Effects of the lunar cycle on ecosystem and heterotrophic respiration in a boreal Sphagnum-dominated peatland

References

• Abrami G. 1972. Correlations between lunar phases and rhythmicities in plant growth under field conditions. Can J Bot. 50:2157–2166. doi: 10.1139/b72-281.
   Google Scholar
• Balling JRC, Cerveny RS. 1995. Influence of lunar phase on daily global temperatures. Science. 267:481–1483. doi: 10.1126/science.267.5203.1481.
   Web of Science ®Google Scholar
• Ben-Attia M, Reinberg A, Smolensky MH, Gadacha W, Khedaier A, Sani M, Touitou Y, Boughamni NG. 2016. Blooming rhythms of cactus Сereus peruvianus with nocturnal peak at full moon during seasons of prolonged daytime photoperiod. Chronobiol Int. 33:419–430. doi: 10.3109/07420528.2016.1157082.
   PubMed Web of Science ®Google Scholar
• Breitler JC, Djerrab D, Leran S, Toniutt L, Guittin C, Severac D, Pratlong M, Dereeper A, Etienne H, Bertrand B. 2020. Full moonlight-induced circadian clock entrainment in Сoffea arabica. BMC Plant Biol. 20:1–11. doi: 10.1186/s12870-020-2238-4.
   PubMed Web of Science ®Google Scholar
• Burr HS. 1947. Tree potentials. Yale J Biol Med. 19:311–318.
   PubMed Web of Science ®Google Scholar
• Cerveny RS, Balling JRC. 1999. Lunar influence on diurnal temperature range. Geophys Res Lett. 26:1605–1607. doi: 10.1029/1999GL900303.
   Web of Science ®Google Scholar
• Choi JY, Kim NN, Choi YU, Choi CY. 2017. Changes in circadian parameters of humbug damselfish, Dascyllus aruanus according to lunar phase shifts in micronesia. Biol Rhythm Res. 48:475–483. doi: 10.1080/09291016.2016.1275395.
   Web of Science ®Google Scholar
• Dean JF, Garnett MH, Spyrakos E, Billett MF. 2019. The potential hidden age of dissolved organic carbon exported by peatland streams. J Geophys Res. 124:328–341. doi: 10.1029/2018JG004650.
   Web of Science ®Google Scholar
• Deveau AM, Miller-Hope Z, Lloyd E, Williams BS, Bolduc C, Meader JM, Weis F, Burkholder KM. 2016. Antimicrobial activity of extracts from macroalgae Ulva lactuca against clinically important staphylococci is impacted by lunar phase of macroalgae harvest. Lett Appl Microbiol. 62:363–371. doi: 10.1111/lam.12563.
   PubMed Web of Science ®Google Scholar
• Dyre JC. 1995. Lunar phase influence on global temperatures. Science. 269:1284–1285. doi: 10.1126/science.269.5228.1284.
   PubMedGoogle Scholar
• Ehlers I, Augusti A, Betson TR, Nilsson MB, Marshall JD, Schleucher J. 2015. Detecting long-term metabolic shifts using isotopomers: CO2-driven suppression of photorespiration in C3 plants over the 20th century. Proc Natl Acad Sci. 112:15585–15590. doi: 10.1073/pnas.1504493112.
   PubMed Web of Science ®Google Scholar
• Hamard S, Robroek BJ, Allard PM, Signarbieux C, Zhou S, Saesong T, Jassey VE. 2019. Effects of Sphagnum leachate on competitive Sphagnum microbiome depend on species and time. Front Microbiol. 10:2042. doi: 10.3389/fmicb.2019.02042.
   PubMed Web of Science ®Google Scholar
• Hardie SML, Garnett MH, Fallick AE, Ostle NJ, Rowland AP. 2009. Bomb-14C analysis of ecosystem respiration reveals that peatland vegetation facilitates release of old carbon. Geoderma. 153:393–401. doi: 10.1016/j.geoderma.2009.09.002.
   Web of Science ®Google Scholar
• Holzknecht K, Zürcher E. 2006. Tree stems and tides–A new approach and elements of reflexion (reviewed paper). Schweizerische Zeitschrift fur Forstwesen. 157:185–190. doi: 10.3188/szf.2006.0185.
   Google Scholar
• Huang LF, Zheng JH, Zhang YY, Hu WH, Mao WH, Zhou YH, Yu JQ. 2006. Diurnal variations in gas exchange, chlorophyll fluorescence quenching and light allocation in soybean leaves: The cause for midday depression in CO2 assimilation. Sci Hortic. 110:214–218. doi: 10.1016/j.scienta.2006.07.001.
   Web of Science ®Google Scholar
• Järveoja J, Nilsson MB, Crill PM, Peichl M. 2020. Bimodal diel pattern in peatland ecosystem respiration rebuts uniform temperature response. Nat Commun. 11:4255. doi: 10.1038/s41467-020-18027-1.
   PubMed Web of Science ®Google Scholar
• Järveoja J, Nilsson MB, Gažovič M, Crill PM, Peichl M. 2018. Partitioning of the net CO2 exchange using an automated chamber system reveals plant phenology as key control of production and respiration fluxes in a boreal peatland. Global Change Biol. 24:3436–3451. doi: 10.1111/gcb.14292.
   PubMed Web of Science ®Google Scholar
• Joosten H, Clarke D. 2002. Wise use of mires and peatlands. International mire conservation group and international peat society 304.
   Google Scholar
• Kets K, Darbah JN, Sober A, Riikonen J, Sober J, Karnosky DF. 2010. Diurnal changes in photosynthetic parameters of Populus tremuloides, modulated by elevated concentrations of CO2 and/or O3 and daily climatic variation. Environ Pollut. 158:1000–1007. doi: 10.1016/j.envpol.2009.09.001.
   PubMed Web of Science ®Google Scholar
• Kowallik W. 1982. Blue light effects on respiration. Annu Rev Plant Physiol. 33:51–72. doi: 10.1146/annurev.pp.33.060182.000411.
   Google Scholar
• Kuiper JJ, Mooij WM, Bragazza L, Robroek BJ. 2014. Plant functional types define magnitude of drought response in peatland CO2 exchange. Ecology. 95:123–131. doi: 10.1890/13-0270.1.
   PubMed Web of Science ®Google Scholar
• Levy O, Appelbaum L, Leggat W, Gothlif Y, Hayward DC, Miller DJ, Hoegh-Guldberg O. 2007. Light-responsive cryptochromes from a simple multicellular animal, the coral Acropora millepora. Science. 318:467–470. doi: 10.1126/science.1145432.
   PubMed Web of Science ®Google Scholar
• Limpens J, Berendse F, Blodau C, Canadell JG, Freeman C, Holden J, Roulet N, Rydin H, Schaepman-Strub G. 2008. Peatlands and the carbon cycle: from local processes to global implications–a synthesis. Biogeosciences. 5:1475–1491. doi: 10.5194/bg-5-1475-2008.
   Web of Science ®Google Scholar
• Maw MG. 1967. Periodicities in the influences of air ions on the growth of garden cress, Lepidium Sativum L. Can J Plant Sci. 47:499–505. doi: 10.4141/cjps67-090.
   Web of Science ®Google Scholar
• Mironov VL. 2022. Cloud cover disrupts the influence of the lunar cycle on the growth of peat moss Sphagnum riparium. Environ Exp Bot. 194:104727. doi: 10.1016/j.envexpbot.2021.104727.
   Web of Science ®Google Scholar
• Mironov VL. 2024. Geomagnetic Anomaly in the growth response of peat moss Sphagnum riparium to temperature. Plants. 13:48. doi: 10.3390/plants13010048.
   Google Scholar
• Mironov VL, Kondratev AY. 2017. Peat moss Sphagnum riparium follows a circatrigintan growth rhythm in situ: a case report. Chronobiol Int. 34:981–984. doi: 10.1080/07420528.2017.1329208.
   PubMed Web of Science ®Google Scholar
• Mironov VL, Kondratev AY, Mironova AV. 2020. Growth of Sphagnum is strongly rhythmic: contribution of the seasonal, circalunar and third components. Physiol Plant. 168:765–776. doi: 10.1111/ppl.13037.
   PubMed Web of Science ®Google Scholar
• Nilsson M, Sagerfors J, Buffam I, Laudon H, Eriksson T, Grelle A, Lindroth A, Weslien P, Lindroth A. 2008. Contemporary carbon accumulation in a boreal oligotrophic minerogenic mire – a significant sink after accounting for all C‐fluxes. Global Change Biol. 14:2317–2332. doi: 10.1111/j.1365-2486.2008.01654.x.
   Web of Science ®Google Scholar
• Poehn B, Krishnan S, Zurl M, Coric A, Rokvic D, Häfker NS, Jaenicke E, Arboleda E, Orel L, Raible F, et al. 2022. A Cryptochrome adopts distinct moon-and sunlight states and functions as sun-versus moonlight interpreter in monthly oscillator entrainment. Nat Commun. 13:5220. doi: 10.1038/s41467-022-32562-z.
   PubMed Web of Science ®Google Scholar
• Polevoy VV. 1989. Физиология растений [Plant physiology]. Москва (Moskva): Высшая школа [Vysshaya shkola pulishers]. p. 464. [In Russian].
   Google Scholar
• Rankin T, Roulet N, Humphreys E, Peichl M, Järveoja J. 2023. Partitioning autotrophic and heterotrophic respiration in an ombrotrophic bog. Front Earth Sci. 11:1263418. doi: 10.3389/feart.2023.1263418.
   Web of Science ®Google Scholar
• Rydin H, Gunnarsson U, Sundberg S. 2006. The role of Sphagnum in peatland development and persistence. In: Wieder R, Vitt D, editors. Boreal Peatland Ecosystems. Ecological Studies. Vol. 188. Berlin, Heidelberg: Springer. doi:10.1007/978-3-540-31913-9_4.
   Google Scholar
• Serk H, Nilsson MB, Bohlin E, Ehlers I, Wieloch T, Olid C, Schleucher J, Kalbitz K, Limpens J, Moore T. 2021. Global CO2 fertilization of Sphagnum peat mosses via suppression of photorespiration during the twentieth century. Sci Rep. 11:24517. doi: 10.1038/s41598-021-02953-1.
   PubMed Web of Science ®Google Scholar
• Singiri JR, Priyanka G, Trishla VS, Adler-Agmon Z, Grafi G. 2023. Moonlight is perceived as a signal promoting genome reorganization, changes in protein and metabolite profiles and plant growth. Plants. 12:1121. doi: 10.3390/plants12051121.
   Google Scholar
• Smolders AJP, Tomassen HBM, Pijnappel HW, Lamers LPM, Roelofs JGM. 2001. Substrate‐derived CO2 is important in the development of Sphagnum spp. New Phytol. 152:325–332. doi: 10.1046/j.0028-646X.2001.00261.x.
   Web of Science ®Google Scholar
• Špunda V, Kalina J, Urban O, Luis VC, Sibisse I, Puertolas J, Sprtova M, Marek MV. 2005. Diurnal dynamics of photosynthetic parameters of Norway spruce trees cultivated under ambient and elevated CO2: the reasons of midday depression in CO2 assimilation. Plant Sci. 168:1371–1381. doi: 10.1016/j.plantsci.2005.02.002.
   Web of Science ®Google Scholar
• Takeuchi Y, Kabutomori R, Yamauchi C, Miyagi H, Takemura A, Okano K, Okano T. 2018. Moonlight controls lunar-phase-dependency and regular oscillation of clock gene expressions in a lunar-synchronized spawner fish Goldlined spinefoot. Sci Rep. 8:6208. doi: 10.1038/s41598-018-24538-1.
   PubMed Web of Science ®Google Scholar
• Turetsky MR, Wieder RK. 1999. Boreal bog Sphagnum refixes soil-produced and respired 14CO2. Ecoscience. 6:587–591. doi: 10.1080/11956860.1999.11682559.
   Web of Science ®Google Scholar
• Vogt KA, Beard KH, Hammann S, Palmiotto JOH, Vogt DJ, Scatena FN, Hecht BP. 2002. Indigenous knowledge informing management of tropical forests: the link between rhythms in plant secondary chemistry and lunar cycles. AMBIO. 31:485–490. doi: 10.1579/0044-7447-31.6.485.
   PubMed Web of Science ®Google Scholar
• Voss I, Sunil B, Scheibe R, Raghavendra AS, Weber A. 2013. Emerging concept for the role of photorespiration as an important part of abiotic stress response. Plant Biol. 15:713–722. doi: 10.1111/j.1438-8677.2012.00710.x.
   PubMed Web of Science ®Google Scholar
• Yudina L, Sukhova E, Mudrilov M, Nerush V, Pecherina A, Smirnov AA, Dorokhov AS, Chilingaryan NO, Vodoneev V, Sukhov V. 2022. Ratio of intensities of blue and red light at cultivation influences photosynthetic light reactions, respiration, growth, and reflectance indices in lettuce. Biology. 11:60. doi: 10.3390/biology11010060.
   PubMedGoogle Scholar
• Yu Z, Loisel J, Brosseau DP, Beilman DW, Hunt SJ. 2010. Global peatland dynamics since the last glacial maximum. Geophys Res Lett. 37:1–5. doi: 10.1029/2010GL043584.
   Web of Science ®Google Scholar
• Zantke J, Ishikawa-Fujiwara T, Arboleda E, Lohs C, Schipany K, Hallay N, Tessmar-Raible K. 2013. Circadian and circalunar clock interactions in a marine annelid. Cell Rep. 5:99–113. doi: 10.1016/j.celrep.2013.08.031.
   PubMed Web of Science ®Google Scholar
• Zhang XH, Lang DY, Zhang EH, Bai CC, Wang HZ. 2013. Diurnal changes in photosynthesis and antioxidants of angelica sinensis as influenced by cropping systems. Photosynthetica. 51:252–258. doi: 10.1007/s11099-013-0013-6.
   Web of Science ®Google Scholar
• Zürcher E, Schlaepfer R, Conedera M, Giudici F. 2010. Looking for differences in wood properties as a function of the felling date: Lunar phase-correlated variations in the drying behavior of Norway Spruce (Picea abies Karst.) and Sweet Chestnut (Castanea sativa Mill.). Trees. 24:31–41. doi: 10.1007/s00468-009-0376-2.
   Web of Science ®Google Scholar