Diel patterns of reproduction in rotifer populations from a tropical lake

SUMMARY. The diel patterns of reproduction were studied for three rotifer populations from Lake Valencia, Venezuela. Significant departures from uniformity were recorded for egg eclosion and egg deposition rates in Keratella americana and Brachianus calyciflorus , but only from egg deposition rates in B. havanaensis . The existence of non-random reproduction has practical ramifications for studies of population dynamics and secondary production.     

The Uptake of Growth Substances: VI. A COMPARATIVE STUDY OF THE FACTORS DETERMINING THE PATTERNS OF UPTAKE OF PHENOXYACETIC ACID AND 2,4,5-TRICHOLOROPHEN-OXYACETIC ACID, WEAK AND STRONG AUXINS, BY GOSSYPIUM TISSUES2

Using segments of etiolated hypocotyls of Gossypium, a comparativestudy has been made of the processes which determine the patternsof uptake of a very weak auxin, phenoxyacetic acid (POA), anda very powerful one, 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). When segments are placed in solutions of POA-1-¹⁴C, a continuousincrease in the radioactivity of the tissues is accompaniedby the formation of radioactive metabolities which can be separatedfrom POA by techniques of paper chromatography. At the sametime there is a progressive increase in the amount of radio-activitywhich cannot be removed by transferring the tissues to buffer.Uptake is inhibited by low temperature, anaerobiosis, 2,4-dinitrophenol,and iodoacetate. It is concluded that the accumulation of POAinvolves its metabolic conversion to products which do not readilydiffuse out into the external medium. With 2,4,5-T-1-¹⁴C the radioactivity of the segments at firstincreases rapidly but this is followed after two hours by aphase of rapid decrease. No radioactive metoabolites can bedetected by paper chromatography and all of the ¹⁴C taken upcan be rapidly removed by transfer to buffer. The magnitudeof the decrease in radioctivity during the second phase of uptakeis balanced by a release to the medium of a matched amount ofradioactive 2,4,5-T. Uptake of 2,4,5-T is somewhat less sensitiveto temperature and anaerobiosis than uptake of POA and is bycontrast only slightly inhibited by 2,4-dinitrophenol and iodoacetate. Pretreatment of segments in buffer markedly alters the patternof uptake of 2,4,5-T but not that of POA. It reduces both theamount of 2,4,5-T initially taken up and the amount subsequentlyreleased to the medium. In addition, both net loss of radioactivityduring the course of uptake of 2,4,5-T and the reduction inthe extent of uptake following pretreatment are both arrestedby adding streptomycin, but not by the addition of pencillinor chloramphenicol. It is concluded that the uptake of 2,4,5-T involves reversibleaccumulation by a process whose efficiency decreases with time:the most likely systems are a metabolically linked mechanismfor the active transport across a membrane or reversible adsorptionon specific binding sites.     

Epidemiological aspects of blackspot disease of roses caused by Diplocarpon rosae Wolf

Conidia of Diplocarpon rosae Wolf are dispersed mainly by water-splash. Within a crop the spread of the disease can be traced from primary foci. Infection follows the ‘compound interest’ pattern, sensu van der Plank (1963), which is typical of most leafspot diseases. Accumulation of inoculum, together with certain conditions of rainfall and temperature in August, led to a characteristic, rapid development of the disease in September 1963 and 1964, after an incubation period of 2–4 weeks.     

THE BREEDING BEHAVIOUR AND BIOLOGY OF THE SHORT-BILLED FORM OF THE WHITE-TAILED BLACK COCKATOO CALYPTORHYNCHUS FUNEREUS

The breeding biology of the short-billed form of the White-tailed Black Cockatoo was studied at two main study areas, Coomallo Creek, an area with large tracts of uncleared lands, and Manmanning, an area of extensive clearing with little native vegetation remaining. The study was based on individually marked birds. The actions of females selecting and preparing their nest hollow ensured that other females were kept away from the area of that nest, resulting in nests being spaced out through the study areas. Eggs were laid between July and November with birds at Manmanning starting about four weeks after those at Coomallo Creek. Clutch size was a maximum of two and incubation took 28–29 days. Hatching success was higher for two-egg clutches than for one-egg clutches. There were no differences between fledging success for one-egg or two-egg clutches at either area, but fledging success at Manmanning was lower than that of Coomallo Creek. Rates of growth for weight and length of folded left wing were calculated for nestlings from both areas. These rates of growth were compared within areas between years and between areas within years. There were differences in rates of growth of nestlings from Coomallo Creek compared with those from Manmanning and these differences were related to shortages of food at Manmanning. The annual survival of tagged adults was calculated at 61–69% and that of juveniles over the first 12 months after fledging at 15%. The survival figures for adults seemed too low and it is suggested that the wearing of wing-tags may place the individual at a selective disadvantage compared with an untagged individual.     

The timing of larval wandering and puparium formation in the flesh-fly Sarcophaga argyrostoma

ABSTRACT. In mixed-age cultures of the flesh-fly, Sarcophaga argyrostoma (Robineau-Desvoidy), the initiation of larval wandering (exodus behaviour) occurs as a gated circadian rhythm. In light-dark (LD) cycles, most of this activity occurs in the dark, except in very short nights, or in certain phase relationships between the rhythm and light cycle. When transferred from series of LD cycles into continuous darkness (DD), cultures show a weakly persistent free-running rhythm with a period of about 21 h. However, after transfer of first instar larvae from continuous light (LL) to DD, no such rhythm is observed. In contrast to larval exodus, formation of the puparia occurs at any stage of the LD cycle. The physiological mechanisms underlying this gated exodus behaviour, and its possible selective advantages, are discussed.