Select Committee on Agriculture Minutes of Evidence



Examination of witnesses (Questions 40 - 59)

TUESDAY 18 JULY 2000

DR DAVID BUCKERIDGE and MR MIKE RUTHVEN

Mr Todd

  40. If I turn to your statement about your 1999 crop, you make a statement bearing in mind what you have just said that needs to be explored a little further. "A a result, there is no GM impurity in the 1999 harvest of spring oilseed rape seed delivered to Europe." What exactly does that mean?
  (Dr Buckeridge) It means that we ran a test, we took a statistically representative sample, we used a test method in a lab that we had audited and, at the statistical level of confidence which we used, which was a high level, we found no GM impurities.

  41. Could you explain that further? Does that mean that someone running a PCR test on that particular collection of seed would find no GM presence within it?
  (Dr Buckeridge) It is not possible to make that statement, no. All I can say to you is that we did a thorough test. It was an issue of great importance to us.

  42. Using the PCR?
  (Dr Buckeridge) We used a bio-assay test in that particular instance, because we were not confident of the reliability of PCR.

  43. Although you have accepted PCR in the context of this case, because that was how the original occurrence was identified.
  (Dr Buckeridge) Yes, but bear in mind that what we did when we heard the original occurrence was quantified by PCR was that we first of all did a follow-up test, and we also verified using a different method. Practically, as we have said in the submission, the industry is going to have to accept that a variant of PCR testing will be the method that has to be used. The reasons for that are logistical reasons. To turn seed around between seasons is a very tight turnaround, and we will need a test that can deliver a result very quickly. It does not take away the reservations we have about the reliability of the test and the reservations that independent scientists and publications that have come through people like MAFF have about the reliability of the test. There are definite flaws in the methodology. It is not to say that the methodology in five years' time will not overcome those flaws, but right now, as we sit here, particularly looking at brassica crops, there are questions around that methodology.

  44. There is another implication of that statement, which is that, even taking the qualifications you have now put into that about what no GM impurity actually means, it does indicate that the company took risks with the 1998 crop which it chose not to take with the 1999 crop. In other words, it understood the possibility of contamination. As you said earlier in the paragraph, on the basis of precaution rather than any suspicion of possible contamination, you moved your supply within the North American continent to different locations. That does imply a degree of carelessness on the part of your company.
  (Dr Buckeridge) No, it does not. As I said earlier, the environment in the prairies of Canada for producing seed with respect to GM impurities was very different in 1998 compared to 1999. In 1999 55 per cent of the Canadian crop was GM. The land had been subjected to GM crops for a further year. In our opinion, it was not possible to get the level of seed purity protection in 1999 that we could achieve in—

  45. Surely that is a matter of modest degree rather than principle.
  (Dr Buckeridge) No, I do not agree.

  46. In your figures in 1998 the level of GM crops was 35 per cent, so the move from 35 to 55 which triggered your decision to move. So it is a matter of degree, is it not, as to what degree of risk you were prepared to take with your customers?
  (Dr Buckeridge) I think a 60 per cent increase in the acreage is quite significant.

  47. Yes, but 35 per cent available acreage anywhere was quite significant. Your risk analysis would appear to be not as robust as one might wish from a company seeking to sell to customers on a confident basis.
  (Dr Buckeridge) As I say, we made a risk assessment in 1998 in the context of the environment that was there in front of us.

  48. You made a different one in 1999 on the basis of some increase.
  (Dr Buckeridge) On the basis of some increase and on the basis that the fields that were available to us were far more likely to have already grown GM crops, so there was also a risk in those fields.

  49. My own question at this point is that this evidence, not surprisingly, focuses largely on UK reaction, although as we may explore with the Minister, the reaction of Sweden comes into this as well. You presumably sold your seed widely in other parts of Europe, including in Germany, where the problem was detected. We are not party in this evidence to what reaction there has been in other parts of your marketplace.
  (Dr Buckeridge) I would be happy to expand if that is of interest.

  50. I would be interested to know.
  (Dr Buckeridge) When we first learned about the problem in Germany, as I said earlier, we checked through seed lots to find out whether those specific seed lots of that particular variety had been distributed elsewhere. We then did a further check of seed lots when we were suspicious but without evidence that a couple of other varieties could have also been affected. That led us to understand that the seed had been sold, as we knew, in Germany, in the UK, and then there were small acreages in France. We were also concerned about acreages in Sweden and Finland. We checked what had happened to that seed, and in the case of Sweden it was reported to us that no seed had left the distributors' warehouse. This was, I think, to do with the more northerly latitude and the later planting dates. So immediately that seed was stopped. Later on the distributor came back to us and said that they had found some seed from the 1998 production in merchants' warehouses, and that that seed had gone into the ground, but it was a small quantity; that they had immediately notified the Swedish authorities of that event, and that information was received by us on 15 or 16 May. That information was immediately communicated to the UK government so that they were aware of the Swedish situation. We had told them earlier about seed in France and seed in Germany, but we had done the check on Sweden and got a negative response from our distributor. When the distributor came back and said he had found some seed, we immediately informed the UK Government. The Swedish Ministry discussed the issue with the distributor in Sweden and made a public statement on, I think I am right in saying, 16 May.

  51. Within 24 hours. We will touch on that with the Minister. You mentioned France, where presumably sowing had already taken place.
  (Dr Buckeridge) Yes.

  52. What has happened there?
  (Dr Buckeridge) The French situation is that the French Government concluded that it should order the destruction of the crop. The destruction of the crop was ordered in France before—and I would have to check and send you a note on when that decision was made. The French situation is almost identical to the UK situation at this moment, in that we have agreed a compensation plan for the farmers in France, the crops have been ploughed out of the ground in France, and so the situation is very parallel.

  53. The last thing is what level of purity as seed suppliers do you seek for these particular varieties in normal circumstances?
  (Mr Ruthven) Within the existing regulations?

  54. Yes.
  (Mr Ruthven) If it were open pollinated rape, the genetic purity would be 0.3 per cent and the mechanical purity would be 2 per cent. Because of the parentage in hybrid rapes, there is a very high degree of genetic impurity permitted, and that is 10 per cent.

  55. So actually the level of tolerance is very high in these particular varieties.
  (Mr Ruthven) On these particular varieties, yes.

Mr Drew

  56. Given your demand for regulation, it sounds as though you have no confidence whatsoever in the self-regulatory regime, ie drawn up by SCIMAC. Is that true to say?
  (Dr Buckeridge) I think that SCIMAC scheme relates specifically to GM crops and the testing of GM crops or issues of environmental diversity. I think we have confidence in that scheme. We support it. There has been talk about review of the separation distances in that scheme. We think that is appropriate. Even when you have an experience like this, it is always appropriate to look at things like that. I do not think it is fair to say we do not have confidence in the scheme.

  57. But surely SCIMAC must have discussed these arrangements as well. The different bodies within the trade association must have seen this as a potential problem that was bound to arise.
  (Dr Buckeridge) The trade association certainly saw GM impurities as a potential problem and made their views on that clear through their European Association to the Commission in October 1999.

  58. So what degree of regulation would you want to see?
  (Dr Buckeridge) We would like to see a clear threshold set. We would like regulations to specify a testing method, we would like to see regulations specify a statistical analysis of the results of those tests, and we believe the seed industry should comply with that. This is an issue of great public sensitivity. I do not think it is appropriate to have that issue governed by industry self-regulation. I think it is appropriate that there are regulations.
  (Mr Ruthven) Could I add to that? The ordinary seed regulations are well understood and are internationally standardised so that the seed can move around the world, as it does. You have heard, for instance, that we are producing seed now in New Zealand, in Montana and in eastern Canada. Other species may come from a number of different countries. The seed moves around and the regulations are very much the same in all countries. So we believe that the reason the regulation is needed is not only for the reasons Dr Buckeridge has explained, but it does need to be internationally recognised so that when the seed is received in this country or when it is sold in this country and produced locally, its certification can be relied on by the consuming farmer and the consumer in general.

  59. Is it fair to say that if full product liability was in place, that is an alternative way of doing this and you would be in considerable difficulties now? It may well be that you would blame people who have polluted your crop, but is that something you would have to face up to?
  (Mr Ruthven) I think the issues of liability are extremely difficult. The contracts between seed companies internationally have certification on a document called an orange international certificate, and a great deal of reliance can be placed upon the information in that certificate under international rules. If a similar process were adopted for GM, which would probably fit quite comfortably with that sort of regulation, it would be possible to pinpoint the question of liability in the contractual chain.


 
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