A NEW TECHNIQUE FOR ASSESSING THE CONTACT TOXICITY OF MOLLUSCICIDES TO SLUGS

A technique is described to accurately assess the dermal contactdose-mortality response of molluscicides. The technique involvescarbon dioxide anaesthesia of laboratory reared Deroceras reticulatum(Müller) followed by application of test substances insolution to the dorsal surface. The LD₅₀ of the substances testedwere as follows: Sodium pentachlorophenate, 55.9 ng.mg^–1,Copper sulphate, 124.1 ng.mg^–1, Methiocarb, 314.6 ng.mg^–1and Potassium permanganate, 418.9 ng.mg^–1 body weight. (Received 18 August 1988; accepted 17 December 1988)     

Development of Vacuolar Volume in the Root Tips of Pea

Cell and vacuole areas were measured by light microscopy inlongitudinal and transverse sections cut at 0.4-mm intervalsalong the apical 7.2 mm of the primary root of pea. The vacuolararea (or volume) fraction — that is, vacuole area (orvolume) divided by cell area (or volume) — increased fromabout 15 % in cells 0.4 mm from the distal boundary of the apicalmeristem (the cap /root junction), to about 85% in cells situated6.8–7.2 mm from that boundary. At each distance, vacuoledevelopment tended to be greater in the cortex than in the stele.Vacuoles occupied about 22% of the tissue volume in the first1 mm length of root (measured from the cap/root junction), about31 % of the tissue volume in the first 2 mm, and about 45% whensummed over the apical 5-mm length of root. Phosphorus supplyor deprivation produced only minor and non-significant changesin vacuole development. The results have implications affectingprevious estimates of cytoplasmic and vacuolar phosphate concentrationsin pea root tips. Pisum sativum L., pea, root, vacuole, volume     

Carbon isotopes as indicators of elephant diets and African environments

Stable carbon isotope ratios have been successfully used to assess modern animal diets and to reconstruct prehistoric diets of animals and humans (Vogel & van der Merwe, 1977; van der Merwe & Vogel, 1978; Burleigh & Brothwell, 1978; Vogel, 1978a; DeNiro & Epstein, 1978; Tieszen et al., 1979; Tieszen & Imbamba, 1980; Chisholm, Nelson & Schwarcz, 1982; Tauber, 1981). We have used ¹³C/¹²C ratio measurements of bone collagen to study the diets of African elephants in twelve wildlife refuges. These represent most of the habitats in which elephants live, including such diverse plant communities as primary rain forest, savanna woodland and desert. The δ¹³C values were found to have a simple linear relationship with tree density in most cases. When translated into relative amounts of dietary browse (C₃ plants) and graze (C₄ plants), the grass content is seen to be systematically under-represented, presumably due to inefficient metabolism. This does not affect the relationship between elephant diet and tree density, which has implications for the study of elephant-woodland interactions, and for reconstructions of past African environments.     

Are Roots a Source of Abscisic Acid for the Shoots of Flooded Pea Plants?

Flooding the soil for 2–5 d decreased stomatal conductancesof pea plants (Pisum sativum L., cv. Sprite) with six or sevenleaves. This coincided with slower transpiration, increasedleaf water potentials and increased concentrations of abscisicacid (ABA) in the leaves. No increase in ABA was found in theterminal 20 mm of roots of flooded plants over the same timeperiod. Small stomatal conductances associated with increases in foliarABA were also found in plants grown in nutrient solution whenaeration was halted, causing the equilibrium partial pressuresof dissolved oxygen to fall below 05 It Pa. No increase in ABAconcentration in young secondary roots of the non-aerated plantswas detected after 24, 48 or 72 h, even when the shoot, thepresumed site of deposition for any ABA from the roots, wasremoved 5–6 h before analysis. Similarly, ABA concentrations in roots were not increased whenthe nutrient solution was de-oxygenated by continuous purgingwith nitrogen gas. The abscisic acid concentration in leaf epidermis,the tissue most likely to be the recipient of any ABA movingin the transpiration stream from oxygen-deficient roots, waslower than in the remaining parts of the leaf when examinedin the mutant Argenteum which possesses easily removable epidermallayers. It is concluded that the leaves of plants subjectedto flooding of the soil or oxygen shortage in the root environmentare not enriched substantially with ABA from the roots. A moreprobable source of this growth regulator is the leaf itself. Key words: Pisum sativum, flooding, roots, hormones, aeration stress, abscisic acid, Argenteum mutant     

拟澳洲赤眼蜂生殖系统的研究

拟澳洲赤眼蜂(Trichogramma confusum)的体长约0.6mm,腹部长度约0.3mm.雌蜂生殖系统(包括卵巢、生殖腔、受精囊及三种附腺)位于腹部后端,约占腹腔的2/3.成熟的卵巢由两条多滋式的卵巢管组成.两条成熟卵巢的端段细长,扭卷成一条疏松索,基部膨大,内脏贮存大量卵粒.成对的侧输卵管较短,分别开口于生殖腔后方的两侧,中输卵管缺如.受精囊呈梨形,开口于生殖腔后方.雌性生殖系统三种附腺中,第一种附腺是成对的,呈锤状,分别连接于生殖腔前方两侧;第二种附腺,腺体呈球状,其前端以短曲的小管通进膨大的贮腺囊,贮腺囊端部成柄状的弯曲小管,连接于产卵管的基部开口处.第三种附腺的腺体呈棒状,前端为细长的小管,开口于第二种附腺贮腺囊的前端.雄性生殖系统由成对的睪丸,输精管、贮精囊、附腺及单一的射精管组成.蛹的早期到后期至成虫期睾丸的形态结构,各有不同变化.     

蓖麻蚕前胸腺细胞超微结构的变化与蜕皮激素分泌活动的关系

本研究叙述蓖麻蚕Philosamia cythia ricini四龄及五龄幼虫前胸腺蜕皮激素分泌活动各不同时期所显示的腺细胞超微结构变化.从幼虫蜕皮后至进入眠期之间的腺细胞结构可分为三个时期,(1)不活动期:细胞核呈圆形,核内密布染色质及核仁,细胞质内有结构完整的线粒体、粗面及滑面内质网、核糖体和高尔基氏体;细胞外围的细胞间区内有许多小囊泡及多泡囊.(2)活动期:细胞结构变化为细胞核膜出现内陷、外突,形成波浪形的核周膜;线粒体变形,出现内嵴稀疏的空心线粒体.(3)激素释放期:细胞核变形,形成若干长短不一向外伸出的指状突,有些伸达细胞边缘;其余细胞器退化,其后仅余残缺的高尔基氏体,稀疏的核糖体,线粒体的内崤逐渐消失,成为空腔扩大的及空腔内藏“膜轮”的线粒体,和一些溶解体及大形“膜轮”.     

Cold shock and heat shock: a comparison of the protection generated by brief pretreatment at less severe temperatures

Abstract Brief exposure to low (0^oC) or high (40^oC) temperature elicits a protective response that prevents injury when the flesh fly, Sarcophaga crassipalpis Macquart, is subjected to more severe cold (-10^oC) or heat (45^oC). Both the low and high temperature responses were found in all developmental stages of the fly, but were most pronounced in the pupal and pharate adult stages. The protective responses generated by brief exposure to 0 or 40^oC appear similar in that both result in a rapid acquisition of cold or heat tolerance and a loss of protection after the flies are returned to 25^oC. The protection generated by chilling is obvious within 10 min of exposure to 0^oC while a 30 min exposure to 40^oC is required to induce the high temperature protection. High temperature protects against cold shock injury within a narrow range (around 36^oC) but we have no evidence that low temperature can protect against heat injury. We previously demonstrated that the rapid increase in cold tolerance correlates with concomitant increases in glycerol concentration, but in this study we found no significant elevation in glycerol in heat-shocked flies. Thus the physiological and biochemical bases for the rapid responses to cold and heat appear to be different.     

Seed survival and seasonal pattern of seedling emergence in some Leguminosae

Seeds of 11 species of Leguminosae were collected, usually in each of 3 years, and mixed with the top 7·5 cm of sterilised soil confined in cylinders sunk in the ground outdoors and cultivated three times yearly. Emergence was recorded for at least 3 yr. Some seedlings of all species emerged soon after sowing but their numbers varied both within and between species, a probable reflection of the percentage of ‘hard’ seeds in the samples. Appreciable numbers of seedlings appeared in the following 3 yr but few seeds remained viable and dormant after 5 yr. The annual weed Vicia hirsuta was an exception, with an average of 11% of the seeds sown still viable at this time. Most seedlings of Lotus corniculatus, Medicago lupulina, Melilotus altissima, Trifolium repens and Vicia cracca emerged in spring, V. cracca rather later than the others. In contrast, maximum emergence of Trifolium arvense, T. campestre and T. dubium took place from June to September. Limited data indicated a similar pattern for T. striatum and Lathyrus pratensis. Seedlings of Vicia hirsuta emerged from October to May but scarcely at all in summer. Although variation in the percentage of hard seeds influenced the extent of immediate germination and seed persistence, the seasonal patterns in seedling emergence of most species were found to be very consistent.     

Behavioral Aspects of Rodent Population Biology

Five approaches to the study of behavior as a factor in thepopulation biology of rodents are outlined. These approachesare: (1) genetics, (2) physiology, (3) chronobiology,(4) behavioralecology and sociobiology, and (5) the use of intra- and inter-specificcomparisons. For each approach selected examples from the recentliterature, from this symposium and from my own work are usedto illustrate the new directions that are emerging for analyzingbehavior as a factor affecting natality, mortality and emigration/immigrationin rodents. Areas where additional investigations are neededare noted including some questions to be tested by future experiments.A variety of new techniques that have been developed or areinnovative applications of existing techniques are incorporatedinto the examples. Most of the material presented concerns fourgenera of rodents, Microtus, Mus, Peromyscus, and Rattus. Thefollowing major conclusions emerge from an overview of theseapproaches: Most recent research on behavior as a factor inrodent population biology has been concerned primarily withnatality. Few investigators have dealt with mortality and onlya limited number have explored emigration/immigration. Fieldand laboratory studies on behavioral aspects of rodent populationbiology have become more integrated than they were several decadesago. Both proximate and ultimate questions about behavior andpopulation dynamics are now being tested by both laboratoryand field methods. In contrast to some earlier approaches thatoften viewed population control as involving a single factor,most emerging conceptual frameworks have, as a major assumption,that population regulation is a multi-factorial process includingmany behavioral components.     

Some Microscopical Observations of Functioning Sieve Tubes of Heracleum using Nomarski Optics

The study of isolated phloem in Heracleum has been extendedto intact functioning sieve tubes. Techniques of phloem dissectioncombined with Nomarski interference optics have been developedto permit useful visual observations, photomicrography, andciné photographs of sieve tubes which are apparentlynormal. In these preparations, plastids and organelles calledby us ‘marker particles’ are visible in rapid bouncingmotion, and the state of dispersal of these particles is relatedto the amount of damage done to the preparations. The movement of the marker particles and their subsequent fixationshows that they are apparently attached to or restrained byan invisible network in situ. The network is very sensitiveto disturbance and readily collapses around the sieve platesto form slime plugs upon damage to the sieve element. The markerparticles do not move through the cell nor across sieve platesin mature Heracleum. In young cells cyclosis is observable alongthe periphery and this suggests that a vacuole may then be present.In undamaged mature cells there was evidence neither of a vacuolenor of trans-cellular tubules of any size optically detectable. The motion of the particles was greater than Brownian movementand appeared to be under some physiological control. Their movementprobably indicated the presence of an operating transport phenomenon,either because solution was moving past them in the sieve tubeor because they were themselves attached to a contractile networkactively in pulsatory motion. Nearby companion and parenchymacells showed normal cytoplasmic streaming. Proposed mechanisms of translocation involving cytoplasmic streamingdo not seem to be applicable to the phloem of Heracleum. Themovement of the marker particles seemed to agree best with amechanism of ‘activated’ mass flow.