Claytonia rubra, what is that? pt. II

Hi, all — I’ve decided to switch things up and simply chat with you a bit about a topic that has apparently been the most popular on my blog so far: Claytonia rubra (Howell) Tidestrom. You may find yourself now asking the question, “Claytonia rubra, what is that?” Well, there’s a blog post for that.

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Claytonia rubra photographed while flowering, plants growing abundantly in the Pinyon-Juniper belt on the Modoc Plateau, northern California.

But Claytonia rubra may be more than meets the eye, especially if you’ve been paying close attention to it where it grows in different areas, or if you’ve been so lucky as to see it from across its entire geospatial distribution. Let’s think about this for a minute, considering first the global range of Claytonia rubra.

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Range map from Flora of North America Treatment by Miller and Chambers (2003).

It is across this wide and ecologically diverse distribution, north to south from British Columbia to near (probably in) Mexico, and west to east from the San Francisco Bay Area to the Black Hills of South Dakota, that the annual Claytonia rubra displays a seriously diverse range of morphologies. Is it phenotypic plasticity? Is it local adaptation? Is it speciation? Is it hybridization? Is it some mix of all of these? Claytonia rubra is a tough cookie to crack!

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Claytonia rubra photographed while flowering on the Modoc Plateau, northern California. Notice the largest leaf blades (outermost in the rosette) are among the first to have emerged in early development — These lay flat on the ground surface (or nearly so)

Starting with identification, something I’ve found to be fairly characteristic of Claytonia rubra is that its older leaves (outermost in the rosette of basal leaves), which often have the largest blades, tend to lay flat on the ground — some close relatives (like certain subspecies of C. perfoliata) do this too, or something like it, so don’t take this for a smoking gun. Furthermore, some races of C. rubra do not have basal rosettes that lay flat, rather they are elevated ever so slightly above the forest floor. Don’t you just love those kinds of dichotomous key breaks? — Is is erect to ascending (sometimes spreading), or ascending to spreading (sometimes erect)?! — Still, if you see something in the mountains of western North America like in the picture below, where the outermost (older) leaves in the basal rosette lay flat, appressed to the ground, you can be fairly confident that you are looking at something that is quite appropriately called Claytonia rubra.

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Vegetative Claytonia rubra photographed at the Tejon Ranch in the Tehachapi Mountains, southern California.

For effect, compare the leaves of Claytonia rubra plants in the above picture with the leaves of the plant in the picture immediately below, C. perfoliata, both of which were photographed at the Tejon Ranch in somewhat close proximity (either side of the same mountain ridge) — see how Claytonia perfoliata (below) tends to elevate its leaves off the ground?

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Vegetative Claytonia perfoliata photographed at the Tejon Ranch in the Tehachapi Mountains, southern California.

The characteristic of Claytonia rubra have low-growing leaves seems pretty useful, until you come across a putative lineage (sometimes in the same mountain range!) that looks like the plant below — these plants have distinctly erect / ascending leaves, although the proximal portion of their petioles are still appressed to the ground. This gives the leaves a sort of ‘S-curved’ look. Believe it or not, these are another subspecies of Claytonia rubra!

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Claytonia rubra photographed while flowering at the Tejon Ranch in the Tehachapi Mountains, southern California.

This is a time where it comes in handy to know a few other characters that, when used in combination, can help to distinguish Claytonia rubra from similar-looking miner’s lettuce.

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Classic, beet-colored (reddish to purplish) undersides of basal leaves of Claytonia rubra. Whenever possible, try to observe this character in multiple plants — Generally, the basal leaves should be deep green adaxially and reddish abaxially in Claytonia rubra.

For example, the plants photographed above demonstrate another conspicuous characteristic of most lineages of Claytonia rubra — betalain pigmentation is generally evident on the abaxial (lower) surfaces of the basal (and sometimes cauline) leaves, giving them a purple/reddish appearance. This is a sort of ‘no-brainer’ character I tend to point people towards, but just as with the characteristic basal leaf orientation I mentioned above, this morphological character doesn’t always hold true. Plants love exceptions WAY MORE than rules: in this particular case there appears to be an environmental element to variation in Claytonia betalain pigmentation, as evidenced by some unpublished observations I have made in common garden experiments involving C. perfoliata, C. rubra, and some perennials in the C. “peirsonii” complex.

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Variegation on foliage characteristic of some lineages of Claytonia rubra.

OK, so the leaves are sort of laying flat, and kinda red undeneath, but you’re still not totally convinced you are looking at Claytonia rubra and not some other similar-looking miner’s lettuce. Well, you’re in luck — I’ve noticed that many races of Claytonia rubra tend to have the look of variegated leaves, possibly related to a breaking up of the cuticle during development. If you see something like the plant in the picture(s) above, where there are variegated streaks on the leaves of a Claytonia, it is VERY likely that you are indeed looking at Claytonia rubra.

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[From left to right, Claytonia parviflora, C. perfoliata, and C. rubra!] Multiple miner’s lettuce species growing in sympatry in Mill Creek Canyon, San Bernardino Mountains, California.

IF you still can’t be sure about which Claytonia you are looking at — just ask me! That’s what I am here for…

Free data isn’t free… except in this case.

Hey, all y’all! I am VERY excited to announce that I am ready and willing to share ddRADSeq data (double digest, Restriction site Associated DNA Sequences) with anyone and everyone that can benefit from using them. I am currently testing outgroup rooting using ddRADSeq. Thus, I have data for some distant samples (phylogenetically speaking, relative to my interest group Claytonia) from Order Caryophyllales that someone out there on the world wide web might be interested in using. Maybe someone just wants to try their hand at playing with some Next Generation Sequencing data, just to see what it is like, or in order to gain some experience for the evermore competitive post-doc opportunities out there…

More specifically, I have these free data to offer up:

Silene aff. verecunda sp. nov. 1 (Caryophyllaceae) — lane 1, lane 2, and lane 3. (combined total = 657,952 reads).

Silene aff. verecunda sp. nov. 2 (Caryophyllaceae) — lane 1, lane 2, and lane 3. (combined total = 1,450,085 reads).

Silene parishii (Caryophyllaceae) — lane 1, lane 2, and lane 3. (combined total = 2,758,351 reads).

Calandrinia ciliata (Montiaceae) — lane 1, lane 2, and lane 3. (combined total = 1,692,880 reads).

Lewisia rediviva (Montiaceae) — lane 1, lane 2, and lane 3. (combined total = 25,626 reads).

Montia parvifolia (Montiaceae) — lane 1, lane 2, and lane 3. (combined total = 31,848,680 reads).

In the (likely) case that I made an error during the copy-and-paste-athon above, feel free to follow this link to a folder containing all of the data. Also, let me know where the copy/paste errors are and I’ll work quickly to fix them!

Data details: Genomic DNA was digested using EcoRI and MspI enzymes. Window for size selection was +/- 150 base pairs. Libraries were sequenced on an Illumina HiSeq. Entire dataset includes reads from 2 lanes of single-end (lanes one and two) and 1 lane (lane 3) of paired-end sequencing. These data were generated by Global Biologics.

Anything else you want/need to know in order to use these data in a publication, such as voucher information or having the data served in an alternative format, don’t hesitate to ask!

And now something different…

It has been a while since I blabbered about the cotyledons of Claytonia, but I want to let you all in on something I find VERY interesting…IMG_1521… so maybe we should start with a survey, to see what you think. How many cotyledons do you think Claytonia have? Keep in mind, they are dicots.

Claytonia saxosa seedlings2013-12-01 12.10.10If you guessed that Claytonia have 2 cotyledons, you’re right… but you’re not the only one that is right. Technically, those of you that guessed Claytonia have only 1 cotyledon are also correct — that’s right, there is in fact a group of dicots with only 1 cotyledon (probably several, but that question exceeds the scope of this blog post). Claytonia Section Claytonia, otherwise known as the tuberous perennials, lack a second cotyledon present in other species of Claytonia (and all of their closest relatives). To me, this is just another reason why you should believe that Claytonia is the whackiest group of plants this side of the Mississippi River.😉

IMGP9244So who cares, there has been a loss of one of the cotyledons in this group of plants. One time only evolution, and now these plants simply can’t recover that lost cotyledon — I’m over it… right? WRONG! There is something fishy going on here, and it has to do with a certain caudicose perennial I have mentioned before: Claytonia megarhiza (pictured below).

IMG_4012IMG_4025You can see from the second image (the photo immediately above) that Claytonia megarhiza clearly has two cotyledons, not one like the tuberous, perennial Claytonia species I mentioned before. Thus, you’d expect that this species is more closely related to those other Claytonia that have two cotyledons, right? Well…

Print Trees PreviewAbove is a preliminary phylogenetic tree that I presented at the Botanical Society of America Meeting this year in Edmonton, Alberta, Canada. This tree has been developed from ~500 single nucleotide polymorphisms isolated from the nuclear genome of all of the samples included (using ddRADseq). You can see from the tree that the caudicose perennial C. megarhiza (indicated by [morphologically similar, but anatomically quite different] cartoon carrots ) clearly has a close association with the tuberous, perennial Claytonia, albeit the exact area in the tree where they will stabilize is still yet to be determined. Without question, Claytonia megarhiza is nested somewhere in this clade of otherwise tuberous, perennial Claytonia.

So how did C. megarhiza find itself with 2 cotyledons while all of its closest relatives (including those diverging away from the lot much earlier in evolutionary history) have only 1? If you have the answer… I would love to hear it from ya! From my perspective, it is a question that is ‘to be determined’ but I am hopeful that my dissertation will change things.😉

Oops, that took embarassingly long: UPDATE on what’s new with western Claytonia

IMG_0850First off (technically second, after the eye candy above), I need to announce that my research on Claytonia (Montiaceae) has been recently funded [yay!] by the National Science Foundation. You can see the abstract here for #DEB1502085:

http://www.nsf.gov/awardsearch/showAward?AWD_ID=1502085

Second (yes, I know, technically third), we should play my favorite game: compare the above eye candy with the below ridiculously beautiful [spring] beauty… SAME? or different.😉

IMG_2978Now before you answer to yourself, consider that the Claytonia in the above two pictures are considered in the current taxonomy to be the same as the plants in the below picture, all being C. lanceolata [for now]. IMG_2834Check out the variation in those leaves!!! Who cares about the flowers, right? No way…IMG_0865IMG_7563IMG_2825The three photos immediately above correspond respectively with the same three putative taxa [let’s call them operational taxonomic units] in the first three pictures of this blog post. So? SAME or different? Feel free to vote at the bottom, and I welcome any feedback or discussion — I can’t say it all in 140 characters or less.

Third [ok, let’s stop with the sequential nonsense], I took an epic trip across California, Nevada and Oregon during the spring months of 2015 as part of #DEB1502085. While on this trip, I photographed new, mind-boggling [taxonomically speaking], tuberous Claytonia. Almost immediately after that, I took another most epic trip across California, Nevada, Utah, and Colorado (with guest appearances in Arizona and Wyoming) with ‘Los Caryophylleros’. Let’s just say, I can’t wait to get my new morphological and molecular data (RADSeq X 2) up to speed…

Lastly [HA! I win!], I’ll finish this [short] commentary with what has been the most difficult collection of photos I’ve ever had to select from for the purpose of sharing, then I need to finish preparing for presentations at BOTANY and the Caryophyllales meetings…

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Hybridization — are generalist pollinators the key to success?

I’ve been on a bit of a rant lately concerning hybridization in plant species complexes, which recently resulted in my last post suggesting hybridization could be a potential ‘solution’ to the problem of an ever-changing climate. I want to dig a little deeper now and ask the questions — can generalist pollinators have anything to do with the maintenance of a generalized floral form in Claytonia? If so, can this indirectly act as a selective force for increased hybridization among distantly (and closely) related species? If you have seen the ‘face shots’ from a recent ‘Spring Beauty Pageant‘ than you know what I’m talking about. Maybe you’ve even suggested to a friend, because Claytonia grow like weeds where you are from, that you believe there to be little variation in floral form among species in the genus. I’d agree with you, to a certain extent… but then again, maybe there is so much intra-population variation in floral morphology (coloration, petal shape) that we are blind to see the true pattern of differentiation in floral form among closely related taxa. I’ve touched upon the subject of within-population variation of the flowers of one member of the C. “peirsonii” complex from the southern Sierra Nevada, but now I want to expand on this subject with photographs taken within a single population of C. lanceolata sensu lato on the Great Continental Divide in Montana. As you can easily tell from the first picture below, in which all of the white spots are Claytonia flowers, it is not difficult to conduct this sort of ‘experiment’ yourself. In other words, it is easy to get a lot of face-on photographs of Claytonia flowers because they occur in extremely dense populations. This spring, try to see how much your favorite Claytonia varies in its floral form — you may be surprised at what you find!IMG_8497IMG_8570IMG_8449IMG_8582 IMG_8453IMG_8458IMG_8477IMG_8478IMG_8531IMG_8547IMG_8516     Keep in mind that all of the above pictures are of plants that occur in a single population of C. lanceolata sensu lato on the Great Continental Divide in Montana. As evidenced by the last photograph, even merosity can go haywire from time to time. If I showed you just that last picture, you might even confuse the plants for Lewisia. That is a lot of variation! Are these hybrid plants of C. lanceolata (which has retuse petal apices) crossed with another species in the area with entire petals? Good question! Let me get back to you on that one…

All I know is that multiple Claytonia species can occur in sympatry, and intermediate forms can be found in those areas. This is especially true of the annual species of Claytonia. I haven’t observed putative hybrids among the annuals (i.e., the miner’s lettuces) and tuberous perennials (i.e., C. lanceolata species complex), although I have observed them sharing pollinators in southern California. Pictured below are soft-wing flower beetles (Melyridae) visiting both C. rubra (section Limnia, first picture below) and C. “peirsonii (section Claytonia, second picture below) at the same location on the same day in the southern Sierra Nevada, California. You might remember from one of my very first posts: these pollen eaters are quite effective pollinators.

IMG_5457 IMG_5402Too many questions for a single dissertation to address, but I’ll see what I can do!😉

Hybridization — problems, or solutions?

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Claytonia perfoliata species complex on the Tejon Ranch — this is only the beginning of your Montiaceae-related nightmares…

The taxonomy for the annual species of Claytonia (section Limnia) is VERY difficult to work with, mostly because diagnostic characters are not well preserved on herbarium specimens. Unfortunately, a molecular phylogeny that spells out the relationships among taxa in this group is still lacking, but I have added many samples as out-group taxa for my own dissertation studies on section Claytonia (i.e., the tuberous perennial Claytonia)… Is the cause for confusion in field identification due to phenotypic plasticity, hybridization, or both? Is it something else altogether, such as the rapid formation of localized ‘races’ due to poor dispersal capabilities? If the difficulty of accurate field identification is due to hybridization, is this a problem? For taxonomy, the morphological consequences of hybridization are an issue that must be addressed, but for the longevity of lineages, hybridization is probably not a ‘problem’ but rather a solution — it might just be the key to sustaining genetic diversity and promoting adaptation in a forever changing climate — evolutionary success! Before I get too deep into the hole I am digging, we’d better take a look at some nice plant images to really smell what I am stepping in😉

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Claytonia parviflora subsp. viridis — Tejon Ranch. Note the linear basal and cauline leaves of this mildly succulent annual. Were you to collect, you could rest easy with ID of this plant.

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Claytonia parviflora subsp. viridis X C. rubra ?!?!– Tejon Ranch. Note the non-linear basal and cauline leaves of this moderately succulent annual, and the floral morphology of C. rubra. Yet, this plant retains the fully separate leaf pair of C. parviflora subsp. viridis.

Claytonia parviflora subsp. viridis X C. perfoliata ?!?! -- Tejon Ranch. Note the non-linear basal and cauline leaves of this mildly succulent annual.

Claytonia parviflora subsp. viridis X C. perfoliata ?!?! — Tejon Ranch. Note the spatulate basal leaves. I certainly wouldn’t want to be doing a flora of this area, as I’m sure this isn’t the only group with these kinds of ‘problems’ with hybridization😉

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Claytonia exigua (left) and C. exigua X C. perfoliata (right) ?!?! — Tejon Ranch. Note the glaucus basal leaves of the plant on the right, which should otherwise look like the plant in the first picture of this post. Yikes!

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More fun with sympatry on Tejon Ranch!!! Left to right, Claytonia exigua, a diminutive C. perfoliata, and something that approaches C. rubra in morphology — section Limnia is tough!

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Could this possibly even be the same as any taxon we’ve seen elsewhere in this blog post? I’m really not sure, but I would lean toward calling it C. perfoliata-like. The C. perfoliata complex, including also C. rubra and C. parviflora, is probably the most difficult group in section Limnia.

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This is also Claytonia perfoliata! Its first leaves are narrow like these. Under drought conditions it can ‘bypass’ switching to the more mature spatulate leaf condition by going directly into flowering and therefore only producing the perfoliate cauline leaves.

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Contrast (or compare, in case of my suggested hybrids) the above pictures with this one of Claytonia rubra — this appears to be a good example of this species which at one point was treated as C. perfoliata but has been found to be a unique lineage and is treated as such.

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Now, compare the picture immediately above (of Claytonia rubra subsp. rubra) with this one — same or different?! Same! Well, sorta… This is ALSO C. rubra, presumably subsp. depressa, which apparently also occurs on the Tejon Ranch — how exciting!

Okay, so interestingly enough, I took all of these photos (and many, many, many more) in only one day on Tejon Ranch with Nick Jensen, a colleague at Rancho Santa Ana Botanic Garden doing a floristic study of the area. His website can be found here. This is a fascinating area because it serves (or, served) as a biogeographic traffic signal for the Sierra Nevada, the Transverse Ranges AND the San Joaquin Valley and the Mojave Desert. I suspect the evidence for hybridization exhibited by the numerous sympatric Claytonia here is mirrored in other plant groups on the Tejon Ranch where multiple taxa co-occur.

But that isn’t all, of course — the evidence of hybridization reappears in every mountain range I have explored in southern California! It seems to be a battle among divergent lineages to survive and compete for overlapping and limited niche space near the southern part of the geographic distribution of these plants, but maybe a little cooperation wouldn’t hurt for the ‘greater good’ of Claytonia if it increases genetic diversity… In the San Bernardino Mountains, you can find members of the C. perfoliata species complex in sympatry. The evidence for hybridization in this area mirrors what I observed at Tejon Ranch.

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From left to right, Claytonia parviflora, C. perfoliata and C. rubra, all members of the C. perfoliata species complex occurring together in Mill Creek Canyon, San Bernardino Mountains.

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A good example of Claytonia parviflora; note the erect, linear basal leaves that are almost terete in shape, and the cleft in the disc-like cauline leaf-pair resulting from incomplete fusion of two leaves.

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Compared with the picture immediately above, this one looks like a fusion of C. parviflora and presumably one (or both?) of the other two annual species in the area. I tend to think C. perfoliata may have played a role in the formation of this hybrid, but we can only be sure by DNA sequencing or by extensive cytological screening. Note the erect basal leaves that are no longer linear in shape but instead have rather distinct blades — this is NOT C. parviflora in the strictest sense of the name.

In the San Jacinto Mountains, you can find more of the same — members of the C. perfoliata species complex in sympatry and evidence for hybridization that may make you want to tear your hair out if you are working to identify plant specimens collected here. For instance, the pictures below from the San Jacinto Mountains are more or less taken from within ~1 contiguous square mile in Garner Valley.

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An excellent example of C. parviflora subsp. viridis is strutting its stuff roadside in the San Jacinto Mountains. Here, you have more action in the ring coming from the C. parviflora corner than from elsewhere in the C. perfoliata complex — I’m not sure the reason but think it is related to the locality I visited, a recently burned area in Garner Valley with little overstory cover.

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Compare the picture immediately above (of C. parviflora subsp. viridis) with this one of C. parviflora subsp. parviflora — similarly erect basal leaves that approach a terete-linear shape, but a contrastingly perfoliate cauline leaf-pair that is almost completely fused (as opposed to the free cauline leaves of C. parviflora subsp. viridis photographed above). The two appear to have different coloration under the same conditions here as well in both the flowers and foliage. — Garner Valley, San Jacinto Mountains.

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Now, compare the picture immediately above (of C. parviflora subsp. parviflora) with this one of some sort of C. parviflora hybrid — similarly erect basal leaves but these appear to be forming distinct blade and petiolar regions unlike the other two photos above from the same general location… tempting to call them the same, but I imagine this fishiness has both rhyme and reason to it. — Garner Valley, San Jacinto Mountains.

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This plant is OBVIOUSLY different from the rest, but what do you call it?! Under some Jeffrey pines that survived the fire, these plants approach the morphology of C. perfoliata subsp. mexicana but the smaller leaves in the center of the rosette are suggestive of certain races of C. rubra. — Garner Valley, San Jacinto Mountains.

What a wild and wacky world we live in! Claytonia will keep me busy (and happy) for many years to come…

Yukon — too much good stuff!

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Cheers from the Ogilvie Mountains!

Hey, all — I have returned from the Yukon Territory and I want to share with you at least SOME of the highlights regarding my fieldwork there. Ingrid Jordon-Thaden and I summarized most of it in our recent post on Experiment.com (click here to see the lab note), but I wasn’t able share all of the pictures that I wanted to share there — my administrative privileges on Claytonia.org allow me to expand a bit here😉

So what did I see, exactly? Oh gosh, I collected a fair amount of Silene, a few Androsace septentrionalis seeds and vouchers, at least a few Boechera, and I even grabbed an endemic Claytonia to make the trip VERY worthwhile. Claytonia ogilviensis (two pictures below) was my main target, so I was very glad that we were able to collect it. I found at least one population, but I also got the opportunity to sample from some recent herbarium specimens where C. ogilviensis has been collected outside of the range from which it was originally described, each with a slightly different morphology (and geology) to boot — I am VERY excited to see how this all fits into the phylogeny I am developing (with help from collaborators) for Claytonia Section Claytonia.

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Tuber from putatively old individual of Claytonia ogilviensis in the Ogilvie Mountains, Yukon Territory, Canada.

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Basal leaf (left center) and remnants of flowering stem (right center) of Claytonia ogilviensis in the Ogilvie Mountains, Yukon Territory, Canada.

Based on my recent observations in the field, and from scanning herbarium specimens collected all across western North America, I can tell why many people have suggested that Claytonia ogilviensis (pictured above) may be closely related to C. umbellata (pictured below). It doesn’t help that I am not EXACTLY sure about who the REAL C. umbellata is, considering I collected four distinct genotypes (each with their own distinct morphologies) all within about 20 air miles of the vaguely described type locality. To make matters worse (read about it here), my collaborator has found another distinct lineage of C. umbellata in eastern Oregon that is nearly identical (genetically) to the Ogilvie Mountains endemic (C. ogilviensis) that I just collected… Claytonia is a tough cookie to crack!

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Tuber from individual of Claytonia umbellata in the Diamond Mountains, Nevada.

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Basal leaf of Claytonia umbellata from the Diamond Mountains, Nevada.

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Basal and cauline leaves of Claytonia umbellata from the Pine Nut Mountains, Nevada.

Aside from collecting the narrow endemic Claytonia ogilviensis in the Yukon Territory, I also found an interesting population currently treated as C. tuberosa (pictured below) in the area of Keno Hill. In my most recent nrITS phylogeny, it appears that these plants may be more closely related to samples of C. multiscapa from the Rocky Mountains than they are to other samples of C. tuberosa collected just to the west in Alaska — I don’t yet have chloroplast data to support this relationship (the Idaho area C. multiscapa sequences are from GenBank).

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Face-view of flower of Claytonia tuberosa s.l. from the top of Keno Hill, Yukon Territory, Canada.

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Claytonia tuberosa s.l. photographed on top of Keno Hill, Yukon Territory, Canada.

Lastly, I got to see and collect a VERY beautiful Claytonia in the Kluane National Park, a member (and my first sample) of Section Rhizomatosae Claytonia sarmentosa (photographed below). This rhizomatous perennial seems to really prefer talus slopes, not unlike C. ogilviensis, C. umbellata, and the C. “peirsonii” complex.

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Face-view of flower of Claytonia sarmentosa from the Kluane Ranges, Yukon Territory, Canada.

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Claytonia sarmentosa photographed on the King’s Throne Trail, Kluane Ranges, Yukon Territory, Canada.

It was a great trip, but I’m glad to be home — with school about to start, and another spring season just around the corner, it is time to REALLY get some work done!!!

Up Next = Molecular lab + Herbarium work.

It has been a while, but I’ve been busy…

photoIMG_8879Hey, all — I wanted to share a short post with you, some links that detail my activities in the field over the last two weeks in Idaho and Montana. I’ve been on the hunt for Claytonia, Silene, Boechera and Androsace in alpine areas across these two states, including my new favorite mountain range, the Sawtooth Range (pictures above). At the end of this trip in Idaho and Montana I got my first ever glimpse of the alpine Claytonia megarhiza (pictures below) — I’m beginning to think I should have selected that species for a more thorough investigation… I suppose there is life after dissertation, so maybe this can be my next problem child.😉

IMG_8952IMG_8954My collaborator, Ingrid Jordon-Thaden, and I have been to some pretty spectacular places (see links below), but it is only going to get better (I think) when we head north to the Yukon (Canada) following the 2014 Botany Conference. I look forward to keeping you all in the loop!

first update: https://experiment.com/u/0gYspQ

second update: https://experiment.com/u/pdFliA

third update: https://experiment.com/u/itzIEA

Beginning of the end of Silene verecunda sensu lato

Hey, all — I thought I would share with you that my recent manuscript with colleagues (Diana D. Jolles and Heath A. Bartosh) describing a new species of Silene (Caryophyllaceae) has finally been published! You can access our article here, or the whole issue is here. It is a very special issue for the California Fish and Game Journal, #100, and the first ever all botany issue for the journal — some really GREAT articles in there that are worth reading, including an introduction by Governor Jerry Brown. Neat Stuff!

combined_finalAs always, I am interested to know what you think about this topic — the Silene verecunda problem is VERY complex, but fortunately the taxonomy isn’t.