ALBERT

Notes: Biological damage to plants is commonly found from the Devonian but occurs most commonly from the Cretaceous. Damage inflicted on plants whilst they were alive may trigger a pathological response involving the growth of abnormal tissues. Much of the damage is caused by arthropods, particularly insects. Whilst some damage is non-taxon specific, such as simple feeding traces, other damage, such as leaf mines, galls or bark boring, may reveal the co-evolution of host specific taxa and the timing of such interactions. Damaged plants, particularly from the Cretaceous and Tertiary are described and illustrated. The geological history of the evolution of insect-related plant damage is briefly reviewed. Increased variety in the pathological response of plants is seen from the Cretaceous with the evolution of the angiosperms and diversification of numerous insect groups.

Notes: The effect of aerobic mesophilic microfloral concentration on the isolation of Listeria monocytogenes LM82 was studied in 31 (18 cheeses and 7 noncheese) retail foods having standard plate counts of 101 to 108 colony forming units (CFU)/g. Foods were spiked with L. monocytogenes and enriched at 30°C for 24 h in a selective enrichment broth used in a U.S. Food and Drug Administration method. Inoculum levels for isolation on modified McBride agar ranged from 0.1 to 〉 5 × 103 with a geometric mean value of 5 inoculated CFU/g or 1.4 CFU/g. Pure Enterococcus (Streptococcus) faecalis (0 to 6 × 106 inoculated CFU/mL) in the absence of food matrix had no effect on the enrichment of L. monocytogenes. Ease of isolation of LM82 was independent of the food microflora concentration both generally and in the specific food type of 9 Brie cheeses. Competition, when it occurs, therefore, may be due to specific bacterial competitors rather than bacterial numbers.

Notes: When the aggregates of fairly dry, medium-coarse soil were broken down and firmed over the seed by moderate or heavy pressure, slug damage was reduced. Coarse soil aggregates did not break down so well, particularly under heavy pressure; many seeds remained exposed and were damaged. The seed was also protected by deep planting, with the penalty of late emergence of the seedlings.

Notes: The choice of resting places in bare soil of both immature and mature slugs Was influenced by the size of the soil aggregates. A moderate to coarse soil was preferred and it is suggested that response to contact stimuli may be partly responsible for this behaviour. Soil composed of fine aggregates was preferred for egg-laying sites.

Notes: The ability of the herbicide safeners, BAS-145138 (1-dichloroacetyl-hexahydro-3,3,8a-trimethyl-pyrrolo(1,2a)pyrimidin-6(2H)-one), dichlormid (N,N-diallyl-2,2-dichloroacetamide), flurazole (phenylmethyl ester), and MG-191 (2-dichloromelhyl-2-methyl-1,3-dioxolane) for preventing metazachlor injury to maize (Zea mays L.) and sorghum (Sorghum bicolor L.) seedlings were compared with their effects on 14C-metazachlor metabolism to a glutathione (GSH) conjugate, effects on non-protein thiol contents (mainly GSH) and effects on Glutathione S-transferase (GST) activity in these two species.Sorghum shoot growth was reduced by 41% and maize shoot growth was reduced by 54%, by metazachlor concentrations in vermiculite nutrient culture of 0·6 μM and 7·5μM, respectively. In this system, all four compounds had significant activity as safeners for metazachlor in both sorghum and maize seedlings. BAS-145138 and flurazole were the most effective safeners in maize and sorghum, respectively. In the absence of safeners, the rate of non-enzymatic conjugation of metazachlor and GSH was much greater than the enzymatic rate. However, the rate of enzymatic conjugation of metazachlor with GSH was increased by safener treatment in both maize and sorghum. Safener effectiveness was highly correlated with increases in 14C-metazachlor uptake and metabolism in both species. Safener effectiveness was more highly correlated with safener effects on GST activity in maize or sorghum when 14C-metazachlor was used as the substrate than when the non-specific CDNB (1-chloro-2,4-dinitrobenzene) was used as the substrate. Safener effectiveness was also strongly correlated with safener effects on GSH levels in sorghum, but not in maize, possibly because of the greater importance of non-enzymatic conjugation of metazachlor with GSH in sorghum as compared to maize.

Notes: A semi-open circuit system for measuring changes in net CO2 exchange (NCE) in single leaves of intact grasses following herbicide treatment is described and evaluated. There were significant differences in levels of inhibition and subsequent recovery of NCE in maize and eight weedy panicoid grasses following limited root uptake of atrazine (2-chloro-4-ethyl-amino-6-isopropylamino-1,3,5-triazine). cyanazine [2-chloro-4-(1-cyano-1-methylethylamino)-6-ethylamino-1,3,5-triazine] and cyprazine (2-chloro-4-cyclopropylamino-6-isopropyl-amino-1,3.5-triazine). Rate of NCE recovery was positively correlated (P = 0.05) with growth of seedlings in nutrient solution containing the herbicides. Rates of NCE recovery 〉0.9 mg CO2 per dm2 per h/h reflected rapid rates of herbicide detoxification in the leaves and a significant tolerance to preplant incorporated and postemergence applications of atra-zine, cyanazine and cyprazine. In contrast, some species, e.g. large crabgrass [Digitaria sanguinalis (L.) Scop.] and proso millet (Panicum miliaceum L.) treated with cyanazine demonstrated considerable tolerance to these treatments in spite of low NCE recovery rates indicating that factors other than foliar detoxification may play an important role in the tolerance of some grasses to 2-chloro- 1,3,5-triazine herbicides.

Notes: Atrazine [2-chloro-4-(ethylaminol-6-(isopropyl-amino)-s-triazine] resistant biotypes of lamb's quarters (Chenopodium athum L) were reported in the maize growing areas of Ontario, where the herbicide had been used fur a number of years. Field samples from four locations proved tolerant to higber than recommended rates of atrazine in controlled environment screening trials. A resistant biotype was not killed with up to 40 kg/ha atrazine. Diuron at 5 x10-5 M inhibited the Hill reaction with isolated chloroplasts of resisiant and susceptible biotypes of lamb's-quarters. However, with 10-4 M atrazine, the photochemical activity was inhibited in chloroplasts isolated from the susceptible biotype but not in chloroplasts from the resisiant biotype. With maize chloroplasts, inhibition with 10-4 M atrazine was the same as with the susceptible biotype of lamb's-quarters. These studies suggested that a new mechanism of intraspecific resistance in lamb's quarters to atrazine was involved, other than differences in uptake, translocation and metabolism reported with interspecific comparisons involving the s-triazines and other herbicides, It was also concluded that atrazine and diuron did not have precisely the same mechanism of action as photosynthetic inhibitors with lamb's-quarters, and that external and or internal structure or function of chloroplasts in relation to atrazine inhibition can vary significantly even in biotypes of the same species.

Notes: The effect of five herbicide safeners on preventing maize (Zea mays L.) injury by acetochlor [N-(2-ethyl-6-methyl-phenyl)-N-(ethoxymethyl)-chloroacetamide], their influence on herbicide uptake and metabolism to a glutathione (GSH) conjugate as well as on GSH content and glutathione S-transferase activity (GST) in untreated and herbicide with/without safener-pre-treated 4-day-old seedlings were determined. The safeners studied were: AD-67 (N-di-chloroacetyl-1-oxa-4-azaspiro-4-5-decane), BAS-145138 [1-dichloroacetyl-hexahydro-3,3,8a-trimethyl-pyrrolo(l,2-a)pyrimidin-6(2H)-one], dichlormid (N, A,-diallyl-2,2-dichlo-roacetamide), DKA-24 (N, N2-diallyl-N2dichloroacetylglycineamide) and MG-191 (2-dichloromethyl-2-methyl-1,3-dioxolane). All safeners significantly increased [14C]acetochlor uptake and metabolism rate, maize GSH content and GST activity. Seedlings receiving BAS-145138 pre-treatment metabolized almost 70% of the absorbed [14C]acetochlor within 10 min.Safener-enhanced GST activity was always found to be higher when [14C]acetochlor was used as the substrate compared with CDNB (1-chloro-2,4-dinitrobenzene). Although DKA-24 had a significantly lower influence on both herbicide metabolism and GST activity, it was nearly as effective a safener as BAS-145138, while the others provided no or poor protection to maize from acetochlor injury when they were not incorporated in the soil. Effets d'antidotes sur la toxicité, la pénétration et le métabolisme de I'acétochlore chez le mats etsur l'activité glutathion S-transférase Cinq antidotes d'herbicides diminuaient la toxicité de 1'acétochlore [N-(2-éthyl-6-méthyl-phényl)-N-(éthoxyméthyl)-chloroacétamide] à I'égard du maïs (Zea mays L.). Lew effet sur l'absorption de l'herbicide et sur son métabolisme en un conjugué avec le glutathion (GSH), de même que leur effet sur la teneur en GSH et 1'activité glutathion 5-transférase (GST) ont étéétudiés sur des maïs âgés de 4 jours. Les antidotes étaient: l'AD-67 (N-dichloroacétyl-1-oxa-4-azaspiro-4,5-décane), le BAS-145138 [1 -dichloroacétyl-hexahydro-3,3,8a-triméthyl-pyrrolo(l,2-a) pyrimidine-6(2H)-one], le di-chlormide (N, N-diallyl-2,2-dichloracétamide), le DKA-24 (N, N2-diallyl-N2-dichloracétylgly-cineamide] et le MG-191 (2-dichlorométhyl-2-méthyl-l,3-dioxolane). Tous les antidotes augmentaient de manière significative 1'absorption et le métabolisme de I'acétochlore 14C, ainsi que la teneur du maïs en GSH et son activité GST. Les jeunes plantes prétraitées avec le BAS-145138 métabolisaient en 10 min près de 70% de I'acétochlore 14C absorbé. L'activité GST stimulée par 1'antidote était toujours plus élevée avec I'acétochlore 14C comme substrat qu'avec le CDNB (1-chloro-2,4-dinitrobenzène).Le DKA-24 avait un effet significativement plus faible que le BAS-145138 sur le métabolisme de l'herbicide et sur l'activité GSH, mais son action antidote était presque aussi importante. Les autres produits n'apportaient au maïs qu'une protection faible ou nulle contre l'acétochlore quand ils n'étaient pas incorporés au sol. Wirkung von Safenern auf die Phytotoxizität, Aufnahme und Metabolismus von Acetochlor und die Glutathion-S-Transferase-Aktivität in Mais Die Wirkung von 5 Safenern (AD-67, BAS-145138, Dichlormid, DKA-24 und MG-191; chemische Bezeichnungen s.o.) auf die Phytotoxizität von Acetochlor für Mais (Zea mays L.) und ihr Einfluß auf die Aufnahme des Herbizids und Metabolismus zu einem Glutathion-(GSH-) Konjugat und auf die Glutathion-S-Transferase-(GST-)Aktivität wurde an 4 Tage alten Keimpflanzen untersucht. Durch die Vorbehandlung mit den Safenern wurden die [14C]-Acetochlor-Aufnahme- und -Metabolierungsrate, der GSH-Gehalt und die GST-Ak-tivität signifikant erhöht. Mit BAS-145138 vorbehandelte Keimpflanzen metabolisierten fast 70% des absorbierten [14C]-Acetochlor innerhalb von 10 min. Die durch die Safener erhöhte GST-Aktivität bei [14C]-Acetochlor als Substrat war im Vergleich zu Chlordinitroben-zen immer höher. Obwohl DKA-24 einen signifikant geringeren Einfluß sowohl auf den Herbizidmetabolismus als auch auf die GST-Aktivität hatte, war es fast so wirkungsvoll wie BAS-145138, während die anderen ohne Einarbeitung in den Boden für den Mais keinen oder geringen Schutz gegen Schäden durch Acetochlor boten.