988 resultados para Log conformance


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Fecundity (F, number of brooded eggs) and egg size were estimated for Hawaiian spiny lobster (Panulirus marginatus) at Necker Bank, North-western Hawaiian Islands (NWHI), in June 1999, and compared with previous (1978–81, 1991) estimates. Fecundity in 1999 was best described by the power equations F = 7.995 CL 2.4017, where CL is carapace length in mm (r2=0.900), and F = 5.174 TW 2.758, where TW is tail width in mm (r2=0.889) (both n=40; P< 0.001). Based on a log-linear model ANCOVA, size-specific fecundity in 1999 was 18% greater than in 1991, which in turn was 16% greater than during 1978–81. The additional increase in size-specific fecundity observed in 1999 is interpreted as evidence for further compensatory response to decreased lobster densities and increased per capita food resources that have resulted either from natural cyclic declines in productivity, high levels of harvest by the commercial lobster trap fishery, or both.

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We present a method to integrate environmental time series into stock assessment models and to test the significance of correlations between population processes and the environmental time series. Parameters that relate the environmental time series to population processes are included in the stock assessment model, and likelihood ratio tests are used to determine if the parameters improve the fit to the data significantly. Two approaches are considered to integrate the environmental relationship. In the environmental model, the population dynamics process (e.g. recruitment) is proportional to the environmental variable, whereas in the environmental model with process error it is proportional to the environmental variable, but the model allows an additional temporal variation (process error) constrained by a log-normal distribution. The methods are tested by using simulation analysis and compared to the traditional method of correlating model estimates with environmental variables outside the estimation procedure. In the traditional method, the estimates of recruitment were provided by a model that allowed the recruitment only to have a temporal variation constrained by a log-normal distribution. We illustrate the methods by applying them to test the statistical significance of the correlation between sea-surface temperature (SST) and recruitment to the snapper (Pagrus auratus) stock in the Hauraki Gulf–Bay of Plenty, New Zealand. Simulation analyses indicated that the integrated approach with additional process error is superior to the traditional method of correlating model estimates with environmental variables outside the estimation procedure. The results suggest that, for the snapper stock, recruitment is positively correlated with SST at the time of spawning.

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Bycatch taken by the tuna purse-seine fishery from the Indian Ocean pelagic ecosystem was estimated from data collected by scientific observers aboard Soviet purse seiners in the western Indian Ocean (WIO) during 1986–92. A total of 494 sets on free-swimming schools, whale-shark-associated schools, whale-associated schools, and log-associated schools were analyzed. More than 40 fish species and other marine animals were recorded. Among them only two species, yellow-fin and skipjack tunas, were target species. Average levels of bycatch were 0.518 metric tons (t) per set, and 27.1 t per 1000 t of target species. The total annual purse-seine catch of yellowfin and skipjack tunas by principal fishing nations in the WIO during 1985–94 was 118,000–277,000 t. Nonrecorded annual bycatch for this period was estimated at 944–2270 t of pelagic oceanic sharks, 720–1877 t of rainbow runners, 705–1836 t of dolphinfishes, 507–1322 t of triggerfishes, 113–294 t of wahoo, 104–251 t of billfishes, 53–112 t of mobulas and mantas, 35–89 t of mackerel scad, 9–24 t of barracudas, and 67–174 t of other fishes. In addition, turtle bycatch and whale mortalities may have occurred. Because the bycatches were not recorded by some purse-seine vessels, it was not possible to assess the full impact of the fisheries on the pelagic ecosystem of the Indian Ocean. The first step to solving this problem is for the Indian Ocean Tuna Commission to establish a pro-gram in which scientific observers are placed on board tuna purse-seine and longline vessels fishing in the WIO.

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We have formulated a model for analyzing the measurement error in marine survey abundance estimates by using data from parallel surveys (trawl haul or acoustic measurement). The measurement error is defined as the component of the variability that cannot be explained by covariates such as temperature, depth, bottom type, etc. The method presented is general, but we concentrate on bottom trawl catches of cod (Gadus morhua). Catches of cod from 10 parallel trawling experiments in the Barents Sea with a total of 130 paired hauls were used to estimate the measurement error in trawl hauls. Based on the experimental data, the measurement error is fairly constant in size on the logarithmic scale and is independent of location, time, and fish density. Compared with the total variability of the winter and autumn surveys in the Barents Sea, the measurement error is small (approximately 2–5%, on the log scale, in terms of variance of catch per towed distance). Thus, the cod catch rate is a fairly precise measure of fish density at a given site at a given time.

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I simulated somatic growth and accompanying otolith growth using an individual-based bioenergetics model in order to examine the performance of several back-calculation methods. Four shapes of otolith radius-total length relations (OR-TL) were simulated. Ten different back-calculation equations, two different regression models of radius length, and two schemes of annulus selection were examined for a total of 20 different methods to estimate size at age from simulated data sets of length and annulus measurements. The accuracy of each of the twenty methods was evaluated by comparing the back-calculated length-at-age and the true length-at-age. The best back-calculation technique was directly related to how well the OR-TL model fitted. When the OR-TL was sigmoid shaped and all annuli were used, employing a least squares linear regression coupled with a log-transformed Lee back-calculation equation (y-intercept corrected) resulted in the least error; when only the last annulus was used, employing a direct proportionality back-calculation equation resulted in the least error. When the OR-TL was linear, employing a functional regression coupled with the Lee back-calculation equation resulted in the least error when all annuli were used, and also when only the last annulus was used. If the OR-TL was exponentially shaped, direct substitution into the fitted quadratic equation resulted in the least error when all annuli were used, and when only the last annulus was used. Finally, an asymptotically shaped OR-TL was best modeled by the individually corrected Weibull cumulative distribution function when all annuli were used, and when only the last annulus was used.

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刺叶栎( Quercus ilex L.)是地中海的常绿树种,属于古老的第三纪植物区系成份。本文根据苏黎世——蒙特利尔学派的植被学基本原理,全面地研究了分布在整个威尼托(Veneto)大区的剌叶栎林,详细研究刺叶栎林的群落组成、结构及类型划分。同时,对威尼托的刺叶栎林同北京山区的栎林进行了比较研究。最后,着重研究了威尼托刺叶栎林的生物多样性。 威尼托的刺叶栎林主要分布在亚得里亚海沿岸(包括Foci del Tagtiamento和Bosco Nordio e Rosolina Mare两地)、Lago di Garda和Colli Euganei。 在气候上,亚得里亚海沿岸属于半地中海气候。加尔达湖区域(Laqo di Garda)则是接近欧洲中部的大陆性气候,且维持半地中海的气候特点。Co t l i Euganei是这两地气候的过渡类型,且更接近亚得里亚海沿岸的类型。 在亚得里亚海沿岸的刺叶栎林可以分为三类,第一类(I)是一些矮树丛,这是Fraxinus ornus和Quercus ilex混交林的前身,较干旱。第二类群落(II)缺少乔木层,灌木层是由一些盖度不大的刺叶栎代替,更干旱。第三类群落(Ⅲ)是一群在外貌上相同的成熟群落.Fraxinus ornus和Quercus ilex得到充分发展,较中生。 在加尔达湖区的刺叶栎林可划分为三类。第一类群落(I)代表一组耐旱、开敞的矮树丛,含有Sesterio Variae-Ostryelum群丛的特征种,这一类可划分为SesLerio Variae-Ostryetum群 丛,土壤贫脊和干旱。第二类群落(Ⅱ)代表一类较郁闭的矮树丛,含有较多的Prunetalia群落目的成份,土壤较贫脊。第三类群(Ⅲ)代表一类郁闭的群落,乔木具有很大的密度因而林下灌木不能充分发展。SesLerio Variae-Ostryetum群丛和Prunetalia群落目的成份均不多。 在Colli Euganei的刺叶栎林可划分为二类。第一类群落(I)是一些不郁闲的矮树林组成。大体上分为地中海旱生栎林和地中海假灌丛。第二类群落(II)代表了较中生状态的植被,刺叶标种群绝对郁闭。 北京地处华北大平原的西北部。北京山地的气候为温带陆地性季风气候,其地带性的落叶阔叶林是以栎林为典型。虽然这些栎林同意大利威尼托刺叶栎林是两种不同的森林类型,但两者之间是存在着一定的联系。其共有的科有20个,共有属有11个。他们在植物组成中,以禾本科,蔷薇科和豆科的植物种类为最多。在乔木层中,他们都是以壳斗科的栎属(Quercus)为优势,其中木犀科的白蜡属(Fraxinus)和槭树属(Acer)较多。 本文对威尼托大区刺叶栎林的物种多度分布格局进行了全面探讨,计算出刺叶栎林的几何分布模型、Broken-stick分布模型、Log分布模型、Log-normat分布模型等四种物种多度分布的理论模型,并将这些理论分布模型用“序列/多度”图解和“多度/频度”图解表示出来。其中,几何分布模型.Broken-stick1分布模型用“序列/多度”图解表示。Broken-stick2分布模型、Log分布模型、Log-normal分布模型用“多度/频度”图解表示。 对上述四个物种多度的理论分布同实际现察的物种多度分布进行X2分析,在5%的显著性水平上,对整个威托大区的刺叶 栎林,几何分布模型最能代表其物种多度分布,显著性最大;Log-normal分布模型也可以用来代表威尼托刺叶标妹的物种多度分布,其显著性次于几何分布模型的显著性。这表明威尼托的刺叶栎林尚处于演替的早期阶段,这些刺叶栎林曾受到严重破坏,现正在恢复。 通过比较Foci del Tagtiamento和Bosco Nordio加尔达湖区、Colli Euganei四个地方刺叶栎林的物种多度的几何分布模型和Log-normal分布模型,显示出Lago di Garda(加尔达湖区)的刺叶栎林生物多样性最好、Foci del Tagtiamento刺叶栎林生物多样性较好.Bosco Nordio的剌叶栎林生物多样性较差.Colli Euganei的刺叶栎林生物多样性最差。 再利用多样性指数计算全部威尼托大区剌叶栎林的生物多样性。计算的多样性指数有丰富度指数(包括Margalef指数、Men-hinick指数、Monk指数)、多样性指数(Shannon信息指数、Bri llouin个息指数、Gini指数、PIE指数、Mcintosh指数)、优势度指数(Berger-Parker指数、Simpson指数)、均一度指数(Pielou均一度指数、Brillouin均一度指数,PIE的V’均一度指数.PIE的V均一度指数,N2的V’均一度指数,N2的V均一度指数,Mclntosh均一度指数,Hill的F10均一度指数,Hill的E21均一度指数,Hill的F21的一度指数)。通过比较丰富度指数,多样性指数、均一度指数与优势度之间的关系,结果,Simpson优势度指数同Men-hinick物种丰富度指数、Shannon信息指数、Bril-louin信息指数、Pielou均一度指数,Brillouin均一度指数,Mcintosh均一度指数、PIE的V’均一度指数呈负相关关系,因此,上述生物多样性指数可以较好地反映威尼托大区刺叶栎林的生物多样性。反映出的结果是:加尔达湖区刺叶栎林生物多样性最好,Foci del Tagtiamento刺叶栎林生物多样性较好,Bosco Nordio的剌叶栎林生物多样性较差.Colli Euganei的刺叶栎林生物多样性最差。 生物多样性的研究显示出生物多样性同生境状况的密切联系。往往受人为干扰严重的群落生物多样性低、如Coli Euganei和亚得里亚海岸刺叶栋林;而受人为破坏较轻的群落其生物多样性高,如加尔达湖区刺叶栎。 生物多样性的研究还显示出生物多样性同群落演替的发展阶段密切相关,在群落演替初期,由于缺乏优势种,而又有大量物种侵入,物多样性相对较高。在群落演替中期,由于形成了一个或几个优势种,优势度的增加导致了生物多样性相对减低。如Foci del Tagtiamento刺叶栎林生物多样性高于Bosco Nordio刺叶栎林的生物多样性。到演替后期,随着更多物种的侵入,群落结构的复杂化、生物多样性又将逐步提高。

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通过群落生态学和景观生态学方法,结合GIS、RS技术对锡林河流域湿地植被进行了研究。结果表明:流域湿地面积为301.62km2,占流域面积的3%左右。尽管面积相对较小,但是物种丰富,群落结构多样。植被调查数据显示基本确定的植被型4个,植被亚型6个,群系组16个,群系68个,区系成分以泛北极种为主,占69%,相对简单;按照水分生态型划分,中生物种占最多,为44.32%;按生活型分以多年生草本为主占50%以上;科属分布相对复杂,隶属39个科,其中禾本科和菊科是最大的两个科,所占比例仅有17.30%和12.43%,其他科没有明显的优势性,充分说明湿地优越的生境可以满足多种植物共同生长。 多度分布是研究物种多样性分布的重要组分,同时反映了群落结构的特性。以常用的Lognormal、Logseries和Weibull、Exp、Power模型来拟和6个典型草甸群落和踏头草甸群落的物种多度分布,分log-相对多度-物种级数和物种-游程两种形式进行比较;同时,对于典型草甸群落和踏头群落区分常见种、偶然种等进行细化,深入分析群落多度的变化。结果表明,5个模型对于log-相对多度-物种级数在整个群落水平上均不能很好的拟和,50%以上的点都落在95%置信区间以外;但是对常见种和偶然种的拟和情况要好,Weibull、Power和Logseris模型分别对典型草甸群落常见种、偶然种和中间种能很好的拟和,而Logseries和Power模型对于踏头群落的常见种和偶然种拟和较好。5个模型都能较好的拟和物种-游程分布,其中K—S检验结果表明:Lognormal模型对于无脉苔草、针苔草和荸荠这类相对湿润环境下的典型草甸群落拟和较好,对于长叶火绒草和密花风毛菊群落Weibull拟和最好,Power 模型拟和箭叶橐吾最好,踏头草甸拟和最好的是Logseries模型,踏头间拟合最好的是Exp模型。不同的拟和模型应用于不同的群落类型,可以看出湿地群落的复杂性和生境的多样性。区分常见种和偶然种的拟合结果表明典型群落和踏头群落表现一致,即Lognormal模型对所有种拟和是最好的,而Power模型对偶然种的拟和是最好的,同时,Lognormal对典型草甸群落的中间种拟和也是最好。从中可以看出典型草甸群落和踏头群落尽管在表现形式上不同,但是群落的内部仍存在相似的联系,可能跟相似物种的作用有关。 根据湿地表观类型、植被水分状态和航片判别能力,结合实地调查,采用监督分类的方法将锡林河流域的湿地划分为低湿地草甸、盐化草甸和沼泽三种类型。自1984年以来20多年的时间中,锡林河流域的湿地发生了巨大的变化。尽管总的面积没有太大变化,但是湿地类型发生转化。中上游的低湿地草甸面积减少8.94%,沼泽面积减少30.82%,同时,盐化草甸的面积增加了15.98%。增加的盐化草甸主要是另外两种湿地类型转化而成的,中游水库截流,加速中下游草甸的盐化是锡林河流域湿地变化的主要原因。利用GIS技术依据探讨不同湿地的空间变化,分析沙化对湿地变化的影响,结果表明:沙化只对少数湿地有影响,发育良好的湿地即使处在相对强烈的沙化环境下,仍能保持不变。接着,分析了人类直接干扰对湿地变化的影响,缓冲区居民点分析结果表明:近20年来,位于湿地周边的居民点分布格局发生显著的变化。1980年代,居民点分布在盐化草甸周边的最多,到2004年,居民点在沼泽草甸分布数量为最多,该类湿地水、草和资源最为丰富,人类直接的干扰最大,进而转化成另外两类,减少面积最大。低湿地草甸是物种丰富,结构复杂的一种湿地,抗干扰能力强,恢复能力也强,因此相对的变化面积较小。以锡林浩特市水库上下游的湿地植被物种和群落结构的变化,证明了水量减少是湿地数量、结构改变的直接影响因子。

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Estimates of length-weight relationship in Otolithes cuvieri justify separate equations for males (log W =-5.0100+3.1365 log L) and females (log W =-5.2000+3.1006 log L). Relative condition factor "Kn" was found to be 0.877-1.946 in males and 0.879-1.328 in females. High "Kn" values during March to September at 180-220 mm TL in either sexes are indicative of the maturation of gonads. Separate equations for length-weight relationship are also justified for males (log W = -5.1126 + 3.0690 log L) and females (log W = -5.6400 + 3.3070 log L) of Johnius elongatus . "Kn" values were found to be 0.924-1.894 for males and 0.894-1.087 for females. High "Kn" values during January-May and August-September at 130 mm TL onward are indicative of gonadal maturation.

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The gonads of Otolithes cuvieri and Johnius elongatus are described in seven maturity stages. O. Cuvieri spawns once a year from April to September as evidence by ova diameter frequency distribution and GSI values. 50% maturity is attained at 210mm TL in males and 200mm TL in females. Fecundity ranged from 2387 to 104379 with a mean value of 33502. Log-Log relationship between fecundity and total lenght, body weight and ovary weight were determined. An overall sex ratio of 1.54:1.00 was unequal in favour of males. Johnius elongatus spawns twice a year from January-February to Aprile-May and from August to October as evidence by ova diameter frequency distribution and GSI values. 50% maturity is attained at 140-143mm TL in both sexes. Fecundity ranged from 4238 to 167669 with a mean value of 42818. Log-Log relationship between fecundity and total lenght, body weign and ovary weight were determined. An overall sex ratio of 1.00:1.20 was unequal in favour of females.

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During the present study fecundity of 30 ovaries of Euryglossa orientalis was determined. Fecundity ranged from 9922 to 8389 with a mean value of 36361. The number of ova in the dorsal lobe was less than that of ventral lobe. Log-log relationship between fecundity and total length, fish weight, ovary weight and ovary length were determined.

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The length-weight relationship of T. thalassinus differed in the sexes and, therefore separate equations were obtained; for males log W = -5.1728 4- 3.0495 log L; and for females log W = -5.7456 + 3.2798 log L. The spawning period of this species appears to be restricted to a short period from October to November. Fecundity has been found to range from 33 to 55 mature eggs in specimens of the size range 421-564mm. The sex ratio of males to females was 1.8:1. T. thalassinus is a bottom carnivore, crustaceans ranking first in food followed by fishes, mollusc and polychaetes.

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Culture of Magur, Clarias batrachus on an experimental basis was carried out for a total of 159 days in 6 earthen ponds each of 0.02 ha in area, singly in 2 ponds and in combination with Rohu, Labeo rohita in 4 ponds. Three different artificial feeds were used. Growth of Magur varied from 89 to 110 and survival form 93 to 100%. Out of the 3 feeds used, feed formulation 2 yielded better results. Length-weight relationship parameters were found as log W=0.4979067+1.878346 log L; -1.1116438+2.3511497 log L; and -1.238157+2.433125 log L indicating growth to be not isometric. Relative condition factor (K u) was close to or higher than 1.0 only in fishes higher than 200 mm of total length; K. values which were less than 1.0 up to January, reached values greater than 1.0 by March-April. Condition appears to be influenced by spawning rather than feeding.

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The study was conducted to investigate the efficacy of chlorine and UV irradiation in disinfecting aquarium effluent. A non-agglutinating, a virulent strain of Aeromonas salmonicida (NCIMB 11 02) was used as the test organism. Effluents from a fish tank were inoculated with a suspension of test organisms and subsequently treated with different concentrations of hypochlorite and UV irradiation separately and simultaneously. When used alone, 1.0 ppm hypochlorite reduced the viable cell count from 6.5 log to 3.0 log within 20 minutes of contact period. On the other hand, when used in combination with UV irradiation only 0.5 ppm hypochlorite exerted the same bactericidal effect within the same contact period as was observed with 1.0 ppm hypochlorite alone. This result indicated that required dose of disinfectant for the disinfection of aquarium effluents can be considerably reduced when it is used in combination with UV irradiation.

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Growth and mortality rate of Cyprinus carpio (Linnaeus) under five different dietary conditions were studied in fifteen floating net cages in ponds of the Bangladesh Agricultural University Campus, Mymensingh. Growth rate was found to vary under different dietary conditions. The feed with mixture of 25% rice bran, 5% wheat bran, 30% linseed oil cake and 40% water hyacinth leaf meal exhibited the highest growth rate. The gain of log of body weight per unit increase of log of total length was significant. Significant survivals of the fishes were found.

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The length-weight relationship and condition factor of Mylopharyngodon spiceus were determined. The result of the study showed the dependence of weight (W) on the total length (L) in the following form: W= 0.006L(super 3.156) or in the logarithmic form Log W=- 2.1851 + 3.156 Log L. Standard errors of length and weight were 0.674 cm and 3.214 g respectively. The co-efficient correlation "r" was found to be 0.972 which indicated that the relationship between length and body weight of the fish was highly significant. The t-test also indicated that the correlation between length and weight was significant. The range and mean value of condition factor (K) were 0.865 to 1.041 and 0.958 respectively.