Laboratory Studies on Effects of Temperature and Delayed Initial Feeding on Development of Striped Bass Larvae

Author(s):  
Bruce A. Rogers ◽  
Deborah T. Westin
2007 ◽  
Vol 32 (4) ◽  
pp. 808-817 ◽  
Author(s):  
Stephen S. Cheung

Over the past decade, research interest has risen on the direct effects of temperature on exercise capacity and tolerance, particular in the heat. Two major paradigms have been proposed for how hyperthermia may contribute to voluntary fatigue during exercise in the heat. One suggests that voluntary exhaustion occurs upon the approach or attainment of a critical internal temperature through impairment in a variety of physiological systems. An alternate perspective proposes that thermal inputs modulate the regulation of self-paced workload to minimize heat storage. This review seeks to summarize recent research leading to the development of these two models for hyperthermia and fatigue and explore possible bridges between them. Key areas for future research and development into voluntary exhaustion in the heat include (i) the development of valid and non-invasive means to measure brain temperature, (ii) understanding variability in perception and physiological responses to heat stress across individuals, (iii) extrapolating laboratory studies to field settings, (iv) understanding the failure in behavioural and physiological thermoregulation that leads to exertional heat illness, and (v) the integration of physiological and psychological parameters limiting voluntary exercise in the heat.


Plant Disease ◽  
2010 ◽  
Vol 94 (1) ◽  
pp. 54-60 ◽  
Author(s):  
L. L. Granke ◽  
M. K. Hausbeck

Controlled laboratory studies were undertaken to determine the effects of water temperature (2, 9, 12, 19, 22, and 32°C), inoculum concentration (1 × 102, 1 × 103, 5 × 103, 1 × 104, 2 × 104, and 4 × 104 zoospores/ml), and zoospore suspension age (0, 1, 3, and 5 days old) on infection of pickling cucumbers (Cucumis sativus) by Phytophthora capsici. Zoospore motility and mortality in response to commercial algaecides were also investigated. Cucumbers became infected at all temperatures tested, except 2°C, and the highest infection incidence was observed for cucumbers incubated in suspensions held at ≥19°C. Fewer fruit (<40% at ≥19°C, 0% at ≤12°C) became infected when water contained 1 × 102 zoospores/ml. Almost 100% of fruit were infected when water contained ≥5 × 103 zoospores/ml at temperatures ≥12°C. While the incidence of fruit infection declined with the zoospore suspension age, infection still occurred when 5-day-old suspensions were used. Commercial algaecides inhibited zoospore motility and caused significant zoospore mortality in laboratory assays, and show promise for treatment of infested irrigation water. Avoidance of infested irrigation water throughout the growing season is warranted until effective and economically acceptable water treatments are developed for field use.


1979 ◽  
Vol 36 (3) ◽  
pp. 335-342 ◽  
Author(s):  
N. H. Anderson ◽  
Kenneth W. Cummins

Benthic species are partitioned into functional feeding groups based on food-acquiring mechanisms. Effects of food quality on voltinism, growth rate, and size at maturity are demonstrated for representatives of gougers and shredders, collectors, and scrapers. Food quality for predators is uniformly high, but food quantity (prey density) obviously influences their life histories. A food switch from herbivory to predation, or some ingestion of animal tissues, in the later stages is a feature of the life cycle of many aquatic insects. Temperature interacts with both food quality and quantity in effects on growth as well as having a direct effect on control of metabolism. Thus further elaboration of the role of food in life history phenomena will require controlled field or laboratory studies to partition the effects of temperature and food. Key words: aquatic insects, feeding strategies, functional groups, life histories


1963 ◽  
Vol 95 (8) ◽  
pp. 878-881 ◽  
Author(s):  
G. E. Swailes

AbstractLaboratory studies showed that eggs of Hylemya brassicae required 34 and 67 day-degrees at 10° and 30 °C. and 49 day-degrees at 15°, 20°, and 25 °C. to hatch when 7.2 °C. was used as the threshold temperature for development. Factors that were lethal to the eggs were temperatures above 41 °C. for one hour and periods of desiccation of 1, 1, 2, 5, and 9 days at 30°, 25°, 20°, 15°, and 10 °C., respectively.First-instar larvae survived for approximately 2, 3, 5, and 8 days without food at temperatures of 20°, 15°, 10°, and 5 °C. Starvation for 24 hours immediately after hatching reduced initiation of feeding only slightly.


1955 ◽  
Vol 3 (3) ◽  
pp. 295 ◽  
Author(s):  
LF Hitchcock

Laboratory studies of the effects of temperature and relative humidity on the non-parasitic stages of the cattle tick, Boophilus microplus (Canestrini), are described. The pre-oviposition period ranged from 19-39 days at 59-60�F to 2-3 days at 97�F. The duration of oviposition was uninfluenced by relative humidity but varied from a maximum of 44 days at 59�F to a minimum of 4 days at 102�F. The minima at each temperature were exceedingly irregular, due to the deaths of ticks. The number of eggs laid by a female tick was uninfluenced by relative humidity. The peak oviposition mean of 2496 eggs per female occurred at 75�F, fewer eggs being laid at higher and lower temperatures. Daily egg output attained a maximum of 197 at 92�F, but was uninfluenced by relative humidity. The water loss of engorged female ticks was greatly affected by inert dusts and even dusting with a sample of soil chosen at random produced a significant increase in water loss. Developmental period was uninfluenced by order of deposition, but percentage hatch of eggs laid during the last few days of oviposition is lower. Eggs did not hatch at constant relative humidities lower than 70 per cent., but some were able to survive relative humidities lower than this if exposed periodically to a saturated atmosphere. The period of development of eggs varied from a maximum of 146 days at 62�F to a minimum of 14 days at 97�F. Maximum hatch occurred between 85 and 95�F, and at relative humidities above 95 per cent. Exposure of eggs to temperatures below the developmental zero prolonged the period of development merely by the period of exposure. Regular alternation of temperature between the limiting temperatures of 59 and 97�F with a steady rise or fall between the extremes resulted in development at a rate approximately equal to that obtained at constant temperature of 78�F, the arithmetic mean of the above figures. Larval longevity was influenced markedly by temperature and humidity. A maximum of 240 days was recorded at 72�F and 90 per cent. relative humidity. Larvae are able to recoup water losses sustained at low relative humidity by absorption from the atmosphere during subsequent periods of high relative humidity.


1982 ◽  
Vol 6 ◽  
pp. 37-50
Author(s):  
Barun K. Sen Gupta

Benthic foraminifera live in a wide variety of marine habitats, from marshes to abyssal plains. Both epifaunal and infaunal adaptations are present. The distribution of species is controlled by a complex of abiotic and biotic variables of the environment, usually resulting in a depth-zonation of assemblages on continental margins.The composition of the substrate may have a direct or indirect influence on the constitution of the assemblage. Laboratory studies and field observations demonstrate the effects of temperature and salinity variations, particularly on nearshore species. Many calcareous species have algal or chloroplast symbionts; their distribution is partly controlled by light tolerance.Benthic foraminifera are omnivorous and feed mainly by the pseudopodia. Large supply of nutrients, as in areas of upwelling or water mixing, may give rise to large blooms of opportunistic species.Marine marshes of diverse geographic locations support some common species. Deep bathyal or abyssal species are widespread, but dominance patterns are apparently associated with identifiable water masses, although causal relations are unclear.


1999 ◽  
Vol 89 (3_suppl) ◽  
pp. 1217-1229 ◽  
Author(s):  
Ulf Landström ◽  
Kjell Englund ◽  
Bertil Nordstrom ◽  
Anita Stenudd

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