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Thursday, July 23, 2015

Botanizing in Alaska: Dwarf Birch

I found this tree trunk on a rocky outcrop at the top of a mountain just outside Fairbanks, Alaska. The wood was spread over a foot or so, though I didn't have a measuring-tape handy to get a precise measure. The cold and exposed environment suggests that the tree would have grown very slowly and may be anywhere from decades to hundreds of years old.

In this environment, strong winter winds quickly abrade away overly-exposed living material. Dead material doesn't last very long either. Yet this tree remains alive, with vital growth attached to the dead wood at the lower-right and upper-left.

It was only by comparing the above tree to something more youthful (at right) that I was able to identify it as the Dwarf Birch (Betula nana). Forests of this tree can be ancient, but only inches tall.


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Thursday, July 9, 2015

Botanizing in Alaska: Mountain Avens


The Mountain Avens (Dryas octopetala) is a circum-arctic subshrub, growing up to a meter across while reaching only a few centimeters tall. The flowers typically have eight petals (hence the name octopetala) and track the arctic sun as it rolls around the summer sky. This heliotropism is thought to help the flower warm up so it can mature its seeds more quickly. There are several subspecies, including the Alaskan form (D. octopetala ssp. alaskensis), but little information is available about the differences between the forms.

Since I found them after the flowers were long gone, identification was a bit trickier. The seed-heads reminded me of those from the Pasqueflower (Pulsatilla), so I started my searches there. The leaves are distinctly different, however, so I meandered into looking at images of arctic wildflowers from Alaska until I found an image that had the right leaves. I was lucky in that the site included an ID of the plant, which I rapidly confirmed elsewhere.

Supposedly the plant takes well to garden culture, though its short-stature would make it sensitive to being overgrown by aggressive weeds when in a warmer climate. I did collect a few seeds, so I hope to see how it does here.


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Saturday, July 4, 2015

Botanizing in Alaska: Wild Iris

I just returned from a week-long trip to Fairbanks in central Alaska. I quickly noted the abundant wild irises (Iris setosa interior) in bloom around the city. The species is endemic through much of Alaska, with a few regional subspecies/varieties. It goes by a few different common names. "Beachhead Iris" seems to be the most common, though I prefer "Alaska Iris" for the plants I encountered because it more clearly refers to the specific Alaskan sub-species.

While I was there, the local paper (Fairbanks Daily News-Miner) published an article about Jack Finch, a metalworking instructor at the local university, who has a long-running hobby of breeding I. setosa.

www.newsminer.com/features/our_town/an-eye-for-irises-grower-pulls-a-rainbow-of-varieties/article_db950be2-1d65-11e5-8207-4ff1af2d6​4db​.html

Though we tend to refer to all the colorful floral structures of a typical garden iris as "petals", the structures are botanically divided into the true petals (upright standards) and petaloid sepals (descending falls). In I. setosa, the botanical petals are reduced so severely that the flower appears to have only three "petals". Jack Finch occasionally sells plants in Fairbanks, which probably helps explain the diversity of colored forms I found in gardens during my week.


NewsMiner photo.
In addition to numerous shades, Jack Finch also isolated a recessive mutation which converts the tiny petals of the wild flower into full-sized sepals (thus producing an attractive and larger flower). I never did find an example of this flower, but the newspaper published a photo which nicely illustrates the variation.

During my trip I was able to collect seeds from several plants with different colored flowers. As the plants were in full bloom, the only seeds to be found were those left-over from the previous season or two. Hopefully they remain viable so that when I plant them this fall (for cold-stratification) they can start growing in spring.



The Iris genus is subdivided into several sub-genera, which are then in turn subdivided into several series of species. For the wild Iris setosa I was so admiring, the full nomenclature is something like: [Genus = Iris] [Subgenus = Limniris] [Series = Tripetalae] [Species = setosa] [Subspecies = interior].

Species definitions in plants are often less strict than they seem to be for animals. Some research from a few years ago sought to identify how I. setosa was related to other North American wild irises. They found I. setosa was most likely one of the parents (with I. virginica) of I. versicolor. I. setosa and I. virginica are both diploid with 38 (19/19) and 70 (35/35) chromosomes, respectively. The hybrid between the two species is infertile due to mis-paired chromosome sets (19/35). But like in other cases (http://the-biologist-is-in.blogspot.com/2015/01/hybrid-sterility-and-speciation.html), that infertility can be resolved by a whole genome duplication like that which appears to have happened in the ancestors of modern I. versicolor.



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Friday, June 19, 2015

Roses, Wild and Moreso

I've been very busy lately with the new full-time job and the ongoing efforts in my yard and garden areas. Unfortunately, this means my blog has drifted back to things I think about but don't spend much time on.

I did get to spend a recent weekend camping and hiking with the love of my life and some friends. I took lots of photos that will likely be scattered through several less-intensive biology posts than I started the blog with. I expect to do longer-form postings and have several that are in the works, but they may become less common until I get some of the house/yard duties done with.

So, what is that lovely flower you've been looking at in the photos at left? It is a wild rose I found growing in Devil's Lake State Park, just south of Baraboo, WI. It produces small white flowers in large numbers. Those small flowers are followed later by equally small rose hips (at right). The species grows wild over much of the USA, but it is only here because we brought it from its native range in eastern Asia. The large numbers of flowers produced in each cluster give it its name, Rosa multiflora.

The tiny rose-hips are spread by many small birds and the stupendous number of the fruit that a mature plant can produce helps to ensure that it grows densely (and spreads) whenever it is given the chance.

I'm somewhat interested in what a cross between R. multiflora and some smaller rose (like the presumed native rose at right, also from Devil's Lake) might look like, as well as the mix of traits that would crop up in the F2 generation.

I have plenty of interesting rose seeds already that I need to grow, so I probably don't need to start collecting breeding projects for them just yet.


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Wednesday, June 3, 2015

Strawberries Galore

I've been thinking a lot about what I wanted to do with my recently acquired property. Aside from the usual house and yard parties, and just relaxing under the shade of our lovely cottonwood tree, I've been thinking about installing some berry gardens.

Strawberries in particular are often in my thoughts. The plants produce numerous attractive flowers in early spring and the berries themselves are a wonderful treat. When I was a young child one of the neighbors had an amazing raised-garden full of strawberry plants, so there is also some nostalgia for me in the idea of picking ripe strawberries out in the yard.

Biologically, strawberries are in the same family as roses, raspberries, and blackberries. Remarkably, they can even hybridize with raspberries, though the reported hybrid have been completely sterile. The sterile hybrids produce wonderful flower displays, however, so they're not without value. As well, there remains the potential to correct the sterility and produce some [presumably] novel-tasting fruit. (http://the-biologist-is-in.blogspot.com/2015/01/hybrid-sterility-and-speciation.html)

With all that in mind, I've been collecting wild strawberry plants during my travels around the mid-west. I like the thought of discovering something 'new' and distinct from what I would get at the local garden center. I have also acquired a batch of modern domesticated plants from a fellow gardener in Minneapolis, because no matter how much I like the wild plants, I really do want to get some nice large berries out of this project.

  1. Wild strawberry from swamp in central Wisconsin.
    • Found growing on a raised trail in the center of a swamp in central Wisconsin. The plants filled in large areas of the trail and produced scattered small fruit held above the leaves. The flowers have petals facing more forward than the typical domesticated strawberry. The three leaflets of each leaf are narrower and more forward pointing than the typical domesticated strawberry.
  2. Wild strawberry from lake-shore in Brainerd, MN.
    • Found growing above the waterline in very sandy soil where they would experience periodic dryness. The plants formed wide colonies, but were small enough they could possibly be maintained in a mowed lawn. Ripe berries weren't seen, but several small ones are now developing.
  3. Wild strawberry from woodland in Brainerd, MN.
    • Found on the other side of the house from the other Brainerd sample, these were growing in deep shade underneath pines. The plants are large, similar to domesticated types.
  4. Wild strawberry from woodland in Duluth, MN.
    • Found growing in open woods. Large, flat-faced flowers are reminiscent of domesticated types. The plants are large, similar to domesticated types.
  5. Wild strawberry from open woods in Saint Paul, MN.
    • Found growing under tree cover adjacent to open area where it had spread across a low slope. The plants run wildly, but otherwise appear as a domesticated strawberry. Ripe berries have not been observed.
  6. Wild strawberry from Fairbanks, AK.
    • I don't actually have this plant yet, but I will be visiting central Alaska in the coming months and totally expect to do some botanizing while I'm there. The locals tell me that there are wonderful wild strawberries and I plan to pick up a few plants. They should be very cold-hardy and produce berries very early in the season. The big question is if they will be able to survive the heat of a mid-west summer.
  7. Domesticated strawberries (mixed varieties) from Minneapolis, MN.
    • These appear to be producing large berries, like you might find in stores. Some of the plants were described as being "alpine" strawberries, but their lack of distinction from the others makes me question this claim. For now the "alpine" variety is planted separately.
I've got some photos of the various plants, but a comprehensive photo-shoot will have to wait until I get them all planted in a soon-to-be-constructed garden bed (with some way to keep the deer at bay) for them.

The other day I made the pleasant discovery that one of my raspberry plants is in flower at the same time as the various strawberries. I've got too much going on (in and out of the garden) to attempt crossing my strawberries to it this spring, but it is definitely in the plans for next year.

Friday, May 22, 2015

The Color of Peppers

Since writing this post, I took some nice photos of chiles I collected or grew this year, found more interesting mutations to talk about, and have generally filled out my understanding of the story of pepper color genetics. All this has been included in a new post at: the-biologist-is-in.blogspot.com/2015/11/the-color-of-peppers-2.html



I previously posted about some of the genetics involved in determining the color of tomatoes (http://the-biologist-is-in.blogspot.com/2014/04/the-color-of-tomatoes.html). Here we'll be looking at the colors of chile peppers.

Ripe chile peppers come in a very similar range of colors to ripe tomatoes. Both vegetables (along with potatoes, tomatillos, and ground-cherries) belong to the Solanaceae family of plants. Because of the close relationship of the plants, there are strong similarities in how the basic biology of color operates in each of them.

The red color of a classic ripe tomato is due to lycopene. The red color of a classic ripe pepper is not due to lycopene, but instead due to a combination of Capsanthin and Capsorubin. These are produced by the carotenoid pathway like lycopene, but they're produced further along the pathway. The figure at right illustrates the carotenoid pathway in peppers, to the degree I've been able to learn about it from reading primary research literature. Most of the pathway here is identical to that seen in tomatoes (and other plants), but with an extension after Zeaxanthin.



Compared with tomatoes, there is less research available to elucidate the genetics of color in pepper. The following figures are close-up versions of the main figure above, highlighting the placement of a series of mutations in the pathway which result in color changes. The mutations are indicated by a large negative, highlighted in red, at the location of the change to the pathway.

Mutant "y".
The first major mutation (left) is responsible for the difference between red and most yellow-orange peppers. The recessive mutant generating the "yellow" ("y") trait is caused by a defect in the gene Capsanthin-Capsorubin Synthase (CSS), which normally converts lighter colored Antheraxanthin and Violaxanthin into the Capsanthin and Capsorubin which are responsible for the typical rich red color.

Papers discussing mutations in CSS refer to the resulting fruit as yellow or sometimes orange. I'm pretty sure this is due to the actual color ranging between orange and yellow depending on the actions of other genes (like those described below).

The next major color mutations are abbreviated as "c1" and "c2". The "c1" trait results in a reduction in red pigment to about 1/10 of the wild-type level. The "c2" trait results in a reduction in red pigment to about 1/100 of the wild-type level. In an otherwise red fruit (with the "Y" allele), the actions of these two genes can result in a range of colors from light-red, to orange and pale-orange. In an otherwise yellow fruit (with the "y" allele), the actions of these two genes can result in a range of colors from pale-orange-yellow, to lemon-yellow and white.
Mutant "c2".

The "c2" mutation has been determined to likely be a defect in the Phytoene Synthase gene. This interferes with the production of a very early stage of the carotenoid pathway, resulting in a strong suppression of every later product in the pathway. Mutations in the same gene in tomatoes is also responsible for the production of yellow and white fruit. Though the phenotypes are different in the two species, they share the common aspect of having a much reduced output of the carotenoid pathway.

Mutant "bc".
Another mutation that results in an orange pepper and doesn't have the complications of the "y"/"c1"/"c2" genes is associated with a large increase in β-Carotene. This mutation is in the β-Carotene Hydroxylase 2 (BCH2) gene and interferes with the conversion of β-Carotene into β-Cryptoxanthin. Because of the increase in β-Carotene, the trait is called "bc".

There's also a pair of genes, called "B" and "t" that interact to result in a high level of β-Carotene, but so far I haven't been able to find any useful research to clarify how the mutations do so.
Mutant "cl".

The chlorophyll that makes a typical immature pepper green is broken down during maturation of the fruit. A mutation that interferes with this breakdown is called "chlorophyll retainer" ("cl"). When it is found in an otherwise red pepper, the result is a ripe pepper with a chocolate-brown color. When it is found in an otherwise yellow pepper, the result is a ripe pepper with an olive-green color.

There are several pepper varieties that have purple or black immature fruit. This trait is driven by two genes. The first mutant ("A") allows the plant to produce anthocyanin pigments in its leaves, stems, and purple immature fruit. The second mutant is a modifier of "A" ("MoA") that increases the amount of anthocyanins produced and results in a black immature fruit. These anthocyanins are broken down as the fruit matures. There is a very rare trait which interferes with this breakdown (seen in variety "Pimenta De Neyde") and so results in ripe fruit that remain purple. I haven't been able to find any publications describing this trait, so I've decided to refer to it as "anthocyanin retainer" and abbreviate as "an". I think it is likely to be a recessive trait, but I'll have to perform some crosses to be sure.



Looking at the β-Carotene enhancing mutant 'bc' in the pathway, I wonder if there are any mutations around which interfere with the conversion of Lycopene into β-Carotene. Such a mutation wouldn't be visible in the normal genetic backround of red peppers, as the red color of Lycopene is very similar to the red color of Capsanthin and Capsorubin. However, such a mutation would be very visible in the bright-orange background of a strain with the 'bc' trait.

Alternately, instead of searching for such a mutation, one could be engineered into the lycopene-cyclase gene to slow down its activity and result in a fruit which has a mix of Lycopene, Capsanthin, and Capsorubin.




pale-orange; orange; red.
Habanero-type chiles exist in a wide range of shades. I'd really like to breed up some standard-shaped Habanero chiles in the few missing colors (white, lilac, purple, and black). There is a variety called "Habanero White", but it doesn't have the shape of the classic Habanero. There is also a variety called "Black Habanero", but it has a rich brown color instead of black because it lacks the anthocyanin pigments necessary to generate the most darkly-colored fruit.

Pepper color genotypes I have.
yclc1c2AMoAan-ripe-fruit-color
+++++++red ("Habanero" from Dominican Republic)
+++c2+++orange ("Habanero" from grocer)
++c1c2+++pale-orange ("Habanero" from grocer)
y++c2+++lemon-yellow ("Devil's Tongue"; "Datil")
++++AMoAanpurple ("Pimenta De Neyde")
-
Habanero color genotypes I'd like to have.
yclc1c2AMoAan-ripe-fruit-color
y+c1c2+++white
y+c1c2A+anlilac
++++AMoAanpurple
+cl++AMoAanblack

I expect different combinations of the "y", "c1", "c2", and "MoA" genes would result in a range of shades between a light lilac all the way to a visually black fruit.



I don't have any pictures of the various pepper colors, but I am growing several peppers this year and expect to get a few nice photos. I have red, pale-orange, and purple fruited plants well-established and I'll soon be starting some of the orange and lemon-yellow types I have seed for.

If I can get my gardens built soon enough, as well as find a way to keep them protected from deer, I'll be able to think about doing some of the initial crosses I would need to make progress towards the few remaining novelty colors.

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Saturday, May 9, 2015

Violet Surprise

I've been very busy lately. Between looking for a job and working on the yard, I haven't found time to write any blog posts. I've had lots of ideas, but none of them have worked their way into something I wanted to post. Stress leads to writer's block, among other consequences.



Today I was out working in the garden, pulling buckthorn and extracting the broken remains of a thin glass gazing sphere that the previous homeowner had somehow smashed into the soil. The broken glass was a pretty blue and I managed to only cut myself once.

While pulling yet another buckthorn, I noted a violet flower that appeared to be coming from a plant (at right and below) with leaves I didn't recognize. The common yard violet in this area is Viola sororia (Common Blue Violet). Its flowers are often seen in shades of blue/purple, sometimes mixed with white. For several years I've been interested in collecting the forms I've found with different colored flowers, but until recently I didn't have a permanent enough place to keep them. (The plants don't survive winter well in pots or as houseplants.) I've never heard of a version with a modified leaf form, however.

There is a closely related violet species (V. triloba) that has cut leaves, but it differs from this plant in that the species starts and ends the season with regular, uncut leaves (like in this photo). Even the youngest leaves on the plant I found have the cut shape. The pattern of the leaf shape also appears to differ from that seen in all the photos I've found of V. triloba, though this is a less certain distinction.

Another slightly less-related violet species (V. pedata, "Bird's Foot Violet") also has cut leaves. However, the pattern of cuts in the leaf shape are distinct from the plant I found and the flowers are very distinct. [This paragraph was added after a relative mentioned V. pedata as a possible ID.]

My current assessment is that this plant represents a leaf mutant in V. sororia. The presence of related species with cut leaves hints that there is a pathway to producing this phenotype hidden in their normal development, just waiting to be revealed by some mutation. Mutations happen all the time, but it can take a somewhat practiced eye to see their results as significant and worth preserving.

I'll be transplanting this little plant to a place I can better keep an eye on and protect it.


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