Weed control with selected herbicides in acetolactate synthase-resistant sorghum

The recent development of grain sorghum hybrids with resistance to acetolactate synthase (ALS)-inhibiting herbicides has allowed for the use of several post-emergence applied (POST) ALS-inhibitors to control weeds in the crop. Field experiments were conducted at four sites in Kansas in 2008 to evaluate the efficacy of nicosulfuron and nicosulfuron + rimsulfuron applied alone or in combination with dicamba, metsulfuron methyl, and atrazine. All POST treatments slightly injured sorghum 2 weeks after treatment (WAT) at Garden City and Hesston, whereas at Hays and Manhattan, only treatments that included dicamba caused injury. Nicosulfuron + rimsulfuron applied alone provided 41, 83, 74, and 93% control of grasses 4 WAT at Garden City, Hays, Hesston, and Manhattan, respectively. However, to obtain the highest level broadleaf weed control, nicosulfuron or nicosulfuron + rimsulfuron need to be applied with other broadleaf herbicides. POST treatment of nicosulfuron + metsulfuron methyl + dicamba + atrazine provided 90% or greater control of all broadleaf weeds at sorghum flowering. Sorghum grain yield was greater following all herbicide treatments compared with the weedy check. The POST treatment that provided the highest yield at Garden City was nicosulfuron + rimsulfuron + atrazine, whereas in Hesston and Manhattan, nicosulfuron + metsulfuron methyl + dicamba + atrazine provided the highest yields. This research showed that many grasses can be effectively controlled with POST applications of nicosulfuron or nicosulfuron + rimsulfuron in ALS-resistant sorghum. The research also indicated that broadleaf weed control is greater when nicosulfuron or nicosulfuron + rimsulfuron are applied with other broadleaf-control herbicides such as dicamba, metsulfuron methyl, and atrazine.     

Application of (15NH4)2SO4 to study N dynamics in hoop pine plantation and adjacent native forest of subtropical Australia: the effects of injection depth and litter addition

Purpose

Hoop pine (Araucaria cunninghamii) is a nitrogen (N)-demanding native Australian softwood plantation species. Litter quality and its effects on soil mineral N and ¹⁵N transformations have not been well studied in the hoop pine plantation and adjacent native forest. The present study was conducted to determine the impact of ¹⁵N injection depth and litter additions on the dynamics and fate of mineral ¹⁵N and also to compare the difference in litter quality, ¹⁵N dynamics, and fate between the hoop pine plantation (HP) and the adjacent native forest (NF).

Materials and methods

The experiments were done in the Yarraman State Forest (26°52′ S, 151°51′ E), southeastern Queensland. Materials of litter addition were prepared on the basis of ten random samples of litters taken from the NF and HP sites using a 1?×?1-m quadrat. Litter additions were defined as: SL represented the average condition of forest floor in the forest ecosystems and DL represented the double average amount of litters in the forest ecosystem. Experiment 1 covered 2 forest types (NF and HP)?×?3 litter rates (nil litter, SL, and DL)?×?3 ¹⁵N injection depths (0, 2.5, and 5.0 cm). Experiment 2 included 2 forest types (NF and HP)?×?2 litter rates (nil litter and SL)?×?3 injection depths (0, 2.5, and 5.0 cm) of distilled water. The in situ core incubation method was used with an incubation period of 28 days. The isotope ratio of mineral N or/and total N (soil and litter) were analyzed using an isotope ratio mass spectrometer with a Eurovector elemental analyzer (Isoprime-EuroEA 3000).

Results

Total N and δ ¹⁵N were significantly higher, and C/N ratios and δ ¹³C were significantly lower in the NF litters than in the HP litters. The NF litters had significantly lower total ¹⁵N and total ¹⁵N recovery than the HP litters after ¹⁵N addition. Litter addition had no significant effect on mineral ¹⁵N transformations and δ ¹⁵N in the NF soil, but decreased ¹⁵NO ₃ ^? –N, mineral ¹⁵N, and δ ¹⁵N and increased immobilized ¹⁵N in the HP soil. The depth of added ¹⁵NH ₄ ⁺ significantly altered total ¹⁵N, δ ¹⁵N, and total ¹⁵N recovery in the litters, whereas it did not influence ¹⁵NH ₄ ⁺ –N, ¹⁵NO ₃ ^? –N, mineral ¹⁵N, or immobilized ¹⁵N in soils in the two forest ecosystems.

Discussion

The NF litters had significantly higher δ ¹⁵N than the HP litters, indicating that the NF soil had a higher rate of nitrification than the HP soil. Higher litter quality in the NF was an important driving force for N cycling to promote strong N dynamics in the NF soil over the HP soil. The HP litters had significantly higher total ¹⁵N than the NF litters after ¹⁵N addition, implying that soil mineral N was relatively deficient in the HP in comparison with the NF. Litters decreased nitrification and increased immobilization in the HP soil, showing forest litters resulted in more N immobilization to prevent the loss of substantial quantities of NO ₃ ^? through leaching or denitrification. The depth of ¹⁵N injection did not significantly alter concentrations of ¹⁵NH ₄ ⁺ –N, ¹⁵NO ₃ ^? –N, mineral ¹⁵N, and immobilized ¹⁵N in the NF and HP soils, suggesting that the depth of ¹⁵N injection had no significant influence on the evaluation of soil N transformations.

Conclusions

The NF litters had significantly higher total N and δ ¹⁵N and lower C/N ratios and δ ¹³C than the HP litters. Mineral N was relatively insufficient in the HP soil relative to the NF soil. The HP litters facilitated more N immobilization in the soil to reduce the loss of substantial quantities of NO ₃ ^? through leaching or denitrification. The depth of ¹⁵N added did not significantly alter concentrations of ¹⁵NH ₄ ⁺ –N, ¹⁵NO ₃ ^? –N, mineral ¹⁵N, and immobilized ¹⁵N in the NF and HP soils. The application of ¹⁵N solution by uniform sprinkling onto the soil surface can be used to study in situ field N (including mineral ¹⁵N) transformations in the 10-cm depth soils of both forest ecosystems.     

国际禽病研究的进展

疫病是世界养禽生产效率的主要限制因素。尽管分子生物学方面的基础研究导致了新型疫苗的出现，但集约化生产体系仍受到新的和变异疫病的危害，这常常是多因子感染造成的。本文综述了一些重要疫病复合症的研究进展并对商品蛋鸡群和肉鸡生产效益的影响作一评述。     

Effects of pH, temperature, and salinity on persistence of avian influenza viruses in water

The combined effects of water temperature, salinity, and pH on persistence of avian influenza virus (AIV) were evaluated in a model distilled-water system using three isolates from ducks sampled in Cameron Parish, Louisiana. Variables were tested within the ranges normally associated with surface water. Differences were detected between temperature (17 C and 28 C), pH (6.2, 7.2, 8.2), and salinity (0 ppt and 20 ppt), with a strong interactive effect observed between pH and salinity. Estimated persistence of infectivity for 1 x 10(6) mean tissue-culture infective dose of A/mottled duck/LA/38M/87 (H6N2) was longest at 17 C/0 ppt/pH 8.2 (100 days) and shortest at 28 C/20 ppt/pH 8.2 (9 days). Differences in the response to these variables were apparent between viruses. The ability of AIV to persist in surface water was also evaluated using samples collected from varied waterfowl habitats in coastal Louisiana. Observations were consistent with the model system, with duration of infectivity decreasing with increased salinity and pH. This suggests that experimental results may have application to field conditions.     

Avian influenza viruses from migratory and resident ducks of coastal Louisiana

Cloacal and tracheal swabs were collected from 1389 hunter-killed ducks in Cameron Parish, Louisiana, during the 1986 and 1987 waterfowl seasons. Twenty-eight avian influenza viruses (AIVs) were isolated from 605 blue-winged teal (Anas discors), 75 mottled ducks (A. fulvigula), 375 gadwalls (A. stepera) and 334 green-winged teal (A. crecca). Prevalence estimates of AIV in ducks sampled during September, November, and December through January were 3.1%, 2.0%, and 0.4%, respectively. Differences in prevalence were detected by season (P = 0.044) and age class (P = 0.036). Two isolations from resident mottled ducks document transmission of AIV on these wintering areas. Much subtype diversity was present, with nine of 13 hemagglutinin (HA) and nine of nine neuraminidase (NA) subtypes recovered. Predominant HA and NA subtypes were typical of AIVs commonly associated with waterfowl. Results indicate that AIVs are transmitted in the wintering areas, and, although prevalence is low, these viruses continue to circulate within these duck populations during winter.     

The occurrence of Clostridium perfringens in the intestine of chicks

Commercial broiler chicks brooded either on wire or on used or new litter demonstrated a 75% (62/75) incidence of recovery of "perfringens-like" colonies from the intestine during a 5-week period. Eleven Clostridium spp. were identified from among these "perfringens-like" organisms, which were cultured on SPS selective agar medium. Clostridium perfringens was positively identified only infrequently (five isolates) from among the "perfringens-like" colonies. In contrast, "perfringens-like" colonies were not recovered from the intestinal contents of specific-pathogen-free chicks reared in an isolation unit. However, C. perfringens was isolated from the yolk sac of one embryonated egg and from the intestine of a single 7-day-old chick, indicating the possibility of vertical transmission of this potential pathogen.     

Elimination of false-positive polymerase chain reaction results resulting from hole punch carryover contamination.

The collection of biological material (e.g., blood) directly onto filter paper for subsequent use in laboratory assays such as polymerase chain reaction (PCR), has become a common practice. Dried cells or fluid on the paper can be readily rehydrated and retrieved into a standard volume of an appropriate elution buffer but introduces a dilution factor to the sample. The use of a common cutting instrument for excising a standard-sized piece of paper that contains the material also introduces the potential for transferring biological material from one sample to subsequent samples, causing false-positive results by PCR. In the present study, filter-paper-collected blood that contained beak and feather disease virus was used to determine if viral DNA could be transferred between samples by a hole punch used to excise sequential filter papers. It was determined that false-positive results could be obtained at least 13 times after a positive sample. Subsequently, the efficacy of 4 methods of hole punch disinfection, flaming, VirkonS, bleach, and a bleach-ethanol combination, was assessed. The only effective and practical method to destroy DNA was a method where the hole punch was agitated in commercial bleach, rinsed in water, the water was displaced with 100% ethanol and air-dried. This method was simple, cheap, and relatively rapid, and allowed for the use of a single hole punch for a series of samples, without carryover contamination and consequent false-positive results.     

Acute polyneuromyopathy with respiratory failure secondary to monensin intoxication in a dog

Objective

To describe a successfully managed case of polyneuropathy and respiratory failure secondary to presumed monensin intoxication.

Case Summary

A 9‐month‐old Australian Shepherd was evaluated for progressive generalized weakness and respiratory distress. Several days preceding presentation, the dog was seen playing with a monensin capsule, and had free access to a barn where the product was stored and where chewed capsules were subsequently found. The dog was presented with flaccid tetraparesis, hyperthermia, and severe respiratory distress. Bloodwork and urinalysis revealed marked increase in serum creatine kinase concentration and presumed myoglobinuria. Cardiac troponin I level was markedly increased. Management included mechanical ventilation for 5 days, fluid‐therapy, active cooling, antimicrobial therapy, analgesia, gastroprotectants, antiemetics, enteral feedings, continuous nursing care, and physiotherapy. Intravenous lipid rescue therapy was administered with lack of improvement in respiratory function and muscle strength. The patient completely recovered and was discharged after 12 days of hospitalization.

New or Unique Information Provided

Monensin intoxication should be considered in the differential diagnosis of acute polyneuromyopathy and respiratory failure in dogs with access to this compound. Respiratory failure secondary to monensin intoxication does not necessarily carry a poor prognosis if mechanical ventilation can be provided as a bridge until return of respiratory function is achieved.