abdomen black, with whitish lateral bands with wavy edges and narrow arrowhead-shaped patch of golden-brown urticating setae (Fig. 2F).

Remarks and variation –

males. The paratype male from a locality near that to the holotype presents eight labial cuspules and a more rounded sternum (Fig. 4D, E). The carapace shares the wittish setae on margins but it is covered by iridescent purple setae (Fig. 4A, F); lateral abdominal stripes and pale margins are so more conspicuous (Fig. 4B, C) and the urticating patch is slightly displaced towards the central portion of the dorsal abdomen (Fig. 4B). Both the holotype and paratype males share ventral maxillae with the apical half covered by short spiniform setae (Fig. 4E) as well as short, stout setae on the dorsal metatarsi encircling the trichobothria (Fig. 4H). The tibial apophyses have some differences, the male paratype has a more curved RB along with a stout spine on the apical portion (Fig. 5). In relation to the palp configuration, the male paratype has a more developed cymbial projection on the retrolateral face (Fig. 6A) and the palpal bulb has a PS slightly more distinct than in the holotype male and a well-developed tegular projection along with a more serrated SA keel (Fig. 7A–D).

Description – female.

Female paratype (MUSA-AR 318). Total length: 19.10. Carapace: length 7.40, width 6.34. Chelicerae with 11–12 teeth on promargin; cheliceral teeth pattern from the basal end: right side: V-V-VvvvvVVV-V, left side: v-V-VVvvvvvVV-V. Anterior eye row procurved, posterior recurved (Fig. 8A). Eye sizes and interdistances: AME 0.23, ALE 0.26, PME 0.20, PLE 0.27, AMEAME 0.14, AMEALE 0.09, PMEPME 0.55, PMEPLE 0.08, ALEPLE 0.19, AMEPME 0.10, OQ length 0.46, width 0.76. Ocular tubercle oval and slightly elevated (Fig. 8A), length 0.89, width 1.12, clypeus narrow, length 0.22. Fovea transverse, deep, procurved (Fig. 8A), width 1.16. Labium length 0.89, width 1.60, anterior third with 4 cuspules (Fig. 8D), maxillae right/left with 66/71 cuspules, ventral maxillae covered with short spiniform setae located on apical half (Fig. 8B, D). Sternum: length 4.01, width 3.32, with three pairs of oval sigillae (Fig. 8B). Abdomen (Fig. 8C): length 11.7, width 8.84. PLS three-segmented, length 3.34, basal segment 1.27, middle segment 0.92, apical segment 1.15, all digitiform. PMS (one segment), length 0.79. Abdomen with type III urticating setae located in a narrow arrowhead-shaped patch (Fig. 8C), length 3.79, width 2.66. Leg pattern: IV>I>II>III (Table 2). — Scopulae: Tarsi I–II fully scopulated and entire with a row of thin setae, tarsi III–IV without scopula. Metatarsi I 1/3 scopulated, metatarsi II 1/5 scopulated, metatarsi III–IV without scopula. — Spination: Femora I–IV and femora of palps 0. Patellae and patellae of palps 0. Tibiae I 0; II 0; III v 0-0-(0-1) (apical); IV 0. Metatarsi I v 0-0-1 (apical); II v 0-0-4 (apical), p 0-0-(1-0) (apical); III v 0-(3-1)-(6-5) (apical), p 0-(0-1)-2 (apical), r 0-1-(1-2); IV v (1-0)-(1-3)-4 (3-4 apical), p 0-0-2 (1 apical), r 0-(0-1)-1. Tarsi I–IV and tarsi of palps 0. — Spermathecae: with a single subquadrate dome-shaped receptacle with large granules (Fig. 8E) — Coloration (in life): Carapace blackish-brown, with whitish pubescence extending from the anterior margin of the ocular tubercle to the fovea, and long whitish setae along the margins; chelicerae dorsally covered with whitish setae (Fig. 9). Legs and palps blackish-brown; femora with faint whitish pubescence; patellae, tibiae, metatarsi, and tarsi with whitish pubescence (Fig. 9). Femora of legs and palps with three parallel longitudinal stripes (two dorsal, one retrolateral); patellae I–II and palpal patella with two nearly equal parallel longitudinal stripes, patellae III–IV with two unequal diagonal stripes; tibiae with two parallel longitudinal stripes; metatarsi I–II with a longitudinal stripe extending to midlength, metatarsi III–IV with a stripe extending to about one third of their length; palpal tarsi with a stripe reaching about one fourth of the segment (Fig. 9). Abdomen dark brown, with whitish lateral bands with wavy edges, and a blackish-brown longitudinal band similar running along the midline, adjacent to a golden brown arrowhead-shaped patch of urticating setae, near the posterior end (Fig. 9). Urticating patch small, lanceolate, composed of golden-brown setae (Fig. 9).

Table 2.

Kiskalla ignacioi sp. nov., holotype male (MUSA-AR 317). Lengths of palpal and leg segments.

Femur Patella Tibia Metatarsus Tarsus Total
Palp 3.76 1.92 3.34 1.90 10.92
Leg I 6.10 2.63 3.52 3.21 2.21 17.67
Leg II 4.42 2.54 2.91 2.52 2.32 14.71
Leg III 3.82 2.58 2.12 2.70 2.12 13.34
Leg IV 4.84 2.68 3.52 3.48 2.61 17.13
Table 3.

Kiskalla ignacioi sp. nov., paratype female (MUSA-AR 318). Lengths of palpal and leg segments.

Femur Patella Tibia Metatarsus Tarsus Total
Palp 4.35 2.68 2.61 2.43 12.07
Leg I 5.19 3.68 3.56 2.81 1.93 17.17
Leg II 5.12 3.43 2.99 2.75 1.68 15.97
Leg III 4.24 2.52 2.42 2.70 2.26 14.14
Leg IV 5.39 3.07 3.65 3.78 2.66 18.55

Remarks and variation – females.

One of the paratype female (Fig. 10) from a locality near the type site presents five to seven labial cuspules (Fig. 10E), a more strongly procurved fovea (Fig. 10A) and more conspicuous lateral abdominal stripes (Fig. 10B, D). Possibly due to preservation conditions, the females from the Chacaconiza community (MUBI 313, 314) have the entire abdomen covered by short plumose setae, given a “fluffy” appearance (Figs 10B, 10D, 11), a feature not evident in one of the other female paratype (Fig. 8C). Aside from these specific differences, all examined females share the same general morphology; ventral maxillae covered with short spiniform setae restricted to the apical half (Fig. 10E), tarsi IV with only slightly developed scopulae (Fig. 10G) and the spermathecae with a single subquadrate seminal receptacle (Fig. 10H).

Figure 11. 

Detail of plumose setae covering ventral abdomen of Kiskalla ignacioi sp. nov. Photos: N. Ferretti.

Natural history and distribution.

Kiskalla ignacioi sp. nov. is known from Corani locality at Puno department, Peru (Fig. 16), found at elevations of 4360–4570 m a.s.l. The habitat is characterized by a cold and mountainous environment, with a mean annual temperature of –6°C to 12°C. The vegetation comprises mainly grasslands near to wetlands known as “bofedales” (Fig. 2E). The male holotype was found under a stone without any apparent retreat, the female paratype was found under a stone inside a burrow without discernible webbing and ranged in length between 18–20 cm. Male and female paratypes were found in the field between 2014 and 2024 in areas near the community of Chacaconiza, Corani District, Carabaya Province, Puno Department, Peru. The species inhabited puna grassland formations including tussock grass (pajonal), puna turf, and cryoturbated zones, always associated with rocky outcrops or scattered medium to large-sized stones. Individuals were found beneath stones, usually in small burrows excavated under them, at depths ranging from 20 to 80 mm. During field observations, wasps of the family Pompilidae (known as tarantula hunters) were also recorded in the vicinity of the species’ habitat. It is worth noting that in the area of occurrence, there are plans for the development of two medium-scale open-pit mining projects, which may pose a potential threat to populations of this species.

Kiskalla yeisoni sp. nov.

Figures 12, 16; Table 4

Type material.

Holotype: PERU • 1♀; Puno, San Antonio de Putina, Putina; 4000 m a.s.l.; 07.V.2022; O. M. Quispe-Colca col.; MUSA-AR 319.

Table 4.

Kiskalla yeisoni sp. nov., holotype female (MUSA-AR 319). Lengths of palpal and leg segments.

Femur Patella Tibia Metatarsus Tarsus Total
Palp 3.29 2.18 2.24 1.88 9.59
Leg I 4.40 2.63 3.22 1.90 1.54 13.69
Leg II 3.74 2.21 2.50 1.76 1.62 11.83
Leg III 3.15 2.20 2.33 1.54 1.82 11.04
Leg IV 4.38 2.54 2.92 2.60 2.23 14.67

Additional material examined.

PERU • 1♀; same data as for holotype; MUSA-AR 321.

Etymology.

This species is named in honor of Yeison A. Calizaya Melo, a close friend of Oscar M. Quispe-Colca, who regards him as a younger brother.

Diagnosis.

Females of Kiskalla yeisoni sp. nov. differ from congeners by the distribution of short spiniform setae covering most of the surface of maxillae (Fig. 12E), whereas in K. ignacioi sp. nov. and K. zukuapasanka sp. nov., these setae are restricted to the apical half. Kiskalla yeisoni sp. nov. also differs from K. ignacioi sp. nov. by its coloration: carapace, legs, and palps dark-brown; abdomen pale brown, lacking lateral bands (Fig. 12G); and spermathecae consisting of a single dome-shaped receptacle with small granules (Fig. 12F), instead of a sub-quadrate receptacle with large granules. Females of K. yeisoni sp. nov. resemble those of K. zukuapasanka sp. nov. in the general aspect of the spermathecae, but can be easily distinguished by the lower number of labial and maxillary cuspules (Fig. 12E), a shorter fovea (Fig. 12A), and a slightly elevated caput (Fig. 12A).

Figure 12. 

Kiskalla yeisoni sp. nov., AG holotype female (MUSA-AR 319). A Carapace, dorsal view; B sternum, ventral view; C abdomen, dorsal view; D eyes, dorsal view; E labium and maxillae, ventral view; F spermathecae, dorsal view; G habitus; H habitat at type locality in San Antonio de Putina, Puno. Scale bars = 1 mm. Photos: O. Quispe-Colca.

Description – female.

Female holotype (MUSA-AR 319): Total length: 15.78. Carapace (Fig. 12A): length 6.17, width 5.28. Chelicerae with 10–11 teeth on promargin; cheliceral teeth pattern from the basal end: right side: V-V-VvvvVVV-V, left side: V-V-VvvvVVVV-V. Anterior eye row procurved, posterior recurved. Eye sizes and interdistances: AME 0.26, ALE 0.23, PME 0.14, PLE 0.22, AME-AME 0.12, AME-ALE 0.10, PME-PME 0.47, PME-PLE 0.07, ALE-PLE 0.21, AME-PME 0.10, OQ length 0.48, width 0.64. Ocular tubercle oval and slightly elevated (Fig. 12D), length 0.76, width 0.97. Clypeus narrow, length 0.08. Fovea transverse, deep, procurved (Fig. 12A), width 0.88. Labium length 0.82, width 1.43, anterior third with 4 cuspules (Fig. 12E), maxillae right/left with 99/97 cuspules, ventral maxillae widely covered with short spiniform setae (Fig. 12E). Sternum (Fig. 12B): length 3.11, width 2.87, with three pairs of oval sigillae. Abdomen (Fig. 12C): length 9.61, width 7.38. PLS three-segmented, length 2.95, basal segment 1.14, middle segment 0.85, apical segment 0.96, all digitiform. PMS (one segment), length 0.72. Abdomen with type III urticating setae located in a medial dorsal arrowhead-shaped patch (Fig. 12C), length 2.27, width 1.36. Leg pattern: IV>I>II>III (Table 3). — Scopulae: Tarsi I–II fully scopulated with a row of thin setae, tarsi III 2/3 scopulated, tarsi IV 1/3 scopulated located on margins. Metatarsi I 1/3 scopulated, metatarsi II 2/3 scopulated, metatarsi III–IV without scopula. — Spination: Femora I–IV and femora of palps 0. Patellae and patellae of palps 0. Tibiae I 0; II 0; III v 0-0-(1-0) (apical), p 0-(1-0)-0, r 0-(1-0)-0; IV p 0-1-0. Metatarsi I v 0-0-2 (apical); II v (0-1)-0-(3-4) (apical); III v 0-(3-2)-4 (apical), p 0-1-1, r (1-0)-(1-0)-(0-1); IV v 1-(3-2)-(5-3) (4-2 apical), p 0-0-(1-0), r 0-1-(0-1). Tarsi I–IV and tarsi of palps 0. — Spermathecae: a single lowered rectangular receptacle with small granules (Fig. 12F). — Coloration (in life): Carapace dark brown with long pale brown setae along the margins; chelicerae dorsally covered with pale brown setae (Fig. 12G). Legs and palps dark brown with long pale brown setae, especially on femora. Femora of legs and palps with three parallel longitudinal stripes (two dorsal and one retrolateral); patellae I–II and palpal patella with two nearly equal parallel longitudinal stripes, patellae III–IV with two unequal diagonal stripes; tibiae of legs and palps with two parallel longitudinal stripes; one longitudinal stripe reaching about one third of the metatarsi I–II length, and about one third of the metatarsi III–IV length; and one longitudinal stripe on palpal tarsi reaching about one third of the segment (Fig. 12G). Abdomen pale brown with a dark brown band running along the midline, adjacent to a light brown arrowhead-shaped patch of urticating setae (Fig. 12G).

Male.

Unknown.

Natural history and distribution.

Kiskalla yeisoni sp. nov. is known only from Putina locality at Puno department, Peru (Fig. 16), found at elevation of 4000 m a.s.l. The habitat is characterized by a cold and mountainous environment, with a mean annual temperature of –5°C to 17°C. The vegetation comprises mainly scrubs and grasslands near to relict “queñua” forest (Polylepis incarum Bitter and P. triacontandra Bitter) (Fig. 12H), however, there are also nearby crop areas as well as grazing of cattle, sheep and camelids. The entrance to the burrow of the female holotype was found under a rock without any discernible webbing, at a depth between 15 and 20 cm below the ground.

Kiskalla zukuapasanka sp. nov.

Figures 13, 14, 15, 16; Table 5

Type material.

Holotype: PERU • 1♀; Puno, Abra Sallaco; 4000 m a.s.l.; 10.X.2023; N. Ferretti, J. Chaparro and R. West cols.; MUBI 226.

Table 5.

Kiskalla zukuapasanka sp. nov., holotype female (MUBI 226). Lengths of palpal and leg segments.

Femur Patella Tibia Metatarsus Tarsus Total
Palp 4.12 2.16 1.97 1.85 10.11
Leg I 4.92 2.65 3.49 2.14 1.7 14.9
Leg II 4.27 2.66 2.58 1.96 1.68 13.15
Leg III 3.77 2.34 1.82 2.21 1.71 11.85
Leg IV 4.75 2.67 3.16 2.52 1.64 14.74

Additional material examined.

PERU • 3♀♀; Puno, Cuyo Cuyo, Quiscupunco; 4211 m a.s.l.; 25.XI.2019; J. Chaparro and J. Richards cols.; MUBI 103 • 3♀♀; Puno, Sandia, Abra Sallaco; 11.X.2023; N. Ferretti, J. Chaparro and R. West cols.; MUBI 211 • 2♀♀; Puno, Abra Sallaco; 4000 m a.s.l.; 10.X.2023; N. Ferretti, J. Chaparro and R. West cols.; MUBI 226.

Etymology.

The specific name zukuapasanka is derived from the Quechua words zuku, meaning “grey-haired,” and apasanka, a local name for tarantulas. The epithet refers both to the general appearance of the species, characterized by its greyish setae, and to the common name used by local communities for these spiders.

Diagnosis.

Females of Kiskalla zukuapasanka sp. nov. resemble those of K. yeisoni sp. nov. in the general aspect of the spermathecae (Fig. 13H) and those of K. ignacioi sp. nov. in having the ventral maxillae with short spiniform setae restricted to the apical half (Fig. 13F). However, K. zukuapasanka sp. nov. can be easily distinguished from its congeners by the higher number of labial cuspules (8–24 in K. zukuapasanka sp. nov. versus 4–7 in K. ignacioi sp. nov. and K. yeisoni sp. nov.), a broader fovea (Fig. 13A), a highly elevated caput (Fig. 13A, C) and booklung openings bordered by short, stout setae (Fig. 13D).

Figure 13. 

Kiskalla zukuapasanka sp. nov., holotype female (MUBI 226). A Carapace, dorsal view; B abdomen, dorsal view; C carapace, lateral view; D abdomen, ventral view, green square shows detail of the stout setae around the booklung opening (green arrows indicate the setae); E sternum, ventral view; F labium and maxillae, ventral view; G eyes, dorsal view; H spermathecae, dorsal view. Scale bars = 1 mm. Photos: N. Ferretti.

Description – female.

Female holotype (MUBI 226): Total length: 10.49. Carapace (Fig. 13A, C): length 5.74, width 5.42. Chelicerae with 10 teeth on promargin and 14 small denticles; cheliceral teeth pattern from the basal end: right side: VvvV-VVVVVV, left side: V-VVvvvVVV-V. Anterior eye row procurved, posterior recurved (Fig. 13G). Eye sizes and interdistances: AME 0.18, ALE 0.19, PME 0.18, PLE 0.27, AME-AME 0.15, AME-ALE 0.14, PME-PME 0.5, PME-PLE 0.11, ALE-PLE 0.17, AME-PME 0.95. Ocular tubercle oval and slightly elevated (Fig. 13G), length 1.05, width 1.32. Clypeus wide, length 0.58. Fovea transverse, wide, deep, procurved and displaced to proximal carapace making cephalic region highly elevated (Fig. 13A, C), width 2.19. Labium length 0.91, width 1.56, anterior third with 20 cuspules (Fig. 13F), maxillae right/left with 168/170 cuspules on basal proximal margin, ventral maxillae covered with short spiniform setae on apical half (Fig. 13F). Sternum (Fig. 13E): length 3.52, width 3.22, with three pairs of sigillae, first and second pairs circular, third pair oval. Abdomen (Fig. 13B, D): length 4.75, width 3.8. PLS three-segmented, length 2.42, basal segment 0.76, middle segment 0.74, apical segment 0.92, all digitiform. PMS (one segment), length 0.77. Abdomen with type III urticating setae located in a medial dorsal arrowhead-shaped patch (Fig. 13B), length 1.44, width 1.07. Leg pattern: IV>I>II>III (Table 4). — Scopulae: Tarsi I–IV fully scopulated, tarsi I with scopulae divided by a row of about 5 long setae, tarsi II with scopulae divided by a row of about 5/6 long setae, tarsi III–IV with scopulae divided by a row of about 9 long setae. Metatarsi I 1/2 scopulated divided by a row of about 3 long setae, metatarsi II 1/3 scopulated divided by a row of about 3 long setae, metatarsi III 1/4 scopulated, divided by a row of about 6 long setae, metatarsi IV without scopula. — Spination: Femora I d 1-0-0; II–IV 0, palp 0. Patellae of legs and patellae of palps 0. Tibiae I v 1-0-0; II 0; III p 0-0-1; IV v 1-0-1, r 0-0-1. Metatarsi I v 0-0-2; II v 0-2-0 (4 apical); III v 0-1-1-0 (5 apical); IV v 1-2-1 (4 apical), r 0-0-1. Tarsi I–IV and tarsi of palps 0. — Spermathecae: a single lowered rectangular and wide receptacle with large granules (Fig. 13H). — Coloration (in life): Carapace dark brown with long light brown setae along the margins; chelicerae dorsally covered with grey setae (Fig. 14). Legs and palps dark brown with short pale brown setae (Fig. 14). Femora of legs and palps with two nearly equal parallel longitudinal stripes; patellae I–IV with two unequal diagonal stripes; tibiae of legs and palps with two parallel longitudinal stripes (Fig. 14). Abdomen dark greyish brown, with a black longitudinal band extending along midline, adjacent to a grey arrowhead-shaped patch of urticating setae, and with three short lateral bands that do not extent to the margins (Fig. 14).

Figure 14. 

Kiskalla zukuapasanka sp. nov., holotype female (MUBI 226), habitus. A, B Lateral views; C frontal view; D dorsolateral view. Scale bars = 1 cm. Photos: J.C. Chaparro.

Male.

Unknown.

Natural history and distribution.

Kiskalla zukuapasanka sp. nov. is known only from Abra Sallaco and Cuyo Cuyo localities at Puno department, Peru (Fig. 16), found at elevations of 4000–4220 m a.s.l. The habitat is damp and mountainous featuring steep valleys with rocky talus slopes (Fig. 15A) with seasonal temperatures ranging from a low of –4°C to a high of 17°C. Vegetation is sparse and consists of patches of mosses and low grasses. Females and subadults were found in ground retreats under large angular rocks laying on the ground surface. These retreats lacked any discernible webbing at the entrance and appeared to be self-excavated. The retreats under the rock ranged in length from 20 to 40 cm with the end angling deeper into the ground (Fig. 15B).

Figure 15. 

Kiskalla zukuapasanka sp. nov., holotype female (MUBI 226). A Habitat at type locality in Abra Sallaco, Puno; B burrow under a stone from an adult female at type locality; C holotype female in natural environment, habitus. Scale bar = 1 cm. Photos: R.C. West.

Figure 16. 

Distribution map of the known species of Kiskalla gen. nov.

4. Discussion

The Peruvian Andes are widely recognized as a key biogeographic region shaping the independent evolutionary trajectories of populations, largely due to their role as a major geographic barrier along western South America (Hazzi et al. 2018; Alencar et al. 2024; Salazar et al. 2025). The remarkable biodiversity of this region reflects, in part, its extreme topographic complexity, which spans from sea level to above 6000 m a.s.l. and encompasses a correspondingly broad spectrum of climatic niches (Rahbek et al. 2019). Although the family Theraphosidae is the largest and most studied group of mygalomorph spiders, comprising nearly a thousand species (World Spider Catalog 2026), Peru has long attracted the attention of arachnologists because of the exceptional diversity of this family within Andean environments. In recent years, numerous new species and even new genera of Theraphosidae have been described, several of which are endemic to Peru (Kaderka et al. 2023).

This “hidden” diversity result from two main factors: (i) the scarcity of taxonomic specialists working on Theraphosidae in the Andes, and (ii) the lack of intensive sampling and long term fieldwork, which has limited representation of taxa in scientific collections. Peru illustrates both conditions. However, recent years have seen growing taxonomic interest combined with systematics fieldwork, substantially increasing the availability of specimens deposited in scientific collections, which has allowed for an increase in the description of new species in recent years.

Our study contributes to filling this gap by combining the examination of existing museum material with new field collections aimed at documenting the diversity of high-Andean tarantulas. During 2022–2023, we discovered several intriguing dwarf theraphosids that superficially resembled small Hapalotremus. A detailed morphological analysis of these specimens, coupled with a molecular phylogenetics, confirmed the distinctiveness of this lineage and justified the recognition of a new genus.

Kiskalla gen. nov. shares with Hapalotremus certain reproductive traits, such as the general shape of the male palpal bulb and the presence of a single spermathecal receptacle in females. Nevertheless, it differs consistently in several respects. The distinctive coloration pattern, particulary the arrowhead-shaped dorsal patch of urticating setae has not been reported in Hapalotremus. Moreover, while both genera share a globose tegulum and retrolaterally curved embolus, the subapical keel is highly developed and serrated, whereas the prolateral superior keel is vestigial. Similarly, females possess a single spermathecal receptacle, but in Kiskalla gen. nov. this structure is quadrate or subquadrate and consistently lacks the apical and lateral projections characteristics of Hapalotremus.

In addition, Kiskalla gen. nov. exhibits traits not observed in other closely related genera: numerous spines on all legs (specially in males), an apical crown of robust spines on the apical metatarsi, short stout setae encircling the trichobothria on the dorsal metatarsi and a weakly-developed scopulae on tarsi IV restricted to the margins. Other features, such as the reduced number of labial cuspules and the pattern of spiniform setae on the ventral maxillae, are reminiscent of other high-Andean genera (e.g. Antikuna Kaderka et al., 2021, Bistriopelma Kaderka, 2015, and Chinchaysuyu Ferretti et al., 2023).

Although the preliminary molecular phylogeny presented here is limited to just one marker (COI), we recovered some representatives of Hapalopini grouped sister to one genus of Grammostolini, as was reported by Kaderka et al. (2023). Arguably, this result will change in future analyses of broader taxonomic sample because we only included the genus Bistriopelma as representative of Grammostolini and some Hapalopini genera that were not included here. The basal placement of Antikuna within Hapalopini, as observed in our analysis, agrees with both the molecular evidence of Kaderka et al. (2023) and the morphological cladistic study of Hapalotremus by Ferretti et al. (2025). Kiskalla gen. nov. represents a distinct high-Andean lineage within Hapalopini, occurring around 4,000 m a.s.l., alongside other high-altitude genera such as Antikuna, Hapalotremus, and Urupelma. Its phylogenetic position as sister to Hapalotremus suggests a close evolutionary relationship, possibly derived from a common ancestor that colonized montane habitats and subsequently diversified across different high-Andean ecological niches. To clarify the evolutionary dynamics of high-Andean tarantulas, including colonization events and potential downslope migration into lower elevations, broader sampling of montane Hapalopini taxa and additional genetic markers will be essential.

5. Acknowledgements

We are grateful to Yeison Andru Calizaya Melo for his help on field trips. To Lizbeth G. Quispe-Colca, who helped us to prepare the distribution maps. To Diana Silva Dávila and Luis Ramírez Montano from the Museo de Historia Natural, Lima, Peru, for their support and facilitating the use of equipment at the MUSM. Juan Carlos Chaparro is thanked for supplying transportation during that fieldtrip and accommodation in Cusco. Josh Richards is thanked for collecting and donating some of the specimens to MUBI used in this study. Thanks to Aarón J. Quiróz for his valuable help during the collection of some specimens, and to Josh Richards for collecting some specimens. Nelson Ferretti thanks Agencia I+D+i for funding through the projects PICT 2018-1751 and PICT 2021-0407, the Secretaría de Ciencia y Técnica, Universidad Nacional del Sur for the grant PGI 24/ZB00, and Rick West for his private funding supporting the fieldwork. This work was possible through collecting permits R.D.G. N° D000636-2021-MIDAGRI-SERFOR-DGGSPFFS, R.D.G. N° D000425-2021-MIDAGRI-SERFOR-DGGSPFFS and DGGSPFFS, RD-000123-2022-MIDAGRI-SERFOR-DGGSPFFS-DGSPFS.

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Quispe-Colca and Ferretti contributed equally to this work and are to be regarded as co-first authors.
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