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Article

Fertilization and Shading Trials to Promote Pinus nigra Seedlings’ Nursery Growth under the Climate Change Demands

1
Laboratory of Silviculture, Department of Forestry and Natural Environment, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
2
Faculty of Forestry, University of Belgrade, 11030 Belgrade, Serbia
*
Author to whom correspondence should be addressed.
Sustainability 2021, 13(6), 3563; https://doi.org/10.3390/su13063563
Submission received: 18 January 2021 / Revised: 4 March 2021 / Accepted: 12 March 2021 / Published: 23 March 2021
(This article belongs to the Special Issue Climate Adaptive Reforestation and Plant Material Production)

Abstract

:
Pinus nigra is one of the most widely used tree species for reforestation within its geographical distribution, as well as being a potential substitute for other tree species in Central Europe under future climate scenarios. P. nigra is transplanted into the field as two-year or three-year old seedlings because of its relatively low growth rate in the nursery. This study investigated the effects of fertilization programs and shading on P. nigra seedlings, aiming to accelerate early growth, and thus to reduce the nursery rearing time. The experiment (a completely randomized block design) was conducted in an open-air nursery by sowing seeds from Grevena, Northern Greece, in Quick pots filled with peat and perlite in a 2:1 ratio. The seedlings were subjected to two levels of fertilization—5 and 10 g L−1 NPK (30-10-10)—and two shading levels: 50% and 70%. At the ends of the first and second nursery growing season, we recorded the seedlings’ above- and below-ground morphology and biomass data. The results show that the application of all of the treatments produced seedlings which met the targeted quality standards for outplanting. However, the combination of a high fertilization rate and low shading level resulted in seedlings of a higher morphological quality, which is often considered to be an indicator for a successful seedling establishment in the field.

1. Introduction

Wildfires are a common phenomenon worldwide, and their frequency is expected to increase under the climate change [1,2]. They usually occur in forest ecosystems which are adapted to them, but in recent years, many fires have occurred in global forest ecosystems which have not developed adaptation mechanisms to wildfires, especially to crown fires. Some typical cases are the ecosystems of black pine (Pinus nigra J.F. Arnold) and fir forests (Greek fir—Abies cephalonica Loud. and King Boris fir—Abies borisii regis Mattf). The seeds of both pine and fir species mature during the autumn and disperse in the spring, so in the case of a summer fire there are no mature seeds to ensure regeneration [3]. At the same time, these species cannot regenerate asexually and, as a result, there is the risk of the forest not being able to re-establish itself [4], causing significant consequences such as loss of biodiversity and natural resources (i.e., soil due to erosion) and landscape degradation.
Pinus nigra J.F. Arnold is a conifer species with a relatively wide, but fragmented, distribution [5] across Europe and Asia Minor, predominantly in mountain areas. Because of its ecological flexibility and economic importance in southern Europe, it is one of the most widely used tree species for reforestation within its geographical distribution [6,7,8]. Furthermore, it is considered to be a potential substitute for other indigenous coniferous species in Central Europe under future climate scenarios. After a wildfire in a black pine forest, secondary succession results in the development of a non-forest ecosystem. Following a fire in a black pine forest in Turkey, secondary succession led to the dominance of the shrub species Cistus laurifolius in the burnt pine areas [9]. Retana et al. [10] also reported that there is a decline of black pine presence in burnt areas in Spain due to the lack of regeneration of the species in post-fire conditions, and a great percentage of burnt black pine forests has a significant probability of turning into shrubland. Fyllas et al. [11] reported that, 13 years after the fire (in 2007) in a black pine forest at Olympos Mountain on Lesvos island, the burnt area was dominated by mixed stands of Pinus brutia and evergreen broadleaves. Similar observations were made in Greece for many burnt black pine forests [6].
Based on the available data, the recurrence of large wildfires is threatening the conservation of P. nigra ecosystems, as very little natural regeneration occurs in these species’ forests after wildfires. Because the black pine is a non-serotinous pine, and because it has no adaptive mechanisms to crown fires, the natural regeneration of the species is limited to a short distance from the unburnt stands [3,10,12]. Seed dispersal models have shown that the natural regeneration of the black pine occurs at distances no greater than 100 m, depending on the following factors: the side seeding potential, site characteristics (soil fertility, moisture, slope, etc.), germination success, competing vegetation, survival and growth of the germinants, and anthropogenic interventions (fires, grazing, etc.) [10,13,14].
The ecosystems formed by black pine are a priority habitat type on a European level according to the Habitats Directive (Directive 92/43/EEC). Tackling the problem of the species’ conservation is imperative, because a greater number of fires are expected to appear in these ecosystems in the future, due to climate change [15]. This gives rise to an urgent need to prepare and perform effective reforestation projects for the restoration of the burnt black pine forests within its geographical distribution. The preferred option for black pine reforestation is planting [3].
In forestry practice, P. nigra seedlings are transplanted into the field as two or three-year old seedlings because of their relatively low growth rate during the first few years [16,17,18,19]. Larger planting stock has a higher nutrient and carbohydrate content, which can promote field performance [20]. In the study of Devetaković et al. [21], taller and slender P. nigra seedlings survived at a higher rate, because in environmental conditions with a lack of vegetation control, the greater seedling height can be consider as an advantage [22,23].
Fertilization at the nursery phase is of great importance in producing seedlings of high quality with the potential for favorable field performance [23,24,25], due to good growth, nutrient storage reserves, and resistance to biotic and abiotic stresses [20]. However, unlike the vast literature on the effect of fertilization on pine seedling nursery growth [26,27,28,29], the effects on seedling above- and below-ground-morphology of P. nigra seedlings are poorly known [29,30].
P. nigra is a semi-shade tolerant tree species, and is considered to have similar behavior to that of shade-tolerant species [6,31]. Shading is used in Mediterranean nurseries as a common technique to protect seedlings from leaf damage and water loss due to the excessive radiation during the summer months. During the nursery phase, shading increases the shoot:root ratio, the leaf area, and the shoot height of the seedlings [26,32,33,34]. Therefore, identifying the tolerance degree of the species to specific shading conditions during the seedlings’ production could provide information for both the species’ plasticity and the best level of shading to produce vigorous high quality seedlings in a shorter time [35].
The specific main objectives of this study are to evaluate any possible effect of the application of different nitrogen-concentration fertilizers, different levels of shading, and their combined effects at the nursery phase, on the above- and below-ground growth of P. nigra seedlings, and accordingly, to identify whether the above treatments effectively accelerate the early seedlings’ growth and reduce the time needed for them to gain a plantable size and quality.

2. Materials and Methods

The experiment was conducted in an open-air nursery of the Laboratory of Silviculture of the Aristotle University of Thessaloniki, northern Greece (40°5385618′ N, 22°99705299′ E). Undamaged P. nigra seeds originating from the Grevena area, Northern Greece (Figure 1), were sown in March (2017) in plastic trays (Quick pots with 24 cavities each, a cavity volume of 330 cm3, and a depth 16 cm). All of the pots were filled with peat and perlite (2:1, v/v).
The seedlings were subjected to the following treatments: two fertilization regimes with two high doses (5 g and 10 g) [36] of water-soluble fertilizer N:P:K 30:10:10 + micronutrients per liter of substrate (486 mg seedling−1 and 972 mg seedling−1 respectively), and two shading regimes: 50% and 70%. Half the amount of fertilizer was incorporated into the substrate prior to sowing, and the other half was applied by watering during the rapid growth period of the seedlings. The shading treatments were applied from the beginning of June to the end of September. The four treatments (applied as a 2 × 2 factorial) were arranged in a completely randomized block design, and there were 10 blocks (i.e., 10 trays) per treatment, and a total of 222 seedlings per treatment. All of the seedlings were irrigated by an overhead irrigation system as needed.
At the end of the first growing season in the nursery (October 2017), the seedlings’ above- and below-ground morphology and biomass were measured and recorded [8,37]. The measurements included: the shoot height (SH ± 0.1 cm), root collar diameter (RCD ± 0.1 mm), and percentage of mature needles of all of the seedlings. Furthermore, for a number of the sampled seedlings (seven seedlings per treatment) [26], and after a destructive sampling, the following quality parameters were measured: the central root length (CRL), number of first-order lateral roots longer than 1 cm (FOLR), number of root tips, and above and below- ground biomass. For the destructive sampling, the seedlings were extracted from the pots, and the root system was carefully separated from the substrate, under a gentle water jet, using a sieve to collect any root fragments detached from the system [37]. Then, the shoot and roots were separated (cut) at the root collar. The CRL, FOLR, and number of root tips were manually measured, as accurately as possible. Then, the shoots and the separated roots were dried at 70 °C for 72 h for the dry biomass measurements (accuracy of 0.01 g).
During the second growing season, 14 and 20 months after sowing (May 2018 and December 2018, respectively), the shoot height (SH) and root collar diameter (RCD) were measured on all of the seedlings.
A two-way ANOVA was used to determine the main treatment effects and their interaction. We considered the treatment’s effect to be significant when p < 0.05. The trend of the seedlings’ SH and RCD growth over time, during the 20 months after sowing in the nursery in the two doses of fertilization and two shade regimes, were investigated by regression analysis. Several linear and non-linear models were tested, and we selected the simplest significant (p < 0.01) models that best interpreted each relationship. All of the models were evaluated for goodness of fit by the graphical analysis of residuals. The best fitting model was selected with the highest coefficient of determination (R2), and the lower root mean square error in prediction (RMSE) [37]. The statistical analysis was performed using the SPSS program (v. 23, SPSS Inc., Chicago, IL, USA).

3. Results and Discussion

The P. nigra seedlings at the end of the growth period (seven months after sowing, October 2017), reached a size ranging from 8.5 (±0.5) to 10.1 (±0.6) cm in height, and from 2.0 (±0.1) to 2.4 (±0.008) mm in root collar diameter. The produced one-year-old container seedlings subjected to the specific fertilization and shade regimes were found to be shorter but thicker in diameter (Table 1), and with a greater number of FOLR (Table 2) than those of the same age reported by Kolevska et al. [38], whose SH fluctuated between 11.2 and 13.0 cm, RCD was between 1.90 and 1.97 mm, and number of FOLR was between 12.4 and 15.9. Furthermore, Ivetić et al. [18] reported much lower dimensions for the same age of black pine container seedlings (RCD 1.92 mm and SH 7.25 cm) than those of the current study. However, in both studies, the black pine seedlings were raised in smaller containers in volume and depth compared to those used in the present study. Larger containers generally result in better seedling nursery growth and field survival [39,40,41]. Therefore, the greater diameter and number of FOLR of the current study seedlings could be attributed to the influence either of the N fertilization and shading regimes, or to the greater container capacity.
At this point, all of the studied seedlings cannot be considered plantable [42], according to the Serbian standard SRPS D.Z2.111:1968), as no treatment resulted in the seedling’s RCD being higher than the crucial limit of 3 mm (Turkish Standards Institute TS 2265/March 1976 and TS 2265/February 1988, [43]). This is not surprising for black pine seedlings, taking into consideration the eco-physiological attitudes of the species and the low endogenous growth rate during the first year [43].
The seedlings’ RCD and mature needles significantly increased under the higher fertilization dose, while the number of FOLR was significantly reduced (Table 1 and Table 2). Toca et al. [29,30] reported for black pine seedlings supplied with 150 mg 20N–20P2O5–20K2O fertilizer that they developed larger root systems by maintaining a greater number of growing roots, rather than by increasing the elongation rate of the individual roots. Puértolas et al. [40] found that SDW, RDW, RCD, and SH increased with the fertilizer application rate in P. halepensis seedlings. However, we must mention that the effect of the nursery treatments (nutrient supply and growing density) in the root development of P. nigra seedlings is difficult to interpret, because they present a high variability of root length and number of root tips [44].
Regardless of the fertilization dose, the shade level affected the majority of the seedlings’ attributes. The seedlings raised under 50% shade were significantly shorter, but presented significantly greater RCD, shoot dry mass, root fresh and dry mass (and therefore a greater root:shoot ratio), and number of root tips than those under 70% shading. Santelices et al. [36] also reported that Nothofagus leonii seedlings grew more efficiently under 50% shade. Puértolas et al. [34], who studied two Mediterranean species with contrasting shade tolerance, found that the quality of the seedlings of Quercus ilex (a shade tolerant species) and P. halepensis (shade intolerant) grown under 60% shade was not affected. Meanwhile, a previous study [33] on Quercus ilex seedlings concluded that 45% shading during the nursery growth significantly affected only the shoot:root ratio.
The shoot fresh weight and CRL showed no change with the applied treatments. P. nigra, as with most pine species, is tap-rooted at a young age, and the development of the central root of the seedlings was limited by the container depth [45], resulting in a similar length for all of the treatments.
Seedling root growth and fibrosity (FOLR, root tips) are valuable indicators of seedlings’ quality [39,46]. However, in this study, even though the interpretation of the treatments effect on root branching is complex, it is quite clear that the seedlings raised under 50% shade presented significantly greater RCD, root biomass, and number of root tips than those under 70% shading.
During the second growth period, 14 months after sowing, the shade regimes significantly affected the seedlings’ SH and RCD, while the higher N fertilization dose significantly increased the seedlings’ RCD in both shade regimes (Table 3). The seedlings raised under 50% shade were found to be thicker and higher. However, almost all of the seedlings could be considered plantable14 months after sowing, because they had a diameter of 3.5–4.0 mm—a decisive factor for transplanting success—and a satisfactory height of approximately 14 cm. This may be interesting in some cases, when reforestation concerns areas of high elevation in an oro-Mediterranean climate, where plantings are carried out in spring [47].
At the end of the second growth period (twenty months after sowing) the produced seedlings achieved the dimensions needed for transplanting into the field. Almost all of the applied treatments produced seedlings of a satisfactory size, because their RCD exceeded 5 mm, and their SH exceeded 25 cm (Table 4). These studied container seedlings were found to be thicker and taller, and to have a greater number of FOLR than two-year-old container [8,18,43,48,49] and bareroot or tubed [50] black pine seedlings.It is of great importance that the achieved seedlings’ size, in all of the treatments applied in this study, is considered well balanced in terms of diameter and height, and quite high for an effective field transplant [42], as they excel the minimum standard values proposed as suitable for black pine seedlings by the Greek Forest Service, as well as by the Turkish Standards Institute [43] and Serbian Standards [18]. The produced seedlings can not only be considered plantable but they are also morphologically improved Grade 1 seedlings, because almost all of the seedlings presented RCD greater than 5 mm, a value which is considered as fundamental for that characterization [42]. These seedlings usually have a higher root:shoot ratio, and are characterized by more fibrous roots [51]. Jinks and Kerr [49], who studied the field performance of P. nigra var. maritime seedlings, concluded that the initial seedling size was the most important factor determining the future growth in the field. Similarly, many previous studies have shown that the seedling performance after outplanting in the field was related to the initial seedling size at planting, even in the Mediterranean environments [18,20,37,52,53]. According to Villar-Salvador et al. [23],a seedling’s size is an important attribute because it strongly determines the plant’s photosynthesis and nutrient storage capacity and, consequently, resource mobilization and growth capacity. The above responses could be critical in enhancing the ability of seedlings with larger root and shoot systems to grow quickly and occupy site resources during the establishment phase in the field [39,54].
Regardless of the shading treatment, twenty months after sowing, the higher fertilization dose was favorable for the seedlings’ size (Table 4). This is evident from the seedling’s growth trend during the whole period in the nursery (Figure 2 and Figure 3): the higher the N fertilization dose, the larger the seedlings. However, the seedlings’ SH and RCD were significantly greater only under 50% shade (Table 4). Our observations agree with the previous studies which found thatthe SH and RCD of pine seedlings increased with increasing fertilization rates applied during the nursery phase [28,55]. Similarly, González Orozco et al. [27] found that ahigh dose with 8 g L−1 of Multicote TM (18-6-12) per liter of substrate improved the seedlings’ height, diameter, total biomass, and Dickson quality index of Pinus cooperi Blanco. Many studies have indicated that an increase in seedling size and tissue nutrient concentration improves plants’ survival in Mediterranean forest plantations [20,33]. The seedlings’ SH and RCD were also significantly affected by the applied shade regimes (Table 4). During the same nursery period, regardless of the fertilization dose, the shade effect was significant. The 50% shade regime better favored the growth of the seedlings’ RCD. Similarly to the first growing season, the combination of a higher fertilization dose (10 g per lit substrate) and 50% shade produced significantly thicker (RCD 6.35 mm) and taller seedlings (SH 28.6 cm).
Concerning the seedlings’ growth trend during the 20 months after sowing in the nursery, 50% shade contributed to the exponential growth of the seedlings’ SH (R2 = 0.90, p < 0.01) and RCD (R2 = 0.97, p < 0.01) (Figure 4 and Figure 5). In case of 70% shade, the seedlings’ SH also increased exponentially with the time (R2 = 0.85, p < 0.01), while their RCD increased linearly (R2 = 0.94, p < 0.01). It is worthwhile to point out that the seedlings grew not only during the typical growth period (May to October, for northern temperate regions), but also during the rest of the months of the year. This type of growth was apparent for the seedlings’ height and diameter. However, there was more evidence for diameter increment.

4. Conclusions

In the open nursery environment, at the end of the 2nd growth period, the containerized P. nigra seedlings overcame the target morphology (>25 cm in SH and >5 mm in RCD), with dimensions that have not been reported by other studies so far. The treatments applied—fertilization with high N participation, and shade—both had a significant effect on the seedlings’ morphological characteristics. The higher the N fertilization dose the larger the seedlings produced. The 50% shade exponentially increased the seedlings’ SH and RCD with the time, regardless of the fertilization. The results of this study suggest that the combination of a high fertilization dose (10 g water-soluble fertilizer per litre of substrate) and intermediate shade (50%) accelerate the seedlings’ growth and result in more robust and large seedlings in terms of their above- and below-ground morphological characteristics, which are considered to be indicators for a successful seedling field performance. However, taking into consideration the threat of climate change and the expected increase of wildfires, the need for species conservation is imperative. The results of this research contribute to an efficient production method of black pine seedlings of suitable size and quality, which is recommended for the restoration of burnt species’ ecosystems.

Author Contributions

Conceptualization, P.G. (Petros Ganatsas); methodology, P.G. (Petros Ganatsas) and M.T.; software, M.T.; validation, M.T. and V.I.; formal analysis, P.G. (Petros Ganatsas), M.T.; investigation, P.G. (Petros Ganatsas), M.T., P.G. (Panagiota Giannaki), N.K.; data curation, M.T., P.G. (Panagiota Giannaki), N.K.; writing—original draft preparation, P.G. (Petros Ganatsas), M.T., V.I.; writing—review and editing, M.T., V.I.; supervision, P.G. (Petros Ganatsas). All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable. The study did not require ethical approval.

Informed Consent Statement

Not applicable.

Acknowledgments

We would like to thank the three anonymous referees whose comments contributed to improve this manuscript. Also, we would like to thank Despina Paitaridou (Ministry of Environment and Energy, General Directorate of Forest, Greece) for seeds supply. The work of Vladan Ivetić in this study was supported by the Ministry of Education, Science and Technological Development of the Republic of Serbia according to the agreement number 451-03-9/2021-14/200169.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Location of the sampled Pinus nigra seeds from the Grevena area in Greece.
Figure 1. Location of the sampled Pinus nigra seeds from the Grevena area in Greece.
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Figure 2. Seedlings’ SH growth trend (means ± standard error) during the 20 months after sowing in the nursery, in the two shade regimes (50% and 70%). Continuous line: 10 g fertilization dose; dashed line: 5g fertilization dose.
Figure 2. Seedlings’ SH growth trend (means ± standard error) during the 20 months after sowing in the nursery, in the two shade regimes (50% and 70%). Continuous line: 10 g fertilization dose; dashed line: 5g fertilization dose.
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Figure 3. Seedlings’ RCD growth trend (means ± standard error) during the 20 months after sowing in the nursery, in the two shade regimes (50% and 70%). Continuous line: 10 g fertilization dose; dashed line: 5 g fertilization dose.
Figure 3. Seedlings’ RCD growth trend (means ± standard error) during the 20 months after sowing in the nursery, in the two shade regimes (50% and 70%). Continuous line: 10 g fertilization dose; dashed line: 5 g fertilization dose.
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Figure 4. Seedlings’ SH growth trend during the 20 months after sowing in the nursery, in the two doses offertilization (5 g and 10 g) and the two shade regimes (50% and 70%). The error bars represent the std error of the mean.
Figure 4. Seedlings’ SH growth trend during the 20 months after sowing in the nursery, in the two doses offertilization (5 g and 10 g) and the two shade regimes (50% and 70%). The error bars represent the std error of the mean.
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Figure 5. Seedlings’ RCD growth trend during the 20 months after sowing in the nursery, in the two doses of fertilization (5 g and 10 g) and the two shade regimes (50% and 70%). The error bars represent the std error of the mean.
Figure 5. Seedlings’ RCD growth trend during the 20 months after sowing in the nursery, in the two doses of fertilization (5 g and 10 g) and the two shade regimes (50% and 70%). The error bars represent the std error of the mean.
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Table 1. Effects of fertilization and shade regimes, and their interaction on P. nigra seedlings’ shoot morphology and biomass at the end of the first growing season in the nursery, 7 months after sowing (October 2017).
Table 1. Effects of fertilization and shade regimes, and their interaction on P. nigra seedlings’ shoot morphology and biomass at the end of the first growing season in the nursery, 7 months after sowing (October 2017).
Shade 50%
Fertilization Level per Lit SubstrateShoot Height SH, (cm)Root Collar Diameter, RCD, (mm)Percentage of Mature Needles (%)Fresh Weight (g)Dry Weight (g)
5 g9.3 ± 0.472.1 ± 0.0872.0 ± 4.61.7 ± 0.100.5 ± 0.03
10 g8.5 ± 0.492.4 ± 0.0887.5 ± 6.71.6 ± 0.130.6 ± 0.04
p value0.267* 0.043* 0.0450.7080.079
Shade 70%
5 g10.1 ± 0.531.9 ± 0.0957.0 ± 3.41.3 ± 0.150.4 ± 0.04
10 g10.1 ± 0.602.0 ± 0.1090.9 ± 8.81.6 ± 0.170.4 ± 0.05
p value0.9850.207* 0.0490.1660.369
Shade effect
p value
* 0.024** 0.0010.0900.252* 0.016
Fertilization effect
p value
0.458* 0.047* 0.0320.3340.066
Fertilization X Shade
p value
0.4420.2940.0870.1600.625
The means are followed by the ± standard error of the mean, (n = 222 and n = 7 for fresh and dry weight). The symbols * and ** mean significant effect at p < 0.05 and 0.01, respectively.
Table 2. Effects of the fertilization and shade regimes, and their interaction on P. nigra seedlings’ root morphology and biomass at the end of the first growing season in the nursery, 7 months after sowing (October 2017).
Table 2. Effects of the fertilization and shade regimes, and their interaction on P. nigra seedlings’ root morphology and biomass at the end of the first growing season in the nursery, 7 months after sowing (October 2017).
Shade 50%
Fertilization Level per Lit SubstrateCentral Root Length (cm)FOLRNumber of Root TipsFresh Weight (g)Dry Weight (g)
5 g17.6 ± 0.6838.5 ± 2.08661.4 ± 80.70.9 ± 0.100.3 ± 0.03
10 g18.3 ± 0.7229.6 ± 2.21723.9 ± 85.71.0 ± 0.100.4 ± 0.03
p value0.278** 0.0010.6270.733** 0.007
Shade 70%
5 g18.4 ± 0.7736.9 ± 2.36658.1 ± 91.60.7 ± 0.100.2± 0.03
10 g16.7 ± 0.8724.4 ± 2.67323.5 ± 103.30.6 ± 0.110.2± 0.03
p value0.279* 0.010* 0.0110.4990.449
Shade effect
p value
0.6190.150* 0.030* 0.010** 0.000
Fertilization effect
p value
0.503** 0.0000.1400.8200.119
Fertilization X Shade
p value
0.1160.461* 0.0330.483* 0.013
The means are followed by the ± standard error of the mean, (n = 7). The symbols * and ** mean significant effect at p < 0.05 and 0.01, respectively.
Table 3. Effects of fertilization and shade regimes, and their interaction on P. nigra seedlings’ shoot morphology14 months after sowing (May 2018).
Table 3. Effects of fertilization and shade regimes, and their interaction on P. nigra seedlings’ shoot morphology14 months after sowing (May 2018).
Shade 50%
Fertilization Level per Lit SubstrateShoot Height (cm)Root Collar Diameter (mm)
5 g13.8 ± 0.53.6 ± 0.10
10 g13.9 ± 0.64.0 ± 0.11
p value0.932* 0.033
Shade 70%
5 g14.0 ± 0.43.4 ± 0.07
10 g12.9 ± 0.73.6 ± 0.16
p value* 0.0220.358
Shade effect
p value
* 0.041** 0.003
Fertilization effect
p value
* 0.040* 0.026
Fertilization X Shade
p value
0.2730.315
The means are followed by the ± standard error of the mean (n = 215). The symbols * and ** mean significant effect at p < 0.05 and 0.01, respectively.
Table 4. Effects of the fertilization and shade regimes, and their interaction on P. nigra seedlings’ shoot morphology 20 months after sowing (December 2018).
Table 4. Effects of the fertilization and shade regimes, and their interaction on P. nigra seedlings’ shoot morphology 20 months after sowing (December 2018).
Shade 50%
Fertilization Level per Lit SubstrateShoot Height (cm)Root Collar Diameter (mm)
5 g25.5 ± 0.55.9 ± 0.16
10 g28.6 ± 0.76.5 ± 0.18
p value** 0.001** 0.003
Shade 70%
5 g26.0 ± 0.65.2 ± 0.13
10 g27.0 ± 0.75.4 ± 0.15
p value0.5980.504
Shade effect
p value
* 0.020** 0.000
Fertilization effect
p value
* 0.018* 0.009
Fertilization X Shade
p value
* 0.011* 0.046
Means are followed by the ± standard error of the mean (n = 215). The symbols * and ** mean significant effect at p < 0.05 and 0.01, respectively.
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Tsakaldimi, M.; Giannaki, P.; Ivetić, V.; Kapsali, N.; Ganatsas, P. Fertilization and Shading Trials to Promote Pinus nigra Seedlings’ Nursery Growth under the Climate Change Demands. Sustainability 2021, 13, 3563. https://doi.org/10.3390/su13063563

AMA Style

Tsakaldimi M, Giannaki P, Ivetić V, Kapsali N, Ganatsas P. Fertilization and Shading Trials to Promote Pinus nigra Seedlings’ Nursery Growth under the Climate Change Demands. Sustainability. 2021; 13(6):3563. https://doi.org/10.3390/su13063563

Chicago/Turabian Style

Tsakaldimi, Marianthi, Panagiota Giannaki, Vladan Ivetić, Nikoleta Kapsali, and Petros Ganatsas. 2021. "Fertilization and Shading Trials to Promote Pinus nigra Seedlings’ Nursery Growth under the Climate Change Demands" Sustainability 13, no. 6: 3563. https://doi.org/10.3390/su13063563

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