Rice (Oryza sativa) is the staple food for more than 3.5 billion people worldwide. Yield levels in Asia have tripled and are expected to increase by 70% over the next 30 years due to population growth. In the US, Arkansas accounts for more than 50% of rice production. Over the last 68 years, rice production has continued to grow in Mississippi, placing it in fourth place after Arkansas, Louisiana, and California. Due to increasing rice acreage, regionally and worldwide, the need to develop abiotic stress tolerant rice has increased. Unfortunately, current rice breeding programs lack genetic diversity, and many traits have been lost through the domestication of cultivated rice. Currently, stressors stemming from the continued effects of climate change continue to impact rice. This chapter highlights current research that strives to discover abiotic and biotic stress tolerant rice. This chapter calls for directed research in genetics and genomics to address the need to discover biotic and abiotic stress tolerant traits. While many genes have been uncovered to arm rice against these stresses, decreased genetic variability in current rice traits presents a small gene pool for discovery.
Rice is a staple food for more than 3.5 billion people worldwide, with Asia producing almost 90% of the global rice yield. In the US, rice is primarily produced in four regions: Arkansas Grand Prairie, Mississippi Delta, Gulf Coast, and Sacramento Valley of California. Arkansas currently accounts for more than 50% of the rice produced in the US. As global temperatures continue to rise and fluctuate, crop-breeding programs must continue to evolve. Unfortunately, sudden submergence due to climate change and unpredictable flash flooding can cause yield reduction up to 100% and affect 20 million ha of agricultural farmlands. Similarly, it has been demonstrated that temperatures higher than 34°C can cause spikelet infertility resulting in up to 60% reduction in yield. One major drawback to developing abiotic stress-tolerant rice is the loss of critical traits such as vegetative vigor, spikelet fertility, and grain quality, which are essential in increasing economic return for farmers. To replace traits lost in past breeding endeavors, weedy rice (WR) has been proposed as a source for novel trait discovery to improve rice breeding programs. Therefore, the goal of this study was to screen and identify heat- and submergence-tolerant WR accessions. A WR mini germplasm consisting of seedlings at the 3–4 leaf stage was exposed to heat (38°C) and complete submergence for 21 days. After each treatment, height was recorded every 7 days for 28 days, and biomass was collected 28 days after treatment. The average height reduction across all accessions was 19 and 21% at 14 and 28 days after treatment (DAT) for the heat-stress treatment. The average height reduction across all accessions was 25 and 33% for the complete submergence stress. The average biomass reduction across all accessions was 18 and 21% for heat and complete submergence stress, respectively. Morphologically, at 28 DAT, 28% of the surviving WR accessions in the heat-stress treatment with <20% height reduction were straw-colored hull types without awns. Under complete submergence stress, 33% of the surviving WR accessions were blackhull types without awns. These specific biotypes may play a role in the increased resilience of WR populations to heat or submergence stress. The results presented in this paper will highlight elite WR accessions that can survive the effects of climate change.
Weedy rice is conspecific, the most troublesome weed of cultivated rice identified as a threat to global rice production. The weed has inherited high reproductive ability and high dormancy by outcrossing with modern rice cultivars and wild cultivars, respectively. Traits such as rapid growth, high tillering, enhanced ability to uptake fertilizers, asynchronous maturation, seed shattering, and long dormancy periods make weedy rice more competitive than cultivated rice. Weedy rice infesting rice fields are morphologically diverse with different hull color, awn length, plant height, and variable tiller number. Morphological diversity in weedy rice can be attributed to its high genetic diversity. Introgression of alleles from cultivated rice into weedy has resulted in high genetic and morphological diversity in weedy rice. Although variations among weedy rice populations make them difficult to control, on the brighter side, competitive nature of weedy rice could be considered as raw genetic materials for rice breeding program to develop vigorous rice plants able to tolerate high biotic and abiotic stresses.
Increasing agricultural productivity is indispensable to meet future food demand. Crop improvement programs rely heavily on genetic diversity. The success of weeds in the ecosystem can be attributed to genetic diversity and plasticity. Weedy rice, a major weed of rice, has diverse morphology and phenology, implying wide genetic diversity. Study was conducted to genotype weedy rice accessions (n = 54) previously phenotyped for herbicide tolerance and allelopathic potential using 30 SSR markers. Cultivated rice (CL163, REX) and allelopathic rice (RONDO, PI312777, PI338047) were also included in the study. Nei’s genetic diversity among weedy rice (0.45) was found to be higher than cultivated rice (0.24) but less than allelopathic rice (0.56). The genetic relationship and population structure based on herbicide tolerance and allelopathic potential were evaluated. Herbicide-tolerant and susceptible accessions formed distinct clusters in the dendrogram, indicating their genetic variation, whereas no distinction was observed between allelopathic and non-allelopathic weedy rice accessions. Weedy rice accession B2, which was previously reported to have high allelopathy and herbicide tolerance, was genetically distinct from other weedy rice. Results from the study will help leverage weedy rice for rice improvement programs as both rice and weedy rice are closely related, thus having a low breeding barrier.
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