The translocation and root exudation of leaf-applied sublethal concentrations of 14C-labeled clopyralid (3,6-dichloropicolinic acid) and 14C-labeled 2,4-D [(2,4-dichlorophenoxy)acetic acid] were compared in Canada thistle [Cirsium arvense (L.) Scop. var. horridum Wimm. and Grab. ♯ CIRAR] at the rosette stage over a period of 9 days. The rate of absorption and export of 14C out of the treated leaf was similar for both herbicides. However, the distribution of the herbicides throughout the plant was very different. After 9 days, 15 vs. 3% of the applied 14C from 14C-clopyralid vs. 14C-2,4-D, respectively, was isolated from the foliage of the treated leaf. In the roots, twice as much 14C was recovered from the 14C-clopyralid treatments as from the 14C-2,4-D treatment at all sampling times, with 33 vs. 15% being recovered, respectively, after 9 days. When the plants were grown hydroponically, 20% of the 14C-clopyralid vs. 48% of the 14C-2,4-D was recovered in the nutrient solution during a 9-day period. No metabolites of either herbicide were recovered from the foliage, root system, or nutrient solution. Large differences in translocation of these herbicides may account for the unequal toxicity to young Canada thistle plants.

Adventitious root bud development and assimilate translocation were studied in Canada thistle [Cirsium arvense (L.) Scop. ♯ CIRAR] grown in nutrient solution in controlled environments using combinations of two photoperiods (PP) (13 and 15 h), three day/night shoot temperatures (ST) (15/5, 25/15, and 30/22 C), and three root temperatures (RT) (10, 20, and 30 C). Total root bud elongation increased with RT and length of PP and was greatest (65 cm/plant) at 25/15 C ST, 15-h PP, and 30 C RT. The number of root buds produced was greatest at 20 C RT (7.3 to 10.3 buds/plant), whereas variations in PP and ST had little effect. Total dry-matter production was greatest (7.2 g/plant) at 15-h PP, 30/22 C ST, and 20 C RT. To study phloem translocation, photoassimilates were labeled in Canada thistle plants by exposing mature leaves to 14CO2. Net assimilate translocation from a source leaf following 24-h temperature acclimation was affected little by RT and ST, but was greater under the 13-h PP than under the 15-h PP. After 7 days of temperature preconditioning, net translocation of 14C-assimilates increased with both RT and ST, but no effects due to PP were noted. With 24-h temperature acclimation, net assimilate accumulation in roots was enhanced by 13-h PP and low ST (15/5 C), whereas RT itself had no effect. In temperature-preconditioned plants, 10 C RT enhanced assimilate accumulation in roots, but ST and PP had no effect.

Translocation of 14CO2-labeled photoassimilates was compared to movement of 14C-glyphosate [N-(phosphonomethyl)glycine] in Canada thistle [Cirsium arvense (L.) Scop. ♯ CIRAR] under field and controlled-environment conditions. Field-grown Canada thistle plants were treated on mature upper leaves at the midflower stage in mid-June and harvested 8 days later. No differences were found in glyphosate and assimilate distribution, and movement was primarily basipetal. Of the glyphosate and photoassimilates translocated from the treated leaves, 25 and 31%, respectively, were recovered from the roots, while 59 and 58%, respectively, were found in the shoot tissue below the treated leaf. Concentration of labeled glyphosate in the roots as much as 95 cm from the treated shoot was as high as at the base of the treated shoot. Photoperiods that induce flowering (15 h) or maintain vegetative growth (13 h) did not differentially affect the distribution of photoassimilates or glyphosate in 7-week-old Canada thistle plants in the growth chamber. In growth chamber-grown plants equivalent amounts of glyphosate and assimilates were translocated out of treated leaves; however, relatively more glyphosate than photoassimilates accumulated in the roots.

Dark germination of light-requiring lettuce seeds (Lactuca sativa L. ‘Grand Rapids’) was stimulated by SAN 9789 [4-chloro-5-(methylamino-2-(α,α,α-trifluoro-m-tolyl)-3(2H)-pyridazinone] and to a minor degree by BASF 13761 [4-chloro-5-methoxy-2-phenyl-3(2H)-pyridazinone] and BASF 44521 [4-chloro-5-methoxy-2-(α,α,α-trifluoro-m-tolyl)-3(2H)-pyridazinone], but not by’ pyrazon [5-amino-4-chloro-2-phenyl-3(2H)-pyridazinone], SAN 9785 [4-chloro-5-(dimethylamino)-2-phenyl-3 (2H)-pyridazinone], SAN 9774 [5-amino-4-chloro-2-(α,α,α-trifluoro-m-tolyl)-3(2H)-pyridazinone], or SAN 6706 [4-chloro-5-(dimethylamino)-2-(α,α,α-trifluoro-m-tolyl)-3(2H)-pyridazinone]. SAN 9789 stimulation was inhibited by cis-4-cyclohexene-1,2-dicarboximide (CHDC), and abscisic acid (ABA) at 1 × 10-4 M. Red light nullified the inhibitory effect of CHDC (1 × 10-4 M) but not the inhibitory effect of ABA (1 × 10-4 M) on SAN 9789 stimulated germination. Gibberellic acid (GA3) and kinetin (6-furfurylaminopurine) increased the germination stimulatory effect of SAN 9789 in darkness. Temperatures above 25 C decreased the effect of SAN 9789, with a temperature of 35 C completely inhibiting germination. The inhibitory effect of CHDC was strongly decreased at temperatures below 20 C. SAN 9789-induced germination in darkness was always the same (25 to 26% units increase in germination) even though the red light-stimulated germination differed with the seed batch.

From 1976 to 1981, emergence date, height, and dry weight per plant were taken for eight weed species grown at Bushland, TX, at two stand densities. Height and dry weight per plant were related to precipitation and degree-days for air and soil temperatures using base temperatures of 10, 15.5, or 21 C. Kochia [Kochia scoparia (L.) Schrad. ♯ KCHSC] emerged early in March and was followed by poison suckleya [Suckleya suckleyana (Torr.) Rydb. ♯ SUKSU], sunflower (Helianthus annuus L. ♯ HELAN), and common cocklebur (Xanthium pensylvanicum Wallr. ♯ XANPE) in early April. Buffalobu(Solanum rostratum Dunal. ♯ SOLCU), puncturevine (Tribulus terrestris L. ♯ TRBTE), lanceleaf sage (Salvia reflexa Hornem. ♯SALRE), and barnyardgrass (Echinochloa crus-galli L. Beauv. ♯ECHCG) emerged in late April. The weeds began to increase in height during May but plants did not start increasing in weight until June. Kochia, common cocklebur, and sunflower grew tallest, produced most dry matter, made most efficient use of water, and weighed most per plant. Heat unit accumulations were strongly correlated with plant height.

The seed composition in the upper 15-cm soil horizon was determined and correlated with weed seedlings growing with fieldbeans (Phaseolus vulgaris L. ‘Valley’). The total seed reservoir averaged 250 seed/kg of soil, and 19 species were represented. Seed occurring with the most frequency were redroot pigweed (Amaranthus retroflexus L. ♯ AMARE), common lambsquarters (Chenopodium album L. ♯ CHEAL), and common purslane (Portulaca oleracea L. ♯ POROL). Seed from these plants accounted for over 85% of the seed found. The number of barnyardgrass [Echinochloa crus-galli (L.) Beauv. ♯ECHCG], buffalobur (Solanum rostratum Dunal ♯ SOLCU), common lambsquarters, common purslane, and common sunflower (Helianthus annuus L. ♯ HELAN) seed in the soil was correlated with the number of plants growing in the field with fieldbeans. A correlation occurred between redroot pigweed, yellow foxtail [Setaria lutescens (Weigel.) Hubb. ♯ SETLU], and barnyardgrass growing in corn (Zea mays L.) fields in the fall of the year and plants growing in the field with fieldbeans the following year.

Field experiments were conducted to measure the grain yield of wheat (Triticum aestivum L. ‘ANZA’) at various wild oat (Avena fatua L. ♯ AVEFA) and wheat plant densities. Wheat yield declined as wild oat plant density increased. Wheat yield increased in wild oat-infested plots as wheat plant density increased. Regression models were developed to describe the combined effect of wheat and wild oat plant densities on wheat grain yield. Wheat yields were best described by a nonlinear regression model using the relative density of wild oat in the weed-crop stand as the dependent variable. Inclusion of crop stand as a competitive factor significantly improved the fit of all regression models tested. Wild oat were more competitive against wheat in these experiments than in experiments reported by others. Possible reasons for differences in observed competitiveness are discussed.

The depth distribution of weed seed, their location in relation to soil aggregates, and the size distribution of soil aggregates were determined in fields that had been under continual conventional or reduced tillage for more than 12 years. Soil samples were taken at three depths in the spring and fall of 1982, and soil aggregates were classified into seven size classes by dry, rotary sieving. Subsamples were deflocculated and washed through sieves to recover weed seed. In the spring, 85% of all seed in the reduced-tillage and 28% of those in the conventional-tillage soil were in the 0- to 5-cm-depth layer. Conventional tillage incorporated weed seed uniformly into various soil aggregate classes, whereas with reduced tillage more seed accumulated in the unaggregated fraction of the soil. In the fall, weed seed distribution in relation to soil depth and among soil aggregate classes was similar for both tillage regimes.

Growth chamber and laboratory experiments evaluated the effects of seed-soil microsite characteristics on seed germination. When corn (Zea mays L. ‘Pioneer 3541’), soybean [Glycine max (L.) Merr. ‘Corsoy 79’], velvetleaf (Abutilon theophrasti Medic. ♯ ABUTH), and giant foxtail (Setaria faberi Herrm. ♯ SETFA) were seeded among soil aggregates 2.50 to 1.25 cm in diameter in the growth chamber, there was decreased seedling emergence with decreasing frequency of irrigation. These same species seeded inside artificial soil aggregates showed increased seedling emergence with decreasing frequency of irrigation. The germination of corn and soybean seed inside 0.4-g, fully moist soil aggregates incubated in the laboratory under high relative humidity conditions was significantly decreased relative to seed incubated in the absence of soil. Velvetleaf and giant foxtail germination was significantly reduced by 0.1-g soil aggregates. Rice (Oryza sativa L.) had 68% emergence from 1.0-g, fully moist soil aggregates, whereas larger seeded corn and soybean had only 20 and 10% emergence, respectively. Germination inhibition of giant foxtail seed by fully moist soil was partially reversed by incubating seed-containing aggregates in an atmosphere of 75% oxygen.

Because environmental factors facilitating the breaking of dormancy of seed of catclaw mimosa (Mimosa pigra L. ♯ MIMPI) under field conditions were unknown, the effect of constant temperatures (2 to 44 C) on germination of scarified and unscarified seeds, and the effect of diurnally fluctuating temperatures on unscarified seeds were examined. Temperatures fluctuated diurnally by 10 and 20 C in these latter experiments. Germination was less than 10% at all constant temperatures except 44 C, which had 40% germination. Scarification increased germination to 100% at constant temperatures greater than 12 C. Germination of unscarified seed was significantly lower (0 to 23%) when day/night temperature ranges fluctuated by 10 C than when they fluctuated by 20 C. Optimum temperature for germination was 40/20 C, where 93% germination occurred within 4 days.

Common cocklebur (Xanthium pensylvanicum Wallr. ♯ XANPE), velvetleaf (Abutilon theophrasti Medic. ♯ ABUTH), and jimsonweed (Datura stramonium L. ♯ DATST) are weeds that grow taller than soybeans [Glycine max (L.) Merr.] and compete for limited resources such as light. These weeds have an average area of influence of 0.5 m2, thus a density of 1 to 2 plants/m2 forms a full canopy of weed leaves above the soybeans that intercept 44 to 56% of the sunlight. Shade of 44 to 56% without weeds, placed above soybeans late in the season corresponding to times of weed shading, reduced soybean yield 19 to 26%. Since reported soybean yield reductions at weed densities of 0.7 to 2.5 plants/m2 were 18 to 54% for common cocklebur and 12 to 31% for jimsonweed and velvedeaf, it was concluded that most of the interference from jimsonweed and velvetleaf infestations in soybeans could be ascribed to competition for light, but only about one-half the interference was due to competition for light for common cocklebur. Soybean photosynthesis in the field was reduced about twice as much as soybean yield at equivalent levels of shading.

Interference studies utilizing manipulated and natural infestations of giant foxtail (Setaria faberi Herrm. ♯ SETFA) in soybeans [Glycine max (L.) Merr. ‘Williams’] were conducted at Urbana, IL, in 1982 and 1983. Giant foxtail clumps, each consisting of 3 to 6 plants per dm2, were used to determine the effect of clump density on giant foxtail dry weight and soybean seed yield. In both years, regression equations predicted a soybean seed yield loss of 0.8% for each giant foxtail clump per 9 m of row. The highest density of 30 clumps per 9 m of row reduced soybean yield 26%. In a second study, fluazifop {(±)-2-[4-[(5-(trifluoromethyl)-2-pyridinyl)oxy]phenoxy]propanoic acid} at 0.28 kg ai/ha or fluazifop + alachlor [2-chloro-2’,6’-diethyl-N-(methoxymethyl)acetanilide] at 0.28 + 2.24 kg/ha applied 10 or 15 days after emergence gave maximum giant foxtail control with little or no reduction in soybean seed yield. Interference from uncontrolled giant foxtail began to reduce soybean dry-matter accumulation 15 days after emergence under favorable growing conditions in 1982. Under less favorable conditions in 1983, similar effects were not observed until 25 days after emergence.

In greenhouse and controlled-environment tests, velvetleaf (Abutilon theophrasti Medic. ♯ ABUTH) and prickly sida (Sida spinosa L. ♯ SIDSP) control with Fusarium lateritium Nees ex Fr. was affected by inoculum concentration and plant growth stage at the time of inoculation, by postinoculative air temperature, and by dew period duration and temperature. A higher level of control of both weeds was obtained with inoculum concentrations of 7.5 × 105 and 1.5 × 106 macroconidia/ml when the weeds had fewer than seven true leaves. Postinoculative air temperatures above 25 C significantly reduced control of both weeds. Mortality of both species was higher at dew temperatures of 25 C than at temperatures of either 15 or 35 C. At least 12 h of dew at 25 C was required to achieve satisfactory control of prickly sida, while a dew period of 16 h was required to achieve a comparable level of control of velvetleaf.

In four tests conducted in 2 years, Alternaria cassiae Jurair and Khan effectively controlled sicklepod (Cassia obtusifolia L. ♯ CASOB) as indicated by stand counts of the weed and by soybean [Glycine max (L.) Merr.] yields. The number of sicklepod seedlings was reduced more than 90% within 14 days after foliar applications of A. cassiae conidia were banded (46 cm) at rates of 4.2 and 2.1 kg/ha (9.4 and 4.7 kg/ha broadcast, respectively). One banded application of 0.04 or 0.4 kg/ha (0.09 or 0.9 kg/ha broadcast, respectively) did not satisfactorily control sicklepod. These results indicate that sicklepod control may be enhanced by multiple applications of A. cassiae.

Space-planted johnsongrass [Sorghum halepense (L.) Pers. ♯ SORHA] was clipped back to a height of 26 cm after flowering and, when 45 to 61 cm in height, was treated with various rates of the sodium salt of dalapon (2,2-dichloropropionic acid), MSMA (monosodium methanearsonate), or the sodium salt of asulam (methylsulfanilylcarbamate). Treatments were reapplied as needed during the growing season whenever a majority of surviving plants in a plot had initiated new foliar growth. Most plants were not killed by a single application of any herbicide, although rhizome development, as measured by the number of rhizome buds, was inhibited by the initial herbicide treatments. MSMA at 4.5 kg ai/ha was more phytotoxic to johnsongrass than other herbicide treatments or MSMA at 2.3 kg ai/ha; a single application at the higher rate reduced the original number of rhizome buds on plants by 50 to 60%, and two applications killed 86 to 93% of the plants. Asulam at 4.5 and 6.7 kg ae/ha and dalapon at 6.7 and 9.0 kg ae/ha primarily controlled plants by inhibiting growth for an extended period. After two or three applications of asulam or dalapon at 6.7 kg ae/ha, only about 40% of the plants had been killed, but the original number of rhizome buds on surviving plants had been reduced by about 80%.

The herbicides 2,4-D [(2,4-dichlorophenoxy) acetic acid], dalapon (2,2-dichloropropionic acid), glyphosate [(N-phosphonomethyl)glycine], paraquat (1,1’-dimethyl-4,4’-bypiridinium ion), and pronamide [3,5-dichloro-(N-1,1-dimethyl-2-propynyl)benzamide] were applied at selected rates and dates to quackgrass [Agropyron repens (L.) Beauv. ♯ AGRRE]-infested alfalfa (Medicago sativa L.) sod in 1979 and 1980 to suppress vegetation for subsequent establishment of alfalfa without tillage. The influence of herbicides on weed control, alfalfa seedling density and visual stand, and forage yield and quality was assessed for 3 yr. During establishment, all herbicides except 2,4-D effectively controlled quackgrass. Glyphosate applied broadcast increasingly suppressed the existing sod as the rate was increased from 0.6 to 1.6 kg ai/ha. The effectiveness of herbicides as measured by total (old and new) plant density was closely related to the suppression of the sward. While the substitution of new alfalfa plants for old ones was not necessary under dense (40 plants/m2) alfalfa stands, completely controlling the vegetation with glyphosate resulted in sustained productivity throughout the experimental period. After 3 yr, alfalfa percentage and yield were highest when glyphosate was broadcast at 1.6 kg/ha. Improvement in forage quality, as estimated by the concentrations of crude protein and neutral-detergent fiber, was closely related to grass control.

Preemergence and postemergence application of metribuzin [4-amino-6-tert-butyl-3-(methylthio)-as-triazine-5(4H)-one] at 0.6 and 1.1 kg ai/ha controlled downy brome (Bromus tectorum L. ♯ BROTE) in winter wheat (Triticum aestivum L. ‘McDermid’) but caused considerable injury without the use of activated carbon over the seeded row. Activated carbon applied in 5-cm bands over the seeded row at 84, 167, and 336 kg/ha protected winter wheat at Pendleton on a silt loam soil. On a sandy loam soil, only a 336 kg/ha rate provided protection from metribuzin. Metribuzin toxicity to winter wheat was more difficult to neutralize when applied preemergence. Downy brome control was not reduced by carbon applied over the wheat row. The best treatment in this study was carbon at 336 kg/ha applied preemergence over the row followed by metribuzin at 0.6 or 1.1 kg/ha postemergence. A 10-week delay between preemergence carbon banding and postemergence metribuzin protected winter wheat from chemical injury.

Field experiments were conducted in 1982 and 1983 on a Dothan sandy loam (Plinthic Paleudult) at Headland, AL, to investigate minimum-tillage production of peanuts (Arachis hypogaea L.). The experiments included two peanut varieties: a) ‘Pronto’ (an earlier maturing Spanish type), and b) ‘Florunner’ (a later maturing runner type). Two row-spacing patterns were used: a) conventional 91-cm rows, and b) a modified twin 18-cm row pattern. A constant seeding rate (140 kg/ha) was used regardless of row spacing. Six herbicide systems were evaluated within each combination of variety and row spacing. The Florunner variety outyielded the Pronto variety across both years and weed management systems. Modified twin 18-cm rows outyielded conventional 91-cm rows across years and peanut varieties. Two of the six weed management systems were successful: 1) paraquat (1,1’-dimethyl-4,4’-bipyridinium ion) + oryzalin (3,5-dinitro-N4,N4-dipropylsulfanilamide) (preemergence), paraquat (ground cracking), naptalam (N-1-naphthylphthalamic acid) + dinoseb (2-sec-butyl-4,6-dinitrophenol) (postemergence); and 2) paraquat + pendimethalin [N-(1-ethylpropyl-3,4-dimethyl-2,6-dinitrobenzenamine] (preemergence), acetochlor [2-chloro-N(ethoxymethyl)-6’-ethyl-o-acetotoluidide] + dinoseb (ground cracking), and cyanazine {2-[[4-chloro-6-(ethylamino)-s-triazine-2-yl]amino]-2-methylpropionitrile} (early postdirected spray). Both systems provided the best overall control of Texas panicum (Panicum texanum Buckl. ♯ PANTE), Florida beggarweed [Desmodium tortuosum (Sw.) DC. ♯ DEDTO], and sicklepod (Cassia obtusifolia L. ♯ CASOB) and were acceptable for use in minimum-tillage peanut production.

Oxadiazon [2-tert-butyl-4(2,4-dichloro-5-isopropoxyphenyl)-δ2-1,3,4-oxadiazolin-5-one] applied to dormant bermudagrass [Cynodon dactylon (L.) Pers. ‘Tifway’ ♯ CYNDA] retarded early foliar growth more than other herbicides evaluated. When bensulide [O,O-diisopropyl phosphorodithioate S-ester with N-(2-mercaptoethyl)benzenesulfonamide] treatments were delayed until after bermudagrass initiated spring growth, foliar growth and quality were generally lower than when the treatments were applied to dormant turf. Retardation of early foliar bermudagrass growth by 2,4-D [(2,4-dichlorophenoxy)acetic acid] + mecoprop {2-[(4-chloro-o-tolyl)oxy] propionic acid} + dicamba (3,6-dichloro-o-anisic acid) was generally the same whether applied to dormant or semidormant turf. This combination of herbicides reduced the quality and density of bermudagrass when applied to growing but not to dormant turf. Atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine] did not retard bermudagrass growth or affect density whether applied to dormant or semidormant turf, but turf quality was slightly lower when atrazine was applied to semidormant turf.

Single and sequential applications of mefluidide {N-[2,4-dimethyl-5-[[(trifluoromethyl)sulfonyl] amino] phenyl] acetamide} and acifluorfen {5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid} were evaluated in the field for velvetleaf (Abutilon theophrasti Medic. ♯ ABUTH) and common cocklebur (Xanthium pensylvanicum Wallr. ♯ XANPE) control in soybeans [Glycine max (L.) Merr. ‘Williams’]. Acifluorfen was applied at 0.4 or 0.6 kg ai/ha alone or 3, 5, or 7 days following application of 0.1 or 0.3 kg ai/ha mefluidide. Acifluorfen applied alone provided acceptable control of velvetleaf and common cocklebur in the two- and three-leaf stage of growth, but acifluorfen was not as effective when applied to weeds with five to eight true leaves. Sequential applications of mefluidide and acifluorfen often increased velvetleaf and common cocklebur control, compared to either herbicide applied alone.