Modification and testing of a domestic freezer for use in studies of plant growth and survival at low temperatures

Modifications of a domestic freezer are described, which convert it to a versatile controlled environment chamber capable of maintaining temperatures between ambient and - 18 °C and therefore useful in investigations both of plant growth at low positive temperatures and of survival of sub-zero temperatures. The temperature control mechanism can provide a wide range of diurnal temperature regimes and of cooling and warming rates. Measurements in two such chambers showed air temperatures were always uniform to within ° 1 °C of set temperature except in a 6 cm band round the inside walls, where they were lower by 0°6 °C, at most; CO₂ concentration was always close to 300 v.p.m.; relative humidity was usually in the range 80–90% and photon flux densities during the light period were 180 ° 10 μmol m^-2 s^-1. The uniformity of environmental conditions within each chamber was confirmed by measurements of leaf growth and plant survival of tillers of a single genotype of perennial ryegrass growing in pots of compost. These tests also confirmed the lower temperature of the 6 cm band adjacent to the chamber walls. Although temperature settings were identical, air and compost temperatures were 0°3 °C higher in one of the two chambers tested. Although this difference did not result in significant differences in plant survival, significant differences in leaf lamina extension were found between cabinets. Problems encountered in the design and testing of the chambers are discussed.     

Genetic variation in populations of the terrestrial planarian Artioposthia triangulata (Dendy), and evidence for passive dispersal in Northern Ireland

Genetic variation in 12 populations of the terrestrial planarian Artioposthia triangulata from Northern Ireland and one in the Republic of Ireland were assessed using starch-gel electrophoresis. Seven enzymes - adenylate kinase, aspartate aminotransferase, enolase, malate dehydrogenase, phosphoglucose isomerase, phosphomannose isomerase and superoxide dismutase - provided consistent, resolved stains. Coefficients of genetic identity were similar for all comparisons suggesting that the populations did not belong to distinct taxa. There was no relationship between genetic distance and geographic distance for populations, thus confirming the role of passive dispersal in the spread of A. triangulata. Average percentage polymorphic loci and mean heterozygosities were higher in the east of the Province (41.4% and 0.240), than the west (37.5% and 0.185) suggesting that the planarian had spread westwards after an initial colonisation in the east.     

15N natural abundance of plant and soil components of a Banksia woodland ecosystem in relation to nitrate utilization, life form, mycorrhizal status and N2-fixing abilities of component species

Studies of the variation in δ¹⁵N values for plants from a fire-prone Banksia woodland in South West Australia showed that pioneer herbaceous, non-mycorrhizal species which were active in nitrate reduction and storage, had the highest values (1.81%c). A detailed study of one such species Ptilotus polystachus demonstrated a close correspondence between the δ¹⁵N values of soil nitrate, xylem nitrate and leaf total nitrogen, suggesting an exclusive reliance on nitrate ions as nitrogen source. These pioneer species also showed a preponderance of the chloroplastic isoform of glutamine synthetase while woody species generally had higher activity associated with the cytosolic isoform. The group comprising monocotyledonous hemicryptophytes and geophytes contained species with slightly positive δ¹⁵N values and moderately active in nitrate reduction and storage. Nitrogen-fixing species had the lowest δ¹⁵N values (–0.36‰), irrespective of their apparent utilisation of nitrate. However, woody resprouter species which had low levels of nitrate reduction and storage had δ¹⁵N values which fell within the range of values obtained for the miscellaneous assemblage of N₂-fixing species. Consequently, ¹⁵N abundance values failed to distinguish N₂ fixing from non-fixing woody species, and therefore, could not be used in the ecosystem to determine the dependence of putative nitrogen fixing species on N₂ fixation. The study demonstrated complex patterns of nitrogen utilization in the ecosystem in which exploitation of different nitrogen resources related to plant life form and the physiological attributes of nitrogen assimilation by component species.     

A carbon balance model of the sorghum-Striga hermonthica host-parasite association

Abstract. Growth and gas exchange measurements are used to formulate a carbon balance model to describe the sorghum- Striga hermonthica host-Parasite association. S. hermonthica reduces the growth and radically alters the architecture of infected sorghum plants. Grain and stem weight are reduced, whilst leaf and root biomass are maintained. Losses in host productivity result from two processes: export of carbon to the parasite and Parasite-induced reductions in host photosynthesis. The latter occurs before the emergence of the Parasite above ground and accounts for 80% of the Predicted loss in production over the lifecycle of the association. S. hermonthica is dependent on carbon exported from the host, since the plant has low rates of photosynthesis coupled with high rates of respiration. Host-derived carbon accounts for approximately one-third of the total parasite carbon requirement.     

Phytophagous insect communities in the canopies of three Eucalyptus forest types in south-eastern Australia

Intensive sampling of tree canopies for phytophagous insects was carried out in three contrasting eucalypt forest types comprised of species widely distributed in sub-alpine forests in Victoria and New South Wales (Eucalyptus delegatensis, E. dives, and E. pauciflora). The number of phytophagous insects present in the canopies of these forest types was low, with a seasonal average of 20 individuals per kg of foliage (dry weight). Numbers were much lower than expected from past literature reporting‘chronically high’levels of defoliation in eucalypt forests. Microlepidoptera, Geometridae, Chrysomelidae, and Curculionidae were the major leaf-chewing groups recorded. Most sap-feeders were either leafhoppers (Cercopidae and Cicadellidae) or in the superfamily Fulgoroidea. Psyllidae and gall-making species were rare. Leafhoppers made up a very large portion of the phytophagous insect communities in each forest type, particularly in the E. dives forest. Microlepidoptera was the most commonly encountered defoliator group in all three forest types making up 33-44% of the total count. Non-phytophagous arthropods accounted for 44-48% of all individuals encountered. The density of insect defoliators was greater in the lower crown than upper crown. The E. dives canopy supported many more phytophagous insects per unit weight of foliage, as well as more per hectare, than the other two forest types. The greatest number of phytophagous species was also encountered in E. dives canopy. The E. delegatensis canopy supported the lowest number of phytophagous insects per unit weight of foliage as Well as numbers per hectare. Abundance of insect defoliators in the eucalypt forest types in this study was similar to published figures of insect defoliators in northern temperate forests.     

Body Form and Locomotion in Sharks

A revised interpretation of the mode of action of the heterocercaltail in sharks shows that the upturned tail axis tends to producea thrust directed downwards behind the centre of balance ofthe fish and thus gives a moment turning the head upwards. Thisis countered in two ways—by the rotation of the tail alongits longitudinal axis during each lateral beat, and throughthe action of the ventral hypochordal lobe. The shape of thetail and the mode of action of the tail in all sharks so farconsidered reflects a balance between these three factors, inall of them the net effect being the production of a forwardthrust from the tail that passes directly through the centreof balance of the fiish. There is normally therefore no tendencyfor the fish to turn around the centre of balance in a sagittalplane but there is a net sinking effect that is countered bythe planning effect of the pectoral fins and the ventral surfaceof the head. A study of 56 species of sharks shows that the tail is constructedaccording to a remarkably consistent common plan, the extremesbeing the high angled rather symmetrical tail of pelagic sharkssuch as hums, Lamna and Rhincodon and the straight tails ofbenthic sharks such as Ginglymostoma in which a ventral hypochordallobe is absent. When the general body shape of sharks, includingthe position of insertion of the median and paired fins andthe pattern of growth of fin surface areas is considered, theuniformity of the shark body plan and locomolor function isfurther emphasised. Four patterns of body form in sharks are recognised: 1) Thefast swimming pelagic sharks and the whale sharks have a tailwith a high aspect ratio, a conical head, a lateral fluke onthe caudal peduncle. 2) The generalised sharks typified by theCarcharhinidae, have lower heterocercal angles, a flattenedventral surface on the head and lack the caudal fluke. 3) Thedemersal sharks typified by the catsharks (Scyliorhinidae) havea very low, almost straight tail. The ventral hypochordal lobeis absent and the first dorsal fin is posterior in position.4) The squalomorph sharks are distinct in the absence of theanal fin, presence of a marked epicaudal lobe in the tail andoften an elevated insertion of the pectorals. The anal and second dorsal fins are always the smallest finsand the pectorals grow at the fastest rate. In general thereis an inverse relationship between size and rale of growth ofall fins and the ventral surface of the head. In hammerheadsthe growth data confirms that the head has a significant planingaction in swimming. The pectoral, second dorsal and anal finsshow an extreme constancy of position of insertion in all sharksstudied. The locomotor mechanism of sharks is adapted for anefficient cruising swimming but at the same time, the potentialinstability in the sagittal plan allows for the production ofturning moments that are used in attack and feeding.