Research Article |
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Corresponding author: Oscar M. Quispe-Colca ( oscarqc07@gmail.com ) Academic editor: Lorenzo Prendini
© 2026 Oscar M. Quispe-Colca, Nelson E. Ferretti, Juan C. Chaparro, José A. Ochoa, Rick C. West.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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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.
Andes, Araneae, Kiskalla, Puno, South America, southern Peru, Taxonomy
Peru is recognized as a megadiverse country, harboring an exceptional number of endemic animal and plant species, likely driven by its complex topography (
The family Theraphosidae Thorell, 1869 represents the most species-rich group of mygalomorph spiders, currently comprising 1,193 species in 187 genera (
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.
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.
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 (
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
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
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 | OR178610 | ||
| Antikuna majuski | OR178637 | ||
| Thrixopelma ockerti | OR178629 | ||
| Bistriopelma matuskai | OR178612 | ||
| Bistriopelma sp. | OR178614 | ||
| Urupelma sanctimariae | OR178633 | ||
| Urupelma machiguenga | OR178631 | ||
| Urupelma johannae | OR178627 | ||
| Urupelma awanqay | OR178630 | ||
| Cyriocosmus itayensis | OR178619 | ||
| Cyriocosmus peruvianus | OR178621 | ||
| Cyriocosmus aueri | OR178616 | ||
| Cyriocosmus elegans | OR178618 | ||
| Cyriocosmus leetzi | OR178620 | ||
| Cyriocosmus bicolor | OR178617 |
Sequence alignments of the COI fragments were generated with MAFFT v7.017 (
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.
The phylogenetic analyses recovered the tribes Grammostolini and Hapalopini as monophyletic, both with high support values (Fig.
Order Araneae Clerck, 1757
Infraorder Mygalomorphae Pocock, 1892
Family Theraphosidae Thorell, 1869
Subfamily Theraphosinae Thorell, 1869
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.
Kiskalla ignacioi sp. nov.
The new genus differs from all remaining Theraphosinae genera by the following combination of characters: the presence of lateral abdominal stripes (Figs
Kiskalla ignacioi sp. nov., A–D holotype male (
Kiskalla ignacioi sp. nov., holotype male (
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.
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.
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.
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 (
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.
Kiskalla ignacioi sp. nov., K. yeisoni sp. nov. and K. zukuapasanka sp. nov.
Holotype: PERU • 1♂; Puno, Carabaya, Corani; 4360 m a.s.l.; 19.IV.2022; Y. A. Calizaya Melo col.;
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.
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.
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
Male holotype (
males. The paratype male from a locality near that to the holotype presents eight labial cuspules and a more rounded sternum (Fig.
Female paratype (
Kiskalla ignacioi sp. nov., holotype male (
| 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 |
Kiskalla ignacioi sp. nov., paratype female (
| 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 |
One of the paratype female (Fig.
Kiskalla ignacioi sp. nov. is known from Corani locality at Puno department, Peru (Fig.
Holotype: PERU • 1♀; Puno, San Antonio de Putina, Putina; 4000 m a.s.l.; 07.V.2022; O. M. Quispe-Colca col.;
Kiskalla yeisoni sp. nov., holotype female (
| 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 |
PERU • 1♀; same data as for holotype;
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.
Females of Kiskalla yeisoni sp. nov. differ from congeners by the distribution of short spiniform setae covering most of the surface of maxillae (Fig.
Kiskalla yeisoni sp. nov., A–G holotype female (
Female holotype (
Unknown.
Kiskalla yeisoni sp. nov. is known only from Putina locality at Puno department, Peru (Fig.
Holotype: PERU • 1♀; Puno, Abra Sallaco; 4000 m a.s.l.; 10.X.2023; N. Ferretti, J. Chaparro and R. West cols.; MUBI 226.
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 |
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.
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.
Females of Kiskalla zukuapasanka sp. nov. resemble those of K. yeisoni sp. nov. in the general aspect of the spermathecae (Fig.
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.
Female holotype (MUBI 226): Total length: 10.49. Carapace (Fig.
Unknown.
Kiskalla zukuapasanka sp. nov. is known only from Abra Sallaco and Cuyo Cuyo localities at Puno department, Peru (Fig.
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 (
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
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.