Changes in Stoichiometry, Cellular RNA, and Alkaline Phosphatase Activity of Chlamydomonas in Response to Temperature and Nutrients.

Phytoplankton may respond both to elevated temperatures and reduced nutrients by changing their cellular stoichiometry and cell sizes. Since increased temperatures often cause increased thermal stratification and reduced vertical flux of nutrients into the mixed zone, it is difficult to disentangle these drivers in nature. In this study, we used a factorial design with high and low levels of phosphorus (P) and high and low temperature to assess responses in cellular stoichiometry, levels of RNA, and alkaline phosphatase activity (APA) in the chlorophyte Chlamydomonas reinhardtii. Growth rate, C:P, C:N, N:P, RNA, and APA all responded primarily to P treatment, but except for N:P and APA, also temperature contributed significantly. For RNA, the contribution from temperature was particularly strong with higher cellular levels of RNA at low temperatures, suggesting a compensatory allocation to ribosomes to maintain protein synthesis and growth. These experiments suggest that although P-limitation is the major determinant of growth rate and cellular stoichiometry, there are pronounced effects of temperature also via interaction with P. At the ecosystem level, nutrients and temperature will thus interact, but temperatures would likely exert a stronger impact on these phytoplankton traits indirectly via its force on stratification regimes and vertical nutrient fluxes.

Introduction

Elemental composition and temperature are key factors that affect growth and stoichiometry in class="Species">algae. The ambieclass="Chemical">nt coclass="Chemical">nceclass="Chemical">ntratioclass="Chemical">n class="Disease">ns and ratios of key elements, such as carbon (C), nitrogen (N), and phosphorus (P) will have major impacts of phytoplankton elemental ratios and thus growth (Sterner and Elser, 2002; Klausmeier et al., 2008). Nutrient uptake and demands in autotrophs do also depend on ambient temperatures. The direct responses of temperature related to growth rate and stoichiometry are primarily governed by kinetic responses, i.e., enzyme activity, cell division, and nutrient uptake that may occur at higher rates with elevated temperature. However, also macromolecular make-up, rate of protein synthesis, and storage of elements may respond to temperature, which in this way also indirectly affect growth and cellular stoichiometry (Woods et al., 2003; Klausmeier et al., 2004; Toseland et al., 2013).

In class="Species">higher plants aclass="Chemical">nd multicellular class="Chemical">n class="Species">algae, there has been observed a general decline in specific N and P contents when moving from cold, high latitudes, toward the warmer, equatorial regions (Reich and Oleksyn, 2004; Borer et al., 2013). The decrease in P content with elevated temperatures is higher than that of N, however, causing an increase in the overall N:P ratio with increased temperature (or decreased latitude). Several studies have revealed a similar positive correlation between the overall N:P ratio of marine phytoplankton and global temperature (Martiny et al., 2013; Toseland et al., 2013; Yvon-Durocher et al., 2015), but there are few comparative lake studies, despite the fact that a strong increase in lake temperatures has been recorded worldwide (O’Reilly et al., 2015). A higher N:P with elevated temperature is likely associated with the increased enzyme efficiency at higher temperatures that cause a lower cellular density of P-rich ribosomes because fewer ribosomes are then needed to maintain a certain level of protein synthesis (Toseland et al., 2013; Thrane et al., 2016, 2017). If true, levels of RNA would also be reduced with elevated temperature, but again this response could be confounded by ambient nutrient concentrations.

Decreased phytoplankton cell size is another proposed respoclass="Disease">nse to warmiclass="Chemical">ng (Atkiclass="Chemical">n class="Disease">nson et al., 2003; Daufresne et al., 2009; Sheridan and Bickford, 2011; Forster et al., 2012). The causality for smaller cell size, notably at the intraspecific level, remains obscure however. Experimental studies on phytoplankton indicate contributions both from ambient nutrient levels and temperature per se to cell size (Peter and Sommer, 2013, 2015), but it is difficult to disentangle the drivers based on in situ studies because warming also will affect thermal stratification, mixing depth, and thus vertical nutrient fluxes in aquatic ecosystems (Galbraith and Martiny, 2015). Reduced concentrations of ambient nutrients in response of reduced mixing would promote smaller cells owing to their higher surface-to-volume ratios and thus higher nutrient affinities (Raven, 1998; Marañón et al., 2012; Marañón, 2015). Hence in a “global change” context, both temperature and nutrient fluxes will change, with expected effects on the stoichiometry, growth and size of phytoplankton, yet likely with several confounding interactions (Sommer et al., 2016).

With this study, we aim to disentangle the effects of temperature and nutrients on phytoplankton growth and stoichiometry under controlled experimental conditioclass="Disease">ns. To assess the respoclass="Chemical">n class="Disease">nses in stoichiometry and growth, and the related responses [RNA, alkaline phosphatase activity (APA), and cell size] we conducted a factorial experiment with the chlorophyte Chlamydomonas reinhardtii, under high and low temperatures and high and low concentrations of phosphorus.

Materials and Methods

For the experiments, we used the unicellular chlorophyte C. reinhardtii (strain CC-1690 wild type mt+) obtained from the class="Species">Chlamydomonas Resource Ceclass="Chemical">ntre (Uclass="Chemical">niversity of Miclass="Chemical">nclass="Chemical">nesota). The species, aclass="Chemical">nd class="Chemical">notably this straiclass="Chemical">n, is widely used for experimeclass="Chemical">ntal studies. While this species clearly may class="Chemical">not be represeclass="Chemical">ntative for all phytoplaclass="Chemical">nktoclass="Chemical">n respoclass="Chemical">n class="Disease">nses, it is commonly found across a variety of freshwater habitats and widely used also in ecologically relevant experiments.

The experiment was designed as a cross factorial setup with two P treatments (5 μmol P L-1 or 25 μmol P L-1), hereafter low P (class="Chemical">LP) aclass="Chemical">nd high P (class="Chemical">n class="Chemical">HP), and two temperature treatments (13 or 19°C), designated low temperature (LT) and high temperature (HT), respectively. While the concentrations of P only differ by a factor of 5, the use of chemostats and turbidostats produced P-limited and P-sufficient cultures by design (see details below), and hence the actual P-concentrations were not critical in this context. A wider temperature gradient would likely provide stronger temperature responses, but the applied temperature represent a “realistic” span in epilimnetic summer temperatures of temperate lakes. Each treatment had three replicates. The experiments were run as semicontinuous cultures in 40 ml tissue bottles (Nunclon Delta filtercap, Thermo Scientific). We used a modified version of Guillard and Lorenzen’s (1972) WC medium with filtered water from a high-alkalinity lake as a base to minimize the risk of CO2-deficiency. Excess N was ensured by keeping N:P well above Redfield ratio (Redfield, 1958). A concentration of 1000 μmol NO3 was used in both the high and LP treatments yielding molar N:P-ratios of 40:1 and 200:1, respectively. The lake water was initially filtered on Whatman GF/F and then sterile filtered (0.2 μm pore width) prior to additions of macronutrients, trace elements, and vitamins according to the WC medium recipe.

The class="Species">algae were cultivated iclass="Chemical">n two climate-coclass="Chemical">ntrolled rooms of LT aclass="Chemical">nd HT (13 aclass="Chemical">nd 19°C, respectively) with a 12:12 h light-dark cycle aclass="Chemical">nd a light iclass="Chemical">n class="Disease">nsity of approximately 85 μE m-2 s-1 of PAR (both cool and warm white light). For the LP treatment, a semicontinuous culture with a fixed dilution of 50% 3 days per week was applied. In this chemostat-type of dilution the algae are kept in a stationary growth phase below the carrying capacity. For the HP treatment we used a turbidostat-type of dilution where the culture was diluted to a fixed cell number (50,000 cells ml-1) 3 days per week. The turbidostat design is beneficial by a maintaining a fixed density of algae in a non-limited condition with regard to nutrients, light and CO2, thus avoiding the pitfalls of high-nutrient chemostats.

For all dilutioclass="Disease">ns, the cultures were traclass="Chemical">n class="Disease">nsferred to new bottles to avoid or minimize “bottle effects” like wall growth. Analysis of cell number (for growth estimates) and cell size were done at each day of dilution (3 days a week), samples for elemental ratios (C:N:P) were taken 14 days after inoculation, while samples for RNA and APA were taken 21 days after inoculation. However, because the APA results for two of the replicates in the HT × LP treatment had to be discarded due to a mistake made in the experimental procedure, we included a second sampling and analysis both for APA and RNA.

The cell number and size was measured by an electronic cell counter (CASY TT, Schärfe, Germany). A regular 12:12 h light:dark cycle was applied to synchronize cell division, and samples for estimatioclass="Disease">ns of cell declass="Chemical">n class="Disease">nsities and sizes were taken at the same time point each harvesting day. The specific growth rate was determined as the ln of relative change in cell abundance between two points in time (see Supplement for formula), and averaged for the duration of the experiment. As measures of cell size, we recorded both the mean and the peak (mode) of the size distribution of the algal samples.

For analysis of particulate C and N content, class="Species">algae were collected oclass="Chemical">n a GF/C filter (Whatmaclass="Chemical">n, Sigma-Aldrich), aclass="Chemical">nd aclass="Chemical">nalyzed usiclass="Chemical">ng aclass="Chemical">n elemeclass="Chemical">nt aclass="Chemical">nalyzer (Thermo Ficlass="Chemical">nclass="Chemical">negaclass="Chemical">n EA 1112 series flash, Thermo Fisher scieclass="Chemical">ntific). P-coclass="Chemical">nteclass="Chemical">nt was estimated by digesticlass="Chemical">ng the samples iclass="Chemical">n a solutioclass="Chemical">n of class="Chemical">n class="Chemical">potassium peroxydisulfate (K2S2O8) before colorimetric analyses using an autoanalyzer (Bran Luebbe, Norderstedt Germany). In this case, the samples were soaked in 10 ml of a 1% solution of potassium peroxydisulfate for 30 min at 120°C.

Cellular contents of RNA were included in the study both as a proxy of growth rate and to judge the effect of P-limitation. In addition, the total RNA serves as an indicator of the amount of ribosomal RNA in the cell (Flynn et al., 2010). For the RNA analyses, we applied a modified version of the RiboGreen fluorescence protocol (Turner BioSystems) (cf. Gorokhova and Kyle, 2002). Depending on cell declass="Disease">nsity, we sampled 1–4 ml from each culture. The sampled volume was filtered oclass="Chemical">n a class="Chemical">nitrocellulose membraclass="Chemical">ne (0.65 μm class="Chemical">n class="Chemical">DAWP, Millipore) and the filter stored in nuclease tubes before snap-frozen in liquid N. Prior to analysis, 120 μl of the extraction buffer was added (1% sarcosyl, Sigma) and, while still frozen, the samples were homogenized by ice-cold sonification (Branson Sonifier) for 2 min. The samples were again put on ice and diluted with TE buffer in a 1:5 ratio (10 mM Tris-HCL, 1 mM EDTA, pH 7.5). For each sample, we extracted 2 × 75 μl into two separate slots of a 96-well plate (655076 Greiner Bio-one, USA). The duplicates were inserted pairwise in the columns following the first, which was reserved for standard. In the first set of duplicate samples, we added a total of 20 μl RNase-free water (Gibco BRL1071), and in the other set of duplicates 20 μl of 0.1% RNase A (A7973, Promega). Immediately after the RNase mixture was added, the well plate was incubated at 37°C on a shaking table with the output 400RPM to ensure homogenous dispatch of the RNase and digestion of RNA. After the incubation, 75 μl of 100 × diluted RiboGreen dye (R-11490, Molecular Probes, USA) was added to each well by the use of an automatic eight-channel pipette. The RNA content was then analyzed by the use of a fluorescence microplate reader (Synergy MX, BioTek Instruments, USA) with an excitation wavelength of 480 nm and an emission wavelength of 525 nm.

class="Gene">Alkaline phosphatase activity was iclass="Chemical">ncluded iclass="Chemical">n the study as aclass="Chemical">n iclass="Chemical">ndepeclass="Chemical">ndeclass="Chemical">nt biomarker for P-limitatioclass="Chemical">n (Thiclass="Chemical">ngstad aclass="Chemical">nd Maclass="Chemical">ntoura, 2005; Litchmaclass="Chemical">n aclass="Chemical">nd Nguyeclass="Chemical">n, 2008; Waclass="Chemical">ng aclass="Chemical">nd Liaclass="Chemical">ng, 2014). This eclass="Chemical">nzyme is used to split the class="Chemical">n class="Chemical">ester bound in phosphomonoesters, thus removing phosphate groups from macromolecules scaled with the degree of P-deficiency (Hoppe, 2003). APA was analyzed by the CDP-star chemo-luminescence method according to the protocol of Wojewodzic et al. (2011). Samples for APA were collected as in the RNA analysis and stored at -80°C prior to analysis. For analysis, 0.3 ml of Triton X-100 solution (T8787, Sigma) was added to each sample (while kept on ice) and then sonified corresponding to the RNA procedure described above. The standards for the calibration curve were then prepared by using a concentration gradient AP type VII-S from bovine intestinal mucosa (P5521, Sigma). After the preparation of the standards, 20 μl of both the standards and the samples was transferred to a pyrophosphate-free 96-well plate (Nunc, 236105) kept on ice. Next 20 μl of the 0.4 mM CDP-star solution was dispensed with and automatic eight-channel pipette to all the wells. The APA contents of the cells were then analyzed using a fluorescence microplate reader (Synergy Mx, BioTek Instruments, USA). All statistical analysis and plotting were performed in the R programming environment v3.2 (R Development Core Team, 2016). The full script with additional data is given in the Supplementary Material.

Results

We found an overall strong effect of P-treatment on growth rates of class="Species">algae, but with temperature aclass="Chemical">nd the iclass="Chemical">nteractioclass="Chemical">n betweeclass="Chemical">n P-treatmeclass="Chemical">nt aclass="Chemical">nd temperature as importaclass="Chemical">nt explaclass="Chemical">natory factors coclass="Chemical">ntributiclass="Chemical">ng to differeclass="Chemical">nces iclass="Chemical">n growth (Figure ; Table ). At class="Chemical">n class="Chemical">HP × HT, growth rates stabilized at ca. 1.2 d-1, dropped to 0.77 d-1 at HP × LT, and further to 0.32 d-1 in the LP treatments. The growth rate responses remained stable during the 3 weeks course of the experiments (see Supplementary Figure S1).

Mean growth rates for the three replicates in each of the experimental treatments.

The cell-specific content of C, N, and P all responded to P treatments, yet in different fashioclass="Disease">ns (Figure ; Table ). The respoclass="Chemical">n class="Disease">nse in cell-specific C was modest, yet with somewhat lower C-content at LP × HT (Figure ). The same pattern was seen for cellular N, although in this case response was stronger, notably at HT, where cell-specific N was twice as high in the HP-treatment (Figure ), and for cellular P the differences were even stronger (Figure ). For N and P, there was also a positive interaction with temperature, where HP × HT yielded the highest cell-specific content of nutrients. This effect was most prominent for P. Since the cell sizes differed somewhat between treatments, and notably with reduced cell size at HT × HP (cf. Supplementary Figure S5), the estimates of cell specific elemental contents were corrected for cell size (using the mean of the cell size distribution). The correction was also applied for the other cell-specific responses (RNA and APA). The cell-specific results (not corrected for size) are given in the supplementary in the plot to the left in Supplementary Figures S6–S8 and S13 and S14. The size correction considerably changed the patterns for the C, N, and P contents, whereas RNA and APA basically displayed the same patterns as the non-corrected.

Volume corrected contents of class="Chemical">carbon (A), class="Chemical">n class="Chemical">nitrogen (B), and phosphorus (C) expressed as fraction of wet weight for each of the three replicates (gray circles) in the four experimental treatments. Points in black and dashed horizontal lines denote the mean in each group.

These respoclass="Disease">nses to the T × P treatmeclass="Chemical">nts yielded stroclass="Chemical">ng respoclass="Chemical">n class="Disease">nses in elemental ratios, and unsurprisingly with the largest deviation in C:P, primarily in response to P-treatment, and for C:N and C:P also with modest contribution from temperature (Figures ; Table ). The responses in N:P was consistent across temperature treatments with a fourfold decrease in N:P in the HP treatments. Also C:N responded strongly with lower ratios in the HP treatments, likely as a response to higher N-demands for protein synthesis with high access to P. In this case temperature also contributed, notably in the LP treatment with elevated C:N.

The elemental ratios for class="Chemical">carbon:class="Chemical">n class="Chemical">nitrogen (A), carbon:phosphorus (B), and nitrogen:phosphorus (C) for each of the three replicates (gray circles) in the four experimental treatments. Points in black and dashed horizontal lines denote the mean in each group. All ratios in molar units.

Cellular RNA responded strongly both to temperature and class="Chemical">phosphorus with higher levels at class="Chemical">n class="Chemical">HP and LT (Figure ; Table ). While RNA corresponded well with cellular P (Figure ), it deviated from the growth rate responses (cf. Figure ). Note that despite higher growth rates at HT (19°C), the RNA-concentration was higher at LT (13°C). APA ranged almost two orders of magnitude in response to P-treatment, with almost negligible contributions from temperature (Figure ; Table ).

Volume corrected RNA contents (A) and n class="Gene">alkaline phosphatase activity (APA)/eclass="Chemical">nzyme coclass="Chemical">nteclass="Chemical">nt (B) expressed as fractioclass="Chemical">n of wet weight for two sampliclass="Chemical">ng times. Poiclass="Chemical">nts iclass="Chemical">n black aclass="Chemical">nd dashed horizoclass="Chemical">ntal liclass="Chemical">nes declass="Chemical">note the meaclass="Chemical">n iclass="Chemical">n each group (vertical liclass="Chemical">nes = staclass="Chemical">ndard deviatioclass="Chemical">n).

The combined respoclass="Disease">nse for all variables to temperature aclass="Chemical">nd class="Chemical">n class="Chemical">phosphorus treatments can be summarized by a principal component analysis (Figure ). The analysis clearly supports that P treatment was the experimental factor that explained most of the variation in RNA and nutrient contents (the separation of points along PCA axis 1, which captures 82% of the variance, primarily reflects P treatment). Growth rate and APA activity is included in the plot as passive variables (i.e., they did not influence the ordination) and clearly convey a strong positive relationship between P availability and growth rate, and a negative one between P availability and APA.

Principal component analysis for respon class="Disease">nses related to RNA aclass="Chemical">nd elemeclass="Chemical">ntal coclass="Chemical">nteclass="Chemical">nt (size corrected) with growth rate aclass="Chemical">nd APA as passive variables.

Discussion

The overall conclusion from these experiments is that P-limitation is the major determinant of growth rate as well as stoichiometry and indicators thereof (RNA and APA), but that temperature also exerted a significant impact on most parameters. The cultures were maintained as chemostats (although semicontinuous) and turbidostats for the class="Chemical">LP aclass="Chemical">nd class="Chemical">n class="Chemical">HP treatments, respectively, to ensure chronically P-deficient and P-saturated cells. The APA analysis clearly showed that these premises were fulfilled with a striking deviation between HP and LP cultures under both temperatures. While APA only marginally responded to temperature, suggesting that this enzymatic response is not sensitive to a temperature span from 13 to 19°C, cellular RNA was much elevated at LT under both HP and LP, indicating a compensatory mechanism to maintain the rate of protein synthesis and thus growth at reduced temperature. Still growth rates were consistently lower at LT for the HP treatment (while not for LP).

The respoclass="Disease">nses iclass="Chemical">n RNA were also reflected iclass="Chemical">n the cell quotas of P, aclass="Chemical">nd heclass="Chemical">nce also the cellular stoichiometry. It is however class="Chemical">noteworthy that the respoclass="Chemical">n class="Disease">nse in C:P was not only related to cellular quotas of P, but also of C (Figure ). The fact that also C:N were impacted by elevated P likely reflects its effect on growth and protein synthesis. Cellular processes, such as transcription and translation require a coupling of N and P, where P is needed for mRNA synthesis while N is required for protein synthesis.

The causal relatioclass="Disease">nship betweeclass="Chemical">n the close correlatioclass="Chemical">n class="Disease">ns typically found between growth rate, P-content and RNA in small heterotrophs, such as bacteria, crustacean zooplankton, and other invertebrates (Elser et al., 2000), is not straightforward, i.e., high growth rate could promote high RNA-content, but also be a consequence of other factors promoting elevated growth rates (in both cases this presupposes that sufficient P is available for making RNA). Also the availability of N would modify the relationship between RNA and growth rate, since the rate of protein synthesis may be constrained by the access to N (amino acids).

The contrasting temperature respoclass="Disease">nses we fouclass="Chemical">nd betweeclass="Chemical">n cell-specific P-coclass="Chemical">nteclass="Chemical">nt relative to that of RNA is strikiclass="Chemical">ng, however, aclass="Chemical">nd with the proviso that we here oclass="Chemical">nly tested oclass="Chemical">ne species, aclass="Chemical">nd that cryophilic species might respoclass="Chemical">nd differeclass="Chemical">ntly, this support the “RNA-efficieclass="Chemical">ncy” hypothesis (cf. Woods et al., 2003; Cotclass="Chemical">ner et al., 2006). This meaclass="Chemical">n class="Disease">ns higher demands of RNA at low temperature to maintain the levels of protein synthesis. This may further result in decreased N:P-ratios at lower temperatures, or thus vice versa as a response of warming (Martiny et al., 2013; Toseland et al., 2013; Yvon-Durocher et al., 2015), which is supported by the observed trend of decreased N:P in foliage or macroalgae when moving pole-wards (Reich and Oleksyn, 2004; Borer et al., 2013). For pelagic autotrophs, however, the stoichiometric responses may be confounded by the aforementioned change in mixing regimes along temperature gradients, and our study on Chlamydomonas suggest no impact at all of temperature on N:P. The chlorophyte Chlamydomonas may, however, not necessarily be representative of responses in other taxa. Different species and taxa of phytoplankton may have different strategies and responses with regard to N and P acquisition together with the N:P ratio of nutrient availability (Klausmeier et al., 2004; Thrane et al., 2016). In a more detailed assay with the same strain of Chlamydomonas grown in microwells along a wide gradient of temperatures and ambient N:P in the media, the optimum N:P ratio shifted from 27 to 37 (atomic ratio) over a temperature gradient from 11 to 18°C (Thrane et al., 2017). Yet, as pointed out in their paper, there are differences in measured optimal demand ratios for maximum growth and the ratio of total cellular pools of N:P in cells. Very strong deviations in N:P should basically not be expected, however, due to the mutual demands for N and P under transcription and translation as well as other cellular processes. I.e., also APA may ultimately be influenced by N-availability (Marklein and Houlton, 2012), and while photosynthetic capacity may be limited by the high N-demands of the photosynthetic machinery, so may P-limitation constrain the production of Rubisco (Reich et al., 2009). Corresponding temperature responses in stoichiometry and RNA has been observed in heterotrophic bacteria (Cotner et al., 2006).

Among the parameters tested in this study, RNA gave the strongest temperature respoclass="Disease">nse with elevated cellular coclass="Chemical">nceclass="Chemical">ntratioclass="Chemical">n class="Disease">ns at LT, but also growth rate and C:P showed a relatively strong response to temperature. Since growth rate was positively related to temperature, especially at HP (Figure ), this does indeed suggest a stronger allocation of P to RNA under low temperature. The fact that it did not result in a corresponding decrease in N:P suggest that N-uptake and protein synthesis kept pace with P-uptake and RNA synthesis. RNA did not correspond well with growth rate across temperatures, and to which extent the growth rate hypothesis (GRH) holds for autotrophs is still a matter of controversy (Ågren, 2004; Matzek and Vitousek, 2009; Flynn et al., 2010). It is, however, important to note that the GRH was explicitly formulated to hold within temperatures (Elser et al., 2000), hence within temperature (either 13 or 19°C) growth rate clearly match RNA content (and P).

Whether or not temperature per se affect cell size, or indirectly via lower ambient nutrient concentratioclass="Disease">ns, is aclass="Chemical">n issue of major coclass="Chemical">ncerclass="Chemical">n iclass="Chemical">n the coclass="Chemical">ntext of global warmiclass="Chemical">ng. Iclass="Chemical">n our experimeclass="Chemical">nts, smaller cells were fouclass="Chemical">nd uclass="Chemical">nder class="Chemical">n class="Chemical">HP × HT, but this response likely reflects the higher rate of cell division in this treatment. Still this implies that systems with higher temperatures could give smaller cells, but only when sufficient nutrients are available to promote strong growth.

Although temperature poses a direct impact on phytoplankton traits, notably on growth rate and cellular RNA, judged from these experiments, temperature would be expected to exert the strongest impact on phytoplankton indirectly via changes in stratification regimes and vertical nutrient fluxes.

Author Contributions

class="Disease">DH had the idea of the experimeclass="Chemical">nt, aclass="Chemical">nd placlass="Chemical">nclass="Chemical">ned the desigclass="Chemical">n together with TA. OH was the maiclass="Chemical">n respoclass="Chemical">n class="Disease">nsible for conducting the experiment with help from CB, NS, and MW, and was also instrumental in the analysis of the data together with input from the other authors. CB run the final scripts, stats, and figures in discussion with TA and DH. DH wrote up the manuscript with input from all co-authors.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relation class="Disease">nships that could be coclass="Chemical">n class="Disease">nstrued as a potential conflict of interest.

Table 1

Fraction of total variance explained by temperature and P limitation treatments, and their interaction.

Variable	Growth rate (per day)	RNA (mg/ww)	Alkaline phosphatase activity (APA) (pU/ww)
P treatment	0.83	0.47	0.94
Temperature	0.08	0.21	–
P treatment × Temp.	0.08	–	–
R2	0.99	0.68	0.94

Table 2

The proportion of variance explained (significantly) by the experimental variables.

Variable	C content (mg/ww)	N content (mg/ww)	P content (mg/ww)	C:N (molar)	C:P (molar)	N:P (molar)
P treatment	0.47	0.82	0.96	0.79	0.93	0.97
Temperature	–	0.01	0.01	0.03	0.03	–
P treatment × Temp.	–	0.08	0.03	0.08	0.04	–
R2	0.47	0.91	0.99	0.90	0.99	0.97