Translator Disclaimer
1 September 2006 Response from Soleri and colleagues
Author Affiliations +

Ortiz-García and colleagues (2005a) agreed with us that variance effective population size (Ne(v)), not census population size (n), should be used to estimate transgene frequency (Vencovsky and Crossa 1999), and reanalyzed their data using Ne(v) with two additional statistical tests. The first was based on the assumption that sampled maize populations had no significant structure, which is not valid (Cleveland et al. 2005). The second, Fisher's combined probability test, gave a minimum detection level for seeds in 2004 of approximately 1% (0.00775, P < 0.05) (Ortiz-García et al. 2005b), close to our estimate of approximately 1%–4% (0.00961–0.03586, P < 0.05) across individual locations, accounting for population structure (Cleveland et al. 2005), and contrasted with their original estimate of 0.01%, P = 0.00003 (Ortiz-García et al. 2005a). Therefore, there is no evidence to refute our conclusion that “we still do not have any data to support the proposition that transgenes are not present at other localities, or at frequencies below 1–4% in the localities in the Ortiz-García et al. study” (Cleveland et al. 2005, p. 205).

Although Ortiz-García and colleagues assume that Quist and Chapela's study showed transgenes “common in traditional maize varieties,” that study was based on a very small, nonrandom sample; the study showed only transgene presence and thus cannot be used to estimate changes in transgene frequency (Cleveland et al. 2005).

It is important to see the debate about transgene presence from unintended gene flow in a wider policy context: Commercialization of transgenic varieties, especially in centers of origin, may have difficult-to-predict effects—many irreversible—on landrace diversity and farmer well-being. Therefore, wide scientific discussion of research methodologies and results is critical.

References cited

  1. D. A. Cleveland, D. Soleri, F. Aragón Cuevas, J. Crossa, and P. Gepts . 2005. Detecting (trans)gene flow to landraces in centers of crop origin: Lessons from the case of maize in Mexico. Environmental Biosafety Research 4:197–208. Google Scholar

  2. S. Ortiz-García, E. Ezcurra, B. Schoel, F. Acevedo, J. Soberón, and A. A. Snow . 2005a. Reply to Cleveland et al.'s “Detecting (trans)gene flow to landraces in centers of crop origin: Lessons from the case of maize in Mexico.”. Environmental Biosafety Research 4:209–215. Google Scholar

  3. S. Ortiz-García, E. Ezcurra, B. Schoel, F. Acevedo, J. Soberón, and A. A. Snow . 2005b. Absence of detectable transgenes in local landraces of maize in Oaxaca, Mexico (2003–2004). Proceedings of the National Academy of Sciences 102:12338–12343. Google Scholar

  4. R. Vencovsky and J. Crossa . 1999. Variance effective population size under mixed self and random mating with applications to genetic conservation of species. Crop Science 39:1282–1294. Google Scholar


[1] The authors thank José Crossa for comments on this letter.

DANIELA SOLERI, DAVID A. CLEVELAND, and FLAVIO ARAGÓN CUEVAS "Response from Soleri and colleagues," BioScience 56(9), (1 September 2006).[709:RFSAC]2.0.CO;2
Published: 1 September 2006

Back to Top