Sicklepod is a competitive and prolific weed that emerges throughout the crop season. Glyphosate applications to flowering sicklepod greatly reduce seed production, but there is limited information on glyphosate translocation in flowering weeds. Therefore, a laboratory study was conducted to document the absorption and translocation of 14C-glyhosate in flowering sicklepod. Flowering sicklepod plants were treated with a 14C-glyphosate solution, and 14C-glyphosate absorption and translocation was quantified by scintillation spectrometry. Absorption and translocation of 14C-glyphosate in flowering sicklepod were similar for both 0.21 and 0.42 kg ae ha−1 glyphosate. Although the treated leaflets retained approximately 50% of the recovered 14C-glyphosate, movement of the herbicide was both acropetal and basipetal, with the highest 14C-glyphosate concentrations in the shoot below the treated leaf and the roots. By 96 h after treatment, sicklepod buds and flowers had abscised, but analysis of the structures revealed accumulation of 2% of the recovered 14C-glyphosate. Based on results of the study, effects of glyphosate accumulation in buds and flowers combined with plant stress associated with the primary and secondary effects of glyphosate result in bud and flower abscission, drastically reducing sicklepod seed production.

A threefold glyphosate tolerance was identified in two Italian ryegrass populations, T1 and T2, from Mississippi. Laboratory experiments were conducted to characterize the mechanism of glyphosate tolerance in these populations. The T1 population absorbed less 14C-glyphosate (43% of applied) compared to the susceptible (S) population (59% of applied) at 48 h after treatment (HAT). The T2 population absorbed 14C-glyphosate at levels (56% of applied at 48 HAT) that were similar to both T1 and S populations, but tended to be more comparable to the S population. The amount of 14C-glyphosate that remained in the treated leaf was significantly higher in both T1 (67% of absorbed) and T2 (65% of absorbed) populations compared to the S population (45% of absorbed) at 48 HAT. The amount of 14C-glyphosate that moved out of treated leaf to shoot and root was lower in both T1 (25% of absorbed in shoot and 9% of absorbed in root) and T2 (25% of absorbed in shoot and 11% of absorbed in root) populations compared to the S population (40% of absorbed in shoot and 16% of absorbed in root) at 48 HAT. There were no differences in epicuticular wax mass among the three populations. Treating a single leaf with glyphosate solution at the field use rate (0.84 kg ae ha−1) as 10 1-µl droplets killed the S plant but not the T1 and T2 plants (33 and 55% shoot fresh-weight reduction, respectively). Shikimic acid accumulated rapidly at higher levels in glyphosate-treated leaf segments of the S population compared to the T1 population up to 100 µM glyphosate. However, above 500 µM glyphosate, the levels of shikimate were similar in both the S and T1 populations. Furthermore, shikimic acid content was three- to sixfold more in whole plants of the S population treated with 0.22 kg ae ha−1 glyphosate compared to the T1 and T2 populations. No degradation of glyphosate to aminomethylphosphonic acid was detected among the tolerant and susceptible populations. These results indicate that tolerance to glyphosate in the T1 population is partly due to reduced absorption and translocation of glyphosate and in the T2 population it is partly due to reduced translocation of glyphosate.

In order to explore the physiological mechanism of paraquat resistance in tall fleabane, a widespread weed in Taiwan where resistance to this herbicide has been observed since 1980, the role of the antioxidative system was assessed. The susceptible (S) and resistant (R) biotypes of tall fleabane were distinguished clearly by the relative distribution frequency of injury index caused by 78 µM paraquat. Although malondialdehyde, an indicator for peroxidation damage to the plant, in the the R-biotype was not changed, in the S-biotype malondialdehyde increased within 2 h after treatment of 50 µM paraquat. Analysis of several antioxidants and pertinent enzymes revealed that ascorbate peroxidase activity was decreased by paraquat treatment in the S-biotype; and a lower basal level of ascorbate was present in the S-biotype as well. The maintenance of a high ratio of reduced glutathione to total glutathione, coupled with a pronounced and rapid increase of glutathione reductase (GR) activity in the the R-biotype, suggests that an active reduced glutathione/oxidized glutathione (GSH/GSSG) cycle is critical to paraquat resistance of tall fleabane. The decisive contribution of a functional GSH/GSSG cycle to paraquat resistance through an enhancement of GR activity in this weed was further confirmed by an experiment of exogenous application of ascorbate.

Sorghum genes responsive to purple witchweed parasitism were isolated, and their expression was analyzed. Using the suppression-subtractive hybridization strategy, 30 genes that were up-regulated in response to purple witchweed parasitism were isolated from the roots of a susceptible sorghum cultivar ‘Abu 70’. The changes in the expression of each gene were investigated in the roots and leaves of the sorghum cultivars ‘Wad Ahmed’ and ‘Tabat’ were parasitized by purple witchweed. Tabat is more susceptible and Wad Ahmed is less susceptible to purple witchweed than Abu 70. Further, the changes in the gene expression and host susceptibility to purple witchweed were studied in the roots of the three sorghum cultivars after treatment with salicylic acid (SA) or methyl jasmonate (MeJA). Purple witchweed parasitism induced jasmonic acid (JA)-responsive genes and suppressed SA-responsive genes in the roots of the cultivars Abu 70 and Tabat. In contrast, purple witchweed parasitism in the less-susceptible cultivar Wad Ahmed induced SA-responsive genes and induced JA-responsive genes to a small extent. SA, but not MeJA, decreased the susceptibility of all the sorghum cultivars to purple witchweed. Systemic expression of a few genes was observed in the leaves of the purple witchweed–parasitized sorghum cultivars.

Tembotrione inhibits 4-hydroxyphenyl-pyruvate-dioxygenase (HPPD) and was recently registered for use in all types of corn. Some sweet corn hybrids are killed by tembotrione, yet a mechanistic understanding of sensitivity has not been reported. Sensitivity of mesotrione, another HPPD-inhibitor, is conditioned by a single allele. Two hypotheses were tested: (1) response to tembotrione and mesotrione are conditioned by alleles at the same or closely linked loci and (2) the extent of early-season injury from tembotrione and mesotrione is similar on hybrids. The first hypothesis was tested by comparing responses to tembotrione and mesotrione in 136 F3:5 families derived from a cross of mesotrione-sensitive and mesotrione-tolerant sweet corn inbreds. F3 families cosegregated for responses to tembotrione and mesotrione: 94% of the families had the same response to both herbicides. Thus, the same gene or very closely linked genes condition response to both herbicides. On the basis of chi-square goodness of fit tests, responses of families to tembotrione fit a 3 : 2 : 3 sensitive : segregating : tolerant ratio (P = 0.24), which would be expected if sensitivity to tembotrione was conditioned by a single recessive allele. The second hypothesis was tested in six field experiments by quantifying the extent of early-season injury to 249 sweet corn hybrids 1 wk after treatment (WAT) of tembotrione (184 g ha−1) or mesotrione (210 g ha−1). One hundred ninety-three hybrids were tolerant to both herbicides. Seven sensitive hybrids that were severely injured by both herbicides 1 WAT differed in their response 3 to 4 WAT; sensitive hybrids treated with mesotrione had apparently resumed normal growth, whereas those treated with tembotrione died. Conversely, hybrids with intermediate levels of injury (> 10 to 50%) 1 WAT with mesotrione had no visual symptoms of injury from applications of tembotrione. Despite the common genetic basis for response to mesotrione and tembotrione, hybrids with sensitive or intermediate responses to mesotrione did not have identical responses to tembotrione.

Resistance to protoporphyrinogen oxidase (PPO)-inhibiting herbicides in waterhemp has been shown previously to be the result of a unique mechanism. Specifically, a three–base-pair (3-bp) deletion in the PPX2L gene, a gene encoding both plastid- and mitochondria-targeted PPO enzymes, confers herbicide resistance in this species. Furthermore, when this unique mechanism was initially characterized it was presumed that waterhemp contained three PPX genes, PPX1, PPX2S, and PPX2L, and that the resistant biotypes were missing PPX2S. Here, allele testing and examination of genetic sequence data demonstrate that there are likely only two PPX genes in waterhemp, PPX1 and PPX2L. Next, to determine the prevalence of this mechanism of resistance in Illinois waterhemp, we developed an allele-specific polymerase chain reaction (PCR) marker that amplifies only the 3-bp deletion allele, ΔG210, of PPX2L. By utilizing this marker, we show that the ΔG210 PPX2L allele correlated with whole-plant resistance to PPO inhibitors in each of four other waterhemp populations evaluated from Illinois.

Nicosulfuron, mesotrione, dicamba plus diflufenzopyr, and carfentrazone are postemergence herbicides from different chemical families with different modes of action. An association between the sensitivity of sweet corn to these herbicides was observed when 143 F3 : 4 families (F4 plants) derived from of a cross between Cr1 (sensitive inbred) and Cr2 (tolerant inbred) were evaluated in greenhouse trials. The ratio of tolerant : segregating : sensitive families was not significantly different from a 3 : 2 : 3 ratio, which would be expected if a single gene conditioned herbicide response. Families cosegregated for responses to these herbicides. In field studies with 60 F3 : 5 families in 2005 and 120 F3 : 5 families in 2007, responses to these herbicides and foramsulfuron and primisulfuron were associated. Responses to bentazon in field trials were similar to the aforementioned herbicides for tolerant families, but differences were noted for families that were sensitive or segregated for responses to nicosulfuron, foramsulfuron, primisulfuron, mesotrione, dicamba plus diflufenzopyr, and carfentrazone. The gene(s) affecting herbicide sensitivity in Cr1 maps to the same region of chromosome 5S as a previously sequenced cytochrome P450 gene, where alleles previously designated nsf1 and ben1 were associated with sensitivity to nicosulfuron and bentazon and appear to be the result of a 392–base-pair insertion mutation. This work supports the hypothesis that a single recessive gene or closely linked genes in the sweet corn inbred Cr1 condition sensitivity to multiple cytochrome P450 enzyme-metabolized herbicides.

Experiments were conducted to determine the influence of various environmental factors on seed germination and seedling emergence of eclipta. Seed germination was completely inhibited in the dark, whereas in the light/dark it was 76, 93, and 87% at 25/15, 30/20, and 35/25 C alternating day/night temperatures, respectively. Germination was greater than 80% up to a temperature of 140 C, when seed were placed in an oven for 5 min followed by incubation at 30/20 C for 14 d, but declined progressively with a further increase in exposure temperature with no germination at 200 C. Seed germination was tolerant of salt stress but highly sensitive to water stress. Seed germinated (87 to 93%) over a pH range of 4 to 10. Seedling emergence was greatest (83%) for the seed placed on the soil surface but declined thereafter, and no seedlings emerged from a depth of 0.5 cm. Seedling emergence was slower and lower with the addition of 4 to 6 t ha−1 of plant residue. The information gained from this study identifies some of the factors facilitating eclipta becoming a widespread weed in the humid tropics and might contribute to its control.

Laboratory experiments were conducted to determine the effects of temperature, light, cold stratification, dry storage, solution pH, solution osmotic potential, and planting depth on germination and emergence of dame's rocket. Maximal germination (> 80%) of fresh seeds occurred at alternating temperatures ≥ 25/15 C in both alternating light/dark and continuous darkness. However, < 10% of seeds germinated at or below 20/10 C, with lower germination in the presence of light than in darkness. Cold stratification at 4 C for 4 to 16 wk enhanced germination at low alternating temperatures (≤ 20/10 C), but depressed germination at warm temperature regimes (≥ 25/15 C). After 1 yr of dry storage (after-ripening), germination exceeded 94% and did not differ significantly among temperature regimes. Germination exceeded 60% in solutions with pH 3 to 10. Germination was reduced below 50% in solutions with osmotic potentials below −0.6 MPa. Percent emergence was greater than 56% at burial depths in soil of 0 to 5 cm, with maximal emergence (93 to 99%) at 0 to 2 cm. Dame's rocket seeds possess non-deep physiological dormancy at maturity, but when dormancy is alleviated, the seeds are capable of germinating in a variety of climatic and edaphic conditions.

Intraspecific genetic variation may contribute significantly to invasiveness and control problems, but has been characterized to date in relatively few invasive weed species. We examined 56 intersimple sequence repeat (ISSR) loci in 220 individuals from 11 invading populations of yellow toadflax sampled across five western states. All populations showed high levels of genetic diversity. Estimated values for Shannon's diversity measure ranged from 0.217 to 0.388, and for expected heterozygosity from 0.178 to 0.260. Nei's total gene diversity index (HT), on the basis of all individuals across all populations, was 0.267. Partitioning of genetic variance using analysis of molecular variance revealed 1.7% of genetic variation among regional population groups, 29.1% among populations within groups, and 69.2% within populations, consistent with expectations for an outcrossing species but suggesting little geographic differentiation. Pairs of adjacent individuals identical at all ISSR loci that appeared to be ramets of a single clone were detected in only one population. This indicates that patch expansion in yellow toadflax is driven more by sexual reproduction via seed than by rhizomatous clonal spread, at least at the spatial scale of sampling for this study. Eight populations had significant values for Mantel's R at P = 0.05, suggesting some fine-scale positive genetic structuring, possibly from restricted gene flow. Population clustering on the basis of Nei's genetic distance between populations and unweighted pair group method with arithmetic mean did not reflect geographic location. It is likely that multiple introductions of this species have occurred across the Intermountain West, followed by extensive genetic recombination. High levels of genetic diversity within yellow toadflax populations pose management challenges, as already seen in reports of variable response to herbicide application and limited impacts of biocontrol agent releases.

Intercropping is an eco-friendly approach for reducing weed problems through nonchemical methods. Intercrop effects on weed community structure have rarely been studied. A 6-yr study was initiated in 1999 and the response of aboveground weed flora (1999–2002 and 2005) and seed bank (2005) to the intercropping of saffron and black zira, two perennial crops was investigated. Mixtures consisted of 0/100, 25/75, 50/50, 75/25, and 100/0 saffron/black zira ratios, each planted at three densities: 30, 50, and 70 plant m−2. The effect of planting density on weed populations was variable and in most cases not significant. However, mixture ratios caused drastic species compositional changes in the weed community for which univariate and multivariate analyses explored four major associations: (1) weeds that favored a higher ratio of saffron in mixtures (e.g., grasses, field bindweed, pigweeds), (2) weeds that preferred a higher ratio of black zira in mixtures (e.g., Persian speedwell, Brassicaceae complex, Polygoaceae complex, and earthsmoke), (3) weeds that were more abundant in 50/50 mixtures (e.g., Caryophyllaceae complex), and (4) weeds that showed no specific pattern (e.g., common lambsquarterss). Pigweeds, prostrate knotweed, and common lambsquarters dominated the viable seed bank with relative densities of 48, 28, and 8%, respectively. The seed bank of most weed species responded to mixture ratios in a similar manner to those of their corresponding aboveground flora. Seed density decreased as soil depth increased, leading to the accumulation of 66, 22, and 12% of viable seeds in soil layers of 0–5, 5–15 and 15–25 cm, respectively. Greater weed and seed densities were found in more pure stands of black zira. These findings contribute to improving current understanding of crop–weed community structures and may help in developing weed management practices.

The influence of soybean row width and glyphosate application timing was determined on survival, biomass, and seed production of cohorts from a mixed population of Palmer amaranth and pusley species (Florida and Brazil pusley) along with soybean seed yield. The first Palmer amaranth and pusley cohort comprised plants that emerged from soybean planting through the V3 (3 wk after soybean emergence [WAE]) soybean stage (cohort 1). The second cohort comprised plants that emerged between the V3 to V6 (5 WAE) soybean stages (cohort 2), and the third cohort emerged after the V6 through the R2 soybean stage (cohort 3). Glyphosate at 840 g ae ha−1 was applied at V3; V6; V3 and V6; and V3, V6, and R2 in rows either 19 or 97 cm wide. A nontreated control was included for comparison in each row width. Sequential glyphosate applications at V3 and V6 or at V3, V6, and R2 soybean stages resulted in 1 to 3% survival of cohort 1 compared with 23 to 28% survival after a single glyphosate application. Vegetative biomass production by cohort 1 accounted for 71% of the total pusley biomass produced in the nontreated plots. Cohort 1, 2, and 3 contributed 68, 31, and 1%, respectively, of the total 37,900 seeds m−2 produced by pusley plants in nontreated plots. Delaying a glyphosate application to the V6 stage resulted in higher biomass and more than twice the seed produced from cohort 1 when compared with cohort 2. Glyphosate applied at V3 and V6 stages prevented pusley seed production from cohort 1, and an additional glyphosate application at the R2 stage prevented seed production from cohorts 2 and 3. No Palmer amaranth emergence occurred after the V6 soybean stage in either row width. A single glyphosate application at the V3 or V6 stage eliminated cohort 1 of Palmer amaranth in narrow rows. Palmer amaranth plants from cohort 1 in wide rows that survived the V3 glyphosate application produced 3.3 g m−2 biomass and 600 seeds m−2. Averaged over years and row widths, soybean yields after sequential glyphosate applications were 2,490 to 2,640 kg ha−1 compared with 1,850 to 2,020 kg ha−1 after a single glyphosate application at the V3 or V6 stage. This research confirms that sequential glyphosate applications are superior to a single application for minimizing pusley and Palmer amaranth survival, biomass, and seed production along with an improvement in soybean yields.

The variability of 12 Echinochloa populations with respect to certain morphological and physiological characteristics, sensitivity to certain POST rice herbicides, and activity of selected enzymes was studied. Three distinct groups (each one represented by four populations from different areas) were studied: E. crus-galli, E. oryzoides, and E. phyllopogon. All the E. oryzoides and E. phyllopogon populations showed earlier seed germination and higher germination percentages than the E. crus-galli populations. All the E. oryzoides and E. phyllopogon populations showed reduced susceptibility to propanil, cyhalofop, clefoxydim, and bispyribac compared with the E. crus-galli populations. With respect to plant prostrateness, the species order, averaged over the four populations, was E. crus-galli prostrate > E. oryzoides relatively erect > Ε. phyllopogon phyllopogon. erect, while the species order with respect to leaf length and tillering ability was E. crus-galli ≥ E. oryzoides > Ε. phyllopogon. Regarding leaf width, time of panicle emergence, height, and biomass accumulation, the order was E. crus-galli > E. oryzoides > Ε. phyllopogon, while that of seed weight, length and width was E. oryzoides > Ε. phyllopogon > E. crus-galli. The order of species susceptibility (averaged over the four populations) to most of the herbicide treatments was E. crus-galli > E. oryzoides > E. phyllopogon, which was exactly the opposite of that relating to their antioxidant enzyme activity. Finally, the order of herbicide efficacy, averaged over all Echinochloa populations, was penoxsulam > clefoxydim > bispyribac > cyhalofop > propanil. Variability in a number of traits among the most common Echinochloa species of rice fields in northern Greece as a result of different adaptive strategies of each species may be related to differential sensitivity to herbicides. This variability should be taken into account for the elaboration of effective weed management programs in rice. Where mixed populations of these species are present in a field, difficulties may arise in the successful chemical control of the Echinochloa complex in rice due to species differences in biology and herbicide sensitivity.

The effects of nitrogen (N) rate and weed interference on the grain yield of four corn genotypes were investigated in 2002 and 2003 at Ikenne (7°38′N, 3°42′E), Shika (11°11′N, 7°38′E), and Samaru (10°24′N, 7°42′E) in Nigeria. Nitrogen (N) at 0, 30, 60, and 90 kg N ha−1 were the main plot treatments. Weed-free (weeded weekly), low (intrarow weeds only), and high (zero weeding) weed pressure were the subplot treatments. Four corn genotypes (ACR8328 BN C7, Low-N-Pool C2, Oba Super II, TZB-SR) were the sub-subplot treatments. Weed density was higher at Shika and Samaru than at Ikenne, and the order of average weed biomass 8 to 10 weeks after planting was Samaru (271 g m−2) > Ikenne (236 g m−2) > Shika (161 g m−2). Corn genotype and N rate had no effect on weed biomass except at Samaru where fertilized treatments had higher weed biomass than the unfertilized treatments. Corn leaf area (LA) increased with increasing N rate at all locations regardless of weed pressure and genotype, except at Shika where ACR8328 BN C7, Oba Super II, and TZB-SR did not show any clear N response; LA was highest in the weed-free and lowest in the unfertilized treatments for all genotypes and locations, and weed pressure treatments. Low-N-Pool C2 had the highest LA, which was 1.3 times larger than in Oba Super II, which had the lowest LA. Nitrogen rate, weed pressure, and genotypes significantly affected corn leaf chlorophyll content. Chlorophyll content was higher in the fertilized treatments than the unfertilized treatments, and higher in the weed-free treatments than the low or high weed pressure treatments. ACR8328 BN C7 and Oba Super II had significantly more chlorophyll than the other genotypes. Low-N-Pool C2 showed a linear grain yield response with the increase in N rates. ACR8328 BN C7 did not respond to N application. Compared with the results in the weed-free treatment, high weed pressure reduced grain yield in all genotypes by more than 65% at Samaru, 50% at Shika, and 35% at Ikenne.

Three major hypotheses were examined in this study: (1) the density of summer annual weeds is reduced in crop rotation systems that include winter wheat compared to those with strictly summer annual crops, (2) the integration of a red clover in cropping systems reduces weed seedbank densities, and (3) changes in weed seedbanks due to crop rotation system have greater impact on future crops that are managed with cultivation alone, compared to those managed with herbicides. To test these hypotheses, five 3-yr rotation sequences were examined in central New York state: continuous field corn (FC); field corn with red clover (FC + CL); field corn–oats–wheat (FC/O/W); sweet corn–peas–wheat (SC/P/W), and SC/P/W with red clover (SC/P/W + CL). In the fourth year, sweet corn, snap beans, and cabbage were planted in subplots with three levels of weed management as sub-subplots: cultivation alone, reduced-rate herbicides (1/2×), and full-rate herbicides (1×). The trial was carried out in two separate cycles, from 1997 to 2000 (cycle 1) and from 1998 to 2001 (cycle 2). Crop rotations with strictly summer annual crops (FC) did not result in consistently higher weed seedbank densities of summer annual weeds compared to rotations involving winter wheat (FC/O/W; SC/P/W; SC/P/W + CL). Integration of red clover in continuous field corn resulted in higher weed seedbanks (cycle 1) or emergence (cycle 2) of several summer annual weeds compared to field corn alone. In contrast, integration of red clover in the SC/P/W rotation led to a 96% reduction in seedbank density of winter annuals in cycle 1, although this effect was not detected in cycle 2. Observed changes in weed seedbank density and emergence due to crop rotation resulted in increased weed biomass in the final year in only one case (sweet corn, cycle 2), and did not result in detectable differences in crop yields. In contrast, final year weed management had a strong effect on weed biomass and yield; cultivation alone resulted in yield losses for sweet corn (32 to 34%) and cabbage (0 to 7%), but not snap beans compared to either 1/2× or 1× herbicides.

Cover crop systems were investigated in 2004 and 2005 for their effects on the activity-density (a function of movement and density) of a promising group of weed biocontrol organisms, the ground beetles collectively known as carabids, with particular emphasis on a beneficial carabid species Harpalus rufipes DeGeer. Marked H. rufipes released into pea/oat–rye/vetch cover crop plots were more than twice as likely to be recaptured within the same plots as beetles released in nonvegetated fallow plots (18 and 8%, respectively). Marked beetles released into fallow plots were more than twice as likely to leave their plots and be recaptured in pea/oat–rye/vetch plots as vice versa (13 vs. 5%), indicating a clear preference for habitat with vegetative cover. Overall recapture rates were not different between treatments. Unmarked H. rufipes activity-density was also higher in pea/oat–rye/vetch compared to fallow plots. Additionally, five cover crop systems, including the fallow and pea/oat–rye/vetch treatments, and two residue management methods (conventional and zone tillage) were investigated from June to August in 2005 for their effects on H. rufipes activity-density. Corn was planted in 2005 into residues of the five cover crop systems grown in 2004. H. rufipes activity-density was higher in zone and conventionally tilled corn planted in pea/oat–rye/vetch residues and conventionally tilled corn planted in red clover/oat residues than in any other cover crop and residue management combination. Pea/oat–rye/vetch cover crop systems are apparently beneficial for H. rufipes during the cover crop year as well as in subsequent crops planted into this cover crop's residues. This system was not the least disturbed system but, based on the number of tillage events, represented a medium level of disturbance among the various systems. Thus, some level of disturbance might be beneficial for H. rufipes, but how and when that soil disturbance occurs requires further research to determine the best means of conserving this species.

Invasive plants can respond to injury from natural enemies by altering the quantity and distribution of biomass among woody materials, foliage, fruits, and seeds. Melaleuca, an Australian tree that has naturalized in south Florida, has been reunited with two natural enemies: a weevil introduced during 1997 and a psyllid introduced during 2002. We hypothesized that herbivory from these and other adventive organisms (lobate-lac scale and a leaf-rust fungus) would alter the distribution and allocation of biomass on melaleuca trees. This hypothesis was tested by temporally assessing changes in aboveground biomass components in conjunction with the presence of natural enemies and their damage to melaleuca trees. Melaleuca trees of different diameters representing the range (1 to 33 cm diam at 1.3 m height) within study sites were harvested during 1996, prior to the introduction of herbivorous insects, and again during 2003 after extensive tree damage had become apparent. Aboveground biomass, partitioned into several components (woody structures, foliage, fruits, and seeds), was quantified both times in Broward, Miami–Dade, and Palm Beach county sites located in south Florida. The two harvests within each site were performed in closely-matched melaleuca stands, and changes in biomass components were compared between years. Total biomass and woody portions decreased in Broward, whereas they increased in Miami–Dade and Palm Beach sites. Reductions in foliage (on all trees) and seed biomass (among seed-bearing trees) were greatest at Broward and least at Miami–Dade County site. Hence, overall seed and foliage production was severely reduced at the Broward site where both the natural enemy incidence and damage were more abundant compared to other sites. We therefore attribute the reduced foliar biomass and reproductive capability of melaleuca trees to infestations of natural enemies. These findings highlight the role that natural enemies can play in the long-term management of invasive tree species.

Field experiments were conducted in northern Greece during 2001 and repeated in 2002 and 2004 to evaluate the effects of pronamide on sugar beet. Total leaf area, leaf area index (LAI), leaf and root dry weights, photosynthetic yield (quantum yield of photochemical energy conversion in photosystem II), chlorotic index, and yield components of sugar beet were monitored after pronamide application. Three sugar beet cultivars, ‘Avantage’, ‘Dorothea’, and ‘Bianca’, requiring short, intermediate, and long vegetative periods, respectively, were subjected to treatment. Pronamide was applied on sugar beet either as a double application of 0.63 kg ai ha−1 at the two- to four-leaf and 0.63 kg ai ha−1 at the four- to six-leaf stage or as a single application of 1.26 kg ai ha−1 performed at the latter leaf stage. Both application procedures were combined with a split application of phenmedipham at 0.04 kg ai ha−1 plus desmedipham at 0.04 kg ai ha−1 plus metamitron at 0.70 kg ai ha−1 plus ethofumesate at 0.10 kg ai ha−1 plus mineral oil at 0.50 L ha−1 applied POST at the cotyledon–to–two-leaf as well as at the four-leaf growth stages. Pronamide (both single and double application) initially caused chlorosis and reduction of sugar beet growth. LAI and photosynthetic yield were also significantly affected for a 2-mo period following the final application, after which the negative effects caused by pronamide were ameliorated. At harvest, sugar beet root and sugar yield, sucrose, K+, Na+, and N-amino acid concentrations were not affected by the herbicide treatments compared with those produced in weed-free and herbicide-free plots, indicating that all cultivars managed to overcome the transient pronamide stress. Regarding sugar beet cultivars, root and sugar yield of Avantage and Dorothea at harvest were higher than that of Bianca, whereas sucrose concentration of Avantage was the lowest. There was not an apparent relationship between the order of sugar yield per cultivar (Dorothea > Avantage > Bianca) and the length of the vegetative period (Avantage < Dorothea < Bianca).

Control of weeds growing around field edges to limit seed production is an important component of preventative weed management. POST herbicide rates that are effective on weeds growing within a dense corn or soybean canopy may not be high enough to control weeds at the edge of a field. A study was conducted from 2004 through 2006 to compare velvetleaf growth and fecundity at the edge of the field as opposed to within the crop in response to a range of glyphosate rates. Treatments included position (plot center or edge), time of emergence (VE or V4 crop growth stage) and glyphosate rate (0 to 900 g ae ha−1). Without herbicide application, velvetleaf plants grown on the edge flowered earlier, had thicker stems, and produced more seed capsules than plants grown in the center of the plots. At glyphosate application rates of 200 to 900 g ha−1, the percentage of plants surviving and reproducing was higher on the edge than within the crop. Edge plants treated with 900 g ha−1 of glyphosate produced more seeds than center plants that received no herbicide. Dose–response curves were used to estimate the glyphosate rate that would reduce seed production of surviving plants to 80% of the untreated plants. Plants emerging at the VE stage were estimated to require 300 g ha−1 within the corn or soybean canopy and 668 g ha−1 on the crop edge, whereas plants emerging at the V4 stage would require 0 g ha−1 within the canopy and 280 g ha−1 on the crop edge.