» Articles » PMID: 11559838

Temporal and Spatial Overlap Between Monarch Larvae and Corn Pollen

Overview
Specialty Science
Date 2001 Sep 18
PMID 11559838
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

To assess the likelihood that monarch larvae will be exposed to Bacillus thuringiensis (Bt) pollen, we studied milkweed and monarch densities in habitats which comprise much of the land available to breeding monarchs, e.g., cornfields, cornfield edges, other agricultural fields, and nonagricultural areas, in four regions of the monarch breeding range. We found that monarchs use milkweed in cornfields throughout their breeding season, and that per plant densities are as high or higher in agricultural habitats as in nonagricultural habitats. As a result of the prevalence of agricultural land, most of the monarchs produced in the upper Midwest are likely to originate in cornfields or other agricultural habitats. There was a greater temporal overlap between susceptible monarchs and corn anthesis in the northern than the southern part of the summer breeding range, because of earlier pollen shed in the south. The importance of agricultural habitats to monarch production suggests that, regardless of the impact of genetically modified crops, agricultural practices such as weed control and foliar insecticide use could have large impacts on monarch populations.

Citing Articles

Differences in drought avoidance rather than differences in the fast versus slow growth spectrum explain distributions of two Asclepias species.

Matzner S, Konz E, Marts S, Eversman H, Kasuske K, Atkins T Physiol Plant. 2024; 177(1):e70034.

PMID: 39723722 PMC: 11800957. DOI: 10.1111/ppl.70034.


Processes for regulating genetically modified and gene edited plants.

Caradus J GM Crops Food. 2023; 14(1):1-41.

PMID: 37690075 PMC: 10761188. DOI: 10.1080/21645698.2023.2252947.


Different factors limit early- and late-season windows of opportunity for monarch development.

Yang L, Swan K, Bastin E, Aguilar J, Cenzer M, Codd A Ecol Evol. 2022; 12(7):e9039.

PMID: 35845370 PMC: 9273743. DOI: 10.1002/ece3.9039.


Lessons learned from the introduction of genetically engineered crops: relevance to gene drive deployment in Africa.

Quemada H Transgenic Res. 2022; 31(3):285-311.

PMID: 35545692 PMC: 9135826. DOI: 10.1007/s11248-022-00300-2.


Host Plant Species Mediates Impact of Neonicotinoid Exposure to Monarch Butterflies.

Prouty C, Barriga P, Davis A, Krischik V, Altizer S Insects. 2021; 12(11).

PMID: 34821799 PMC: 8623494. DOI: 10.3390/insects12110999.


References
1.
Hellmich R, Siegfried B, Sears M, Daniels M, Mattila H, Spencer T . Monarch larvae sensitivity to Bacillus thuringiensis- purified proteins and pollen. Proc Natl Acad Sci U S A. 2001; 98(21):11925-30. PMC: 59744. DOI: 10.1073/pnas.211297698. View

2.
Pleasants J, Hellmich R, Dively G, Sears M, Mattila H, Foster J . Corn pollen deposition on milkweeds in and near cornfields. Proc Natl Acad Sci U S A. 2001; 98(21):11919-24. PMC: 59743. DOI: 10.1073/pnas.211287498. View

3.
Hansen Jesse L, Obrycki J . Field deposition of Bt transgenic corn pollen: lethal effects on the monarch butterfly. Oecologia. 2014; 125(2):241-248. DOI: 10.1007/s004420000502. View

4.
Wassenaar L, Hobson A . Natal origins of migratory monarch butterflies at wintering colonies in Mexico: new isotopic evidence. Proc Natl Acad Sci U S A. 1998; 95(26):15436-9. PMC: 28060. DOI: 10.1073/pnas.95.26.15436. View

5.
Losey J, Rayor L, Carter M . Transgenic pollen harms monarch larvae. Nature. 1999; 399(6733):214. DOI: 10.1038/20338. View