黑翅土白蚁踪迹信息素组分数量的柱层析分离和活性测定分析

本文分析了在活性限浓度进行生物活性测定时,黑翅土白蚁Odontotermes formosanu Shiraki对踪迹信息素的行为反应特点以及使用不同踪迹线载体对踪迹信息素活性的影响。并设计标准生物活性测试方法,测定了采用柱层析方法分离的黑翅土白蚁踪迹信息素各分离馏分的活性,发现黑翅土白蚁踪迹信息素用22%乙酸乙酯/正己烷洗脱液等度洗脱分离后的各馏分中包含两个强活性区段,推测黑翅土白蚁踪迹信息素至少包含2个有轻微极性差异的组分。     

七种抑制剂对两种白蚁谷胱甘肽S-转移酶活性抑制作用的比较

利用分光光度酶动力学方法,确定了白蚁谷胱甘肽S-转移酶（GSTs）的最适反应条件,并进一步研究了7种抑制剂对黑翅土白蚁Odontotermes formosanus (Shiraki)和黑胸散白蚁Reticulitermes chinensis Snyder GSTs活性的体外影响。结果表明：白蚁GSTs测定的最适反应条件为pH 6.5,温度25℃,最适反应时间2 min。黑翅土白蚁GSTs的米氏常数(K_mCDNB和K_mGSH)分别为0.11±0.02 mmol/L和0.81±0.16 mmol/L,最大反应速度(V_maxCDNB和V_maxGSH)分别为425.92±19.67 nmol/(min·mg)和534.86±39.05 nmol/(min·mg)。黑胸散白蚁GSTs的米氏常数(K_mCDNB和K_mGSH)分别为0.12±0.03 mmol/L和1.03±0.31 mmol/L,最大反应速度(V_maxCDNB和V_maxGSH)分别为544.39±37.19 nmol/(min·mg)和715.45±83.68 nmol/(min·mg)。浓度为2×10^-5 mol/L时,槲皮素和辛硫磷对黑胸散白蚁GSTs活性的抑制作用要强于黑翅土白蚁,对黑胸散白蚁GSTs活性的抑制作用分别为62.28％和44.89％,对黑翅土白蚁GSTs活性的抑制作用分别为54.96％和28.36％。高效氯氰菊酯、甲氰菊酯、啶虫脒和单宁酸对黑翅土白蚁GSTs活性的抑制作用要强于黑胸散白蚁,对黑翅土白蚁GSTs活性的抑制作用分别为39.43％,72.07％,52.24％和82.19％;对黑胸散白蚁GSTs活性的抑制作用分别为14.96％,40.23％,39.96％和57.80％。阿维菌素对黑翅土白蚁和黑胸散白蚁GSTs活性的抑制作用没有显著差异,对黑翅土白蚁和黑胸散白蚁GSTs活性的抑制作用分别为76.21％和76.88％。这表明两种白蚁对药剂的敏感性完全不同。实验结果还表明,在3.2×10^-8～2×10^-5 mol/L内,上述植物次生物质和杀虫剂对两种白蚁GSTs活性的抑制率存在明显的剂量-效应关系。     

黑翅土白蚁乙酰胆碱酯酶最佳反应体系的建立及药剂敏感度比较

用正交试验方法研究了酶浓度、底物浓度、反应体系pH值、反应温度、反应时间5个因素对黑翅土白蚁Odontotermes formosanus (Shiraki)乙酰胆碱酯酶(AChE)活性测定的影响。通过对正交试验结果进行极差和方差分析,明确了测定黑翅土白蚁AChE活性的最适反应条件是酶浓度为12.5 g/L,底物浓度为8 mmol/L,pH值8.0,反应温度40℃,反应时间5 min。此外,研究了6种药剂对黑翅土白蚁体内AChE活性的影响。结果表明：灭多威、辛硫磷、三唑磷、丙溴磷、马拉硫磷和氧化乐果6种药剂对黑翅土白蚁AChE抑制中浓度(IC₅₀)分别为3.52×10^-4,1.86×10^-3,5.13×10^-3,9.55×10^-4,8.81×10^-3,和1.39×10^-2 mol/L。在3.3×10^-7～5×10^-3 mol/L的浓度范围内,上述6种药剂对黑翅土白蚁体内AChE活性的抑制作用都具有明显的剂量效应关系。     

黑翅土白蚁的跟踪信息素

黑翅土白蚁Odontotermes formosanus(Shiraki)严重危害堤坝,有明显跟踪行为,其分泌跟踪物质的腹板腺位于腹部第5节腹板前沿中部,分泌细胞呈长形,与腹板呈垂直方向排列。用滤纸双圈法测定黑翅土白蚁跟踪行为。跟踪物质的抽提以正己烷较好,丙酮和二氯甲烷次之。从抽提液柱层析、薄层层析和微化学反应结果推测,其跟踪物质可能是含有双键的醇类化合物。密褐褶孔菌及其感染的腐木块抽提液及白蚁跟踪信息化合物——顺,顺-3,6-十二碳双烯醇都对黑翅土白蚁有较强的跟踪活性。肖若散白蚁和家白蚁抽提液均对黑翅土白蚁有跟踪活性,但肖若散白蚁和家白蚁对黑翅土白蚁抽提液及其柱层析和薄层层析的活性馏份无活性反应。     

四种植物精油对黑翅土白蚁触杀和驱避作用

为筛选出高效防治黑翅土白蚁的天然植物精油,减少有机合成农药的使用,该文研究了大蒜精油、肉桂油、丁香油和印楝素油四种植物精油对黑翅土白蚁的触杀效果和驱避作用。结果表明:大蒜精油、肉桂油和丁香油的浓度为5和10 mg·m L~(-1)时,处理2 h后,黑翅土白蚁的校正死亡率达100%,而相同浓度的印楝素油和对照处理的黑翅土白蚁校正死亡率低于5%。随着处理时间延长,浓度为1.25和2.5 mg·m L~(-1)的大蒜精油、肉桂油和丁香油处理6 h时,黑翅土白蚁的校正死亡率仍达100%,而此时对应的印楝素油和对照处理的黑翅土白蚁校正死亡率仅为10%,说明大蒜精油、肉桂油和丁香油对黑翅土白蚁具有较强的触杀效果。大蒜精油、丁香油和肉桂油在处理黑翅土白蚁2 h后LC_(50)值(半致死量)分别为1.572、1.05和1.03mg·m L~(-1),说明肉桂油对黑翅土白蚁的毒性相对最大,触杀效果最好。此外,10 mg·m L~(-1)的大蒜精油、肉桂油、丁香油和印楝素油的驱避试验表明,处理4、6、8和12 h后,大蒜精油、肉桂油和丁香油三精油处理区的黑翅土白蚁数均显著低于对照区的,驱避率总体93%,而对应的印楝素油的驱避率总体28.5%,表明大蒜精油、丁香油和肉桂油三种植物精油对黑翅土白蚁均有显著的驱避活性。综上可知,四种植物精油中大蒜精油、肉桂油和丁香油在防治黑翅土白蚁方面应用潜力很好,是开发绿色环保白蚁防治药剂的可选材料。     

氯化钠含量对黑翅土白蚁生存的影响

【目的】为摸清堤坝土埝中氯化钠对黑翅土白蚁Odontotermes formosanus Shiraki生存的影响,合理确定防治黑翅土白蚁危害堤坝的氯化钠含量值,确保堤坝工程安全运行。【方法】选取有黑翅土白蚁生存和无黑翅土白蚁生存两类堤坝的土埝,进行土埝中氯化钠含量的测试。【结果】有黑翅土白蚁生存的堤坝土埝氯化钠含量在0.02%以下,无黑翅土白蚁生存的堤坝土埝氯化钠含量在0.19%以上。【结论】研究成果对黑翅土白蚁危害堤坝的防治具有很好的实用价值。     

黑翅土白蚁巢群觅食群体大小与工蚁体长呈正相关

【目的】明确黑翅土白蚁Odontotermes formosanus巢群的觅食群体大小与工蚁体长之间的关系,为进一步研究其生态学特点以及更好地开展防治提供依据。【方法】在杭州植物园内选择5处有黑翅土白蚁活动区域作试验点,诱捕并以中性红(neutral red)标记捕获的白蚁工蚁,通过“捕获-标记-释放-重捕”试验测定黑翅土白蚁的觅食群体大小。【结果】5个试验点中有4个成功实施了“捕获-标记-释放-重捕”试验,4个试验点黑翅土白蚁巢群的觅食群体个体数量分别为443 133±45 469, 495 360±67 429, 674 345±101 703和1 224 662±93 112头。黑翅土白蚁觅食群体大小(Y)与觅食工蚁的体长(X)呈正相关,拟合的指数函数方程式为：Y=1.8389e^0.7185X(R²=0.7834)。【结论】本研究明确了黑翅土白蚁的觅食群体大小以及工蚁体长之间的函数关系,为开展区域防治提供了依据。     

烯啶虫胺肠衣饵剂对黑翅土白蚁的防治效果

[目的]为了开发一种高效环保型白蚁饵剂.[方法]选定烯啶虫胺和溴虫腈对黑翅土白蚁Odontotermes formosanus进行室内毒力测定,根据室内毒力测定结果筛选毒力较高药剂进行驱避试验,并制备3种不同剂量的肠衣饵剂,开展室内白蚁毒杀效果试验和园林白蚁防治效果试验;选用合适剂量肠衣饵剂进行堤坝黑翅土白蚁诱杀试验,并用挖巢法检测肠衣饵剂对堤坝黑翅土白蚁的诱杀效果.[结果]1.6tg/mL烯啶虫胺处理黑翅土白蚁72 h后校正死亡率达100％,16 μtg/mL溴虫腈处理72 h后黑翅土白蚁校正死亡率也达到100％.室内毒力测定结果表明烯啶虫胺对黑翅土白蚁的LC5o值低于溴虫腈,100 μtg/mL烯啶虫胺处理8h后对黑翅土白蚁无显著驱避作用.3种剂量烯啶虫胺肠衣饵剂处理72 h后,黑翅土白蚁校正死亡率均在60％以上.将不同剂量的烯啶虫胺肠衣饵剂投放到园林中45 d后,肠衣饵剂基本被食空,施药点周围无白蚁及活动迹象.在福建省水库大坝周围投放60 μtg/g烯啶虫胺肠衣饵剂,3个月后肠衣饵剂未发霉且基本被食空,6个月后挖巢发现蚁道内无黑翅土白蚁活动,白蚁巢体出现死亡和坍塌情况.[结论]60 μg/g烯啶虫胺肠衣饵剂对园林和堤坝中的黑翅土白蚁具有良好的诱杀效果,是一种高效环保型白蚁肠衣饵剂.     

氟虫腈、吡虫啉作为黑翅土白蚁诱杀药剂的效果

毒力测定结果表明,0.025~0.4μg/mL氟虫腈和吡虫啉分别在药后3 d和5 d对黑翅土白蚁Odontotermes formosanus表现出明显的毒杀效果,氟虫腈和吡虫啉药后1 d的LC50分别为药后5 d的509倍和63.8倍,2种药剂对黑翅土白蚁的毒杀效果均比较缓慢。毒性传递试验表明,0.5μg/g毒沙处理白蚁1 h后,氟虫腈和吡虫啉的致死毒性均可被传毒白蚁传递给受毒白蚁。驱避作用试验表明,50μg/mL氟虫腈对黑翅土白蚁无明显的驱避作用,而50μg/mL吡虫啉对黑翅土白蚁表现出了明显的驱避作用。可见,2种供试药剂中,氟虫腈是较理想的白蚁诱杀药剂。     

水库堤坝白蚁的防治研究

本工作是根据水库堤坝的生态环境特点,研究土牺白蚁中黑翅土白蚁[Odontotermes(O.)formosantts(Shiraki)]和黄翅大白蚁(Macrotermes barneyi Light)的分布情况、活动规律和防治措施,其中包括以黑光灯诱杀成虫和药剂灌巢。     

Discrimination of female sex pheromone by male Trichoplusia ni (Hubner)

The olfactory discrimination process of male cabbage loopermoths, Trichoplusa ni (Hübner), was assessed by measuringtheir response to one of two emission sources within a windtunnel. The males discriminated between (1) Z7–12:Ac concentrations;(2) Z7–12:Ac alone and the volatile emission from excisedfemale sex pheromone glands; and (3) Z7–12:Ac and theemission from a mixture of six synthetic pheromone componentsthat mimics the volatile emissions of a female gland. Althoughmales could discriminate between a freshly excised female sexpheromone gland and 7.4x 10^–11 M Z7–12:Ac, theycould not discriminate between a gland and 78.5x10^–11M Z7–12:Ac. Males also could not discriminate betweenthe mixture of six volatile compounds and 28.7x10^–11 Mof Z7–12:Ac. The data show that male cabbage looper mothshave difficulty discriminating between Z7–12:Ac aloneand in mixtures with other female-emitted volatile compounds.     

旋花蛾性信息素成分的鉴定

提取和鉴定了杂草田旋花Convolvulus arvensis的天敌旋花蛾Tyta luctuosa的性信息素主要成分,并应用风洞实验对雄蛾进行了测试。结果表明,腺体提取物和雌蛾求偶时所释放的主要性信息素成分均为2种化合物：顺-9-十四碳烯醛（Z9-14∶Ald）和顺-11-十六碳烯醛（Z11-16∶Ald）。腺体提取物中2种化合物的总量在个体间差异很大（22～167 ng）,但二者的比率相对稳定（Z9-14∶Ald/Z11-16∶Ald=0.3±0.15）。雌蛾所释放的性信息素量及比率在个体间也存在差异。每只雌蛾求偶时平均每小时释放94 ng Z9-14∶Ald和45 ng Z11-16∶Ald,平均比率为2.2。风洞实验结果显示,48%的雄蛾可被合成的性信息素混合物（0.4 μg Z9-14∶Ald, 2 μg Z11-16∶Ald）引诱完成逆风飞行并最终触及刺激源,而2种对照组（以求偶期雌蛾或性信息素腺体提取物为刺激源）的引诱率则分别为62%和44%。     

Purification and Characterization of a Novel Sex Pheromone that Induces the Release of Another Sex Pheromone during Sexual Reproduction of the Heterothallic Closterium peracerosum-strigosum-littorale Complex

A sex pheromone, PR-IP Inducer, which is released from mating-typeminus cells of Closterium, was purified by monitoring its biologicaleffect on the induction of the release of protoplast-release-inducingprotein (PR-IP) from mating-type plus cells. The purified PR-IPInducer had an apparent molecular mass of 22 kDa and of 18.7kDa as determined by SDS-PAGE and mass-spectrometric analysis,respectively. Staining with periodic acid-Schiff reagent indicatedthat PR-IP Inducer included a glycan chain. From the analysisof a dose-response curve, it seemed that PR-IP Inducer was ableto exert its activity over quite wide range of concentrations(1 x 10^–10–3 x 10^–7 M). It appears that PR-IPInducer is a novel glycoproteinaceous pheromone, as is PR-IP,and that it exerts its effect at the earliest stages of thesexual reproduction of the Closterium peracerosum-strigosum-littoralecomplex. ¹Recipient of a Fellowship for Japanese Junior Scientists fromthe Japan Society for the Promotion of Science.     

Purification, Identification, Concentration and Bioactivity of (Z)-7-Dodecen-1-yl Acetate: Sex Pheromone of the Female Asian Elephant, Elephas maximus

In their natural ecosystems, adult male and female Asian elephants,Elephas maximus, live separately. For several weeks prior toovulation, female elephants release a substance in their urinewhich elicits a high frequency of non-habituating chemosensoryresponses, especially flehmen responses, from male elephants.These responses occur prior to, and are an integral part of,mating. Using bioassay-guided fractionation, quantitativelydependent on these chemosensory responses, a specific sex pheromonewas isolated and purified by an alternating series of organicand/or aqueous extractions, column chromatography, gas chromatographyand high-performance liquid chromatography. Using primarily¹H-proton nuclear magnetic resonance (NMR) spectrometry andgas chromatography-mass spectrometry (GC-MS) of the urine-derivedpheromone and its dimethyl disulfide derivative, we determinedthe structure of the active compound to be (Z)-7-dodecen-1-ylacetate (Z7-12:Ac). Concentrations of Z7-12:Ac in the femaleurine increased from non-detectable during the luteal phaseto 0.48µg/ml (0.002 mM) early in the follicular phaseand to 33.0µg/ml (0.146 mM) just prior to ovulation. Bioassayswith commercially available authentic synthetic Z7-12:Ac, using10 Asian male elephants at several locations in the US, demonstratedquantitatively elevated chemosensory responses that were robustduring successive tests, and several mating-associated behaviors.Bioassays with Z7-12:Ac with adult male elephants dwelling inmore natural social situations in forest camps in Myanmar revealedsome differing contextual pre-mating behavioral components.The remarkable convergent evolution of this compound suggeststhat compounds identified in mammalian exudates that are alsopresent in pheromone blends of insects should be re-evaluatedas potential mammalian chemosignals. Chem. Senses 22: 417–437,1997.     

Effects of algal concentration, bacterial size and water chemistry on the ingestion of natural bacteria by cladocerans

Journal of Plankton Research, 11, 1273–1295, 1989. The values of P/U⁰ (Table I) and fluid velocity used to calculatethe energy required for sieving (pp. 1289–1290) and severalequations (footnote b of Table I; p. 1290, lines 3–4)are incorrect. The corrected table appears below: Table I. Filter setule measurements (mean and within specimenstandard deviation) of the gnathobases for the cladocerans studied^aGnathobaseof trunklimb number. ^bP = 8µU₀/(b(1 – 21nt + 1/6(t²) - 1/144(t⁴))), whereP = pressure drop in dyn cm^–2, =3.1416, U₀ = fluid velocityin cm s^–1, b = distance between setule centres in cm,t = ( x setule diameter)/b and µ = 0.0101 dyn s^–1cm^–2. Formula from Jørgensen (1983). The text (p. 1289, line 19 to p. 1290, line 10) should read: organism. Using a similar argument, a 0.5 mm Ceriodaphnia witha filter area of 0.025 mm² (Ganf and Shiel, 1985) and pressuredrop P = 2757 dyn cm^–2 (with fluid velocity of 0.07 cms^–1) allocates only 2171 ergs h^–1 to filtrationof a total energy expenditure of 10⁴ ergs h^–1 [filtrationenergy (ergs h^–1) = area (cm²) x pressure drop (dyn cm^–2)x 3600 (s h^–1) x 1/0.2 (efficiency of conversion of biochemicalinto mechanical work); total energy (ergs h^–1) = respiration(0.05 µl O₂ ind^–1 h^–1 consumed; Gophen, 1976)x conversion factor (2 x 10⁵ ergs µl^–1 O₂). Withan estimated 0.034 mm² in filter area, fluid velocity of 0.041cm s^–1 and respiration of 1.8 x 10⁴ ergs h^–1 (calculatedfrom Porter and McDonough, 1984), a 0.5 mm Bosmina uses <4%of its metabolism to overcome filter resistance. The velocities used in the original examples (0.4 cm s^–1for Ceriodaphnia, 0.2 cm s^–1 for Bosmina) were derivedfrom literature values of appendage beat rate and estimatesof the distance travelled by the appendages during each beatcycle. This approach unnecessarily assumes that all water movedpasses through the filter. In the new calculations, the flowacross the filter needed for food to be collected by sieving(0.07 cm s^–1 for Ceriodaphnia and 0.041 cm s^–1 forBosmina) was determined from the maximum clearance rate/filterarea. The amended energy expenditures, although higher, do notrefute the sieve model of particle collection.     

Carbon and nitrogen content of Noctiluca scintillans in the Seto Inland Sea, Japan

The carbon and nitrogen content of Noctiluca scintillans cellsfrom the Seto Inland Sea, Japan was investigated in order toestimate its biomass in natural samples. The carbon contentof N.scintillans ranged from 123 to 627 ng C cell^–1 witha mean value of 353 ng C cell^–1, or 1.12 to 2.67 fg Cµm^–3 with a mean value of 1.98 fg C µm^–3.The nitrogen content ranged from 36.0 to 232 ng N cell^–1with a mean value of 131 ng N cell^–1, or 0.499 to 0.910fg N µm^–3 with a mean value of 0.694 fg N µm^–3.Total cell carbon and nitrogen increased but the carbon andnitrogen per cell volume decreased with increasing cell volume.The C/N ratio of the cells ranged from 2.3 to 4.4, which wasrelatively low compared with the Redfield ratio. The carbonand nitrogen content was extremely low (91.2 ng C cell^–1,41.8 ng N cell^–1) for starved cells, whereas it was extremelyhigh (528 ng C cell^–1, 205 ng N cell^–1) for cellswhich had ingested the large diatom, Coscinodiscus wailesii.Our results suggest that the carbon and nitrogen content ofN.scintillans varies depending on its physiological conditionand the type of food that it has recently consumed.     

Diffusional permeability of rabbit mesothelium

Diffusional permeability (P) to sucrose(P_suc) andNa⁺(P_Na⁺)was determined in specimens of rabbit sternal parietal pericardium,which may be obtained without stripping. Specimens were mounted in anUssing apparatus with ³H-labeledsucrose and²²Na⁺in a luminal (L) or interstitial (I) chamber.P_suc was 2.16 ± 0.44 for LI and 2.63 ± 0.45 (SE) × 10⁵ cm/s for IL,i.e., ~10 times smaller than that previously obtained in strippedspecimens of pleura despite the similarity of intercellular junctionsin pericardium and pleural mesothelium of various species. Thesefindings suggest that previousP_suc wasoverestimated because stripping damages the mesothelium.P_Na⁺ (×10⁵ cm/s) was 7.07 ± 0.71 for LI and 7.37 ± 0.69 × 10⁵ cm/s for IL.Measurements were also done with phospholipids, which are adsorbed onthe luminal side of mesothelium in vivo. With phospholipids in L,P_suc was 0.75 ± 0.10 and 0.65 ± 0.08 andP_Na⁺was 3.80 ± 0.32 and 3.76 ± 0.15 × 10⁵ cm/s for LI andIL, respectively, i.e., smaller than without phospholipids.With phospholipids in I (where they are not adsorbed), P_suc (2.33 ± 0.42 × 10⁵ cm/s) andP_Na⁺(7.01 ± 0.45 × 10⁵ cm/s) were similar tothose values without phospholipids. Hence, adsorbed phospholipidsdecrease P of mesothelium. If themesothelium were scraped away from the specimen,P_suc of theconnective tissue would be 13.2 ± 0.76 × 10⁵ cm/s.P_suc of themesothelium, computed fromP_suc of theunscraped and scraped specimens, corrected for the effect of unstirredlayers (2.54 and 19.4 × 10⁵ cm/s, respectively),was 2.92 and 0.74 × 10⁵ cm/s without and withphospholipids, respectively. Hence, most of the resistance to diffusionof the pericardium is provided by the mesothelium.

     

Biological Activities of the Methyl Ester of Gibberellin A73, a Novel and Principal Antheridiogen in Lygodium japonicum

The synthetic methyl ester of GA₇₃ (GA₇₃-Me) and the naturalantheridiogen of Lygodium japonicum showed almost the same activityto induce the formation of antheridia in dark-grown protonemataof L. japonicum at concentrations of 10^-14 M and higher. Thus,it appears that the principal antheridiogen in L. japonicumis GA₇₃-Me. GA₇₃-Me inhibited formation of ar-chegonia in light-grownprothallia of L. japonicum at concentrations of 10^-11 M andhigher and induced germination of spores in the dark in thisspecies at the same range of concentrations. GA₇₃(free acidform) promoted growth of seedlings of dwarf rice and hypocotylsof cucumber seedlings at dosages of and above 1 and 100 ng/plant,respectively. Eight compounds related to GA₇₃-Me, includingantheridiogens of Anemia phyllitidis and Anemia mexicana, wereactive in inducing an-theridial formation in L. japonicum, althoughtheir activities were considerably lower than that of GA₇₃-Me. (Received August 24, 1988; Accepted November 28, 1988)     

Specific Labeling of Cell Wall Polysaccharides with myo-[2-3H] Inositol during Germination and Growth of Phaseolus vulgaris L.

myo-[2-³H]Inositol was fed to bean seeds by imbibition and itsmetabolic fate was studied during germination and seedling growth.The largest amount of myo-inositol was taken up from a 500 HIMsupply (8 mg/seed) and the highest percentage was from 1 HIM(29%). myo-Inositol was incorporated to new cell wall polysaccharidesof hypocotyl and roots, mostly as uronic acid and pentose residues.In the 80% ethanolinsoluble cell walls of hypocotyls at 3, 4and 5 days after imbibition, 47 to 52% of ³H was detected asuronic acids, 20 to 24% as arabinose and 11 to 19% as xylose.Glucogenesis from myo-inositol was low: less than 6% was recoveredas hexoses. The ³H in uronic acid and arabinose residues decreasedwith increasing age (i.e. 0 to 6 cm from cotyledons) and increasedin older segments (further than 6 cm from cotyledons). In theoldest segment of 5-day-old hypocotyl (> 10 cm), ³H in thesugar residues was more than that in the youngest part (0–2cm). On the other hand, ³H in xylose residues increased steadilyin the older part, but did not exceed that in arabinose. The results show that the myo-inositol oxidation pathway functionsin growing hypocotyls and roots of bean seedlings to provideexclusively uronic acid and pentose units for cell wall synthesis.Results also show that incorporation of arabinose and uronicacids derived from myo-[2-³H]inositol to cell wall polysaccharidesis active in two regions of the hypocotyl; first, for the constructionof the primary walls in the young, growing region of the hypocotyl,and second, for thickening of the walls after completion ofelongation growth. ¹Supported by NSERC of Canada. (Received April 10, 1984; Accepted June 12, 1984)     

Predation and respiration by the small cyclopoid copepod Oithona similisr: How important is feeding on ciliates and heterotrophic flagellates?

Feeding on natural plankton populations and respiration of thesmall cyclopoid copepod Oithona similis were measured duringthe warm season in Buzzards Bay, Massachusetts, USA. AlthoughO.similis did not significantly ingest small autotrophic andheterotrophic flagellates (2–8 µn), this copepodactively fed on >10 µm particles, including autotrophic/heterotrophic(dino)flagel-lates and ciliates, with clearance rates of 0.03–0.38ml animal^–1 h^–1. The clearance rates increased withthe prey size. O.similis also fed on copepod nauplii (mainlycomposed of the N1 stage of Acartia tonsa with a clearance rateof 0.16 ml animal^–1 h^–1. Daily carbon ration fromthe combination of these food items averaged 148 ng C animal^–1day^–1 (41% of body C day^–1), with ciliates and heterotrophicdino-flagellates being the main food source ({small tilde}69%of total carbon ration). Respiration rates were 020–0.23µl O₂ animal^–1 day^–1. Assuming a respiratoryquotient of 0.8 and digestion efficiency of 0.7, the carbonrequirement for respiration was calculated to be 125–143ng C animal^–1 day^–1, close to the daily carbon rationestimated above. We conclude that predation on ciliates andheterotrophic dinoflagellates was important for O.similis tosustain its population in our study area during the warm season.