Interactions between seed priming treatments and nine seed lots of carrot, celery and onion. II. Seedling emergence and plant growth

Samples of three seed lots of each of three cultivars of carrot, celery and onion were primed in polyethylene glycol solution for two weeks at 15 °C. Seedling emergence was recorded in the field for carrot and onion and in the glasshouse for celery. Compared to the untreated control, priming increased the percentage seedling emergence in certain poorly-emerging seed lots of carrot and celery, but had no effect on onion. Mean emergence times were reduced by priming in all seed lots, by 3–5, 5–8 and 3–9 days in carrot, celery and onion respectively. The largest effects occurred in the slowest-emerging seed lots. There were significant interactions between priming and seed lots within cultivars in carrot and celery and between priming and cultivars in celery and onion. Priming generally reduced the spread of emergence times, but the effects were not statistically significant in carrot. Drying back the primed seeds had no effect on percentage emergence in onion, but reduced it (compared to primed seed which had not been dried-back) in certain carrot and celery seed lots. Primed and dried-back seeds emerged later than primed seeds, by up to 1·5, 2·6 and 2·6 days in carrot, celery and onion respectively. The spread of emergence times was generally larger for primed and dried-back seeds than for primed seeds, but the differences were not always statistically significant. Plant fresh weights were recorded 9, 7 and 12 wk after sowing for carrot, celery and onion, respectively. In each species, mean plant weight was inversely related to seedling emergence time; thus plants grown from primed seed were always heavier than the controls, by up to 33%, 182% and 47% in carrot, celery and onion respectively.     

A Theft-Resistant Adjustable Security Box for Digital Cameras

Abstract: Remote camera traps are becoming an increasingly popular, affordable, and valuable tool for wildlife research. However, theft and vandalism of these camera systems can result in substantial financial loss and loss of valuable data. We developed an adjustable steel camera security box to protect our Cuddeback® (Non Typical, Inc., Park Falls, WI) digital scouting cameras. Our cameras were deployed for 160 days and experienced no theft or vandalism during that time. Our armored camera box successfully protected our equipment and data, can be sized to accommodate any brand of camera, and can be used in a variety of field situations.     

Effect of different soil and nitrogen fertilizer conditions on 32P-labelled phosphate uptake by two grass species

In two years of trials, roots of ryegrass took up more ³²P-labelled phosphate than roots of fescue. Application of 672 kg N ha^-1 increased phosphate absorption compared with application of 112 kg N ha^-1. Roots in mineral soil absorbed more phosphate than those in peat soil. In both soils uptake decreased as depth of phosphate injection increased from 5 to 30 cm. An interaction occurred whereby roots in the intermediate depth (10–22-5 cm) in peat absorbed less phosphate than in mineral soil and this was apparently unrelated to the exchange or sorption properties of the soil.     

Assessment of body condition in live birds; measurements of protein and fat reserves in the mute swan, Cygnus olor

Condition in animals is often measured in relation to various demands, such as reproduction, migration and cold weather. Usually, indices of protein and fat reserves have to be measured on dead animals. Measurements on live animals enable variations in the condition of individuals to be monitored over time, and can be related to their life histories.
In birds, the size of the breast muscle is the most commonly used measure of protein reserves. A technique for measuring breast muscle thickness was developed, using ultrasound, and was tested on mute swans. The measurements were accurate and highly repeatable. Breast muscle thickness was positively related to the lean dry weight of the breast muscle, and is likely to be a good indicator of total protein reserves.
A system of fat scoring by colour was developed to assess the size of the subcutaneous fat layer. Although the method relies on subjective judgements, the results were highly correlated with the percentage of fat in the subcutaneous layer, and with other measures of fat reserves.
Measurements were made on live, non-breeding swans to monitor seasonal variations in reserves. The seasonal pattern of fat reserves was similar to the normal cycle of weight changes; high in winter and low in summer. There was no change in relation to the moult. No distinct seasonal variation in muscle thickness was found.
There is an unusual pattern of change in the relative size of reserves during emaciation in swans. Muscle reserves appear to be depleted to a greater extent than fat reserves. This is possibly due to the effects of lead poisoning, causing protein necrosis and preventing muscle regeneration.     

Estimating consumable biomass from body length and order in insects and spiders

1. Current models used to estimate insect prey biomass for diet studies use whole weight. However, a large proportion of an arthropod's body is taken up by an indigestible exoskeleton, leading to erroneous estimation of the food intake of insectivorous animals. 2. Linear mixed effect models were used to obtain equations to predict consumable biomass from body length for a variety of Neotropical insects and spiders. These data were obtained by feeding taxa of various orders to groups of 100 social spiders and comparing pre‐ and post‐consumption weights using size‐matched controls. 3. Significant linear relationships were found relating body size to consumed biomass for all orders, with slopes ranging from 1.276 to 4.011 and R² values from 0.476 to 0.929. For orders other than spiders and Orthoptera, the increase in weight with size exhibited negative allometric scaling, suggesting a decrease in tissue density, or an increase in internal air space, with size. 4. Although there were significant differences across taxonomic orders in the proportion of biomass consumed, within most orders the proportion consumed did not differ significantly with body size. The estimated regression coefficients may be used by other workers to estimate consumable biomass of arthropod prey for studies requiring large sample sizes or non‐lethal sampling of rare or endangered species.     

Modelling and analysing evolution of dispersal in populations at expanding range boundaries

Abstract 1. Species would be expected to shift northwards in response to current climate warming, but many are failing to do so because of fragmentation of breeding habitats. Dispersal is important for colonisation and an individual‐based spatially explicit model was developed to investigate impacts of habitat availability on the evolution of dispersal in expanding populations. Model output was compared with field data from the speckled wood butterfly Pararge aegeria, which currently is expanding its range in Britain. 2. During range expansion, models simulated positive linear relationships between dispersal and distance from the seed location. This pattern was observed regardless of quantity (100% to 10% habitat availability) or distribution (random vs. gradient distribution) of habitat, although higher dispersal evolved at expanding range margins in landscapes with greater quantity of habitat and in gradient landscapes. Increased dispersal was no longer evident in any landscape once populations had reached equilibrium; dispersal values returned to those of seed populations. However, in landscapes with the least quantity of habitat, reduced dispersal (below that of seed populations) was observed at equilibrium. 3. Evolutionary changes in adult flight morphology were examined in six populations of P. aegeria along a transect from the distribution core to an expanding range margin in England (spanning a latitudinal distance of >200 km). Empirical data were in agreement with model output and showed increased dispersal ability (larger and broader thoraxes, smaller abdomens, higher wing aspect ratios) with increasing distance from the distribution core. Increased dispersal ability was evident in populations from areas colonised >30 years previously, although dispersal changes were generally evident only in females. 4. Evolutionary increases in dispersal ability in expanding populations may help species track future climate changes and counteract impacts of habitat fragmentation by promoting colonisation. However, at the highest levels of habitat loss, increased dispersal was less evident during expansion and reduced dispersal was observed at equilibrium indicating that, for many species, continued habitat fragmentation is likely to outweigh any benefits from dispersal.     

THE STRUCTURE OF FISH GILLS IN RELATION TO THEIR RESPIRATORY FUNCTION

1. The general structure of the gills of different fishes is compared and it is concluded that, though essentially the same, there are certain differences by which they can be recognized. Possible ways in which they may have evolved from one another are considered. 2. A detailed account is given of the structure of the secondary lamellae, where gaseous exchange takes place, and it is shown that two epithelial sheets are separated by a vascular axis mainly composed of pillar cells overlain by a basement membrane on each side. Blood pathways through the gills are discussed in relation to their respiratory function. 3. The embryonic development of gills is described and evidence regarding homo-logies of different structures, particularly the pillar cells, is reviewed. 4. The gills of fish having different modes of life show variations in (a) the number of arches, (b) the number and length of the gill filaments, and (c) the size and frequency of the secondary lamellae. Ways in which measurements of gill area may be carried out and some of the complications involved are reviewed and a summary given of measurements made for a wide variety of species. Measurements of the thickness of the water-blood barrier are also discussed; the more active fish generally have thinner water-blood barriers and larger gill areas. 5. The different mechanisms of gill ventilation are summarized and characteristics of gill resistance in elasmobranchs and teleosts are compared. Gas exchange is discussed in relation to available techniques and the current terminology and symbols, and to indicate the value of analogies between gill exchangers and systems studied by engineers. 6. It is outlined how studies of the functioning of gills during coughing, parasitic infection, and in polluted waters add to knowledge of their role in respiration.