Evidence that global warming has altered the phenology of the biosphere, possibly contributing to increased plant production in the northern hemisphere, has come from a diversity of observations at scales ranging from the view of the back yard to satellite images of the earth. These observations, coupled with an understanding of the effects of temperature on plant phenology, suggest that future changes in the atmosphere and climate could alter plant phenology with unknown or unpredictable consequences. We assessed the effects of simulated climatic warming and atmospheric CO 2 enrichment on the spring and autumn phenology of maple trees (Acer rubrum and A. saccharum) growing for four years in open-top field chambers. CO 2 enrichment ( 1 300 ppm) had no consistent effects on the timing of budbreak and leaf unfolding in the spring or leaf abscission in the autumn. Warming ( 1 4 1C) usually had predictable effects: in two of the three years of assessment, budbreak occurred earlier in warm chambers than in ambient temperature chambers, and leaf abscission always occurred later. The lengthening of the growing season could contribute to increased productivity, although effects of temperature on other physiological processes can concurrently have negative effects on productivity. In 1995, budbreak was unexpectedly delayed in the warmer chambers, apparently the result of advanced budbreak leading to injury from a late-spring frost. Likewise, there was increased risk associated with longer leaf retention in the autumn: in 1994, leaves in the warm chambers were killed by freezing temperatures before they had senesced. These observations support the premise that global warming could increase the length of the growing season. Phenological responses should, therefore, be part of any assessment of the possible consequences of global change, but our results also suggest that those responses may not always have positive effects on production.

Dermatophytosis is the most common contagious and infectious skin disease of cats. It is of particular importance in animal shelters because it is a known zoonosis, highly contagious, and easily transmitted. In this open clinical trial, 58 cats with confirmed Microsporum canis dermatophytosis and 32 uninfected bonded pairs or littermates were treated with a combination of 21 days of oral itraconazole (10 mg kg(-1)) and twice weekly lime sulphur rinses until cured. Cats were not clipped in this treatment programme. Fungal cultures were obtained once weekly on all cats, and cats were considered cured when they had two consecutive negative weekly fungal cultures. Cats were held in the facility and received continued topical treatment until the fungal cultures were finalized. None of the cats developed oral ulcerations as a result of grooming the lime sulphur rinses. Oral ulcerations only developed in cats with clinical signs associated with upper respiratory disease. None of the uninfected cats living in contact with infected cats became culture positive or developed skin lesions. When data were examined retrospectively and the number of days to finalize the cultures was subtracted (21 days) from the total number of days the cats were housed in the annex, the mean number of days of treatment required for cure was 18.4 +/- 9.5 SEM (range 10-49 days). Cats with more severe infections required longer therapy. In this shelter, the combination of oral itraconazole and topical lime sulphur rinses for the treatment of dermatophytosis was effective and safe.

SLIT treatment produced clinical improvement in dogs with dust mite-associated AD and was associated with serological changes supporting this improvement. Further studies in larger numbers of dogs and those with polysensitization are warranted.

In an open non-randomized study, 90 cats with severe dermatophytosis were treated with 21 days of oral itraconazole at 10 mg/kg and one of three topical antifungal rinses applied twice weekly: lime sulphur (LSO); reformulated lime sulphur with an odour-masking agent (LSR); or a 0.2% miconazole nitrate and 0.2% chlorhexidine gluconate rinse (MC). Weekly examinations and fungal cultures were used to monitor the cats' response to therapy. If at day 42 of treatment cats were still strongly fungal culture positive and/or developing new lesions, they were retreated with oral itraconazole and LSO. Cats were not prevented from licking the solutions and none developed oral ulcerations. Thirty-one cats were treated with LSO, 27 with LSR and 32 with MC. The median number of days to cure was 30 (range 10-69 days) and 34 (range 23-80 days) for LSO and LSR, respectively. Thirty-two cats were treated with MC, and 13 of 32 cats required repeat treatment because of persistent culture-positive status and development of new lesions. Median number of days of treatment for the 19 cats that cured with MC was 48 (range 14-93 days). When the number of days to cure was compared between the groups, there was a significant difference between cats treated with LSO and LSR (P=0.029) and cats treated with LSO and MC (P=0.031), but no significant difference between the number of days to cure for cats treated with LSR and MC (P=0.91).

In this study, isolated infective Microsporum canis spores were used in an in vitro test model to compare the sporocidal activity of two commercial topical antifungal rinses. The two commercial test solutions used in the study were a lime sulphur solution 97.8% (LymDyp) and miconazole base 5.2%/chlorhexidine gluconate 5.9% mixture (Malaseb Concentrate Rinse). Water and household bleach were used as controls. Isolated infective spores were harvested from infected hairs and 500 microL of the spore suspension was incubated with an equal volume of dilutions of lime sulphur or the miconazole/chlorhexidine gluconate combination for 5 min and 4 h followed by fungal culture. There were too many to count colonies on the water control plates. Lime sulphur was 100% sporocidal at all test dilutions at both times. Miconazole/chlorhexidine gluconate was 100% sporocidal at all but the 1 : 128 dilution after 5 min of incubation and 100% sporocidal when incubated with spores for 4 h. It is not known if the two products have similar antifungal activity against infective spores on or within hairs; however, based on the findings of this study there is good evidence to recommend either rinse as an adjuvant topical therapy in a dermatophyte treatment and control program.

Objectives The goal of this study was to determine how frequently Microsporum canis was isolated after 1, 2 and 3 weeks of incubation on dermatophyte culture medium either from untreated cats or cats during treatment. Methods This was an observational retrospective study. Toothbrush fungal culture results were examined from two data pools: untreated cats with suspect skin lesions and weekly fungal cultures from cats being treated for dermatophytosis. Results Results from 13,772 fungal cultures were reviewed and 2876 (20.9%) were positive for M canis. Of these, 2800 were confirmed as positive within 14 days of incubation and only 76 (2.6%) required >14 days for confirmation of M canis. In pretreatment specimens, 98.2% (1057/1076) of M canis isolates were recovered within 14 days of incubation in specimens from cats not known to have received prior antifungal treatment. For cats receiving treatment, 96.8% (1743/1800) of M canis isolates were recovered within 14 days of incubation. Of the 57 cultures that required >14 days for finalization, 21 required extra incubation time because cultures were grossly abnormal, 12 had concurrent contaminant growth delaying microscopic confirmation and 24 had no growth in the first 14 days. Of these 24, 19 had 1-2 colony-forming units (cfu)/plate and the remaining five plates had 5 to >10 cfu/plate, all with abnormal morphology. Conclusions and relevance The findings of this study show that it is not necessary to hold pretreatment or post-treatment fungal cultures for 21 days before finalizing cultures for no growth. Growth requiring >14 days had grossly abnormal morphology.

In this study, 5/6 commercially available fungal culture media were comparable with respect to first growth, first colour change, and first sporulation when inoculated with three strains of Microsporum canis, one strain of Microsporum gypseum, and one strain of Trichophyton species when incubated at either 25°C or 30°C. Five of six plates showed 100% growth at both temperatures. Five of six plates showed 100% growth when inoculated with naturally infective M canis hairs and spores. One commercial product packaged as a self-sealing incubation plate showed growth in only 65.4% of times and the plates were prone to desiccation. M canis inoculated plates were incubated under four different light exposures (24h of light, 24h of dark, 12h light/12h dark, and room lighting) and no differences in growth or sporulation were noted.

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