Newcastle disease in Cyprus: A review     

K. Polydorou 《Tropical animal health and production》1979,11(1):37-41

Summary The first Newcastle disease epidemic in Cyprus was reported in 1949 to 1950 and between 1953 and 1959 there was a second. In November 1977 another Newcastle disease outbreak occurred. Measures implemented immediately were: quarantine of all foci of infection, destruction of diseased and in-contact birds, disinfection of premises and island-wide (Government controlled) vaccination. Within a month the epidemic was brought under control. In all 47 outbreaks were recorded with the loss of about 35,000 birds. Only 2 commercial units were affected, the remaining outbreaks occurring in premises of back-yard poultry keepers. The virus was the Asiatic type.

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La Enfermedad De Newcastle En Chipre: Revisión De La Literatura

Resumen La primera epidemia de Newcastle en Chipre se describio en 1949–50 y la segunda entre 1953 y 1959. En Noviembre de 1977 ocurrio otro brote. Las medidas tomadas fueron: cuarentena de todos los focos de infección, destrucción de todas las aves enfermas y en contacto, desinfección de los galpones y vacunación general. La epidemia se controló en un mes. En los 47 brotes diagnosticados, hubo una pérdida calculada de 35 000 aves. La enfermedad se diagnosticó en dos empresas comerciales y en unidades pequeñas familiares. El virus aislado fue el tipo Asiático.

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La Maladie De Newcastle A Chypre—Revue

Résumé La première appartition de la maladie de Newcastle à Chypre, a eu lieu en 1949–1950, avec une seconde vague entre 1953 et 1959.La maladie est répparue en 1977. Les mesures assitôt prises ont été: la mise en quarantaine des foyers d'infection, la destruction des animaux malades et des animaux contaminés, la désinfection des locaux et une large vaccination, sous contrôle officiel, des volailles de l'Ile. En l'espace d'un mois la maladie a été enrayée. Pour les 47 foyers constatés les pertes se sont élevées à environ 35 000 têtes. Deux élevages commerciaux ont seulement été atteints, les autres foyers étant apparus dans les poulaillers des petits éleveurs.

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Plasma concentration of sulphadimethoxine in pigs after multiple dosing and during injections of Escherichia coli endotoxin     

O. Ladefoged 《Veterinary research communications》1979,3(1):73-77

The effect of endotoxin induced fever on the steady state concentration of sulphadimethoxine in pigs has been studied.Sulphadimethoxine 20 mg/kg b.wt. was injected at 9 a.m. in an ear vein each day for eleven days. From day 6 until the end of the experiment, endotoxin fromEscherichia coli 1.5 g/kg b.wt. was injected at 9 a.m. and at 3 p.m. The plasma concentration versus time curves were calculated by means of a computer program, assuming a two-compartment model. During the endotoxin injections the plasma concentrations were simulated and compared with those calculated.It was not possible to show any clinically significant changes in pharmacokinetics of sulphadimethoxine after the start of endotoxin injections.  相似文献   

Tom-cat odour and other pheromones in feline reproduction     

K. P. Bland 《Veterinary research communications》1979,3(1):125-136

The function and suppression of urine spraying by cats is discussed as also is the source of tom-cat odour. It seems unlikely that tom-cat odour is derived from the lipid in the proximal convoluted tubule of the kidney, however its production by the anal glands has not yet been proven. Although male cats show a flehmen response when sniffing urine, smell seems to play a more important role in reproduction in the female than the male. The available data suggests that valeric acid may function as a female/female pheromone in cats by inducing or facilitating oestrus. Nepetalactone, the active ingredient of catnip, is probably not related to any naturally occurring pheromone in the cat but simply acts as an hallucinogenic drug.  相似文献   

小麦丛矮病研究之三:灰飞虱同发病的关系     

蔡祝南  魏德忠  林志亮  杨莉  梅汝鸿  裘维蕃 《植物保护学报》1979,6(2):35-46

1976—1977年河北晋县贺家寨大队小麦春季灰飞虱的传带病毒率为31—52%,不同地块同代灰飞虱的带毒率异差较大:而秋苗期则为12—35.4%,其中不同地块上同代(四代成虫)灰飞虱的带毒率的差异从33.3%至35.4%则不太大。灰飞虱的有效传毒指数(即虫口数×自然带毒率)同田间小麦发病率的相关性是非常显著的,其r=0.9769。1975—1976两年调查及计算分析结果,其直线回归公式如y=4.12x-2.577。在有效传毒指数0.7—20.9之间用于予测发病率有效。人工分期侵染试验证明小麦在生长发育过程中受侵愈早,病情愈重,其中死株率也愈大。秋季侵染的死株率达95.6%,病指为99.6;夏季侵染的死株率为0,病指为57.6。秋季小麦出苗前后的大量虫口形成小麦10月中下旬的一个发病高峰,第二年春季4月中旬的虫口高峰形成5月上旬的一个发病高峰。3月下旬的一个发病高峰是越冬前受侵的。病毒在小麦植株中的潜育期的长短随小麦的生长速度而异。温度不过其中因素之一,最短5—8天,最长30—40天。侵染后如小麦进入越冬期,即不表现症状,一直要到返青以后。介体灰飞虱在河北晋县以第五代3—4龄若虫在冬麦地及草荒中越冬。夏季在玉米上可以产卵并孵化,但不能长期存活,主要在地头沟边及夏作物荫蔽下的禾草上越夏。冬麦治虫防病的重点应在秋季麦苗出土前,春季则应在3月中旬左右。冬麦适当推迟播种有利于减少发病率。棉间作麦比平作的病情重六倍而粮麦间作的病情比平作的重九倍。  相似文献   

西藏的小麦白秆病     

徐雍皋 《植物保护学报》1979,6(2):25-33,66

小麦白秆病是在青藏高原上为害小麦的一种新病害,在受害的叶、叶鞘及茎秆上产生草黄色条斑和椭圆形至长方形斑点两种症状。经鉴定病害由壳月孢属(Selenophoma)真菌引起。病菌在15℃黑暗条件下的马铃薯葡萄糖琼脂上培养,形成粘质状菌落,生长缓慢,不形成分生孢子器,而在菌丝上芽殖分生孢子;在15℃黑光灯照射下的燕麦琼脂等培养基上培养,形成分生孢子器。分生孢子器分生孢子新月形,无色,单胞,大小为17.9-26×2.6-3.6μ;而芽殖分生孢子的大小及形态变异较大。病菌的生长温度范围为0—20℃,以15℃为最适宜。其寄主有小麦、黑麦及冰草等。种子和幼苗经接种后,均产生系统性条斑症状。根据病菌的形态和寄主范围,小麦白秆病菌即Selenophoma donacis(pass)sprague efA.G.Johnson,由于S.donacis 只产生斑点症状,而小麦白秆病菌产生特有的系统性条斑症状,且发生温度偏低,所以认为小麦白秆病菌是在青藏高原特殊的生境条件下,形成的一个Selenophoma donacis(pass)sprague et A.G.Johnson的“白秆(albo-culmo)生态型。  相似文献   

利用磷肥厂副产氟硅酸防治小麦锈病的研究     

屠予钦  魏岑 《植物保护学报》1979,6(1):57-70

作者于1966半报告了氟硅酸对小麦条锈病具有良好药效,氰硅酸是磷肥厂副产,资源丰富、成本低廉。1971年又用氟硅酸与尿素制成便于运输和贮存的晶态的氟硅脲,其分子式为[(NH_2)_2CO]_4·H_2SiF_6。十多年来经过15个省市的田间试验,肯定了氟硅酸和氟硅脲对小麦三种锈病均有效。在山东烟台地区和四川内江地区的大面积推广试用均取得良好效果。防治有效浓度按H_2SiF_6计为0.05～0.10%,药液中须加入湿润剂。除扬花期不可喷药外,其它生育期均可喷药。对小麦的增产效果显著。小麦种子中未发现氟的反常残留。经卫生部门测定,十个样本中有6个氟残留量为0.71～1.98ppm,有1个样本中为3.47ppm,系过量喷药所致。其余3个样本中未检出氟。本文讨论了使用无机氟剂的环境保护问题。根据地球化学和环境化学的最近研究成果,在本文所建议采取的使用浓度下,用氟硅酸防治小麦锈病并无引起环境污染之虞。  相似文献   

棉铃虫田间分布型及在实践中的应用——2.棉铃虫田间卵量调查及序贯抽样检定防治标准的方法     

袁锋  汪世泽  魏建华 《植物保护学报》1979,6(1):37-50

在调查分析了解棉铃虫卵在田间呈核心理论分布型的基础上,研究了卵量调查方法的改进,应用序贯抽样检定防治标准,及统计资料的代换方法。根据棉铃虫卵在田间呈核心分布型,为了提高田间调查准确度,改进我国已经应用的田间取样方式,提出田间卵量调查方法是:以200株为取样量,采用平行线式,40个样点,每点单行五株。因为这样增多了样点和卵分布核心相遇的机会,经与原采用的单对角线式,双对角线式,棋盘式,分行式取样比较,平行线式取样准确度最高,降低了样本平均数代表性误差。为了节省田间卵量检查时间,可采用调查着卵株率计算百株卵量的办法,或对不同卵量密度的田块区别对待,百株卵量10粒以上检查100株,10粒以下检查200株。以田间百株卵量15粒或着卵株率11.77%为达到防治标准;卵量10粒或着卵株率8.36%为未达到防治标准,制定了序贯抽样检定防治标准的方法。检查卵量序贯抽样确定防治标准的方程:d_o=0.1127n-8.5353d_1=0.1127n 8.5353检查着卵株序贯抽样确定防治标准的方程:d_o=0.0998n-6.4228d_1=0.0998n 6.4228为了使用方便,制定了每次检查五株为单位的序贯抽样确定防治标准的田间实用检定表。实例计算表明,对棉铃虫卵和田间调查资料,进行变量分析,用对数和平方根代换均可。根据卵呈核心或嵌纹分布的特点,对数代换更为合理些。  相似文献   

小麦对条锈病的水平抗病性研究初报   总被引：4，自引：0，他引：4  

曾士迈  王沛有  武修英  张万义  王吉庆  宋位中  王生元 《植物保护学报》1979,6(1):1-10

将小麦品种采用随机区组的田间设计种于小种病圃中,以鉴定和测定其水平抗性。根据各个“品种——小种”组合的相对病情指数的方差分析的结果,有些品种,如农大311、西农6028和丰产3号,其品种——小种互作高度显著,被鉴定为具有垂直抗性,另外一些品种,对试验所用的小种并无专化性,并且在大田生产中已显出20多年的持久的中度抗性,初步推测为属水平抗性。在后一类中,有些品种,如平原50,表现为中等反应型,其余则属于呈典型感病的迟锈慢锈类型。在迟锈慢锈品种的病指的对数矫正值(logits)和病圃的锈病强度(以感病对照品种的病指表之)的对数矫正值之间发现了直线回归。  相似文献   

Virus eradication from some Pelargonium zonale cultivars by meristem-tip culture     

F. A. Hakkaart  Gusta Hartel 《European journal of plant pathology / European Foundation for Plant Pathology》1979,85(2):39-46

On the older leaves ofPelargonium zonale chlorotic rings and flecks are common, especially during spring and fall. From such plants an isometric virus can be isolated that causes local lesions on the leaves ofChenopodium quinoa. An attempt was made to produce symptomless plants, reacting negatively onC. quinoa. Meristem tips on a basal medium supplemented with α-naphthalene acetic acid and coconut milk produced abundant callus, but no plantlets. However, on media containing low concentrations of indole acetic acid and kinetin or benzyl adenine, some plants were produced that fulfilled the above requirements. Those selected on horticultural properties, are considered as valuable mother plants. Of twenty-one cultivars such plants were obtained. They may prove an important contribution to the improvement of theP. zonale industry in the Netherlands.  相似文献   

Direct electron microscopy and serology with plant viruses in leaf material dried and stored over calciumchloride     

Dr. L. Bos  Dr. M. P. Benetti 《European journal of plant pathology / European Foundation for Plant Pathology》1979,85(6):241-251

Most of 43 viruses could easily be detected directly in 53 out of 66 leaf samples dried and stored over CaCl₂ for varying periods of time up to 20 1/2 years. Detection usually was with PTA pH 6.5, but alfalfa mosaic, cucumber mosaic and tomato aspermy viruses required PTA pH 3.0 to 4.0. Bean common mosaic, cowpea aphid-borne mosaic and cowpea mosaic viruses were also easily observed in newly dehydrated samples obtained for diagnosis from Morocco and Tanzania.Broad bean wilt virus, cowpea mosaic virus and cucumber mosaic virus were detected with agar gel-diffusion tests in dry leaf material ground in buffer. This serological assay demonstrated a high concentration of cucumber mosaic virus in leaf material dried over CaCl₂ 20 years ago. This paper further coroborates the value of the CaCl₂ method of dehydration and storage of plant viruses in leaf material.Samenvatting Zeer uiteenlopende plantevirussen kunnen goed worden bewaard in bladmateriaal van geïnfecteerde planten dat is gedroogd en bewaard boven CaCl₂. Bij rechtstreekse elektronenmicroscopische toetsing van 66 monsters met verschillende isolaten van 43 virussen konden in 53 monsters gemakkelijk virusdeeltjes worden waargenomen (Tabel 1 en Fig. 1 en 2). Meestal lukte dit met fosforwolfraamzuur pH 6,5 dat doorgaans voor in ruw plantesap voorkomende virussen wordt gebruikt. Bij luzernemozaïekvirus en komkommermozaïek virus gelukte dit alleen maar bij lagere pH (3,0 en 4,0). Ook het tomate-aspermievirus was dan veel gemakkelijker aantoombaar. Methylaminewolfraamzuur gaf geen beter resultaat.Draden van bonerolmozaïekvirus en van cowpea aphid-borne mosaic virus en bolletjes van cowpea mosaic virus waren snel waarneembaar in elektronenmicroscopische preparaten gemaakt van bladmateriaal van recent uit Marokko en Tanzania ontvangen monsters.Cowpea mosaic virus, tuinboneverwelkingsvirus en komkommermozaïekvirus konden eveneens gemakkelijk en snel serologisch worden aangetoond in met bufferoplossing vermalen droog blad van respectievelijk cowpea, erwt en tabak. Het laatstgenoemde, reeds 20 1/2 jaar geleden gedroogde bladmateriaal, bleek in vergelijking met pas geïnoculeerd vers blad van komkommer enChenopodium quinoa zelfs zeer veel serologisch actief virusmateriaal te bevatten (Fig. 3).De beschreven waarnemingen bevestigen nogmaals de waarde van de toegepaste methode van virusbewaring en tonen aan dat het mogelijk is vele virussen te herkennen in van elders ontvangen gedroogde bladmonsters, zonder het risico te lopen van virusontsnapping, zoals altijd aanwezig bij werk met toetsplanten in de kas.Guestworker from Istituto Sperimentale per la Patologia Vegetale, Rome, Italy, participating in the investigations from September 21 to December 21, 1977.  相似文献