Effects of starvation on larval growth, survival and metamorphosis of Ivory shell Babylonia formosae habei Altena et al., 1981 (Neogastropoda: Buccinidae)

Zheng, Huaiping; Ke, Caihuan; Zhou, Shuiqin; Li, Fuxue

doi:10.1016/j.aquaculture.2004.10.010

Cited by 32 publications

(24 citation statements)

References 37 publications

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“…stylized facts empirical evidence feeding during starvation, organisms are able to reproduce animals: Kjesbu et al (1991), Hirche & Kattner (1993) and Kirk (1997) during starvation, organisms are able to grow animals: Stromgren & Cary (1984), Russell & Wootton (1992), Roberts et al 2001, Dou et al (2002, Gallardo et al (2004) and Zheng et al (2005) during starvation, organisms are able to survive for some time animals: Stockhoff (1991) and Letcher et al (1996) bacteria: Kunji et al (1993) growth the growth of isomorphic organisms at abundant food is well described by the von Bertalanffy growth curve Putter (1920) andvon Bertalanffy (1938) animals: Frazer et al (1990), Strum (1991), Chen et al (1992), Schwartz & Hundertmark (1993), Ferreira & Russ (1994) and Ross et al (1995) for different constant food levels the inverse von Bertalanffy growth rate increases linearly with ultimate length Putter (1920) animals: Summers (1971), Galluci & Quinn (1979), Weindruch et al (1986), Hubert et al (2000) and Kooijman (2010, pp.48) many species do not stop growing after reproduction has started, i.e. they exhibit indeterminate growth Heino & Kaitala (1999) and Kozlowski (1996) animals: Shine & Iverson (1995) and Jorgensen & Fiksen (2006) holometabolic insects are an exception foetuses increase in weight approximately proportional to cubed time Huggett & Widdas (1951) animals: Huggett & Widdas (1951) and Zonneveld & Koo...…”

Section: (D) Acquisition Homeostasismentioning

confidence: 99%

Dynamic energy budget theory restores coherence in biology

Sousa¹,

Domingos²,

Poggiale

et al. 2010

Phil. Trans. R. Soc. B

220

185

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We present the state of the art of the development of dynamic energy budget theory, and its expected developments in the near future within the molecular, physiological and ecological domains. The degree of formalization in the set-up of the theory, with its roots in chemistry, physics, thermodynamics, evolution and the consistent application of Occam's razor, is discussed. We place the various contributions in the theme issue within this theoretical setting, and sketch the scope of actual and potential applications.Keywords: dynamic energy budget theory; biology; metabolism; ecology; evolution; energetics REACHING OUT FOR GENERALITYIn physics, there is a quest for a unified theory. Physical theories have a broad spectrum of application, a strong mathematical background and are subject to numerous empirical tests. By contrast, in biology, mathematical theory has played a secondary role because biology is frequently seen as a science of exceptions and particular cases, with little interest in abstraction and generalization. Exceptions are the research being done in the fields of theoretical biology and mathematical biology. However, theoretical and mathematical biology have frequently been carried out without a concern for empirical testing. When this concern appears, models are of narrow application, reducing their theoretical breadth. The dynamic energy budget (DEB) theory starts from the Dutch tradition of theoretical and mathematical biology, but couples it with a fundamental concern in producing general theory that is subjected to careful empirical testing.DEB theory aims to capture the quantitative aspects of metabolism at the individual level for organisms of all species. It builds on the premise that the mechanisms that are responsible for the organization of metabolism are not species-specific (Kooijman 2001(Kooijman , 2010. This hope for generality is supported by (i) the universality of physics and evolution and (ii) the existence of widespread biological empirical patterns among organisms . Table 1 synthesizes the essential criteria for any general model for the metabolism of individuals. We explore the links between DEB theory and each of the proposed criteria in the following paragraphs. DEB theory is explicitly based on the conservation of mass, isotopes, energy and time, including the inherent degradation of energy associated with all processes. So it complies to criteria 1, table 1.The DEB theory is biologically implicit, so it applies to all species. Species-specific restrictions of DEB models are explained and predicted by the theory (criterion 5, table 1). For example, consider the most important difference between DEB models, the number of reserves (biomass components that fuel metabolism) and structures (biomass components that have maintenance needs) that are delineated. This depends on the degree of coupling of the various substrates an organism needs. Animals feed on other organisms, which couples uptake of the various substrates (proteins, carbohydrates, lipids, nutrients) tightly and ex...

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Section: (D) Acquisition Homeostasismentioning

confidence: 99%

Dynamic energy budget theory restores coherence in biology

Sousa¹,

Domingos²,

Poggiale

et al. 2010

Phil. Trans. R. Soc. B

220

185

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show abstract

“…Starvation resistance in larvae was usually examined by point-of-no-return (PNR) and point-of-reserve saturation (PRS) experiments (Yin and Blaxter 1987;Abrunhosa and Kittaka 1997;Mookerji and Rao 1999;Zheng et al 2005;Vidal et al 2006). In crustaceans, there have been a considerable number of reports concentrating on starvation resistance (Anger et al 1981;Anger 1987Anger , 1995Anger and Spindler 1987;Giménez 2002;Liddy et al 2003).…”

Section: Introductionmentioning

confidence: 99%

Starvation resistance and metabolic response to food deprivation and recovery feeding in Fenneropenaeus chinensis juveniles

Zhang

et al. 2008

Aquacult Int

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Starvation resistance in the juveniles of Chinese shrimp, Fenneropenaeus chinensis Osbeck, was studied by point-of-no-return (PNR) and point-of-reserve-saturation (PRS) experiments. Changes in oxygen consumption rate, ammonia-N excretion rate, and oxygen consumed to nitrogen excreted (O:N) ratio were investigated immediately before and after the period of recovery feeding for each regime to assess metabolic response during starvation and refeeding. There was a significant change in survival rate and wet weight of test shrimp throughout the PNR and PRS experiments (P \ 0.05). The estimated PNR and PRS for F. chinensis juveniles could be directly calculated from the selected equations as PNR 50 = 7.86 days, PNR 100 = 21.42 days, PRS 0 = 1.16 days, and PRS 50 = 11.75 days. A decrease in metabolic rate during starvation as a means of conserving energy was found in F. chinensis juveniles. Furthermore, although F. chinensis juveniles only utilized protein as an energy source during starvation, they showed a shift from pure protein during starvation to an equal utilization of protein and lipid or a lipid-carbohydrate mixture during later satiate feeding. The results in the present study indicate that F. chinensis juveniles have the ability to withstand and recover from relatively prolonged starvation after longer initial feeding periods. The knowledge derived from the understanding of starvation resistance and the corresponding metabolic response of F. chinensis juveniles will be useful in the design of feeding regimes in this species.

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“…It is suggested that starvation reduced larval growth rates largely by increasing the duration of the larval period relative to the opportunities for acquiring food (McEdward & Qian, 2001). The prolonged starvation may cause permanent detrimental damage on larval feeding ability, such as the ability of larval cilia to collect and ingest food particles, and further inhibit energy generation for continuing development (Zheng et al, 2005). The irreversible damage on the starved larvae in this study was likely to be responsible for the low survival rates in those groups that were delayed first feeding for 96 h or more.…”

Section: Discussionmentioning

confidence: 80%

“…However, when larvae were fed after being starved for more than 72 h, growth rates were significantly smaller, half or less than the growth of the control group. Similarly, growth recovery of larvae for short-duration starvation was observed in Ivory shell Babylonia formosae habei (Zheng et al, 2005), Manila clam Ruditapes philippinarum (Yan et al, 2009), and hard clam Meretrix meretrix (Tang et al, 2006). The possible explanations for the ability of larvae to achieve normal growth after short periods of starvation are mainly attributed into three parts.…”

Section: Discussionmentioning

confidence: 83%

“…For marine invertebrates, larvae depend largely on their endogenous yolk reserves to support the energy for developing the feeding ability and physiological mechanisms, which will help to start the normal first feeding, growth and survival (Olson & Olson, 1989). Previous studies on delayed first feeding or starvation in early larval development may have profound effects on subsequent larval growth, development, and survival (Zheng et al, 2005;Tang et al, 2006;Yan et al, 2009). In the present study, when delayed first feeding for 24, 48 and 72 h, the growth rates of P. yessoensis larvae following short periods of starvation recovered to the level of the non-starved larvae.…”

Section: Discussionmentioning

confidence: 99%

See 1 more Smart Citation

Effects of Delayed First Feeding on Larval Growth and Survival of Yesso Scallop (Patinopecten yessoensis)

Cai¹,

Sun²,

Yang³

2014

IJB

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The time of first feeding is an important factor for establishing successful initial feeding in molluscan hatcheries. The effects of delayed first feeding on larval growth and survival in the larvae of Yesso Scallop Patinopecten yessoensis were investigated in this study. Groups of larvae were fed at early stage of D-shaped larvae or delayed for 24, 48, 72, 96, 120 and 144 h. When first feeding was delayed for less than 72 h, the P. yessoensis larvae grew as rapidly as those non-starved larvae. When delayed first feeding for more than 72 h, the growth rates of larvae were significantly reduced (less than 2 µm day -1 ), half or less than those of the non-starved group. The survival rates decreased sharply with the prolonged starvation period and the extremely low survival rates were observed in the groups that were delayed first feeding for more than 72 h. The results indicate that the prolonged starvation had a deleterious impact on the larval growth and survival when delayed first feeding for 96 h or more. To avoid mass mortality and obtain adequate growth and survival, food availability within 72 h after early D-shaped larvae is critical important for the successful initial feeding in commercial culture of this species.

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Effects of starvation on larval growth, survival and metamorphosis of Ivory shell Babylonia formosae habei Altena et al., 1981 (Neogastropoda: Buccinidae)

Cited by 32 publications

References 37 publications

Dynamic energy budget theory restores coherence in biology

Dynamic energy budget theory restores coherence in biology

Starvation resistance and metabolic response to food deprivation and recovery feeding in Fenneropenaeus chinensis juveniles

Effects of Delayed First Feeding on Larval Growth and Survival of Yesso Scallop (Patinopecten yessoensis)

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