Abstract
For spores, like seeds, the moisture level and storage temperature seem to be crucial factors responsible for their survival. However, in chlorophyllous spores in particular, the problem is not yet fully understood. The aim of this study was to investigate the effect of moisture content (MC; 6.6 and 4.6 %) and storage temperature (15 and −196 °C) on spore germination and gametophyte development in Osmunda regalis. The MC (fresh weight basis) in freshly released spores was 7.5 %, and decreased to 6.6 and 4.6 % during 2 weeks of spore storage at 42 and 18 % relative humidity, respectively. Those spores germinated at 99.9 % within 28 h. The spores with 6.6 and 4.6 % MC were used for the storage at 15 and −196 °C. The deterioration of spores, maintained with 6.6 % MC, proceeds within 1.5 years of storage at 15 °C, starting with month 8. For the spores with 4.6 % MC serious disturbances in germination and capacity to gametophyte development were postponed for more than 6 months. The time required for spore germination increased with the age of the spores, ranging from 28 h in fresh spores to 10 days in spores stored for more than 11 months. Following 7-year-long cryostorage, spore viability remained at 99.9 %, the time taken for germination remained unaltered and gametophyte development was normal. The viability and vigor of spores were directly correlated with their age, the moisture content and storage temperature.
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Introduction
Ferns are an important component of the ecosystem and are among those plants whose genetic diversity often becomes extremely narrow, thus leading to a potentially higher risk of extinction. The royal fern (Osmunda regalis L., Osmundaceae) is one such plant. O. regalis is a sub-cosmopolitan species, with a sub-Atlantic distribution in Europe. It also occurs around the Mediterranean basin, in southern Africa, America, Asia, and New Zealand (IUCN 2014). The species is declining in many parts of Europe and has become rare or threatened with extinction as a result of wetland drainage, forest clearance and habitat destruction due to agriculture. According to the International Union for Conservation of Nature and Natural Resources (IUCN 2014), O. regalis is included in the national Red Lists of many countries including Poland (Mirek et al. 2006).
Over the last decade, the importance of fern preservation has been considered more seriously (Quintanilla et al. 2002; Pence 2008a, b; Li et al. 2010; Barnicoat et al. 2011; Ballesteros 2011; Gabriel y Galán and Prada 2011; Ibars and Estrelles 2012; Li and Shi 2014, 2015). Among those discussed, species belonging to the family Osmundaceae takes a special place. Soil spore-banks do not play a very important role in the conservation of these species owing to the inability of their spores to survive long periods under wet conditions (Ibars and Estrelles 2012; Gupta et al. 2013). Consequently, several ex situ conservation methods have been studied for Osmunda spp., including recovery of viable germplasm from herbarium specimens (Magrini et al. 2010), in vitro propagation (Morini 2000; Soare 2008), gametophyte banking with cryopreservation (Mikuła et al. 2011), and spore banking under various storage temperature conditions (Pence 2000; Ballesteros et al. 2011; Magrini and Scoppola 2012; Li and Shi 2014, 2015).
Species belonging to Osmundaceae are one of those ferns that produce chlorophyllous (green, photosynthetic) spores (Lloyd and Klekowski 1970). Such spores not only germinate faster than their non-chlorophyllous (non-green) counterparts, but also lose their viability very quickly. Green spores exhibit a tendency to germinate 1 or 2 days after sowing, and their average viability is only 48 days (Lloyd and Klekowski 1970; Windham et al. 1986). The results of previous life-span studies of O. regalis spores vary greatly. For example, it was shown that spores stored without any pre-treatment at 25 or 15 or 5 °C retained their capacity to germinate at about 3 % for only 1 month (Magrini and Scoppola 2012). On the other hand, about 5 % viability was reported for O. regalis spores maintained for 3.5 years at 4 °C (Stokey 1951). Furthermore, Magrini et al. (2010) showed that 2 % of O. regalis spores was capable of germination and subsequently developing into gametophyte even after 5 years of storage in a herbarium. Li and Shi (2014, 2015) paid attention to that the viability of O. japonica spores can be affected not only by extending the storage period and temperature conditions, but also by the moisture content of the spores. These authors first reported evidence of the effect of water content of green spores before and after desiccation on their germination ability.
The storage of fern spores in liquid nitrogen (LN) appears to be the most appropriate for the maintenance of fern species. However, our knowledge of spore viability, especially those ephemeral, during long-term LN protection is still poor. A few reports devoted to this problem showed that the viability of O. regalis and O. japonica green spores could be successfully maintained for at least 12 (Li and Shi 2014, 2015), 18 (Pence 2000) and even 24 months (Ballesteros et al. 2011) in LN storage. In contradiction, the non-green spores of three fern species, i.e. Pteris sp., Cyrtomium falcatum and Polystichium tsus-sinense, were capable of germination after 75 months of storage at −196 °C (Pence 2000). However, the studies of Ballesteros et al. (2011) showed that LN storage prolonged viability of Equisetum ramosissimum green spores effectively for only 1 year. After that time, a serious decline in spore viability was observed. It was shown that 1-year-long cryostorage of non-green spores of Alsophila spinulosa and A. gigantea resulted in a comparatively small loss of viability, but for this period, the viability of ephemeral spores of A. podophylla was lost (Li et al. 2010). This indicates that the monitoring of spore viability during their long-term storage in LN is absolutely essential.
Chlorophyllous spores are the object of not only ex situ conservation programmes, but also of physiological investigations as short-living, yet quickly deteriorating, unique plant material. It seems that the main factors affecting spore viability during storage, i.e. moisture and storage temperature, are similar to those described for seeds. However, there is still so little known about the effect of moisture content on green spore viability and also about the decline in their vigor. The aim of this study was to investigate the effect of moisture content and storage temperature on spore germination and gametophyte development in O. regalis.
Materials and methods
Plant material
Mature fertile fronds of O. regalis, green at the top and cinnamon-colored at the bottom, were collected at the end of May at Polish Academy of Sciences Botanical Garden—CBDC field collection. The experiments were started in 2008. Freshly collected fronds were stored in a paper envelope for 2 days at ambient room conditions (24 ± 5 °C; RH ca. 45–80 %) until the sporangia dehisced and spores were released. For spore cleaning, a sieve of mesh size 100 µm was used. The spores were kept in darkness, in a climatic chamber at controlled temperature of 25 ± 1 °C, and under two different relative humidity conditions: 42 ± 2 or 18 ± 2 % for 2 weeks. The equilibrium relative humidity of spores (eRH) and their moisture content (MC) were determined (Table 1). These spores were used for experiments as a control.
Spore storage conditions
Samples of spores with two various initial moisture levels were placed in the dark, in two storage environments:
-
1.
A climatic chamber with controlled temperature (15 ± 1 °C) and a relative humidity (RH) of 18 ± 2 %;
Spores which were initially kept for 2 weeks at 42 ± 2 % RH were stored in a very tight polypropylene vials (10 ml) with screw cap and rubber seal. The vials were opened for 1–2 s every 2 weeks for exchange of gases. The second spore samples, which were initially kept at 18 ± 2 % RH, were stored in open Petri dishes.
The eRH of both type of spores was measured every month during the time of their storage. The final values of eRH of spores after 18 months of storage are shown in the last line of Table 1.
-
2.
Liquid nitrogen (−196 °C).
For those samples to be stored at a temperature of −196 °C, the 2 ml polypropylene cryovials, each containing about 0.1 ml of freshly collected spores, were directly immersed in LN. Spores were thawed quickly by placing the cryovials in a 38 °C water bath for 3 min (Mikuła et al. 2009).
Viability assays
The spore ability to germinate (germinability), the time of germination and the ability of germinated spores to develop into gametophytes were assessed for both storage conditions and moisture tested. The tests were performed every month, on un-disinfected spores sown in sterile, distilled water (5 ml) in glass Petri dishes (9 cm in diameter). For samples stored at a temperature −196 °C more than 2 years, the viability tests were carried out every year. Germination was performed in a climatic chamber at 22 ± 2 °C with a 16-h photoperiod of light intensity 50 μM m−2 s−1.
All spores, whether live or dead, were counted by scoring 16 fields of vision under a light microscope using 3 independent replicates for each storage time and storage condition (at least 600 spores per replicate). An ability to germinate was calculated as the ratio of germinating spores to the total spores scored and expressed as a percentage. Spores were considered to be germinated when their cell wall was ruptured and at least one cell division happened. A detection of germinated spores was carried out with the help of an epifluorescence microscope (Vanox AHBT3, Olympus, Japan) equipped with computer image analysis system (cellSens Standard ver. 1.7). Fluorescence was induced by blue-violet light (BV filter 400–440 nm).
Time of germination was expressed as the minimum time required for germination of all living spores. The number of gametophytes emerging daily was counted from the day of planting the spores onto the film of water till the time the spore germination was completed. Spores were examined using an epifluorescence microscope.
The ability of germinated spores to develop into gametophytes was assessed starting from the first day of spore germination until the time the development of gametophytes was advanced. Gametophyte development was expressed as a percentage of spores that developed into gametophytes over the total number of spores germinated.
Monitoring of spore moisture status
For monitoring of spore moisture status, the rapid and non-destructive method of equilibrium relative humidity (eRH) assessment was used (Probert et al. 2003). The relative humidity (RH) of the air at equilibrium with spores held in a sealed chamber of a hygrometer was measured at a prescribed temperature of +21 ± 2 °C by means of a digital humidity sensor Hygrolab with probe AW-DIO (Rotronic AG). The eRH of spores was determined every 24 h for the first 2 days (i.e. until all spores from sporangia were released), and next after 2 weeks. The eRH of spores was monitored every month of storage.
The initial spores and spores stored for 18 months in a climatic chamber with controlled temperature of 15 ± 1 °C were used for MC determination. About 100 mg spores was dried at 85 °C to a constant weight (24 h). Three replicates were performed. Moisture content (MC) was expressed as the percentage mass fraction of water of total spore mass according to the equation: [(FW − DW)/FW] × 100.
Statistical analysis
The spore germination and prothallus developmental data were shown as the mean ± standard deviation of three or two independent replicates, representing 16 fields of view through a microscope per replicate. Results were evaluated by means of single-factor analysis of variance (ANOVA) and Fisher’s Least Significant Difference Test (LSD) using Statgraphics Plus software. Significance was stated at P < 0.05.
Results
Germination and development of freshly collected spores
After 28 h post-sowing, all freshly collected spores of O. regalis had germinated on the film of water (Fig. 1a–d). Imbibed spores were green inside and rich in lipid droplets (Fig. 1a). Their chlorophyll autofluoresced red, and their spore coats blue in response to blue-violet light (Fig. 1b). This was the first sign of spore viability and their willingness to germinate. The first visual sign that the spores were about to germinate was the rupture of the spore coat and the appearance of a rhizoidal cell (Fig. 1c). The first division of this spore cell was unequal, giving rise to a small cell that differentiated to form a rhizoid and a larger cell that occupied much of the spore volume. Control spores germinated quickly and evenly. After 28 h post-sowing, all spores germinated (Fig. 1d). For a short time following the first cell division of the spore, both protonemal and rhizoidal cells contained chloroplasts (Fig. 1d).
The first division of the protonemal cell was almost equal and transverse to the polar axis of the germinated spore (Fig. 1e). It occurred simultaneously with the elongation of the rhizoidal cell. The second division was parallel to its axis (Fig. 1e). In contrast to the protonemal cells, the elongated rhizoid cell did not divide and contained few chloroplasts (Fig. 1f).
Next, several divisions of protonemal cells led to the formation of a young prothallus (Fig. 1g). The cells of gametophytes contained abundant chloroplasts and lipid droplets (Fig. 1h). The gametophytes formed more than one rhizoid per 8 days of growth (Fig. 1i). After 16 days, most rhizoids lacked chloroplasts (Fig. 1j) and gametophytes started to form a meristematic zone (Fig. 1k). Finally, at 2 months, gametophytes reached maturity.
The spore moisture content in O. regalis
The eRH of freshly harvested O. regalis spores which were gradually released from sporangia, decreased rapidly from 69.8 to 48.6 % during 2 days of storage at ambient room conditions (24 ± 5 °C; RH 45–80 %) (Table 1). The water content in those spores amounted to 7.5 %. The spores exhibited clear responsivity to the relative humidity of storage air, and the MC during storage was decreasing fast until equilibrium has been reached. In a climatic chamber (25 ± 1 °C; RH 42.0 ± 2 %), the eRH and MC of spores stored for 2 weeks in open Petri dishes dropped to 41 and 6.6 %, respectively. When the spores were stored at temperature of 25 ± 1 °C and RH of 18.0 ± 2 %, both studied parameters decreased from 48.6 and 7.5 % to 18.5 and 4.6 %, respectively. After equilibration, spore moisture remained at almost constant level until the end of storage period (i.e. 18 months).
The effect of moisture content and storage temperatures on spore vitality
The total germination of freshly released O. regalis spores at the original moisture content (7.5 %) was 99.9 %, and it was equal to germinability of spores desiccated for 2 weeks under relative humidity of storage air (Table 2). The spores germinated within 28 h (Fig. 2), and the germination was uniform (Fig. 1c, d).
Spores kept at 15 °C for 18 months differed in their ability to germinate depending on MC (Table 2). The germination of spores was complete (nearly 100 %) until month 8 of their storage. Germinability of spores in which the MC amounted to 6.6 % decreased gradually between months 8 (98.5 %) and 16 (to 71.4 %) of spore storage, reaching 20.1 % by the end of month 18. Spores of water content 4.5 % exhibited more than 90 % viability until month 16 of their storage. Significant decrease in germination capacity of the spores at months 17 and 18 (to 81.3 % and 74.3, respectively) was observed (Table 2).
Variation in the timing of O. regalis spore germination was well noticeable when the spores were stored at 15 °C (Fig. 2). The time required for spore germination increased with the age of the spores, ranging from 28 h to 10 days. After month 8 of storage, the period between water imbibition and spore germination increased rapidly, reaching a maximum of 10 days following months 17–18 of storage.
When spores were stored at 15 °C, the higher moisture content in spores (MC = 6.6 %) caused faster reduction in the formation of gametophytes (Table 2). At month 10, almost 84 % of those spores germinated, but more than 30 % of them did not develop into gametophytes. For spores with lower moisture content (MC = 4.5 %), the 30 % reduction in the ability of gametophytes development was observed after 16 months. At the end of storage period, 33.2 % of spores with lower MC was still capable of forming gametophytes, while it was almost totally stopped by the end of month 17 in the second type of spores.
Long-term spore storage at temperature of 15 °C contributed to disturbances in their germination. Spores with MC = 6.6 % and MC = 4.5 %, did not display uniform germination since months 10 and 16 of storage, respectively. Instead, all the following stages were visible simultaneously: imbibed spores (1), recently germinated spores with ruptured coat (2) and multicellular young gametophytes (3) (Fig. 3a, b). The germinating spores developed into young prothallia in the next few days (Fig. 3c). Some prothalli showed disturbances in rhizoid formation but their later growth was normal. Development of gametophytes from spores incapable of fast germination (no 1. on the Fig. 3a, b) was arrested after the first (Fig. 3d) or second (Fig. 3e) or fourth cell division (Fig. 3f). In abnormally growing 2–5-celled prothalli, chloroplasts were very scant (Fig. 3d–f).
When spores with higher moisture content (MC = 6.6 %) were stored in LN, their survival was high (99.9 %) and the time required for germination was constant (Table 2; Fig. 3g). Germinability and germination time did not change for the whole period of storage, i.e. 7 years. Growth of gametophytes obtained from cryostored spores was normal (Fig. 3h). An apical cytoplasmic cap containing dense cytoplasm was clearly visible in actively growing rhizoids (Fig. 3h). All gametophytes developed normally (Fig. 3i), attained maturity and finally were able to reproduce sexually.
Discussion
Desiccation tolerance of green spores
Green spores of ferns are more tolerant of desiccation than was originally thought (Raghavan 1989). Pence (2000) discovered that spores of O. regalis are able to survive exposure to low relative humidity (below 20 % overnight). Encapsulated spores survived 18 h of osmotic dehydration and 4 h of air desiccation. However, the moisture status of the spores was not assessed by her. Recently, Li and Shi (2014) showed for the first time the changes in water content in green spores during desiccation process. The water content in the fresh spores of O. japonica was 11.2 %, and it decreased rapidly to 6.6 and 4.4 % after desiccation by silica gel for 12 and 48 h, respectively (Li and Shi 2015). The desiccation level of spores (from 19.4 to 4.8 % MC) was also modified by equilibrating at different RH levels (from 96 to 10 %) using saturated salt solutions for a week (Li and Shi 2015). Their studies and ours demonstrated that an internal relative humidity of green spores, similar to that of non-green (Ballesteros and Walters 2007b; Ballesteros et al. 2012), can be easily manipulated by equilibration at different relative humidity values. The critical MC for mature spores of O. japonica was determined to be about 4.8–6.6 % (Li and Shi 2015). For comparison, our study revealed that the spore germination of O. regalis (99.9 %) was not affected even by desiccation to 4.6 % MC (eRH = 18.5 %). According to Lebkuecher (1997) the chlorophyllous spores of Equisetum hyemale can be desiccated almost completely following storage at 25 °C and 2 % RH. Ninety percent of the spores survived that extreme, however, not longer than 1-week-long, desiccation to 4 % relative water content. Thus, the studies show that the moisture content in green spores could be comparable to those described in the non-green spores of Polypodium vulgare (6.5 %) (Smith and Robinson 1975), Alsophila spinulosa (7.45 %), A. gigantea (5.85 %) and A. podophylla (5.95 %) (Li et al. 2010). By comparison, for recalcitrant seeds, the critical MC values below which dehydration injury occurs waver between 32 and 50 % (Pritchard et al. 1995). For pollen, like orthodox seeds, critical moisture level waver between 5 and 10 % (Metz et al. 2000). Although an intolerance of desiccation is one of the crucial factors suspected of causing the rapid loss of viability in recalcitrant seeds (Pritchard et al. 1995), this factor seems not to be directly responsible for the decline in the ability to germinate of green spores.
Reduction of storage temperature is a first step towards spore longevity
Temperature is one of the crucial factors affecting the viability of fern spores during storage. Its reduction leads to extension of the spore longevity. The effect of various temperatures on O. regalis spore germination and developmental behaviour was commenced at ambient temperature (25 °C), progressing through 15, 2–6, −20 or −25, −40, −80 °C and finally −196 °C (LN) (Stokey 1951; Pence 2000; Ballesteros et al. 2011; Magrini and Scoppola 2012).
The retention of vitality of O. regalis spores increased along with decreasing storage temperature. An ambient temperature is not effective for the long-term preservation of green spores. Magrini and Scoppola (2012) showed that only up to 5.9 % of O. regalis spores survived 1 month of storage at 25 °C. In contradiction, the studies of Ballesteros et al. (2011) and ours (data not shown) demonstrated that spores of this species retained their capacity to germinate even 3 months at 25 °C, but lost it completely during the next month. Our study indicated that the germination of spores was, independent of their MC, complete (nearly 100 %), uniform and rapid until month 8 of storage at 15 °C. Several sources report that a very small part of green spores can survive longer than 2 years at temperatures ranging from 2 to 6 °C. The viability of fully hydrated spores of O. regalis was about 10 % after 28 months of storage at 5 °C (Magrini and Scoppola 2012). Stokey (1951) demonstrated that the survival of O. regalis and O. claytoniana spores maintained for more than 3.5 years at 2–6 °C was about 4–5 and 1 %, respectively. However, other papers reported that viability of O. regalis spores stored at 4 °C seriously began to decline after about 6 months, and that after 12 months, only 2 % spores germinated (Ballesteros et al. 2011). Temperatures ranging from −20 to −25 °C were beneficial for preserving O. regalis spore germination and capacity for gametophyte development for a period of 24–28 months (Ballesteros et al. 2011; Magrini and Scoppola 2012). However, a 20–50 % reduction in viability was reported at that time. In general, temperatures as low as −25 °C are insufficient to prevent deterioration of spore survival effectively because of triacylglycerols crystallization (Ballesteros and Walters 2007a).
The life span of O. regalis spores could be effectively prolonged by storing at temperatures between −80 and −196 °C (Ballesteros et al. 2011). In this case, there was no loss of viability and vigor of over a 2-year-long period of storage. Unlike the spores of O. regalis, the spores of Equisetum ramosissimum were short-lived even in LN (Ballesteros et al. 2011). After month 24 of cryostorage, a significant decline in viability of those spores was noticed. For non-green spores of Alsophila spinulosa and A. gigantea, storage in LN for 1 year resulted in 10–20 % loss of their viability, and in complete loss of it for A. podophylla (Li et al. 2010). More than 10–50 % reduction in survival of O. japonica spores after 1 year of LN storage was observed by Li and Shi (2015). These authors demonstrated that the level of maturity and desiccation process can have an impact on the viability of green spores during LN storage. The viability of mature spores was always higher than those of post-mature spores. Moreover, their study showed that the mature spores can tolerate LN freezing independently of the desiccation process (Li and Shi 2015). Our results seems to be consistent with their achievements. When mature and fully capable of germinating spores of O. regalis (eRH = 41 %; MC = 6.6 %) were used for cryostorage, their survival remained at 100 % for at least 7 years. It indicates that LN is the best option for the long-term storage of O. regalis spores. Furthermore, the spores may be put into LN immediately after harvest and without any additional treatment, thus making the conservation of genetic material, and hence biodiversity of this species, very simple, quick and safe.
Effects of increasing age of spores
Factors affecting viability of spores, such as genotype, age, temperature, storage humidity and moisture content (Gabriel y Galán and Prada 2011), lead to an increase in delay in germination, a decrease in the rate of germination, and a decline in germination ability (Stokey 1951; Smith and Robinson 1975; Beri and Bir 1993; Magrini et al. 2010; Ballesteros et al. 2011). These factors also contribute to an increase in the proportion of abnormal gametophytes, a postponement of early gametophyte development (Camloh 1999; Ballesteros et al. 2011) or disruption of gametophyte morphology (Smith and Robinson 1975; Li et al. 2010). An understanding of spore longevity and dynamics of vitality deterioration is crucial to the investigation of mechanisms of spore aging. According to our results, the green spores of O. regalis and the storage temperature as high as 15 °C seems to be the best for that purpose. The deterioration of the spore germination, maintained with 6.6 (eRH = 41 %) and 4.6 % MC (eRH = 18.5 %), proceeds smoothly within a year and a half of storage, starting with month 10 and 11, respectively. In contrast to O. regalis green spores, the visible decline in germination in non-green spores of Polypodium vulgare was observed after about 2 years of storage at 4 °C (Smith and Robinson 1975). A clearly noticeable deterioration in the vigor of O. regalis spores maintained with 6.6 % MC occurred by the end of month 8 of storage at 15 °C. For spores stored with 4.6 % MC, significant disturbances in the capacity for gametophyte development were postponed for 3 months, however, still more than 90 % of normal gametophytes was obtained. By comparison, only 25 % of germinating spores of O. regalis developed into gametophytes after 12 months of storage at 4 °C and about 65 % RH (Ballesteros et al. 2011). The studies reveal that the capacity for germination and normal gametophyte development by spores stored at temperature higher than zero are directly correlated with their MC.
We also found that the time required for spore germination increased with the age of the spores, ranging from 28 h in fresh spores to 9–10 days in spores stored for more than 11 months at 15 °C. These results are in agreement with those obtained by Stokey (1951), Magrini et al. (2010), Ballesteros et al. (2011) and Beri and Bir (1993) who also showed a significant lengthening of germination time in both green (O. regalis) and non-green (Pteris vittata) spores. The 34- and 130- and 150-day-old spores of O. regalis germinated in 4 days and 7 days and 20 days, respectively (Stokey 1951). Time to 50 % of maximum germination (T50) increased to 15 days for O. regalis spores stored for 12 months at 4 °C and about 65 % RH (Ballesteros et al. 2011). According to Magrini et al. (2010), the time required for the germination of 5-year-old spores of this species, stored in closed polyethylene bags with an internal RH equal to 52 %, was 20 days. After 17 years of storage, less than 1 % of these spores germinated within 30 days and died shortly after germination (Magrini et al. 2010). Our data showed that most of the germinating aging spores were able only to complete the first 2–4 cell divisions (Fig. 3d–f). Sometimes, the 3–5-celled prothalli had normally developed rhizoids, but these were not capable of further divisions and gametophyte formation. Some authors state that the loss of viability of green spores may be attributed to rapid changes in the moisture content (Beri and Bir 1993) and a failure to recover photosynthetic activity following desiccation (Lebkuecher 1997). Our study showed that although the spore humidity was maintained at a constant level during 18 months of storage (ca. 4.5 % MC), the differences in spore vitality were clearly visible. It may suggests that the changes in desiccation level per se during storage of spores were not a direct cause of their deterioration. It is more probable that the spore MC was still enough to maintain a high rate of respiration. The degree of respiratory activity could be the main limiting factor in chlorophyllous spores that are constantly physiologically active (Hauke 1963; Lloyd and Klekowski 1970). In non-germinated spores, soluble sugars, free amino acids, storage proteins and lipids, as well as starch grains in chloroplasts, are present in significant quantities in order to satisfy demands for energy and substrates for germination (Gantt and Arnott 1965; DeMaggio et al. 1980). The high metabolic activity during germination causes the depletion of storage reserves what has been demonstrated for green spores of Onoclea sensibilis (DeMaggio et al. 1980) and non-green spores of Pteris vittata (Beri and Bir 1993). And as the storage compounds become totally depleted, the spores become non-viable (Lloyd and Klekowski 1970). The resulting deficiency in respiratory substrates leads to an irreversible loss of membrane permeability (Kato 1976), many biochemical impairments (i.e. inactivation of various enzymes and growth substances), or genetic disruption, as has been studied for aging seeds (Murthy et al. 2003). The delay in germination of seeds is thought to reflect the time required for repair of damaged membranes and for a potentially costly reallocation of internal resources during rehydration (Berjak and Villiers 1972). Therefore, the aged seeds which germinate may develop after a delay into normal or weak seedlings. Similarly, in aging spores, recovery of gametophytes can be incomplete, and the accumulation of defects may eventually lead to death of cell/spore.
Conclusion
We conclude that storage conditions for O. regalis green spores can be optimized not only by lowering the temperature of spore maintenance, but also by controlling their water content. It is possible to achieve full arrestment of aging process in spores of O. regalis for at least 7 years using ultra-low temperature of LN. Thus, LN is the most appropriate for the conservation of O. regalis genetic diversity in ex situ conditions.
On the other hand, O. regalis spores, because of their unicellular structure and rapid loss of viability, can probably be a better object than seeds for investigating the deterioration during aging. The spores themselves could be considered as a valuable material for fundamental research into structural, biochemical and molecular mechanism of the process of aging. Knowledge of the dynamics of O. regalis spore deterioration, that has been provided with this work, is an important first step in such studies.
Author contribution statement
The authors have made the following declarations regarding their contributions: Conceived and designed the experiments: AM. Performed the experiments: KT, DM, MN, AM. Contributed to the writing of the manuscript: AM, KT, JJR.
Abbreviations
- eRH:
-
Equilibrium relative humidity of spores
- LN:
-
Liquid nitrogen
- MC:
-
Moisture content
- RH:
-
Air relative humidity
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Mikuła, A., Tomiczak, K., Makowski, D. et al. The effect of moisture content and temperature on spore aging in Osmunda regalis . Acta Physiol Plant 37, 229 (2015). https://doi.org/10.1007/s11738-015-1985-6
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DOI: https://doi.org/10.1007/s11738-015-1985-6