WEBVTT

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lost in the fog of a cosmic storm floating on

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whimsical wavelengths is the norm dancing through

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the stars chasing spectrums of light riding the

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waves that are just out So one of the things

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that I've noticed is that I don't introduce myself

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very often. And for all those new listeners out

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there that show up from time to time, my name's

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Dr. Jeffrey Zurich. I'm the host of Whimsical

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Wavelengths. And today is all about the white

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sturgeon. Because, you know, I've spent the vast

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majority of my life living along the major rivers

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in southern British Columbia, Canada. The Kootenai

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and the Columbia Rivers and now the Fraser River.

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These rivers have a lot in common from the ecology

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standpoint with respect to salmon and the subject

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of today's episode, the white sturgeon. And these

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fish are amazing. I've spent a lot of time fishing

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the Columbia for trout and walleye, also known

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as pickerel in other parts of Canada. But I've

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never interacted with a sturgeon. To me, they've

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always been mysterious fish of the river. I know

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they are there, but I've never seen them. The

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Loch Ness of the Columbia and the Fraser River.

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And I've always wanted to learn more about these

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creatures. You know, this group, sturgeon, and

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their family group, they first appeared in the

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late Cretaceous, with the oldest seen in the

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fossil record at 100 million years ago, found

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in Alberta. canada in fact they look today very

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similar to what they looked in the late cretaceous

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they join a short list of creatures that have

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not at least outwardly significantly changed

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their body shapes or their large scale building

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blocks in a very long time like the crocodile

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whose modern body shape came together 80 to 90

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million years ago or the horseshoe crab which

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has been around a lot longer nearly 400 million

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years Besides being what some term a living dinosaur,

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they're also polyploidy, meaning they can have

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different numbers of chromosomes. This whole

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part of it actually makes my head hurt. Give

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me the simplicity of a wave equation. Thankfully,

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in a few minutes, I have a guest to help me understand

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it. But let me attempt to set this up. So they,

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the white sturgeon, are scientifically amazing

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already. And we haven't even gotten into what

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the species do. Above and beyond what the local

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rivers mean to us. There are culturally important

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food for First Nations of North America and harvested

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for caviar in other places. The caviar can go

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for $1 ,000 to $5 ,000 Canadian per pound. A

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true luxury item. that starts its history almost

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2500 years ago when the persians ate them in

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a belief that it provided strength later becoming

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a prized delicacy of european nobility sturgeon

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are predators and scavengers using barbells or

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whisker -like sensory organs that smell and taste

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to detect on the riverbed things like salmon

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carcasses eggs lamprey crayfish clams and worms

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some might call them a keystone scavenger aiding

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in keeping riverbeds healthy for other species

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now we have the geologic time perspective and

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the culture perspective and how they are important

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to the river systems they inhabit what about

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their population i can anecdotally attest to

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these fish being rare In fact, they're threatened

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as a species due to overfishing and habitat modification.

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The Columbia River has many, many dams along

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it due to the Columbia River Treaty. All right,

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time to bring in the guest. To help us understand

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about these enigmatic fish, their populations,

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and their genetics, please welcome a fisheries

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geneticist with the Hagerman Genetics Lab, Dr.

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Stuart Willis. Hi, Jeff. Always excited to talk

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about sturgeon. Yay. Before jumping into the

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science, I always think it's important to like

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see how someone comes by their chosen subject.

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I mean, careers in STEM, we need to make them

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less scary in general. And science is always

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a human endeavor. I grew up living beside a river.

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But what about you? Was there a river, a body

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of water? Was it fishing? What brought you to

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studying fish and their ecosystems? Yeah, so

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I did a lot of fishing with my dad as a kid back

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in Texas, except I always wanted to bring our

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catch home and keep them in an aquarium to learn

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more about them. So as a teenager, I did keep

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a lot of aquarium, but mostly South American

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river fishes, not our North American native fishes.

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And so then when I went to college, I got hooked

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up with a professor who had a graduate student

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doing phylogenetic and evolutionary ecology work

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on South American fishes, and I was hooked. And

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so I did my graduate work on phylogenetics and

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population genetics of South American fishes.

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But in academia, as you know, you sort of have

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to go where the money is. And so that eventually

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led into the work that I do today for a consortium

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of tribal nations for whom fish, and particularly

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salmon, are an integral part of their culture.

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They've taken a lead role in managing the natural

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resources within their ancestral territories

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in the Columbia River Basin. And as a part of

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that work, I manage our genetic investigations

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of white sturgeons, which are the largest freshwater

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fish in North America. Okay. So, I mean... I

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grew up next to the Columbia. I fully support

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this sort of research and keeping those ecosystems

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at least understandable, what's happening to

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them, monitor them and make sure they're there

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for the next generation. But are you also looking

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at different opportunities to do other research

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outside of those drainage catchments as well?

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I mean, yes, you follow the money, but, you know,

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I also want to go back one day and do some volcano

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research that might take years and years and

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years and years to actually come to fruition.

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I mean, that's the nature. of sometimes playing

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science. It's a long game. Yeah, I still do collaborate

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on occasion with people from my past. I still

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have a project that I'm working on looking at

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photosensory evolution in shallow and deep walling

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reef fishes and things like that. But for the

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most part, I stay within what the tribes need

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and the tribes are focused on fisheries in the

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Columbia River Basin. A lot of what I do day

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to day is... salmon genomics. And there's a huge

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community of people, as you can imagine, that

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are interested in all things salmon, everything

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we find out about salmon. White sturgeon is a

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little bit smaller of a community, but to me,

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because there's so much less known about white

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sturgeon, it sort of feels more like a voyage

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of discovery, much more like the things that

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I did as a graduate student, where I was going

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out into the Amazon and finding things for the

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first time, seeing places that no scientist had

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collected fish before, at least. A lot of new

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stuff. Hard, difficult, but new. Right. And I

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will get into how you managed to find these fish,

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hopefully eventually here. But I want to pivot

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a little bit to the rivers themselves that are

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kind of the focus of this study and your work

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in general. The mighty Fraser and the Columbia,

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two rivers here on the west coast of North America.

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I really felt like I needed to add a little bit

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Canadian content from the political past. It's

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kind of a fun little tidbit. The two rivers are

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separated by only about 45 meters of elevation.

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Like there's a divide right near Vail Mount,

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British Columbia. In the 1960s, British Columbia

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actually made a public threat in taking the Columbia's

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water in a negotiating tactic for the Columbia

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Basin River Treaty. In a geographic sense, the

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rivers are very similar. Yet today... are very

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different. Perhaps let's start there. What is

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kind of like the state of the two rivers? Yeah.

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So both the Fraser and Columbia basins face increasing

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pressure from urbanization and other intentional

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and unintentional modifications, as well as changing

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precipitation and temperature patterns that make

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life as an aquatic organism exponentially harder.

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The Fraser, fortunately, doesn't have the same

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level of damming that Columbia does, particularly

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the main channels. Thanks, and going back to

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your... comment on Canadian politics, as I understand

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it, to push back from the public about the effects

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that would have on aquatic species and the people

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that depend on them. Which is not to say that

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Fraser is in pristine shape. Channel modification

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and pollution are a big issue and anagimous fisheries

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have been on the decline for a number of years.

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Some of the factors for that are local and some

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of them probably regional. The Columbia, on the

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other hand, is strongly segmented by hydroelectric

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facilities from the tributaries through the main

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channel. And on top of that, as well as urbanization

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and other habitat degradation, not to mention

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climate change, invasive species have really

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started chasing their toll. Some intentionally

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introduced by well -meaning but short -sighted

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state agencies like Channel Catfish and Chad.

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Some introduced by well -meaning but ignorant

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bucket biologists like walleye. And some completely

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unintentional hitchhikers, like quagga mussels

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and Siberian ponds. So the answer to your question,

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the state of the rivers is probably middling

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to struggling, respectively. Right. But maybe

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where I was kind of wondering is like, what's

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the effect of those dams? Because that's like,

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all things being equal, they have, I mean, yeah,

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I could say that Columbia, at least in its lower

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reaches, has more population pressure. And they're

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very similar in their geographic and everything

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else, but the Fraser's dirty. It has a lot of

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sediment. I wouldn't say dirty. Dirty is the

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wrong word necessarily because it's not like

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it's polluted or anything, but you have all these

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dams in the Columbia that are causing all that

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sediment to settle out. And that's, you know,

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I've heard it said that a dam gives a river a

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stroke. You can partially recover from that stroke,

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but you're never going to get all the way back.

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Right. So there are great diversity of dams on

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the Columbia. Sort of the two main types are

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run of river dams that sort of don't have a big

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difference in elevation. And then dams that have

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a large body of water that are held behind them.

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And those in particular have major effects on

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the river ecosystems because. Not only do they

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slow down their water, which means that fish

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now have to swim rather than just being in the

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current, but they also allow the water to heat.

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And that hot water is really hard for these very

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cold -specific species, cold -adapted species,

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because they get in hot water, their retazolums

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ramp up, their parasite load is more difficult

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to manage. And so they're very different, both

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at a very small -scale endocrine level and then

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at a major ecological level. And then, of course,

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there are a number of dams that don't even have

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fish passage at all. So it's hard to be an anagimous

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fish when you can't even get over the dam in

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the first place. Okay. I was going to move on

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to the next question, but I need to check the

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word. Anagimous? So anagimous is a term that

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just means fish that start out in freshwater,

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go and live part of their life in saltwater,

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and then come back to spawn in saltwater. It's

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a subset of what we call diadromous fish, so

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fish that have sort of two different parts to

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their life history strategy or life cycle. The

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alternative is catadromous fish that live in

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saltwater as adults, spawn, they're young, go

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into freshwater for some period of time, and

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then return back to saltwater response. I think

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the American eel is a catadromous fish. They

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all spawn out in the ocean. They're young, spend

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most of their life in freshwater. So then what

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would salmon be? Salmon are anadromous fish.

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They spawn in fresh water. The young go out to

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the ocean, grow up, and then come back to adults.

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And this is sort of getting off on a tangent.

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There are some salmon that don't, right? Like

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rainbow trout. Anything we call a trout is because

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they can't complete their life cycle in fresh

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water. The reason that they go to the ocean is

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because there are so much more nutrients in the

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ocean. So there's an advantage to going out to

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the ocean. to be able to grow faster or have

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greater access to nutrients. And so all of that

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life history differences are adaptations that

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these fish sort of manage across time as environments

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changed. Right. Okay, well, to pivot to the topic

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of the day, the white sturgeon. Who are they

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and what role do they fill in the ecosystem of

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these two rivers? Yeah, sturgeon are very charismatic

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fishes for those who are lucky enough to live

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where they do. As you mentioned in your intro,

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they look very prehistoric. And indeed, as a

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group, the order as a pincer of forms, which

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includes sturgeons and paddlefish, had been around

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for a long time, being one of the earliest groups

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of bony fishes to break off at least 300 million

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years ago. So before the divergence of the dinosaurs

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from other reptiles. But I personally don't like

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the term. living fossil or living dinosaur that

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sometimes gets applied because they are, in fact,

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highly modified both from other fishes and from

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their own ancestors. For example, they have a

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mostly cartilaginous skeleton, like sharks, but

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that's a feature that they evolved after diverging

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from other fishes. It's a secondary characteristic.

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Similarly, while fish recognizable as asapensirthons

00:13:57.529 --> 00:14:00.190
have existed since at least the early Jurassic,

00:14:00.840 --> 00:14:03.620
Modern sturgeon and paddlefish were as different

00:14:03.620 --> 00:14:06.279
from those forms as sturgeon and paddlefish are

00:14:06.279 --> 00:14:09.460
from each other today. But, you know, as you

00:14:09.460 --> 00:14:11.279
say, they have been around for a long time, and

00:14:11.279 --> 00:14:14.039
they have some neat features beyond their unique

00:14:14.039 --> 00:14:17.860
appearance. For example, they still retain electrosensory

00:14:17.860 --> 00:14:21.240
organs on their head called ampullae of Lorenzini.

00:14:21.820 --> 00:14:24.740
that allow them to sense the weak electric field

00:14:24.740 --> 00:14:27.399
emitted by other aquatic organisms, a feature

00:14:27.399 --> 00:14:29.860
that they share with sharks and rays and one

00:14:29.860 --> 00:14:31.820
of the group of early diverging fawny fishes.

00:14:32.279 --> 00:14:35.159
And you can imagine that feature helps them to

00:14:35.159 --> 00:14:38.320
find fish in the deepest, darkest parts of large

00:14:38.320 --> 00:14:41.100
rivers where they're found. And that leads into

00:14:41.100 --> 00:14:43.620
their ecological roles, which change depending

00:14:43.620 --> 00:14:46.899
on their life stage. As eggs, larvae, and fry,

00:14:47.000 --> 00:14:50.250
they are food for a lot of other creatures. But

00:14:50.250 --> 00:14:51.950
they grow really fast in the first couple of

00:14:51.950 --> 00:14:54.549
years of life, usually reaching 30 to 40 centimeters

00:14:54.549 --> 00:14:57.889
in the first year and a meter within three to

00:14:57.889 --> 00:15:01.090
five years. And after that, especially as adults

00:15:01.090 --> 00:15:04.009
that reach three or four or even more meters

00:15:04.009 --> 00:15:06.769
long, they don't have a lot of natural predators.

00:15:07.190 --> 00:15:09.649
So they can sit at the top of the aquatic food

00:15:09.649 --> 00:15:12.230
chain, eating basically anything that can hoover

00:15:12.230 --> 00:15:14.370
up into their mouth that smells good, which could

00:15:14.370 --> 00:15:17.330
be live or dead. And so they are both top predators

00:15:17.330 --> 00:15:22.860
and scavengers. All right, so I guess they're

00:15:22.860 --> 00:15:25.259
kind of like a keystone species to some extent

00:15:25.259 --> 00:15:29.279
for these two rivers. You know, it's hard to

00:15:29.279 --> 00:15:30.899
say keystone species because that sort of depends

00:15:30.899 --> 00:15:32.539
on your perspective. I mean, you could say that

00:15:32.539 --> 00:15:34.539
salmon are a keystone species for these ecosystems

00:15:34.539 --> 00:15:38.539
because they bring all of those marine direct

00:15:38.539 --> 00:15:43.440
nutrients. They're an apex species, right? They

00:15:43.440 --> 00:15:45.039
sit at the top of the food chain, and certainly

00:15:45.039 --> 00:15:48.289
they have effects on the ecosystem. You know,

00:15:48.289 --> 00:15:51.169
Keystone is sort of an amorphous concept. So

00:15:51.169 --> 00:15:54.610
I'd be cautious to venture out and say that for

00:15:54.610 --> 00:15:57.289
sure. Well, how long does it take for them to

00:15:57.289 --> 00:15:59.710
get to adulthood? Because I know that they're

00:15:59.710 --> 00:16:03.110
long living. And generally speaking, those species

00:16:03.110 --> 00:16:06.450
who are long living, you know, they take a long

00:16:06.450 --> 00:16:08.370
time to reach adulthood. They take a long time

00:16:08.370 --> 00:16:10.809
to reproduce. Is that the same for this species

00:16:10.809 --> 00:16:15.240
as well? It is. As a survival strategy, you avoid

00:16:15.240 --> 00:16:18.159
being prey yourself. White sturgeons grow as

00:16:18.159 --> 00:16:21.879
fast as they can to get into a size so that they're

00:16:21.879 --> 00:16:24.500
less likely to be eaten. But once they do, they

00:16:24.500 --> 00:16:26.320
slow down their growth and just sort of chill.

00:16:26.679 --> 00:16:29.779
Since prehistorically, at least, mortality amongst

00:16:29.779 --> 00:16:33.059
sub -adults and adults was really low. While

00:16:33.059 --> 00:16:35.940
conversely, finding food to maintain such large

00:16:35.940 --> 00:16:40.740
bodies is a full -time job. So they are a type

00:16:40.740 --> 00:16:42.799
of fish that exhibit what we call a periodic

00:16:42.799 --> 00:16:45.379
life history strategy, which means that they

00:16:45.379 --> 00:16:48.120
reproduce at regular intervals, usually in the

00:16:48.120 --> 00:16:50.559
late spring when snow melt is high but the water

00:16:50.559 --> 00:16:53.519
is warming. But the local conditions that help

00:16:53.519 --> 00:16:57.440
their young to survive can be unpredictable spatially.

00:16:57.779 --> 00:17:00.340
And so it's really advantageous to produce a

00:17:00.340 --> 00:17:03.360
ton of eggs that get spread out across space

00:17:03.360 --> 00:17:06.720
to mitigate risk. And for organisms like that,

00:17:06.759 --> 00:17:10.460
for which egg number or secondity is a determining

00:17:10.460 --> 00:17:14.200
factor in reproductive success, size at reproduction,

00:17:14.460 --> 00:17:17.000
which generally also means age, also becomes

00:17:17.000 --> 00:17:19.819
a determining factor, which explains why sturgeon

00:17:19.819 --> 00:17:22.660
males, for whom size is slightly less of a constraining

00:17:22.660 --> 00:17:26.000
factor, don't mature to around 12 to 20 years

00:17:26.000 --> 00:17:29.019
of age, while sturgeon females don't usually

00:17:29.019 --> 00:17:32.220
start to mature around at least 15, usually 18,

00:17:32.259 --> 00:17:35.779
but can hit the 30 years. to mature and then

00:17:35.779 --> 00:17:39.400
once they do because that kind of pulse reproductive

00:17:39.400 --> 00:17:42.599
effort is so taxing females in the wild will

00:17:42.599 --> 00:17:45.420
usually only reproduce every three to six years

00:17:45.420 --> 00:17:48.500
or so and some of those years would be good recruitment

00:17:48.500 --> 00:17:52.480
years and some will be bad and based on prevailing

00:17:52.480 --> 00:17:55.240
environmental conditions so the reason why they

00:17:55.240 --> 00:17:58.859
succeed is because they can live so long Long

00:17:58.859 --> 00:18:02.660
enough for a few fry to survive from a few of

00:18:02.660 --> 00:18:05.799
the 70, even 100 years that they're going to

00:18:05.799 --> 00:18:09.319
live. But that's in natural conditions and rivers

00:18:09.319 --> 00:18:12.380
unaltered by dams and dredging and pollution,

00:18:12.460 --> 00:18:14.859
invasive species, et cetera, et cetera. So how

00:18:14.859 --> 00:18:17.619
that continues to function in our modern river

00:18:17.619 --> 00:18:20.799
ecosystems is something we are actively studying.

00:18:21.920 --> 00:18:23.940
I have a feeling I'm about to jump the shark

00:18:23.940 --> 00:18:25.720
here with this question because you kind of brought

00:18:25.720 --> 00:18:31.210
it up. take decades to like humans have a couple

00:18:31.210 --> 00:18:34.130
of years and we you know sexually mature like

00:18:34.130 --> 00:18:36.849
it's it's it's a standard window it's not exactly

00:18:36.849 --> 00:18:39.769
the same between individuals but it's pretty

00:18:39.769 --> 00:18:43.630
close like it's not decades and you just gave

00:18:43.630 --> 00:18:47.609
a range that were potentially decades long that

00:18:47.609 --> 00:18:52.490
it takes to mature like that seems Could you

00:18:52.490 --> 00:18:56.009
imagine being a teenager for decades? And one

00:18:56.009 --> 00:18:58.809
person or one fish goes through that in 12 years.

00:18:58.869 --> 00:19:03.049
The next one takes 20 years. We make jokes about

00:19:03.049 --> 00:19:05.250
us men taking a lot longer to mature, but this

00:19:05.250 --> 00:19:07.609
is taking it to the whole next level, right?

00:19:08.069 --> 00:19:12.390
It is. Yeah. And so some of that is probably

00:19:12.390 --> 00:19:15.549
environmental conditions. If you grow quickly,

00:19:15.690 --> 00:19:17.829
you're more likely to mature quickly if your

00:19:17.829 --> 00:19:20.460
growth rate is sort of... set at an early age

00:19:20.460 --> 00:19:22.500
to be slow. You're going to take longer to reproduce.

00:19:22.759 --> 00:19:26.460
But sometimes that can be an advantage. You know,

00:19:26.480 --> 00:19:28.680
we talk about keeping it back to salmon because

00:19:28.680 --> 00:19:30.200
that's one of the other things that I work on.

00:19:30.259 --> 00:19:34.460
Salmon have very distinct peaks in age at maturity,

00:19:34.579 --> 00:19:38.019
but larger fish have larger precondities. They

00:19:38.019 --> 00:19:39.920
produce more eggs. And so it can actually be

00:19:39.920 --> 00:19:43.299
an advantage to become sexually mature later.

00:19:43.829 --> 00:19:46.309
And so it's entirely possible that's true for

00:19:46.309 --> 00:19:48.690
sturgeon as well, that it can be an advantage

00:19:48.690 --> 00:19:51.650
to wait to become sexually mature because you're

00:19:51.650 --> 00:19:54.849
larger, you end up having a greater fecundity,

00:19:55.069 --> 00:19:57.829
maybe you weathered out a time period of which

00:19:57.829 --> 00:19:59.690
you wouldn't have been successful reproducing

00:19:59.690 --> 00:20:01.829
anyway because there were cruddy conditions for

00:20:01.829 --> 00:20:04.569
offspring. And so, yeah, that range certainly

00:20:04.569 --> 00:20:07.549
has implications for population dynamics, but

00:20:07.549 --> 00:20:10.309
at an individual level can actually be an advantage.

00:20:11.069 --> 00:20:15.130
And not to get too hard, to jump too far ahead

00:20:15.130 --> 00:20:17.990
into talking about, you know, sort of state of

00:20:17.990 --> 00:20:20.349
the population. One of the things that we're

00:20:20.349 --> 00:20:23.289
seeing in looking at some of these river segments,

00:20:23.390 --> 00:20:25.329
the ones that are sectioned off by dams and that

00:20:25.329 --> 00:20:27.170
kind of thing, is that fish are taking longer

00:20:27.170 --> 00:20:30.230
to mature. And so basically that's probably because

00:20:30.230 --> 00:20:32.750
the ecosystems are not as productive or the fish

00:20:32.750 --> 00:20:35.430
don't have access to the areas where they historically

00:20:35.430 --> 00:20:37.880
would have been able to. get enough for me to

00:20:37.880 --> 00:20:41.680
be able to reproduce at younger ages. So let's

00:20:41.680 --> 00:20:44.019
pivot towards the actual paper, the reason I

00:20:44.019 --> 00:20:46.240
got you onto the show. And to be honest, I really

00:20:46.240 --> 00:20:48.440
struggled with it to understand it. I mean, I

00:20:48.440 --> 00:20:50.220
guess I'm a volcanologist, this to be expected,

00:20:50.339 --> 00:20:52.339
but even the more I learned, the more I was blown

00:20:52.339 --> 00:20:56.220
away. The paper, Genome Assembly and Diagnostic

00:20:56.220 --> 00:20:59.799
DNA Markers for Sex of the Largest Freshwater

00:20:59.799 --> 00:21:04.079
Fish in North America, the White Sturgeon Assenpenser

00:21:04.079 --> 00:21:07.890
Transmountainous. I know I did the terrible job

00:21:07.890 --> 00:21:10.470
of pronouncing that, but that's okay. So I guess

00:21:10.470 --> 00:21:13.329
let's start with the hardest thing that I had

00:21:13.329 --> 00:21:15.650
wrapping my head around and I made a joke. Give

00:21:15.650 --> 00:21:20.130
me wave equations instead. What exactly is ploidy?

00:21:20.730 --> 00:21:25.369
Yeah. So this paper is our first attempt at reconstructing

00:21:25.369 --> 00:21:27.789
the genome of white sturgeon so that we could

00:21:27.789 --> 00:21:30.390
develop new genomic tools for their conservation.

00:21:30.390 --> 00:21:33.130
But we really couldn't do that without confronting

00:21:33.130 --> 00:21:37.339
the issue of ploidy. And so hopefully I can explain

00:21:37.339 --> 00:21:39.180
that without getting too much into the weeds

00:21:39.180 --> 00:21:42.119
and feel free to jump in if I'm getting entirely

00:21:42.119 --> 00:21:46.019
too nerdy and esoteric. But we fully embrace.

00:21:46.519 --> 00:21:49.900
Don't worry about that. Esoteric. Well, to a

00:21:49.900 --> 00:21:51.740
point, because we have to understand it, too.

00:21:51.859 --> 00:21:54.160
Well, that's my that's my wife's euphemistic

00:21:54.160 --> 00:21:57.440
term for me. So, you know, that's just how I.

00:21:57.500 --> 00:22:03.519
Yeah. But ploidy refers to the number of complete.

00:22:04.190 --> 00:22:07.829
sets of chromosomes in a cell, whatever complete

00:22:07.829 --> 00:22:10.789
is for that species. And I'm using air quotes

00:22:10.789 --> 00:22:13.470
when I say complete. My voice does not convey

00:22:13.470 --> 00:22:16.130
that. And I'll come back to that in a moment.

00:22:16.190 --> 00:22:18.210
But to give you an example you're familiar with,

00:22:18.269 --> 00:22:21.130
humans, like most multicellular organisms, are

00:22:21.130 --> 00:22:24.650
diploid, diploid, di meaning two. That is, we

00:22:24.650 --> 00:22:27.329
get one complete set of chromosomes from mom

00:22:27.329 --> 00:22:30.309
and one from dad. So the final set contains pairs

00:22:30.309 --> 00:22:35.400
of each unique or homologous. chromosome, meaning

00:22:35.400 --> 00:22:38.299
what each mom and dad contributes, eggs and sperm,

00:22:38.599 --> 00:22:42.119
are, in this case, monoploid, mono meaning one,

00:22:42.220 --> 00:22:46.380
one complete cell. Now, technically, we use the

00:22:46.380 --> 00:22:50.519
term haploid to refer to the complement of chromosome

00:22:50.519 --> 00:22:55.240
in a gamete, an egg or a sperm, meaning half.

00:22:55.440 --> 00:22:59.240
And what the combined gametes produce, somatic

00:22:59.240 --> 00:23:03.450
cells, are called duploid. The root U, meaning

00:23:03.450 --> 00:23:07.289
true or even. And then we call instances where

00:23:07.289 --> 00:23:10.390
there are incomplete sets of chromosomes aneuploid

00:23:10.390 --> 00:23:14.490
or not even. For example, in humans, we may be

00:23:14.490 --> 00:23:17.089
familiar with trisomy, where there are three

00:23:17.089 --> 00:23:24.170
copies of a chromosome. And the trisomy, three

00:23:24.170 --> 00:23:28.450
bodies of chromatome or chromosome, which creates

00:23:28.450 --> 00:23:31.690
uneven sets of chromosome or even. aneuploidy.

00:23:31.710 --> 00:23:33.869
And this is usually a problem developmentally,

00:23:33.930 --> 00:23:37.069
like trypsin via chromosome 21 in humans produces

00:23:37.069 --> 00:23:40.789
Down syndrome, because gene regulation, as it

00:23:40.789 --> 00:23:44.730
turns out, is frequently dosage dependent, meaning

00:23:44.730 --> 00:23:47.609
the regulation and expression of genes has evolved

00:23:47.609 --> 00:23:51.569
to be balanced in a copy number dependent manner,

00:23:51.690 --> 00:23:54.849
and aneuploidy messes up the typical dosage.

00:23:55.650 --> 00:23:58.369
But going back to the air quotes, complete...

00:23:58.970 --> 00:24:01.309
set of chromosomes, when we look across animal

00:24:01.309 --> 00:24:04.430
and plant species, we see wildly different numbers

00:24:04.430 --> 00:24:08.029
of chromosomes and genome sizes. Some of these

00:24:08.029 --> 00:24:10.849
differences are because chromosomes have expanded

00:24:10.849 --> 00:24:13.910
or contracted individually, or some chromosomes

00:24:13.910 --> 00:24:17.089
have split or combined. And so we see relatively

00:24:17.089 --> 00:24:19.950
moderate changes in chromosome numbers among

00:24:19.950 --> 00:24:22.910
related species. But those changes don't affect

00:24:22.910 --> 00:24:25.720
the ploidy. because it's not changing how many

00:24:25.720 --> 00:24:28.640
sets of chromosomes are in each cell, rather

00:24:28.640 --> 00:24:32.880
just the numbers that make up each set. But sometimes

00:24:32.880 --> 00:24:36.200
the genome sizes changes because of polypoidization,

00:24:36.420 --> 00:24:39.640
poly meaning many, in this case many sets, where

00:24:39.640 --> 00:24:42.619
the number of chromosomes goes up by entire sets

00:24:42.619 --> 00:24:46.119
all at once. And there are two main ways this

00:24:46.119 --> 00:24:50.460
can happen. In allopolypoidization, allo meaning

00:24:50.460 --> 00:24:54.150
different, in this case different species, Two

00:24:54.150 --> 00:24:57.049
moderately divergent species hybridize, and through

00:24:57.049 --> 00:24:59.970
some cell developmental magic, the progeny end

00:24:59.970 --> 00:25:02.509
up with twice the combined set of chromosomes

00:25:02.509 --> 00:25:05.930
from both parental species. And this form of

00:25:05.930 --> 00:25:08.230
polyploidy is fairly rare in animals, though

00:25:08.230 --> 00:25:11.029
there's at least one group of fishes, the Catastomidae,

00:25:11.029 --> 00:25:14.769
or suckers, that are thought to be allopolyploids.

00:25:15.529 --> 00:25:17.710
But it's actually fairly common in plants, including

00:25:17.710 --> 00:25:20.109
some you might know, like wheat. Wheat is an

00:25:20.109 --> 00:25:23.900
allopolyploid. If, on the other hand, polyploidization

00:25:23.900 --> 00:25:27.519
happens without hybridization, by the doubling

00:25:27.519 --> 00:25:32.019
of a genome within a species, we call that autopolyploidization.

00:25:32.440 --> 00:25:36.259
Auto meaning cell. And autopolyploidization has

00:25:36.259 --> 00:25:38.599
happened repeatedly, not only in plants, but

00:25:38.599 --> 00:25:40.940
also in vertebrates, especially in fishes, and

00:25:40.940 --> 00:25:46.650
in particular in sturgeons. So based on mapping

00:25:46.650 --> 00:25:48.589
of chromosome counts across the phylogenetic

00:25:48.589 --> 00:25:50.730
tree of fishes, that is the relationships among

00:25:50.730 --> 00:25:54.450
species of fish, we can estimate the ancestor

00:25:54.450 --> 00:25:57.150
of the Acipensia reforms, that was sturgeons

00:25:57.150 --> 00:26:00.970
and paddlefish, had a euploid or complete number

00:26:00.970 --> 00:26:05.650
of chromosomes around 60. But all modern Acipensia

00:26:05.650 --> 00:26:08.750
reforms have at least 120 chromosomes in their

00:26:08.750 --> 00:26:11.029
genome. And many sturgeons, like the white sturgeon,

00:26:11.529 --> 00:26:15.069
normally have at least 240 chromosomes in themselves.

00:26:15.329 --> 00:26:18.869
So approximately double to quadruple the ancestral

00:26:18.869 --> 00:26:23.069
number. So if we presume that that ancestor with

00:26:23.069 --> 00:26:25.910
60 chromosomes was diploid, which is a reasonably

00:26:25.910 --> 00:26:28.710
safe bet for a reason we can talk about, then

00:26:28.710 --> 00:26:32.369
the species with around 120 chromosomes would

00:26:32.369 --> 00:26:36.369
be evolutionary or ancestral tetraploids. That

00:26:36.369 --> 00:26:40.170
is relative for complete sets to that ancestor

00:26:40.170 --> 00:26:43.170
that had two. And species with 240 or so chromosomes

00:26:43.170 --> 00:26:47.109
would be ancestral octoploids, the eight complete

00:26:47.109 --> 00:26:51.730
sets. And so the haploid number for those organisms,

00:26:51.930 --> 00:26:54.670
what's found in an egg or a sperm, and what's

00:26:54.670 --> 00:26:57.609
half the euploid number, and all of that, is

00:26:57.609 --> 00:27:02.230
multiple complete sets relative to the ancestors.

00:27:02.809 --> 00:27:07.529
And big jumps like that from 60 to 120 to 240

00:27:07.529 --> 00:27:10.730
as the euploid number are the hallmark of...

00:27:11.119 --> 00:27:16.059
polyp organization. Okay. To be honest, I had

00:27:16.059 --> 00:27:19.059
a hard time following. I think it's just because

00:27:19.059 --> 00:27:22.279
it's like, there's not enough numbers. No. And

00:27:22.279 --> 00:27:26.339
I also couldn't spell any of those words. Like,

00:27:26.420 --> 00:27:28.859
I just come back to like the human idea here.

00:27:28.980 --> 00:27:31.339
And we talk about human genetics when we end

00:27:31.339 --> 00:27:35.380
up with, like, it seems like the more you have,

00:27:35.440 --> 00:27:37.680
the more things that can go wrong. Or is it the

00:27:37.680 --> 00:27:42.599
more you have, the more Fail safes you have like

00:27:42.599 --> 00:27:48.859
Yeah, how does that work? So it's what's really

00:27:48.859 --> 00:27:51.700
interesting is that in most of the ancestor polyploids

00:27:51.700 --> 00:27:54.279
we know in both plants and animals the genome

00:27:54.279 --> 00:27:58.480
actually acts as functional diploids made the

00:27:58.480 --> 00:28:02.319
same two pairs of chromosomes Pair up and split

00:28:02.319 --> 00:28:04.920
for distribution in gametes rather than in sets

00:28:04.920 --> 00:28:07.279
of multiples on random parable the original multiple

00:28:08.109 --> 00:28:12.170
We call this process redeploytization. And although

00:28:12.170 --> 00:28:14.430
the reasons for why this seemed to inevitably

00:28:14.430 --> 00:28:18.470
happen are an active area of research, we think

00:28:18.470 --> 00:28:22.230
that it's some combination of fixing what dosage

00:28:22.230 --> 00:28:25.769
problems were created by polypoidization, particularly

00:28:25.769 --> 00:28:29.349
around sex regeneration, and the redeployment

00:28:29.349 --> 00:28:32.390
of what duplicated genes are retained for distinct

00:28:32.390 --> 00:28:36.130
purposes. And indeed, in an ancestral tetrapoid

00:28:36.130 --> 00:28:38.450
European sturgeon called the sterlet, for which

00:28:38.450 --> 00:28:40.269
we have a pretty good genome sequence, there's

00:28:40.269 --> 00:28:42.269
pretty clear evidence that most of the genome

00:28:42.269 --> 00:28:46.970
has at least redeployed that. But white sturgeon,

00:28:47.009 --> 00:28:49.990
the subject of our paper, to get to be an ancestral

00:28:49.990 --> 00:28:52.710
octopoid has probably undergone two polyphoretization

00:28:52.710 --> 00:28:56.410
events. The first prior to its split its sterlet,

00:28:56.470 --> 00:28:58.369
so a shared one, and then one that's more recent

00:28:58.369 --> 00:29:02.910
and exclusive to Pacific sturgeon. But if sterlet

00:29:02.910 --> 00:29:06.670
are ancestral tetraploids, functional diploids,

00:29:06.829 --> 00:29:10.910
what does that make white sturgeon? So what we've

00:29:10.910 --> 00:29:12.950
gained from our genome assembly from white sturgeon

00:29:12.950 --> 00:29:15.190
is that there's evidence both that the majority

00:29:15.190 --> 00:29:19.309
of the genome seems to exist in four copies or

00:29:19.309 --> 00:29:23.789
relative to the sterlet sturgeon, that's a template,

00:29:23.930 --> 00:29:27.230
your diploid number, which makes white sturgeon

00:29:27.230 --> 00:29:31.119
technically tetraploid. There's also evidence

00:29:31.119 --> 00:29:36.200
that four ancestral chromosomes don't recombine

00:29:36.200 --> 00:29:38.900
much during meiosis, suggesting that enough of

00:29:38.900 --> 00:29:42.700
the genome has rediploidized for the machinery

00:29:42.700 --> 00:29:45.299
of cell division to treat them as two pair rather

00:29:45.299 --> 00:29:48.400
than four of a kind. So notwithstanding that

00:29:48.400 --> 00:29:51.559
there's ambiguity in our results, because shockingly,

00:29:51.599 --> 00:29:54.859
it's really hard to assemble an octoploid genome.

00:29:55.500 --> 00:29:57.599
It looks like the white sturgeon genome is in

00:29:57.599 --> 00:29:59.720
sort of an intermediate phase of rediploidizing

00:29:59.720 --> 00:30:02.940
from being functionally petroploid to the most

00:30:02.940 --> 00:30:06.819
recent autopletoplasmic event. So I guess what

00:30:06.819 --> 00:30:08.039
I'm trying to say in answering your question

00:30:08.039 --> 00:30:11.359
is that it's hard and it creates problems, but

00:30:11.359 --> 00:30:14.339
it seems that most of the time genomes go back

00:30:14.339 --> 00:30:20.859
to being diploid across time. polyploidy is an

00:30:20.859 --> 00:30:24.319
important factor. Evolutionary is sort of a different

00:30:24.319 --> 00:30:29.599
question, but in terms of how it sort of rejiggers

00:30:29.599 --> 00:30:32.859
the machinery, it does that by becoming rediploid,

00:30:32.980 --> 00:30:37.259
going back to being diploid over time. So it

00:30:37.259 --> 00:30:40.920
tries to simplify over time genetically. Right,

00:30:40.940 --> 00:30:46.160
yeah. In the, what's the word, I guess the background

00:30:46.160 --> 00:30:48.670
research that I tried to do in I don't pretend

00:30:48.670 --> 00:30:50.390
to understand it. They made the case that perhaps

00:30:50.390 --> 00:30:56.869
this sort of branching ploidy is to deal with

00:30:56.869 --> 00:31:01.509
evolutionary or environmental conditions. So

00:31:01.509 --> 00:31:05.450
I guess the argument is plants began that process

00:31:05.450 --> 00:31:08.869
when they came onto land. Is that kind of where

00:31:08.869 --> 00:31:11.089
we're going here? The environment changes so

00:31:11.089 --> 00:31:13.390
much that the genetics had to change really quickly.

00:31:13.509 --> 00:31:16.670
And one way to do that is to have more chromosomes

00:31:16.670 --> 00:31:20.059
that can drift and change with the environment?

00:31:20.200 --> 00:31:25.880
Yeah. And I, the broad answer to your question

00:31:25.880 --> 00:31:29.180
is maybe, um, I don't want to get into what one

00:31:29.180 --> 00:31:32.839
might call, um, an adaptationist or selection

00:31:32.839 --> 00:31:36.619
paradigm, um, because not every trait that an

00:31:36.619 --> 00:31:40.440
organism has is necessarily adaptive. Sometimes

00:31:40.440 --> 00:31:44.859
it's just neutral. Um, or maybe even disadvantageous,

00:31:44.859 --> 00:31:46.920
but developmentally connected to a trait that

00:31:46.920 --> 00:31:50.640
is advantageous. In addition, for any trait to

00:31:50.640 --> 00:31:53.920
actually being adapted, it has to be advantageous

00:31:53.920 --> 00:31:58.200
at an individual level. That is, it has to give

00:31:58.200 --> 00:32:01.339
that individual an edge over competitors within

00:32:01.339 --> 00:32:05.420
its own species. So that trait can't just appear

00:32:05.420 --> 00:32:08.819
to be beneficial for the population as a whole.

00:32:09.359 --> 00:32:11.859
And the same here goes with coity. It's likely

00:32:11.859 --> 00:32:15.079
that in most cases, these kinds of genomic changes

00:32:15.079 --> 00:32:17.880
are ultimately lethal. And it's only when the

00:32:17.880 --> 00:32:20.859
stars align that a polycoidization event happens.

00:32:21.000 --> 00:32:25.079
That genome is developmentally viable. The phenotype

00:32:25.079 --> 00:32:27.500
it creates is relatively neutral or even has

00:32:27.500 --> 00:32:30.700
some advantage in some environments. And then

00:32:30.700 --> 00:32:33.500
that that individual is fertile and able to reproduce

00:32:33.500 --> 00:32:36.480
either with normal coity individuals or that

00:32:36.480 --> 00:32:39.269
there are enough. other polypoids around that

00:32:39.269 --> 00:32:41.529
tend to reproduce. And those are pretty exceptional

00:32:41.529 --> 00:32:46.069
circumstances. But the answer to the broader

00:32:46.069 --> 00:32:48.329
question of why would this ever possibly work

00:32:48.329 --> 00:32:51.529
out is really the same answer to why we have

00:32:51.529 --> 00:32:53.170
sexual reproduction in the first place, which

00:32:53.170 --> 00:32:54.910
I think is part of what you're talking about.

00:32:55.069 --> 00:32:58.130
And the answer to that is novelty. The most salient

00:32:58.130 --> 00:33:01.309
theory for why we have sexual reproduction, which

00:33:01.309 --> 00:33:04.190
creates generally diploid offspring using material

00:33:04.190 --> 00:33:06.940
from two parents, Why it evolved in the first

00:33:06.940 --> 00:33:09.599
place is because of a race between organisms

00:33:09.599 --> 00:33:13.319
and their generally clonally reproducing parasites

00:33:13.319 --> 00:33:16.799
and pathogens. Combining DNA from two individuals

00:33:16.799 --> 00:33:19.519
creates new variants a lot faster than having

00:33:19.519 --> 00:33:22.759
to mutate them from scratch. And the same is

00:33:22.759 --> 00:33:25.559
true for polypoids. When we look across environments,

00:33:25.740 --> 00:33:28.039
polypoids are associated with two things. As

00:33:28.039 --> 00:33:30.619
you say, extreme environments and also humans.

00:33:31.400 --> 00:33:33.539
Humans, and this is mostly true for agricultural

00:33:33.539 --> 00:33:35.960
species like the wheat that I mentioned, because

00:33:35.960 --> 00:33:38.460
when we find weirdos that have traits that we

00:33:38.460 --> 00:33:40.960
like, even if those traits would have put them

00:33:40.960 --> 00:33:43.859
at a disadvantage out in the wild, we baby them

00:33:43.859 --> 00:33:46.460
and we breed them a bunch. So like with wheat,

00:33:46.559 --> 00:33:49.539
most grasses have tiny dinky little seeds, and

00:33:49.539 --> 00:33:52.519
most of what's adaptive about them is their ability

00:33:52.519 --> 00:33:55.900
to delay germination, to resist being eaten or

00:33:55.900 --> 00:33:58.200
resist digestion if they are eaten, or to spread

00:33:58.200 --> 00:34:01.150
as far as possible. But wheat, on the other hand,

00:34:01.250 --> 00:34:03.750
has these giant honking brains that we love,

00:34:03.869 --> 00:34:06.069
but are pretty terrible for avoiding being eaten

00:34:06.069 --> 00:34:09.670
or dispersed. And it turns out the same goes

00:34:09.670 --> 00:34:12.650
in extreme environments. A lot of polypoids,

00:34:12.769 --> 00:34:15.610
where they are viable, have exaggerated characteristics

00:34:15.610 --> 00:34:18.070
compared to those normal voiding individuals

00:34:18.070 --> 00:34:20.730
in their next seasons. So think like wheat with

00:34:20.730 --> 00:34:23.789
the giant seeds. They're often what Stephen Jay

00:34:23.789 --> 00:34:27.110
Gould once called hopeful monsters, obvious mutants

00:34:27.110 --> 00:34:28.789
that are just looking for the right environment.

00:34:29.469 --> 00:34:31.769
And in places where you're competing with normal

00:34:31.769 --> 00:34:33.670
-point individuals in an ancestral environment,

00:34:33.829 --> 00:34:36.369
you may be at a disadvantage. But if you happen

00:34:36.369 --> 00:34:39.650
to disperse into an extreme environment, extreme

00:34:39.650 --> 00:34:42.429
here simply meaning beyond the normal environmental

00:34:42.429 --> 00:34:45.369
tolerances for that species, immediately you've

00:34:45.369 --> 00:34:47.610
got less competition than the normal -point individuals.

00:34:47.989 --> 00:34:50.409
And if those exaggerated characteristics make

00:34:50.409 --> 00:34:52.889
you better suited for that environment than normal

00:34:52.889 --> 00:34:55.010
-point individuals, then you're off to the races.

00:34:55.550 --> 00:34:57.429
Ecologists would say you're exploiting a new

00:34:57.429 --> 00:35:00.849
niche. But to bring it home to Sturgeon, why

00:35:00.849 --> 00:35:03.429
Sturgeon specifically exhibit this kind of ploidy

00:35:03.429 --> 00:35:07.349
variation, my guess is that this is genomic flexibility.

00:35:07.389 --> 00:35:10.510
It has more to do with a slow mutation rate and

00:35:10.510 --> 00:35:13.929
a compound history of polyploidy than an adaptively

00:35:13.929 --> 00:35:16.889
retained ability to tolerate or utilize changes.

00:35:17.349 --> 00:35:20.070
Though, sort of to your broader point, whether

00:35:20.070 --> 00:35:23.150
that has given them an advantage to weather the

00:35:23.150 --> 00:35:25.530
many changes that they have seen over 300 million

00:35:25.530 --> 00:35:27.929
years, that's an open question. Yeah, I don't

00:35:27.929 --> 00:35:29.230
think we really have the answer for that yet.

00:35:29.730 --> 00:35:32.570
Okay, I'm going to go on a short tangent because

00:35:32.570 --> 00:35:34.369
I don't know if you have the answer. You mentioned

00:35:34.369 --> 00:35:37.349
extreme environments and environments where you

00:35:37.349 --> 00:35:41.309
can change quickly, where you have less, you

00:35:41.309 --> 00:35:44.989
know, other animals and plants being in competition

00:35:44.989 --> 00:35:48.130
with you. What about things like ocean islands

00:35:48.130 --> 00:35:51.070
that, you know, volcanic, they're wiped clean.

00:35:51.389 --> 00:35:54.250
Is this another type of environment where Ploody

00:35:54.250 --> 00:35:58.019
can take it? So I'm thinking Galapagos, I'm thinking

00:35:58.019 --> 00:36:01.880
Hawaii, I'm thinking those sorts of really extreme

00:36:01.880 --> 00:36:05.420
but yet isolated environments. Yeah, so islands

00:36:05.420 --> 00:36:07.780
have always been sort of a natural laboratory

00:36:07.780 --> 00:36:13.179
for evolutionary diversification and adaptation.

00:36:13.559 --> 00:36:15.960
And there are a number of reasons for that. Islands,

00:36:16.199 --> 00:36:19.059
as you say... They often have less competition

00:36:19.059 --> 00:36:20.960
because there are so many fewer species, which

00:36:20.960 --> 00:36:24.000
means that there are a lot of unoccupied niches.

00:36:24.039 --> 00:36:26.260
They tend to be very isolated, so there's not

00:36:26.260 --> 00:36:28.840
a lot of input from other populations that would

00:36:28.840 --> 00:36:31.239
prevent you from adapting to those new environments.

00:36:31.699 --> 00:36:34.599
And they often have very small population sizes.

00:36:34.800 --> 00:36:37.599
And so you have, it's technically inbreeding,

00:36:37.659 --> 00:36:39.679
but essentially what's happening in populations,

00:36:39.679 --> 00:36:42.969
you always have a balance between. Things that

00:36:42.969 --> 00:36:44.769
are happening because of genetic drift. So these

00:36:44.769 --> 00:36:47.250
are just numerical things that gene frequencies

00:36:47.250 --> 00:36:50.070
change because they're just a limited number

00:36:50.070 --> 00:36:52.969
of individuals and natural selection. Natural

00:36:52.969 --> 00:36:56.349
selection is creating adaptation. And so those

00:36:56.349 --> 00:37:00.489
factors are often in conflict with one another

00:37:00.489 --> 00:37:04.110
because a drift will often sort of accidentally

00:37:04.110 --> 00:37:09.550
take you away from the adaptive. field that you're

00:37:09.550 --> 00:37:11.650
looking for. I don't want to anthropomorphize

00:37:11.650 --> 00:37:17.449
it. That is optimal. And so in large populations,

00:37:17.869 --> 00:37:21.510
natural selection is less opposed by drift, and

00:37:21.510 --> 00:37:23.670
therefore it can be more effective. And in small

00:37:23.670 --> 00:37:25.809
populations, drift is a much bigger force. And

00:37:25.809 --> 00:37:28.190
what that can sometimes mean is you can drift

00:37:28.190 --> 00:37:31.829
over into different phenotypes that are actually

00:37:31.829 --> 00:37:35.750
better for niches, unoccupied niches that you

00:37:35.750 --> 00:37:38.119
wouldn't have been able to exploit before. And

00:37:38.119 --> 00:37:41.559
that can be true for polyploidy as well. Think

00:37:41.559 --> 00:37:44.860
of polyploidy as being sort of the oddballs that

00:37:44.860 --> 00:37:46.719
normally they would get selected out. But when

00:37:46.719 --> 00:37:48.699
you're in these isolated environments where you're

00:37:48.699 --> 00:37:51.300
not getting input from a lot of nomoploidy individuals,

00:37:51.639 --> 00:37:54.460
it doesn't take that many polyploid individuals

00:37:54.460 --> 00:37:57.860
to start an entire new population. So that combined

00:37:57.860 --> 00:38:00.280
with the unoccupied niches, with the isolation,

00:38:00.719 --> 00:38:03.380
all those kinds of things, gives them an opportunity

00:38:03.380 --> 00:38:06.159
that they wouldn't normally have in mainland

00:38:06.159 --> 00:38:10.449
environments. Cool. All right. So we know they

00:38:10.449 --> 00:38:13.889
have complex genetics and I don't really want

00:38:13.889 --> 00:38:15.969
to get into it, but I will just kind of drop

00:38:15.969 --> 00:38:17.969
it. We have a society that has gotten confused

00:38:17.969 --> 00:38:20.409
when talking about the rare cases in human genetics

00:38:20.409 --> 00:38:25.829
when it comes to sex. But with four or six different

00:38:25.829 --> 00:38:32.940
pairs or chromosome groups like. Can they switch

00:38:32.940 --> 00:38:35.820
sexes like other species? Is there some combination

00:38:35.820 --> 00:38:38.139
of chromosomes that kind of try to determine

00:38:38.139 --> 00:38:39.900
this? Like, it's got to be way more complicated

00:38:39.900 --> 00:38:44.420
for them than it is for us. It is. I mean, it's

00:38:44.420 --> 00:38:47.139
also in some ways sort of fundamentally different

00:38:47.139 --> 00:38:49.400
because, as I alluded to, sex is one of the primary

00:38:49.400 --> 00:38:52.360
reasons that genomes are forced to restructure

00:38:52.360 --> 00:38:56.030
after a polyploidization event. So, for example,

00:38:56.050 --> 00:38:59.110
in mammal species, which have an XY sex chromosome

00:38:59.110 --> 00:39:02.570
system like humans, females, which of course

00:39:02.570 --> 00:39:05.809
have two X chromosomes, one of them is generally

00:39:05.809 --> 00:39:09.110
completely turned off during development or silent

00:39:09.110 --> 00:39:12.309
to maintain the same dosage as in males, which

00:39:12.309 --> 00:39:14.789
only have a single act, right? And an interesting

00:39:14.789 --> 00:39:17.070
manifestation of this, if you've ever seen a

00:39:17.070 --> 00:39:19.329
tortoiseshell cat, which have that attractive

00:39:19.329 --> 00:39:22.170
black and orange spotting. It's because of that

00:39:22.170 --> 00:39:26.469
gene or colors on the X chromosome in cats. And

00:39:26.469 --> 00:39:30.250
which X chromosome is silenced can vary across

00:39:30.250 --> 00:39:32.769
the body in early development in females, which

00:39:32.769 --> 00:39:35.710
leads to different versions of the gene being

00:39:35.710 --> 00:39:38.929
expressed in different patches of skin. But to

00:39:38.929 --> 00:39:41.070
your question, part of the reason why it's very

00:39:41.070 --> 00:39:43.409
different in sturgeons to a degree is because

00:39:43.409 --> 00:39:48.320
they show a ZW sex determination system. Birds

00:39:48.320 --> 00:39:50.760
generally have a ZW sex determination system,

00:39:50.920 --> 00:39:54.380
and that's where the female is the sex with the

00:39:54.380 --> 00:39:57.539
two different sex chromosomes rather than the

00:39:57.539 --> 00:40:00.019
male. And so just to be obvious about that, we

00:40:00.019 --> 00:40:03.940
say ZW instead of XY in these female heterogametic

00:40:03.940 --> 00:40:07.460
species. And we know that that's true, that sturgeons

00:40:07.460 --> 00:40:10.280
have a ZW sex determination system because you

00:40:10.280 --> 00:40:14.239
can actually feminize or masculinize fish using

00:40:14.239 --> 00:40:18.280
hormones. So when feminized males are used, so

00:40:18.280 --> 00:40:21.079
this would be a fish that only has the ZZ chromosome,

00:40:21.360 --> 00:40:23.940
they produce all male offspring because there

00:40:23.940 --> 00:40:27.360
are no W chromosomes amongst them. Whereas if

00:40:27.360 --> 00:40:31.659
you masculinize females and make ZW females be

00:40:31.659 --> 00:40:35.480
male, they produce both male and female offspring,

00:40:35.619 --> 00:40:37.500
although the ratio is messed up because there

00:40:37.500 --> 00:40:40.619
are now more W chromosomes than there would usually

00:40:40.619 --> 00:40:44.039
be. And indeed, in the sterlet sturgeon, that

00:40:44.039 --> 00:40:46.820
diploid European sturgeon that I may have mentioned

00:40:46.820 --> 00:40:50.360
before, there is a region on one chromosome that's

00:40:50.360 --> 00:40:54.079
only present in females, as expected. And it

00:40:54.079 --> 00:40:55.900
happens to be a gene that's strongly expressed

00:40:55.900 --> 00:40:59.739
in the sex organs of some other fishes. And then

00:40:59.739 --> 00:41:02.079
we found the same region present in white sturgeon,

00:41:02.099 --> 00:41:05.119
too. And it seems to predict sex pretty well,

00:41:05.199 --> 00:41:07.119
depending on which population you're looking

00:41:07.119 --> 00:41:10.000
at. But all of that being said... It's true.

00:41:10.099 --> 00:41:13.280
We don't know how much environment may play a

00:41:13.280 --> 00:41:16.360
role in determining sex of sturgeon. It is possible

00:41:16.360 --> 00:41:18.559
that this genomic region that we found, both

00:41:18.559 --> 00:41:22.139
in these two seasons of sturgeon, can be mediated

00:41:22.139 --> 00:41:25.619
or completely overridden in certain environments.

00:41:25.860 --> 00:41:29.199
And that could cause some noise around what the

00:41:29.199 --> 00:41:31.900
markers that we develop from this predict in

00:41:31.900 --> 00:41:36.599
terms of sex. Interesting. All that to say is

00:41:36.599 --> 00:41:40.639
it's possible, but we don't know. It is possible.

00:41:40.820 --> 00:41:44.960
So as I thought this earlier and didn't get a

00:41:44.960 --> 00:41:48.820
chance, the other wonky thing about sturgeon

00:41:48.820 --> 00:41:53.139
is that not only are they probably functional

00:41:53.139 --> 00:41:55.579
tetraploids themselves, they also show spontaneous

00:41:55.579 --> 00:41:58.420
autopolyploids. So these are the fish with the

00:41:58.420 --> 00:42:01.119
six N chromosomes that you were talking about.

00:42:01.639 --> 00:42:05.079
And these spontaneous autopoly, what we know

00:42:05.079 --> 00:42:07.760
is that they have one and a half times. the normal

00:42:07.760 --> 00:42:10.579
amount of dna normal for white turkish which

00:42:10.579 --> 00:42:13.920
is of course a sort of a more of this concept

00:42:13.920 --> 00:42:16.960
but these individuals then one and a half times

00:42:16.960 --> 00:42:19.960
would either be um hexaploid the six in you mentioned

00:42:19.960 --> 00:42:21.880
or if you're talking ancestrally they could be

00:42:21.880 --> 00:42:24.340
dodecaploid 12n or if you consider that white

00:42:24.340 --> 00:42:27.280
spirits are normally diploid they are triploid

00:42:27.280 --> 00:42:30.659
but and i can i can talk about how we think that

00:42:30.659 --> 00:42:32.820
actually happens is spontaneous auto polyploidy

00:42:32.820 --> 00:42:36.780
but the weirder part is as a rule triploid fish

00:42:36.780 --> 00:42:39.480
are sterile right in fact triploid fish you may

00:42:39.480 --> 00:42:41.860
have heard of these rainbow trout brass carp

00:42:41.860 --> 00:42:44.900
atlantic salmon are often stocked in the wild

00:42:44.900 --> 00:42:47.400
specifically because they're sterile because

00:42:47.400 --> 00:42:50.000
they won't invade habitats or interbreed with

00:42:50.000 --> 00:42:52.599
wild fish and they're sterile because having

00:42:52.599 --> 00:42:54.760
three sets of chromosomes when they go to make

00:42:54.760 --> 00:42:57.119
their haploid gametes the chromosomes get all

00:42:57.119 --> 00:42:59.519
shuffled up in unpredictable ways and their gametes

00:42:59.519 --> 00:43:02.539
end up having uneven set that is their aneuploid

00:43:03.019 --> 00:43:05.320
But I guess nobody told white sturgeon, because

00:43:05.320 --> 00:43:08.179
while we've found that these one and a half times

00:43:08.179 --> 00:43:11.179
variants are rare in the wild, they're still

00:43:11.179 --> 00:43:13.880
present, but they're rare. They're pretty common

00:43:13.880 --> 00:43:16.619
in hatcheries, common enough that they've been

00:43:16.619 --> 00:43:19.699
unintentionally crossed with normal ploidy sturgeon.

00:43:19.820 --> 00:43:22.179
And lo and behold, they produce five offspring

00:43:22.179 --> 00:43:24.360
with an intermediate ploidy, which is probably

00:43:24.360 --> 00:43:28.159
safest to call pentaploid, I guess, which is

00:43:28.159 --> 00:43:30.119
five sets of chromosome. And we don't really

00:43:30.119 --> 00:43:32.940
know a lot about these pentaploids except that

00:43:32.940 --> 00:43:35.800
they're viable. So it's sort of an open question

00:43:35.800 --> 00:43:37.880
as to whether or not they could be important

00:43:37.880 --> 00:43:41.119
evolutionarily if they were created out in the

00:43:41.119 --> 00:43:43.460
wild and half the population. But the point,

00:43:43.539 --> 00:43:46.639
you know, to your point is that those spontaneous

00:43:46.639 --> 00:43:49.880
autopolyploids, the one and a half times fish,

00:43:50.059 --> 00:43:53.019
that are hexaploid, dodecaploid, triploid, whatever

00:43:53.019 --> 00:43:56.019
you call them. are at least viable and partly

00:43:56.019 --> 00:43:59.059
fertile. And you can sort of imagine that there

00:43:59.059 --> 00:44:02.480
are situations where enough of them were accumulating

00:44:02.480 --> 00:44:04.579
out there in sort of an isolated environment

00:44:04.579 --> 00:44:06.980
that they actually could create an entirely new

00:44:06.980 --> 00:44:10.860
population. And so that sort of gives you a bridge

00:44:10.860 --> 00:44:14.119
or a window to how these higher ploidies could

00:44:14.119 --> 00:44:16.300
have formed in the first place. And you have

00:44:16.300 --> 00:44:18.619
these sort of strange cellular developmental

00:44:18.619 --> 00:44:23.340
things going on that result from sort of... breakdowns

00:44:23.340 --> 00:44:25.960
in environmental conditions and just create this

00:44:25.960 --> 00:44:29.639
sort of convergence of conditions where new set

00:44:29.639 --> 00:44:32.900
of OED variants happen to start reproducing and

00:44:32.900 --> 00:44:38.119
diverge from the original population. Okay, so

00:44:38.119 --> 00:44:40.880
let's go back to the paper. You're using DNA

00:44:40.880 --> 00:44:44.559
markers to figure out whether or not individuals

00:44:44.559 --> 00:44:48.960
are male or female. And according to this, you're

00:44:48.960 --> 00:44:51.730
like, you can't. see, I would imagine, a fish,

00:44:51.769 --> 00:44:53.269
whether it's male or female, just by looking

00:44:53.269 --> 00:44:56.369
at it. And so you're using genetics and you're

00:44:56.369 --> 00:44:59.989
96 % accurate for females, but only 81 % for

00:44:59.989 --> 00:45:03.250
males. Why is it easier to spot the female genetically?

00:45:03.409 --> 00:45:06.530
And is it a null result sometimes instead of

00:45:06.530 --> 00:45:09.309
like, say, a false positive or false negative?

00:45:09.769 --> 00:45:12.489
Yeah, it's certainly possible that some cases

00:45:12.489 --> 00:45:15.710
where our sex markers aren't 100 % accurate could

00:45:15.710 --> 00:45:19.699
be. because of the failure of the molecular assay,

00:45:19.699 --> 00:45:22.900
something that we call a null allele, where the

00:45:22.900 --> 00:45:25.519
genomic region is there in that individual, but

00:45:25.519 --> 00:45:29.239
our assay simply fails to pick it up. And that

00:45:29.239 --> 00:45:33.000
would explain why some females were predicted

00:45:33.000 --> 00:45:36.739
to be males, but not why males would be predicted

00:45:36.739 --> 00:45:40.119
to be females. In those cases, it's not the assay

00:45:40.119 --> 00:45:42.239
that's failing, since we can clearly see that

00:45:42.239 --> 00:45:46.190
the genomic region is present. but rather a failed

00:45:46.190 --> 00:45:50.530
association of the genomic region with phenotypic

00:45:50.530 --> 00:45:53.489
sex. And I think what's actually going on is

00:45:53.489 --> 00:45:58.030
any or all of three things. One, it's possible

00:45:58.030 --> 00:46:00.829
that the sex data for our samples are wrong for

00:46:00.829 --> 00:46:02.730
some populations. That is, which are males and

00:46:02.730 --> 00:46:04.489
which are females was just misrecorded. As a

00:46:04.489 --> 00:46:06.349
scientist, you have to be upfront about the fact

00:46:06.349 --> 00:46:08.869
that your data may just be flawed in some cases.

00:46:09.010 --> 00:46:12.519
And the fact that our markers are... 100 % accurate

00:46:12.519 --> 00:46:15.260
for fish whose sex I have personally confirmed,

00:46:15.579 --> 00:46:18.300
not by looking under the hood, but through offspring

00:46:18.300 --> 00:46:21.460
of known crosses, sort of indicates that in some

00:46:21.460 --> 00:46:25.260
cases. But two, as we said earlier, it's possible

00:46:25.260 --> 00:46:28.179
that in some cases environment may play more

00:46:28.179 --> 00:46:30.760
of a role in determining sex than we understand.

00:46:31.239 --> 00:46:33.619
But three, and this is my preferred hypothesis,

00:46:33.920 --> 00:46:36.159
or at least the one I'm most interested in pursuing,

00:46:36.400 --> 00:46:40.380
that how far down the process of re -diploidization

00:46:40.989 --> 00:46:43.170
and specifically how much exchange between those

00:46:43.170 --> 00:46:46.829
ancestral sex chromosomes there still is, varies

00:46:46.829 --> 00:46:50.110
from one population to another. And so the association

00:46:50.110 --> 00:46:53.710
of our markers and perhaps even how that genomic

00:46:53.710 --> 00:46:58.469
region mediates sex may vary from one sturgeon

00:46:58.469 --> 00:47:01.230
population to another. And indeed, some of the

00:47:01.230 --> 00:47:03.710
data that we use to make our genome assembly

00:47:03.710 --> 00:47:06.550
indicate that at least in the Middle Snake River

00:47:06.550 --> 00:47:09.099
in Idaho, which is one of the places where our

00:47:09.099 --> 00:47:11.840
sex markers aren't 100 % accurate. There is still

00:47:11.840 --> 00:47:14.739
some recombination between those ancestral sex

00:47:14.739 --> 00:47:17.980
chromosomes. Okay, well, let's try to give this

00:47:17.980 --> 00:47:22.559
a little bit more real world heft to it now.

00:47:23.860 --> 00:47:26.480
How does this, I guess I'm going to add something

00:47:26.480 --> 00:47:28.980
to my original question is like, how does this

00:47:28.980 --> 00:47:32.300
further our understanding of genetics in the

00:47:32.300 --> 00:47:35.719
animal kingdom? And how do we use this to like

00:47:35.719 --> 00:47:39.079
help? conservation of the species like how do

00:47:39.079 --> 00:47:42.500
we how do we use this information in practice

00:47:42.500 --> 00:47:47.179
yeah it's you know been a few decades now since

00:47:47.179 --> 00:47:51.800
we sequenced the human genome and we know a lot

00:47:51.800 --> 00:47:54.260
more than we did then but every day we sort of

00:47:54.260 --> 00:47:56.679
find out that our understanding of what genomes

00:47:56.679 --> 00:48:00.639
are how they work what's wrong and that's science

00:48:00.639 --> 00:48:02.820
that's how that's supposed to work you know so

00:48:02.820 --> 00:48:06.650
for example these days we're interested in structural

00:48:06.650 --> 00:48:08.710
variation. So structural variation of genomes

00:48:08.710 --> 00:48:12.929
is entire sections of the genome that are present

00:48:12.929 --> 00:48:15.969
in one individual or missing in another, or regions

00:48:15.969 --> 00:48:18.429
that are, you know, reversed so that they're

00:48:18.429 --> 00:48:21.210
in the opposite direction from one individual

00:48:21.210 --> 00:48:23.829
to another. We sort of originally thought that

00:48:23.829 --> 00:48:26.050
genomes were basically the same, except, you

00:48:26.050 --> 00:48:29.030
know, I've got an A and you've got a T, and over

00:48:29.030 --> 00:48:31.309
here you've got a G and I've got a C, that they're

00:48:31.309 --> 00:48:33.730
very small differences. It turns out that even

00:48:33.730 --> 00:48:35.469
among individuals of some species, there can

00:48:35.469 --> 00:48:39.090
be huge, very big differences in the chromosomes

00:48:39.090 --> 00:48:42.050
between individuals. And so that is particularly

00:48:42.050 --> 00:48:45.110
true for polypoids, where not only is that happening

00:48:45.110 --> 00:48:48.630
between just very small homologous chromosomes,

00:48:48.769 --> 00:48:52.070
but chromosomes that have a much larger ancestral

00:48:52.070 --> 00:48:55.949
relationship. And so the way the genomes evolve

00:48:55.949 --> 00:49:00.610
or redepoidize following polypoidization provides

00:49:00.610 --> 00:49:03.420
a good window into understanding that. But as

00:49:03.420 --> 00:49:05.800
to the conservation of this species, which, of

00:49:05.800 --> 00:49:08.239
course, is what I'm interested in on behalf of

00:49:08.239 --> 00:49:10.980
the tribe, it's easier to imagine that folks

00:49:10.980 --> 00:49:12.920
running commercial caviar farms would like to

00:49:12.920 --> 00:49:16.239
know which fish are female as early as possible

00:49:16.239 --> 00:49:18.820
so they can maximize their root hormone on investment.

00:49:19.039 --> 00:49:21.559
But that's not really our target audience. On

00:49:21.559 --> 00:49:23.260
behalf of the tribes, we're focused on trying

00:49:23.260 --> 00:49:25.880
to maintain or rebuild the fisheries of these

00:49:25.880 --> 00:49:28.610
species and understanding. Population dynamics

00:49:28.610 --> 00:49:31.230
is a critical part of that, like the sex ratio

00:49:31.230 --> 00:49:34.409
of wild populations or how many females reproduce

00:49:34.409 --> 00:49:37.449
in a year and with how many males. And being

00:49:37.449 --> 00:49:39.869
able to take a thin clip and predict sex rather

00:49:39.869 --> 00:49:42.969
than having to do an abdominal biopsy makes that

00:49:42.969 --> 00:49:45.449
data a lot more accessible. But beyond that,

00:49:45.530 --> 00:49:47.590
because there are a lot of populations that are

00:49:47.590 --> 00:49:50.269
slowly declining because of a lack of consistent

00:49:50.269 --> 00:49:53.969
recruitment and reproduction, a number of conservation

00:49:53.969 --> 00:49:57.739
aquaculture programs. hatcheries that are specifically

00:49:57.739 --> 00:50:01.099
focused on rebuilding wild populations have been

00:50:01.099 --> 00:50:03.219
developed to supplement those wild populations.

00:50:03.420 --> 00:50:05.639
And while they have become very adept at producing

00:50:05.639 --> 00:50:08.019
many young sturgeons, they're very effective.

00:50:08.400 --> 00:50:11.659
We don't know whether those aquaculture practices

00:50:11.659 --> 00:50:15.000
bias the resulting offspring towards one sex

00:50:15.000 --> 00:50:17.679
or another. For example, it's possible that male

00:50:17.679 --> 00:50:20.289
sturgeon grow faster than female. And at high

00:50:20.289 --> 00:50:22.650
densities, like there are atrophied males, may

00:50:22.650 --> 00:50:24.750
out -compete females and produce, therefore,

00:50:24.869 --> 00:50:26.710
a male -biased population. You don't want to

00:50:26.710 --> 00:50:28.969
dump a whole bunch of males back into the wild

00:50:28.969 --> 00:50:32.489
because that screws up the population. So since

00:50:32.489 --> 00:50:34.909
you can't sex young sturgeon until they're basically

00:50:34.909 --> 00:50:37.630
begun to mature, having a molecular assay, like

00:50:37.630 --> 00:50:40.610
we've developed from this marker, is a much more

00:50:40.610 --> 00:50:42.610
effective way of doing that at earlier life stages.

00:50:43.750 --> 00:50:46.329
Okay, so you're providing the information needed

00:50:46.329 --> 00:50:49.349
for those that are making the policy decisions

00:50:49.349 --> 00:50:51.889
about how to do the conservation. You're giving

00:50:51.889 --> 00:50:54.460
them the tools to make those decisions. Yeah,

00:50:54.559 --> 00:50:57.820
we're much more focused on sort of the state

00:50:57.820 --> 00:50:59.940
agencies that are putting into action policies,

00:50:59.940 --> 00:51:02.019
something that we need to be people who have,

00:51:02.099 --> 00:51:04.639
you know, in a higher pay grade. Right. But you're

00:51:04.639 --> 00:51:06.739
giving them the information to make those policy

00:51:06.739 --> 00:51:09.139
decisions. I mean, in a volcanology sense, a

00:51:09.139 --> 00:51:11.119
volcanologist isn't the one telling people to

00:51:11.119 --> 00:51:13.500
evacuate. The volcanologist is telling them,

00:51:13.539 --> 00:51:15.460
OK, this is what's happening. This is the likely

00:51:15.460 --> 00:51:18.219
outcome. And then the policy people who make

00:51:18.219 --> 00:51:20.239
a lot more money typically, not always, but typically

00:51:20.239 --> 00:51:22.420
make the decision whether or not you need to

00:51:22.420 --> 00:51:26.099
get out of town. Yes, yes, exactly. We provide

00:51:26.099 --> 00:51:28.559
as much information as we can, and what they

00:51:28.559 --> 00:51:31.280
choose to do with it is beyond our purview, unfortunately.

00:51:31.780 --> 00:51:36.199
Exactly, exactly. Okay, so I'm kind of glad to

00:51:36.199 --> 00:51:38.980
see that it's working similarly in two completely

00:51:38.980 --> 00:51:41.699
different disciplines, actually. That's science,

00:51:41.840 --> 00:51:46.199
yes. For better or worse. It goes both ways.

00:51:46.340 --> 00:51:48.260
Sometimes you really don't want the scientists

00:51:48.260 --> 00:51:50.480
making the decision for people sometimes, and

00:51:50.480 --> 00:51:54.840
sometimes it would actually be better. I'm biased

00:51:54.840 --> 00:51:57.579
there, I guess. Yeah, no, having everybody at

00:51:57.579 --> 00:51:59.320
the table is not the right way to do it. It's

00:51:59.320 --> 00:52:01.539
just being able to respect everyone's opinions

00:52:01.539 --> 00:52:07.860
is sometimes the challenge. Yeah. On that note,

00:52:08.000 --> 00:52:11.699
I'm going to skip one of my questions because

00:52:11.699 --> 00:52:14.019
I think it's kind of wrapped up here in the same.

00:52:14.360 --> 00:52:16.659
So the Fraser River, it's a river that connects

00:52:16.659 --> 00:52:19.559
my home turf and more broadly for my local river.

00:52:20.119 --> 00:52:21.699
What is the future for this species? Because

00:52:21.699 --> 00:52:24.239
you've mentioned the Snake River already being

00:52:24.239 --> 00:52:27.639
already quite different. But I know you're focused

00:52:27.639 --> 00:52:30.239
more on the Columbia and its tributaries. But

00:52:30.239 --> 00:52:33.300
what can you say about the Fraser and what needs

00:52:33.300 --> 00:52:37.719
to happen to protect it? Yeah. So as we said,

00:52:37.840 --> 00:52:40.079
the Columbia has a major challenge of having

00:52:40.079 --> 00:52:43.199
all of these dams. And you can imagine that.

00:52:43.900 --> 00:52:46.000
prehistorically a five meter fish could go basically

00:52:46.000 --> 00:52:49.079
anywhere it wanted in in the basin you know if

00:52:49.079 --> 00:52:50.860
there are different sections of the river basin

00:52:50.860 --> 00:52:54.639
that are better for reproduction for growth or

00:52:54.639 --> 00:52:57.139
you know hanging out in hot summer temperatures

00:52:57.139 --> 00:52:59.159
that kind of thing you could choose that and

00:52:59.159 --> 00:53:01.059
you put in dams in the way well now you just

00:53:01.059 --> 00:53:03.519
got to deal with whatever is available and unfortunately

00:53:03.519 --> 00:53:06.360
in many of these sections there's not enough

00:53:06.360 --> 00:53:09.630
good habitat for rearing in the early life stages,

00:53:09.849 --> 00:53:11.690
that they're getting a lot of recruitment. And

00:53:11.690 --> 00:53:13.710
so what is there is getting older and older,

00:53:14.210 --> 00:53:16.710
and as a result, the populations diminish over

00:53:16.710 --> 00:53:20.170
time. The Frasier does not have that problem

00:53:20.170 --> 00:53:23.010
of damming. From my understanding, the biggest

00:53:23.010 --> 00:53:25.650
threats to the Frasier white sturgeon are habitat

00:53:25.650 --> 00:53:29.170
degradation and the diminishing runs of the naturalist

00:53:29.170 --> 00:53:31.949
fish, particularly chum, phantom, and eucalon.

00:53:32.480 --> 00:53:35.320
It may be strange to think of a freshwater fish

00:53:35.320 --> 00:53:38.860
as being dependent on marine species, but these

00:53:38.860 --> 00:53:41.820
interior Pacific ecosystems have evolved with

00:53:41.820 --> 00:53:44.800
that regular influx of marine -derived nutrients.

00:53:45.079 --> 00:53:46.820
And that's especially true for white sturgeon,

00:53:46.940 --> 00:53:50.300
which depend on those returning fish, their carcasses,

00:53:50.420 --> 00:53:53.639
their eggs, their offspring for food. And as

00:53:53.639 --> 00:53:58.099
those runs diminish, it's likely that sturgeon

00:53:58.099 --> 00:54:01.139
will continue to do so too, unfortunately. And

00:54:01.139 --> 00:54:06.980
we're already hearing reports of, and I should

00:54:06.980 --> 00:54:09.420
say, that's not something that conservation aquaculture

00:54:09.420 --> 00:54:11.940
can overcome. You can dump a bunch of young fish

00:54:11.940 --> 00:54:13.940
in the river, but if there's nothing for them

00:54:13.940 --> 00:54:17.900
to eat, then you're just spinning your wheels.

00:54:18.119 --> 00:54:20.599
And we're already hearing reports this year of

00:54:20.599 --> 00:54:24.239
another warm water blob developing off of California

00:54:24.239 --> 00:54:27.679
and the prediction of a super El Nino later this

00:54:27.679 --> 00:54:31.679
year. So it seems to be that while there are

00:54:31.679 --> 00:54:34.059
things that we can do to give the Fraser River

00:54:34.059 --> 00:54:37.219
or the Columbia River sturgeon the best chance

00:54:37.219 --> 00:54:40.719
we can, their fate, like the fate of so many

00:54:40.719 --> 00:54:42.699
other species, is going to depend on whether

00:54:42.699 --> 00:54:46.119
we humans can get our act together as a species

00:54:46.119 --> 00:54:48.619
and realize that we're not entitled to be the

00:54:48.619 --> 00:54:50.440
center of the universe and start acting like

00:54:50.440 --> 00:54:55.099
good stewards, like we should be. So we could

00:54:55.099 --> 00:54:57.260
sum it up with essentially climate change. Yeah.

00:54:57.599 --> 00:54:59.940
I mean, that's certainly the train coming down

00:54:59.940 --> 00:55:02.679
the tracks, right? It's how long do we need to

00:55:02.679 --> 00:55:04.239
see the train before we decide that we're going

00:55:04.239 --> 00:55:08.579
to get off of it, off the tracks. And I'm actually

00:55:08.579 --> 00:55:10.460
more of an optimist than a doomsayer because

00:55:10.460 --> 00:55:15.739
I think being a doomsayer paralyzes action. We

00:55:15.739 --> 00:55:17.840
are doing stuff. Things are changing. It's just

00:55:17.840 --> 00:55:20.079
changing too slowly, to be fair. Yeah. Well,

00:55:20.239 --> 00:55:22.500
I mean, the science is there and it's really

00:55:22.500 --> 00:55:24.460
just a matter of political will when it comes

00:55:24.460 --> 00:55:27.260
down to it, which is both. promising and depressing.

00:55:27.659 --> 00:55:34.780
Yeah, it's both simultaneously. One of these

00:55:34.780 --> 00:55:37.000
days, actually, as a plug, I don't know if it'll

00:55:37.000 --> 00:55:39.699
be my last episode of the season, but because

00:55:39.699 --> 00:55:41.440
of just the nature of when things need to be

00:55:41.440 --> 00:55:43.320
published, because we're going to I have another

00:55:43.320 --> 00:55:44.900
one that I have to record that I don't know what

00:55:44.900 --> 00:55:47.480
I can get out. It's going to be all about volcanoes

00:55:47.480 --> 00:55:50.579
and climate change and how we know that volcanoes

00:55:50.579 --> 00:55:53.230
do not put out. nearly as much co2 as humans

00:55:53.230 --> 00:55:56.349
i'm going to go through the the nerdy math and

00:55:56.349 --> 00:55:58.170
the melt inclusions and the whole nine yards

00:55:58.170 --> 00:56:01.429
so that that i don't know if it'll help but you

00:56:01.429 --> 00:56:05.210
know what i mean yeah no dispelling any alternative

00:56:05.210 --> 00:56:07.909
then we're doing it to ourselves is definitely

00:56:07.909 --> 00:56:11.530
part of the puzzle okay so we're nearing the

00:56:11.530 --> 00:56:14.130
end and it's time for call outs this is your

00:56:14.130 --> 00:56:18.030
chance to flag cool projects something you're

00:56:18.030 --> 00:56:20.690
working on something completely random it's whatever

00:56:20.690 --> 00:56:23.039
you want Yeah, I mean, really, I just want to

00:56:23.039 --> 00:56:24.860
acknowledge all the people that have contributed

00:56:24.860 --> 00:56:28.340
to this. What we do with sturgeon is a team effort,

00:56:28.380 --> 00:56:31.599
and we have a number of irons in the fire. You

00:56:31.599 --> 00:56:33.719
know, we're looking at spontaneous autopolycoiding

00:56:33.719 --> 00:56:36.780
in wild fish because it seems to be happening

00:56:36.780 --> 00:56:40.280
in the wild as well in really hot weather years.

00:56:40.969 --> 00:56:45.449
We're continuing to look at how things like shad,

00:56:45.730 --> 00:56:47.570
which are the big thing in the Columbia River

00:56:47.570 --> 00:56:50.429
Basin now, huge, huge runs of shad that turn

00:56:50.429 --> 00:56:53.130
out to have a lot of something called thiaminase

00:56:53.130 --> 00:56:57.630
in their tissue. And that thiaminase causes the

00:56:57.630 --> 00:57:00.550
eggs to be thiamin deficient and for these fish

00:57:00.550 --> 00:57:04.900
to die or grow weird. So we have a number of

00:57:04.900 --> 00:57:07.699
projects that we're working on, and all of them

00:57:07.699 --> 00:57:10.619
depend on our collaborations with state agencies

00:57:10.619 --> 00:57:13.880
and universities to work. And in particular,

00:57:13.980 --> 00:57:16.860
I want to acknowledge the leadership of Janella

00:57:16.860 --> 00:57:19.719
Miller, who's now a manager with Pritvik, but

00:57:19.719 --> 00:57:22.219
was formerly with the Yakima Nation Fisheries

00:57:22.219 --> 00:57:24.599
when they developed their conservation aquaculture

00:57:24.599 --> 00:57:28.840
program. And she has been... Just a huge, steadfast

00:57:28.840 --> 00:57:31.159
champion for understanding and rebuilding white

00:57:31.159 --> 00:57:33.460
surgeon populations. I'm really glad to be able

00:57:33.460 --> 00:57:37.440
to work with her. Awesome. You know what that

00:57:37.440 --> 00:57:40.679
means. It's time for the infamous question. The

00:57:40.679 --> 00:57:43.539
one that I warn every single guest is coming.

00:57:43.699 --> 00:57:47.239
I warn it before they even see what kind of topics

00:57:47.239 --> 00:57:49.400
I'm going to ask them or anything else. It is

00:57:49.400 --> 00:57:53.420
the traditional last question. What is your favorite

00:57:53.420 --> 00:57:57.239
science joke? Yeah. I don't know if I would call

00:57:57.239 --> 00:58:02.139
it a joke or a lament, but I have always enjoyed

00:58:02.139 --> 00:58:04.199
the description of the kind of work that I do

00:58:04.199 --> 00:58:06.679
by a guy named John Shepard, who's sort of a

00:58:06.679 --> 00:58:11.059
famous fishery professor. He said that studying

00:58:11.059 --> 00:58:14.340
fish populations is exactly like studying forests,

00:58:14.679 --> 00:58:18.760
except you can't see them and they move, which

00:58:18.760 --> 00:58:21.739
I guess makes white sturgeon like the giant sequoias

00:58:21.739 --> 00:58:24.460
of the freshwater fish world. So I'm glad to

00:58:24.460 --> 00:58:29.219
be working on that. Perfect. Well, thank you

00:58:29.219 --> 00:58:31.780
so much for taking the time to come on and teaching

00:58:31.780 --> 00:58:34.380
me a lot about white surgeon. Yep. I'm always

00:58:34.380 --> 00:58:36.360
happy to talk about surgeon and genetics. My

00:58:36.360 --> 00:58:40.159
favorite things. And that brings the second to

00:58:40.159 --> 00:58:45.659
last episode of season two to an end. Okay. So

00:58:45.659 --> 00:58:49.039
that means that next episode is the last of season

00:58:49.039 --> 00:58:52.159
two and it's going to be a solo episode. All

00:58:52.159 --> 00:58:58.659
about volcanoes and CO2 and climate change. A

00:58:58.659 --> 00:59:01.719
little bit of a historical romp, I guess, through

00:59:01.719 --> 00:59:06.000
how we can prove that volcanoes do not put out

00:59:06.000 --> 00:59:09.079
anywhere near the amount of CO2 that humans do.

00:59:09.360 --> 00:59:14.980
A fitting way to end Season 2. At any rate, just

00:59:14.980 --> 00:59:17.059
remember that over the summer there will be encore

00:59:17.059 --> 00:59:20.300
editions to kind of fill the feed to make sure

00:59:20.300 --> 00:59:23.409
that the... Computer overlords are still happy

00:59:23.409 --> 00:59:25.889
with whimsical wavelengths. And then we'll be

00:59:25.889 --> 00:59:28.150
back in September. There are a few things that

00:59:28.150 --> 00:59:30.090
could get into the mix, and I'll repeat these

00:59:30.090 --> 00:59:32.849
next time, because I'm also expecting a surgery

00:59:32.849 --> 00:59:35.510
somewhere over summer, and I really don't know

00:59:35.510 --> 00:59:38.190
when that'll happen. So hopefully everything

00:59:38.190 --> 00:59:40.889
lines up, and I'll be able to start Season 3

00:59:40.889 --> 00:59:46.489
on time September 14th. All right. I'll see you

00:59:46.489 --> 00:59:53.250
again in two weeks. so chaotic so misbehaved

00:59:53.250 --> 01:00:00.349
echoes of melodies remind us it's always colors

01:00:00.349 --> 01:00:08.090
weave stories painting the sky swaying to rhythms

01:00:08.090 --> 01:00:27.650
as the galaxies fly by deep in our bones through

01:00:27.650 --> 01:00:34.789
this melodic maze our minds explore change
