Population genomics of yellow-eyed penguins uncovers subspecies divergence and candidate genes linked to respiratory distress syndrome
nature ecology & evolution
Article
https://doi.org/10.1038/s41559-026-03062-w
Population genomics of yellow-eyed
penguins uncovers subspecies divergence
and candidate genes linked to respiratory
distress syndrome
Received: 19 October 2025
A list of authors and their affiliations appears at the end of the paper
Accepted: 27 March 2026
Published online: xx xx xxxx
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Yellow-eyed penguins (hoiho/takaraka, Megadyptes antipodes) are among
the world’s rarest penguins and considered taonga (treasured) species in
Aotearoa New Zealand. Since 2019, chicks on the New Zealand mainland have
been affected by a deadly neonatal disease, respiratory distress syndrome,
contributing to a decline to fewer than 115 breeding pairs. To investigate
the putative genetic basis of this disease, we generated high-quality
whole-genome data from 249 individuals spanning the species range,
including New Zealand mainland (Northern range) and sub-Antarctic
Enderby (Auckland Islands) and Campbell Islands (Southern range).
Population genomic analyses unexpectedly revealed three deeply
divergent lineages with negligible gene flow, which is consistent with
recognition of three distinct subspecies. Phylogenetic divergence dating
suggests that these splits predate human arrival by several millennia,
with the Northern lineage diverging from the Southern populations
5–16 thousand years. Genome scans for local adaptation revealed regions
of strong differentiation, while genome-wide association analyses
identified candidate immune and respiratory genes linked to respiratory
distress syndrome. In partnership with Ngāi Tahu, who hold Indigenous
guardianship over yellow-eyed penguins, we recommend recognition
of three subspecies, urgent conservation action for the critically small
and rapidly declining Northern subspecies and the need for immediate
population size and trend assessments for the Auckland and Campbell
Island populations.
Yellow-eyed penguins (Megadyptes antipodes) are an endangered species endemic to Aotearoa New Zealand1. They are regarded as taonga
(treasured) by Māori, the Indigenous peoples of New Zealand, who
named them hoiho or takaraka. As one of the rarest penguin species
in the world, yellow-eyed penguins serve as an important indicator of
ecosystem health, with their population trajectories reflecting broader
ecosystem change1–3. Therefore, protecting yellow-eyed penguins is
critical for biodiversity conservation and maintaining the integrity
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of coastal ecosystems. They are also an icon of the regional wildlife
tourism industry, substantially contributing to the local economy4.
Therefore, their decline represents a biodiversity crisis and a cultural
and economic loss.
Yellow-eyed penguins have been delineated into two management
groups: the Northern population found on the New Zealand mainland
(throughout Te Waipounamu/South Island and Rakiura/Stewart Island)
and the Southern population distributed across the Maukahuka/Motu
Article
Maha/Auckland Islands, including Enderby Island, and Motu Ihupuku/
Campbell Island (Fig. 1a). The Department of Conservation estimates
that fewer than 3,000 individuals remain, with approximately 115
breeding pairs remaining within the Northern distribution, and fewer
than 20% of Northern chicks surviving to adulthood5. As the sole surviving species of the Megadyptes genus, the yellow-eyed penguin is not
only endangered6,7, but also at risk of extinction within its Northern
range within the next two decades because of threats of habitat loss,
dietary change8–11, disease12–18, bycatch19–21 and climate change22,23.
Since 2019, a deadly neonatal respiratory disease known as respiratory distress syndrome (RDS) has presented an additional threat
to the persistence of the Northern population. RDS results in severe
breathing difficulties, with necropsies revealing lung congestion and
haemorrhage along with lymphoid depletion24. The causative agent is
probably a non-enveloped DNA virus in the Anelloviridae family known
as yellow-eyed penguin gyrovirus (YPGV)24. In contrast, although YPGV
is endemic across all regions, the Southern population shows no clinical signs consistent with RDS, and YPGV can be detected in apparently
healthy individuals, including both adults and chicks, throughout
the species range. Whether the Northern population is genetically
more susceptible to developing RDS, or the differences in disease
presentation are due to other causes (such as environmental variables
or differences in viral lineages), remains an open question requiring
species-wide genomic studies.
Previous genetic studies have suggested that yellow-eyed penguins migrated to their Northern range approximately 500 years
ago, after the extinction of the closely related Megadyptes antipodes
waitaha, coincident with human arrival on the mainland25–28. In this
recent-immigrant model, the mainland population is viewed as having established via a peripheral northward range expansion of the
species and is potentially maladapted to warmer conditions. Under
this hypothesis, conservation strategies for the Northern population could involve replacement, translocation or genetic rescue from
Southern populations, noting that at the present time, no such strategies have been proposed29. Yet, before such interventions can be
realistically considered, the genetic basis of the populations’ apparent differential susceptibility to developing RDS must be resolved
because this remains a key knowledge gap that could directly inform
conservation decision-making.
In this study, deep sequencing of 249 yellow-eyed penguin
genomes further resolved the species demographic history and allowed
us to investigate the genetic basis of susceptibility to developing RDS.
We combined phylogenetic molecular dating, genome-wide association studies30, selective sweep scans31 and ancestral recombination graph (ARG) inference32,33 to capture both long-term and recent
evolutionary dynamics. Among these, ARGs were particularly suited to
our aims because they enabled the estimation of the time to the most
recent common ancestor both within and between populations. This
fine-scale approach offers substantially greater resolution of divergence, migration and adaptation over the last few dozen generations
than traditional population genetic methods34,35.
Through this framework, we revealed the presence of three genetically distinct populations of yellow-eyed penguins. These lineages
are characterized by deep divergence, minimal genomic evidence of
ongoing migration and signatures of local adaptation. The scale of
genomic differentiation strongly supports their recognition as three
genomically and geographically distinct subspecies, with the split
between the Northern and Southern populations occurring much
earlier than previously considered25. We identified genetic variants that
underlie differential responses to infection with YPGV, highlighting
the role of host genetics (...truncated)