Journal of Threatened Taxa | www.threatenedtaxa.org | 26
April 2026 | 18(4): 28719–28723
ISSN
0974-7907 (Online) | ISSN 0974-7893 (Print)
https://doi.org/10.11609/jott.10190.18.4.28719-28723
#10190 |
Received 01 October 2025 | Final received 09 February 2026| Finally accepted 09
March 2026
First record of leucism in Rock Hyrax Procavia
capensis from Ibex Reserve Protected Area, Saudi
Arabia
Zaffar R. Mir 1, Naif Alajmi 2, Ali Alahmari 3, Ahmad Alobaid
4, Khalid Almaliki 5,
Farah Niaz 6, Naif Alqahtani 7 &
Ahmed Boug 8
1–8 National Centre for Wildlife,
P.O. Box 4508, Makkah Mukarramah Road, Riyadh 12411,
Saudi Arabia.
1 zaffarmir@ncw.gov.sa
(corresponding author), 2 n.m.alajmi@ncw.gov.sa, 3 a.alahmari@ncw.gov.sa,
4 a.alobaid@ncw.gov.sa,
5 k.almalki@ncw.gov.sa, 6 farah@ncw.gov.sa, 7
n.a.alqahtani@ncw.gov.sa, 8 boug@ncw.gov.sa
Editor: Bhargavi Srinivasulu, Zoo Outreach Organisation,
Hyderabad, Telangana, India. Date of publication: 26 April 2026 (online & print)
Citation: Mir, Z.R., N. Alajmi,
A. Alahmari, A. Alobaid, K.
Almaliki, F. Niaz, N. Alqahtani
& A. Boug (2026).
First record of leucism in Rock Hyrax Procavia capensis
from Ibex Reserve Protected Area, Saudi Arabia. Journal of Threatened Taxa 18(4): 28719–28723. https://doi.org/10.11609/jott.10190.18.4.28719-28723
Copyright: ©
Mir et al. 2026. Creative Commons Attribution 4.0 International License.
JoTT allows unrestricted use, reproduction, and
distribution of this article in any medium by providing adequate credit to the
author(s) and the source of publication.
Funding: None.
Competing interests: The authors declare no competing interests.
Acknowledgements: We are highly grateful to the management and the staff of Ibex Reserve Protected Area for their contribution.
Abstract: Pigment anomalies such as leucism and albinism are rare in wild mammals, often linked
to genetic or developmental factors and sometimes carry ecological
consequences. Here, we report the first record of leucism
in the Rock Hyrax Procavia capensis from Saudi Arabia. The observation was made
during routine monitoring in the Ibex Reserve Protected Area on 17 May 2025. The
individual, an adult with pale pelage and normal dark eyes, was classified as leucistic. Given the healthy and non-fragmented hyrax
population in the reserve, this case is likely an isolated anomaly rather than
evidence of inbreeding or population-level genetic issues. This record extends
the taxonomic and geographic range of leucism to P.
capensis in central Saudi Arabia and
underscores the importance of continued monitoring and systematic documentation
of aberrant colour morphs in wildlife.
Keywords: Genetic variation, Hyracoidea,
Mammalia, phenotypic anomaly, pigmentation anomaly, Procaviidae,
wildlife monitoring.
Pigmentation
anomalies such as leucism and albinism are rare but
have been recorded in many vertebrate groups. These conditions, often
collectively referred to as hypopigmentation, arise from a reduction in pigment
production and can manifest as albinism, leucism, or piebaldism in birds and mammals (Abreu et al. 2013; Van Grouw 2013). Leucism is characterised by partial or complete loss of integumentary
pigment while typically retaining normal eye colour,
in contrast to albinism, which also involves a loss or reduction of ocular
pigmentation (Van Grouw 2013). Recording such
observations improves understanding of their frequency, causes and possible
conservation implications. The extreme rarity of leucistic
morph in the animal kingdom could be linked with their odds of getting selected
in nature, as these individuals may suffer from reduced foraging opportunities
and communication, increased threats, affected organ development as well as
physiological disadvantages, which are often poorly understood (Caro 2005; Fan
et al. 2023). Hence, it is imperative to document the presence of such colour anomalies in different taxa and determine the causal
factors, in addition to their distribution and survival probability.
In most
animals, colouration plays a crucial role in
camouflage, predator avoidance, and enhancing foraging efficiency (Ruxton et
al. 2004; Stevens & Cuthill 2006). However,
individuals exhibiting leucism or albinism may face
survival disadvantages, as their conspicuous appearance makes them more easily
detected by both predators and prey (Camargo et al. 2014). This heightened
visibility can reduce survival prospects and, in some cases, disrupt normal
social interactions (Barreto et al. 2023). Despite being relatively rare,
pigment anomalies have been documented across a wide range of mammalian orders,
including Carnivora (Talamoni et al. 2017; Descalzo et al. 2021; Chaudhuri
et al. 2024), Chiroptera (Rocha et al. 2013; Romano
et al. 2015), Primates (Aximoff
et al. 2020; Barros-Diaz et al. 2022), and Rodentia (Camargo et al. 2014; Samson
et al. 2017; Beninato et al. 2020). Comparable cases
have also been observed in avifauna, with Islam et al. (2015) reporting leucism in the Houbara Bustard Chlamydotis
macqueenii from Saudi Arabia. Notably, leucism has not previously been recorded in any member of
the order Hyracoidea.
Study
area
The Ibex
Reserve Protected Area, located within the Tuwaiq
Escarpment landscape in Riyadh, Saudi Arabia, covers an area of 1,842 km² (Cunningham
& Wronski 2009) (Image 1). The reserve is
characterized by undulating limestone plateaus interspersed with canyon wadis (Wronski et al. 2012). Vegetation is sparse and during
summer (May to October), temperatures average around 40 oC
(Wronski et al. 2012). Rainfall is sporadic, peaking
in winter with an annual average of around 60 mm (Wronski
et al. 2012). In terms of its mammal diversity, the protected area has been the
focus of a key conservation and reintroduction program of the vulnerable Nubian
Ibex Capra nubiana. The area is also inhabited
by important populations of the Arabian Wolf Canis
lupus, and Arabian Gazelle Gazella
arabica in addition to other mammal species. The protected area also
supports a healthy population of Rock Hyrax Procavia
capensis.
Observation
and Discussion
In Saudi
Arabia order Hyracoidea is only represented by Rock
Hyrax which is distributed along the western mountains extending from the Gulf
of Aqaba down southward reaching the Yemen border. It is also associated with
the rocky terrain of Tuwaiq mountains in central
Saudi Arabia. The distribution of the Rock Hyrax is limited by the presence of
rocky terrain with steep mountains. The Rock Hyrax is a robust,
rabbit-like mammal with short ears and a short tail, weighing around 4
kg. Typically, it has thick, grey-brown fur that varies in shade depending
on the environment. The species is assessed as ‘Least Concern’ by the IUCN Red
List (Butynski et al. 2015), but it is listed as Near
Threatened in the National Red List of Saudi Arabia.
Here, we
present the first record of a leucistic Rock Hyrax,
from a central Saudi Arabian protected area. During routine trail monitoring on
17 May 2025 at Ibex Reserve Protected Area (approximate coordinates: 23.492° N,
46.348° E), we detected an unusually pale Rock Hyrax individual. The animal, an
adult Procavia capensis,
was observed on a rocky outcrop at 1700 h. It was readily identified as leucistic by its partially white pelage and normal dark
eyes (Image 2). The individual’s unique pattern of pale fur provided a natural
visual marker, allowing us to reliably distinguish this hyrax from conspecifics
during subsequent monitoring and to avoid duplicate observations. The Ibex
Reserve is known for its rugged Tuwaiq escarpment
habitat, which is ideal for the Rock Hyrax. The hyrax population in this
reserve is good, reflecting effective protection.
The retained
dark eye colour in the observed rock hyrax, combined
with its pale/white pelage, supports classification as leucism
rather than albinism. Leucism in wild mammals is
uncommon and has been linked to a range of causes, including genetic factors
such as recessive alleles, genetic drift in small or isolated populations, and
occasional developmental anomalies (Caro & Mallarino
2020). Ecological effects, such as increased detectability to predators, have
been noted for some species. However, leucistic
individuals are capable of reaching adulthood and reproducing successfully, and
isolated observations do not necessarily indicate underlying population-level
genetic issues.
In the
present case, the Ibex Reserve supports a healthy and non-fragmented Rock Hyrax
population, making it unlikely that this single observation reflects inbreeding
or other genetic bottlenecks. Instead, it is best regarded as a rare,
individual anomaly. Continued monitoring and the systematic archiving of
photographic vouchers will be valuable for documenting any future occurrences
and understanding possible patterns.
Comparable
records of leucism and other pigment anomalies in
wildlife have been reported from diverse regions and taxa. For example, Barreto
et al. (2023) described the first known case of leucism
in a Brazilian rodent Kerodon rupestris, Chaudhuri et al. (2024) reported a leucistic Sloth Bear Melursus
ursinus in India, and Al-Sheikhly
et al. (2018) documented aberrant white plumage in the endangered Basra Reed
Warbler Acrocephalus griseldis.
Each of these studies stresses that although pigment anomalies are rare, their
documentation is important for understanding both proximate causes and broader
ecological implications. Similarly, Abreu et al. (2013) and Barreto et al.
(2023) highlight that recording such events contributes to knowledge of
environmental contexts in which they arise. Our report extends the taxonomic
and geographic record of leucism to P. capensis in Saudi Arabia.
While some
studies note higher leucism frequency in small or
isolated populations due to reduced genetic diversity, the current observation
confirms that such individuals can survive to adulthood without obvious growth
limitations. The hyrax in question appeared fully mature and in good condition,
indicating no apparent developmental disadvantage in this case. Interestingly,
Ortiz-Hoyos et al. (2020) suggest that in diurnal
species, leucistic and albino individuals may
experience reduced predation risk compared to nocturnal species, as the latter
are more visible in low-light environments. This may help explain how visibly
distinctive individuals like this hyrax can persist in the wild.
FOR
IMAGES – CLICK HERE FOR FULL PDF
References
Abreu, M.S.L., R. Machado, F. Barbieri, N.S. Freitas & L.R. Oliveira
(2013). Anomalous colour in Neotropical mammals: a
review with new records for Didelphis sp. (Didelphidae,
Didelphimorphia) and Arctocephalus
australis (Otariidae,
Carnivora). Brazilian Journal of Biology 73: 185–194. https://doi.org/10.1590/S1519-69842013000100020
Aximoff, I., M.T. Zaluar, A. Pissinatti, P.A.
Bastos, T. de A. Morais, C.A. da Rosa, L.C. Oliveira,
D.S. Teixeira & M.M. Vale (2020). Anomalous
pigmentation in invasive and native marmosets, Callithrix jacchus, Callithrix penicillata
(Primates, Callitrichidae), and their hybrids in Brazil. Folia Primatologica 91(2): 149–158. https://doi.org/10.1159/000501186
Barreto, H.F., Y. R. Meneses, A.B. Galina, S.F. Ferrari & R. Beltrão-Mendes (2023). Leucism in rodents: the first record for the mocó (Kerodon rupestris
Wied-Neuwied, 1820), a rodent endemic to
Brazil. Notas sobre Mamíferos Sudamericanos 5(1): 2–12. https://doi.org/10.31687/SaremNMS23.6.3
Barros-Diaz, C., S. Vela, A. Gallo-Pérez, M.
Chiquito, X. Cornejo, D. Mosquera-Muñoz
& J. Perez-Correa (2022). Hypopigmentation
in mantled howler monkeys Alouatta palliata (gray 1849): First documented cases of whole-body leucism in South America. Ecology and Evolution
12(12): e9628. https://doi.org/10.1002/ece3.9628
Beninato, V. A., G.A. Rivero-Castro, M.A. Pérez, C.E.
Borghi & S.M. Giannoni (2020). First
records of leucism in small rodents for Argentina. Therya Notes 1: 62–66. https://doi.org/10.12933/therya_notes-20-15
Butynski, T., H. Hoeck, L. Koren & Y.A. de
Jong (2015). Procavia capensis. The
IUCN Red List of Threatened Species 2015: e.T41766A21285876. https://doi.org/10.2305/IUCN.UK.2015-2.RLTS.T41766A21285876.en. Accessed
on 13.i.2026.
Camargo, I., E. Rios, C. Cornejo-Latorre &
S.T. Álvarez-Castañeda (2014). First record
of leucism in the genus Peromyscus
(Mammalia: Rodentia). Western North American Naturalist 74: 366–368.
https://doi.org/10.3398/064.074.0301
Caro, T. & R. Mallarino (2020). Coloration in Mammals. Trends in
Ecology & Evolution 35: 357–366. https://doi.org/10.1016/j.tree.2019.12.008
Chaudhuri S, S. Dutta & K. Ramesh (2024). First record
of leucistic Sloth Bear Melursus
ursinus Shaw, 1791 (Mammalia: Carnivora: Ursidae) in Panna Tiger Reserve, India. Journal of
Threatened Taxa 16(9): 25882–25887. https://doi.org/10.11609/jott.9349.16.9.25882-25887
Cunningham P.L. & T. Wronski (2009). Blanford’s fox confirmed in the At-Tubaiq
Protected Area (northern Saudi Arabia) and the Ibex Reserve (central Saudi
Arabia). Canid News 12(4): 1–7.
Descalzo, E., F.N. Muñóz, M.M. Huete, J.F. Sánchez,
J.C. Urones, J. Jiménez, M.D. Mateos,
F.D. Ruiz & P. Ferreras (2021). First
records of anomalous colouration in the Egyptian
mongoose (Herpestes ichneumon). Galemys 33: 57–60. https://doi.org/10.7325/Galemys.2021.N6
Fan, W., Y. He, J. Su, Y. Feng, T. Zhuo, J.
Wang, X. Jiao, Y. Luo, J. Wu & Yi Geng (2023). Effects of leucism on organ development and molecular mechanisms in
Northern snakehead (Channa argus) beyond pigmentation alterations. Scientific
Reports 13: 19689. https://doi.org/10.1038/s41598-023-46608-9
Islam, M.Z., A. Boug & H.V. van Grouw (2015). A white Houbara Bustard Chlamydotis macqueenii
(Jacquin, 1784) in Saudi Arabia. Sandgrouse
37(1): 90–93.
Ortiz-Hoyos, R.D., Á.M. Mejía-G., D.C. Stasiukynas,
B.J. Lizarazo & E. Payá
n-Garrido (2020). Primer registro de leucismo en Didelphis marsupialis Linnaeus, 1758 (Didelphimorphia: Didelphidae) en Colombia. Galemys
32: 1–5. https://doi.org/10.7325/Galemys.2020.N2
Rocha, P.A., J.A. Feijó, C.R. Donato & S.F.
Ferrari (2013). Leucism in Seba’s
short-tailed bat, Carollia perspicillata (Linnaeus, 1758), from a rock shelter in
northeastern Brazil. Chiroptera Neotropical 19(1): 1151–1153.
Romano, M.C., M.E. Montani, M.C. Cordini & S. Auil
(2015). First record of albinism in Tadarida
brasiliensis (Chiroptera:
Molossidae) in South America and new records of leucism in central Argentina. Chiroptera
Neotropical 21(1): 1312–1319.
Ruxton, G.D., T.N. Sherratt & M.P. Speed
(2004). Avoiding Attack: The Evolutionary Ecology of Crypsis,
Warning Signals and Mimicry, 1st
Edition. (Oxford 2004; online ed., Oxford Academic,
1.ix.2007). https://doi.org/10.1093/acprof:oso/9780198528609.001.0001. Accessed
on 12.i.2026.
Samson, A., B. Ramakrishnan & S. Bargavi
(2017). Leucism in the three-striped palm squirrel (Funambulus palmarum)
at Gudalur Forest Division, Tamil Nadu, Southern
India. Therya 8: 261–262. https://doi.org/10.12933/therya-17-503
Sheikhly, O.F.A.,
M.K. Haba, N.A. Fazaa &
R.H. Al-Asady (2018). First record
of colour aberration in Basra Reed Warbler Acrocephalus griseldis
(Hartlaub, 1891) (Passeriformes: Acrocephalidae)
from the Central Marshes of southern Iraq. Journal of Threatened Taxa
10(13): 12800–12804. https://doi.org/10.11609/jott.4353.10.13.12800-12804
Stevens, M. & I.C. Cuthill (2006). Disruptive
coloration, crypsis and edge detection in early
visual processing. Proceedings of the Royal Society, Series B 273(1598):
2141–2147. https://doi.org/10.1098/rspb.2006.3556
Talamoni, S., P.I.M.
Viana, C.G. Costa, L. Palú, R.B. Oliveira & L.M. Pessôa (2017). Occurrence
of leucism in Eira
barbara (Carnivora, Mustelidae) in Brazil. Biota Neotropica
17: e20170328. https://doi.org/10.1590/1676-0611-BN-2017-0328
van Grouw, H. (2013). What colour is that bird? The cause and recognition of common colour aberrations in birds. British Birds 106:
17–29.
Wronski, T., K. Alageel, M. Plath & M.A. Sandouka (2012). Twenty years of monitoring a
re-introduced population of Mountain Gazelles, Gazella
gazella (Pallas, 1776), in the Ibex Reserve,
Saudi Arabia. Zoology in the Middle East 55: 3–18. https://doi.org/10.1080/09397140.2012.10648912