Effects of light path lengths and initial culture density on the cultivation of Chaetoceros muelleri (Lemmermann, 1898)

被引:26
作者
Göksan, T [1 ]
Durmaz, Y [1 ]
Gökpinar, S [1 ]
机构
[1] Ege Univ, Fac Fisheries, Dept Aquaculture, TR-35100 Izmir, Turkey
关键词
Chaetoceros muelleri; photobioreactor; light path; initial cell density;
D O I
10.1016/S0044-8486(01)00854-7
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
In the cultivation of a marine diatom Chaetoceros muelleri (Lemmermann, 1898), flat plate vertical glass reactors with light path lengths of 1 or 3 cm were used in the laboratory under a constant photon flux density (PFD) of 190 mumol photon m(-2) s(-1). In the first experiment, equal inocula were added in the two bioreactors (1 and 3 cm light path); by the end of the second day, cell concentration was low in the 1-cm light path bioreactor, possibly indicating photoinhibition, since growth of the culture increased in the 3-cm light path bioreactor. As for in the second trial, the areal volumes were equal, that is, the cell concentration was increased three-fold in 1 cm light path to equalize the areal optic densities in both reactors. After the harvest started, average of the volumetric output rates in 1 cm (P-V1 (cm)) and 3 cm light paths (P-V3 (cm)) were calculated to be 0.22 and 0.10 g l(-1) day(-1), and areal output rates in 1 cm (P-A1 (cm)) and 3 cm (P-A3 (cm)) light paths were calculated to be 1.80 and 2.53 g m(-2) day(-1), respectively. The optimal population density was obtained by a daily harvest of 5% of culture volume to be 2.39 g m(-2) day(-1) in 1 cm light path and 3.27 g m(-2) day(-1) in 3 cm light path. Light path length of 3 cm was found optimal in both with low and high initial cell densities. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:431 / 436
页数:6
相关论文
共 18 条
[1]  
Borowitzka Michael A., 1996, Journal of Marine Biotechnology, V4, P185
[2]   Nutritional properties of microalgae for mariculture [J].
Brown, MR ;
Jeffrey, SW ;
Volkman, JK ;
Dunstan, GA .
AQUACULTURE, 1997, 151 (1-4) :315-331
[3]   Dual sparging laboratory-scale photobioreactor for continuous production of microalgae [J].
Eriksen, NT ;
Poulsen, BR ;
Iversen, JJL .
JOURNAL OF APPLIED PHYCOLOGY, 1998, 10 (04) :377-382
[4]   CELL FRAGILITY - THE KEY PROBLEM OF MICROALGAE MASS-PRODUCTION IN CLOSED PHOTOBIOREACTORS [J].
GUDIN, C ;
CHAUMONT, D .
BIORESOURCE TECHNOLOGY, 1991, 38 (2-3) :145-151
[5]  
Hu Q, 1996, BIOTECHNOL BIOENG, V51, P51, DOI 10.1002/(SICI)1097-0290(19960705)51:1<51::AID-BIT6>3.0.CO
[6]  
2-#
[7]  
Hu Q., 1994, J APPL PHYCOL, V6, P391, DOI DOI 10.1007/BF02182155
[8]   HIGH-DENSITY PHOTOAUTOTROPHIC ALGAL CULTURES - DESIGN, CONSTRUCTION, AND OPERATION OF A NOVEL PHOTOBIOREACTOR SYSTEM [J].
JAVANMARDIAN, M ;
PALSSON, BO .
BIOTECHNOLOGY AND BIOENGINEERING, 1991, 38 (10) :1182-1189
[10]   A LABORATORY-SCALE SYSTEM FOR MASS-CULTURE OF FRESH-WATER MICROALGAE IN POLYETHYLENE BAGS [J].
MARTINEZJERONIMO, F ;
ESPINOSACHAVEZ, F .
JOURNAL OF APPLIED PHYCOLOGY, 1994, 6 (04) :423-425