Showing posts with label ecology. Show all posts
Showing posts with label ecology. Show all posts

Thursday, December 15, 2016

Last EXEB-meeting in 2016 on December 20: hard and soft selection revisited


Posted by Erik Svensson

Nathalie and I decided to have a final EXEB-meeting of the year next week anyway, even though nothing was planned. Nathalie will bring "fika", and I will introduce a review paper (hopefully a light read) on "hard" and "soft" selection; two very important concepts that illustrate the difference between ecological and population genetic views of how selection works. Title and Abstract of the paper follows below.

When: Tuesday, December 20 at 10.00
Where: "Darwin, 2nd floor, Ecology Building

 Hard and Soft Selection Revisited: How Evolution by Natural Selection Works in the Real World

by David Reznick ( J Hered doi: 10.1093/jhered/esv07)

Abstract

The modern synthesis of evolutionary biology unified Darwin’s natural selection with Mendelian genetics, but at the same time it created the dilemma of genetic load. Lewontin and Hubby’s (1966) and Harris’s (1966) characterization of genetic variation in natural populations increased the apparent burden of this load. Neutrality or near neutrality of genetic variation was one mechanism proposed for the revealed excessive genetic variation. Bruce Wallace coined the term “soft selection” to describe an alternative way for natural selection to operate that was consistent with observed variation. He envisioned nature as presenting ecological vacancies that could be filled by diverse genotypes. Survival and successful reproduction was a combined function of population density, genotype, and genotype frequencies, rather than a fixed value of the relative fitness of each genotype. My goal in this review is to explore the importance of soft selection in the real world. My motive and that of my colleagues as described here is not to explain what maintains genetic variation in natural populations, but rather to understand the factors that shape how organisms adapt to natural environments. We characterize how feedbacks between ecology and evolution shape both evolution and ecology. These feedbacks are mediated by density- and frequency-dependent selection, the mechanisms that underlie soft selection. Here, I report on our progress in characterizing these types of selection with a combination of a consideration of the published literature and the results from my collaborators’ and my research on natural populations of guppies.

Monday, June 11, 2012

Scientific misconceptions, publication stress and criticism of molecular ecology as a research field





Posted by Erik Svensson

At Juha Merilä's research group blog, EGRU-blog, one often finds very interesting and provocative posts, that stimulates self-reflection and critical thinking. Here is one such post, which raises some critical questions about the field of molecular ecology and the lack of rigour among some of the scientists defining themselves as belonging to this novel field.

This short post actually refers to a recent Invited Review, which is likely to upset some molecular ecologists, as it is very provocative and questions much of the research practices in this very young and technologically-oriented discipline. I do not necessarily endorse everything in this article, and some points that are discussed are beyond my expertise and research interests. As for myself, I do not get very upset or feel very threatened by the message, because I am not a molecular ecologist (and will never become one), even though we have used molecular techniques in our research lab for several years now, and published several papers in the journal Molecular Ecology as well (e. g. this, this and this).

But using molecular techniques, like we have done in these studies, and even endorsing them, is not the same thing as being a molecular ecologist, in my opinion. It is not even enough to publish in the journal Molecular Ecology, I think. I, for myself,  would never define myself as molecular ecologist. Rather, I define myself as an old-fashioned evolutionary biologist interested in the ecological aspects of evolutionary change. Or sometimes I simply define myself an evolutionary ecologist, who is prepared to use observations, field and lab experiments, quantitative genetics and molecular techniques, depending on what is needed and what question that is being adressed.

In contrast, molecular ecology as a field, as I perceive it, is a primarily a discipline defined by techniques and the use of molecular markers, rather than being defined by research questions. And that is why I have never been very interested in this field, as I tend to be more interested in conceptual problems in ecology and evolution, while not being hostile towards new techniques, when they help to solve these classical problems (which is not always the case, however). Molecular Ecology partly grew out from behavioural ecology during the eighties and nineties, as new molecular methods for determining paternity in birds and other animals were developed (first DNA-fingerprinting and later microsattelites). Later, the field came to include many other research questions being adressed by the use of molecular markers, such as phylogeography and molecular population genetic structure etc.

The current review is - interestingly - published in Molecular Ecology - which I think is to the benefit of this outlet as it shows some self-criticism of the same field that the journal is built upon. Hopefully, this article will help to promote self-reflection and critical thinking, both among molecular ecologists (the main target), but also other biologists using molecular techniques. The paper is Open Acess and can be downloaded here. 

 Here are some excerpts, and quite critical and provocative quotations from the paper (Abstract and full reference given below this post):

"Many misconceptions in the various subdisciplines of molecular ecology arise as a consequence of the huge amount of data that can be relatively easily and rapidly generated and analysed. There are many more automated DNA sequencers than classes in population genetic theory, and as self-educated molecular ecologists contribute in professional service, we sometimes see misconceptions perpetuated by journal authors, reviewers and editors."

And:

"At the end of this review, many readers will still believe that if they can properly format data for mega (Tamura et al. 2011) or arlequin(Excoffier et al. 2005), they do not need population genetic theory, they can pick it up along the way, or all the information they need is in the manual. Considering the high error rate (49.9%) in publications of a simple calculation of a population genetic parameter revealed bySchenekar & Weiss (2011), our answer is this: about half of you are right."


Finally, here is some very harsh criticism against the data publication culture in the field of molecular ecology,  and the tendency to crank out too many papers, with too many authors and ignoring much of the classic work that has already been published and which would be relevant to cite:





Abstract: The field of molecular ecology has burgeoned into a large discipline spurred on by technical innovations that facilitate the rapid acquisition of large amounts of genotypic data, by the continuing development of theory to interpret results, and by the availability of computer programs to analyse data sets. As the discipline grows, however, misconceptions have become enshrined in the literature and are perpetuated by routine citations to other articles in molecular ecology. These misconceptions hamper a better understanding of the processes that influence genetic variation in natural populations and sometimes lead to erroneous conclusions. Here, we consider eight misconceptions commonly appearing in the literature: (i) some molecular markers are inherently better than other markers; (ii) mtDNA produces higher FST values than nDNA; (iii) estimated population coalescences are real; (iv) more data are always better; (v) one needs to do a Bayesian analysis; (vi) selective sweeps influence mtDNA data; (vii) equilibrium conditions are critical for estimating population parameters; and (viii) having better technology makes us smarter than our predecessors. This is clearly not an exhaustive list and many others can be added. It is, however, sufficient to illustrate why we all need to be more critical of our own understanding of molecular ecology and to be suspicious of self-evident truths.

Sunday, May 9, 2010

A new synthesis between community ecology and evolutionary biology?

On the lab-meeting this coming Wednesday (12 May, 2010), I would like to discuss a review article in TREE about the (possible) new and emerging synthesis between community ecology and evolutionary biology. You can download this article here. Hopefully, we can have a good and conceptually rich dicussion about the general message in this paper.

The lab-meeting the week after this one (i. e. May 17, 2010), I was planning to have a lab-meeting outdoors, meet the spring and (hopefully!) see the first emerged odonates of the year, followed by lunch at cosy outdooor museum and restaurant Kulturens Östarp. Stay tuned, more info soon.

Time and place for the coming lab-meeting the current week as usual:

Where: "Darwin"-room, 2nd floor, Ecology Building
When: May 10 2010, 10.15

Any fika-volunteer?