Ergovaline does not alter the severity of ryegrass staggers induced by lolitrem B

AIM: To investigate a possible interaction between lolitrem B and ergovaline by comparing the incidence and severity of ryegrass staggers in sheep grazing ryegrass (Lolium perenne) containing lolitrem B or ryegrass containing both lolitrem B and ergovaline.

METHODS: Ninety lambs, aged approximately 6 months, were grazed on plots of perennial ryegrass infected with either AR98 endophyte (containing lolitrem B), standard endophyte (containing lolitrem B and ergovaline) or no endophyte, for up to 42 days from 2 February 2010. Ten lambs were grazed on three replicate plots per cultivar. Herbage samples were collected for alkaloid analysis and lambs were scored for ryegrass staggers (scores from 0–5) weekly during the study. Any animal which was scored ≥4 was removed from the study.

RESULTS: Concentrations of lolitrem B did not differ between AR98 and standard endophyte-infected pastures during the study period (p=0.26), and ergovaline was present only in standard endophyte pastures. Ryegrass staggers was observed in sheep grazing both the AR98 and standard endophyte plots, with median scores increasing in the third week of the study. Prior to the end of the 42-day grazing period, 22 and 17 animals were removed from the standard endophyte and AR98 plots, respectively, because their staggers scores were ≥4. The cumulative probability of lambs having scores ≥4 did not differ between animals grazing the two pasture types (p=0.41).

CONCLUSIONS AND CLINICAL RELEVANCE: There was no evidence for ergovaline increasing the severity of ryegrass staggers induced by lolitrem B. In situations where the severity of ryegrass staggers appears to be greater than that predicted on the basis of concentrations of lolitrem B, the presence of other tremorgenic alkaloids should be investigated.     

Effect of Stocking Density on Growth,Survival, and Condition of the Mexican Cichlid Cichlasoma beani

The Mexican cichlid Cichlasoma beani is currently exploited regionally as food and can be commercialized in the aquarium trade. Natural populations of C. beani may already be negatively affected by anthropogenic alteration of the areas in which it is distributed. The aim of the present study was to examine the effect on growth, survival, and condition of C. beani cultured in three stocking densities: three (D3), six (D6), and nine (D9) fish per each 40 L tank. At the end of a 6‐wk trial the fish cultured in D3 were longer, heavier, and grew faster than the rest of the treatments but their survival was the lowest compared to D6 and D9. The mortalities were caused by a strong aggressive behavior in D3.     

Use of stem diameter variations to detect plant water stress in tomato

The sensitivity of stem diameter variations (SDV) measured with linear variable transducer (LVDT) sensors as indicators of plant water status in tomato was evaluated. Two tomato crops were grown sequentially in a sandy loam soil in an unheated plastic greenhouse. These were an autumn–winter tomato crop (autumn crop) and a spring–summer tomato crop (spring crop). One drying cycle of 61 days was imposed to the autumn crop in winter at 92 days after transplanting (DAT). Two drying cycles, each of 29 days, were applied to the spring crop, to young (58 DAT) and mature plants (121 DAT). For each drying cycle, four replicate plots did not receive irrigation, and four were well watered. During each drying cycle, LVDT sensors continuously measured SDV, and daily measurements were made of leaf (Ψ _leaf) and stem water potential (Ψ _stem). SDV data was interpreted using the SDV-derived indices, maximum daily shrinkage (MDS) and stem growth rate (SGR). The response of SDV-derived indices to water deficit differed with (1) climatic conditions during stress imposition and (2) crop age. In the winter drying cycle of the autumn crop, the responses of the SDV-derived indices to soil drying were relatively small and slower than Ψ _leaf and Ψ _stem. Under warmer conditions, the SDV-derived indices were much more responsive to soil drying. In rapidly growing young plants, where SDV was characterized by high SGR and small MDS, SGR was the most sensitive SDV-derived index. In more mature plants with little stem growth, MDS was the most sensitive SDV-derived index. In mature plants grown in warm to hot conditions, MDS (1) responded at a similar time or earlier than Ψ _leaf and Ψ _stem and (2) had larger “signal” values (ratio of values from unwatered to control plants) than Ψ _leaf and Ψ _stem. However, there was appreciably more “noise” (coefficient of variation, CV) associated with the SDV-derived indices, giving lower “sensitivity” values, determined from “signal” to “noise” ratios, than for Ψ _leaf and Ψ _stem. Regression analysis between MDS of well-watered plants and climatic variables gave best results for a linear relationship between MDS and daily maximum vapor pressure deficit. There were strong linear relationships between MDS and Ψ _leaf for each drying cycle. The slopes of these relationships differed with crop age indicating that there was no constant relationship between MDS and Ψ _leaf for a whole season. Overall these results demonstrated that MDS and SGR can be sensitive indicators of the water status of tomato crops under conditions of moderate to high evaporative demand. However, the variability associated with the SDV-derived indices and the changing MDS–Ψ _leaf relationship with crop age represent major issues regarding the development of irrigation scheduling protocols for tomato.     

Thermal preference and tolerance of green abalone Haliotis fulgens (Philippi, 1845) and pink abalone Haliotis corrugata (Gray, 1828)

The thermoregulatory behaviour of green abalone Haliotis fulgens and pink abalone H. corrugata was investigated. Haliotis fulgens juveniles ranging in wet weight from 3.0 to 3.3 g and from 28.7 to 30.5 mm shell length and of H. corrugata 2.0 g and 25.7 mm in shell length were exposed to 19°C for 30 days in a flow‐through water system. Temperature preference was determined in a horizontal thermal gradient and was found to be 25.4°C for green abalone and 25.0°C for pink abalone. Displacement velocity was 4.3 cm h⁻¹ for H. fulgens and 12.8 cm h⁻¹ for H. corrugata. The optimum temperature for growth calculated for both abalone species was 24.6 and 24.5°C respectively. The critical thermal maxima (CTMax) of H. fulgens and H. corrugata were determined as a measure of thermal tolerance. Abalones were subjected to increasing water temperatures at a rate of 1°C on 30 min until they detached from the substrate. The CTMax at 50% were 33.6 and 32.0°C for green and pink abalone respectively. The results are discussed in relation to site selection and commercial rearing.