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Short Day Lengths (short + day_length)
Selected AbstractsAffective and Adrenocorticotrophic Responses to Photoperiod in Wistar RatsJOURNAL OF NEUROENDOCRINOLOGY, Issue 2 2008B. J. Prendergast The present study tested the hypothesis that seasonal intervals of exposure to modest changes in photoperiod, typical of those experienced by humans living in temperate latitudes (10,14 h light/day), engage changes in emotional behaviour of Wistar rats, a commonly-used animal model for investigations of affective physiology. Short day lengths (, 12 h light/day) induced behavioural despair in a forced-swim test, exploratory anxiety in an open field arena, and anhedonia in a two-bottle sucrose preference task, relative to longer day lengths. Plasma adrenocorticotrophic hormone was lower in short-day relative to long-day rats, but testosterone and corticosterone concentrations were comparable across treatments. In common with animals that engage reproductive responses to day length, reproductively nonresponsive mammals such as Wistar rats exhibit changes in affective state following small changes in day length. Wistar rats may provide an animal model for the study of seasonal mood regulation because the neuroendocrine, depressive, anxious and anhedonic responses of Wistar rats to short days bear similarities to those observed in some human populations. Standard laboratory husbandry practices (exposure to a 12 : 12 h light/dark cycle) may inadvertently deliver a chronic background depressive and anxiogenic stimulus. [source] Sex Differences in Feeding Activity Results in Sexual Segregation of Feral GoatsETHOLOGY, Issue 5 2008Robin I. M. Dunbar Sexual segregation is common in ungulates. We show, in a high latitude population of feral goats where behavioural synchrony and fission rates have been shown to be the best explanation for segregation, that it is differences explicitly in the feeding time requirements of the two sexes (but not those for other activities) that best explains the variations in monthly frequencies of segregation. However, this effect is less marked during winter months when short day length forces the time budgets of the two sexes to converge. We argue that the various explanations for segregation can best be interpreted as separate factors in a multivariate model in which species- and habitat-specific weightings influence the relative importance of these variables, and thus the likelihood that segregation will occur. [source] Effect of day length on development and reproductive diapause in Nysius huttoni White (Heteroptera, Lygaeidae)JOURNAL OF APPLIED ENTOMOLOGY, Issue 8 2004X. Z. He Abstract:,Nysius huttoni White is endemic to New Zealand and an important pest of wheat and brassica crops. To provide critical information for pest forecast, management and quarantine inspection, we investigated the effect of day length on the growth, development and reproductive diapause of this pest under a series of photoperiodic regimes: 16 : 8, 14 : 10, 12 : 12 and 10 : 14 h [light : dark (L : D)]. Long day lengths [16 : 8 and 14 : 10 h (L : D)] promote a continuous lifecycle while short day lengths [12 : 12 and 10 : 14 h (L : D)] slow up the growth and development, prolong the pre-mating period, and induce the reproductive diapause. The absence of oviposition for approximately 30 days is recognized as the criterion for N. huttoni reproductive diapause definition. When all life stages are kept under the short day length conditions, only 60,73% of females enter reproductive diapause; if the exposure to short day lengths starts in late instar nymphs, 100% of females enter reproductive diapause. If only adults experience short day lengths, does diapause incidence fall in between, with up to 26% of females laying a few eggs before entering diapause. The critical photoperiod for the induction of reproductive diapause falls between 13.3 : 10.7 and 13.5 : 10.5 h. [source] 160 Copepodology for the Phycologist with Apologies to G. E. HutchensonJOURNAL OF PHYCOLOGY, Issue 2003P. A. Tester Heterocapsa triquetra is one of the most common bloom forming dinoflagellates found in estuaries and near shore regions around the world. In order to bloom, H. triquetra optimizes a suite of factors including low grazing pressure, increased nutrient inputs, alternative nutrient sources, and favorable salinity and hydrodynamic conditions, as well as the negative factors of temperature-limited growth, short day lengths, and periods of transient light limitation. The prevailing environmental conditions associated its wintertime blooms are largely the result of atmospheric forcing. Low-pressure systems moved through coastal area at frequent intervals and are accompanied by low air temperatures and rainfall. Runoff following the rainfall events supplies nutrients critical for bloom initiation and development. Heterocapsa triquetra blooms can reach chl a levels >100 mg L,1 and cell densities between 1 to 6×106 L,1. As the blooms develop, nutrient inputs from the river became insufficient to meet growth demand and H. triquetra feeds mixotrophically, reducing competition from co-occurring phytoplankton. Cloud cover associated with the low-pressure systems light limit H. triquetra growth as do low temperatures. More importantly though, low temperatures limit micro and macrozooplankton populations to such an extent that grazing losses are minimal. [source] Effects of temperature, irradiance and photoperiod on growth and pigment content in some freshwater red algae in culturePHYCOLOGICAL RESEARCH, Issue 2 2001Marcelo Ribeiro Zucchi SUMMARY The responses of relative growth rate (% day-1) and pigment content (chlorophyll a, phycocyanin and phycoerythrin) to temperature, irradiance and photoperiod were analyzed in culture in seven freshwater red algae: Audouinella hermannii (Roth) Duby, Audouinella pygmaea (Kützing) Weber-van Bosse, Batrachospermum ambiguum Montagne, Batrachospermum delicatulum (Skuja) Necchi et Entwisle,,Chantransia' stages of B. delicatulum and Batrachospermum macrosporum Montagne and Compsopogon coeruleus (C. Agardh) Montagne. Experimental conditions included temperatures of 10, 15, 20 and 25°C and low and high irradiances (65 and 300 ,mol photons m,2 s,1, respectively). Long and short day lengths (16:8 and 8:16 LD cycles) were also applied at the two irradiances. Growth effects of temperature and irradiance were evident in most algae tested, and there were significant interactions among treatments. Most freshwater red algae had the best growth under low irradiance, confirming the preference of freshwater red algae for low light regimens. In general there was highest growth rate in long days and low irradiance. Growth optima in relation to temperature were species-specific and also varied between low and high irradiances for the same alga. The most significant differences in pigment content were related to temperature, whereas few significant differences could be attributed to variation in irradiance and photoperiod or interactions among the three parameters. The responses were species-specific and also differed for pigments in distinct temperatures, irradiances and photoperiods in the same alga. Phycocyanin was generally more concentrated than phycoerythrin and phycobiliproteins were more concentrated than chlorophyll a. The highest total pigment contents were found in two species typical of shaded habitats: A. hermannii and C. coeruleus. The expected inverse relationship of pigment with irradiance was observed only in C. coeruleus. In general, the most favorable conditions for growth were not coincident with those with highest pigment contents. [source] | ||||||||||