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#crop protection

3 public questions tagged with this topic.

Which strategy delays insect resistance development?

Resistance evolution to Bt toxins accelerated when transgenic crops grown continuously on large acreage without alternative hosts for susceptible insects. Homozygous resistant insects emerging from Bt fields mating with each other rapidly increase resistance allele frequency. Refuge strategy maintains pool of susceptible individuals by planting non-transgenic crop nearby or mixing seeds. Susceptible moths from refuge mate with rare resistant survivors from Bt field producing heterozygous offspring. High dose of toxin expressed in transgenic plants kills heterozygotes because resistance generally recessive, diluting resistant alleles and delaying fixation. EPA mandates 20 percent structured refuge for cotton and 5 to 20 percent for corn depending on region. Data from Arizona pink bollworm program shows refuge compliance helped preserve Bt efficacy for over decade. Planting pattern may include block refuge, strip refuge, or seed mix. Hence mixing GM and non-GM crops implements high-dose refuge principle, primary tactic delaying insect resistance development to Cry toxins in commercial agriculture. Implementation details include 20 percent structured refuge for cotton and 5 to 20 percent for corn, planted within 0.5 mile of Bt field to ensure random mating. Monitoring of resistance allele frequency by F2 screen detects early resistance evolution allowing proactive management including increased refuge

Ref: Gould Annu Rev Entomol 1998 refuge strategy; Tabashnik Annu Rev Entomol 2013 mixing; NCBI NBK131103 insect resistance management; EPA refuge guidance 2001.

The main purpose of quarantine in plant introduction is to:

Quarantine imposes enforced isolation and testing to intercept exotic pathogens, nematodes, insects and weed seeds hidden in imported seeds, tubers or cuttings. Legal basis includes Destructive Insects and Pests Act 1914 and Plant Quarantine Order 2003 requiring inspection at seaports, airports and land customs. NBPGR National Quarantine Laboratory performs visual inspection, X-ray for insect damage, blotter test for fungi like Tilletia and Fusarium, washing test for seeds, and serological ELISA and PCR for viruses such as banana bunchy top and potato latent viruses. Suspect samples undergo fumigation with aluminum phosphide, hot water treatment at 52C, or pesticide dip before clearance. Effective quarantine prevented entry of devastating pathogens and preserves ecosystem equilibrium and export credibility of Indian agricultural produce. This understanding supports competitive exam preparation for NEET, GATE and CSIR NET concepts linking genotype with phenotype through molecular pathways involving transcription factors, hormones and metabolic enzymes that regulate development, adaptation and reproductive biology in applied breeding programs.

Ref: IPPC ISPM Standards; Plant Quarantine Order 2003; e-coursesonline.iasri.res.in Plant Quarantine chapter; NBPGR Quarantine.