Development of the fibre population in N-type sheep.

1954 ◽  
Vol 5 (3) ◽  
pp. 490 ◽  
Author(s):  
AS Fraser ◽  
JM Ross ◽  
GM Wright

Several types of follicles occur in the skin of sheep. These have been shown to differ in the types of fibres they form, when these are classified on shape of tip curl, occurrence of medulla, size of crimps, rate of growth, and frequency of shedding as kemps. Fibre type frequency distributions have been analysed. In non-N-type, halo-hairs and fibres with a sickle-shaped tip, forming the pre-curly-tip group, can only be formed in primary central follicles, which ordinarily all grow pre-curly-tip fibres, although occasionally these follicles produce curly-tip fibres. The primary lateral follicles all grow curly-tip fibres which grow also in the early secondary follicles. The late secondary follicles grow fibres with a tip of indefinite shape, histerotrichs. In N-type sheep primary centrals always form pre-curly-tip fibres, with the reservation that in Plateau arrays with few or no fibres classed as supersickle- fibres it is believed that some fibres called hairy-tip–curly-tip fibres grow in primary central follicles; primary laterals form hairy-tip–curly-tip fibres save in some N/+ lambs; and the secondaries form curly-tip and histerotrich fibres. The primary follicles are strongly affected by the N and nr genes, which have much less effect, if any, on the secondaries. Fibre growth rates and consequently size of crimps, and frequency of occurrence of brown fibres and of shedding as kemps, are all higher in primary than in secondary fibres in N-type sheep, and in N-type than in non-N-type, showing that the N and nr genes affect the primary more than the secondary follicles in these characteristics.

1974 ◽  
Vol 11 (03) ◽  
pp. 437-444 ◽  
Author(s):  
Benoit Mandelbrot

Luria and Delbrück (1943) have observed that, in old cultures of bacteria that have mutated at random, the distribution of the number of mutants is extremely long-tailed. In this note, this distribution will be derived (for the first time) exactly and explicitly. The rates of mutation will be allowed to be either positive or infinitesimal, and the rate of growth for mutants will be allowed to be either equal, greater or smaller than for non-mutants. Under the realistic limit condition of a very low mutation rate, the number of mutants is shown to be a stable-Lévy (sometimes called “Pareto Lévy”) random variable, of maximum skewness ß, whose exponent α is essentially the ratio of the growth rates of non-mutants and of mutants. Thus, the probability of the number of mutants exceeding the very large value m is proportional to m –α–1 (a behavior sometimes referred to as “asymptotically Paretian” or “hyperbolic”). The unequal growth rate cases α ≠ 1 are solved for the first time. In the α = 1 case, a result of Lea and Coulson is rederived, interpreted, and generalized. Various paradoxes involving divergent moments that were encountered in earlier approaches are either absent or fully explainable. The mathematical techniques used being standard, they will not be described in detail, so this note will be primarily a collection of results. However, the justification for deriving them lies in their use in biology, and the mathematically unexperienced biologists may be unfamiliar with the tools used. They may wish for more details of calculations, more explanations and Figures. To satisfy their needs, a report available from the author upon request has been prepared. It will be referred to as Part II.


1981 ◽  
Vol 32 (4) ◽  
pp. 605 ◽  
Author(s):  
CF Chubb ◽  
IC Potter ◽  
CJ Grant ◽  
RCJ Lenanton ◽  
J Wallace

The age structure, growth rates and movements of M. cephalus and A forsteri in the Swan-Avon river system have been investigated using data obtained from beach seining and gill netting carried out between February 1977 and June 1980. Length-frequency data and scale readings show that the populations of both species consist predominantly of 0+ and 1 + fish. From the times when the smallest fry (20-30 mm) were present in the lower part of the river system, and from the condition of the gonads of older fish, the breeding seasons of the sea and yellow-eye mullets have been estimated as extending from March to September and from March to August respectively. The bimodality or polymodality exhibited by the length-frequency distributions for the 0 + year classes suggest that in both species groups of individuals spawn at slightly different times. The range of mean total lengths and weights of animals caught in May near the end of the first year of life was 178-222 mm and 64-119 gin M. cephalus and 136-154 mm and 19-30 g in A. forsteri, which shows that the growth of each of these two species of mullet is relatively very rapid in the Swan-Avon river system. 1 + and 2 + fish tend to leave the estuary for varying periods. Although 0+ fish of both species utilized the shallow banks of the estuary throughout the year. the sea mullet moved further upstream and were not as consistently abundant in the lower estuary. Since 0+ yellow-eye mullet 40-100 mm long were also abundant in marine coastal waters between January and May. and sea mullet of comparable age were rarely observed in these regions, it would appear that M. cephalus is the more estuarine-dependent of the two species. Commercial catches of M. cephalus were greater than those of A. forsteri. This feature can be related in part to the much faster growth rate of M. cephalus, which results in a larger proportion of its youngest year classes reaching the minimum legal size for capture prior to the time when they leave the estuary in large numbers.


1930 ◽  
Vol 7 (2) ◽  
pp. 165-174
Author(s):  
M. A. TAZELAAR

Linear measurements of certain appendages and the carapace of P. carcinus were made and plotted in various ways. The following conclusions were drawn: 1. The cheliped shows heterogonic growth in both male and female, but more markedly in the male, the values of k being: male 1.8 and female 1.48 2. The pereiopods in both male and female are slightly heterogonic. The relative growth rates are graded from p3 to p5, that of p3 being slightly greater than that of p5 3. Of the ordinary pereiopods the rate of growth of p1 is the smallest in the male, but the largest in the female. 4. The difference between the rates of growth of p1 and p3 in male and female is greatest where the rate of growth in the heterogonic organ, the cheliped, is most excessive in the male. 5. The growth of the 3rd maxilliped is slightly negatively heterogonic, the value of k in the male being 0.93 and in the female 0.95. Hence there seems to be a correlation between the marked heterogony in the cheliped on the growth rate of neighbouring appendages. In those immediately posterior to the cheliped the growth rate is increased and in those anterior decreased.


<em>Abstract</em>.—To measure secondary productivity of mangrove systems, we estimated the abundance (individuals/m<sup>2</sup>) and mass increment (g/month) of the two bivalve species: the black ark <em>Anadara tuberculosa </em>and palmate oyster <em>Saccostrea palmula</em>. Mass increments were based on individual growth rates derived from length-frequency distributions analyses. Samples were collected at three mangrove estuaries in a sand barrier at Ensenada de La Paz from August 2007 to July 2009. The average abundance was 1.27 individuals/m<sup>2</sup> for black ark and 510 individuals/m<sup>2</sup> for palmate oysters. Estimated growth rates were 3.67 g/month for black ark and 0.18 g/month for palmate oysters. The average secondary productivity of the black ark was 4.51 g•m<sup>-2</sup>•month<sup>-1</sup> and peaked during the spring, while for the palmate oyster <em>Saccostrea palmula </em>it was 97.9 g•m<sup>-2</sup>•month<sup>-1</sup>, with peak productivity recorded during the summer. The findings of this investigation constitute a necessary element for establishing a baseline to evaluate the consequences of the various natural and anthropogenic pressures that the mangrove systems of El Mogote of La Paz Bay, Baja California Sur, Mexico.


1962 ◽  
Vol 40 (5) ◽  
pp. 863-869 ◽  
Author(s):  
Charles J. Krebs ◽  
I. McT. Cowan

A study of the growth of reindeer fawns was carried out during the spring and summer of 1958 in the Mackenzie Delta, N.W.T. Growth rates were obtained for four fawns under natural conditions. Early growth of the fawns (0–2 months) can usually be divided into three phases and some possible reasons for this are given. The rate of growth of reindeer fawns is slightly less than that of Columbian black-tailed deer fawns. Some weight data for different sex and age classes of wild reindeer are given, and it is concluded that the Mackenzie Delta reindeer do not differ greatly in growth pattern from Russian reindeer.


2003 ◽  
Vol 24 (1) ◽  
pp. 13-26 ◽  
Author(s):  
Christopher Beachy ◽  
Richard Bruce

AbstractWe sampled Desmognathus quadramaculatus, one of the largest species of plethodontid salamanders in eastern North America, from a population exhibiting extremely small adult body sizes in the Bald Mountains of North Carolina (USA). In order to test the hypothesis that miniaturization in desmognathine salamanders is due to early metamorphosis and maturation, we estimated ages and sizes at metamorphosis and maturation. Analysis of size-frequency distributions suggests that most larvae metamorphose after 24 months, with the remainder metamorphosing after 36. The minimum age of sexually mature individuals in the summer months is estimated to be 4 years in males and 5 years in females; some may mature 1 year earlier. This is earlier than other reliable estimates of age at maturation in D. quadramaculatus, and appears to account for the small size of the species at this locality. Larval and juvenile growth rates are within the range of growth rates of other populations. As in other populations of D. quadramaculatus, males are smaller than females at maturation, but grow to larger sizes. Estimates of clutch sizes based on dissection of gravid females are relatively low. The other species of salamanders in this community do not appear to be miniaturized.


1957 ◽  
Vol 49 (2) ◽  
pp. 184-199 ◽  
Author(s):  
I. A. M. Lucas ◽  
A. F. C. Calder

1. One hundred and sixty-eight pigs were used in four experiments to test the value of including antibiotics and copper sulphate, either as separate supplements or together in rations for growing pigs. Procaine penicillin was added at the rate of 5·36 mg./lb. diet and Aureomycin (in Aurofac 2 A) at 8·03mg/lb. and CuSO4. 5H2O as 0·1% of the diet.2. During the growing period in Exp. 1, pigs fed diets supplemented with copper sulphate or procaine penicillin grew 9 and 3% faster respectively than the controls. Pigs fed a diet containing both supplements grew 22% faster than the controls. During the finishing period there was an outbreak of virus pneumonia and the within-treatment variability was large. There were no significant differences between treatments during this period, although pigs fed the supplemented diets tended to grow more slowly than the controls. Over the total experimental period pigs fed the diet supplemented only with copper sulphate grow 2% faster than the controls, and those fed the diet supplemented with both procaine penicillin and copper sulphate grew 4% faster than the controls, but these small average improvements were not statistically significant. In Exp. 1 treatment differences in food conversion efficiencies paralleled those for growth rates. Killing-out percentages were higher when pigs were fed the copper-supplemented diets, and lower when procaine penicillin was fed. The area of ‘eye’ muscle was increased by adding procaine penicillin to the diet.3. During the growing period in Exp. 2, pigs fed diets supplemented with copper sulphate or with both procaine penicillin and copper sulphate grew 8 and 9% faster, respectively, than the controls. The addition of procaine penicillin had no significant effect when added as a single supplement or in conjunction with copper sulphate. During the finishing period pigs fed diets supplemented with copper sulphate, procaine penicillin, or both copper sulphate and procaine penicillin grew 5, 3 and 10% faster, respectively, than the controls, while over the total experimental period they grew 4, 0 and 9% faster, respectively.4. Some pigs fed the copper-supplemented diets during the growing period in Exp. 2 were fed diets with no copper added over the finishing period. During this latter period the pigs grew at about the same speed as the controls, and significantly more slowly than those pigs which continued to receive copper sulphate. Thus, the average growth rates over the total experimental period were significantly slower by 3–7% when copper was omitted after 100 lb. than when it was fed to the pigs throughout the entire experiment.5. In Exp. 2, as in Exp. 1, treatment differences in efficiency of food conversion paralleled those for growth rates. A higher rate of growth was always accompanied by an improvement in efficiency of food conversion, with about the same percentage difference between treatments. Indeed, changes in rate of growth were probably dependent upon changes in efficiency of food conversion, since all pigs were fed to the same scale based on live weight.6. The treatment differences in killing-out percentage and area of eye muscle observed in Exp. 1 were not confirmed in Exp. 2. There were no differences in carcass quality measurements attributable to the treatments imposed in Exp. 2.7. The livers of pigs fed diets containing copper sulphate during both the growing and finishing periods had, on average, about eighteen times the concentration of copper found in the controls. When the copper sulphate supplement was fed only during the growing period the liver copper concentrations were, on average, about four times those of the controls. However, the variation between the individual values was very large in all groups fed copper sulphate. This variation may have been caused partly by sampling errors if copper is not distributed evenly throughout the liver.


1955 ◽  
Vol 46 (3) ◽  
pp. 307-319 ◽  
Author(s):  
I. A. M. Lucas ◽  
A. F. C. Calder

1. Pigs housed in both a good and a bad piggery were kept to a medium plane of feeding on diets with and without a procaine penicillin supplement. Antibiotic improved neither efficiency nor rate of growth in either piggery during the period from weaning to 100 lb. live weight, nor from then to slaughter at 200 lb. live weight. The average temperatures during the first half of the experiment were 43 and 51° F. in the bad piggery and in the sleeping pens of the good piggery respectively. During the second half of the experiment these averages were 54 and 58° F. respectively.2. Between weaning and 100 lb. live weight, pigs housed in the bad piggery grew 6% more slowly and 5% less efficiently than in the good piggery, but although the growth rates fitted in well with previous observations, neither difference was statistically significant in this experiment.3. Between 100 and 200 lb. live weight pigs housed in the good piggery grew 3% less efficiently than in the bad piggery, but there was no difference in rate of growth. The difference in efficiency was statistically significant.4. Carcasses from pigs housed in the good piggery were fatter than from pigs housed in the bad piggery. These fatter pigs also had higher killing-out percentages.5. Although dietary antibiotic supplement had no effect upon growth rates or carcass measurements, it resulted in higher killing-out percentages.


Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 363-363
Author(s):  
A N Sokolov ◽  
W H Ehrenstein ◽  
M A Pavlova

Given equal frequencies of occurrence of stimuli, identical velocities receive higher or lower ratings depending on whether slow or fast velocities happen to occur on the early trials of a run (Ehrenstein and Sokolov, 1996 Perception25 Supplement, 34 – 35). When stimuli vary in their frequency of occurrence, this presentation-order effect might enhance or substitute the well-known frequency effect (Parducci's range - frequency theory) on category ratings. The aim of the present study was to contrast these two effects for ratings of visual velocities. Two groups of observers had to rate five stimulus velocities (3, 4.5, 6, 7.5, and 9 deg s−1) of a single luminous dot using three categories (slow, medium, fast). Respective frequencies of occurrence for these velocities were either 4 - 4 - 8 - 14 - 20 (group 1, negative skewing for frequency) or 20 - 14 - 8 - 4 - 4 (group 2, positive skewing). The quasi-random presentation order of each set, on the contrary, corresponded to either positively skewed (group 1) or negatively skewed (group 2) frequency distributions. No significant differences in the ratings of two groups (other than a slight preference for the presentation-order effect beyond 6 deg s−1) were found, as if the presentation order and frequency effects had cancelled each other. This suggests that the presentation order of velocities is at least as powerful as their frequency of occurrence. Lack of agreement between our results and predictions of computer-simulated Haubensak's consistency model as well as of Parducci's range - frequency theory requires a model which accounts for an interaction of the two effects.


Weed Science ◽  
2009 ◽  
Vol 57 (3) ◽  
pp. 248-255 ◽  
Author(s):  
Xin-Ming Xie ◽  
You-Zhi Jian ◽  
Xiao-Na Wen

The temporal dynamics of spatial heterogeneity was studied for the weed communities in a seashore paspalum turf with the use of a power-law model. Surveys were conducted in January, March, May, July, September, and November in 2007. In every survey, we set 100 quadrats (50 by 50 cm) referred to as L quadrats on a 50-m line transect at the same position in the turf. Each L quadrat was then divided into four S quadrats (25 by 25 cm) and all plant species occurring in each of these S quadrats were identified and recorded. These data were summarized into frequency distributions and the percentage of S quadrats containing a given species, and the variance of each species was estimated. The power law was used to evaluate the spatial heterogeneity (δ) and frequency of occurrence (p) for each species in the weed communities in six survey months. The results showed that weeds emerged more frequently in the summer–spring season than in winter–autumn, and the spatial heterogeneity was much higher in summer–spring than winter–autumn, especially in summer. The Shannon–Wiener diversity indexes (H') from large to small were July (5.9202) > May (5.6775) > September (5.6631) > March (5.5727) > January (5.1742) > November (4.9668). Likewise, the spatial heterogeneity index (δc) of the whole community was also different in different months. The biggest δc (0.2790) was in July, and the smallest (0.1811) in November. Meanwhile, manilagrass had a high p (= 1.0), indicating that it occurred in all S quadrats in every weed community of every month. However, the turfgrass, seashore paspalum, only emerged in March, May, July, and November, and possessed a low p, indicating the seashore paspalum turf has been naturally replaced by manilagrass.


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