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03. Science and Technology (Natural Sciences) Committee

Permanent URI for this communityhttps://repository.unesco.gov.ph/handle/123456789/3

In creating a culture of peace and addressing sustainable development challenges, UNESCO aims to cultivate the generation and application of scientific knowledge among its Member States. At UNACOM, we facilitate access to UNESCO’s international programmes in the sciences, such as the Intergovernmental Oceanographic Commission (IOC), Man and the Biosphere (MAB) Programme, and International Geoscience and Geoparks Programme (IGGP), among others.

Through this sector, the Commission aims to contribute to the following SDGs: 11 - Sustainable Cities and Communities, 13 - Climate Action, 14 - Life Below Water, and 15 - Life On Land. With the overarching vision of the 2023-2028 Philippine Development Plan (PDP), UNACOM targets grassroots-inspired cultural heritage and biodiversity protection and conservation, as well as multi-stakeholder partnerships for SDGs promotion.

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    Diurnal and diel patterns in the photosynthetic performance of the agarophyte Gelidiella acerosa
    Ganzon-Fortes, E. T. (Walter de Gruyter, 1997)
    Photosynthesis of the red alga Gelidiella acerosa was monitored on diurnal (during the day) and diel (24 h period) bases using the oxygen evolution technique in a closed system. Natural sunlight and artificial light were used to assess uniformity in the diurnal photosynthetic responses. Photosynthesis-irradiance (P-I) curves were also determined diurnally. On a diel basis, maximal photosynthetic rates occurred at day time and minimal rates occurred at night. Diurnally, photosynthesis fluctuated in different patterns depending on PFDs used. Under saturating but not photoinhibiting FFDs, photosynthesis exhibited an early morning minimum (a few hours after sunrise), a midday-noon maximum, sustained until late afternoon, then declined at or after sunset. However, when exposure to high PFDs (above 1200 μιηοΐ photons m"~s") were prolonged, i.e. from morning until afternoon, the photosynthetic performance suffered a depression starting from noon and persisting until afternoon. When PFDs lowered late in the afternoon, recovery of photosynthetic performance commenced resulting in increased photosynthetic rates. The P-I curve data corroborate findings of experiments using saturating but not photoinhibiting PFDs. The morning P-I curve had lower Pm and alpha, and higher Ik and Is values than the identical noon and afternoon P-I curves. This suggested that photosynthetic performance was yet inefficient in the morning but performed efficiently near midday until the afternoon. An endogenous circadian clock was implicated to have influenced the diurnal and diel patterns in the photosynthetic performance of G. acerosa. Photoinhibition was the other factor suspected to have altered the diurnal pattern.
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    Temperature-influenced infection rates in the Chondrus crispus-Petersenia pollagaster pathosystem: A regression analysis
    Molina, F. I.; Hughes, G. C.; Craigie, J. S. (Springer, 1988-03)
    Cross-infection experiments were performed to determine the influence of temperature on infection rate in the Chondrus crispus Stackhouse-Petersenia pollagaster (Petersen) Sparrow pathosystem. C. crispus thalli were collected at Pubnico Harbor, Nova Scotia, Canada in the fall of 1981 to 1984. Infective zoospores were used to inoculate healthy thalli at five different temperatures. The highest infection rate was obtained at 20°C, while significantly lower rates were obtained at temperature extremes. The parasite's life cycle, consisting of infection of healthy thalli, endobiotic development, and release of zoospores, was completed in 48 to 72 h at 15° to 20°C.
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    Five new sesquiterpenes from the red alga Laurencia flexilis
    de Nys, Rocky; Wright, Anthony D.; König, Gabriele M.; Sticher, Otto; Alino, Perry M. (American Chemical Society (ACS), 1993-06)
    The red alga Laurencia flexilis, collected from Philippine waters, yielded five new sesquiterpenoid metabolites, 3,4-epoxypalisadin A [1], 5B-acetoxypalisadin A [2], 12-bromopalisadin B [3], palisading C [4], and 5B-hydroxypalisadin B [5]. The known metabolites 6-10 were also isolated The unambiguous assignments of H- and C-nmr spectral data for compounds 7 and 8 are reported for the first time.