A reconsideration of the reptilian relationships of Archaeopteryx

The cladistic relationships of Archaeopteryx , the earliest known bird, are re-examined and previous hypotheses of relationships evaluated. The morphology of Archaeopteryx is redescribed. New interpretations of the fossils are presented, particularly in regard to the morphology of the pectoral girdle, manus, pelvic girdle, tarsus and pes. These new interpretations challenge some of the phylogenetic hypotheses recently presented and a new version of thecodontian relationships is suggested.     

A Non-destructive Sampling Technique for Spodoptera mauritia (Boisduval) (Lepidoptera: Noctuidae) and Herpetogramma licarsisalis (Walker) (Lepidoptera: Pyralidae) in Turf

Experiments were conducted using chemical irritants to develop a non-destructive sampling technique for pests of high quality turf and lawn. POW detergent at a concentration of 35 mL in 3.5 L of water applied to an area of 1,600 cm² was the most effective for sampling Spodoptera mauritia and Herpetogramma licarsisalis and resulted in 84% of S. mauritia larvae surfacing within 4 min of application. No larvae surfaced after 4 min. Kendon pyrethrin SF applied at a concentration of 0.46 mL in 3.5 L of water resulted in similar numbers of larvae surfacing relative to 35 mL POW detergent. However, larvae took up to 20 min to surface. Formaldehyde and the pyrethroid, Mavrik® AF did not cause S. mauritia and H. licarsisalis larvae to surface.     

Responses of lotic periphyton to pulses of phosphorus: P‐flux controlled growth rate

1. The response of stream periphyton to the addition of limiting nutrients has been the focus of many studies. However, the influence of pulsed nutrient additions has not previously been examined. This study investigates the biomass accrual and physiological responses of phosphorus‐limited lotic periphyton to hourly phosphate fluxes. 2. Two pulsing experiments were conducted: (i) a variable flux trial that compared variable hourly P‐fluxes, delivered either continuously at different concentrations or at the same concentration but in pulses of differing duration per hour and (ii) a constant flux trial that compared periphyton responses at a set hourly P‐flux but delivered in pulses of varying concentration and duration. 3. Growth response and alkaline phosphatase activity during the variable flux experiment showed that periphyton responds to the hourly integrated flux of phosphorus, regardless of whether the nutrient is supplied in short concentrated pulses or continuously at much lower concentrations. 4. The constant flux experiment examined the pulse period required to attain maximum biomass for a given phosphorus flux. Periphyton response to 5‐min pulses of phosphate per hour approximated the maximum biomass as that attained when the same hourly flux was added continuously. Compared with the control, there was also a substantial increase in biomass with pulses of only 1 min each hour. These results demonstrate that the hourly average phosphate concentration to which periphyton communities are exposed is paramount in determining P‐limited growth dynamics. 5. Species composition was not significantly different among treatments in each experiment; however, the design was to evaluate monotonic response with increasing phosphorus flux and species diversity may not respond monotonically. The data are therefore preliminary but suggest the need to determine if species diversity is generally lower when there are brief pulses of phosphate. Unlike pulse experiments that mimic lentic situations, nutrient additions were not used to completion and species success and composition was more dependent on their ability to acquire limiting nutrients rapidly rather than on their ability to take up nutrients at the lowest concentration.     

Respiration of maleic hydrazide treated and untreated onion bulbs during storage

Respiration rates were determined at a range of temperatures on onion bulbs cv. Rijnsburger sampled from a cool-stored bulk over a period of 8 months. In the first 5 months of storage, respiration rates were low and showed a small increase with temperature. During this period there was little or no difference between untreated bulbs and those treated with maleic hydrazide (MH) prior to harvest. Subsequently there was a rise in respiration rates, which preceded sprouting, but this was not evident in MH-treated bulbs. A relationship between respiration and dormancy was suggested by the correlation between respiration rate in January and sprouting in June for four cultivars.