Analysis of Histones from the Endosymbiont Nucleus of a Binucleate Dinoflagellate1,2

Histones were prepared from chromatin of the eukaryotic (endosymbiont) nucleus of Peridinium balticum (Levander) Lemmermann. The amino acid composition of whole histone was rich in lysine and similar to that of Olisthodiscus luteus and Euglena gracilis. Electropheretic analysis of these proteins in acidic-urea disc gels revealed four major bands: one with a mobility slightly lower than that of calf thymus HI; and three others which comigrated with calf H2B, H2A, and H4, respectively. The low mobility band was soluble in 5% perchloric acid and was sensitive to FeCl₃ destaining. Electrophoresis in slab gels containing 0.1% SDS revealed five major components, with approximate molecular weights of 23,000, 20,000, 15,000, 13,000, and 11,000, respectively. The 15,000 and 11,000 dalton histones had mobilities identical to those of calf H3 and H4, respectively. The two highest molecular weight components were soluble in 5% perchloric acid. No bands were found to comigrate with calf H2A or H2B but a band was present that migrated to a position intermediate between calf H2A and H4 (13,000 dalton histone). Two-dimensional gels consisting of acidic-urea gels in the first dimension and SDS gels in the second dimension revealed that the 20,000 dalton component and the 13,000 dalton component are not resolved in the acidic-urea gel. As a working hypothesis, it is suggested that two of the five bands seen in SDS gels represent an H1-like doublet, and two are analagous to H3 and H4, respectively. The remaining histone may replace H2A and H2B.     

The Onset of Germination Ability in Developing Wheat

The ability of primary wheat grains (cv. Sappo) to germinatewas determined at different times from anthesis. Fresh, prematurelyharvested grains germinated best at low temperatures (<10°C). The temperature range over which appreciable germinationtook place broadened and the maximum percentage germinationachieved increased with lengthening time between anthesis andharvest. Chilling and exogenous applications of GA₃ each affectedthe rate of germination and the maximum percentage germinationof grains in their own ways. The results are discussed in relationto the identification of ‘dormancy’ in wheat grains.     

Reversed animal-plant interactions: the evolution of insectivorous and ant-fed plants

Insectivorous plants and ant-fed plants represent the two ways in which plants have evolved to utilize directly nutrients derived from animals. This paper addresses the limitations under which selection acts to favour the evolution of one or the other of these nutrient-gathering tactics. Both tactics have evolved independently at least six times under similar ecological conditions, indicating that the evolutionary solutions to ecological problems are limited by the historical make-up of communities and are, to some extent, predictable. Both insectivorous and ant-fed plants evolve in environments with very low levels of availability of nutrients in the substrate; the primary use of the animal-food is probably nitrogen; the vast majority of species are perennial, and most species are tropical or subtropical, although some insectivorous genera are primarily temperate.
Although these two nutrient-gathering tactics evolve in response to similar ecological problems, whether plants evolve an insectivorous habit or the ant-fed habit depends on the growth forms of the plants and the habitats in which they grow. Most insectivorous plants evolve as herbs in wet, sterile soils or in sterile aquatic habitats; ant-fed plants evolve as epiphytes on trees in open-canopied habitats. These kinds of animal-plant interactions are relatively rare because the environments in which they are favoured by selection are uncommon.     

The genetics of colour-patterns in the grasshopper Chorthippus brunneus

Several alleles were found to determine the colour of the dorsal pronotum in Chorthippus brunneus; there was evidence for at least two loci (C and V). Brown (C^B)was the universal recessive and green (C^C) was dominant to all other colours. The white allele (C^W)was codominant with green(C^G)and purple (C^P). Wing-patterns were determined by a separate, probably linked locus (W). A dominant plain wing-pattern (W^P) was associated with colours other than brown. Striped(W^S)and mottled(W^mo) were codominant and a plain recessive allele (W^P) was also found. All three alleles were associated with the brown phenotype. A purple-sided allele (S^Pu) was sometimes obmd with C^pu.. S^Pu was dominant to brown sides (S^B), A series of markings on the dorsal and lateral pronotum (linea intermedia, fascia postocularis, linea media, carina media and zona lateralis) were investigated and found to be controlled at separate loci which may be linked to W. These characters were expressed by dominant alleles. Epistatic effects by modifier loci were shown to have an important effect on the determination of wing phenotype. Allele Wo⁺, for example, suppressed the stripe-wing pattern, linea media, carina media and zona lateralis. It was concluded that colour patterns appear to be under genetic control and that dominant alleles were rare in the wild. Changes in shades of colours were shown to be age-dependent and minor.     

Host plant specificity, oviposition behaviour and egg parasitism in some leafhoppers of the genus Eupteryx (Hemiptera: Cicadellidae)

Abstract.

• 1 Three species of Eupteryx, E.aurata, E.cyclops and E.urticae are regularly found on stinging nettles in South Wales.
• 2 E.aurata host alternates between nettles in spring and autumn, and Heraclewn, Eupatorium and Mentha species in summer. E.cyclops and E.urticae attack only nettles.
• 3 All species are host specific during oviposition and show preferences to lay eggs in discrete plant regions.
• 4 A Mymarid egg parasite of the genus Anagrus was reared more commonly from eggs laid in nettles than from eggs laid in alternative hosts.

     

Colour polymorphism in nymphs of the genus Eupteryx (Hemiptera: Cicadellidae)

Abstract.

• 1 The colour morphs of fourth and fifth instar nymphs of E. cyclops and E. urticae are described and their geographic distributions in southeast Wales are examined.
• 2 Morph frequencies are influenced by Chalarus parasites (Diptera: Pipunculidae).

     

Adaptive dispersal and appetitive flight in the green lacewing, Chrysopa cornea

Abstract.

• 1 The flight behaviour of Chrysopa cornea Steph. (Neuroptera: Chrysopidae) with regard to dispersal activity has been investigated in field experiments. There are three main types of flight activities.
• 2 Shortly after emergence (in the first two nights) the adults perform adaptive dispersal flights which are straight downwind flights mostly at elevations higher than 3 m above ground. The lacewings do not react to the presence of honey dew in the crop.
• 3 After 2—3 days the scent of honeydew becomes a strong landing stimulus. The flight is now an appetitive downwind flight which usually is lower than 3 m above ground.
• 4 Once landed, the lacewings' subsequent flights are toward the source of the kairomone which signals honeydew. This can be termed appetitive upwind flight. It is a low stepwise flight within the ‘boundary layer’ which rarely exceeds 1 m above crop level.
• 5 Dispersal takes place in a continuous ‘rolling’ downwind movement of the whole lacewing population. The immigration rate into a field is thus not a function of the quality of that field but rather of upwind fields. Emigration, however, strongly depends on the presence of honeydew (retaining of ovipositing immigrants) and the density of aphids or other food for the larvae (production of new adults).

     

The Conservation of Sea Turtles: Practices and Problems

The various techniques in common use for conservation and restorationof depleted sea turtle populations are reviewed, namely: banninginternational commerce; operating artificial hatcheries, bothin the natural beach environment and in styrofoam and othertypes of incubators; "head-starting" of hatchlings in captivity;protection of nesting females by means of beach patrols; andtranslocation of eggs or hatchlings to distant areas from whichturtles have been extirpated or to which it is desired to introducenew colonies. The difficulties of monitoring the results ofall of these techniques are discussed, and potential dangersor disadvantages of each approach are reviewed. It is concludedthat, until unequivocal data become available, turtle conservationistsshould continue to pursue common sense or logically sound restorationprograms, but should constantly re-evaluate their actions inthe light of the latest available knowledge and modify or desistfrom current approaches as necessary.     

THE INUNDATION ZONE OF THE NIGER AS AN ENVIRONMENT FOR PALAEARCTIC MIGRANTS

Of at least 350 species so far recorded within the boundaries of the Niger Inundation Zone, no less than 108 (31%) are wholly or partially of Palaearctic origin. Five main habitats are recognized in the region: wetland, hygrophilous grassland, transition zone, non-flooded areas and aerial. The habitats, the Palaearctic migrants and their possible Ethiopian competitors are described and discussed. The annual Niger flood regime enables Palaearctic waterbirds to find suitable habitats somewhere within the region during all seasons, but most widely during the autumn and winter months of the flood recession. Non-aquatic species inhabiting flood plain grassland are scarce during the Palaearctic autumn, when the growth of vegetation reaches its maximum, becoming commoner and more diverse during the winter months. Wetland warblers of the genera Acrocephalus and Locustella have not been recorded on autumn passage. It is suggested that in some years at least, these and other trans-Saharan migrants from the West Palaearctic overfly the Sahelian latitudes of mid-West Africa. Species inhabiting the transition zone (which increases in area during years of below average rains and floods) are most in evidence at the end of the winter period and during the spring hot dry season, prior to northward trans-Saharan migration. Habitats and species encountered in the non-flooded areas are similar to those recorded in the Sahel zone elsewhere in West Africa. Aerial habitat is utilized by Common Swifts arriving en masse in early August, at the maximum development of the south-westerly monsoon airstream. Several aquatic species and the first few trans-Saharan migrants also occur during the summer rainy season. Some species (e. g. Whiskered Tern, Lesser Kestrel, Turtle Dove, Short-toed Lark and Sand Martin) are most numerous during the late winter and spring hot seasons, when conditions provided by the Inundation Zone may be more suitable for pre-migration feeding than in other parts of the Sahel zone. As yet there is virtually no information available to determine any effects that drought seasons or flood variation may have on the migrant populations.     

SEASONALITY, DENSITY AND DIVERSITY OF BIRDS OF A PAPYRUS SWAMP IN WESTERN KENYA

The commoner birds of a western Kenya papyrus swamp are listed. This avifauna is probably as rich as in any papyrus habitat, dominated by warblers (Sylviinae) in which interspecific competition between species of similar size is reduced by preference for swamp-edge rather than interior habitats, preference for papyrus over standing water, or vertical habitat partitioning. Comparisons with other west Kenyan habitats show that it is a specialized avifauna with low species diversity indices and few species. Density figures for common species are higher than in forest undergrowth or thicket. There is little ecological diversity of habitat in uniform stands of papyrus which form ecological islands, and this high density may be interpreted as a density compensation on a speciespoor ‘island’ compared to a species-rich ‘mainland’. Rainfall is the most seasonally variable climatic factor in west Kenyan papyrus habitats. In this climatic area of Uganda and western Kenya there is a modal egg-laying period from March to June coinciding with the long rains, and a postnuptial primary moult period from June to November, which extends into the short rains of October and November. On average, a complete moult of the remiges takes six or seven months. In general the moult of immatures begins and ends about two months later than adult moult, but birds reared during the short rains had primary moult only half complete at the beginning of the following long rains. There is very little evidence of interrupted moult. The 1969 rainfall pattern was exceptional, with the heaviest rainfall in February, and there is evidence of a correspondingly early onset of postnuptial moult in that year. Females moulted significantly earlier than males in 1969 whereas males moulted marginally earlier in other years, suggesting that female moult schedules are more flexible.