logo
Our Changing World: Dissecting the world's rarest whale

Our Changing World: Dissecting the world's rarest whale

RNZ News21-05-2025

It's only the seventh time a spade-toothed whale has been documented worldwide, and the first time a complete specimen has been recovered in good condition for examination.
Photo:
RNZ / Tess Brunton
Follow Our Changing World on
Apple
,
Spotify
,
iHeartRadio
or wherever you listen to your podcasts
The spade-toothed whale: deep diving, rare, and largely unknown to science - until now.
The elusive species, part of the beaked whale family, grabbed worldwide headlines in 2024: first when it washed ashore 30 minutes
south of Dunedin
in July, then again five months later when it was
dissected
.
In December 2024, Our Changing World joined the research team during their week-long scientific dissection efforts to find out what secrets the whale holds.
Beaked whales are some of the most elusive marine mammals on the planet because they are so incredibly well adapted to their long-deep-diving lifestyle.
Satellite tagging studies of
Cuvier's
(or goose-beaked) whales have revealed extraordinary feats of physiology. This includes one dive that lasted a mindboggling 222 minutes - that's longer than the runtime of
The Return of the King
, the third (and longest)
Lord of the Rings
movie.
Cuvier's beaked whales are renowned for their deep and long dives, stretching for more than three hours.
Photo:
Laurent Bouveret / CC BY-SA 4.0 via Wikimedia
Another dive reached a depth of almost three kilometres. Average dives lasted about one hour - impressive breath-holding for an air-breathing mammal.
As for the spade-toothed whale's diving prowess - well, nobody knows. It's never been seen alive in the wild.
Anton van Helden helped give the whale its common name - spade-toothed - because the single tusk-like tooth erupting from the lower jaw of males looks like a whaling tool called a spade.
DOC rangers assess a washed up whale, thought to be a spade-toothed whale, on the beach at Taieri Mouth.
Photo:
Supplied/Department of Conservation
Anton, senior science advisor in the marine species team at the Department of Conservation, had described the outer appearance of the whale from photographs taken of a mother and calf that washed up in the Bay of Plenty in 2010. They were originally mis-identified and buried, before DNA analysis confirmed that they were spade-toothed whales, after which their partial skeletons were exhumed.
This meant that when Anton was sent some snaps of the whale that
washed up in Otago in July 2024
he knew exactly what he was looking at, and what a rare find it was.
The 2024 specimen is only the seventh ever found (with all but one from New Zealand).
Spade-toothed Whale
Photo:
Ōnumia CC BY 4.0 DOC
Hence the hum of excitement in the concrete room at AgResearch's Invermay campus in Mosgiel, just south of Dunedin. For the first time ever, scientists got the chance to dissect an intact spade-toothed whale.
The week begins with photographs and whole-body measurements, followed by cutting into and peeling back the thick layer of blubber.
Scientists are starting the examination in Mosgiel, which is expected to take several days.
Photo:
RNZ / Tess Brunton
Once the blubber is removed, individual muscles are identified and documented. The massive backstrap muscle across the length of the body is then removed, exposing the organs below. These are photographed, examined and weighed.
Each beaked whale species seems to have a unique stomach plan. This dissection revealed that the spade-toothed whale has nine stomachs. Squid beaks and eye lenses were found inside, along with some parasites that are now at the University of Otago, awaiting identification.
During the week the intact head was removed and brought to the onsite CT scanner.
The tens of thousands of images that come out of the scan, along with the subsequent head dissection, will help the researchers dig into some of the many questions they have around the whale's evolution, how they make and use sound, and how they feed.
The whale head is lifted into the CT scanner.
Photo:
Claire Concannon / RNZ
For example, tiny vestigial teeth were found in the jawbone of this whale - a throwback to their early evolutionary days when they had more teeth. Now they have evolved to be suction feeders, using sound to echolocate their prey and then employing their piston-like tongue to alter the water pressure and suck them in.
While the focus was scientific dissection, rather than autopsy, the team did find bruising around the neck and head, and a broken jawbone, indicating that the whale had suffered some head trauma that was likely the cause of death.
A large team participated in the whale's recovery and dissection: Te Rūnanga o Ōtākou hapū members and rangatahi, staff from Tūhura Otago Museum, local and international whale scientists, University of Otago staff and scientists, Māori whale experts (tohunga), and staff from the Department of Conservation.
With the blubber removed, the team start investigating the muscles below.
Photo:
Claire Concannon / RNZ
Experts from both knowledge systems - mātauranga Māori and western science - worked alongside each other, with learning going both ways, says Tumai Cassidy from Te Rūnanga o Ōtākou. He was excited to learn from Ngātiwai tohunga Hori Parata and his son Te Kaurinui who answered Te Rūnanga o Ōtākou's call to assist with the dissection.
The whale was named Ōnumia by the rūnanga, after the te reo Māori name for the native reserve stretch of coastline it was found on. The whale's skeleton has been gifted to Tūhura Otago Museum, but it will be a while before it will go on display.
Right now, the bones are in Lyttelton in the care of Judith Streat. Three months in bacteria-filled baths have stripped the bones of flesh, but there is a lot of oil in deep-diving whales, so the process will take several more years.
Tumai Cassidy from Te Rūnanga o Ōtākou says the whale was found on their native reserve land on the Taieri.
Photo:
RNZ / Tess Brunton
The kauae, or jawbone, will stay with Te Rūnanga o Ōtākou, says Rachel Wesley.
"Being able to claim the kauae, you know, as mana whenua, under our rakatirataka and in line with old practices from the past has been a huge step forward from what our hapū has been able to do in the past."
A 3D-printed version of the jawbone will complete the skeleton in the museum.
Sign up to the Our Changing World monthly
newsletter
for episode backstories, science analysis and more.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Genetic marker found for rare children's brain disease
Genetic marker found for rare children's brain disease

RNZ News

time20 hours ago

  • RNZ News

Genetic marker found for rare children's brain disease

A New Zealand-led research team has found new information about the cause of microcephaly, a disease that affects brain growth and function in children. Photo: Image by Gerd Altmann from Pixabay An Otago-led team has uncovered a genetic cause for a rare children's brain disorder. University of Otago associate professor Louise Bicknell, co-author of the study, said the international research team were investigating microcephaly, a developmental disorder where children's brains fail to grow. Dr Louise Bicknell says new research has helped pinpoint a genetic cause of the devastating children's brain disease microcephaly. Photo: Supplied/ University of Otago - Sharron Bennett They pinpointed specific changes in a gene called CRNKL1, and their findings were recently published in the prestigious American Journal of Human Genetics. It was the culmination of a seven-year study of a New Zealand family, Bicknell said. "Their wee girl had really severe microcephaly. Her brain was much smaller than we'd hoped for, and there were quite a few structural things that were abnormal about her brain, so quite unusual." Researchers compared her brain structure with that of nine children overseas who also had the condition. "It was only then that, we realised they all had similar features, of a really small brain, as well as these structural [aspects] of other parts of the brain not being so usual." In a striking discovery, nine of the families also showed genetic changes in the exact same spot in the CRNKL1 gene. It proved there was a strong link between these specific genetic changes and the disorder, and it was an exciting breakthrough, she said. "That's when the heart starts racing and you know you are onto something. Your gut instinct kicks in and says, this can't be a coincidence, this must be something." Lead author Dr Sankalita Ray Das, a postdoctoral fellow at Otago's Rare Disorder Genetics Laboratory, said the research findings clearly showed that CRNKL1 was "crucial" for healthy brain development. "Importantly, this knowledge has provided understanding for families affected by these severe conditions and lays the foundation for further research into why just the brain is affected by these genetic changes." The researchers received funding from the Neurological Foundation of New Zealand, Cure Kids and the University of Otago, Bicknell said. Sign up for Ngā Pitopito Kōrero, a daily newsletter curated by our editors and delivered straight to your inbox every weekday.

Approaching life-changing diagnosis for "missing millions" with ME/CFS
Approaching life-changing diagnosis for "missing millions" with ME/CFS

RNZ News

time2 days ago

  • RNZ News

Approaching life-changing diagnosis for "missing millions" with ME/CFS

Photo: Professor Warren Tate Photo: Supplied Anyone who has or knows someone with ME, chronic syndrome fatigue or long covid knows that being believed is one of the toughest parts of having the condition. University of Otago Emeritus Professor Warren Tate has dedicated his life to researching ME/CFS and is considered a leading authority on long covid. Along with his team, he has been developing a diagnostic test, that so far has shown promising results. If implemented, it would be life-changing. Warren and his co-researcher Dr Katie Peppercorn have also released a one-of-a-kind book to help clinicians and researchers find ways of better understanding post-viral conditions and improve the lives of those 'missing millions' affected with ME/CFS and most recently long covid.

Approaching life-changing diagnosis for 'missing millions'
Approaching life-changing diagnosis for 'missing millions'

RNZ News

time2 days ago

  • RNZ News

Approaching life-changing diagnosis for 'missing millions'

Photo: Professor Warren Tate Photo: Supplied Anyone who has or knows someone with ME, chronic syndrome fatigue or long covid knows that being believed is one of the toughest parts of having the condition. University of Otago Emeritus Professor Warren Tate has dedicated his life to researching ME/CFS and is considered a leading authority on long covid. Along with his team, he has been developing a diagnostic test, that so far has shown promising results. If implemented, it would be life-changing. Warren and his co-researcher Dr Katie Peppercorn have also released a one-of-a-kind book to help clinicians and researchers find ways of better understanding post-viral conditions and improve the lives of those 'missing millions' affected with ME/CFS and most recently long covid.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into a world of global content with local flavor? Download Daily8 app today from your preferred app store and start exploring.
app-storeplay-store