Pete Jorgensen

Plant Science & Horticulture

The Biological Effects of Magnetic Fields on Plant Growth

The use of magnetic fields may be unfamiliar territory to many working within standard horticultural areas. The exact mechanisms of magnetic interactions are not yet well understood, but it is unequivocal that organisms from all five kingdoms respond, in some way, to magnetic fields (Buchachenko, 2016; Kishkinev, et al., 2015; Merrill, 2010; Binhi & N, 2002; Edmonds, 2001; L Kirschvink, et al., 1985).

Magnetic fields influence on plant growth

Higher crop yields have been measured from plants grown following magnetic field treatment compared to those which were not including tomato (Jedlička, et al., 2015) (Hozayn, et al., 2016), chick peas and fava beans (Hozayn, et al., 2016).

Increased germination rates and/or speeds have been observed in tomato (De Souza, et al., 2010), asparagus (Soltani, et al., 2006), pea (Iqbal, et al., 2012), sunflower (Vashisth & Nagarajan, 2010), soybeans (Shine, et al., 2011), snow pea and chick pea (Grewal & Maheshwari, 2011). Increased seedling vigour has been reported in soybean (Shine, et al., 2011), sunflower (Vashisth & Nagarajan, 2010), tomato (Jedlička, et al., 2015), snow pea and chick pea (Grewal & Maheshwari, 2011).

These studies show potential for producing crops that mature more quickly, become more robust at an earlier stage and produce higher crop yields. These benefits could become increasingly important if trends towards organic production techniques continue (Reganold & Wachter, 2016; Gay, 2016; Bilalis, et al., 2013; PAN Europe, 2007).

The effect of magnetic fields on plants is still very much an area of nascent development and may be subject to very complex interactions; similar treatments may cause opposite effects depending on field strength and in combination with other variables such as the plant species. The variation of results even within the same study where germination rates were increased, decreased, or not significantly affected for different treatments with no explicable correlation (Gholami, et al., 2010; Martínez, et al.).

Potential explanations of how magnetism affects plant physiology

Proposed explanations include effects on the lipid order of the cell plasma membrane (Poinapen, et al., 2013) , changes to intercellular ion homeostasis and mitochondrial activity (Belyavskaya, 2004), and cryptochrome-induced changes to rates of protein expression (Solov’yov, et al., 2007). The area remains confusing and largely incomprehensible due to much contradictory experimental data and a notable failure of experiments to be consistently reproducible (Belyavskaya, 2004) (Harris, et al., 2009) (Buchachenko, 2016). Examples of poor practice in one study includes the use of only six plants per test group and no attempt to define or quantify the EMF levels being applied as a treatment (Rio & Rio, 2013).

Scientific investigation into the interaction of magnetic fields with plants continues and a recent review by Buchachenko (2016) gives an excellent overview of current idea. One strongly endorsed idea is that magnetic fields affect electron spin, which in turn can influence biochemical reactions; the review provides a thorough explanation of how the comparative low energy of magnetic fields may influence biochemistry. A recent laboratory-based study has shown that chemical reactions involving cryptochrome can be influenced by a magnetic field strength as low as 1mT and with very significant effects at 30mT (Maeda, et al., 2012). There is still need for more research. Some of this will involve subatomic processes, and require high levels of technology and cross-disciplinary collaboration. Definite verifiable explanations are likely to be elusive for some time to come, but this should not prevent further scientific enquiry which may contribute to the body of knowledge relating to the effects of magnetic fields on plants. By way of comparison the mechanisms of photosynthesis have only recently become well understood and explanations about the electron transfer process that are currently taught at graduate level are still uncertain (Peltier, et al., 2016) - this does not prevent enquiry into the effects of light quality on plant growth (Arena, et al., 2016).

Field Strength and Measurement

There are several methods for measuring the strength of magnetic fields. The SI unit for measuring magnetic flux density is the tesla (T); it is also very common for the centimetre–gram–second (CGS) unit - gauss(G) - to be used; 1T = 10,000G (Gregersen, 2011). Another common measurement is the pull force (Fpull) – the amount of force required to pull a magnet free from a flat steel plate. Most studies on the effects of magnetic fields on plants use mT (millitesla) as per table AA2 in the appendix.

It is important to make a distinction between magnetic flux (φ) and magnetic flux density (B). El Taher’s doctoral thesis (El Taher, 2015) measures magnetic flux in the SI unit of webers (Wb) as well as noting the magnetic flux density measured in tesla (1T=1Wb/m2) of the magnets being used. This is important because the use of different sized magnets with equal B gives rise to different levels of φ; it is notable that this distinction is not made in most studies including (Harris, et al., 2009). However, El Taher’s thesis fails to account for the altered field strength caused by the distance of seeds sown from the surface of the magnet: the magnets were in the bottom of the pots and seeds sown towards the top – there is no mention of the height of the pot or the distance between the seed and the surface of the magnet. She has merely calculated the magnetic flux (table 5-1 in the paper) at the surface of the magnet (φ = BA). It would be impossible to replicate this experiment based on the described methods.

A summary of studies is shown in table AA2 in the appendix, including plant types and field strengths (Maffei, 2014). While the range of field strength studied is extensive, and over 25 of the experiments have been carried out using field strengths in the range 1mT-250mT, all have shown significant results. Harris, et al. (2009) did not find significant results using 100mT, but was not included in the table.

Lower field strengths require more sophisticated equipment both in terms of measurements, and shielding (to ensure outside sources / GMF do not influence the experiment). Higher levels above 1T also require pricey equipment, and levels above 2T are currently recognized as harmful to human health (ICNRP, 2009). Use of a static magnetic field around the 100mT is more affordable, measurable and is many orders of magnitude above any magnetic field that would normally be present in the natural environment.

Field Source

Some studies use AC induction coils (Moon & Chung, 2000), others (Aladjadjiyan, 2010) fail to state to the source of the magnetic field, only confirming the strength. Ring magnets were employed by Gholami, et al. (2010) - they fail to state what type of magnet, but do provide the dimensions and B at the magnet surface. Their figures suggest they were using neodymium magnets. However, they have not specified this.

Permanent neodymium magnets in the region of 100mT have been used in experiments on the cryptochrome response of Arabidopsis thaliana to magnetic field (Harris, et al., 2009) and for investigating the effect of magnetic flux on Sorghum bicolor, Zea mays, Eruca sativa, Portulaca oleracea and Corchorus olitorius (El Taher, 2015). They are affordable, convenient, have an excellent field strength to size ratio. Provided they are not subject to excessive environmental or mechanical stress, they can be reused for many years (Jha, 2014).

Exposure Time to Magnetic Field

There is considerable variation in the exposure times used in studies, and it is difficult to find any justification for the times selected. Often different exposure times are used and form an independent variable within the experimental design, but most commonly are between 1 and 15 minutes (see table AA3 in the appendix). Based on these studies, exposure times of 0,1,3 and 5 minutes are suggested.

Magnetic Pole Orientation

The orientation of poles is rarely mentioned in studies. All static magnetic fields have a consistent direction of flow (Getzlaff, 2008). The term ‘pole’ is not mentioned at all in the ‘gold standard’ study by Harris, et al. (2009): this was despite the use of neodymium magnets for part of that study. This lack of information effectively make the experiment unreplicable. One short study into the growth of cress showed a significant difference between growth response for plants treated with a south pole compared to those treated with a north pole (Krótki, et al., 2015). This study used imprecise measurements of comparison, including analysis of the greenness of photographs and diameter of growth area as viewed from above. These are tentative and imprecise measures. Chlorophyll meters were not used; plant weights and other growth indices were not measured. The study also fails to provide any explanation of a ‘synergistic effect with the magnetic field of the planet’; zero references were attached to this statement. The orientation of GMF in the northern hemisphere is south (Shipman, et al., 2016). From reviewing current literature, it is difficult to envisage how pole direction at a level which is several orders of magnitude higher than GMF could influence experimental outcome, but it would still seem pertinent to mention pole orientation within the experimental process.

Magnetism, Water, and Plant Growth

Some experiments treat seeds following imbibition (Martínez, et al., 2014); (Iqbal, et al., 2012); (Aladjadjiyan, 2010); (Gholami, et al., 2010) others during imbibition (Isaac, et al., 2011); (Aksyonov, et al., 2001). A correlation between longer seed exposure to water before treatment has been found (Aksyonov, et al., 2001). Water has been found to reduce surface tension when exposed to magnetic fields (Cai, et al., 2009). Experiments have been carried out on irrigation using magnetized water with significant results as reviewed by Hozayn, et al. (2014). It is therefore proposed that seeds are pre-soaked prior to treatment.

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Appendices

Table AA1: Typical magnetic field strengths - adapted from Table 1.1-I in Magnetic Fields: A Comprehensive Theoretical Treatise for Practical Use By Heinz E. Knoepfel (Knoepfel, 2000). * Expected surface field strength (K&J Magnetics Inc).

Table AA2: Summary of the effects of magnetic field on plants (Maffei, 2014).

Table AA3: A table of studies using magnetism on plants, showing the exposure times used.

Figure 1A: Equation to calculate the magnetic flux density (B) at a given distance (z) from the pole of a static cylinder magnet with radius R and depth / height D.