Chronobiology and the Design of Marine Biology Experiments Audrey M

Chronobiology and the Design of Marine Biology Experiments Audrey M

Chronobiology and the design of marine biology experiments Audrey M. Mat To cite this version: Audrey M. Mat. Chronobiology and the design of marine biology experiments. ICES Journal of Marine Science, Oxford University Press (OUP), 2019, 76 (1), pp.60-65. 10.1093/icesjms/fsy131. hal-02873899 HAL Id: hal-02873899 https://hal.archives-ouvertes.fr/hal-02873899 Submitted on 18 Jun 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. ICES Journal of Marine Science (2019), 76(1), 60–65. doi:10.1093/icesjms/fsy131 Food for Thought Chronobiology and the design of marine biology experiments Downloaded from https://academic.oup.com/icesjms/article-abstract/76/1/60/5116189 by guest on 18 June 2020 Audrey M. Mat 1,2,* 1LEMAR, Universite´ de Bretagne Occidentale UMR 6539 CNRS/UBO/IRD/Ifremer, IUEM, Rue Dumont D’Urville, 29280 Plouzane´, France 2Ifremer, Centre de Bretagne, REM/EEP, Laboratoire Environnement Profond, ZI de la Pointe du Diable, CS 10070, 29280 Plouzane´, France *Corresponding author: tel: þ33 (0)2 98 22 43 04; e-mail: [email protected]. Mat, A. M. Chronobiology and the design of marine biology experiments. – ICES Journal of Marine Science, 76: 60–65. Received 15 May 2018; revised 24 August 2018; accepted 29 August 2018; advance access publication 5 October 2018. Marine habitats are shaped by several geophysical cycles ranging from a few hours (tidal and solar cycles) to a year (seasons). These cycles have favoured the selection of endogenous biological clocks. Such a clock is a molecular time-keeping mechanism that consists of a set of core clock genes whose expression oscillates. The clocks produce biological rhythms and influence virtually all metabolic, physiological, and behavioural functions in organisms. This work highlights the importance to take chronobiology into account in experimental marine biology to avoid faulty results, misinterpretation of results, and/or to strengthen observations and conclusion. A literature survey, based on 150 articles, was conducted and showed that, despite the pervasive imprint of biological rhythms in marine species, environmental cycles such as the 24 h-light/dark cycle and the seasonality are rarely considered in experimental designs. This work emphasizes that better integrat- ing the temporal organization and regulation of marine species within the marine biology community is essential for obtaining representative results. Keywords: biological rhythms, environmental cycles, experimental settings, marine biology, marine chronobiology. Introduction Biological rhythms are considered to be adaptive (Woelfle et al., The Sun, the Moon, and the Earth’s immutable rotation on their 2004) in that they allow the anticipation of cyclic environmental orbits deeply influence our living world. The pervasive alternation changes, and ensure consistency in organisms’ physiology, metab- of nights and days has favoured the selection of an endogenous olism, and behaviour (Rosbash, 2009). An example of synchroni- circadian clock. The genetic basis of the circadian clockwork zation and anticipation is the daily rhythm of body temperature mechanism was first discovered in fruit flies (Hardin et al., 1990; in human: the trough occurs at night, it starts rising in anticipa- Sehgal et al., 1995; Allada et al., 1998; Rutila et al., 1998): transla- tion of wakening, reaches a peak in the early evening, and drops tion and transcription feedback loops of core clock genes set the in anticipation of sleep (Refinetti and Menaker, 1992). tempo for cells, tissues, and ultimately the whole organism Marine species are influenced not only by environmental cycles (Chaix et al., 2016; Kumar, 2017). Mechanistically, the clock associated with the solar day, but also by moon-related environ- varies between species, but its formal principle is ubiquitous from mental cycles, which include the tidal cycle (with period of 12.4 cyanobacteria, to plants, and animals (Young and Kay, 2001). h), the lunar day (24.8 h, the time it takes for the moon to com- Although ubiquitous among taxa, biological clocks probably plete an orbit around the earth), and the semi-lunar/lunar cycles evolved independently at least twice (Rosbash, 2009). The clock is (14.8/29.5 days; Tessmar-Raible et al., 2011). The seasons also synchronized to the Earth’s 24 h-revolution by external cues deeply influence both terrestrial and marine habitats; in called zeitgebers (time-givers), such as the light/dark cycle. Crassostrea gigas, for example, temperature and photoperiod Without zeitgeber, the clock free-run at its endogenous period (i.e. the duration of the light phase of a light/dark cycle) regulate that is circa 24 h, meaning approximately 24 h. Endogenous peri- oyster annual reproduction (Fabioux et al., 2005). All these cycles ods can vary between individuals (Aschoff, 1981; Johnson et al., make the marine biotope a very complex, yet predictable, cyclic 2004). The circadian clock drives organisms’ biological rhythms, environment. Whereas a deep understanding of the mechanisms including the sleep/wake or hormonal cycles (Kumar, 2017). underlying the circadian clockwork has been provided in VC International Council for the Exploration of the Sea 2018. All rights reserved. For permissions, please email: [email protected] Chronobiology and the design of marine biology experiments 61 terrestrial species, the timing mechanisms in marine organisms I searched for these elements in the Material and methods section, still need to be deciphered (Tessmar-Raible et al., 2011; de la and scanned the text according to keywords (“light”, “dark”, Iglesia and Johnson, 2013). However, endogenous rhythms corre- “cycle”, “photo*” for either photoperiod or photons, “C”, sponding to all of these environmental cycles have been described “temperature”, “fed”, “feed”, “food”, each month and season, in a variety of marine organisms including annelids (Last et al., “lab*” for lab or laboratory, “center”, “instit*” for either institu- 2009), molluscs (Connor and Gracey, 2011), arthropods (Zhang tion or institute, “hous*” for housed). The purpose of this analy- et al., 2013), chordates (Vera et al., 2013), phytoplankton (Bouget sis was to assess the integration of biological rhythms within et al., 2014), and manifest in many phenotypes including locomo- marine biology. tor and feeding activity, as well as metabolism and reproduction. In the laboratory, incubation conditions affect biological rhythms. However, despite the importance of environmental Results cycles in driving major rhythms of marine organisms, they are of- The results are summarized in Table 1; detailed information is Downloaded from https://academic.oup.com/icesjms/article-abstract/76/1/60/5116189 by guest on 18 June 2020 ten neglected in the design of marine biology experiments. Such a gathered in Supplementary Table S1. Out of the 150 articles practice may lead to desynchrony within the group under study if reviewed, 32% did not provide information about the presence/ no environmental cycle is implemented, add some undesired var- absence of a light/dark cycle in the experiment. Another 10% pro- iance among individuals if irregular sampling is performed, or al- vided only partial information such as for a specific time period ter the parameter studied if unnatural incubation conditions during the experiment (i.e. acclimation or incubation), a particu- are implemented. These can potentially alter all observations. lar development stage (for adults but not for their progeny) or Therefore, the objective of the present study was twofold: (1) to for a subset of the studied organisms. Information on a diel cycle evaluate in which way chronobiological information was men- was rarely missing for plants (13% and 8%) or chromists (2% tioned or rather neglected, and (2) to show examples of misinter- and 9%) while it was often missing for animals (52% and 9%), pretation of results when not considering the biological revealing a strong difference in treatment between photosynthetic rhythmicity in marine organisms. and non-photosynthetic organisms. Of all articles analysed, 52% reported experiments run under a light/dark cycle while 6% of the experiments were explicitly run either under constant light or constant darkness. Only 1 article provided an explicit reason to Material and methods work under constant conditions. The photoperiod was given in only 47% of the 150 articles: some articles specified the presence A literature survey of experimental laboratory work (n ¼ 150 of a light/dark cycle but only mentioned a natural photoperiod articles; Supplementary Table S1) on marine and brackish species without detail, for example. The information was not relevant for (according to the World Register of Marine Species, http://www. studies conducted under continuous conditions. The type of marinespecies.org) was performed, using articles which were pub- light, either in terms of intensity or spectrum and when continu- lished between July and December 2017 in the top 20 journals in ous light or light/dark cycles were implemented, was

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