The accessions in Spain fall mainly everywhere

My ex-colleagues at the Crop Trust have a very nice animation on the Genesys blog-type thing showing the progress of landrace collecting around the world over the past 125 years.

Do please read the post for the details of how it was done, and some observations on the results.

Here I just wanted to highlight something that has always intrigued me: how did Spain get so heavily collected? It’s really striking how in any global map of collecting localities, Spain looks like a solid carpet, with genebank accessions from practically every nook and cranny. More so than most neighbouring countries, I would say.

Well, it’s a little difficult to be sure because there’s no slider on the animation to take it backwards and forwards at will, but it looks like a burst of collecting first in the 40s, and then some filling in of gaps in the 80s, are responsible for the blanket coverage.

Maybe someone more familiar with the history of germplasm collecting in Spain can explain more.

Brainfood: Mapping edition

Mind the conservation gap

In the interest of completeness, I feel it incumbent upon me to complement the post on gap analysis for crop diversity conservation that I put up a few days ago with a couple of additional links.

The Crop Trust and FAO elearning Academy have collaborated on a course on the Global Crop Conservation Strategies that includes a lesson on “Crop coverage assessments and gap analysis.”

And the Crop Trust has also made available a “Curriculum of an online lesson for gap analysis.”

So there’s really no excuse for not doing your own gap analysis, is there? And add to the storied history of the field.

A brief history of gap analysis for crop diversity conservation

Many thanks to long-time friend-of-the-blog Dr Colin Khoury for this latest contribution.

Conservation gap analysis using Geographic Information System (GIS) tools relies on several sources of biological and environmental data, including in situ species occurrences and climatic and other environmental variables used to conduct species distribution modeling, as well as passport data from ex situ collections. While species distribution modeling and associated methods had been in development since at least the 1970s (see Rebelo, 1994 and Booth et al., 2013), the widespread use of these tools was not possible until such biological and environmental data were more easily and widely accessible, for example through GBIF, WorldClim, and Genesys.

Genebank scientists, often in collaboration with academic researchers, began to apply available GIS-based tools to PGRFA conservation around the turn of the century, proceeding to develop new methods, software, and datasets (for early examples, see Guarino, 1995; Greene and Guarino, 1999; Guarino et al., 2002). Global climate datasets were compiled at relatively high spatial resolution (e.g., Hijmans et al., 2005), providing key inputs for species distribution modeling. Current distribution models for plant genetic resources began to be calculated, for example for wild relatives of potatoes and peanuts, while future distributions under climate change also began to be modeled, for example for wild peanuts, potatoes, and cowpeas. Field collecting was informed through these tools, for example for wild clover and wild chile pepper expeditions.

The focus on wild relatives of food and agricultural crops was not haphazard. These species were receiving increasing conservation attention at the time in recognition of their value as genetic resources for crop breeding, and because many wild relatives were known to be threatened in their natural habitats and were underrepresented in ex situ repositories. International conservation targets for crop wild relatives had been set at the Convention on Biological Diversity (CBD) (for 2011 to 2020 and again for 2020 to 2030) and in the United Nations Sustainable Development Goals (SDGs) (for 2015 to 2030). At the same time, species distribution modeling methods had primarily been developed for wild species, i.e. taxa whose distributions are mainly driven by climatic, edaphic, and other environmental factors, rather than human preferences (which are more difficult to model), therefore the application of these methods to crop wild relatives was relatively straightforward and a logical starting point for the agricultural research community.

Programs such as DIVA-GIS and FloraMap were created to make the methods more accessible to researchers and practitioners without extensive GIS experience and computing power. Such efforts continue, for example by CAPFITOGEN.

Through an international genebank initiative called the Global Public Goods Project II, run from 2007-2010, the distributions of the wild relatives of ten CGIAR mandate crops were mapped, with priorities for further collecting for ex situ conservation identified. A major milestone of that project was the publication of a standardized, replicable gap analysis methodology for the ex situ conservation of crop wild relatives, which made use of herbarium and other biodiversity observations acquired through GBIF and other sources, as well as genebank passport data, and which embraced recent advancements in species distribution modeling methods.

Continue reading “A brief history of gap analysis for crop diversity conservation”

Himalayan maize: The saga continues

I decided to dig a little deeper into the climatic adaptation of Himalayan maize. You may remember from my last post on this that Genesys has 96 maize accessions from over 2000 masl in the Himalayas, collected at some 50-odd unique localities. When I ran these accessions through the Subsetting Tool in Genesys, I got the following histogram.

What struck me — and surprised me — was the spike of sites way at the left hand of the precipitation plot. So I took a closer look at the results of the subsetting analysis. And the clustering algorithm it uses to look for similar sites did in fact identify two climatically quite different groups of locations: 45 of the unique high altitude maize collecting sites (the blue ones) are indeed drier than the other 7 (in orange).

Much drier. (And also colder actually, but that’s another story.)

They’re the ones mainly collected in Pakistan and Afghanistan.

Now, I don’t know whether these areas really get 135 mm of annual precipitation, which seems really low, and in any case the agriculture there is clearly irrigated.

But those maize samples, mainly now conserved at CGN in the Netherlands incidentally, the results of something called the 1976 Netherlands-Pakistan Expedition by the Stichting voor Plantenveredeling, do seem to have some very unique adaptations.