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PERSPECTIVE article

Front. Microbiol., 25 April 2017
Sec. Aquatic Microbiology
This article is part of the Research Topic Progress in Ecological Stoichiometry View all 34 articles

Ecological Stoichiometry beyond Redfield: An Ionomic Perspective on Elemental Homeostasis

  • 1Department of Integrative Biology, Oklahoma State University, Stillwater, OK, USA
  • 2Department of Biology, University of Texas at Arlington, Arlington, TX, USA
  • 3Water Resources Science Program, University of Minnesota, St. Paul, MN, USA
  • 4School of Natural Resources and Environment, University of Michigan, Ann Arbor, MI, USA
  • 5Department of Ecology, Evolution, and Behavior, University of Minnesota, St. Paul, MN, USA

Elemental homeostasis has been largely characterized using three important elements that were part of the Redfield ratio (i.e., carbon: nitrogen: phosphorus). These efforts have revealed substantial diversity in homeostasis among taxonomic groups and even within populations. Understanding the evolutionary basis, and ecological consequences of such diversity is a central challenge. Here, we propose that a more complete understanding of homeostasis necessitates the consideration of other elements beyond C, N, and P. Specifically, we posit that physiological complexity underlying maintenance of elemental homeostasis along a single elemental axis impacts processing of other elements, thus altering elemental homeostasis along other axes. Indeed, transcriptomic studies in a wide variety of organisms have found that individuals differentially express significant proportions of the genome in response to variability in supply stoichiometry in order to maintain varying levels of homeostasis. We review the literature from the emergent field of ionomics that has established the consequences of such physiological trade-offs on the content of the entire suite of elements in an individual. Further, we present experimental data on bacteria exhibiting divergent phosphorus homeostasis phenotypes demonstrating the fundamental interconnectedness among elemental quotas. These observations suggest that physiological adjustments can lead to unexpected patterns in biomass stoichiometry, such as correlated changes among suites of non-limiting microelements in response to limitation by macroelements. Including the entire suite of elements that comprise biomass will foster improved quantitative understanding of the links between chemical cycles and the physiology of organisms.

Introduction

Ecological stoichiometry considers individuals as collections of chemical elements akin to a very large molecule. At the most fundamental level, ecological stoichiometry is the study of the sub-organismal mechanisms, and supra-organismal consequences of the principle of mass balance. It operates on the axiom that living entities are not a passive conduit of chemical supply, but rather actively regulating their elemental stoichiometry, referred to as elemental homeostasis (Sterner and Elser, 2002). Elemental homeostasis is the fulcrum for most stoichiometric models predicting processes at the level of the individual- (e.g., Frost et al., 2005), population- (e.g., Andersen et al., 2004), community- (e.g., Elser and Urabe, 1999), ecosystem- (e.g., Sterner et al., 1992), and global (e.g., Doney et al., 2009; Galbraith and Martiny, 2015) levels of organization. Indeed, without elemental homeostasis “ecological stoichiometry would be a dull subject” (Sterner and Elser, 2002).

At least two different approaches have been used to quantify the degree of elemental homeostasis (Sterner and Elser, 2002; Meunier et al., 2014). We quantify it using the slope of the log-log relationship between resource and consumer stoichiometry (Figure 1). Most stoichiometric models assume osmotrophs at the base of food webs exhibit relaxed stoichiometric homeostasis compared to phagotrophs occupying higher trophic levels. While this assumption has been a subject of debate and found to be of negligible relevance to stoichiometric models in consumers (Wang et al., 2012) the great diversity in the degree of elemental homeostasis (e.g., Frost et al., 2005; Scott et al., 2012; Godwin and Cotner, 2014, 2015; Meunier et al., 2014) remains largely unexplained. Such diversity is surprising because nutrient supply environments can impose strong selection on elemental quotas and consumption, which may be linked to stoichiometry. For example, Godwin and Cotner (2015) found that P content of isolating medium selected for strains of heterotrophic bacteria differing in P homeostasis and elemental quotas. The eco-evolutionary processes that maintain such substantially divergent phenotypes in natural populations is a central frontier in ecological stoichiometry.

FIGURE 1
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Figure 1. (A) Schematic representation of carbon: phosphorus (C:P) homeostasis in relation to supply C:P in homeostatic (solid line) and non-homeostatic (dotted line) consumers. (B) Hypothesized correlated shifts in carbon: sulfur (C:S) stoichiometry in the same consumer, showing no effect of P on S (dotted line), decrease in S under P limitation (dashed line), and increase in S under P-limitation (solid line).

Variation in genomic architecture has a major effect on physiological responses of both autotrophs (e.g., Arabidopsis; Misson et al., 2005) and heterotrophs (e.g., Daphnia; Roy Chowdhury et al., 2014) to changes in supply stoichiometry with important implications for homeostasis and fitness (e.g., Jeyasingh et al., 2009). Although, several informative loci for P use have been identified in crop plants (recently reviewed in van de Wiel et al., 2016), it is important to note that different genes and physiological pathways can underlie similar homeostatic and fitness outcomes among genotypes in autotrophs (Glycine max; Li et al., 2016) and heterotrophs (Daphnia pulicaria; Sherman et al., in review). This raises the possibility that genotypes exhibiting differing degrees of elemental homeostasis can vary in other traits. At the simplest level, we can think of elements that share similar properties that can be replaced when supply of one is limiting (e.g., substituting P-lipids with S-lipids under P limitation; Van Mooy et al., 2009; Bellinger et al., 2014). It is possible that a homeostatic genotype can maintain P content via efficient use of P, while a flexible genotype decreases P content, but increases S content to maintain basic cellular functions (Figure 1). As such, we need to understand coupled elemental quotas (such as P and S), as well as selection operating on such pathways for a complete understanding of the processes maintaining phosphorus homeostasis in populations.

Potential for correlated changes in homeostasis along multiple elemental axes is perhaps more apparent when one considers the complex physiological adjustments organisms make to maintain net anabolism in limiting conditions of elemental supply. Seminal studies in E. coli revealed the complex nature of responses to P limitation (Van Bogelen et al., 1996), involving differential expression of ~400 proteins orchestrating not only P use physiology, but also those involving other bulk and trace elements. Such complex physiological responses appear to be common. For example, studies in Pseudovibrio (Romano et al., 2015), Saccharomyces (Boer et al., 2010), Chlamydomonas (Moseley et al., 2006), Arabidopsis (Misson et al., 2005), and Daphnia (Jeyasingh et al., 2011), reveal that organisms differentially express a significant proportion of genes and metabolic pathways depending on P supply, often by several-fold. While several candidate P-stress response genes are up-regulated (e.g., P transporters, phosphatases; reviewed in Jeyasingh and Weider, 2007), so are several hundreds of other genes involved in a variety of pathways. Merchant and Helmann (2012) provided a comprehensive treatise on the diversity of microbial strategies to variation in elemental supply. An important message arising from this work is the fundamental interconnectedness of elements in biomass. In other words, acclimatory or adaptive responses to supply stoichiometry often involve changes in the physiological processing of many elements.

In this perspective, we ask whether such broad physiological changes in response to supply stoichiometry alters the entire suite of elements encompassing an individual. Defined as the mineral nutrient and trace element composition of an organism, the ionome represents all the elements of cellular and organismal systems (Salt et al., 2008). As such, the ionome is a dynamic network of elements that underlies the morphological, anatomical, and physiological state of an organism, which are ultimately controlled by the genome in response to the environment. We review evidence in the literature as well as analyze experimental data to illuminate the dynamic nature of the ionome, and discuss its implications for elemental homeostasis specifically, and the framework of ecological stoichiometry in general.

Evidence in the Literature

Ionomics is a relatively new field that has focused primarily on plants (see Huang and Salt, 2016 for a recent review). Ionomics was first employed to better understand the genomic architecture underlying mineral and trace element use in Arabidopsis, because studying the use of one element resulted in an incomplete picture of the genotype-to-phenotype map (Lahner et al., 2003). This approach has since been used as a low-cost, multi-proxy diagnostic tool in agronomy (Baxter et al., 2014) as well as medicine (Malinouski et al., 2014). Ionomics connects genetic potential and evolutionary history to growth, physiology and fitness in contemporary ecological conditions. Studies on both Saccharomyces cerevisiae (Eide et al., 2005; Yu et al., 2012) and Arabidopsis thaliana (Baxter et al., 2008) clearly show that both genetics and supply stoichiometry alter ionomes. Specifically, Eide et al. (2005) characterized the ionomes of over 4,000 yeast strains and found considerable variation in all 13 elements quantified, with both strong positive (e.g., P-Co) and negative (e.g., P-S) correlations under optimal growth conditions. Furthermore, they found that genotypes with mutations in similar functional categories (e.g., vacuolar, mitochondrial) showed similar ionomic signatures. Yu et al. (2012) utilized gene deletion and open reading frame overexpression collections of yeast (~5,000 strains) and found general patterns in the genomic basis of ionomic divergence. Mutations in genes involved in protein metabolism or transport had the largest impacts on the ionome, followed by changes in gene copy number. Baxter et al. (2008) found that Arabidopsis exhibited consistent ionomic patterns depending on supply stoichiometry such that the nature of nutrient stress could be predicted based on the ionome. While P content of leaves decreased under P limitation, there was considerable variation among genotypes, making P content a poor predictor of physiological status compared to a six element (As, B, Co, Cu, P, Zn) model, which included strong positive (e.g., P-Cu) and negative (e.g., P-Zn) correlations among elements. Considering combinations of elements as phenotypes, as opposed to considering single elements at a time, allows for greater sensitivity in identifying stoichiometric variation because of the fundamental interconnectedness among elements in biomass (Baxter, 2015).

An underappreciated component in understanding ionomes is likely to be transmembrane elemental transport systems, with transporters possessing multi-element specificity found to be more common than previously appreciated (Morrissey et al., 2009; Mitani-Ueno et al., 2011). As such, ionomic approaches are well suited to illuminate the complex physiological adjustments that organisms make in response to changes in supply stoichiometry. For example, P limitation increases the expression of several high-affinity phosphate transporters, which are also known to take up As (Muchhal et al., 1996) and thus explains increased As content in P-limited plants. Similarly, plants are known to scavenge metals such as Zn to minimize the formation of complexes with P (Misson et al., 2005) which could underlie the observed increase of Zn content under P limited conditions.

Evidence for ionome-wide shifts from the field are also available. Synechococcus cells collected from regions of the Sargasso Sea that vary in N and P supply exhibited several-fold cell quota differences in a variety of elements (e.g., Mn, Ni, Zn) (Twining et al., 2010). In addition, utilizing a global dataset, Loladze (2014) reported striking changes in the ionomes of C3 plants from four continents in response to elevated atmospheric CO2. In general, elevated CO2 significantly decreased not only N and P content, but also several other elements, including K, Ca, S, Mg, Fe, Zn, Cu, and Mn. These observations clearly indicate that supply stoichiometry alters entire suites of elements, beyond the commonly studied Redfield elements. Understanding the dynamics and regulation of these minor elements is important not only in understanding the ecology and evolution of microbes and plants, but as discussed by Loladze (2014), the variation in the composition of trace elements plays an important role in the nutrition of consumers, including humans (Myers et al., 2014).

Experimental Evidence

Are there patterns in ionomic architecture relevant to key parameters in stoichiometric theory such as homeostasis of Redfield elements? The staggering diversity of stoichiometric physiologies discovered among strains of heterotrophic bacteria inhabiting glacial lakes in northern U.S.A (Godwin and Cotner, 2015) provides an ideal testbed for answering such questions. We studied a subset of strains that were found to exhibit divergent homeostatic coefficients in terms of phosphorus (5 flexible, heterostoichs; 4 inflexible, homeostoichs) at two levels of P supply (C:P = 100 and 10,000; see Supplementary Material for methods). The nine strains used in this study represented three unique genera (Brevundimonas, Flavobacterium, and Sphingomonas) with three strains coming from each genus. All three of the Brevundimonas strains were characterized as flexible, whereas Flavobacterium and Sphingomonas each had two strains characterized as inflexible and one strain as flexible. Although we expected strong strain-specific responses, we generally predicted that homoestoichs should exhibit greater changes in other elements (e.g., S) between high and low P supply conditions compared to heterostoichs due to upregulation of compensating mechanisms. Each strain was originally isolated from lakes within Minnesota using either agar plates or dilution isolation as described previously (Godwin and Cotner, 2015).

A total of 25 elements were detected, of which nine (Co, Cr, K, Mg, Mn, Na, P, S, Zn) were present above detection limits in all samples and were used for further analyses. As expected, there was considerable strain-specific variation in biomass P content (Figure 2). Considerably more genotypic replicates are required to rigorously test for systematic differences among P homeostasis and correlated changes in the content of other elements.

FIGURE 2
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Figure 2. Flexibility of nine elements in relation to each other in nine strains of freshwater heterotrophic bacteria. We define flexibility as the log10[elemental content (mass/mass) at C:P of 10,000:1/ elemental content at C:P of 100:1]. Negative values represent a reduction in element quota under C:P = 10,000, zero means homeostasis, and positive values indicate that the quota increased under P-limitation. Symbols denote strains that are relatively flexible (open circles) or inflexible (closed circles) in phosphorus content. ρ = Spearman's rank coefficient.

Nevertheless, important trends were apparent in this dataset. We quantified the magnitude of elemental change in each strain and compared the differences between the two levels of homeostasis (hereto- vs. homeostoichs). Although considerable strain-specific responses preclude identification of any robust patterns, the response of the two homeostoich phenotypes appear to be distinct (Figure 2). Closer examination revealed that certain groups of elements were positively correlated with each other, namely Mg-Na-K, and to a lesser degree, Zn-S and Cr-Co-Mn (Figure 2). Of particular interest was how flexibility in P content related to flexibility of other elements (leftmost column in Figure 2). Consistent with previous studies (Godwin and Cotner, 2015), P content of all strains was lower under the C:P = 10,000 treatment. Interestingly, strains differed in the responses of other elements, with roughly half of the strains becoming more concentrated while the other half becoming less concentrated for the eight other elements. However, no systematic patterns with regard to the P homeostasis phenotype (flexible vs, inflexible) were apparent. We note that this preliminary result needs to be rigorously verified because the experiment had limitations (see Supplementary Material).

Discussion

It is clear that ionomes are sensitive to both the external environment as well as the genomic composition. Whether such changes in the ionome are ecologically relevant is an important question worthy of attention by both empirical and theoretical practitioners of ecological stoichiometry. Studies with plants indicate that individual growth, even under strong P limitation is better predicted, not by P use efficiency alone, but by the uptake of a few other elements as well (Baxter et al., 2008). We posit that the correlated nature of elements in biomass predisposes organisms to tradeoffs in maintaining homeostasis of a particular element. If these tradeoffs occur, being homeostatic along one axis should be associated with changes in homeostasis along other elemental axes. At this point, we do not understand ionomes sufficiently to make robust predictions about what the most relevant trade-offs are. An understanding of the role and relevance of these other elemental axes, and the costs associated with the trade-offs among axes certainly is important to understanding the stoichiometry of organisms and ecological systems. The nature of such changes will depend on the material demands of biochemical pathways utilized to maintain homeostasis. Such an inclusive perspective of elemental homeostasis is required for understanding the diverse stoichiometric physiologies observed in both osmotrophic and phagotrophic populations (e.g., Frost et al., 2005; Godwin and Cotner, 2014, 2015; Meunier et al., 2014), and reflects the current state of evolutionary biology wherein the multifarious nature of selection is a prerequisite for understanding trait evolution (e.g., Kaeuffer et al., 2012).

As our understanding of nutrient limitation shifts from single nutrient models, to more complex, multiple nutrient models predicting co-limitation (e.g., Saito et al., 2008; Harpole et al., 2011; Bracken et al., 2015), the importance of attention to ionomic patterns in natural systems is magnified. Although there is a paucity of ionomic data in natural ecosystems, such data should reveal important patterns that could illuminate the mechanisms underlying co-limitation, which is increasingly common and should replace the Leibig paradigm (Kaspari and Powers, 2016). As such, simultaneous limitation of multiple elements may be strong sources of selection structuring populations with important implications for contemporary nutrient budgets. Nevertheless, it is unlikely that all of the 25-odd elements represented in biology will impart the same magnitude of selection or ecological significance. Although an organism should acquire all elements from the environment, some elements (e.g., copper) can be recycled within the organism quite efficiently that it may not need to be constantly acquired from the environment (Nose et al., 2006), while others (e.g., phosphorus) are excreted as a byproduct of metabolic processes and need to be constantly acquired from the environment. However, if P and Cu are coupled, then the evolutionary and ecological importance of Cu is amplified. Thus, focusing on correlations among elements may be a particularly informative approach.

Ionomic data from both the literature and our experiment reveal several correlations, although the functional basis for such correlations appears to be more complex than what can be predicted by linkages based on cellular physiology of element processing. For example, sodium dependent phosphate uptake by cells is a well-established mechanism (discussed in the context of ecological stoichiometry in Jeyasingh and Weider, 2007), yet sodium and phosphorus do not appear to be correlated at the ionome level. Clearly, much more remains to be understood about the complex processes underlying such patterns. For example, Malinouski et al. (2014) studied HeLa cell lines to characterize mechanisms that regulate trace elements by performing a genome-wide siRNA/ionomics screen to identify the major pathways. They analyzed a total of 21,360 human gene knockdowns for changes in trace elements in HeLa cells and detected many known genes involved in transport and regulation of trace elements while also identifying several novel genes that regulate the processing of trace elements. As such, the mechanisms underlying correlations among elements in an ionome is difficult, and perhaps of little ecological relevance. However, general patterns in correlations among elements at the level of the ionome will have important ecological ramifications. Discovering such patterns and associated ecological implications should be viewed as a central challenge.

Genotype-specific effects common in ionomic studies discussed above are similar to discoveries about intraspecific variation in biomass C:N:P stoichiometries (e.g., Bertram et al., 2008; Goos et al., 2014; Downs et al., 2016) which are shaped by selection (e.g., El-Sabaawi et al., 2012; Tobler et al., 2016), and generate discernable patterns at higher levels of organization (e.g., Elser et al., 2000). While genetic recombination can produce endless varieties of biota, organismal evolution is bounded by principles of physics and chemistry (Williams and Frausto da Silva, 2006). Ecological stoichiometry, by virtue of abstracting such complexity, has unraveled general patterns linking elements such as phosphorus with fitness-relevant traits and subsequent ecological consequences. The focus on only three of the ~25 elements represented in biology is limited, however, and perhaps has misrepresented both patterns and processes in ecological stoichiometry. Whether, and to what extent, predictions of stoichiometric models are enhanced, similar to those predicting individual growth (e.g., Baxter et al., 2008), by inclusion of the entire suite of elements remains to be seen. Advances in low-cost, high throughput elemental analyses already enable an ionomic view of ecological stoichiometry, and such data will be required to make sense of central parameters in stoichiometric models in light of genomic information, and perhaps also metagenomic data using meta-ionomics, for a more comprehensive genes-to-ecosystems picture of the biosphere.

Author Contributions

All authors made equal, substantial contributions toward the creation of this manuscript, and approve its publication.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

This perspective was catalyzed by a group discussion at the Conference on Biological Stoichiometry in 2015, Trent University, Canada. Support from National Science Foundation grant #1256867 to PJ and #1257571 to JC facilitated this manuscript.

Supplementary Material

The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fmicb.2017.00722/full#supplementary-material

References

Andersen, T., Elser, J. J., and Hessen, D. O. (2004). Stoichiometry and population dynamics. Ecol. Lett. 7, 884–900. doi: 10.1111/j.1461-0248.2004.00646.x

CrossRef Full Text | Google Scholar

Baxter, I. R. (2015). Should we treat the ionome as a combination of individual elements, or should we be deriving novel combined traits? J. Exp. Bot. 66, 2127–2131. doi: 10.1093/jxb/erv040

PubMed Abstract | CrossRef Full Text | Google Scholar

Baxter, I. R., Vitek, O., Lahner, B., Muthukumar, B., Borghi, M., Morrissey, J., et al. (2008). The leaf ionome as a multivariable system to detect a plant's physiological status. Proc. Natl. Acad. Sci. U.S.A. 105, 12081–12086. doi: 10.1073/pnas.0804175105

PubMed Abstract | CrossRef Full Text | Google Scholar

Baxter, I. R., Ziegler, G., Lahner, B., Mickelbart, M. V., Foley, R., Danku, J., et al. (2014). Single-kernel ionomic profiles are highly heritable indicators of genetic and environmental influences on elemental accumulation in maize grain (Zea mays). PLoS ONE 9:e87628. doi: 10.1371/journal.pone.0087628

PubMed Abstract | CrossRef Full Text | Google Scholar

Bellinger, B. J., Van Mooy, B. A. S., Cotner, J. B., Fredricks, H. F., Benitez-Nelson, C. R., Thompson, J., et al. (2014). Physiological modifications of seston in response to physicochemical gradients within Lake Superior. Limnol. Oceanogr. 59, 1011–1026. doi: 10.4319/lo.2014.59.3.1011

CrossRef Full Text | Google Scholar

Bertram, S. M., Bowen, M., Kyle, M., and Schade, J. D. (2008). Extensive natural intraspecific variation in stoichiometric (C : N : P) composition in two terrestrial insect species. J. Insect Sci. 8, 1–7. doi: 10.1673/031.008.2601

PubMed Abstract | CrossRef Full Text | Google Scholar

Boer, V. M., Crutchfield, C. A., Bradley, P. H., Botstein, D., and Rabinowitz, J. D. (2010). Growth-limiting intracellular metabolites in yeast growing under diverse nutrient limitations. Mol. Biol. Cell 21, 198–211. doi: 10.1091/mbc.E09-07-0597

PubMed Abstract | CrossRef Full Text | Google Scholar

Bracken, M. E. S., Hillebrand, H., Borer, E. T., Seabloom, E. W., Cebrian, J., Cleland, E. E., et al. (2015). Signatures of nutrient limitation and co-limitation: responses of autotroph internal nutrient concentrations to nitrogen and phosphorus additions. Oikos 124, 113–121. doi: 10.1111/oik.01215

CrossRef Full Text | Google Scholar

Doney, S. C., Lima, I., Moore, J. K., Lindsay, K., Behrenfeld, M. J., Westberry, T. K., et al. (2009). Skill metrics for confronting global upper ocean ecosystem- biogeochemistry models against field and remote sensing data. J. Mar. Syst. 76, 95–112. doi: 10.1016/j.jmarsys.2008.05.015

CrossRef Full Text | Google Scholar

Downs, K. N., Hayes, N. M., Rock, A. M., Vanni, M. J., and Gonzalez, M. J. (2016). Light and nutrient supply mediate intraspecific variation in the nutrient stoichiometry of juvenile fish. Ecosphere 7:e01452. doi: 10.1002/ecs2.1452

CrossRef Full Text | Google Scholar

Eide, D. J., Clark, S., Nair, T. M., Gehl, M., Gribskov, M., Guerinot, M. L., et al. (2005). Characterization of the yeast ionome: a genome-wide analysis of nutrient mineral and trace element homeostasis in Saccharomyces cerevisiae. Genome Biol. 6:R77. doi: 10.1186/gb-2005-6-9-r77

PubMed Abstract | CrossRef Full Text | Google Scholar

El-Sabaawi, R., Kohler, T., Zandoná, E., Travis, J., Marshall, M., Thomas, S., et al. (2012). Environmental and organismal predictors of intraspecific variation in the stoichiometry of a neotropical freshwater fish. PLoS ONE 7:e32713. doi: 10.1371/journal.pone.0032713

PubMed Abstract | CrossRef Full Text | Google Scholar

Elser, J. J., O'Brien, W. J., Dobberfuhl, D. R., and Dowling, T. E. (2000). The evolution of ecosystem processes: growth rate and elemental stoichiometry of a key herbivore in temperate and arctic habitats. J. Evol. Biol. 13, 845–853. doi: 10.1046/j.1420-9101.2000.00215.x

CrossRef Full Text | Google Scholar

Elser, J., and Urabe, J. (1999). The stoichiometry of consumer-driven nutrient recycling: theory, observations, and consequences. Ecology 80, 735–751. doi: 10.2307/177013

CrossRef Full Text | Google Scholar

Frost, P. C., Evans-White, M. A., Finkel, Z. V., Jensen, T. C., and Matzek, V. (2005). Are you what you eat? Physiological constraints on organismal stoichiometry in an elementally imbalanced world. Oikos 109, 18–28. doi: 10.1111/j.0030-1299.2005.14049.x

CrossRef Full Text | Google Scholar

Galbraith, E. D., and Martiny, A. C. (2015). A simple nutrient-dependence mechanism for predicting the stoichiometry of marine ecosystems. Proc. Natl. Acad. Sci. U.S.A. 112, 8199–8204. doi: 10.1073/pnas.1423917112

PubMed Abstract | CrossRef Full Text | Google Scholar

Godwin, C. M., and Cotner, J. B. (2014). Carbon:phosphorus homeostasis of aquatic bacterial assemblages is mediated by shifts in assemblage composition. Aquat. Microb. Ecol. 73, 245–258. doi: 10.3354/ame01719

CrossRef Full Text | Google Scholar

Godwin, C. M., and Cotner, J. B. (2015). Stoichiometric flexibility in diverse aquatic heterotrophic bacteria is coupled to differences in cellular phosphorus quotas. Front. Microbiol. 6:159. doi: 10.3389/fmicb.2015.00159

PubMed Abstract | CrossRef Full Text | Google Scholar

Goos, J. M., French, B. J., Relyea, R. A., Cothran, R. D., and Jeyasingh, P. D. (2014). Sex-specific plasticity in body phosphorus content of Hyalella amphipods. Hydrobiologia 722, 93–102. doi: 10.1007/s10750-013-1682-7

CrossRef Full Text | Google Scholar

Harpole, W. S., Ngai, J. T., Cleland, E. E., Seabloom, E. W., Borer, E. T., Bracken, M. E. S., et al. (2011). Nutrient co-limitation of primary producer communities. Ecol. Lett. 14, 852–862. doi: 10.1111/j.1461-0248.2011.01651.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, X. Y., and Salt, D. E. (2016). Plant ionomics: from elemental profiling to environmental adaptation. Mol. Plant 9, 787–797. doi: 10.1016/j.molp.2016.05.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Jeyasingh, P. D., and Weider, L. J. (2007). Fundamental links between genes and elements: evolutionary implications of ecological stoichiometry. Mol. Ecol. 16, 4649–4661. doi: 10.1111/j.1365-294X.2007.03558.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Jeyasingh, P., Ragavendran, A., Paland, S., Lopez, J., Sterner, R., and Colbourne, J. (2011). How do consumers deal with stoichiometric constraints? Lessons from functional genomics using Daphnia pulex. Mol. Ecol. 20, 2341–2352. doi: 10.1111/j.1365-294X.2011.05102.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Jeyasingh, P., Weider, L., and Sterner, R. (2009). Genetically-based trade-offs in response to stoichiometric food quality influence competition in a keystone aquatic herbivore. Ecol. Lett. 12, 1229–1237. doi: 10.1111/j.1461-0248.2009.01368.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaeuffer, R., Peichel, C. L., Bolnick, D. I., and Hendry, A. P. (2012). Parallel and nonparallel aspects of ecological, phenotypic, and genetic divergence across replicate population pairs of lake and stream stickleback. Evolution 66, 402–418. doi: 10.1111/j.1558-5646.2011.01440.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaspari, M., and Powers, J. S. (2016). Biogeochemistry and geographical ecology: embracing all twenty-five elements required to build organisms. Am. Nat. 188, S62–S73. doi: 10.1086/687576

PubMed Abstract | CrossRef Full Text | Google Scholar

Lahner, B., Gong, J. M., Mahmoudian, M., Smith, E. L., Abid, K. B., Rogers, E. E., et al. (2003). Genomic scale profiling of nutrient and trace elements in Arabidopsis thaliana. Nat. Biotechnol. 21, 1215–1221. doi: 10.1038/nbt865

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, H. Y., Yang, Y. M., Zhang, H. Y., Chu, S. S., Zhang, X. G., Yin, D. M., et al. (2016). A genetic relationship between phosphorus efficiency and photosynthetic traits in soybean as revealed by QTL analysis using a high-density genetic map. Front. Plant Sci. 7:924. doi: 10.3389/fpls.2016.00924

PubMed Abstract | CrossRef Full Text | Google Scholar

Loladze, I. (2014). Hidden shift of the ionome of plants exposed to elevated CO2 depletes minerals at the base of human nutrition. Elife 3:e02245. doi: 10.7554/eLife.02245

PubMed Abstract | CrossRef Full Text | Google Scholar

Malinouski, M., Hasan, N. M., Zhang, Y., Seravalli, J., Lin, J., Avanesov, A., et al. (2014). Genome-wide RNAi ionomics screen reveals new genes and regulation of human trace element metabolism. Nat. Commun. 5:3301. doi: 10.1038/ncomms4301

PubMed Abstract | CrossRef Full Text | Google Scholar

Merchant, S., and Helmann, J. (2012). Elemental economy: microbial strategies for optimizing growth in the face of nutrient limitation. Adv. Microb. Physiol. 60, 91–210. doi: 10.1016/B978-0-12-398264-3.00002-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Meunier, C. L., Malzahn, A. M., and Boersma, M. (2014). A new approach to homeostatic regulation: towards a unified view of physiological and ecological concepts. PLoS ONE 9:e107737. doi: 10.1371/journal.pone.0107737

PubMed Abstract | CrossRef Full Text | Google Scholar

Misson, J., Raghothama, K. G., Jain, A., Jouhet, J., Block, M. A., Bligny, R., et al. (2005). A genome-wide transcriptional analysis using Arabidopsis thaliana Affymetrix gene chips determined plant responses to phosphate deprivation. Proc. Natl. Acad. Sci. U.S.A. 102, 11934–11939. doi: 10.1073/pnas.0505266102

PubMed Abstract | CrossRef Full Text | Google Scholar

Mitani-Ueno, N., Yamaji, N., Zhao, F. J., and Ma, J. F. (2011). The aromatic/arginine selectivity filter of NIP aquaporins plays a critical role in substrate selectivity for silicon, boron, and arsenic. J. Exp. Bot. 62, 4391–4398. doi: 10.1093/jxb/err158

PubMed Abstract | CrossRef Full Text | Google Scholar

Morrissey, J., Baxter, I. R., Lee, J., Li, L. T., Lahner, B., Grotz, N., et al. (2009). The ferroportin metal efflux proteins function in iron and cobalt homeostasis in Arabidopsis. Plant Cell 21, 3326–3338. doi: 10.1105/tpc.109.069401

PubMed Abstract | CrossRef Full Text | Google Scholar

Moseley, J. L., Chang, C. W., and Grossman, A. R. (2006). Genome-based approaches to understanding phosphorus deprivation responses and PSR1 control in Chlamydomonas reinhardtii. Eukaryot. Cell 5, 26–44. doi: 10.1128/EC.5.1.26-44.2006

PubMed Abstract | CrossRef Full Text | Google Scholar

Muchhal, U. S., Pardo, J. M., and Raghothama, K. G. (1996). Phosphate transporters from the higher plant Arabidopsis thaliana. Proc. Natl. Acad. Sci. U.S.A. 93, 10519–10523. doi: 10.1073/pnas.93.19.10519

PubMed Abstract | CrossRef Full Text | Google Scholar

Myers, S. S., Zanobetti, A., Kloog, I., Huybers, P., Leakey, A., Bloom, A., et al. (2014). Increasing CO2 threatens human nutrition. Nature 510, 139–142. doi: 10.1038/nature13179

PubMed Abstract | CrossRef Full Text | Google Scholar

Nose, Y., Kim, B. E., and Thiele, D. J. (2006). Ctr1 drives intestinal copper absorption and is essential for growth, iron metabolism, and neonatal cardiac function. Cell Metab. 4, 235–244. doi: 10.1016/j.cmet.2006.08.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Romano, S., Schulz-Vogt, H. N., Gonzalez, J. M., and Bondarev, V. (2015). Phosphate limitation induces drastic physiological changes, virulence- related gene expression, and secondary metabolite production in Pseudovibrio sp strain FO-BEG1. Appl. Environ. Microbiol. 81, 3518–3528. doi: 10.1128/AEM.04167-14

PubMed Abstract | CrossRef Full Text | Google Scholar

Roy Chowdhury, P., Lopez, J. A., Weider, L. J., Colbourne, J. K., and Jeyasingh, P. D. (2014). Functional genomics of intraspecific variation in carbon and phosphorus kinetics in daphnia. J. Exp. Zool. A Ecol. Genet. Physiol. 321, 387–398. doi: 10.1002/jez.1869

PubMed Abstract | CrossRef Full Text | Google Scholar

Saito, M. A., Goepfert, T. J., and Ritt, J. T. (2008). Some thoughts on the concept of colimitation: three definitions and the importance of bioavailability. Limnol. Oceanogr. 53, 276–290. doi: 10.4319/lo.2008.53.1.0276

CrossRef Full Text | Google Scholar

Salt, D., Baxter, I., and Lahner, B. (2008). Ionomics and the study of the plant ionome. Annu. Rev. Plant Biol. 59, 709–733. doi: 10.1146/annurev.arplant.59.032607.092942

PubMed Abstract | CrossRef Full Text | Google Scholar

Scott, J. T., Cotner, J. B., and LaPara, T. M. (2012). Variable stoichiometry and homeostatic regulation of bacterial biomass elemental composition. Front. Microbiol. 3:42. doi: 10.3389/fmicb.2012.00042

PubMed Abstract | CrossRef Full Text | Google Scholar

Sterner, R. W., and Elser, J. J. (2002). Ecological Stoichiometry : the Biology of Elements from Molecules to the Biosphere. Princeton, NJ: Princeton University Press.

Google Scholar

Sterner, R. W., Elser, J. J., and Hessen, D. O. (1992). Stoichiometric relationships among producers, consumers and nutrient cycling in pelagic ecosystems. Biogeochemistry 17, 49–67. doi: 10.1007/BF00002759

CrossRef Full Text | Google Scholar

Tobler, M., Alba, D. M., Arias-Rodriguez, L., and Jeyasingh, P. D. (2016). Using replicated evolution in extremophile fish to understand diversification in elemental composition and nutrient excretion. Freshw. Biol. 61, 158–171. doi: 10.1111/fwb.12691

CrossRef Full Text | Google Scholar

Twining, B., Nunez-Milland, D., Vogt, S., Johnson, R. S., and Sedwick, P. N. (2010). Variations in Synechococcus cell quotas of phosphorus, sulfur, manganese, iron, nickel, and zinc within mesoscale eddies in the Sargasso Sea. Limnol. Oceanogr. 55, 492–506. doi: 10.4319/lo.2010.55.2.0492

CrossRef Full Text | Google Scholar

Van Bogelen, R. A., Olson, E. R., Wanner, B. L., and Neidhardt, F. C. (1996). Global analysis of proteins synthesized during phosphorus restriction in Escherichia coli. J. Bacteriol. 178, 4344–4366. doi: 10.1128/jb.178.15.4344-4366.1996

PubMed Abstract | CrossRef Full Text | Google Scholar

van de Wiel, C. C. M., van der Linden, C. G., and Scholten, O. E. (2016). Improving phosphorus use efficiency in agriculture: opportunities for breeding. Euphytica 207, 1–22. doi: 10.1007/s10681-015-1572-3

CrossRef Full Text | Google Scholar

Van Mooy, B. A. S., Fredricks, H. F., Pedler, B. E., Dyhrman, S. T., Karl, D. M., Koblízek, M., et al. (2009). Phytoplankton in the ocean use non-phosphorus lipids in response to phosphorus scarcity. Nature 458, 69–72. doi: 10.1038/nature07659

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, H., Sterner, R. W., and Elser, J. J. (2012). On the “strict homeostasis” assumption in ecological stoichiometry. Ecol. Modell. 243, 81–88. doi: 10.1016/j.ecolmodel.2012.06.003

CrossRef Full Text | Google Scholar

Williams, R. J. P., and Frausto da Silva, J. J. (2006). The Chemistry of Evolution: the Development of Our Ecosystem. Amsterdam; Boston, MA: Elsevier.

Google Scholar

Yu, D., Danku, J. M., Baxter, I., Kim, S., Vatamaniuk, O. K., Vitek, O., et al. (2012). High resolution genome-wide scan of genes, gene-networks and cellular systems impacting the yeast ionome. BMC Genomics 13:623. doi: 10.1186/1471-2164-13-623

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: elemental profiling, freshwater heterotrophic bacteria, ionome, ionomics, nutrient limitation, phosphorus supply

Citation: Jeyasingh PD, Goos JM, Thompson SK, Godwin CM and Cotner JB (2017) Ecological Stoichiometry beyond Redfield: An Ionomic Perspective on Elemental Homeostasis. Front. Microbiol. 8:722. doi: 10.3389/fmicb.2017.00722

Received: 01 February 2017; Accepted: 07 April 2017;
Published: 25 April 2017.

Edited by:

Télesphore Sime-Ngando, Centre National de la Recherche Scientifique (CNRS), France

Reviewed by:

Cedric Leo Meunier, Alfred Wegener Institute, Germany
Ivan Baxter, Agricultural Research Service (USDA), USA

Copyright © 2017 Jeyasingh, Goos, Thompson, Godwin and Cotner. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Punidan D. Jeyasingh, puni.jeyasingh@okstate.edu

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