Palmer amaranth (Amaranthus palmeri) is a major weed in corn (Zea mays) fields in the southern Great Plains of the United States. Field studies were conducted in 1996, 1997, and 1998 near Garden City, KS, to evaluate the effects of Palmer amaranth density and time of emergence on grain yield of irrigated corn and on seed production of Palmer amaranth. Palmer amaranth was established at densities of 0.5, 1, 2, 4, and 8 plants m−1 of corn row both concurrently at corn planting and when corn was at the three- to six-leaf stage. The control plots were weed free. The Palmer amaranth planted with corn emerged with corn, whereas that planted later emerged at the four-, six-, and seven-leaf stages of corn. The Palmer amaranth emerging with corn reduced yield from 11 to 91% as density increased from 0.5 to 8 plants m−1 of row. In contrast, yield loss from Palmer amaranth emerging later than corn was observed only when the emergence occurred at the four- and six-leaf stages. The corn leaf area index (LAI) decreased as Palmer amaranth density increased. Reduction in corn LAI from Palmer amaranth interference was smaller for the second emergence date than for the first emergence date. Seed production per Palmer amaranth plant decreased with greater density, but seed per unit area increased from 140,000 to 514,000 seeds m−2 at densities of 0.5 and 8 plants m−1 of row, respectively, when Palmer amaranth emerged with corn and from 1,800 to 91,000 seeds m−2 at the same densities for later emergence dates. Although Palmer amaranth is highly competitive in corn, this study shows that yield loss is affected more by time of emergence than by density.

A study was conducted near Garden City, KS, under irrigated conditions to determine the effect of full-season Palmer amaranth infestation on corn water use efficiency and light interception in a fully developed corn canopy. Palmer amaranth at densities of 0, 0.5, 1, 2, 4, and 8 plants m−1 was established at corn planting in 1996 and 1997 and at two locations in 1998. Soil water was monitored 240 cm deep in 30-cm increments with a neutron probe each year and at each location every 10 d. Photosynthetic photon flux was measured in 1997 and 1998 by using a circular and a linear quantum sensor for above canopy and in four 50-cm increments for within canopy, respectively. Palmer amaranth reduced corn yield from 11 to 91% as density increased from 0.5 to 8 plants m−1. Water use efficiency of corn declined with increased Palmer amaranth density. Regardless of Palmer amaranth density, soil water extraction was greatest in the top 30 cm of the soil profile. The pattern of corn leaf area distribution was similar across Palmer amaranth densities, with 15, 70 to 75, and 5 to 15% of the total leaf area occurring 1.5 m, 0.5 to 1.5 m, and 0 to 0.5 m above the ground, respectively. In weed-free corn, over 60% of light was intercepted from 0.5 to 1.5 m above the ground. In contrast, in mixed canopies 60 to 80% of light was intercepted 1 m above the ground, where 80% of Palmer amaranth leaf area was concentrated. Under the conditions of this study, water was not a limiting factor. The effect of Palmer amaranth density on total light interception was not significant. However, within each treatment, light interception at different heights differed, emphasizing the importance of evaluating the vertical distribution of light through the canopy to assess the effect of weed height on light competition.

Gene flow from imidazolinone (IMI)-resistant domestic sunflower to IMI-susceptible common sunflower and prairie sunflower was studied. Under greenhouse conditions, pollen from IMI-resistant domesticated sunflower was applied to flower heads of IMI-susceptible common and prairie sunflower. In addition, field studies were conducted in 2000 and 2001 near Manhattan, KS, to evaluate IMI-resistant gene flow from IMI-resistant domesticated sunflower to common and prairie sunflower under natural conditions. Common and prairie sunflower were planted in concentric circles at distances of 2.5, 5, 15, and 30 m around a densely planted IMI-resistant domesticated sunflower species. For both greenhouse and field studies, IMI-resistant gene flow was determined by treating the progeny of both wild species with 40 g ai ha−1of imazamox. Greenhouse crosses made by hand showed that 94% of common sunflower and 79% of prairie sunflower were resistant or moderately resistant. The resistant plants were allowed to grow in the greenhouse and were backcrossed with the corresponding susceptible wild parents. Progeny of the backcross showed a 1:1 ratio of resistant to susceptible plants. In the field, gene flow was detected up to 30 m from the pollen source for both species, and it decreased as distance from the pollen source increased. In 2000, 11 to 22% of the progeny were resistant at 2.5 m from the pollen source and 0.3 to 5% were resistant at 30 m. In 2001, the number of resistant progeny did not exceed 7 and 2% at 2.5 and 30 m from the pollen source, respectively. The results of this study showed that IMI-resistant domesticated sunflower outcrosses with common and prairie sunflower over distances typically encountered near production fields. Also, backcrosses of resistant hybrids with wild parents are successful, further increasing the potential for the spread of IMI-resistant feral sunflowers.

Resistance to imidazolinone (IMI) herbicides has been incorporated recently into domesticated sunflower through conventional breeding methods. However, there are concerns regarding gene flow of the IMI-resistance trait to wild species and possible accompanying ecological consequences. Hybrids of domesticated sunflower with both common sunflower and prairie sunflower were created, with and without the imazamox-resistance trait. The relative fitness of imazamox-resistant (IMI-R) hybrids was compared with their imazamox-susceptible (IMI-S) counterparts. Greenhouse experiments were conducted to study the growth of IMI-R and IMI-S common and prairie sunflower hybrids under noncompetitive conditions. The photosynthesis rate of IMI-S prairie sunflower was slightly higher than that of IMI-R plants. However, relative growth rate, net assimilation rate, leaf area, and total dry weight were similar in IMI-R and IMI-S common and prairie sunflower, whereas plant height of IMI-S hybrid was greater than that of IMI-R common sunflower hybrids. A replacement series study was conducted under field conditions in 2001 and 2002 to evaluate the relative competitiveness of IMI-R and IMI-S common and prairie sunflower. IMI-R and IMI-S hybrids of both sunflower species were equally competitive. The results suggest that, in the absence of IMI herbicides, genes controlling IMI-R do not reduce or increase the competitive ability of either common or prairie sunflower. Therefore, if the IMI-resistant trait is incorporated in these species, the frequency of IMI-resistance genes is unlikely to decrease, even in the absence of IMI selection pressure.

Drought threatens the world's food production, particularly in Sub Saharan Africa low external input and rain fed agricultural systems, where cowpea (Vigna unguiculata (L.) Walp.) is an important food crop. In the context of growing concerns regarding climate changes implications on water availability, this study aimed at 1) to evaluate the drought responses in cowpea landraces with contrasting drought tolerance levels (A55high sensitivity; A80 -mild sensitivity; A116 -tolerant), 2) using an integrated physiological (leaf gas exchanges; chlorophyll a fluorescence) and biochemical (photoprotective pigments; RuBisCO activity; primary metabolite profiling) analysis to identify drought tolerance probes, in plants submitted to three water availability levels (well-watered, WW; mild drought, MD; severe drought, SD). A116 plants maintained a better water status under drought, what could justify the higher P n and P nmax values in MD, as well as higher photochemical use of energy (reflected in the photochemical quenching (q L ) and in the quantum yield of non-cyclic electron transport (Y (II) )), and the lower need of photoprotective thermal dissipation mechanisms (given by the non-photochemical quenching (q N ), and the quantum yield of regulated energy dissipation at photosystem PSII (Y (NPQ) )), in MD and SD plants. Greater declines of net (P n ) and potential (P nmax ) photosynthesis were observed in A55 plants, which frequently showed significant impacts already under MD conditions in most parameters, whereas A80 usually displayed and intermediate behaviour. Still, even A55 showed some acclimation response, regarding photoprotective mechanisms associated with high contents of zeaxanthin, lutein, and carotenes, and high Y (NPQ) , and q N values, supporting the absence of an increase in the non-regulated energy dissipation at PSII (Y (NO) did not increased) even in SD plants. Additionally, A55 was not significantly affected in RuBisCO activity, which showed to be quite resilient in cowpea. A primary metabolite profiling, complemented with a partial least square discrimination analysis (PLS-DA), allowed a better separation of A116 and A55 plants according to their degree of drought tolerance. In response to drought, A116 showed the greatest accumulation of most responsive metabolites, 14 in total, with sucrose, fucose, urea, alanine and putrescine being exclusively increased in this genotype, suggesting that they can be candidates as drought tolerance proxies. Other compounds, as proline, valine, isoleucine (among amino acids), and rhamnose and raffinose (among sugars) showed close increase patterns