What next for DNA barcoding?

I’m a late adopter of DNA barcoding. As a botanist it has often felt that DNA barcoding wasn’t really for me. Unlike in animals, where the mitochondrial gene CO1 often tracks species boundaries, in plants, there is rarely an exact match between DNA barcode sequence and plant species identity. A more general issue is that the use of one or a few regions of non-recombining organellar DNA just doesn’t cut it for answering the population genetic questions I’m most interested in.

But it’s now becoming clear that the scalability of DNA barcoding that allows it to be used on hundreds or thousands of specimens at a reasonable cost may make it a primary tool to accelerate species discovery and to describe biodiversity patterns in the face of massive species extinctions. Perhaps equally important to me is that the plant DNA barcode isn’t set in stone and new sequencing technologies will allow us to find better options for using DNA to tell plant species apart (Hollingsworth et al., 2016).  

Given my new-found enthusiasm for DNA barcoding, last month I went to the 8thInternational Barcoding of Life Conference in Trondheim, Norway, to find out the new developments in this field. Here’s what I learnt:

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It's all because of the holobiont

It’s conference season at the Molecular Ecologist. I went for the first time to a Gordon Research Conference (GRC). GRCs @GordonConf are well known for their efforts to foster an informal and inclusive atmosphere where frontier research in the biological, chemical, physical, and engineering sciences is discussed. Isolated venues and long breaks in the afternoons promote networking and give room for social activities and breakout sessions. Researchers are encouraged to present unpublished results and the contributions are off-record, that means that nobody is allowed to take photos, record sound or video, or share the presentations on social media. And here I am writing about it.

I attended the Animal-Microbe Symbioses Conference #GRCAnimalSymbioses. I went first and most of all because of the incredible line-up of presenters (almost 50% women). Second, I’ve heard that Gordon Research Conferences are especially family-friendly. I was not disappointed.

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Five years as a new PI

Life as a new Principal Investigator (PI) in science is full of surprises. On any given day you’ll be dealing with the past (finishing off manuscripts from your postdoc), present (helping current students) and anticipating the future (working on the next grant). I’ve heard various people say that it’s both the most exciting, and the most stressful, time in someone’s scientific career. The excitement comes from having the opportunity to steer science the way you want to, having well-developed skills to work with the data, and some time to do the analyses. The stress comes from wanting to build a successful new lab, and learning to balance new roles such as teaching and admin while doing the science we all love. In compiling a list of things I’ve learnt I wanted to look beyond the woes of grant writing and rejection, and challenges of work-life balance, which seem to get the most coverage. So, five years in, here are five things that I’ve learnt:

Obsessing about efficiency is not efficient. Time as a new PI seems precious. There are many things to juggle, and there’s no one breathing down your back as to when to do them. So, it’s natural to want to be efficient. We’ve all read lists of 10 tips on managing your time, or lifestyle posts on how ‘successful’ people live. The reality of it though is that a routine of getting up at 5am, going for a run, checking emails once, blocking out time for writing, and generally saying ‘no’ to every request, is going to make you miserable and unpopular. I’ve learnt that most efficiency tips aren’t helpful and end up being a distraction. I make sure that I write most days, and I always have a pet project on the go so that I’m always handling data, but beyond that I go with the flow. Letting go of efficiency targets has made me more productive, and leads to the occasional guilt-free long-lunch with colleagues or coffee break with a student, which can only be a good thing. I also think that giving research time to evolve, rather than pressing to publish as soon as possible, leads to better manuscripts in the end.

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Molecular ecologists — and molecular ecology — at Evolution 2019

The Providence skyline. (Flickr: Timothy Burling)

June means summer is well underway in the northern hemisphere, and those of us tied to the academic calendar are off to fieldwork, buckling down for summer teaching or grant-writing or just writing — and planning for conferences. Evolution, the joint annual meeting of the American Society of Naturalists, Society of Systematic Biologists, and Society for the Study of Evolution, is a big one for molecular ecology and molecular ecologists, and as in many years multiple contributors to this very blog will be present and presenting in Providence, Rhode Island. Here’s a quick rundown of which TME contributors and alumni will be speaking at Evolution 2019, and what events on the program schedule have us excited. Look for our coverage of the conference itself when we converge on the [checks Wikipedia] "Ocean State" on Friday, June 21.

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The state of coral: A mini-review

Coral reefs are one of the main harbingers of the climate crisis.  As such, there have been numerous studies, TED talks, Blue Planet episodes, podcasts, et cetera, about the state of corals. I’ve condensed a select few research findings for a mini-review to highlight some of the most recent results. This is by no means a comprehensive review of the coral literature, obviously.  I will, no doubt, egregiously fail to mention some rock stars who are making great strides in coral biology and conservation.  It’s a big group – both of scientists and of species.

A quick background on coral endosymbionts

Shallow water corals are considered holobionts, comprised of the host coral, endosymbiotic dinoflagellates (often referred to colloquially as zooxanthellae), bacterial and archaea communities. The endosymbionts provide the fixed carbon for the coral via photosynthesis.  When water temperature increases above average for a prolonged time, the endosymbionts are expelled from the coral polyps, leaving bleached coral behind. Corals can rely upon heterotrophy to get their nutrients and fixed carbon, but this is not sustainable over long stretches of time. They can reuptake endosymbionts and recover if temperatures return to normal in a short enough time span.  Most corals obtain their endosymbionts from the environment (horizontally) either during their larval stage in the water column or shortly after settling. Others inherit endosymbionts vertically from their parents. The most reported and studied coral endosymbionts historically have belonged to the genus Symbiodinium, but a recent revision has split the several clades within the genus into seven distinct genera.

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Hybridization in the depths of the last glacial period created a world-conquering clover

White clover, Trifolium repens, in a Los Angeles city park, a hemisphere away from the glacial refugia where it originated. (jby)

Plants’ flexibility with the structure of their genome — able to cope with proliferating transposons, whole-genome duplications, or even acquisition of complete sets of chromosomes from another species — is a big source of evolutionary novelty. Duplication of a single gene allows the duplicate and its template to evolve new functions; adding a whole additional genome provides that much more raw material. That may be the secret of the success of one worldwide weed we’ve seen featured on this blog before, Trifolium repens, or common white clover. A new paper in The Plant Cell delineates two fairly intact progenitor genomes within the T. repens genome, and reconstructs the history of an evolutionary mashup that created a wildflower you can very likely find by simply stepping outside and walking to the nearest well-watered lawn.

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Posted in adaptation, evolution, genomics, hybridization, speciation | Tagged | 1 Comment

Introducing Molecular Ecology Spotlight

Today, the Molecular Ecology journals are launching a new venue for highlights and behind-the-scenes looks at the research they publish. Molecular Ecology Spotlight fills a niche as the official blog of Molecular Ecology and Molecular Ecology Resources, publishing author summaries and interviews linked to noteworthy new papers in the journals — and a Twitter feed that will broadcast all new papers as they’re published.

The new blog is a project of the Junior Editorial Board, formed last year with early-career researchers who were recognized in the Harry Smith Prize competition. The goal is that this will provide another way to follow research results from the journals, and context and background for papers of particular interest; where The Molecular Ecologist has always defined itself as a forum for the field of molecular ecology writ broadly, Molecular Ecology Spotlight will, as the name implies, shine a light on the best work in Molecular Ecology and Molecular Ecology Resources specifically.

You can find Molecular Ecology Spotlight at molecularecologyblog.com, and on Twitter at @molecology.

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Go north, young salamander

Plethodon shenandoah (Wikimedia Commons)

Shenandoah salamanders are a case study in restricted distributions, known only from three mountainsides in Shenandoah National Park, in the Appalachian Mountains of Virginia. What’s keeping them in such a restricted range? A new paper in the journal Ecology and Evolution aims to answer that question using population genetics.

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Bigger bees bumble by barriers, end up with lower population genetic differentiation

Look at the dispersal ability on that lad! What an absolute unit. (Flickr: Viv Lynch)

Population structure is the core of ecological genetics, as it’s practiced today. Genetic differentiation between populations in different places is our null hypothesis and one of our most widely used indirect signals that environmental factors are impacting the evolution of those different populations. Oh, and it’s also a first step to the origin of new species.

The huge body of published datasets testing for population structure is a great resource for synthetic work, that identifies broad general patterns about population genetic processes. Last year we saw one such study link locomotion mode and genetic differentiation — confirming that bird populations are less likely to differentiate, given a particular geographic distance, than populations of land-bound vertebrates. Now, freshly out in Molecular Ecology, we have a similar project in a more specific taxonomic scope: bees.

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Move or adapt to changing climate? These chipmunks have had to do both

Tamias alpinus (Flickr: Eric Sonstroem)

Climate change threatens to land many, many species in conditions for which they’re not adapted — too warm, too dry, too stormy, too flood-prone — and traditionally the ways that living things might respond to this are framed as a choice between moving to more suitable habitat elsewhere, adapting to the new conditions in the current habitat, or dying out. These are a false choice, of course; it’s possible to move and adapt, and it’s possible that even doing both won’t be enough to avoid extinction. A new study of one rare chipmunk in the Sierra Nevada mountains pinpoints exactly such a case.

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