Hybrid Pine (Pinus attenuata × Pinus radiata) Somatic Embryogenesis: What Do You Prefer, Mother or Nurse?

Abstract

Development of hybrid pines of Pinus radiata D. Don for commercial forestry presents an opportunity to diversify the current resource of plant material. Climate change and different land uses pose challenges, making alternative species necessary to guarantee wood and non-wood products in the future. Pinus radiata var. cedrosensis × Pinus attenuata hybrid possesses different attributes, such as tolerance to drought conditions, better growth and resistance to snow damage at higher altitudes, and more importantly, different wood quality characteristics. Embryogenic cell lines were successfully initiated reciprocal hybrids using as initial explants megagametophytes, excised zygotic embryos and excised zygotic embryos plus nurse culture. However, the questions raised were: does the initiation environment affect the conversion to somatic plantlets months later? Does the mother tree or the cross have an effect on the conversion to somatic plantlets? In the present work we analysed the maturation rate, number of somatic embryos, germination rate, and the ex-vitro growth in cell lines derived from different initiation treatments, mother tree species, and crosses. Differences were not observed for in vitro parameters such as maturation and germination. However, significant differences were observed due to the mother tree species in relation with the ex-vitro growth rates observed, being higher those in which P. radiata acted as a mother. Moreover, embryogenic cell lines from these hybrids were stored at −80 °C and regenerated after one and five years.

1. Introduction

Pinus spp. are frequently used in reforestation programs and, specifically, Pinus radiata D. Don is one of the most cultivated species in New Zealand and Spain because of its fast growth and wood production. However, several stresses derived from climate change can affect the productivity of plantations. This has contributed to a growing interest in the potential of pine hybrids. For instance, the commercial development of the P. patula × P. tecunumanii hybrid in South Africa to improve Fusarium circinatum (Pitch canker) resistance of susceptible P. patula has been a major success story in plantation forestry [1,2]. Hybrids of US southern pines with Mexican pines [2,3,4] may offer opportunities to improve wood properties and create ‘‘varieties’’ better adapted to specific exotic environments or to variable climatic conditions. According to the predictions, climatic change will increase the incidence and severity of droughts in ecosystems worldwide [5]. Different pine species, in comparison with radiata pine, possess different attributes, such as tolerance to subtropical climatic conditions, better growth at higher altitudes, susceptibility to disease, and, importantly, different wood quality characteristics [6]. P. attenuata, for instance, can potentially contribute to drought, cold and snow damage resistance acquisition in P. radiata, which does not have those attributes [6]. In this sense, hybrid pines have been recognised as an opportunity for the future [7,8]. Bearing in mind the information about P. attenuata pure species, some years ago we started studying the drought stress tolerance mechanism of the hybrid P. attenuata × P. radiata trying to understand the mechanisms involved in this process [9]. This hybrid showed higher drought tolerance than breeds from pure species from different geographical and climatological growth areas [10,11,12]. Moreover, some field studies have been carried out to evaluate the performance of the P. attenuata × P. radiata hybrid for afforestation in New Zealand [7].

Conifer propagation methodologies such us somatic embryogenesis (SE) facilitate multiplication and storage of embryogenic tissue while field testing takes place. These technologies are well established for P. radiata [13,14,15] but have not been developed for the Pinus radiata × Pinus attenuata hybrid. For this reason, SCION (New Zealand) and Neiker (Spain) focused on testing and modifying existing P.radiata protocols to produce hybrid plants for field trials [8].

Several studies carried out in our lab in Pinus spp. have showed the effect of environmental conditions during initiation of SE process in the subsequent stages of the process [16,17,18]. Taking into account our previous studies, we were interested in following the effect of the physical and chemical environment of SE process in P. radiata × P. attenuata hybrid and in answering to the following questions:

• Does the presence of initiation environment inhibit or enhance the success of the process?
• What is the effect of the mother (i.e., P. radiata or P. attenuata as the female parent) in embryonal mass conversion to somatic plants?

2. Materials and Methods

2.1. Plant Material

Proseed, a commercial seed orchard located at Amberley (North Canterbury, New Zealand) provided all the test material for this investigation. Green cones were collected from two hybrid crosses, Pinus attenuata × P. radiata var. cedrosensis and Pinus radiata var. cedrosensis × P. attenuata. Both hybrid crosses were control pollinated with a mixture of pollen parents (polycross) of the respective species. Details of crosses in respect to their relatedness were described in [8].

Green cones were stored at 4 °C for one-three days depending on when each cross was put into culture [19]. As described in [8] four collections were made from December to January corresponding to zygotic embryo stages 1 to 6 according to scoring system given by [13].

2.2. Culture Conditions and Initiation of Embryonal Masses

Immature seeds were aseptically removed from the seed coat and given one of the following three treatments (treatment and media details follow the treatment outlines):

Treatment 1:

Megagametophyte + Glitz medium

Treatment 2:

Excised zygotic embryo (ZE) + Glitz medium

Treatment 3:

Excised ZE + Glitz medium + Nurse

Glitz medium [13] is a modified Litvay medium [20] (

Table 1. Basal media composition for the different media used along the somatic embryogenesis process in Pinus attenuata × Pinus radiata and the reciprocal hybrid: Glitz medium, embryo development medium (EDM) and half-strength modified Lepoivre medium (LP ½ Modified).

Chemicals (mg/L)	Glitz	EDM	LP ½ Modified
Ca(NO3)2·4H2O			417.5
CaCl2·2H2O	11	25
KNO3	950	1431	900
MgSO4·7H2O	925	400	220
NaNO3		310
NH4H2PO4		225
NH4NO3	825		200
KH2PO4	170		337.5
FeSO4·7H2O	30	30	30
Na2EDTA·2H2O	40	40	40
ZnSO4·7H2O	43	25	8.6
H3BO3	31	8	6.2
MnSO4·4H2O	21	3.6	1
CuSO4·5H2O	0.5	2.4	0.025
KI	4.15	1	0.08
CoCl2·6H2O	0.125	0.2	0.025
Na2MoO4·H2O	1.25	0.2	0.25
Thiamine HCl	5	5	0.1
Nicotinic acid	5	5	0.5
Pyridoxine HCl	0.5	0.5	0.5
Casein hydrolisate	1000
Glutamine *	500	550
Asparagine *		525
Arginine *		175
L-Citrulline *		19.75
L-Ornithine *		19
L-Lysine *		13.74
L-Alanine *		10
L-Proline *		8.75
Myo-inositol	100	1000	100
Sucrose	30,000	60,000	30,000
Medium pH	5.7	5.7	5.8

* Filter-sterilised stock solution was added after autoclaving and cooling to 60 °C.

) supplemented with 4.5 µM 2,4-dichlorophenoxyacetic acid, 2.7 µM benzyladenine, and 3 g L⁻¹ of gellam gum (Gelrite^®; Duchefa, Haarlem, The Netherlands). Amino acids were filter-sterilised but not pH-adjusted and were added to the autoclaved medium.

For treatment 3 each dissected ZE was placed on a sterile piece (3 cm × 3 cm) of Nybolt nylon screen (Scapa Filtration, 30-µm-diameter mesh) on top of a P. radiata nurse culture. The nurse tissue used consisted of a vigorously growing P. radiata cell line that had been maintained by routine subculture to Glitz 2 [8] at 14-day intervals for approximately ten years. This line has no regenerative capability using current Scion somatic embryo maturation protocols. There were three individual nurse cultures per Petri dish, each consisting of approximately 150–250 mg of fresh tissue with a square of Nybolt lightly pressed on to the top of the callus tissue; care was taken to ensure that the callus was vented, and the nylon screen was not forming a complete seal on the media surface. The nurse treatments were applied for seven days and then the screen was shifted to a fresh dish of Glitz for further culture.

Following the initial application of treatments, cultures were incubated under low light (5 μmol m⁻² s⁻¹) at 24 ± 1 °C. Four weeks after initiation, all responding explants were transferred to Glitz medium and sub-cultured at 14-day intervals (Figure 1a,b). Following 8–10 weeks of subculture, the embryogenic cell lines (ECLs) had to have in excess of 50 mg of tissue to be scored as established, the results were shown in previous studies [8].

2.3. Maturation and Germination of Embryos

ECLs from each of the initiation treatments (1,2 and 3) were subjected to maturation; 23 ECLs from treatment 1 (12 with P. attenuata as the mother tree, 11 with P. radiata var. cedrosensis as the mother tree), 19 ECLs from treatment 2 (8 with P. attenuata as the mother tree, 11 with P. radiata var. cedrosensis as the mother tree), and 23 ECLs from treatment 3 (10 with P. attenuata as the mother tree, 13 with P. radiata var. cedrosensis as the mother tree). ECLs with P. attenuata as the mother tree belonged to three crosses (887.301, 887.302, 887.315) and ECLs with P. radiata var. cedrosensis as the mother tree belonged to four crosses (886.975, 886.977, 886.981, 886.987). Maturation and germination were performed following the methodology described by [14]. For maturation, samples of 100 mg of proliferating embryogenic tissue, 14 days after their last transfer to fresh medium, were placed in 5 mL of liquid embryo development medium (EDM) ([21], Table 1) devoid of growth regulators and gently suspended. The suspension was then poured onto a filter paper (Whatman no. 2, 70 mm) in a Büchner funnel; a vacuum pulse was applied for 10 s, and the filter paper with the attached tissue was transferred to maturation medium. Maturation medium was EDM medium supplemented with 60 µM abscisic acid (ABA) and 9 g L⁻¹ Gelrite^® (Duchefa, Haarlem, The Netherlands); medium was poured in 90 mm × 9 mm × 20 mm Petri dishes. Four Petri dishes per ECL were assayed, giving a total of 260 Petri dishes. Cultures were incubated at 22 °C in the dark. Mature somatic embryos (Se’s) were harvested 15 weeks later (Figure 1c) and placed on half strength macronutrients LP medium [22] modified by [23] (1/2 LP, Table 1) with 2 g L⁻¹ of activated charcoal and 9 g L⁻¹ of gellan gum (DifcoAgar^®; Becton Dickinson; Franklin Lakes, NJ, USA). Petri dishes (90 mm × 9 mm × 15 mm) were used as containers, with the root caps of the Se’s pointing downwards at an angle of approximately 60° and placed under dim light (10 µmol m⁻² s⁻¹) for seven days. Twenty embryos Petri dish were cultured, the number of Petri dishes cultured depended on the number of Se’s obtained for each ECL. After six weeks, germinated Se’s (Figure 1d) were subcultured to glass jars with medium of the same composition (seven somatic plantlets per jar). Cultures were maintained 5 weeks at 23 °C under 16 h photoperiod at 100 µmol m⁻² s⁻¹ provided by cool white fluorescent tubes (TFL 58 W/33).

2.4. Acclimatization

After 12 weeks from the start of germination stage, plantlets showing roots and an aerial part of more than 15 mm were considered suitable to be transplanted to 43 cm³ pots containing a wet sterile peat: perlite mixture (3:1, v/v). After transplanting, the plantlets were acclimatized in a greenhouse under controlled conditions at 21 ± 2 °C and progressively decreasing humidity from 100% to 70% over four weeks. Then, after two months in the greenhouse the plants were transplanted to bigger pots and six months later in the greenhouse, the height (cm) was measured in 368 plants coming from different mother species and treatments (Figure 1e,f).

2.5. Long Term Conservation at −80 °C

43 ECLs were chosen, 17 EMs from P. radiata × P. attenuata (14 of them used in maturation experiments) and 26 EMs from P. attenuata × P. radiata were used for this study, (21 of them used in maturation experiments). Conservation of EMs at −80 °C was carried out following the procedure described by [24]. Briefly, 1.5 g of vigorously growing EMs were resuspended in 5.4 mL of EDM liquid medium supplemented with 180 g L⁻¹ sucrose. After one hour of incubation in this medium, the same volume of EDM liquid medium containing 180 g L⁻¹ sucrose plus 15% dimethyl sulfoxide was gradually added (3 times 1.8 mL in 15 min intervals) to reach a final concentration of 7.5%. The suspension was maintained in darkness in an ice bath on a shaker at 120 rpm during this process.

Finally, the suspension was pipetted into cryovials (six times 1.8 mL), and five cryovials, each containing 250 mg fresh mass of tissue, were arranged in a Mr. Frosty container (Nalgene^® Labware; Thermo Fisher Scientific, Waltham, MA, USA) and then in an ultra-low temperature freezer (Sanyo V.I.P.™; Osaka, Japan) at −80 °C. After 90 min, the cryovials with cell suspensions were rapidly removed from the Mr. Frosty and plunged into liquid nitrogen for 5 min. Then the cryovials were stored again in the ultra-low temperature freezer (−80 °C) for one year and for five years. Thawing of samples was carried out after one and five years as follows: cryovials were removed from the −80 °C freezer and left at room temperature for 1 min. Then, they were immersed in a water bath at 40 °C for 3 min. Finally, the suspension was poured onto a filter paper disc (Whatman^® no. 2.70 mm; Maidstone, UK) in a Büchner funnel. A vacuum pulse was applied for 10 s, and the filter paper with the attached tissue was transferred to EDM basal medium supplemented with a combination of 4.5 μM 2, 4-dichlorophenoxyacetic acid, 2.7 μM 6-benzylaminopurine, 30 g L⁻¹ sucrose and 3.5 g L⁻¹ gellan gum (Gelrite^®; Duchefa, Haarlem, The Netherlands). After 24 h, the filter papers were transferred to fresh EDM medium and the cultures were kept in darkness at 23 ± 1 °C.

Control samples (one cryovial per ECL) treated as frozen ones but not cooled in the Mr. Frosty or immersed in liquid nitrogen, were subjected to the same procedure in order to assess whether they had lost regeneration potential prior to storage at −80 °C.

2.6. Data Collection and Analysis

After 15 weeks on maturation medium, the ECLs producing Se’s were recorded and the percentage of maturation was calculated by dividing the number of ECLs that produced mature Se’s by the total number of ECLs subjected to maturation.

After 15 weeks on maturation medium, the number of Se’s in ECLs producing Se’s was counted and the number of Se’s per gram of fresh tissue was calculated. Regarding the number of Se’s, two analyses were conducted. Firstly, a linear mixed effects model including the cross as a fixed effect and the ECL as a random effect to cope with variability was fitted. Additionally, the number of Se’s was transformed using the square root. Secondly, a similar linear mixed effects model including the treatment, the mother, and their interaction as fixed effects, and the ECL as a random effect was considered to evaluate the effect of the treatment on the number of Se’s. The same square root transformation was applied to the number of Se’s to reduce variability.

To assess the effect of the cross on the germination percentage, a logistic mixed model including the ECLs a random effect was considered. The ECL was included to improve the fit and to cope with variability. The effects of the treatment, the mother and their interaction were assessed using a logistic mixed model including the ECLs a random effect. In this model the treatment, the mother, and their interaction were fixed effects.

The height of somatic plantlets after six months in the greenhouse was evaluated by two-way analysis of variance (ANOVA). Data were transformed by LN (height). Significant differences between means were determined by Tukey’s post hoc test at a significance level of 5%.

For data on ECL storage at −80 °C after one year and five years, the number of ECLs that showed growth two months after thawing was recorded (Figure 1b) and the regeneration percentages were calculated.

3. Results

The analyses on the effect of treatment, the mother species and the cross were reported previously [25]; as described in this study, there was a significant effect of treatment, and cross and an interaction among these factors.

To evaluate the effect of the cross on the maturation percentage, an initial exploratory data analysis was conducted revealing that this percentage was above 80% for all levels of cross but one. Moreover, the maturation percentage was 100% in two levels of cross. With these data, it was not possible to fit any model. Regarding the effect of the treatment and the mother, the exploratory analysis revealed that in four out of the six levels defined by the interaction of both factors, the maturation percentage was above 80% with one level reaching 100%. Therefore, results were based on descriptive statistics. Maturation percentages for the different mother trees and crosses are shown in Figure 2a. Maturation percentages by treatment and mother are shown in Figure 2b (three crosses when P. attenuata acted as the mother tree and four crosses when P. radiata var. cedrosensis acted as the mother tree). Different ECLs analysed for each cross showed a different maturation rate ranging from 67 % (cross 887.302, P. attenuata as mother tree) to 100% (cross 887.301 with P. attenuata as mother tree and cross 886.975 with P. radiata as the mother tree, ECLs from the rest of crosses showed maturation rates between 83 and 89% (Figure 2a). On the other hand, different initiation treatments provoked a variation in the success of the process depending on the species that acted as mother; Treatment 1 was the most successful when P. attenuata was the mother and the worst when this species was the father. As it can be observed in Figure 2b, there was an opposite effect of the treatments: maturation percentage decreased from 1 to 3 when P. attenuata acted as mother and increased when P. radiata was the mother. So, there was a strong effect of the species that acted as mother in the maturation rates obtained.

When the effect of mother, cross and treatment on the number of Se’s was analysed, significant differences were not found (p > 0.05), even when the interaction was analysed (p > 0.05).

Table 2. Number of somatic embryos g⁻¹ fresh weight in embryogenic cell lines in which P. attenuata acted as the mother tree (crosses 887.301, 887.302, 887.315) and in which P. radiata var. cedrosensis acted as the mother (crosses 886.975, 886.977, 886.981, 886.987). Sample mean and its standard error.

Mother Tree	Cross	Sample Mean ± Standard Error
P. attenuata	887.301	80.728 ± 14.995
P. attenuata	887.302	189.123 ± 37.872
P. attenuata	887.315	376.549 ± 98.988
P. radiata	886.975	353.125 ± 51.390
P. radiata	886.977	230.052 ± 49.358
P. radiata	886.981	329.393 ± 73.431
P. radiata	886.987	248.116 ± 35.880

displays the sample mean (and its standard error) of the number of Se’s for the levels of cross and the two mothers.

Table 3. Number of somatic embryos g⁻¹ fresh weight for the different levels of mother and initiation treatments (1, 2, and 3). Sample mean and its standard error.

Mother Tree	Treatment	Sample Mean ± Standard Error
P. attenuata	1	172.997 ± 33.339
P. attenuata	2	370.332 ± 115.092
P. attenuata	3	97.882 ± 19.893
P. radiata	1	271.589 ± 41.779
P. radiata	2	394.495 ± 74.453
P. radiata	3	211.397 ± 30.642

displays the same information for the treatment levels and the two mothers. Though at first glance, some differences seem to be important, the statistical models did not detect such apparent discrepancies. The reason is that the variability within the levels of cross and the combination of treatment and mother were rather large, and the statistical model could hardly cope with it. Much of this variability persisted even with a square root transformation of the data (which typically reduces variance) and the introduction of the ECL as a random effect. However, it is noticeable that within the ECLs from each mother tree (P. attenuata or P. radiata) the best results were obtained in ECLs from treatment 2 and the lowest number os Se’s were recorded in ECLs from treatment 1.

The germination percentage did not show significant differences when the cross was analysed for each mother (

Table 4. Analysis of deviance of the mixed logistic regression for germination (%) according to cross, mother tree, treatment and their interaction.

Source	X2 Test	df	p Value
Cross	3.163	6	0.788
Mother	0.002	1	0.967
Treatment	0.533	2	0.767
Mother × Treatment	1.312	2	0.519

and Figure 3a). In the same way, when the mother, treatment and interaction were evaluated not significant differences were found (Table 3 and Figure 3b). In both cases, the germination percentages were always above 75%.

Table 5. Height of somatic plants (cm) from embryogenic cell lines in which P. attenuata or P. radiata var. cedrosensis acted as the mother and from different initiation treatments (1, 2 and 3) after six months in the greenhouse.

Mother Tree	Treatment	Height (cm)
P. attenuata	1	8.89 ± 1.48 b
P. attenuata	2	9.37 ± 2.31 b
P. attenuata	3	9.23 ± 1.99 b
P. radiata	1	13.99 ± 4.16 a
P. radiata	2	13.29 ± 3.33 a
P. radiata	3	12.17 ± 3.07 a

Different letters indicate significant differences by Tukey’s post hoc test (p < 0.05).

and

Table 6. Height of somatic plants (cm) from embryogenic cell lines in which P. attenuata or P. radiata var. cedrosensis acted as the mother and from different initiation treatments (1, 2 and 3) after six months in the greenhouse.

Mother Tree	Cross	Height (cm)
P. attenuata	887.301	9.39 ± 0.66
P. attenuata	887.302	9.45 ± 0.42
P. attenuata	887.315	9.03 ± 0.20
P. radiata	886.975	12.35 ± 0.46
P. radiata	886.977	15.67 ± 0.67
P. radiata	886.981	13.26 ± 0.31
P. radiata	886.987	11.96 ± 0.42

show the height of plants coming from different treatments and from different crosses when each species acted as mother, respectively. No significant differences were found between initiation treatments. However, when P. radiata acted as mother, plants showed a significantly higher height (13.1 cm on average) than when P. attenuata was the mother (9.2 cm on average). When P. radiata acted as a mother somatic plants from ECLs from cross 886.977 displayed where significantly higher than somatic plants from the other crosses tested.

The regeneration percentage in samples before freezing (controls) was 100%. After one year of storage at −80°C, regeneration percentages were 82% and 81% in ECLs from P. radiata and P. attenuata mother trees, respectively. After five years of storage the regeneration percentages decreased to 12% and 8% in embryogenic cell lines from P. radiata and P. attenuata mother trees, respectively.

4. Discussion

There is very little information on the effect of the mother on the development of embryogenic processes in Pinus spp. hybrids, these together with the fact that there is also little information on the effect that a certain treatment applied at initial steps of SE might have on the subsequent steps of the process, led us to carry out this study.

We found that the initiation treatment did not affect the in vitro conversion of EMs to somatic plants, this is in agreement with results reported in Pinus halepensis [26] and opposite the effect of environmental conditions at initial stages of SE process on plant conversion reported by different authors [26,27]. Although a great variability was observed among ECLs, this is common in SE with conifer species and the strong effect of genotype has been reported by several authors [28,29]; this is why a high number of genotypes (65 ECLs) were screened in this study.

Regarding maturation percentages, the lowest was obtained when P. attenuata acted as mother (63%) in one of the crosses tested, however the rest of crosses assessed presented maturation percentage above 80% regardless of the species that acted as a mother. These results are high when compared with those reported in other Pinus species such as P. pinea [30] or P. nigra [31] but in accordance with those reported previously in this species [14,17]. The number of Se’s produced by different ECLs showed a high variability, this fact has been widely reported in the literature [32]. However, it was observed that independently of the species used as mother, initiation treatment 2 (excised zygotic embryo) was the one that gave the best results. Our results are in line with those reported by [33] in the hybrid Pinus elliottii var. elliottii × P. caribaea var. hondurensis where they reported a high variability in somatic embryo production among the genotypes tested; these authors also observed that there was a significant effect of proliferation medium on the obtaining of Se’s. On the other hand, while the nurse culture seems to be beneficial in certain occasions at initial stages of the process [8] the ECLs developed from this treatment presented the lowest number of Se’s.

Germination was carried out without any post-maturation treatment such as desiccation and the percentages obtained in this study were high (always above 75%) considering that this phase has been reported as a bottleneck for the SE process in this genus [34]. Germination percentages did not depend on the initiation treatment, the mother species or de cross. As reported for white spruce [34], variation among cell lines will be apparent in all stages of the SE process, affecting the overall effective yield of somatic plants, however this variance due to ECLs seems to be higher for SE initiation, lower for maturation and still lower for germination. Although an effect of the environment at proliferation stage on germination percentage was described in P. halepensis [26] or in P. pinaster [27], our results are in line with those reported for P. radiata in previous studies in our laboratory [19].

Size of somatic plantlets after six months of hardening was significantly higher in crosses in which P. radiata was the mother, showing the same behaviour as pure species; in this sense, P. attenuata grows much more slowly on most New Zealand sites where commercial forests are grown, when compared with P. radiata [35]. However, even when growth is slower than in P. radiata, P. attenuata is drought, snow and frost tolerant, and also capable of growing on poor soils [35]. Although in gymnosperms it has been believed that the mitochondrial DNA is inherited from the female parent and the chloroplast DNA is only inherited from the male [36], recent studies in Pinus mugo × Pinus sylvestris hybrid [37] have shown a biparental inheritance of chloroplast DNA. It could be interesting for future research to study the plastid inheritance in our reciprocal hybrids to try to elucidate the origin of the better ex vitro growth of the P. radiata × P. attenuata hybrids.

Finally, in this work we have also explored the possibility of storing ECLs from the hybrid at −80 °C. After one year, regeneration percentages were similar to those found by [24] in P. radiata using the same methodology and storage time. This storage time, although insufficient for carrying out ex vitro testing of clones, enables a preliminary assessment of the in vitro performance of different ECLs. Results are encouraging as with this storage period and with the development of genomic techniques even an early selection could be performed [38]. Although there are several studies were conifer ECLs has been cryopreserved in liquid nitrogen [39], this is the first report where regeneration of embryogenic tissues has been reported after a long storage period at −80 °C (five years). Regeneration percentages were very low after this storage period, further research will be carried out to try to improve regeneration by means of evaluating different protectant solutions for storage and testing other post-thawing treatments. Additionally, the use of nurse will be evaluated for thawing ECLs stored at −80 °C as it has been successful used for the regeneration of cryopreserved cell lines of P. radiata [24].

5. Conclusions

The physical and chemical environment derived from the presence of megagametophytes and/or nurse did not provoke any effect on the maturation percentages, the number of Se’s developed or the germination percentages. However, P. radiata × P. attenuata somatic plantlets growing in the greenhouse showed significantly higher heights than P. attenuata × P. radiata plantlets.

It is possible to preserve ECLs at −80 °C for one year without loss of regeneration capacity. Regeneration has also been obtained from some ECLs stored at −80 °C up to five years. The application of this technique could represent a great economic saving because it does not require cryotanks with liquid nitrogen.