Common Cocklebur Plants Research Articles

Ankara ayçiçeği ekim alanlarında sorun olan domuz pıtrağı (Xanthium strumarium L.)‘nın meydana getirdiği ürün kayıpları ve ekonomik zarar eşiğinin belirlenmesi

High nutritive content, using in various industrial sectors and adaptation of various regions of sunflower ( Helianthus annuus L.) have allowed of cultivation and consumption at high scale. One of the important problems of sunflower prevalently cultivated in Marmara and Central Anatolia Regions is weeds. Among the weeds, common cocklebur ( Xanthium strumarium L.) is very important because it has a competitive character, and there is only one herbicide registered to control this weed. The field study was carried out to determine the economic threshold of common cocklebur in sunflower from 2013 to 2015 in Ankara. According to the three-year study values, the highest sunflower plant length (138.33 cm), head diameter (14.4 cm) and 1000-seed weight (85.03 g) were obtained from the control parcels while the lowest plant length (104.17 cm), head diameter (10.41 cm) and 1000-seed weight (62.81 g) were taken from the parcels consisted of 16 common cocklebur plants. The economic thresholds were calculated using the current sunflower price and the herbicide, imazamox (40 g l -1 SL), price. The economic threshold in 2013, 2014 and 2015 were computed as 1.22 plant m -2 (Y=-7.139x+142.23), 0.61 plant m-2 (Y=-8.041x+145.84), 1.97 plant m -2 (Y=-9.78x+140.26). To control common cocklebur economically in Ankara herbicide applications should be done when the intensity of common cocklebur reaches the values, 0.61-1.97 plant m -2 .

Influence of Increasing Common Ragweed (Ambrosia artemisiifolia) or Common Cocklebur (Xanthium strumarium) Densities on Forage Nutritive Value and Yield in Tall Fescue Pastures and Hay Fields

Separate field trials were conducted in 2007 and 2008 to investigate the effects of increasing densities of common ragweed or common cocklebur on total yield and forage nutritive values in tall fescue pastures. Common ragweed densities ranged from 0 to 188 plants m−2, and common cocklebur densities ranged from 0 to 134 plants m−2. Total biomass yields (weeds plus tall fescue) were determined in response to each weed density and species; pure samples of tall fescue, common ragweed, or common cocklebur were also hand collected from each plot at the time of the total biomass harvest. Near-infrared spectroscopy was used to predict crude protein (CP) concentration and in vitro true digestibility (IVTD) of the total harvested biomass, pure tall fescue, and pure weed species in each plot. Results indicate that biomass yields may increase by as much as 5 kg ha−1with each additional common ragweed plant m−2within a tall fescue stand. Additionally, CP concentration of the total harvested biomass, pure weed species, and tall fescue decreased by 0.2 to 0.4 g kg−1with each additional increase in common ragweed or common cocklebur plant per m−2. As weed densities increased, IVTD of pure tall fescue samples increased only minimally (0.04%), regardless of the weed species. An increase in common ragweed density also resulted in the CP concentration of pure samples of common ragweed to decrease by 0.2 g kg−1for each additional plant per m2and by 0.4 g kg−1for each additional common cocklebur per m2. Overall, results from these experiments indicate that plant biomass yield and nutritive values of the total harvested biomass are only marginally influenced by increasing common ragweed or common cocklebur densities.

Common Cocklebur Competition in Forage Maize

Common cocklebur is a new weed in irrigated maize grown for forage in the hot, dry region of northwest Pakistan. We conducted experiments in the Khyber Pakhtunkhwa Province, Peshawar, Pakistan, during 2006 and 2007 to evaluate the interaction of common cocklebur density and maize density on biomass, leaf area index (LAI), and plant height of forage maize. Seven common cocklebur densities (0, 2, 4, 6, 8, 10, and 12 plants m−2) in maize planted at four densities (5, 7.5, 10, and 12.5 plants m−2) were evaluated. An ANOVA for both years revealed significant main effects and interactions for all variables. Regression of measured variables against common cocklebur density showed that maize biomass declined linearly as common cocklebur density increased from 0 to 12 plants m−2, with an increasing rate of decline for high maize densities and low maize densities. Combined data for all maize densities revealed that the relationship between maize biomass and common cocklebur biomass fit a linear function, with 1.28 to 1.35 kg ha−1loss in maize biomass for each kilogram per hectare increase in common cocklebur biomass from about 1,500 to 3,200 kg ha−1. Above 8 to 10 common cocklebur plants m−2, weed biomass declined, presumably due to intraspecific competition. An increase in common cocklebur density decreased maize LAI about 0.15 to 0.3 units for each additional common cocklebur plant per square meter in 2006, and 0.11 to 0.24 units in 2007. Common cocklebur LAI increased in a linear fashion as density of the weed increased. Results suggest that the effect of common cocklebur interference on maize biomass was associated with a change in allocation of resources, resulting in increased crop height growth at the expense of a reduction in LAI and presumably potential light interception by the crop as common cocklebur density increased.

Southern Root-Knot Nematode (Meloidogyne incognita) Affects Common Cocklebur (Xanthium strumarium) Interference with Cotton

Southern Root-Knot nematode and common cocklebur interfere with cotton growth and yield. A greater understanding of the interaction of these pests with cotton growth and yield is needed for effective integrated pest management (IPM). An additive design was used in outdoor microplots with five common cocklebur densities (0, 1, 2, 4, and 8 plants per plot) growing in competition with cotton, with and without the presence of southern Root-Knot nematode. Differences in cotton height could not be detected among common cocklebur densities or nematode presence at 3 wk after transplanting (WAT); however, differences in crop height were observed at 5 WAT between nematode treatments. In the absence of nematodes, the relationship between cotton yield loss and common cocklebur density was described by a rectangular hyperbolic regression model (P < 0.0001). Maximum yield loss from common cocklebur in the absence of nematodes exceeded 80%. In the presence of nematodes, there was a linear relationship between cotton yield loss and common cocklebur density (P = 0.0506). The presence of nematodes at each common cocklebur density increased cotton yield loss 15 to 35%. Common cocklebur plant biomass was 25% greater in nematode treatments, likely because of the reduced competitiveness of the cotton plants in these plots. This study demonstrates that multiple pests can interact to cause an additive reduction in crop yield.

Management of Acetolactate Synthase (ALS)–Resistant Common Cocklebur (Xanthium strumarium) in Soybean

A fixed-plot management study for control of acetolactate synthase (ALS)–resistant common cocklebur in soybean was initiated in 1994 at Fayetteville, AR. Three susceptible and three imazaquin-resistant common cocklebur plants were transplanted into the field, and seed (burs) were distributed throughout the plots in the fall of 1994. Herbicide treatments included imazaquin, chlorimuron, and chlorimuron plus metribuzin applied each year from 1995 through 1999 and herbicide rotations containing ALS inhibitors and herbicides with alternative modes of action. Effectiveness of management systems and the dynamics of the development of common cocklebur resistance, including development of resistance to imazaquin and chlorimuron, were evaluated. Imazaquin controlled susceptible common cocklebur populations in 1995 but not the resistant population, resulting in significant soybean yield reduction. By the end of the 1996 season, the resistant biotype dominated imazaquin plots, and a high level of cross-resistance to chlorimuron was observed in the population. Resistant populations were reduced by non-ALS herbicide programs of sulfentrazone plus clomazone applied preemergence (PRE), metribuzin plus clomazone applied PRE followed by bentazon applied postemergence (POST), and transgenic herbicide programs of glyphosate and glufosinate applied POST. Rotating ALS inhibitors with non–ALS-inhibiting heribicides may slow the development of resistance, but resistant individuals may eventually dominate the population.

Intraspecific variability of the acetolactate synthase gene

Common ragweed and common cocklebur plants were collected at two sites each in Illinois, Minnesota, and Ohio to analyze intraspecific variability of the gene encoding acetolactate synthase (ALS). A 385-nucleotide fragment within the coding sequence ofALSwas compared among 24 plants of each of these two species from the six locations. Common ragweedALSwas highly variable, with polymorphisms observed at 48 (12.5%) of the 385 nucleotides among the 24 plants. Despite the numerous nucleotide polymorphisms, only two inferred amino acid polymorphisms were identified. No apparent population structure was suggested by theALSsequence data, indicating widespread gene flow consistent with the wind-pollinated nature of common ragweed. In contrast to common ragweed, noALSpolymorphisms were identified among the common cocklebur plants used in this study. As a basis for comparing the extremes observed between common ragweed and common cocklebur,ALSintraspecific variability also was investigated in 10 plants each of tall waterhemp and smooth pigweed. Normalized to the number of plants analyzed, the number of nucleotide polymorphisms for both tall waterhemp and smooth pigweed was greater than that in common cocklebur but less than that observed in common ragweed. Information on variability of herbicide target-site genes may be useful in predicting the likelihood for herbicide-resistance development. However, all four of the species investigated in this study have evolved resistance to ALS-inhibiting herbicides, despite the different levels ofALSvariability observed.

Variability in Photosynthetic Rates and Accumulated Biomass Among Greenhouse-Grown Common Cocklebur (Xanthium strumarium) Accessions1

Common cocklebur is an adaptable and competitive weed with variable morphology. To learn how the rate of net photosynthesis (Pn) by common cocklebur relates to traits that may influence competitiveness, we compared Pn, accumulation of biomass (shoot mass, root mass, and total plant mass), and total leaf area among six accessions of common cocklebur grown in a greenhouse. There were highly significant (P ≤ 0.01) differences among accessions for all measured traits. Correlations of each measure of biomass with total leaf area were positive and highly significant, but correlations of Pn with each biomass measure and with total leaf area were negative. The negative correlations were largely a result of relatively low biomass accumulation by the two accessions with the highest Pn. This contrasted with results from a previous experiment on field-grown common cocklebur plants, in which the correlation of Pn with shoot mass was positive (r = 0.64). Despite the negative Pn-to-biomass correlations in the greenhouse study, the rank among accessions for Pn in the greenhouse was nearly the same as with the field-grown plants (Spearman rank correlation r = 0.89). We conclude that the relative Pn rates among common cocklebur accessions grown in the greenhouse may be used to predict their relative Pn rates in the field, but relationships of Pn with biomass or leaf area observed in the greenhouse may not be a reliable indicator of relationships in the field.Nomenclature: Common cocklebur, Xanthium strumarium L. #3 XANTH.Additional index words: Biotype, competitiveness, leaf area, photosynthesis, stomatal density.Abbreviations: CDT, Central Daylight Time; Pn, net photosynthetic rate; PPFD, photosynthetic photon flux density; TOD, time of day.

Influence of planting date on common cocklebur (Xanthium strumarium) interference in early-maturing soybean (Glycine max)

Field studies were conducted to determine the effect of common cocklebur interference in early-maturing (maturity group IV) soybean planted in April, May, and July. Common cocklebur density and length of interference did not affect soybean height, canopy width, or node number at any planting date. Removal of common cocklebur 4 weeks after emergence (WAE) prevented reduction of soybean leaf area, stem dry weight, dry leaf weight, dry pod weight, and seed yield. Aboveground biomass for common cocklebur emerging in July was less than biomass of April or May plantings. Common cocklebur planted into soybean 2, 4, or 8 wk after soybean emergence did not reduce soybean yield. Under parameters of this study, planting date was not a significant factor in yield reduction. Interference from one common cocklebur plant per 1.8, 0.9, and 0.3 m of soybean row for 8 wk reduced yields 7, 14, and 30%, and full-season interference reduced yields 16, 33, and 65%, respectively. The Arkansas Weed Management Computer program closely predicted actual yield loss for early-maturing soybean.

Soybean (Glycine max), common cocklebur (Xanthium strumarium), and sicklepod (Senna obtusifolia) sap flow in interspecific competition

Two field experiments were conducted to examine the competitive effect of common cocklebur and sicklepod in soybean. Factors examined included sap flow of both the weed and the crop, as well as the traditional parameters of weed and crop growth and crop yield. The intent was to determine to what extent competitive effects could be attributed to differential water utilization. In the first study, soybean planted at 20 plants m−1row was infested with either sicklepod at 10 plants m−1row or common cocklebur at two plants m−1row. Sicklepod reduced soybean sap flow and yield 53 and 49%, respectively. Common cocklebur reduced soybean sap flow and yield 31 and 38%, respectively. Within a weed species, weed-induced yield and sap flow reductions were comparable, indicating that water deprivation was the primary detriment that these weeds inflicted on soybean. Individual common cocklebur plants were 3.9 times more competitive than sicklepod with respect to reducing soybean yield. However, sap flow of individual common cocklebur plants was only 1.4 times more than that of sicklepod, indicating that water deprivation was not the only causal factor in weed-crop competition. In the second experiment, sicklepod was planted in soybean (fixed density) and clipped to either half the height, same height as soybean, or left unclipped, in an attempt to simulate herbicide-induced stunting. Clipping sicklepod had a positive effect on soybean sap flow and yield. Thus, the benefits of reduced weed competition were achieved without killing sicklepod.

Shoot and Root Interference of Common Cocklebur (Xanthium strumarium) and Soybean (Glycine max)

Field experiments were conducted in 1986 and 1987 to determine the effects of shoot and root interference of common cocklebur and soybean. Plants were grown in porous membrane envelopes. Common cocklebur plants had a longer vegetative growth period than soybean and were twice as tall as soybean at maturity. Soybean root and shoot dry weight and seed yield were reduced by shoot and whole plant (root and shoot) interference of common cocklebur, with whole plant interference giving the greatest reduction. Common cocklebur growth was affected little by soybean interference. Common cocklebur shoot interference alone reduced total soybean seed weight by 48%, the amount caused by common cocklebur whole plant interference.

Interference of Common Cocklebur (Xanthium strumarium) and Cotton (Gossypium hirsutum)

An area of influence method with biweekly destructive harvests 5 through 19 wk after planting (WAP) was used to monitor the reciprocal interference of common cocklebur and cotton in 1987 and 1988. Plant heights, leaf area, and leaf, stem, boll, fiber, and total plant biomass dry weights were measured in 15-cm increments away from common cocklebur or from a randomly selected cotton plant out to 105 cm. Data indicated that cotton less than 60 cm from common cocklebur was shorter, had less leaf area and lower leaf, stem, boll, and biomass dry weights than cotton beyond 60 cm from common cocklebur or cotton grown without common cocklebur interference. Differences in leaf area and biomass between cotton grown with and without common cocklebur interference were greater at and beyond 13 WAP sample dates than before 13 WAP. By 15 WAP, cotton leaf area and biomass were reduced an estimated 11% and 15%, respectively, averaged over the entire 105 cm of row. Cotton yield, harvested 27 WAP, was reduced an estimated 31% on plants grown with one common cocklebur plant per 2.1 m. Cotton yield was reduced on plants out to 99 cm from common cocklebur. Common cocklebur and cotton plants grown alone were taller, had greater leaf area, and greater leaf, stem, and biomass dry weight than those respective plants grown adjacent to cotton. Common cocklebur grown alone produced 67% more biomass than did cotton grown alone. Cotton plants grown adjacent to other cotton plants produced 89% and 96% less boll and fiber weight, respectively, than plants grown alone.

Interference Between Soybeans (Glycine max) and Common Cocklebur (Xanthium strumarium) Under Indiana Field Conditions

The effects of interference between soybeans and common cocklebur were investigated. Common cocklebur interference reduced soybean growth at each of four sample dates during the growing season. The area of interference surrounding individual common cocklebur plants within the soybean row fluctuated over time with respect to intensity and spatial distribution. Soybean growth was significantly reduced up to 10 cm away from individual cocklebur plants at 6 weeks after planting (WAP), 30 cm at 8 WAP, 20 to 30 cm at 10 WAP, and 40 cm at 12 WAP. The maximum possible distance of cocklebur influence, determined by regression analysis, also varied during the growing season. When areas of interference from adjacent cocklebur plants overlapped, the cumulative influence was found to be additive, especially late in the growing season. Soybean interference caused a 50 to 90% reduction in the size of common cocklebur plants grown within the soybean row compared to plants grown without interference. At harvest, soybean yield was reduced up to 40 to 50 cm within the row from individual cocklebur plants. The maximum distance of interference on one side of individual cocklebur plants was 75 cm. One cocklebur plant reduced soybean yield 16.0% within 1.5 m of soybean row as the result of full-season interference. Interference of common cocklebur plants spaced 60 cm apart within the row overlapped and caused an additive reduction in soybean seed yield. Across all cocklebur treatments, there was a consistent ratio of approximately 1 kg/ha loss in soybean seed yield for each 4 kg/ha of cocklebur herbage produced.

Common Cocklebur Competition in Soybeans

The competitive effects of common cocklebur (Xanthium pensylvanicumWallr.) on soybeans[Glycine max(L.) Merr. ‘Lee 68′] were studied on Dundee silty clay loam soil from 1970 to 1972. Full-season competition by common cocklebur at 3,300, 6,600, 13,000, and 26,000 plants/ha reduced the 2-year average soybean seed yields 10, 28, 43, and 52%, respectively. Competition from common cocklebur at 100,000 plants/ha for 4, 6, 8, 10, 12, and 16 weeks after soybean emergence reduced soybean seed yields 10, 36, 40, 60, 80, and 80%, respectively. A reduction in soybean stand occurred after 12 or more weeks competition, and an increase in soybean plant height occurred after 10 or more weeks competition. When common cockleburs were removed during the first 4 weeks after soybean emergence, no further removal was required to obtain maximum soybean yield. Bentazon [3-isopropyl-1H-2,1,3-benzothiadiazin-(4)3H-one 2,2-dioxide] at 1.1 to 2.2 kg/ha applied over-the-top of common cockleburs and soybeans was as effective as hand removal in terminating competition provided common cocklebur plants were not flowering.