Environmental limitation on fitness: Reproduction of laboratory mice in benign and stressful ("tropical") conditions

SUMMARY: In general, the environment limits the fitness of individual animals, and environmental limitation leads to selection for "optimal", intermediate values for all traits that matter, whether imposed by natural or artificial selection. We compared the reproduction of laboratory mice in a normal and a hot, humid environment to test this claim. Thirty males and 150 females from a non-inbred line adapted to normal conditions were mated twice (the second time after rerandomisation) to produce the experimental animals. Individual experimental mice from each litter were allocated from weaning (3 weeks) either to the normal or hot environment. At 9 to 12 weeks of age these mice were paired, 1 male with 1 female, until the female had a chance to have 2 litters. 354 pairs in the normal and 362 pairs in the hot environment were mated. All living progeny were weaned at 3 weeks. Average values of reproductive traits, phenotypic correlations between traits, and heritability estimates for many traits were found in each environment. Negative correlations (trade-offs) between litter number and weight of individual progeny in both environments demonstrated clearly that fitness was limited even in the normal laboratory situation. All quantitative measures of reproduction were lower in the hot room showing that it was more stressful. Yet size of individual young and their survival was not reduced. This may be an adaptive mechanism restricted to housemice. Lower heritability estimates in first than in second parities for quantitative measures of litter size show that while the mouse is still growing she has fewer resources available for reproduction, making her more susceptible to environmental stress. This challenges accepted wisdom that animal breeders should select their animals when they are young. They are least likely to respond then. We believe that natural selection causes animals always to push their fitness (reproduction and survival of the progeny) against a limit set by their particular environment. Each environment selects animals that optimally allocate environmental resources there. Problems arise when inappropriate genetic settings cause phenotypes to misallocate metabolic resources. In relatively difficult environments productive animals, including successful transgenics, allocate insufficient resources to fitness. ZUSAMMENFASSUNG: Begrenzung der Fitne? durch die Umwelt: Reproduktion von Laborm?usen in günstigen und schwierigen ("tropischen") Bedingungen Im Normalfall soll die Umwelt der Fitne? eine obere Grenze setzen. Diese Begrenzung führt zu Selektion auf mittlere "Optimalwerte" bei alien wichtigen Merkmalen. Wir untersuchten die Fortpflanzung von Laborm?usen in entweder normaler oder hei?er Umwelt. Aus einer an erstere angepa?ten, nichtingezüchteten Linie wurden 30 M?nnchen mit 150 Weibchen zweimal verpaart (beim zweiten Mal neu randomisiert) um die Versuchstiere zu erzeugen. Individuen aus jedem Wurf wurden zufallsm??ig an die zwei Umwelten verteilt, worin sie ab 3 Wochen aufgezogen wurden. Im Alter zwischen 9 und 12 Wochen wurden sie zufallsm??ig 1:1 verpaart bis die Paare Zeit für zwei Würfe gehabt hatten. An 354 und 362 Paaren im normalen und hei?en Zimmer wurden Daten ihrer Reproduktion erhoben. Alle lebendgeborenen Jungen wurden bis 3 Wochen alt verfolgt. In beiden Umwelten wurden Durchschnittswerte der einzelnen Merkmale, ph?notypische Korrelationen wichtiger Merkmale, und Heritabilit?tswerte der Merkmale errechnet. Starke negative Korrelationen zwischen Anzahl der Jungen im Wurf und Gewicht der einzelnen Jungen im Wurf, in beiden Umwelten, zeigen da? Fitne? auch in normalen Laborverh?ltnissen begrenzt war. Alle quantitativen Ma?e der Würfe waren betr?chtlich niedriger im hei?en Raum, was zeigt, da? diese Umwelt mehr Stre? bot. Jedoch die Gr??e und überlebensrate der einzelnen Jungen im hei?en Raum wurden nicht beeintr?chtigt. Diese adaptive Anpassung an schwierige Bedingungen k?nnte einmalig bei Mus musculus sein. Niedere Heritabilit?ten von quantitativen Ma?en der Wurfgr??e im ersten gegenüber dem zweiten Wurf zeigen, da? noch selbst wachsende Weibchen nur wenig Ressourcen für Fortpflanzung einsetzen k?nnen und deshalb mehr von Umweltdruck abh?ngen. Paradoxerweise versuchen Tierzüchter meistens so Jung wie m?glich Tiere zu selektieren, die solcher Selektion auf Reproduktion am wenigsten folgen k?nnen. Diese Situation sollte erneut durchdacht werden. Uns scheint, da? Tiere, weil natürliche Selektion andauernd fortwirkt, jederzeit ihre Fitne? bis an eine obere Grenze, von der Umwelt gesetzt, schieben. Jede Umwelt selektiert Tiere, die ihre metabolischen Ressourcen darin optimal einsetzen. Probleme entstehen, wenn genetische Information Ph?notype erzeugt, die Ressourcen fehl einsetzen. In relativ schwieriger Umwelt haben Leistungstiere, und auch erfolgreiche transgenische Tiere, ungenügend Ressourcen übrig für Fortpflanzung.     

Effects of Neem Seed Derivatives on Brown Planthopper Symbiotes

Populations of intracellular symbiotes declined significantly in brachypterous females of the brown planthopper,Nilaparvata lugens (Stål), which were stressed during nymphal development by caging them on IR20 rice plants treated with 3% neem oil, 5% neem seed kernel aqueous extract, or 10% neem cake aqueous extract. In addition, nymphs grew poorly and symbiote populations in prospective females declined, when reared on rice plants grown in soil treated with neem cake; this indicates systemic action of bioac-tive neem constituents. Addition of custard-apple oil to neem oil did not enhance the inhibitory effects. The effects of neem derivatives on the symbiotes may be either host-mediated — possibly through disturbed neuroendocrine homeostasis, or direct — leading to perturbations of host-symbiote equilibrium.     

Effects of timing and size of daylength change on brown egg laying domestic hens: Plasma luteinising hormone concentration and sexual maturity

1. Brown egg laying pullets were transferred from an 8‐h photoperiod to an 8‐, 10‐, 13‐ or 16‐h photoperiod at 6, 9, 12, 15, 18 or 20–3 weeks of age. Plasma luteinising hormone (LH) concentrations were measured at transfer and 7 and 14 d afterwards.

2. Significant increases in plasma LH occurred following light stimulations at 6, 9 and 12 weeks of age.

3. Changes in LH concentration 7 d after a light increase from 8 h to 8, 10, 13, 16 h were highly correlated with photoperiod length at 9 and 12 weeks of age.

4. Changes in LH were generally poorly correlated with age at sexual maturity, although the reduced influence on age at first egg of a light increase given close to sexual maturity was reflected in minimal LH responses at 18 and 20.3 weeks.     

Prevalence and spatial distribution of bovine tuberculosis in brushtail possums on a forest-scrub margin

Tuberculosis caused by Mycobacterium bovis was diagnosed in 36 of 68 (53%) brushtail possums (Trichosurus vulpecula) trapped in August 1992 from a population of exceptionally low density (trap catch <3%) on a forest-scrub margin in Westland, New Zealand. The prevalence of tuberculosis in possums, based solely on gross lesions, was at least twice that previously recorded in New Zealand, and was about seven times that recorded from the same population in 1980. More male (66%) than female (33%) possums had grossly visible tuberculous lesions. The distribution of infection appeared continuous along the forest-scrub margin. Both stoats (Mustela erminea) and one of six hares (Lepus europaeus occidentalis) trapped were also infected with M. bovis.     

Application of subjective methods to the determination of the likelihood and consequences of the entry of foot-and-mouth disease into New Zealand

New Zealand has a history of continuous freedom from foot-and-mouth disease and relies on a two-tier system of surveillance to maintain this status. The first involves border control procedures and stringent importation standards, and the second is an exotic disease and pest response programme. As part of an economic evaluation comparing the exotic disease and pest response programme against a hypothetical lower grade ;measured response programme subjective judgements of the risks involved were required. Twenty-eight selected animal health professionals, predominantly veterinarians, were posted a questionnaire that used three techniques (single point estimates, three point estimates and elicitation methods) to determine the risk components in a foot-and-mouth disease outbreak. The two key variables were the probability of an outbreak in New Zealand, and the number of secondary properties to which the disease spread during the epidemic. A Delphi conference of ten selected participants then focused mainly on the two key variables, with a second round postal extension to this group for the first variable. The individual data sets were then analysed and combined using a stochastic simulation technique. The final mean probability of an outbreak was about once in 50 years (0.0199). The mean numbers of farms to which disease would spread during an epidemic under the existing exotic disease and pest response programme, a measured response programme which allowed vaccination and a measured response programme which excluded vaccination were estimated to be 61, 478 and 2230 respectively. The policy implications arising from the quantification of these two key variables are that more expenditure on preparedness is justifiable and current resource planning is barely adequate.     

Observations on three outbreaks of Leptospira interrogans serovar pomona infection in lambs

Sickness and deaths associated with leptospirosis were reported in three lamb flocks in the Manawatu region. The clinical, pathological and serological features of Leptospiru interrogans serovar pomona infection are described. The mucous membranes of affected animals were pale and jaundiced. Haemoglobinuria, haemoglobinaemia and centrilobular hepatocellular necrosis were also consistent findings. All clinically sick lambs had very high titres in the microscopic agglutination test for L. pomona. Circumstantial evidence of pigs being the source of infection was found in one of the three cases.     

A formal method of determining the dietary amino acid requirements of laying‐type pullets during their growing period

1. The amino acid requirements of laying type pullets during the growing period can be estimated by measuring the growth of different components of the body and making use of nutritional constants that define the amount of each amino acid that is required for the production of the tissues being formed.

2. In this experiment, carcase analyses of each of three breeds of pullets were conducted at weekly intervals throughout the growth of the pullets, to 18 weeks of age. Measurements were made of body weight, gut‐fill and feather weight, and chemical analyses consisted of water, protein, lipid and ash measurements of both the body and the feathers. Each age group comprised 10 birds of each breed.

3. Gompertz functions accurately estimated the growth of both body protein and feather protein, to 18 weeks of age, from which the rate of growth of these two components of the body could be estimated. The mature weight of pullets was overestimated by the Gompertz growth curve, which may indicate that a pullet ceases to increase in body protein content once sexual maturity has been reached.

4. Using allometric relationships between the chemical components of the body and of feathers, all the components of growth could be estimated from the growth of body protein and feather protein. These components were then added together to determine the growth rate of the body as a whole.

5. The daily amino acid requirements for 4 functions were calculated, namely, those for the maintenance of body protein and feather protein, and for the gain in body protein and feather protein. These requirements were then summed to determine the requirement of pullets on each day of the growing period.

6. Using the ‘effective energy’ system, the amount of energy required by these pullets was calculated for each day of the growing period, from which the desired daily food intake of the pullets could be predicted. By dividing the amino acid requirement by this daily food intake it was possible to determine the concentration of amino acids that would be needed in the diet in order to meet the requirements of a pullet.

7. The results indicate that the ratio between the requirement for lysine and for methionine and cysteine changes dramatically during the growing period, negating the concept of a fixed ratio between all the amino acids during growth.

8. The above process is the first step in determining the optimal feeding programme for a population of pullets of a given genotype. The constraining effects, of the diet being offered and of the environment in which the pullets are housed, on the food intake and growth rate of each pullet have to be estimated, and such a theory can then be expanded to include all the individuals in the population. Only by the use: of simulation models can all these constraining effects be considered simultaneously.     

Regulation of early flowering in Pinus banksiana

Seedlings of three families of jack pine (Pinus banksiana Lamb.) were subjected to 16 combinations of photoperiod, growth environment (outdoors, greenhouse and biotron) and gibberellin (GA(4/7)) treatment. After 14 months, which included two dormancy induction periods, ovulate flowering was observed. There was a strong positive correlation between flowering and seedling height; female flower production was stimulated by both a declining photoperiod during bud development and GA(4/7) treatment; and there was an interaction between GA(4/7) treatment and family, such that the difference in flowering intensity between a late-flowering and an early-flowering family was eliminated by GA(4/7) treatment. The results suggest that the genetic control over the time of onset of flowering, and GA(4/7)-induction of flowering depend on a common mechanism.