Bioaccumulation of Pb, Cd, Cu, and Cr by Porphyridium cruentum (S.F. Gray) Nägeli | Soeprobowati | International Journal of Marine Science

Bioaccumulation of Pb, Cd, Cu, and Cr by Porphyridium cruentum (S.F. Gray) Nägeli  

Tri Retnaningsih Soeprobowati , Riche Hariyati
Department of Biology, Faculty Science and Mathematics, Diponegoro University, Tembalang - Semarang, Indonesia
Author    Correspondence author
International Journal of Marine Science, 2013, Vol. 3, No. 27   doi: 10.5376/ijms.2013.03.0027
Received: 03 Apr., 2013    Accepted: 02 May, 2013    Published: 02 Jun., 2013
© 2013 BioPublisher Publishing Platform
This is an open access article published under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Preferred citation for this article:

Soeprobowati and Hariyati, 2013, Bioaccumulation of Pb, Cd, Cu, and Cr by Porphyridium cruentum (S.F. Gray) Nägeli, International Journal of Marine Science, Vol.3, No.27 212-218 (doi: 10.5376/ijms.2013.03.0027)


The red microalgae Porphyridium cruentum (S.F. Gray) Nägeli  usually was used as feeds, a pigment for food and cosmetic, and antiviral activity that might be became industrial interest. Similar to another microalgae, P. cruentum has an ability to remediate heavy metals pollution, however research on it still limited. This research was conducted in order to find out the the accumulation of Pb, Cd, Cr, and Cu on the P. cruentum. A laboratory experiment were developed with different concentrations. Based on this research, P. cruentum with the treatment of 1 mg/L had reduced higher Cu, Pb, Cd, and Cr concentrations rather than 3 and 5 mg/L concentrations, respectively. This was also similar to the BCF, that in day 8 in order of Cu > Cr > Cd > Pb, respectively; however, in day 15 was Cu > Pb > Cd > Cr. The length of treatment influenced BCF value. P. cruentum was good for bioremediation of heavy metal pollution, with the advantage of the short of accumulation time. 

Bioaccumulation; Heavy metal; Porphyridium cruentum; Microalgae; Bioremediation; BCF

The concentration of heavy metals in the environment tend to increase due to the industrial development. Heavy metals is a trace element with the density of ≥ 3 g/cm3, which on the low concentration was required by organism, but toxic in the higher concentration for physiological organism (Banvalvi, 2011). One of the water pollution problem in Indonesia was heavy metals, particularly Lead (Pb), Cadmium (Cd), Chromium (Cr) and Cooper (Cu) that often exceeded the Water Quality Standard for drinking water, agriculture and/or fisheries (Soeprobowati et al., 2001; Soeprobowati et al., 2012). Heavy metals in the environment cannot be degraded and tent to accumulate in the organism. This heavy metals pollution can be solved by bioremediation technique.

Bioremediation is the clean up process of the environment biologically from polluted materials by organism that can be done in-situ or ex-situof polluted sites (Crawford and Crawford, 2005). In the earlier development, bioremediation only applied microbes, furthermore, it is more wider application of organism to remediate freshwater, marine, even terrestrial ecosystems. Bioremediation offer effectiveness, low cost and low impact on ecosystem rather than physical and chemical remediation (Leung, 2004). Phytoremediation was more effective and efficient compare with bacteria-based remediation due to no need oxygen and less odor problem (Dwivedi, 2012). Microalgae have potential use to sink or to remove some toxic substances such as heavy metal by accumulate, adsorb or metabolize into substantial level (Priyadarshani et al., 2011). Phycoremediation (remediation that use microalgae) has advantages to remediate heavy metal since these microalgae can be used as fertilizer after remediation process (Riesing, 2006) or biofuels (Priyadarshani et al., 2011; Kumar et al., 2013); the low cost, simple and flexible in the application, and low maintenance (Emienour, 2012). The disadvantages of using microalgae for heavy metal remediation were require of energy for drying when using dead microalgae, need to be immobilized, and has limited application in the batch systems (Brinza et al., 2007).
Bioaccumulation is an absorption process of chemical compound from the environment by organism through respiratory surface and dietary uptake, and chemically elimination process through respiratory exchange, fecal egestion, chemical parent substance biotransformation, and increasing of tissue volume (Arnot and Gobas, 2006). Bioaccumulation can be used for environmental pollution monitoring since there was a correlation between bioaccumulation capacity with polluted environment or waste concentration. Both biosorption and bioaccumulation can be applied to reduce contaminant from the effluent (Chojnacka, 2009).
Microalgae are microscopic lower plants that have an important role in aquatic ecosystem as the largest primary producers and source of oxygen (Priyadarshani et al., 2011). Microalgae were good biosorption due to functional ion that able to bound ionic metal, especially carboxyl, hydroxylamine, sulphudrile immadazole, sulphate, and sulphonate that located on the cell wall (Volesky, 2007); easily found in a big amount, low operational cost, minimum sludge, and no need additional nutrition (Wang and Chen, 2009). However, microalgae has weaknesses due to a small size, low mass index, and easily degraded by microorganism.
Many researches had been conducted for the use of microalgae for environmental remediation, such as bioaccumulation of Cd by Tetraselmis chuii and Spirulina maxima (Costa and Franca, 2003); biosorption of Pb, Cd, Hg by Microcystis aeruginosa (Chen et al., 2005), biosorption Cd, Cr, Cu by Spirulina (Chojnacka et al., 2005); bioaccumulation of Pb and Cd by Chladophora (Lamai et al, 2005); biosorption of Cu by Chlorella vulgaris (Al-Rub et al., 2006); the application of Chlorella vulgaris to remediate textile wastewaters(Lim et al., 2010); bioremediation of Hg, Cd, Pb by Dunaliella (Imani et al., 2011); toxicity, transformation and accumulation arsenic in Scenedesmus (Bahar et al., 2012); Zn and Pb resistance of two ecotype Eustigmatos sp. (Trzeinska and Pawlik-Skowronska, 2012); Cr6+ bioremediation efficiency of Oscillatoria (Miranda et al.; 2012). However, researches on the use of Porphyridium for remediation were still limited. Preliminary study had shown, that Porphyridium had a potential to use in heavy metals bioremediation (Soeprobowati and Hariyati, 2012).
P. cruentum (S.F.Gray) Nägeliis the primitive micro red algae that can be found to live in variety habitats such as sea water, fresh water, or on the surface of moist soil that form a reddish layer, but prefer to live in a saline habitat. The red color of P. cruentum is coming from phycoerythrine pigment, its big chloroplast is surrounded by sulphate polysaccharide; single cell but able to form colonies (Arrad, 1992). P. cruentum had been used for antiviral (Huleihel et al., 2001). P. cruentum had also been used for nutrition source, particularly of polysaccharides, unsaturated fatty acids, carotenoids, and phycobiliproteins. The phycobiliproteinscontent were phycoerythrin, R-phycocyanin, and allophycocyanin that were affected by sodium bicarbonate (Velea et al., 2011).
P. cruentum consisted of proteins (28%~39%), polysaccharides (40%~57%) and lipids (9%~14%) subsumed into dry algal mass (Veleaet al.,2011); phycobiliproteins, exopolysaccharides, long-chain polyunsaturated fatty acids, carotenoids (zeaxanthin, tocopherol, etc.) and vitamins (Wang et al.,2007; Huang and Chen, 2005). The biomass (w/w) contains of 32.1% available carbohydrates, and 34.1% crude protein. 100 g dried P. cruentum biomass contains of 4,960 mg Ca; 1,190 mg K; 1,130 mg Na; 629 mg Mg and 373 mg Zn. A short residence times in the bioreactor, the biomass were rich in protein and eicosapentaenoic acid (Fuentes et al., 2000).
P. cruentum was qualified for bioremediation due to the absence of toxic production, easily to be cultured, ability to grow in extremes of salinity, pH, and temperature, rapid grow in defined media, ability to achieve a high population, and easily of harvesting (Wilde et al., 1988). P. cruentum is promising for bioremediation of heavy metals since it provides double solution to overcome environmental pollution and energy alternative. P. cruentum had a higher tolerance for the agitation than Phaeodactylum tricornutum. The cell damage was related to the rupture of small gas bubbles at the surface of the culture. An increase of agitation rate had reduced the bubble size to produce damaging (Sobczuk et al., 2006).
1 Result and Discussion
P. cruentum tolerated to a high concentration of heavy metal, as seen in Figure 1. After a second peak population growth on day of nine, it seems that the concentration of 5 mg/L Pb had reduced population growth, meanwhile the lower concentration tent to increase its population. This trend was similar to Cd and Cu treatments. On the concentration of 1 mg/L Cu had induced P. cruentum population growth, however, on the concentration of 3 and 5 mg/L had lowered P. cruentum populations (Figure 1). The concentrations of heavy metals in the sea water before treatments were 0.17 mg/L Pb, 0.01 mg/L Cd, 0.15 mg/L Cu, and 0.03 mg/L Cr. Therefore, the initial concentration of heavy metals was the concentration of treatments added with the sea water concentration.

Figure 1 Population (×1 000 ind/L) of Porphyridium cruentum (S.F.Gray) Nägelion the treatment of Pb, Cd, Cr, and Cu, on concentration 1, 3, and 5 mg/L

On the preliminary research, the population growth of P. cruentum on the 0.5 mg/L concentration of Pb, Cd, Cu, and Cr were fluctuated, the peak population growth were on the day of 4, 10, and 13 (Soeprobowati and Hariyati, 2012). The life cycle of Porphyrydium tent to go a day forward in the higher heavy metal concentrations, but with the lower population.
Generally, the culture media of P. cruentum with Pb, Cd, Cu, and Cr 1 mg/L had the highest reduction of heavy metals than on the concentrations of 3 and 5 mg/L, respectively. For P. cruentum, the percentage of heavy metals concentration reduction was highest on Cu treatment (92% in the day of 15, Figure 2). On the 0.5 mg/L of Pb, Cd, Cu, and Cr treatments, P. cruentum culture had shown the highest reduction of Cu and Cd concentrations of 96% and 70%, respectively (Soeprobowati and Hariyati, 2012). On the higher treatment concentrations of this research, the concentration of 3 and 5 mg/L had reduced population growth, and P. cruentum shown the highest reduction of Cu concentration compare with others, therefore P. cruentum was good to remediate Cu pollution.

Figure 2 The percentage of Pb, Cd, Cu, and Cr reduction on the culture media of Porphyridium cruentum (S.F.Gray) Nägeliin day 8 and 15 treatment concentration 1, 3, 5 mg/L

Heavy metals toxicity can be study by BCF approach. The highest BCF occurred for heavy metals treatment on the concentrations of 1 mg/L (Fig
ure 3). However, the length of treatment influenced BCF value. P. cruentum shown the higher toleration on Cu than Pb, Cd, and Cr BCF of P. cruentum in day of 8 from high was in order of Cu>Cr>Cd>Pb, respectively; however, in day 15 was Cu > Pb > Cd > Cr.Heavy metals bioconcentration on the P. cruentum able to figure out the environmental impact of heavy metals. Based on the trend in Figure 3, it seems that Pb required longer time to accumulate, whereas Cu was more faster.

Figure 3 BCF (ppm) of Pb, Cd, Cr, Cu on the concentration 1, 3, and 5 mg/L

BCF had calculated as a homeostatically ratio of heavy metal concentration on the P. cruentum with heavy metal concentration of media. Microalgae had a protection mechanism against heavy metals by development of heavy metals complex with cellular protein
without change its activity (Wang and Chen, 2009; Girard, 2010). On a high concentration, heavy metals had reduced the population or cell growth because P. cruentum can not counterbalance the heavy metals toxicity.
The mechanism of heavy metal entering to the cell was affected by the concentration difference, the negative charged of the surface cell wall and the positive charged metal ion on the microalgal medium. It was shown from this study that P. cruentum demonstrated successfully in the sorption and removal of heavy metals ion from the water, the highest affinity towards Cu which in the day of 8 and/or 15. A reduction of Cu concentration was higher following the time exposure, which accumulate in the cell wall. This was related to the Cu release rate that relatively lower than the Cu absorption. The heavy metals absorption occurred in 2 ways i.e. heavy metal ionic change with cell wall caption, or development covalent bound between heavy metals with active ionic of cell wall. P. cruentum cell wall consists of organic protein, polysaccharide, alginate acid and urinate acid which were able to bind with heavy metals (Wang and Chen, 2009).
Heavy metal accumulation will increase H+ ion concentration. Therefore, an increase of pH media will increase H+ ion production, which in turn will increase heavy metal absorption by Porphyridium. So, heavy metals bioremediation by P. cruentum will be optimum on the alkaline pH (7-8) condition.
Many researches had been done on the effect of heavy metals on the microalgae. A high concentration of Pb and Cd had decreased Cladophora fracta growth, due to induction of peroxides enzyme activity that had an important role on the indoneacetic acid (IAA) degradation. IAA was a hormone that stimulates the growth and vision of microalgae (Lamai et al., 2005). Chlamydomonas reinhardtii, Chlorella salina, Chlorella sorokiniana, Chlorella vulgaris, Chlorella miniata, Chlorococcum sp., Cyclotella cryptica, Lyngbya taylorii, Phaeodactylum tricornutum, Porphyridium purpureum, Scenedesmus abundans, Scenedesmus quadricauda, Scenedesmus subspicatus, Spirogyra sp., Spirulina platensis, Stichococcus bacillaris and Stigeoclonium tenue were a good biosorpant heavy metal ion (Brinza et al., 2007). Spirulina sp was biosorpant of Cr3+, Cd2+ and Cu2+ ions (Chojnacka et al., 2005).
Bioaccumulation is a process of chemical absorption by organisms from all routes in the environment, including from food and chemical elimination from organism through respiratory, fecal excretion, and metabolic biotransformation and growth emasculation (Arnot dan Gobas, 2006). Bioaccumulation can be used to identify the negative impact of environmental degradation to the organism (McGeer et al., 2003). Aquatic organism could accumulate chemical compound directly form the environment through skin and intestinal digestion surface, or indirectly from chemical compound accumulation from food (Ivanciuc et al. , 2006).
Bioaccumulation Factor (BAF) is the ratio of accumulated chemical compound in the organism and the concentration of chemical compound of the environment. There was a fundamental difference between BCF and BAF. BCF is the degree of absorption process of chemical compound by organism from environment through respiration or skin surface. That’s why BCF was used to determine bioaccumulation under controlled laboratory experiment. BAF is similar to BCF, but with dietary chemical exposure, usually measured under field condition (Arnot and Gobas, 2006).
BCF had been used for fish, but it was possible to calculate BCF of microalgae. The concentration of heavy metals on the microalgae reflected the heavy metal concentration on its environment. Research that had been done in the Uganda’s river was similar to the result of this laboratory experiment, that microalgae, particularly P. cruentum was a bioaccumulator of Cu > Pb > Cd (Sekabira et al., 2011).
The BCF value that greater than 1 ppm indicated heavy metal accumulator, however, it will be a good bioaccumulator when the BCF was greater than 1,000 ppm (Conti and Cecchetti, 2003). Based on the Conti and Cecchetti (2003) criteria, result of this research shown that P. cruentum was only in the category of bioaccumulator, rather than good bioaccumulator similar to the result of Sekabira et al (2011). However, it does not mean that P. cruentum do not good bioaccumulator, since Conti and Cecchetti (2003) developed BCF for fish, therefore it was difficult to gain the criteria of good bioaccumulator for microalgae due to the microscopic size that was very difficult to reach BCF of more than 1,000 ppm. However, the short of accumulation time was the advantages of P. cruentum as a good organism to remediate heavy metal pollution.
2 Materials and Methods
P. cruentum stock was collected from Main Center Brackish water Aquaculture Development, Jepara-Indonesia. All equipments had been sterilized to eliminate or minimize the presence of microorganisms or substances bullies on tools and cultivation media during the study. 1 liter sea water with a salinity of 28 ppt that enriched with Walne medium was used as a culture media. During the treatments, pH, temperature, salinity, and light intensity were maintained to be stabile on 7~8, 28?~32?, 32~34 ppt, and 4,200 lux, respectively.
Porphyridium requires trace heavy metals concentration; however, there were many industries that discharged their wastes in high concentration above the waste standard criteria. Indonesia Government Regulation of Ministry of Environment Criteria for industrial waste stated maximum concentration of Pb, Cd, and Cu were 1, 0.1, 2 mg/L. Costa and Franca (2003) used the concentration of 42.3±2.0 and 61.2±1.1 mg/L to determine the Cd uptake by Tetraselmis chuii. Belokobylsky (2004) used Cr concentration of 3 mg/L to determine the accumulation on the Spirulina platensis.Syahputra (2008) treated Chlorella pyrenoidosa with 3.29 mg/L Cu from metal plated industry.
The 1, 3, and 5 mg concentrations of Pb, Cd, Cu, and Cr were exposed to the P. cruentum culture, respectively. These concentrations were arranged based researches mentioned above, and on the preliminary study on the 0.5 mg/L that induced alga growth (Soeprobowati and Hariyati, 2012).
The trace elements were added to the culture media in the form of Pb (NO3), 3Cd SO4.8H2O, CuCl2.2H2O, and CrCl3.6H2O. The initial concentration on the culture media was measured as well as on the day 7 and 14. The initial concentrations were heavy metal concentrations in the sea waters added with treatment concentration. These initial concentrations had used for the following calculation, and mention as 1, 3, or 5 mg/L of heavy metals treatment. However, the initial heavy metals of the cell concentration do not measure. It was assume that there were no heavy metals concentration in the initial cell, caused of the stock had been collected from under control nutrients and environments condition. For further research, the measurement of initial cell concentration will provide more detail data that able to be compared.
Algae cultured in the Walne medium without heavy metals served as controls. All experiments were performed in triplicates. Every day the population was counted for 14 days. In the beginning, day of 8 and end of experiment the concentration of Pb, Cd, Cu, and Cr was measured with AAS.
A reduction of heavy metals was calculated as well as P. cruentum population. Bioconcentration Factor (BCF) was calculated to determine the accumulation of heavy metals in the P. cruentum. BCF is a comparison between chemical concentrations on the organism with the concentration on the environment (Ivanciuc et al., 2006).
BCF Corg/Cmedia
Corg was heavy metals concentration in Porphyridium cruentum (S.F. Gray) Nägeli
Cmedia was heavy metals concentration in the culture media
Author’s Contribution
Authors worked together in the laboratory experiment. TRS was responsible on the P. cruentum population growth and RH for water quality control. TRS drafted the manuscript, and authors read approved the final manuscript.
This project is supported by Indonesian Higher Education through 2012 DIPA UNDIP for Fundamental Research Grant Number: 117b-3/UN7.5/PG/2012 16 February 2012. Thanks for Kenanga Sari and Her Nur Yoga for helping in experimental preparation and data management.
Abu Al-Rub F.A., El-Naas M.H., Ashour I., and Al Marzouqi M., 2006, Biosorption of Copper on Chlorella vulgaris from Single, Binary and ternary Metal Aqueous Solutions, Process Biochemistry, 41: 457-464
Arad S.M., and Yaron A., 1992, Natural pigments from red microalgae for use in foods and cosmetics. Trends in Food Science & Technology, 3: 92-97
Arnot J.A. and GobasF.A.P.C., 2006, A Review of Bioconcentration Factor (BCF) and Bioaccumulation Factor (BAF) Assessments for Organic Chemicals in Aquatic Organisms Environmental Reviews, 14: 257-297
Banfalvi G. 2011. Cellular effects of heavy metals. Springer. London, pp. 364
Belokobylsky A.I., Ginturi E.I., Kuchava N.E., Kirkesali E.I., Mosulishvili, L., Frontasyeva, M.V., Pavlov, M.V., and Aksenova N.G., 2004, Accumulation of selenium and chromium in the growth dynamics of Spirulina platensis, Journal of Radioanalytical and Nuclear Chemistry 259(1): 65-68
Bahar M.M.; Megharaj M. and Naidu R., 2012, Toxicity, transformation and accumulation of inorganic arsenic species in a microalga Scenedesmus sp. Isolated from soil. Journal of Applied Phycology, 25: 913-917
Brinza L., Dring M.J., and Gavrilescu M., 2007, Marine micro- and macro-algal species as biosorpent for heavy metals, Environmental Engineering Management Journal 6: 237-251
Chen J.Z., Tao X.C., Xu J., Zhang T., and Liu Z.L., 2005, Biosorption of lead, cadmium and mercury by immobilized Microcystis aeruginosa in a column, Process Biochemistry40 (12): 3675-3679
Chojnacka K., Chojnacka A., and Gorecka H., 2005, Biosorption of Cr3+, Cd2+ and Cu2+ ions by blue–green algae Spirulina sp.: kinetics, equilibrium and the mechanism of the process, Chemosphere, 59:75-84
Chojnacka K., 2009, Biosorption and Bioaccumulation in Practice,Nova Science Publishers, Inc. New York, pp.149
Conti M.E., and Cecchetti G., 2003, A biomonitoring study: Trace metals in algae and mollusks from Tyrrhenian coastal areas. Environmental Research, 93 (1): 99-112
Costa A.C.A., and Franca F.P., 2003,Cadmium Interaction with Microalgal Cells, Cyanobacterial Cells, and Seaweeds; Toxicology and Biotechnological Potential for Wastewater Treatment, Marine Biotechnology 5: 149-156
Crawford R.L., and Crawford D.L., 2005, Bioremediation: principles and applications, Cambridge University Press, New York, pp. 406
Dwivedi S., 2012, Bioremediation of heavy metal by algae: current and future perspective. Journal of Advance Laboratory Research in Biology, 3(3): 229-233
Mustafa E.M., Phang S.M, and Chu W.L., 2012, Use of an algal consortium of five algae in the treatment of landfill leachate using the high-rate algal pond system, Journal of Applied Phycology 24: 953-963
Fuentes M.M.R., Fernandez G.G.A., Perez, J.A.S. and GuerreroJ.L.G., 2000, Biomass nutrient profiles of the microalga Porphyridium cruentum, Food Chemistry 70: 345-353
Girard J., 2010, Principles of environmental chemistry. 2nd ed. Jones and Bartlett Publishers, LLC, pp. 677
Huang J., Chen B., and You W., 2005, Studies on Separation of Extracellular Polysaccharide of Porphyridium Cruentum and its anti-HBV in vitro, Chine Journal of Marine Drugs, 24(5): 18-21
Huleihel M., Ishanu V., Tal J., and Arad S., 2011, Antiviral effect of microalgal polysaccharides on Herpes simplex and Varicella zoster viruses.Journal of Applied Phycology 13(2):127-134
Imani S., Rezaei-Zarchi S., Hashemi M., Borna H., Javid A., Zand A.M. and Abarghouei, H.B., 2011, Hg, Cd and Pb heavy metal bioremediation by Dunaliella alga,Journal of Medicinal Plants Research 5(13): 2775-2780
Ivanciuc T., Ivanciuc O., and Klein D. J., 2006, Modeling The Bioconcentration Factors and Bioaccumulation Factors of Polychlorinated Biphenyls with Posetic Quantitative Super Structure/Activity Relationship (QSSAR). Molecular Diversity 10: 133-145
Kumar T.S.J., Balavigneswaran C.K., and Srinivasakumar K.P., 2013. Biodiesel Fuel Production from Marine Microalgae Isochrysis galbana, Pavlova lutheri, Dunaliella salina and Measurement of its Viscosity and Density. International Journal of Marine Science 3(5): 33-35
Lamai C. Kruatrachue M., Pokethitiyook P., Upatham E.S., and V. Soonthornsarathool., 2005, Toxicity and Accumulation of Lead and Cadmium in the Filamentous Green Alga Cladophora fracta (O.F. Muller ex Vahl) Kutzing: A Laboratory Study, Science Asia31: 121-127
Leung M., 2004, Bioremediation: Techniques for Cleaning up a mess.BioTeach Journal, 2: 18-22
Lim S.I., Chu W.L., and Phang S.M., 2010, Use of Chlorella vulgaris for bioremediation of textile wastewater, Bioresource Technology 101: 7314-7322
McGeer J. C, Brix K.V., Skeaff J.M., Deforest D.K., Brigham S.I., Adams W.J., and Green A, 2003, Inverse Relationship Between Bioconcentration Factor and Exposure Concentration for Metals: Implications for Hazard Assessment of Metals in The Aquatic Environment. Environmental Toxicoogyl Chemistry 22(5):1017-1037
Miranda J., Krishnakumar G., and Gonsalves R., 2012, Cr6+ bioremediation efficiency of Oscillatoria laete-virens (Crouan and Crouan) Gomont and Oscillatoria trichoides Szafer: kinetics and equilibrium study, Journal of Applied Phycology, 24:1439-1454
Priyadarshani I., Sahu D., and Rath B., 2011, Microalgae bioremediation: current practices and perspectives. Journal of Biochemistry Technology 3(3): 299-304
Riesing T.F., 2006, Cultivating Algae for Liquid Fuel Production,  
Sekabira K., Origa H.O., Basamba T.A, Mutumba G., and Kakudidi E., 2011, Application of algae in biomonitoring and phytoextraction of heavymetals contamination in urban stream water. International Journal of Environmental Science Technology, 8 (1): 115-128
Soeprobowati T.R, Sugondo H., Hendrarto I.B., Sumantri I. and Toha B., 2001, Diatom and Ecological Changes of the River. Seri Penelitian Fakultas Biologi 4(2): 72-97
Soeprobowati T.R., Hadisusanto S. and Gell P., 2012, The diatom stratigraphy of Rawapening Lake, Implying Eutrophication History, American Journal of Environmental Science 8 (3): 334-344
Soeprobowati T.R. and Hariyati R., 2012, The Potential Used Of Microalgae For Heavy Metals Remediation. Proceeding The 2nd International Seminar on New Paradigm and Innovation on natural Sciences and Its Application, Diponegoro University, Semarang Indonesia, 3 October 2012: 72-87
Sobczuk T.M., Camacho F.G., Grima E.M., and Chisti Y., 2006, Effects of agitation on the microalgae Phaeodactylum tricornutum and Porphyridium cruentum (S.F. Gray) Nägeli, Bioprocess & Biosystem Engineering 28: 243-250
Syahputra B., 2008, Pemanfaatan Algae Chlorella pyrenoidosa untuk Menurunkan Tembaga (Cu) pada Industri Pelapisan Logam, Dec. 11, 2011
Trzeinska M., and Pawlik-Skowronska B., 2012, Differences in Zn and Pb resistance of two ecotypes of the microalga Eustigmatos sp. inhabiting metal loaded calamine mine, Journal of Applied Phycology, 25: 277-284
Velea S., Ilie L., and Filipescu L., 2011, Optimization Of Porphyridium cruentum (S.F. Gray) Nägeli Purpureum Culture Growth Using Two Variables Experimental Design: Light And Sodium Bicarbonate, U.P.B. Sciences Bulletin Series B 73(4): 81-94
Volesky B., 2007. Biosorption and me. Water Resources, 41: 4017-4029
Wang J., B. Chen X.R., Huang J., and Li M., 2007, Optimization of culturing conditions of Porphyridium cruentum using uniform design, World Journal of Microbiology and Biotechnology23: 1345-1350
Wang J., and Chen C., 2009, Biosorpents for heavy metals removal and their future. Biotechnology Advanced,27: 195-226

Wilde E.W., Radway J.C., Domingo J.S., Zingmark R.G., and Whitaker, M.J., 1988, Final Report for TTP# SR-16-PL-42 (Formerly SR-141019)- Bioremediation of Aqueous Pollutants Using Biomass Embedded in Hydrophilic Foam (U). DOE Contract No. DE-AC09-89SR18035. US of department Energy, pp. 262

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