A warmer climate impairs the growth performance of Central Europe's major timber species in lowland regions.

Recent hot droughts have caused tree vitality decline and increased mortality in many forest regions on earth. Most of Central Europe's important timber species have suffered from the extreme 2018/2019 hot drought, confronting foresters with difficult questions about the choice of more drought- and heat-resistant tree species. We compared the growth dynamics of European beech, sessile oak, Scots pine and Douglas fir in a warmer and a cooler lowland region of Germany to explore the adaptive potential of the four species to climate warming (24 forest stands). The basal area increment (BAI) of the two conifers has declined since about 1990-2010 in both regions, and that of beech in the warmer region, while oak showed positive BAI trends. A 2 °C difference in mean temperatures and a higher frequency of hot days (temperature maximum >30 °C) resulted in greater sensitivity to a negative climatic water balance in beech and oak, and elevated sensitivity to summer heat in Douglas fir and pine. This suggests to include hot days in climate-growth analyses. Negative pointer years were closely related to dry years. Nevertheless, all species showed growth recovery within one to three years. We conclude that all four species are sensitive to a deteriorating climatic water balance and hot temperatures, and have so far not been able to successfully acclimate to the warmer climate, with especially Douglas and beech, but also Scots pine, being vulnerable to a warming and drying climate.

Fecal Calprotectin Concentrations in Cats with Chronic Enteropathies.

Diagnosis of feline chronic inflammatory enteropathies (CIE) and the differentiation from small cell intestinal lymphoma (SCL) can be challenging. Intestinally expressed calprotectin (S100A8/A9 protein complex) appears to be part of the complex pathogenesis of feline chronic enteropathies (FCE). Fecal calprotectin is a non-invasive biomarker for intestinal inflammation in humans and dogs but has not yet been evaluated in cats. We hypothesized that fecal calprotectin (fCal) concentrations are increased in FCE, correlate with clinical and/or histologic disease severity, and distinguish cases of CIE from SCL. This case-control study included fecal samples and patient data from cats with CIE (n = 34), SCL (n = 17), other gastrointestinal (GI) diseases (n = 16), and cats with no clinical signs of GI disease (n = 32). fCal concentrations were measured using the immunoturbidimetric fCal turbo assay (Bühlmann Laboratories). Compared to healthy cats, fCal concentrations were significantly increased in CIE, SCL, and other diseases (all p < 0.0001), but were not different between these three groups (all p > 0.05), or between cats with extra-GI diseases and healthy controls. These findings suggest that fCal may have utility as a clinical biomarker for FCE but not for intestinal disease differentiation. It further supports the role of calprotectin in the pathogenesis of the spectrum of FCE, which includes CIE and SCL.

Verification of the fCAL turbo immunoturbidimetric assay for measurement of the fecal calprotectin concentration in dogs and cats.

The concentration of calprotectin in feces (fCal) is a clinically useful marker of chronic gastrointestinal inflammation in humans and dogs. No commercial assay is widely available to measure fCal in small animal medicine, to date. Thus, we verified the immunoturbidimetric fCAL turbo assay (Bühlmann) of fCal for canine and feline fecal extracts by determining linearity, spiking and recovery, and intra-assay and inter-assay variability. We determined RIs, temporal variation over 3 mo, and effect of vaccination and NSAID treatment. Observed:expected (O:E) ratios (x̄ ± SD) for serial dilutions of feces were 89-131% (106 ± 9%) in dogs and 77-122% (100 ± 12%) in cats. For spiking and recovery, the O:E ratios were 90-118% (102 ± 11%) in dogs and 83-235% (129 ± 42%) in cats. Intra- and inter-assay CVs for canine samples were ≤19% and ≤7%, and for feline samples ≤22% and ≤21%. Single-sample RIs were <41 µg/g for dogs and <64 µg/g for cats. With low reciprocal individuality indices, using population-based fCal RIs is appropriate, and moderate fCal changes between measurements (dogs 44.0%; cats: 43.2%) are considered relevant. Cats had significant (but unlikely relevant) fCal increases post-vaccination. Despite individual fCal spikes, no differences were seen during NSAID treatment. The fCAL turbidimetric assay is linear, precise, reproducible, and sufficiently accurate for measuring fCal in dogs and cats. Careful interpretation of fCal concentrations is warranted in both species during the peri-vaccination period and for some patients receiving NSAID treatment.