In Vivo Absorption Spectra as Predictors of Algal Biomass and Pigment Content of the Cultured Microalgae Amphidinium carterae, Isochrysis galbana, Nephroselmis sp. and Anabaena sp.

1. Introduction

Microalgae are widely grown throughout the world to either produce raw biomass that can be fed to other organisms (such as rotifers in fish farms, mollusks, and crustaceans) or processed biomass that can be used to extract useful chemical molecules (such as biological pigments, biofuels, proteins, etc.) from the biomass [1,2,3]. It is essential to precisely and efficiently quantify the biomass of cultivated algae in order to assess their growth performance and gather information on their physiological and biochemical processes. An algae culture's growth can be monitored using both invasive and non-invasive methods, whether it's in a lab for research or an industrial plant for production. Which approach is more efficient relies on how carefully the operators use the techniques and how sensitive they are. Noninvasive methods include measuring optical absorbance in a spectrophotometer [10], determining dry weight after filtering, drying, and weighing, and quantifying cells with a hemocytometer [4,5,6,7,8,9]. Any other method that necessitates smashing cells and chemically analyzing their contents (such as those involving pigments, lipids, proteins, etc.) is intrusive. The algal mass can be precisely calculated by counting the cells with a hemocytometer [11,12] or by filtering and weighing the sample after it has dried. Cell counting is considered the most accurate method, although it takes a long time, is prone to misinterpretation, and is not suitable for microalgae that are filamentous, concatenated, or agglomerated [11]. In addition, both cell counting and weighing require some time to prepare and perform, and the challenge increases when there are many samples. Although cell counting based on the principle of suspended particle counting has recently been simplified and made more accurate with a flow cytometer [13,14], the method still requires an expensive, fine calibrated instrument, trained personnel, and can be used mainly only with unicellular microalgae [15,16]. However, the determination of the optical density of the sample using a spectrophotometer greatly simplifies the problem, since the optical density value can be very easily related to either dry weight or cell density if the necessary regression equations have been developed beforehand [9,17,18]. But in addition to biomass estimation at a single wavelength, the absorption spectrum can also be used to obtain relevant information about the composition of photosynthetic pigments. In order to harvest the biomass from a practical and cultural standpoint, it is essential to understand when the desired pigment reaches its peak concentration in the cells. Continuing the cultivation would be a waste of time, effort, and resources with no added benefit. We have no doubt that by simply looking at the absorption spectra, we can determine the density of the culture, the time at which certain pigments reach their peak, and the best time to harvest. This is based on our extensive observations of absorption spectra over a long period of time in various microalgal species. Estimating peak pigments from spectra can save growers time and money, even though it cannot entirely replace a full analytical methodology. However, prior research on individual microalgal species is necessary for the proper application of this method in order to understand how their culture develops under different environmental conditions and how their pigment concentration changes over time. In the current work, we have examined a number of microalgae (eukaryotic and cyanobacterial), all of which have been preliminary shown to be easily cultured and produce useful amounts of pigment. We investigated how the absorption spectra change during the cultivation period for a given set of environmental factors (salinity, temperature, white light intensity) for each particular species. As illumination is a highly representative and influential condition for cultivation, we evaluated the change in spectra during the cultivation period, by comparing two different lighting situations in the case of the cyanobacterium Anabaena sp. The results of the current study can be used as a planning tool for mass production of the microalgae described here, as well as other microalgae that are first subjected to a similar study. The growers using white or colored light and the absorption spectra can determine the best time to achieve the perfect combination of microalgae quantity and pigment content by evaluating the absorption spectra.

2. Materials and Methods

The species of marine microalgae used were the chlorophyte Nephroselmis sp., the dinophyte Amphidinium carterae, the haptophyte Isochrysis galbana and the cyanobacterium Anabaena sp. All 4 species were isolated from a survey in the lagoon of Messolonghi (W. Greece, 38°20′05.16″ N, 21°25′28.51″ E) [19,20] and were kept in the laboratory as monocultures. All were batch cultured indoors (Figure 1) in air-conditioned room at 20-21 ^oC, at salinity of 30 ppt (Amphidinium) or 40 ppt (Nephroselmis, Isochrysis, Anabaena) and 8000 lux white light intensity while for Anabaena 2000 lux were also used. One-liter glass Erlenmeyer flasks or specially configured 1 L plastic bottles (for Amphidinium) were used, , filled to the 0.9 L mark with previously sterilized water enriched with Walne’s medium. Walne's medium formula consists of 3 final stock solutions A, B, and C, each of which was employed in a ratio of 1 mL per liter of culture water. Basic nutrients N, P and K comprise solution A made by dilution of 300 g of NaNO₃, 20 g of NH₄Cl, and 30 g of KH₂PO₄ (Merck, Germany) in 1 L of distilled water. Trace elements (Merck, Germany) in solution B include ZnSO₄.H₂O (30 g), CuSO₄.5H₂O (25 g), CoSO₄.7H₂O (30 g), and MnSO₄.H₂O (20 g) diluted in 1 L of distilled water. Vitamin B12 (100 mg), biotin (100 mg), and thiamine (10 mg) (Merck, Germany) diluted in 1 L of distilled water make up solution C. Cultures and measurements of the various analyses were done in triplicates.

White light emitted by an array of 20 Watt 1600 lm LED lamps was used and the desired intensities of 40 and 160 μmol photons/m²/s (2000 and 8000 lux, respectively in the case of Anabaena) were attained by properly placing the vessels at the proper distance from the lamps. Intensity was measured at the middle of the outer surface of the vessels by means of a luminometer (BIOBLOCK LX-101, Panasonic). The illumination period of 16hL:8hD was controlled by an electric timer switching on/off appropriately the lamps. The cultures were kept in suspension by means of bubbling air (with its natural CO₂ level) through a 2-mL glass pipettes (one in every vessel) at a rate of half culture volume/min. The pipettes were connected through sterilized plastic hoses to the 0.45 μm filtered central air supply system fed by a blower.

A known volume of culture was filtered using 0.45 m GF/C filters in a vacuum pump (Heto-SUE-3Q) to determine the dry weight. The filters were washed with ammonium formate to remove salts and then placed in a 100 ^oC oven for two hours. The dry weight was then calculated as g/L after they had been weighted to the fourth decimal digit.

Chlorophyll-a and total carotenoids in the case of the cyanobacterium Anabaena sp. were extracted with absolute methanol from centrifuged culture samples. In brief, 2mL of cyanobacterial culture was centrifuged at 5000 rpm for 7 min and then 2mL of methanol pre-cooled at 4 ^oC was added to the sediment and vigorously homogenized. Then the tube was covered with foil and incubated for 20 min. at 4 ^oC. The mixture was centrifuged at 5000 rpm at 4 ^oC for 7 min and the supernatant was measured in the spectrophotometer. Their concentrations (μg/mL) were determined using the following equations [21]:

chl-a =12.9447 (A665-A720)

$$\mathrm{T}\mathrm{o}\mathrm{t}\mathrm{a}\mathrm{l} \mathrm{c}\mathrm{a}\mathrm{r}\mathrm{o}\mathrm{t}.=\frac{1000\left(\mathrm{A}470-\mathrm{A}720\right)-2.86\mathrm{c}\mathrm{h}\mathrm{l}\mathrm{o}\mathrm{r}-\mathrm{a}}{221}$$

where: (A) stands for the absorbance (or optical density-OD) of the processed sample at the indicated wave length using a Shimadzu UVmini-1240 UV-visible (Kyoto, Japan) spectrophotometer.

Chlorophyll-a, chlorophyll-b and total carotenoids in the case of the chlorophyte Nephroselmis sp. were extracted with DMSO from centrifuged culture samples. In brief, 2mL of algal culture was centrifuged at 5000 rpm for 7 min and then 2mL of prewarmed at 60 ^oC DMSO was added to the sediment and vigorously homogenized. Then the tube was covered with foil and incubated for 10 min. at 50 ^oC. The mixture was centrifuged at 5000 rpm for 5 min. and the supernatant was measured in the spectrophotometer. Their concentrations (μg/mL) were determined using the following equations [6]:

chl-a = 12.47(A665)−3,62(A649)

chl-b = 25.06(A649)−6.5(A665)

$$\mathrm{T}\mathrm{o}\mathrm{t}\mathrm{a}\mathrm{l} \mathrm{c}\mathrm{a}\mathrm{r}\mathrm{o}\mathrm{t}.=\frac{1000\left(\mathrm{A}480)-1.29(\mathrm{c}\mathrm{h}\mathrm{l}\mathrm{o}\mathrm{r}.-\mathrm{a}\right)-53.78\left(\mathrm{c}\mathrm{h}\mathrm{l}\mathrm{o}\mathrm{r}.-\mathrm{b}\right)}{220}$$

Chlorophyll-a and total carotenoids in the case of the dinophyte A. carterae and the haptophyte I. galbana were extracted with DMSO and determined as above, but for chlorophyll-c, the extraction was done with methanol at 20 ^oC and its concentration (μg/mL) was determined according to the equation [22]:

chl-c = 23.5902(A630)-7.8516(A647)- 1.5214(A664)-1.7443(A691)

The phytocyanin (PC) content was extracted by freezing (-20 ^oC) for 24 hours a concentrated known amount of culture in 0.1 M sodium phosphate buffer (pH 7.1) as solvent at a ratio of 1:10 (algal mass: solvent), and then thawing at 4 ^oC in the dark. The freezing and thawing process was repeated over the period of two days. The sample's slurry was then centrifuged for 5 minutes at 3000 rpm, and the supernatant's concentration of phycocyanin (measured in mg/mL) was calculated using the formula.:

$$\mathrm{P}\mathrm{C}=\frac{{\mathrm{A}615}_{}-0.474{\mathrm{A}652}_{}}{5.34}$$

From the above equation the yield in phycocyanin (PC) in mg PC/g dry weight was calculated using the equation [23]:

$$\mathrm{P}\mathrm{C}\mathrm{y}\mathrm{i}\mathrm{e}\mathrm{l}\mathrm{d}=\frac{\mathrm{P}\mathrm{C}\left(\frac{\mathrm{m}\mathrm{g}}{\mathrm{m}\mathrm{L}}\right)\mathrm{x}\mathrm{V}\left(\mathrm{m}\mathrm{L}\right)}{\mathrm{D}.\mathrm{W}.\left(\mathrm{g}\right)}$$

where: PCyield = mg of phycocyanin per g algal dry weight

V = volume of solvent used (mL)

D.W. = grams of dry weight of the algal mass used

Daily cell counting with a Fuchs-Rosenthal haematocytometer for single-celled species and drying-weighing a sample filtrate of the filamentous cyanobacterium every 3–4 days were used to measure algal growth, which was measured as either cells/mL for single-celled microalgae or dry weight (g/L) for the filamentous cyanobacterium. At the same time, the optical density at 750 nm was recorded in the spectrophotometer (for all species). Using untreated culture samples, the absorption spectra of the cultures at different stages of maturation were recorded in a Shimadzu UV-1800 (Kyoto, Japan) spectrophotometer, and the data were transformed using its UVprobe 3.2 software.3. Statistical calculations of regression lines, Pearson’s correlation coefficient, standard deviation (SD) and standard error (SE) were made with Excel (Microsoft, USA). For comparisons of pigment content ANOVA was used followed by pair wised Tukey’s test using the free PAST3 software.

3. Results

3.1. Amphidinium carterae

A. carterae was cultured for 15 days in 1 L plastic bottles with a salinity of 30 ppt and 8000 lux of illumination. From the second to the fifteenth day of culture, six absorption spectra were recorded, with cell densities ranging from 485,000 cells/mL on the second day to 3,050,000 cells/mL on the fifteenth day (Figure 2). Based on the plot of each spectrum's optical density (OD) at 750 nm versus the corresponding algal densities (Figure 3A), a regression line with R²=0.986 and its first order equation was produced: “cell density (cells/mL) = 3,000,000 x OD750nm - 317,746”.

The overall picture of the spectra displays a uniform shape of the curves with virtually flat shape for the first (2^nd day), and then, in the following days, a gradually increasing peaking at the wave lengths that distinguish the different pigments (675 and 440 nm for chlorophyll-a, 465 nm for carotenoids and 590 nm for chlorophyll-c). In the final spectrum (of the highest algal density), peaks for all the aforementioned wave lengths became significantly more pronounced. Figure 4 shows the values of each pigment for each spectrum's associated wave length and algal density. All pigments clearly increased as the culture matured, and this rise was especially noticeable in the last two spectra with algal densities of 2,460,000 and 3,050,000 cells/mL. Chlorophyll-a was always much higher than chlorophyll-c or total carotenoids at all densities. At the density of 3,050,000 cells/mL, the maximum concentration of all pigments was recorded as: 5.863±0.322(SE) μg/mL chlorophyll-a, 2.183±0.019(SE) μg/mL chlorophyll-c and 4.517±0.099(SE) μg/mL total carotenoids. Using the pigment values, their plot against their corresponding values of 750 nm are depicted in Figure 3B. The regression equations for pigment – OD 750 nm relation: ”Chlor.-a (μg/mL) = 6.0279x(OD 750 nm) - 0.8847” (R² = 0.9833), “Total carot. (μg/mL) = 5.26x(OD 750 nm) - 1.2923” (R² = 0.9865) and “Chlor.-c (μg/mL) = 2.4032x(OD 750 nm) - 0.5071” (R² = 0.9843), are all very predictive as indicated by their very high Pearson’s coefficient (R²>0.98).

3.2. Isochrysis galbana

I. galbana was cultured for 18 days in 40 ppt salinity, 8000 lux illumination, and 1 L glass Erlenmeyer flasks. From the second to the sixteenth day of culture, 8-day absorption spectra were recorded, with cell densities ranging from 1,420,000 cells/mL on the second day to 17,000,000 cells/mL on the sixteenth day (Figure 5). The plot of each spectrum's optical density (OD) versus the corresponding algal densities at 750 nm (Figure 6A) produced a regression line with R²=0.996 and was described by the first order equation: “cell density (cells/mL) = 10⁷ x OD750nm – (6x10⁶)”.

The overall appearance of the spectra displays a uniform shape of the curves with an almost flat shape for the first spectrum (2^nd day), followed by gradual increases in the following days (4^th, 6^th, 7^th, and 9^th) and then an abrupt increase (11^th, 13^th, and 16^th day) in the peaking at the wave lengths that are indicative of its various pigments (680 and 435 nm for chlorophyll-a, 500 nm for carotenoids, 590 and 640 nm for chlorophyll-c). The final spectrum (with the greatest algal density of17 x 10⁶ cells/mL, 16^th day) showed peaks for all of the aforementioned wave lengths that were significantly more pronounced. The values of each pigment for every corresponding wave length and algal density of each spectrum are depicted in Figure 7. There is an obvious increase of all pigments along the maturation of the culture which became much prominent in the last two spectra of algal densities of 10,400,000 and 17,000,000 cells/mL. The value of chlorophyll-a at all densities was always higher than either chlorophyll-c or total carotenoids (P<0.05). The maximum content in all pigments was recorded at the density of 17 x 10⁶ cells/mL with: 11.977±0.052(SE) μg/mL chlorophyll-a, 7.987±0.084(SE) μg/mL chlorophyll-c and 10.113±0.074(SE) μg/mL total carotenoids. Using the measurent pigment concentrations, their plot against their corresponding values of 750 nm are depicted in Figure 6B. The regression equations for pigment – OD 750 nm relation: ”Chlor.-a (μg/mL) = 5.3491x(OD 750 nm) + 2.5417” (R² = 0.9879), “Total carot. (μg/mL) = 6.399x(OD 750 nm) - 1.2655” (R² = 0.9856) and “Chlor.-c (μg/mL) = 3.8151x(OD 750 nm) + 1.3218” (R² = 0.9721), are all very predictive as indicated by their very high Pearson’s coefficient (R²>0.97).

3.3. Nephroselmis sp.

Nephroselmis sp. was cultured for 20 days in 1 L glass Erlenmeyer flasks at a salinity of 40 ppt with 8000 lux illumination. From the second to the nineteenth day of culture, seven absorption spectra were recorded, with cell densities ranging from 6,350,000 cells/mL on the second day to 28,4000,000 cells/mL on the nineteenth day (Figure 8). The plot of each spectrum's optical density (OD) at 750 nm versus the corresponding algal densities (Figure 9A) produced a regression line with R²=0.9947 and was explained by the first order equation: “cell density (cells/mL) = 3x10⁷ x OD750nm - 10⁷”.

The overall appearance of the spectra reveals a consistent unique shape of the curves with barely perceptible peaks in the first one (2^nd day), and then, in the following days, a gradually increasing peaking at the wave lengths that distinguish the different pigments (682 and 440 nm for chlorophyll-a, 491 nm for carotenoids and 627 nm for chlorophyll-b). In the last two spectra, peaks for all of the aforementioned wave lengths became considerably more noticeable (of days 17 and 19 with the highest algal densities). Figure 10 shows the values of each pigment for each corresponding algal density of each spectrum. There is an obvious increase of all pigments along the maturation of the culture which became much prominent in the last two spectra of algal densities of 26,900,000 and 28,400,000 cells/mL. The value of chlorophyll-a at all densities was always higher than either chlorophyll-b or total carotenoids (P<0.05). The maximum content in all pigments was recorded at the density of 28,400,000 cells/mL with: 12.487±0.273(SE) μg/mL chlorophyll-a, 3.733±0.033(SE) μg/mL chlorophyll-b and 7.99±0.064(SE) μg/mL total carotenoids. Using the pigment values, their plots against their corresponding values of 750 nm are depicted in Figure 9B. The regression equations for pigment – OD 750 nm relation: ”Chlor.-a (μg/mL) = 10.205x(OD 750 nm) – 3.166” (R² = 0.9793), “Total carot. (μg/mL) = 8.516x(OD 750 nm) – 4.9908” (R² = 0.987) and “Chlor.-b (μg/mL) = 4.429x(OD 750 nm) – 3.0029” (R² = 0.9716), are all very predictive as indicated by their very high Pearson’s coefficient (R²>0.97).

3.4. Anabaena sp.

The culture of Anabaena sp. lasted 17 days and was done in 40 ppt salinity, illumination of 2000 and 8000 lux and using three 1 L glass Erlenmeyer flasks for each set of illumination. All parameters were examined and recorded separately for each of the light intensities except for the correlation of the dry weight – OD 750 nm where pooled data from both intensities were used.

Absorption spectra of 5 days were recorded covering the period from the 2^nd till the 16^th day of culture, with recorded dry weights from 0.45 and 0.407 g/L the second day up to 1.141 and 1.727 g/L the sixteenth day for low light (L) of 2000 lux and extra light (XL) of 8000 lux, respectively (Figure 11). Based on the 750 nm value of optical density (OD) of each spectrum, their pooled plot against the corresponding dry weight (Figure 12A) resulted in a regression line with R²=0.9989 and described by the first order equation “dry weight (g/L) = 1.2368 x OD750nm + 0.0754”.

The overall picture of the spectra shows a uniform overall shape of the curves with slightly discernable peaks for the first one (2^nd day) and afterwards, in the next days, a gradual increase in the peaking at the wave lengths that characterize the various pigments (679 and 439 nm for chlorophyll-a, 490 nm for carotenoids and 630 nm for phycocyanin). Peaks for all the above wave lengths became much prominent in the last two spectra (of days 12 and 16 with the highest algal densities). The values of each pigment for every corresponding algal density of each spectrum are depicted in Figure 13. There is an obvious increase of all pigments along the maturation of the culture which became much prominent in the last two spectra of algal densities of 1.424 and 2.089 g/L in L and 1.510 and 1.784 g/L in XL.

The value of chlorophyll-a at all densities of both light conditions was always higher than that of total carotenoids. The maximum content was recorded at the dry weight of 2.089 g/L with: 9.713 ± 0.123(SE) μg/mL chlorophyll-a and 4.839 ± 0.095(SE) μg/mL total carotenoids in “L” and at 1.784 g/L with: 8.75 ± 0.323(SE) μg/mL chlorophyll-a and 4.742 ± 0.091(SE) μg/mL total carotenoids in “XL”, values statistically equal (P>0.05) for carotenoids between the two light regimes and higher (P<0.05) in the case of chlorophyll in the “L” regime. In the case of phycocyanin the situation was totally different as the proportion of phycocyanin content in either concentration (mg/mL) or yield (mg/g dw), was significantly higher (P<0.05) in the final stages of the cultures in the condition of low (L) light (2.126 ± 0.078 mg/mL and 29.785 ± 1.687 mg/g d.w.) as compared to high (XL) light (0.943 ± 0.102 mg/mL and 24.697 ± 0.366 mg/g d.w.) (Figure 13).

Using the pigment values, their plot for chlorophyll-a and total carotenoids against their corresponding values of 750 nm using pooled data from both light regimes are depicted in Figure 12B. The regression equations for pigment – OD 750 nm relation: ”Chlor.-a (μg/mL) = 7.6403x(OD 750 nm) – 0.8902” (R² = 0.9847) and “Total carot. (μg/mL) = 4.3358x(OD 750 nm) – 1.1666” (R² = 0.9907), are both very predictive as indicated by their very high Pearson’s coefficient (R²>0.98). The corresponding equations for phycocyanin – OD 750 nm relation (Figure 12C) were calculated separately for “L” and “XL” illumination and resulted in: ”Phycocyanin (mg/mL) = 1.7797x(OD 750 nm) – 0.2299” (R² = 0.9687) in “L” and ”Phycocyanin (mg/mL) = 0.6984x(OD 750 nm) + 0.0765” (R² = 0.9897) in “XL”, both very predictive as indicated by their very high Pearson’s coefficient (R²>0.965), much higher than their respective one using pooled data from both light regimes (R² = 0.6389).

4. Discussion

The ability of each alga to photosynthesize depends on (and is influenced by) the composition of pigments in its photosynthetic system [24] and more generally on the size and shape of cells, especially those of phytoplankton species. Therefore, when two microalgal species are compared in monoculture, their absorption spectra can be expected to have (and do have) a particular shape that distinguishes them from each other. There are many reasons to study the absorption spectra of different microalgae [25]. For example, one can identify the pigments they contain or compare the location and height of a pigment's peak between a live culture sample and the extracted pigment to calculate the extent to which the pigment's absorption properties are altered by coupling to proteins. Applying the absorbance spectrum of a culture sample of a particular microalga to the calculation of important culture parameters (such as culture density, amount of pigment, etc.) cannot be done with absolute precision. This is because various factors, such as turbidity or other water constituents, either mask or introduce "noise" to the true shape of the spectrum as it would be produced by the pigments present alone. Although such a method may be considered inferior to the highest precision of a biochemical analysis, under production conditions it is critical to have a rapid and repeatable means of determining when the maximum algal biomass should be harvested or when the level of a desired pigment reaches its peak. When analyzing an absorption spectrum, two important things can be discovered. First, whether the culture density is expressed as cells/ml or as grams of dry weight per liter, the absorbance value at 750 nm has been shown to be the most accurate in numerous experiments [6,9] as this wavelength avoids the absorption of light by the photosynthetic pigments, which can affect this parameter, and only allows the measurement of the optical density of the cells. The spectra of all varieties of microalgae in the current study were examined and the values around 750 nm were found to have no peaks, making them the best predictors of biomass. The second component is to determine how the pigment peaks changed as the culture successively matured. This allows the grower to decide, or even predict, the best time to harvest the highest yield from the crop. In the current work, it was shown that the correlations between the concentration values of each pigment and the corresponding absorbance values at 750 nm for each absorbance spectrum of a given culture density cannot be ignored. But the next point must be noted. According to this, each absorption spectrum has its own characteristics and predictive value only under certain circumstances (phytoplankton species, temperature, and illumination)since the spectra are shaped differently depending on the conditions with respect to the critical values of absorption at 750 nm and the various other wavelengths that characterize the different pigments. This, together with the fact that not all pigments give rise to the same intense and obvious change in their peaks in the spectra, must make us particularly cautious when applying the predictive power of the spectra in relation to the concentration of the pigments, as shown by the present study. The case of the cyanobacterium Anabaena, where two different illumination intensities were applied, is the most illustrative example supporting the aforementioned claim. While the correlations between dry weight and 750 nm and between chlorophyll-a or total carotenoids and 750 nm with pooled values for both intensities show a very strong relationship with an apparent predictive value, in the case of phycocyanin such a strong correlation is shown only when the correlation of phycocyanin-750 nm is applied separately for the spectral values of each light intensity. The results on the effects of illumination on cyanobacteria in recent works [21,26,27] can also be seen as confirming this phenomenon although culture parameters (light, temperature, salinity, aeration, pH) have a significant effect on cell growth of a given microalgal species and the same is true for pigment content [24,29,30,31], this should not deter researchers from exploring the predictive potential of absorption spectra. However, this should be done only after sufficient time and effort has been invested in the basic biochemical studies in the culture of an algae under conditions found to be suitable so that they can be recorded as reference values in the respective environments. In the current study, selected species of microalgae from different taxa were examined, and it was shown that analysis of absorption spectra can be predictive for all of them, even when pigment content varies. While other researchers have found similar predictive power for cell density and pigment content using the corresponding wavelengths [7,8,32,33,34,35] without looking at the absorption spectra, our study uses similar techniques and an integrated approach that uses the absorption spectra as a comprehensive predictive tool for both qualification and quantification of biomass and pigment content.

5. Conclusions

The measurement of the biomass growth efficiency of 4 microalgae under laboratory circumstances was made possible by spectrophotometric analyses employing the absorption spectra. Monitoring of cell density or dry weight is made possible by using the optical density at 750 nm while also figuring out how much pigment is present in the microalgae that have been developed. On the basis of the data gathered, conclusions about different stages of the growth of the algae population can be made. By analyzing the absorption spectrum of a particular species' culture, under a particular set of conditions, and at a particular stage of growth, the optical density value of 750 nm and the various respective values at the wave lengths characterizing various pigments of each particular spectrum can be used as a reliable predictor of algal biomass and pigment content.