The ability of Na+-, Li+-, K+-, Ca2+- and Mg2+-exchanged sepiolites and acid-activated sepiolites to remove ethylene from storage environments was examined. The sepiolite from Sivrihisar deposit, Turkey, was treated with 1.0 M NaNO3, LiNO3, KNO3, Ca(NO3)2, Mg(NO3)2, HNO3 and H2SO4 solutions at 90°C for 4 h. The mineralogical, chemical and textural properties of the materials were examined using X-ray diffraction, X-ray fluorescence, cation-exchange capacity and nitrogen gas adsorption analyses. The main mineral phase present in the materials was sepiolite, with minor dolomite, and traces of quartz and feldspar minerals and amorphous matter. Adsorption isotherms of ethylene at 273 K were measured on sepiolite samples over a pressure range of 0–100 kPa. As a result of partial blockage of the sepiolite channels, the ethylene adsorption capacity on cation-exchanged sepiolite forms (0.376–0.907 mmol g–1) was less than that of acid-activated sepiolite forms (1.279 and 1.308 mmol g–1). The ethylene adsorption capacities of the sepiolite samples were compared with those of other clay-based materials (0.167–1.817 mmol g–1) reported in previous studies of ethylene removal.

The adsorption of C2H4 and H2 gases by bentonite from the Ünye region, Turkey both as raw (B) and as K+-, Li+-, Ag+- and Mg2+ -exchanged forms, was investigated using automated volumetric equipment and pressures up to 100 kPa at 273 K and 77 K, respectively. X-ray powder diffraction (XRD) and specific surface area measurement (BET) methods were employed to characterize the bentonite samples. The C2H4 and H2 gas adsorption capacities of the original and modified forms were in the ranges 1.817–0.201 mmol g−1 and 0.522–0.388 mmol g−1, respectively. The influence of salt modifications on the gas adsorption properties of bentonite is discussed.

The effects of MSMA on the development of straighthead, yields of rice, and hormonal balance in rice plants were observed in a greenhouse study. MSMA was applied to soil at 0, 6, and 9 kg ai/ha. At 6 kg/ha some straighthead and a 45% yield reduction occurred. At 9 kg/ha straighthead was evident, and yield was reduced by 85%. Analyses were made for ethylene with gas chromatography and for indoleacetic acid (IAA) with high performance liquid chromatography. Concentrations of ethylene and total arsenic detected in the tissue from rice leaves grown in MSMA-treated soil were higher at every growth stage when compared to plants grown in untreated soil. Both treated and untreated plants showed marked increases of these compounds during the reproductive stage and a decrease prior to panicle emergence. Significant changes occurred in IAA levels with the growth stage of treated and untreated samples, but MSMA had no obvious effect on IAA levels at any of the stages examined in this study.

Substituted quinolinecarboxylic acids, including quinclorac (BAS 514H), are a new class of highly selective auxin herbicides, which are chemically similar to naturally occurring compounds isolated from plants and soils. Quinclorac is used in rice to control important dicot and monocot weeds, particularly barnyardgrass. The herbicide has also been developed for application in turfgrass areas, spring wheat, and chemical fallow. Quinclorac is readily absorbed by germinating seeds, roots, and leaves and is translocated in the plant both acropetally and basipetally. By mimicking an auxin overdose, quinclorac affects the phytohormonal system in sensitive plants. The compound stimulates the induction of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase activity and thus promotes ethylene biosynthesis. In susceptible dicots, increased levels of ethylene trigger an accumulation of abscisic acid (ABA), which, as part of the intrinsic auxin activity of quinclorac, plays a major role in growth inhibition and the induction of epinasty and senescence. In sensitive grasses, such as barnyardgrass species, large crabgrass, broadleaf signalgrass, and green foxtail, quinclorac leads particularly to an accumulation of tissue cyanide, formed as a co-product during increased ACC and ethylene synthesis. This causes phytotoxicity characterized by the inhibition of root and particularly shoot growth with tissue chlorosis and subsequent necrosis. These effects were not observed in tolerant rice and a resistant biotype of barnyardgrass. No significant differences in uptake, translocation, or metabolism of quinclorac between resistant and sensitive grasses were found. Hence, a target-site-based mechanism of selectivity is suggested. The induction process of the ACC synthase activity plays the primary role in the selective herbicide action of quinclorac. This is a common effect of auxin herbicides and auxins, which lead to the accumulation of cyanide and/or ABA depending on the plant species and tissues, the compound concentration in the tissue, and their biological activity.

Leaves of coca are the primary source of cocaine. There is interest in using Fusarium oxysporum as a mycoherbicide in addition to other measures to control coca production, but information on coca physiology, including the stress responses of coca leaves, is limited. Deleafing coca plants stimulates rapid production of new leaves, and young expanding leaves readily abscise if treated with ethylene. Commercial preparations of cell wall degrading enzymes, as well as a 24-kDa elicitor from Fusarium oxysporum, induced significant levels of ethylene production by coca leaves. Ethylene pretreatment of coca leaves enhanced the production of ethylene by coca leaves in response to the cell wall degrading enzyme preparation, Driselase, and the 24-kDa elicitor. However, ethylene pretreatment did not enhance the rate of necrosis induced in response to either Driselase or purified 24-kDa elicitor. Driselase failed to elicit levels of necrosis comparable to the 24-kDa elicitor even at 30-fold higher protein concentrations. The response of coca leaves to the 24-kDa elicitor saturated at 6.7 μg ml−1. Age of coca leaves influenced both the level of resulting necrosis and the amount of ethylene produced in response to protein. Very young leaves produced the highest levels of ethylene and necrosis in response to Driselase and the 24-kDa elicitor. The data suggest that responsiveness of coca leaves to control measures may be synchronized over the first few weeks following defoliation.

Ethylene-stimulated germination of witchweed [Striga lutea Lour. = S. asiatica (L.) O. Ktze.] seed first occurred after 13, 10, 6, 3, and 2 days of conditioning in moist sand at day/night temperatures of 20/14, 23/17, 26/20, 29/23, and 32/26 C, respectively. Maximum germination percentages in these regimes were 0.5, 3, 20, 24, and 37%, respectively. No germination occurred at 17/11 C. Witchweed seed survived in sand frozen for 7 weeks at −7 or −15 C and subsequently germinated in response to ethylene or in the presence of corn (Zea mays L., ‘DeKalb B73 × Mo.17H′) roots. The parasites emerged from the soil and flowered when maintained at 29/23 C after the termination of the freezing treatments. In other experiments, witchweed parasitized corn and/or sorghum [Sorghum bicolor (L.) Moench ‘DeKalb E-59+′] root systems in a sandy loam under 26/17, 26/20, 29/20, 32/23, and 32/26 C day/night regimes. Witchweed emerged from the soil with 26/20, 29/20, 32/23, and 32/26 C and flowered with 26/20, 32/23, and 32/26 C day/night regimes. Underground development and subsequent emergence of the parasites were substantially reduced with day/night temperatures below 29/20 C. Winter soil temperatures and growing season soil and air temperatures are unlikely to limit the spread of witchweed into important corn- and sorghum-producing areas of the United States.

In velvetleaf (Abutilon theophrasti Medic. ♯3 ABUTH), accelerated leaf abscission was a conspicuous response following foliar chlorsulfuron {2-chloro-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl] benzenesulfonamide} treatment at 35 g ai/ha. Leaf abscission of treated plants was decreased by AVG [L-2-amino-4-(2-aminoethoxy)-trans-3-butenoic acid], an inhibitor of endogenous ethylene production. Chlorsulfuron stimulated ethylene production in the abscission zone and leaves of treated plants and also increased cellulase activity in the abscission zone. Accelerated leaf abscission of velvetleaf following chlorsulfuron application appears to result from chlorsulfuron-induced increases in endogenous ethylene production and cellulase activity.

Caryopses (seeds) of fall panicum (Panicum dichotomiflorum Michx.) have a dormancy that is not easily overcome. Although accelerated after-ripening for 4 weeks was partially successful in overcoming dormancy, a dark imbibition at 35 C for about a week was more effective and also interacted strongly with an accelerated after-ripening. In either case, activation of phytochrome by red irradiation was required to induce germination. Similarly, alternating temperatures allowed germination of red-treated seeds but constant temperatures did not. More seeds germinated in sealed flasks than in dishes. The enhancement of germination in sealed flasks appeared to be related to increased CO2 levels. The data suggested a multiple dormancy in fall panicum seeds. One dormancy, the most intense, was relieved by high-temperature imbibition. The residual dormancy was relieved by active phytochrome and alternating temperatures.

Germination of dormant wild oat (Avena fatua L. # AVEFA) seed was examined in response to various concentrations of ethephon (2-chloroethylphosphonic acid), KNO3, or both together in the dark at temperatures ranging from 7 to 32 C. Both chemicals significantly (P = 0.05) promoted germination and their effects were additive. Maximum stimulation of germination in response to all treatments occurred at 7 C, with a gradual decrease in reponse as temperature or duration of after-ripening, the seed that retained dormancy during storage remained responsive to ethephon also occurred during storage of mature seed at 3 to 32 C. The rate and extent of this dormancy loss increased with an increase in storage temperature. Regardless of the temperature or duration of after-ripening, the seed that retained dormancy during storage remained responsive to ethephon and KNO3 treatments. Suitable combinations of after-ripening, ethephon, and KNO3 induced over 90% germination of seed that was dormant at maturity. Experimental evidence has been obtained that suggests that this percentage may represent the total number of viable seed in the population. While ethephon promoted seed germination, it severely stunted root and shoot growth of the resulting seedlings. It appears that strategies could be developed to combine the use of ethephon and nitrate with the natural process of after-ripening to enhance and synchronize wild oat germination.

Freshly collected redroot pigweed seeds were buried 5 cm deep in the field in November of 3 yr in succession. Treatments applied to the soil surface included KNO3 (400 kg ha-1) in midwinter, ethephon (11 kg ha-1) in late spring, and a soil cover (polyethylene sheet for 2 wk) in late spring. Seeds were recovered within 1 yr after treatment, examined for in situ germination, and tested for viability. The 3-yr averages for viable seeds remaining by October in the year after treatment with KNO3 or soil cover, either alone or in combination, did not differ from nontreated checks and averaged 47% of the original population. Viable seeds remaining in soil treated with ethephon either alone or combined with KNO3 were reduced to 21% of the beginning population. The most effective treatments were ethephon either combined with a soil cover or with a soil cover plus KNO3 which reduced the viable seeds to an average of 8% of the original. Ethephon plus a soil cover has the potential to reduce greatly redroot pigweed seed populations in the field.

The incidence of auxinic herbicide resistance in plants has increased worldwide. Auxinic herbicides were the first selective organic herbicides developed and have been used in agriculture for over 50 yr, primarily for the selective control of broadleaf weeds in cereal crops. However, the mode of action of auxinic herbicides and the molecular basis of auxinic herbicide resistance remain unknown, although an auxin-binding protein (ABP) is proposed to be the primary target site. Using auxinic herbicide-resistant (R) and -susceptible (S) biotypes of wild mustard as a model system, we have extensively studied the mode of action of auxinic herbicides and the resistance mechanisms at the physiological, biochemical, and molecular genetic levels. There are no differences in uptake, transport, and metabolism of auxinic herbicides between the R and S biotypes. Based on these results, as well as the studies on the role of auxin-enhanced ethylene biosynthesis and calcium in mediating the auxinic herbicide resistance, we hypothesize that resistance of the R biotype to auxinic herbicides is due to an altered target site, possibly an auxin receptor. We have identified and characterized a small ABP gene family as well as their cDNAs from both R and S of wild mustard. Amino acid changes were found in the ABP of the R biotype. Functional and mutational analyses of these genes are underway to determine the role of ABP in mediating auxinic herbicide resistance. In this review, we focus on the mode of action of auxinic herbicides and the molecular basis of auxinic herbicide resistance in wild mustard.

A small assortment of microbial proteins have the ability to activate defense responses and induce necrosis in plant cells through cell signaling pathways. These proteins are of interest because of their potential use as bioherbicides and inducers of plant resistance in agriculture. A 24-kDa protein (Nep1) was purified from culture filtrates of Fusarium oxysporum, and the effects of this protein on weed leaves were investigated. This protein induced necrosis in detached leaves of Papaver somniferum, Lycopersicon esculentum, Malva neglecta, and Acroptilon repens when taken up through the petiole. The pattern and level of necrosis were dependent on the plant species. Treatment with Nep1 induced the production of ethylene in isolated leaves of various species, and the level of ethylene response was shown to be correlated to the concentration of the protein. Pretreating leaves of P. somniferum, L. esculentum, M. neglecta, and Cardaria draba with 100 µl L−1 ethylene enhanced the protein induction of ethylene biosynthesis in those leaves. Application of Nep1 (200 nM) as a spray to intact plants of Abutilon theophrasti, P. somniferum, Centaurea solstitialis, Centaurea maculosa, and Sonchus oleraceus resulted in extensive necrosis of leaves within 48 h. The results of this research are supplemental to our understanding of the role of specific polypeptides in plant/microbe interactions and demonstrates for the first time that a fungal protein can cause extensive necrosis when applied to weed species as a foliar spray.

The interaction between ethylene production and seed germination of sugar beet (Beta vulgaris L.) was studied. For intact fruits, deoperculated fruits and true seeds, ethylene was only produced after the start of radicle emergence. Removal of the operculum or the whole pericarp, likely allowing better water uptake and gas exchange by the true seed, actually increased the time span between the start of radicle emergence and the beginning of ethylene production compared to intact fruits. ACC (1-aminocyclopropane-1-carboxylic acid), AOA (aminooxyacetic acid), AIB (2-amino isobutyric acid) and STS (silver thiosulphate) in the imbibition medium did not influence the germination pattern. Based on these findings, the function of ethylene during the germination of sugar beet is uncertain.

Methods of evaluation of seed quality providing accurate prediction of seed performance under field conditions are needed by the seed industry. Various physiological tests, i.e. germination tests in suboptimal conditions of temperature, oxygenation and water potential of the medium, or accelerated ageing and controlled deterioration allow sensitive differentiation between seed lots. A better understanding of the biochemical, cellular and molecular mechanisms involved in the acquisition of seed vigour during seed development, in the germination process and in seed deterioration during ageing could suggest various markers of seed quality. Among these markers, electrolyte leakage and ethylene production during imbibition, cell-cycle markers (DNA replication, β-tubulin), soluble sugar metabolism (in particular, changes in the raffinose family of oligosaccharides), proteins (11S globulin B-subunit, late embryogenesis abundant protein, heat-shock protein) and the efficiency of reactive oxygen species scavenging through antioxidant defence systems (e.g. catalase activity) have potential for the evaluation of the state of seed maturity, seed performance and effectiveness of seed priming treatments. Use of global approaches such as transcriptomic, proteomic or metabolomic analysis could also result in the identification of new markers.

The transition from the dormant to the non-dormant state of a viable and mature seed can take place at low hydration by exposure to air-dry storage conditions (dry afterripening; AR). The events occurring during this loss of dormancy are of considerable physiological, ecological and agricultural interest. AR may be attributable to increased sensitivity to germination-stimulating factors and a widening of the temperature window for germination. Genetic, –omics and physiological studies on this mode of dormancy breaking provide support for a key role of the balance between gibberellin (GA) and abscisic acid (ABA) metabolism and sensitivity. Recent evidence also supports a possible role for ethylene (ET) in this complex signalling network that is necessary for AR implementation. However, hormone-independent signals, such as reactive oxygen species (ROS), nitrate () or nicotinamide adenine dinucleotide (NAD+), also appear to be involved. The way in which hormone- and non-hormone-signalling pathways affects each other (cross-talk) is still under study. This review provides updated information on the programmes that overcome seed dormancy. Thus, we have reviewed: (1) the –omic status in dry seeds; (2) the relationship between temperature and nitrate signalling and AR; (3) alterations in ABA/GA synthesis and signalling; (4) the action of hormone molecules other than ABA and GA (i.e. ET, salicylic and jasmonic acids); and (5) participation of reactive oxygen species (ROS), NAD+ and protein carbonylation. Taken together, the acquisition and implementation of dry AR involve a complex signalling network that is difficult to disentangle.

Physiological dormancy of scarified seeds of Townsville stylo (Stylosanthes humilis HBK) was released by acidic aluminium (Al3+) solution. Antiethylenic substances inhibited germination of low-pH-stimulated dormant seeds, with a correspondingly low ethylene production and low activity of 1-aminocyclopropane-1-carboxylate (ACC) oxidase in seeds. On the other hand, antiethylenic substances did not decrease the germination of Al3+-stimulated seeds, but ACC oxidase activity and ethylene production by the seeds was decreased to a large extent. These data provide evidence that dormancy breakage by Al3+ differs from that caused by low pH and is not associated with ethylene production. Similarly to Al3+ action, methyl viologen (MV), a reactive oxygen species-generating compound, broke dormancy of Townsville stylo seeds. Sodium selenate and N-acetyl cysteine, antioxidant compounds, largely decreased germination of MV- and Al3+-stimulated dormant seeds. Altogether these data point to oxidative radicals constituting key molecules in the chain of events triggered by Al3+ leading to dormancy breakage.

Seed germination of Grand Rapids lettuce (Lactuca sativa L.) was inhibited at 38°C (thermoinhibition). Thermoinhibition was totally relieved by a combination of 100% oxygen and 10 mg I−1 kinetin, to a lesser extent by a combination of oxygen and ethylene but not at all by oxygen plus GA3. The combination of oxygen with kinetin or ethylene was more effective in preventing thermoinhibition than a combination of all three hormones and CO2 in air. The beneficial effect of oxygen plus kinetin was not related to either increased production of CO2 or ethylene by the seeds. In air, germination was partially inhibited by 2-aminoethoxyvinyl glycine (AVG) or 2,5-norbornadiene (NBD) and totally inhibited by AVG plus NBD. Oxygen plus kinetin almost completely alleviated their inhibitory effects. It was concluded that oxygen plus kinetin caused seeds to bypass an ethylene requirement for germination or increased the sensitivity of seeds to ethylene. In air at 38°C, seeds exhibited a high level of ethanolic fermentation, while in oxygen plus kinetin they respired aerobically. At 38°C in air, contents of ATP and total adenylates were reduced, while in seeds treated with oxygen plus kinetin these contents were similar or higher than in 25°C controls. A similar response was also observed for adenylate energy charge. It was concluded that part of the mechanism of thermoinhibition could be the failure of ATP content to reach a sufficient level to satisfy the requirement for germination at 38°C. It appeared possible that the prevention of thermoinhibition by oxygen plus kinetin could be related to increased ATP content in seeds caused by this treatment.

Totalling more than 3000 species, parasitic angiosperms are a most diverse group of organisms. Classified as either shoot or root parasites according to site of attachment, plant parasites are further classified, according to the degree of parasitism, into one of two divisions: holoparasitic or hemiparasitic. Within these divisions, angiosperm parasites are either obligate or facultative.

Obligate parasites cannot survive to maturity without attaching to a host plant, thus the need to germinate in close proximity to a host first characterizes the specialized germination and seed dispersal strategies of these plants. However, seeds of all species of the rootholoparasitic Orobanchaceae and four genera within the Scrophulariaceae have evolved very specialized germination strategies. Once the seeds have undergone an after-ripening period, they require a prolonged imbibition period at temperatures of approx. 30°C before they acquire the potential to germinate. Minute seeds with very little reserves, they must germinate within millimetres of the host root for successful host attachment and continued survival. To this end, germination only occurs in responseto specific chemical germination triggers released from the host root. In Striga hermonthica (Del.) Benth., the perception of the host-derived trigger results in stimulation of endogenous ethylene production and it is this ethylene that initiates germination. It is proposed that the chemical triggers released from the host be consideredas ‘elicitors’ which function primarily as allelochemicals and that the parasite seeds have become adapted in such a way as to have an absolute requirement for external germination triggers.

Seed germination of the hemiparasitic angiosperm Striga hermonthica is elicited by compounds present in the root exudates of the host plant. A variety of chemicals can substitute for the host-derived signal although the exact mechanism through which these act is unknown. In the present study, thidiazuron (TDZ), a cytokinin-active urea derivative was found to stimulate germination. This thidiazuron-induced germination was shown to be mediated by endogenous ethylene, by a similar mechanism to germination induced by host-root exudate and the synthetic stimulant GR-24. Comparing the effects of TDZ, host-root exudate, GR-24 and the ethylene precursor 1-aminocyclopropane-1-car-boxylic (ACC) suggests that ethylene production increases as a result of increased ACC synthesis and is consistent with a model for Striga seed germination in which host-derived signals and other stimulants act by eliciting the synthesis of ethylene via a stimulation of ACC synthase activity. All germination stimulants tested trigger a rapid increase in O2 uptake by conditioned seeds. The patterns of O2 uptake following TDZ or GR-24 treatments show similarities and three distinct phases of respiration are apparent. In contrast, stimulation of O2 uptake by ethylene results in a different pattern, with no distinct phases obvious following the initial burst of activity.