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Article

Innovative Peat-Free Organic Substrates and Fertilizers Influence Growth Dynamics and Root Morphology of Fagus sylvatica L. and Quercus robur L. Seedlings One Year After Planting

1
Department of Ecology and Silviculture, Faculty of Forestry, University of Agriculture in Kraków, Al. 29 Listopada 46, 31-425 Kraków, Poland
2
Departments of Forestry and Wildlife Management, Faculty of Agriculture, Nasarawa State University, Keffi P.M.B 1022, Nigeria
*
Author to whom correspondence should be addressed.
Forests 2025, 16(5), 800; https://doi.org/10.3390/f16050800 (registering DOI)
Submission received: 15 April 2025 / Revised: 2 May 2025 / Accepted: 9 May 2025 / Published: 10 May 2025

Abstract

:
This study evaluated the effects of six innovative peat-free substrate formulations, combined with either a conventional solid fertilizer or a novel liquid fertilizer developed by the research team, on the early growth and root morphology of Fagus sylvatica L. and Quercus robur L. seedlings. Treatments were analyzed through two-way ANOVA and species-specific linear regression models. Following one year of field growth, survival rates remained high across all treatments. While R22 (a peat-free substrate with liquid fertilizer) exhibited the highest mean values for seedling height and diameter, only height showed statistically significant variation among treatments (p < 0.05), with no significant differences observed for diameter increment. It was further, revealed that seedlings treated with peat-free substrates and liquid fertilizers exhibited adequate survival, with several combinations especially R22 showing comparable performance to traditional peat-based media with solid fertilizer. Root morphological traits, particularly fine root length (≤0.50 mm) were strong predictors of above-ground growth in F. sylvatica, but less so in Q. robur, which relied more on total root length. The results highlight species-specific root–shoot coordination strategies, with beech exhibiting above-ground growth pattern and oak a gravitropic one. The findings concluded that R22 substrates confirmed exceptional performance with enhanced root growth comparable to peat after one year of forest planting, indicating strong potential for future development without the environmental concerns associated with peat use.

1. Introduction

Reforestation and afforestation initiatives are critical to combating climate change, enhancing biodiversity and stabilizing ecosystems [1,2]. Seedling survival after planting constitutes an essential component of the success of forest restoration programs [3,4,5,6]. This survival is strongly influenced by nursery cultural practices and silvicultural techniques, which play an important role in the performance of a seedling immediately after transplanting. [3]. Root system morphology is particularly important because its architecture directly affects water and nutrient uptake, thereby influencing tree seedling’s overall health and resilience [7]. The importance of root characteristics, in predicting seedling survival and adaptability to varying environments cannot be overemphasized [8].
Classifying root diameter is essential for understanding below-ground carbon dynamics [9]. Very fine roots, defined as those less than 0.5 mm in diameter, are more accurate indicators of root function than the broader traditional category of roots under 2 mm [10]. These very fine roots display species-specific traits and exhibit remarkable plasticity, adjusting their biomass and length across soil depths to optimize nutrient and water uptake [10,11,12]. Fine roots, ranging from 0.5 mm to 2 mm in diameter, are vital to nutrient cycling in terrestrial ecosystems [13,14]. Though they make up less than 5% of forest biomass, they are highly dynamic, functioning as both nutrient sources and sinks, and play a key role in carbon cycling and accumulation [10]. In contrast, coarse roots those greater than 2.0 mm in diameter differ significantly in morphology, nutrient content, and decomposition processes. Their size often correlates with aboveground biomass, and factors like tree size and age are commonly used to predict their development [9,15].
Known for its exceptional physical, chemical and biological properties, peat has long been a stable component in nursery substrates. Its superior water-holding capacity and consistent quality make it ideal for plant growth. However, the slow release of carbon from peat soils raises environmental concerns. Europe experienced a dramatic rise in peat excavation, with volumes soaring from 6000 tonnes in 2012 to 20 million tonnes by 2022 [16,17,18] This represents a staggering 333% increase over a decade, underscoring the expansion of peat extraction and its contribution to environmental degradation [19,20]. Consequently, EU Member States have been actively seeking to reduce peat consumption [21,22,23]. With impending restrictions on the availability of peat [24,25,26,27], the need to find alternative materials to replace peat demand an urgent attention, either partially or entirely. In response to this pressing issue, our team has developed and proposed a substrate designed to provide a sustainable solution [7,28].
Despite increasing efforts to promote peat-free substrates in forest nurseries, existing studies have notable limitations. Many studies evaluating peat-free substrates and fertilization strategies primarily assess above-ground parameters such as height, diameter, and biomass accumulation [28,29,30]. However, root system development, remains understudied. While solid fertilizers are widely used in forestry nurseries, recent advancements in liquid fertilizers suggest they may offer improved nutrient uptake efficiency [31,32,33,34,35]. These studies further examined fertilization effects in nurseries but rarely in the context of peat-free organic substrates. This study therefore, provides a direct comparison of solid and liquid fertilizers in combination with innovative organic substrates, assessing their effects on above-ground growth and below-ground root morphology one year after planting in a forest environment.
Therefore, this study aimed to evaluate the performance of innovative peat-free substrates in combination with two contrasting fertilization approaches: a conventional solid fertilizer and a novel liquid fertilizer formulation developed by our research team. The liquid fertilizer was designed specifically to complement the nutrient dynamics of organic peat-free substrates and optimize seedling uptake efficiency. The tested research hypotheses assumed that: (i) these innovative treatments would produce root and shoot traits comparable to conventional methods. (ii) Fagus sylvatica and Quercus robur would respond differently to the treatments due to their distinct growth strategies. (iii) specific root morphological traits may vary in their association with early shoot growth between the studied species.

2. Materials and Methods

2.1. Study Site

The study site was located in Barbarka, Miechow Forest District. The research area is situated at an altitude of approximately 370 m above sea level, in the Olkuska Upland, southern Poland (50°15′54.2″ N 19°53′36.5″ E). The experiment was situated in a forest complex managed by the National Forest Holding. The area was established in several gaps resulting from the clear-cutting of a Populus spp. plantation. The area of the Miechów Forest District is characterized by a diverse, upland landscape. The Olkuska Upland is a compact karst plateau made of limestone and marl. The climate is continental, characterized by significant temperature amplitude (21 °C) and a significant share of rainfall during the growing season. The average annual air temperature for the Forest District is 8.2 °C. The warmest month is July (19.6 °C), while the coldest is January (−3.0 °C).

2.2. Substrate Composition and Preparation

The peat rich in sphagnum used as the control variant (C) for growing the seedlings in this study was obtained from the nursery farm in Nędza (50.167964 N, 18.3138334 E). Its composition consisted of 93% peat and 7% perlite, with the addition of dolomite (3 kg per 1 m3 of substrate) to achieve a pH of 5.5. The elemental content (g/g of 100% dry weight of the growing medium at the beginning of the experiment) of 37.99 ± 0.69 (C), 0.74 ± 0.01 (N), 0.02 ± 0.01 (P) The peat-free substrates (R20, R21, and R22) were sourced from coniferous woody (mainly pine) they composed of a mixture of different components, including shavings, wood chips, straw, bark, perlite, core wood and mixed silage, with varying proportions as shown on Table 1. In total, four substrates (R20, R21, R22, and peat) were utilized, each subjected to two fertilization (S and U) variants. The first set received standard solid fertilization (SR20, SR21, and SR22 variants), while the second set was treated with a novel liquid fertilizer also developed by the University of Agriculture in Kraków (UR20, UR21, and UR22). The peat substrate served as the control in both fertilization scenarios, designated as SC and UC variants (Table 2).
Prior to filling, the substrate was pre-moistened using a line mixer with spray nozzles, and moisture levels were controlled organoleptically by the line staff to ensure the substrate reached the standard moisture level for container filling. The substrate’s moisture content was 75.9 ± 2.1%. The vibration intensity of the vibrating table was kept constant during the filling process, at 12.0 G maximum acceleration, as measured by the Voltcraft DL-131G device with ±0.5 G accuracy. Throughout the experiment, the line’s efficiency remained stable at 400 containers per hour, which is the standard rate at this nursery. All operating parameters line configuration, containers, and substrate types were consistent with those used in a previous experiment [35].

2.3. Seed Sowing and Germination

Using mechanical methods, the containers were filled with substrates and seeds immediately planted on 19 April 2022, at the Nursery Farm in Suków Papiernia (50.79613, 20.71011), Daleszyce Forest District. The experiment utilized V300 Styrofoam containers, which are commonly used in Poland for cultivating deciduous species such as beech and oak. To improve the germination process, oak seeds were scarified before sowing. After sowing, the containers were placed in a greenhouse for 4 weeks before being transferred to an external production field. During the seedling growth period in the nursery, manual weeding was carried out. The seedlings were cultivated for 5 months, following the standard procedure used in container nurseries [36]. Due to a total rainfall of only 78 mm during this period, irrigation was necessary to address the water deficit, and an automatic RATHMAKERS Gartenbautechnik sprinkler ramp was used for this purpose.
Osmocote fertilizer was incorporated into the substrate before sowing, with a total application rate of 3 kg per cubic meter of substrate. This was a mixture of 2 kg of Osmocote 3-4M and 1 kg of Osmocote 5-6M. The Osmocote 3-4M fertilizer had the following composition: 16% nitrogen (N), with 7.1% as N-NO3- and 8.9% as N-NH4+; 9% P2O5; 12% K2O; 2.0% MgO; and included micronutrients (B, Fe, Cu, Mn, Zn, Mo). The Osmocote 5-6M fertilizer contained 15% nitrogen, with 6.6% as N-NO3− and 8.4% as N-NH4+; 9.0% P2O5; 12% K2O; 2.0% MgO; and similar micronutrients. A new liquid fertilizer regimen was also employed, consisting of two different formulations. The first fertilizer contained 4.78% N, 1% P2O5, 2.64% K2O, 2.65% CaO, 1.4% MgO, 0.71% SO3, and 0.14% Na2O. It was initially applied with a total volume of 3.14 dm3 (0.048 dm3 per square meter). The second fertilizer composition included 0.798% N, 0.166% P2O5, 0.440% K2O, 0.441% CaO, 0.234% MgO, 0.118% SO3, and 0.023% Na2O. This was applied with a total volume of 15.09 dm3 (0.229 dm3 per square meter). During the period of seedling production, the first fertilizer variant was applied eight times at 10-day intervals, while the second variant was applied 15 times at 5-day intervals. This fertilization schedule was uniformly applied to both beech and oak seedlings throughout the nursery phase.

2.4. Plantation Establishment and Seedling Collection

After nursery production, the seedling was transported and planted into the forest on 5 September 2022. The field experiment was laid in a randomized complete block design with 8 treatments replicated 3 times. A total of 24 subplots were established for each species. In each subplot, 49 seedlings were planted with 1 × 1.7 m inter and intra-spacing making a total of 147 seedlings per treatment and species. For both species, therefore, were a total of 2352 seedlings were established. The plantation was established at the onset of the autumn season 2022. At the end of the growing season in 2023, 144 seedlings were selected (3 from each subplot) the seedlings were selected according to the average height of each subplot. The seedlings were carefully uprooted to obtain an intact root segment. The mean height of each subplot characterized the selected seedlings. They were carefully chosen from each of the eight treatment groups for onward laboratory analysis. This resulted in a total assessment of 144 seedlings for both species in the laboratory experiment. To reduce the impact of animals on the new forest, the area was fenced after the plantation was established. Above-ground data was collected on plant height, collar diameter, number of seedlings in perfect condition (SPC) total survived seedlings (TSS). The root morphological characteristics examined in this study include total root length (TRL), root surface area (RSA), average root diameter (ARD), and root volume (RV) to assess how different treatments impacted below-ground development. Root morphological diameters were further classified into very fine (≤0.5 mm), fine (0.5–2.0 mm) and coarse root (>2.0 mm).

2.5. Root Sample Preparation and Analyses

In the laboratory, all roots within each block were processed as follows: Root systems were carefully separated from soil and organic matter to keep the root segments intact and maintain attachment to the larger roots (>2 mm in diameter). The intact root segments were then gently rinsed with tap water followed by deionized water to remove residual soil while preserving delicate root tips. Morphological traits of roots in each diameter class were analyzed using WinRhizo™ Pro 2003b image analysis system (Regent Instruments Inc., Ville de Quebec, QC, Canada), an image analysis system specifically designed for root measurements. This analysis was conducted in the Laboratory of Biotechnology, Department of Ecology and Silviculture, University of Agriculture in Kraków.

2.6. Soil Sample Collection and Analysis

A 0.7-hectare research plot was established on a harvested Populus spp. site characterized by uniform parent material and soil type. Soil samples were collected from five different points within each subplot at two depth intervals: 0–10 cm and 10–20 cm, representing the top mineral horizons. Samples were placed in polyvinyl chloride (PVC) bags for transport and analysis. In total, 480 soil samples were collected. Each sample was air-dried, passed through a 2 mm sieve, and ground prior to physicochemical analysis. Soil pH was measured using the potentiometric method in both water and 1M KCl. Hydrolytic acidity was determined using the Kappen method, while exchangeable acidity and base content were assessed using the Sokołow method [37]. Total nitrogen and carbon contents were analyzed with a LECO CNS TruMac Analyzer (LECO Corporation, St. Joseph, MI, USA). The concentrations of alkaline cations (Ca2+, Mg2+, K+, Na+) were determined using 1M ammonium acetate extraction and quantified via inductively coupled plasma optical emission spectrometry (ICP-OES) with an iCAP 6500 DUO instrument (Thermo Fisher Scientific, Cambridge, UK). All analyses were conducted at the Laboratory of Forest Environment Geochemistry and Land Intended for Reclamation, Department of Ecology and Silviculture, Faculty of Forestry, University of Agriculture in Kraków, Poland.

2.7. Statistical Analyses

To analyze the effect of seedling growth on plantation survival, an overall effect of growth was assessed by fitting all sample units (2352 seedlings) in the population. Using destructive sampling method, nine root samples were selected per treatment, resulting in 72 data points analyzed per species for morphological evaluation. From WinRhizo™ Pro 2003b image analysis system (Regent Instruments Inc., Ville de Quebec, QC, Canada) the data were further separated into very fine, fine and coarse roots (≤0.5 mm, 0.5–2.0 mm, >2.0 mm respectively). To meet normality and homogeneity assumptions for further analyses, the Shapiro-Wilk test for compliance of variable distributions with normal distribution was used. The analyzed variables showed compliance with a normal distribution, and therefore, parametric tests were used. To evaluate treatment effects, on root morphological indices and diameter classification of very fine, fine, and coarse roots, two-way Analysis of Variance (ANOVA) was conducted separately for each species, using substrate type (peat-based vs. peat-free) and fertilizer type (solid vs. liquid) as fixed factors, and block as a random effect in a randomized complete block design. Duncan multiple range test (DMRT) was applied post hoc for pairwise comparisons and significance was set at p < 0.05. Multiple linear regression models were developed to explore the predictive relationships between root morphological traits and above-ground performance indicators. All statistical analyses were performed at a significance level of 95% confidence interval.

3. Results

3.1. Soil Properties

At both sites of beech and oak, the soils were slightly acidic, which is typical of forest environments. The pH values at 20 cm are slightly lower compared to those measured at 10 cm. Oak retains a uniform N concentration between both depths. Altogether, C contents were higher both at 10 cm in both sites and decreased at 20 cm as well P levels. Consistent trends in the C/N ratio across depths indicate that C and N cycling within the soil is balanced. Both sites also have more exchangeable cations at 10 cm than at 20 cm indicating that the upper soil layer plays a crucial role in seedling nutrient uptake, particularly in early growth stages. No significant differences were observed between the two sites based on statistical analysis of soil properties, although there were some small numerical differences among depths (Table 3). This implies a similar soil composition across the study area that can serve as a controlled background for comparison of treatment effects on seedling growth.

3.2. Growth Dynamics of F. sylvatica and Q. robur Seedlings One-Year After Forest Plantation

The result of above-ground growth parameters confirm that seedling establishment was successful across all treatments, with survival rates consistently exceeding 70%, the minimum benchmark for acceptable forest regeneration in Poland. The analysis of biometric increments following field transplanting revealed differences in species responses and treatment effectiveness. Notably, seedlings treated with liquid fertilizers exhibited reduced growth in both species, despite showing acceptable survival rates under both fertilization methods. After one year in the forest, treatment had a significant effect on height (p < 0.05), with R22 achieved height increment comparable to the peat-based control across both species. SC and SR22 (solid), UC and UR22 (liquid) were statistically grouped as the top performers for both height and diameter in both species (Table 4).

3.3. Root Morphological Response of F. sylvatica and Q. robur Seedlings One Year After Forest Plantation Establishment

The result of root morphological parameters shows that the effect of solid fertilization was more pronounced on root morphological indices than the liquid once after one year of growth in the forest. The result of total root length revealed the R20 substrates recorded the higher mean length in beech regardless of fertilization method. The response of oak was different, showing different response to different fertilizer. Peat substrate recorded the highest mean under liquid fertilization while with significant variation while SR21 performed best with no Signiant variation (Table 5). For F. sylvatica, RV was the only parameter to show statistically significant differences across treatments under solid fertilization. Although TRL, RSA, and ARD did not yield statistically significant differences (p > 0.05), numerical trends favored the SC treatment. Among the liquid fertilizer treatments, the UC and UR20 demonstrated marginally improved root architecture relative to other liquid combinations, although these differences were less pronounced. The treatment effects were more distinct among solid fertilizer treatments of Q. robur. The SC and SR21 treatments consistently produced superior results across these morphological parameters. TRL under solid fertilization did not differ significantly (p = 0.336), while the liquid fertilization result shows that TRL varied significantly (p = 0.000), with the control variant (UC) and UR20 recording the highest values (Table 5).

3.4. Root Diameter Classification of F. sylvatica and Q. robur Seedlings Under Different Treatments After One Year in the Forest

Root morphological responses across diameter classes showed distinct patterns between F. sylvatica and Q. robur, and were strongly influenced by fertilizer type and substrate combination (Table 6). In both species, seedlings treated with solid fertilizers, particularly under SC and SR22 treatments, exhibited significantly higher values across most diameter classes, especially in total length and surface area within the very fine root fraction (≤0.50 mm). Surface area and volume in this fine class were not significantly enhanced in these solid fertilizer treatments, but significantly enhanced in these liquid fertilizer treatments. Although, the differences were more pronounced in Q. robur of the same class, however, treatments R20 and R21 also demonstrated higher performance in few parameters, after peat-base substrate. Similar to solid once, treatment, UR22 again recorded higher output after UC in most of the accessed root parameters. Across both species, coarse volume (in the >2.00 mm) diameter class was less variable and showed fewer significant differences among treatments (Table 6).
The multiple linear regression models showed a strong association between below-ground root architecture and above-ground growth performance. Among the assessed variables, the abundance of very fine roots (≤0.50) classified by diameter emerged as the most influential factor driving both height and stem diameter development in beech. In oak, however, TRL was the only significant root trait influencing height, while none of the finer root classifications nor did other morphological parameters have a meaningful effect on diameter. This result brings a new perspective to forest nursery evaluations by demonstrating that root traits should not be universally applied as predictors across species. The differentiated role of root classifications especially the functional distinction of very fine, fine and coarse roots offers new practical implications. For beech, promoting fine root proliferation during nursery production may yield tangible benefits in early field performance. For oak, a broader view of establishment factors may be needed, extending beyond root architecture alone (Table 7).

4. Discussion

The findings of this study provide viability of innovative peat-free substrates and a novel liquid fertilizer in supporting early seedling development, in Fagus sylvatica and Quercus robur. Inline with the proposed hypotheses, several peat-free treatments most notably R22 demonstrated shoot growth and survival levels comparable to conventional peat-based controls. Species-specific differences reflected contrasting ecological foraging strategies in both species. F. sylvatica exhibited stronger correlations between shoot growth and very fine root development, while Q. robur’s growth aligned more closely with total root length (TRL). Therefore, root morphological traits predict early developmental dynamics under novel substrate and fertilizer regimes.
The analysis of soil properties showed slight numerical differences; however, these variations were not statistically significant (p-value < 0.05). The differences observed between soil depths and sampling locations did not significantly influence the growth or survival of seedlings [37,38,39,40]. The overall consistency in soil characteristics across both sites and depths suggests that soil conditions were not a major factor contributing to variations in seedling performance. Showing high survival rates across sites, beech and oak seedlings responded healthy to the applied treatments after one year of establishment. This agrees with previous research highlighting that the survival of seedlings is enhanced when individuals of the same species and age are planted together [41]. Moreover, successful root development remains a key factor in enabling seedlings to access soil moisture [41,42,43].
The high survival rates may also be due to the selection of superior seedlings from the nursery, a practice known to enhance field performance [44]. The consistently high survival rate observed across all treatments identified the potential of these innovative materials for successful seedling establishment. The ability of peat-free substrates to support similar survival outcomes to peat established their viability as sustainable alternatives in reforestation practices. This positive relationship between seedling size and survival has been observed in tropical species like Gmelina arborea and Khaya senegalensis [45,46] and in Mediterranean areas [44,47]. The study found a similar relationship in temperate species, likely due to the balance between root and foliar surface area and the ability to develop deep root systems before leaving the nursery [7,42,48]. However, some studies report no significant or even negative relationships between seedling size and survival [49,50].
The differences observed in seedling performance across treatments are in line with previous study [51] that report generally positive effects of peat-based substrates and solid fertilizers on early seeding development, although in this study, not all such trends reached statistical significance. This contradicts the preliminary report of Rotowa [7] on the same seedling after nursery production circle. Earlier investigation has shown that peat-based media provide favorable water retention, aeration, and structural consistency, which support both root elongation and nutrient uptake during the early growth phase [17]. The compositional analysis of the substrates used in this study confirms that peat substrates had more balanced organic matter and stable texture compared to the peat-free alternatives, which may have contributed to the improved morphological outcomes observed in the control treatments. Similarly, the physicochemical analysis revealed that the peat-based substrates maintained more favorable pH and EC ranges, which are known to influence nutrient availability and uptake efficiency, particularly in forest nursery system.
The limited performance of the novel liquid fertilizers, especially in Q. robur, aligns with previous findings that tree species differ in their tolerance to substrate variability and fertilization regimes [51,52,53]. While some studies report moderate success using composted or wood-based substrates, their performance often depends on precise control of nutrient formulation and substrate stabilization [54,55] These factors were optimized in the current experimental conditions. Furthermore, few studies have explored the role of root diameter classification as a predictor of shoot growth [9,10,11,12]. The strong positive association between very fine root length (≤0.50 mm) and shoot development in F. sylvatica provides new insight into the functional importance of absorptive root fractions in early seedling establishment. This suggests that simply measuring total root size may overlook key structural parameters that drive above-ground biomass accumulation. While Q. robur responded to total root length alone as a significant predictor. The effectiveness of these treatments in promoting increased growth reinforces the earlier recommendation by Rotowa et al., [7] to proceed with forest plantation using these seedlings once adequate root system formation was achieved after nursery production cycle. Though, the translation of those early gains into field performance was less consistent to earlier nursery performance. However, this evenness in results is consistent with the findings of previous studies by Kormanek et al., [56] on root growth of Quercus petraea seedlings, as well as studies on forest tree species grown in containers [57,58,59].
While the distinction between solid and liquid fertilizers was crucial to the experimental design, the observed differences in seedling growth are likely due not only to fertilizer form but also to variations in nutrient composition, availability, and release profiles. The solid fertilizer (Osmocote) used in this study is a controlled-release formulation that provides a balanced supply of essential micronutrients [60]. Its slow nutrient discharge over time ensured consistent availability during this crucial developmental stage, supporting stable root and shoot growth [61,62,63,64] In contrast, the liquid fertilizer although applied at regular intervals during nursery production period had lower overall nitrogen content and was more susceptible to leaching, especially in the more porous, peat-free substrates like UR22. Furthermore, previous work by Rotowa et al. [28] reported that this peat-based control substrate exhibited higher baseline nutrient concentrations prior to seed sowing compared to the innovative peat-free mixtures. This initial nutrient advantage, in combination with the solid fertilizer’s slow-release properties, likely created more favorable conditions for early seedling establishment in a new forest.
In this study, Fagus sylvatica and Quercus robur exhibited contrasting responses in below and above-ground coordination, particularly in how specific root traits influenced early shoot development. F. sylvatica showed a strong correlation between very fine root length (≤0.50 mm) and above-ground growth metrics, whereas Q. robur responded more strongly to TRL as a growth predictor. Although, these findings are consistent with prior studies that emphasize the functional importance of specific root traits in early seedling growth [8,10,11]. However, these variances reflect ecological and eco-physiological strategies of the two species. Beech has been reported to be a shade-tolerant, mesic-adapted species with a typically shallow, fibrous root system that facilitates efficient nutrient acquisition in surface soils [65,66,67,68]. Its early growth is often characterized by shoot elongation and crown development, strategies consistent with competitive light acquisition in closed-canopy environments. The observed association between shoot growth and very fine root traits may thus reflect this species’ reliance on dense absorptive roots for rapid resource uptake in the upper soil horizon. In contrast, oak has been reported to be more drought-tolerant, and characteristically develops a deep, vertically structured root system to access subsoil moisture, which is crucial for its establishment in open or water-limited sites [69,70,71,72]. The weaker correlation between very fine roots and shoot growth, and stronger association with total root length, likely reflects this more conservative growth strategy, which emphasizes rooting depth over fine root proliferation.
For effective reforestation, nursery practices should be tailored to meet species-specific ecological demands, particularly under evolving climate and soil conditions. The species-specific responses and root-shoot dynamics observed in this study offer valuable guidance for nursery management and reforestation planning. Fagus sylvatica, promoted fine root development through well aerated and nutrient-balanced substrates. In contrast, Quercus robur benefits from practices that support deep, vertically structured root systems, such as using containers and substrates that mimic natural soil conditions.

5. Conclusions

This study provides clear evidence that substrate and fertilizer choices significantly influence the early field performance of Fagus sylvatica and Quercus robur seedlings, with marked species-specific responses. Solid fertilizers consistently outperformed liquid formulations in promoting root development and shoot growth. The adoption of three root diameter classes identified that, very fine root traits (≤0.50 mm) offered novel predictive insights, especially for F. sylvatica, where strong root shoot harmonization was observed. Conversely, Q. robur showed a more gravitropic growth strategy, with total root length being the most informative predictor. The root systems of seedlings in the innovative substrates (R20, R21 and R22) were as well healthy, notable root growth was observed in R22, with values closely matching those of the peat-based control; however, these differences were not statistically in most cases after one year of planting into the forest, indicating a guaranteed prospect for future growth without environmental drawbacks like peat. While the study successfully captured early morphological responses under field conditions, limitations such as the absence of root: shoot biomass data and the inability to isolate nutrient form from their composition suggest directions for further research. Future studies should incorporate dry weight measurements, nutrient-matched fertilizer comparisons, and longer-term monitoring to strengthen conclusions on substrate and fertilizer efficacy. Overall, the adoption of these innovative substrates will not only reduce the environmental footprint but also aid biodiversity conservation, providing significant benefits in terms of seedling health and environmental sustainability during the early growth stages of forest seedlings in a new forest.

Author Contributions

Conceptualization, O.J.R. and S.M.; Methodology, O.J.R., S.M., J.B. and D.K.; Validation, S.M., M.P. and J.B.; Formal analysis, O.J.R., S.M., J.B., M.P. and D.K.; Investigation, O.J.R., S.M. and D.K.; Data curation, O.J.R. and J.B.; Writing—original draft, O.J.R.; Writing—review & editing, S.M., M.P., D.K. and J.B.; Supervision, S.M.; Project administration, S.M. and J.B.; Funding acquisition, S.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding. However, the peat-free substrates and liquid fertilizer used in this study were developed under the project POIR.04.01.04-00-0016/20, which was funded by the National Centre for Research and Development (NCBiR) from national resources and the European Regional Development Fund.

Data Availability Statement

Data is available upon request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Pérez-Ramos, I.M.; Gómez-Aparicio, L.; Villar, R.; García, L.V.; Maranon, T. Seedling growth and morphology of three oak species along field resource gradients and seed mass variation: A seedling age-dependent response. J. Veg. Sci. 2010, 21, 419–437. [Google Scholar] [CrossRef]
  2. Andres, S.E.; Standish, R.J.; Lieurance, P.E.; Mills, C.H.; Harper, R.J.; Butler, D.W.; Adams, V.M.; Lehmann, C.; Tetu, S.G.; Cuneo, P.; et al. Defining biodiverse reforestation: Why it matters for climate change mitigation and biodiversity. Plants People Planet 2023, 5, 27–38. [Google Scholar] [CrossRef]
  3. Grossnickle, S.C. Why seedlings survive: Influence of plant attributes. New For. 2012, 43, 711–738. [Google Scholar] [CrossRef]
  4. Ivetić, V.; Škorić, M. The impact of seeds provenance and nursery provenance method on Austrian pine (Pinus nigra Arn.) seedlings quality. Ann. For. Res. 2013, 56, 297–306. [Google Scholar]
  5. Banach, J.; Małek, S.; Kormanek, M.; Durło, G. Growth of Fagus sylvatica L. and Picea abies (L.) Karst. seedlings grown in Hiko containers in the first year after planting. Sustainability 2020, 12, 7155. [Google Scholar] [CrossRef]
  6. Palma, A.C.; Laurance, S.G. A review of the use of direct seeding and seedling plantings in restoration: What do we know and where should we go? Appl. Veg. Sci. 2015, 18, 561–568. [Google Scholar] [CrossRef]
  7. Rotowa, O.J.; Malek, S.; Banach, J.; Pach, M. Effect of different innovative substrate mediums on roots characterization of European beech Fagus sylvatica L. and pedunculate oak Quercus robur L. seedlings. Sylwan 2023, 167, 535–548. [Google Scholar]
  8. Comas, L.H.; Eissenstat, D.M.; Lakso, A.N. Assessing root death and root system dynamics in a study of grape canopy pruning. New Phytol. 2000, 147, 171–178. [Google Scholar] [CrossRef]
  9. Jacobs, D.F.; Salifu, K.F.; Seifert, J.R. Relative contribution of initial root and shoot morphology in predicting field performance of hardwood seedlings. New For. 2005, 30, 235–251. [Google Scholar] [CrossRef]
  10. Makita, N.; Hirano, Y.; Mizoguchi, T.; Kominami, Y.; Dannoura, M.; Ishii, H.; Finér, L.; Kanazawa, Y. Very fine roots respond to soil depth: Biomass allocation, morphology, and physiology in a broad-leaved temperate forest. Ecol. Res. 2011, 26, 95–104. [Google Scholar] [CrossRef]
  11. Pregitzer, K.S.; DeForest, J.L.; Burton, A.J.; Allen, M.F.; Ruess, R.W.; Hendrick, R.L. Fine root architecture of nine North American trees. Ecol. Monogr. 2002, 72, 293–309. [Google Scholar] [CrossRef]
  12. Park, B.B.; Yanai, R.D.; Fahey, T.J.; Bailey, S.W.; Siccama, T.G.; Shanley, J.B.; Cleavitt, N.L. Fine root dynamics and forest production across a calcium gradient in northern hardwood and conifer ecosystems. Ecosystems 2008, 11, 325–341. [Google Scholar] [CrossRef]
  13. Ding, Y.; Leppälammi-Kujansuu, J.; Helmisaari, H.-S. Fine root longevity and below-and aboveground litter production in a boreal Betula pendula forest. For. Ecol. Manag. 2019, 431, 17–25. [Google Scholar] [CrossRef]
  14. Zhou, W.; Guan, K.; Peng, B.; Tang, J.; Jin, Z.; Jiang, C.; Grant, R.; Mezbahuddin, S. Quantifying carbon budget, crop yields and their responses to environmental variability using the ecosystem model for US Midwestern agroecosystems. Agric. For. Meteorol. 2021, 307, 108521. [Google Scholar] [CrossRef]
  15. Makela, A.; Valentine, H.T.; Helmisaari, H.S. Optimal co-allocation of carbon and nitrogen in a forest stand at steady state. New Phytol. 2008, 180, 114–123. [Google Scholar] [CrossRef]
  16. Gruda, N. Current and future perspective of growing media in Europe. Acta Hortic. 2012, 960, 37–43. [Google Scholar] [CrossRef]
  17. Soman, C.; Li, D.; Wander, M.M.; Kent, A.D. Long-term fertilizer and crop-rotation treatments differentially affect soil bacterial community structure. Plant Soil 2017, 413, 145–159. [Google Scholar] [CrossRef]
  18. Hirschler, O.; Osterburg, B.; Weimar, H.; Glasenapp, S.; Ohmes, M.F. Peat replacement in horticultural growing media: Availability of bio-based alternative materials (No. 190). In Thünen Working Paper; The Thünen Institute: Braunschweig, Germany, 2022. [Google Scholar]
  19. Gruda, N.S. Increasing sustainability of growing media constituents and stand-alone substrates in soilless culture systems. Agronomy 2019, 9, 298. [Google Scholar] [CrossRef]
  20. van Beek, R.; Quik, C.; van der Linden, M. Drowning landscapes revisited; Correlating peatland expansion, human habitation trends and vegetation dynamics in the Northwest European mainland. Quat. Sci. Rev. 2023, 312, 108170. [Google Scholar] [CrossRef]
  21. FCS. Federal Council of Switzerland (2012) Bericht des Bundesrates in Erfüllung des Postulats 10.3377 Diener Lenz Torfausstiegskonzept. 2012. Available online: https://www.newsd.admin.ch/newsd/message/attachments/29089.pdf (accessed on 9 August 2023).
  22. EPAP. UK Government England Peat Action Plan. 2021. Available online: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/1010786/england-peat-action-plan.pdf (accessed on 9 August 2023).
  23. NMCE. Norwegian Ministry of Climate and Environment. Norway’s Climate Action Plan for 2021–2030: Meld. St. 13 (2020–2021) Report to the Storting (White Paper). 2021. Available online: https://www.regjeringen.no/contentassets/a78ecf5ad2344fa5ae4a394412ef8975/en-gb/pdfs/stm202020210013000engpdfs.pdf (accessed on 9 August 2024).
  24. EU. Regulation (EU) 2018/841 of the European Parliament and of the Council of 30 May 2018 on the Inclusion of Greenhouse Gas Emissions and Removals from Land Use, Land Use Change and Forestry in the 2030 Climate and Energy Framework, and Amending Regulation (EU) No 525/2013 and Decision No 529/2013/EU (Text with EEA Relevance). 2018. Available online: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32018R0841 (accessed on 8 September 2023).
  25. GME. Growing Media Europe. The Role of Peat in Growing Media. 2023. Available online: https://www.growing-media.eu/peat (accessed on 9 August 2023).
  26. Schmilewski, G. Growing media constituents used in the EU in 2013. In Proceeding of the International Symposium on Growing Media, Composting and Substrate Analysis-SusGro2015, Vienna, Austria, 7–11 September 2015; pp. 85–92. [Google Scholar]
  27. Andersen, R.; Farrell, C.; Graf, M.; Muller, F.; Calvar, E.; Frankard, P.; Caporn, S.; Anderson, P. An overview of the progress and challenges of peatland restoration in Western Europe. Restor. Ecol. 2017, 25, 271–282. [Google Scholar] [CrossRef]
  28. Rotowa, O.J.; Małek, S.; Jasik, M.; Staszel-Szlachta, K. Effect of innovative peat-free organic growing media and fertilizer on nutrient allocation in pedunculate oak (Quercus robur L.) and European beech (Fagus sylvatica L.) seedlings. New For. 2024, 56, 17. [Google Scholar] [CrossRef]
  29. Atzori, G.; Pane, C.; Zaccardelli, M.; Cacini, S.; Massa, D. The role of peat-free organic substrates in the sustainable management of soilless cultivations. Agronomy 2021, 11, 1236. [Google Scholar] [CrossRef]
  30. Prasad, R.; Redmile-Gordon, M.; Gush, M.B.; Griffiths, A. Characterisation of peat-free growing media to facilitate the transition to peat-free horticulture. In Proceeding of the I International Symposium on Growing Media, Compost Utilization and Substrate Analysis for Soilless Cultivation, Quebec, QC, Canada, 11–15 June 2023; pp. 153–162. [Google Scholar]
  31. Crowley, K.F.; Lovett, G.M. Effects of nitrogen deposition on nitrate leaching from forests of the northeastern United States will change with tree species composition. Can. J. For. Res. 2017, 47, 997–1009. [Google Scholar] [CrossRef]
  32. Priya, E.; Sarkar, S.; Maji, P.K. A review on slow-release fertilizer: Nutrient release mechanism and agricultural sustainability. J. Environ. Chem. Eng. 2024, 12, 113211. [Google Scholar]
  33. Martínez-Alcántara, B.; Martínez-Cuenca, M.R.; Bermejo, A.; Legaz, F.; Quinones, A. Liquid organic fertilizers for sustainable agriculture: Nutrient uptake of organic versus mineral fertilizers in citrus trees. PLoS ONE 2016, 11, e0161619. [Google Scholar] [CrossRef]
  34. Wang, M.; Li, G.; Liu, Y. Nursery fertilization affected field performance and nutrient resorption of Populus tomentosa Carr. ploidy levels. For.-Bio Geosci. For. 2020, 15, 16. [Google Scholar] [CrossRef]
  35. Kormanek, M.; Małek, S.; Banach, J. The Influence of Vibration and Moisture Content on the Compactness of the Substrate in Nursery Container Cells Determined with a Multipenetrometer. Forests 2023, 14, 1750. [Google Scholar] [CrossRef]
  36. Szabla, K.; Pabian, R. Container Nursery: New Technologies and Techniques in Forestry Nursery; State Forests Information Centre: Warsaw, Poland, 2003; p. 212. ISBN 83-88478-43-5. (In Polish) [Google Scholar]
  37. Kabała, C.; Musztyfaga, E.; Gałka, B.; Łabuńska, D.; Mańczyńska, P. Conversion of Soil pH 1:2.5 KCl and 1:2.5 H2O to 1:5 H2O: Conclusions for Soil Management, Environmental Monitoring, and International Soil Databases. Pol. J. Environ. Stud. 2016, 25, 647. [Google Scholar] [CrossRef]
  38. Ostrowska, A.; Gawlinski, S.; Szczubialka, Z. Methods of Analysis and Assessment of Soil and Plant Properties; Institute of Environmental Protection: Warsaw, Poland, 1991. [Google Scholar]
  39. Staszel, K.; Błońska, E.; Lasota, J. Slope aspect and altitude effect on selected soil organic matter characteristics in Beskid Mountains forest soils. Folia For. Pol. 2021, 63, 214–224. [Google Scholar] [CrossRef]
  40. Towett, E.K.; Shepherd, K.D.; Tondoh, J.E.; Winowiecki, L.A.; Lulseged, T.; Nyambura, M.; Sila, A.; Vågen, T.-G.; Cadisch, G. Total elemental composition of soils in Sub-Saharan Africa and relationship with soil forming factors. Geoderma Reg. 2015, 5, 157–168. [Google Scholar] [CrossRef]
  41. Andivia, E.; Villar-Salvador, P.; Oliet, J.A.; Puertolas, J.; Dumroese, R.K.; Ivetić, V.; Ovalle, J.F. Climate and species stress resistance modulate the higher survival of large seedlings in forest restorations worldwide. Ecol. Appl. 2021, 31, e02394. [Google Scholar] [CrossRef] [PubMed]
  42. Padilla, F.M.; Pugnaire, F.I. Rooting depth and soil moisture control Mediterranean woody seedling survival during drought. Funct. Ecol. 2007, 21, 489–495. [Google Scholar] [CrossRef]
  43. Luis, V.C.; Puértolas, J.; Climent, J.; Peters, J.; González-Rodríguez, Á.M.; Morales, D.; Jiménez, M.S. Nursery fertilization enhances survival and physiological status in Canary Island pine (Pinus canariensis) seedlings planted in a semiarid environment. Eur. J. For. Res. 2009, 128, 221–229. [Google Scholar] [CrossRef]
  44. Villar-Salvador, P.; Planelles, R.; Enrıquez, E.; Rubira, J.P. Nursery cultivation regimes, plant functional attributes, and field performance relationships in the Mediterranean oak Quercus ilex L. For. Ecol. Manag. 2004, 196, 257–266. [Google Scholar] [CrossRef]
  45. Egbewole, Z.T.; Falade, L.O.; Rotowa, O.J.; Kuje, E.D.; Mairafi, H.H. Evaluation of the Effect of Agricultural Crop on the Growth Performance of Gmelina arborea under Agroforestry System. Growth 2018, 18, 22nd. [Google Scholar]
  46. Egbewole, Z.T.; Rotowa, O.J.; Kuje, E.D.; Ogundana, O.A.; Mairafi, H.H.; Yohanna, I. Early germination, growth and establishment of Khaya senegalensis (DESR.) A. Juss in Middle-Belt Zone of Nigeria. J. Energy Nat. Resour. 2018, 7, 75–82. [Google Scholar] [CrossRef]
  47. Oliet, J.A.; Planelles, R.; Artero, F.; Jacobs, D.F. Nursery fertilization and tree shelters affect long-term field response of Acacia salicina Lindl. planted in Mediterranean semiarid conditions. For. Ecol. Manag. 2005, 215, 339–351. [Google Scholar] [CrossRef]
  48. Trubat, R.; Cortina, J.; Vilagrosa, A. Plant morphology and root hydraulics are altered by nutrient deficiency in Pistacia lentiscus (L.). Trees 2006, 20, 334–339. [Google Scholar] [CrossRef]
  49. Navarro, R.M.; Retamosa, M.J.; Lopez, J.; del Campo, A.; Ceaceros, C.; Salmoral, L. Nursery practices and field performance for the endangered Mediterranean species Abies pinsapo Boiss. Ecol. Eng. 2006, 27, 93–99. [Google Scholar] [CrossRef]
  50. Trubat, R.; Cortina, J.; Vilagrosa, A. Nutrient deprivation improves field performance of woody seedlings in a degraded semi-arid shrubland. Ecol. Eng. 2011, 37, 1164–1173. [Google Scholar] [CrossRef]
  51. Rotowa, O.J.; Małek, S.; Jasik, M.; Staszel-Szlachta, K. Substrate and Fertilization Used in the Nursery Influence Biomass and Nutrient Allocation in Fagus sylvatica and Quercus robur Seedlings After the First Year of Growth in a Newly Established Forest. Forests 2005, 16, 511. [Google Scholar] [CrossRef]
  52. Oliet, J.A.; Planelles, R.; Artero, F.; Valverde, R.; Jacobs, D.F.; Segura, M.L. Field performance of Pinus halepensis planted in Mediterranean arid conditions: Relative influence of seedling morphology and mineral nutrition. New For. 2009, 37, 313–331. [Google Scholar] [CrossRef]
  53. Oliet, J.A.; Artero, F.; Cuadros, S.; Puértolas, J.; Luna, L.; Grau, J.M. Deep planting with shelters improves performance of different stocktype sizes under arid Mediterranean conditions. New For. 2012, 43, 925–939. [Google Scholar] [CrossRef]
  54. Arvidsson, J. Nutrient uptake and growth of barley as affected by soil compaction. Plant Soil 1999, 208, 9–19. [Google Scholar] [CrossRef]
  55. Olajuyigbe, S.; Tobin, B.; Hawkins, M.; Nieuwenhuis, M. The measurement of woody root decomposition using two methodologies in a Sitka spruce forest ecosystem. Plant Soil 2012, 360, 77–91. [Google Scholar] [CrossRef]
  56. Kormanek, M.; Głąb, T.; Banach, J.; Szewczyk, G. Effects of soil bulk density on sessile oak Quercus petraea Liebl. seedlings. Eur. J. For. Res. 2015, 134, 969–979. [Google Scholar] [CrossRef]
  57. Clark, M.J.; Zheng, Y. Species-specific fertilization can benefit container nursery crop production. Can. J. Plant Sci. 2015, 95, 251–262. [Google Scholar] [CrossRef]
  58. Fu, Y.; Oliet, J.A.; Li, G.; Wang, J. Effect of controlled release fertilizer type and rate on mineral nutrients, non-structural carbohydrates, and field performance of Chinese pine container-grown seedlings. Silva Fenn. 2017, 51, 1607. [Google Scholar] [CrossRef]
  59. Chu, X.; Wang, X.; Zhang, D.; Wu, X.; Zhou, Z. Effects of fertilization and container-type on nutrient uptake and utilization by four subtropical tree seedlings. J. For. Res. 2020, 31, 1201–1213. [Google Scholar] [CrossRef]
  60. Broschat, T.K.; Moore, K.K. Release rates of ammonium-nitrogen, nitrate-nitrogen, phosphorus, potassium, magnesium, iron, and manganese from seven controlled-release fertilizers. Commun. Soil Sci. Plant Anal. 2007, 38, 843–850. [Google Scholar] [CrossRef]
  61. Benati, J.A.; de Lima, M.A.C.; Lucho, S.R.; Egewarth, J.; Nava, G.; Bianchi, V.J. Optimization the growth and quality of ‘Picual’ olive plants according to the dose of slow-release fertilizer. J. Plant Nutr. 2024, 47, 2608–2619. [Google Scholar] [CrossRef]
  62. Matysiak, B. Growth response of container grown Japanese azalea and euonymus and concentration of nitrates and phosphates in the runoff water under different irrigation and fertilization. J. Hortic. Res. 2015, 23, 21–32. [Google Scholar] [CrossRef]
  63. Jasik, M.; Staszel-Szlachta, K.; Małek, S.; Banach, J. Concentration of Nutrients in Individual Organs of European Beech (Fagus sylvatica L.) Seedlings and Root System Development as a Result of Different Fertilization. Forests 2024, 15, 2016. [Google Scholar] [CrossRef]
  64. Bohne, H. Influence of a peat-free substrate and kind of fertilizer on the nitrogen-and water balance and on plant growth. Eur. J. Hortic. Sci. 2007, 72, 53. [Google Scholar] [CrossRef]
  65. Leuschner, C.; Hertel, D.; Coners, H.; Büttner, V. Root competition between beech and oak: A hypothesis of coexistence based on root niche differentiation. For. Ecol. Manag. 2001, 149, 41–53. [Google Scholar]
  66. Gessler, A.; Keitel, C.; Kreuzwieser, J.; Matyssek, R.; Seiler, W.; Rennenberg, H. Potential risks for European beech (Fagus sylvatica L.) in a changing climate. Trees 2005, 19, 643–648. [Google Scholar]
  67. Eissenstat, D.M.; Wells, C.E.; Yanai, R.D.; Whitbeck, J.L. Building roots in a changing environment: Implications for root longevity. New Phytol. 2000, 147, 33–42. [Google Scholar] [CrossRef]
  68. Brunner, I.; Bakker, M.R.; Björk, R.G.; Hirano, Y.; Lukac, M.; Aranda, X.; Børja, I.; Eldhuset, T.D.; Helmisaari, H.S.; Jourdan, C.; et al. Fine-root turnover rates of European forests revisited: An analysis of data from sequential coring and ingrowth cores. Plant Soil 2015, 394, 169–185. [Google Scholar] [CrossRef]
  69. Kozlowski, T.T.; Pallardy, S.G. Acclimation and adaptive responses of woody plants to environmental stresses. Bot. Rev. 2002, 68, 270–334. [Google Scholar] [CrossRef]
  70. Iversen, C.M. Digging deeper: Fine-root responses to rising atmospheric CO2 concentration in forested ecosystems. New Phytol. 2010, 186, 346–357. [Google Scholar] [CrossRef]
  71. Allen, M.F. How oaks respond to water limitation. PSW-GTR-251. Berkeley, CA: US Department of Agriculture, Forest Service, Pacific Southwest Research Station: 13–22. Gen. Tech. Rep. 2015, 251, 13–22. [Google Scholar]
  72. Wilson, E.R.; Vitols, K.C.; Park, A. Root characteristics and growth potential of container and bare-root seedlings of red oak (Quercus rubra L.) in Ontario, Canada. New For. 2007, 34, 163–176. [Google Scholar] [CrossRef]
Table 1. Composition of the organic peat free substrate.
Table 1. Composition of the organic peat free substrate.
SubstrateSaw Dust Wood Chips Straw Wood Bark Perlite Core Wood Mixed Silage
(%)
R207310-10421
R212063-10421
R2250-1033421
Table 2. Physicochemical properties of substrates used in seedling growth in the Nursery.
Table 2. Physicochemical properties of substrates used in seedling growth in the Nursery.
SubstrateWater Capacity (%)Water Outflow Rate (L/min)Bulk Density (g/cm3)Solid Density (g/cm3)Air Capacity (%)Porosity (%)
R2040.5 ± 2.9 b0.595 ± 0.150 b0.115 ± 0.009 a0.64 ± 0.08 a52.1 ± 3.19 c92.6 ± 0.60 d
R2133.1 ± 2.5 d0.781 ± 0.114 a0.098 ± 0.014 c1.74 ± 0.07 a60.8 ± 3.06 a93.6 ±0.87 c
R2237.8 ± 5.1 c0.594 ± 0.150 b0.104 ± 0.020 b1.66 ± 0.11 a55.8 ± 5.58 b93.9 ± 0.98 b
Control57.7 ± 5.4 a0.417 ± 0.145 c0.085 ± 0.007 d1.69 ± 0.14 a37.0 ± 5.72 d94.7 ± 0.42 a
F387.4556.3265.811.0717295.7976.48
p0.00000.00000.00000.38700.00000.0000
Letters with different alphabet indicate statistically significant differences between means (p < 0.05).
Table 3. Mean and SD of soil properties of sampled plot of oak and beech at Barbarka experimental site.
Table 3. Mean and SD of soil properties of sampled plot of oak and beech at Barbarka experimental site.
Soil Uptake Level (cm) Exchangeable Cations ((cmol[+]/kg)
pH (H20)N (%)C (%)P2O5 (mg/100g)C/NCaKMgNa
Fagus sylvatica site
0–105.21 ± 0.550.36 ± 0.102.41 ± 0.213.14 ± 0.2113.78 ± 0.325.51 ± 0.520.18 ± 0.010.57 ± 0.060.70 ± 0.08
10–205.10 ± 0.570.34 ± 0.091.94 ± 0.152.87 ± 0.1412.90 ± 0.324.81 ± 0.390.16 ± 0.010.42 ± 0.030.63 ± 0.06
Total5.15 ± 0.560.35 ± 0.102.16 ± 0.122.99 ± 0.1213.30 ± 0.234.22 ± 0.320.15 ± 0.010.49 ± 0.030.55 ± 0.07
p-value0.187 ns0.170 ns0.061 ns0.286 ns0.065 ns0.064 ns0.062 ns0.062 ns0.062 ns
Quercus robur site
0–105.14 ± 0.590.45 ± 0.952.14 ± 0.224.70 ± 0.4513.31 ± 0.335.11 ± 0.530.23 ± 0.020.55 ± 0.060.81 ± 0.26
10–205.03 ± 0.610.44 ± 0.091.83 ± 0.144.22 ± 0.4012.23 ± 0.314.65 ± 0.360.21 ± 0.020.46 ± 0.030.82 ± 0.27
Total5.08 ± 0.590.45 ± 0.101.55 ± 0.134.44 ± 0.3012.73 ± 0.233.32 ± 0.320.22 ± 0.010.38 ± 0.030.82 ± 0.29
p-value0.208 ns0.945 ns0.061 ns0.427 ns0.069 ns0.061 ns0.363 ns0.061 ns0.989 ns
ns = not significance.
Table 4. Biometric and increment rate of F. sylvatica and Q. robur seedlings after one year on crop.
Table 4. Biometric and increment rate of F. sylvatica and Q. robur seedlings after one year on crop.
Fertilization Type After 1 Year in the ForestAfter Nursery Production CycleAbsolute Increment (%)
TreatmentSPCTSSRSS (%)Height (cm)Collar Diameter (mm)Height (cm)Collar Diameter (mm)HeightCollar Diameter
Fagus sylvatica
SR20Solid1121238458.12 ± 9.89 b9.11 ± 2.23 a31.46 ± 3.56 a5.63 ± 1.48 a8562
SR211351429759.01 ± 10.42 ab8.93 ± 2.01 a30.25 ± 3.43 a5.70 ± 1.62 a9555
SR221381439761.92 ± 11.61 a9.22 ± 1.96 a31.64 ± 3.29 a5.58 ± 1.15 a9658
SC1331439762.25 ± 12.02 a9.61 ± 2.48 a30.88 ± 3.23 a5.72 ± 1.23 a10268
Total 60.32 ± 11.188.94 ± 2.4431.06 ± 3.235.66 ± 1.26
p-value. 0.033 *0.203 ns0.473 ns0.341 ns
UR20Liquid1381439744.21 ± 7.77 f7.33 ± 1.98 e30.55 ± 3.23 e5.22 ± 0.95 e4540
UR211301369343.32 ± 7.18 f7.41 ± 2.04 e30.24 ± 2.98 e5.36 ± 1.24 e4438
UR221131359250.07 ± 8.49 e7.68 ± 1.86 e31.18 ± 3.19 e5.21 ± 1.07 e6147
UC1181359254.04 ± 8.52 e7.96 ± 1.49 e31.07 ± 3.08 e5.28 ± 0.99 e5651
Total 49.41 ± 3.197.60 ± 1.8230.76 ± 3.175.27 ± 1.07
p-value. 0.024 *0.176 ns0.253 ns0.316 ns
Quercus robur
SR20Solid1291349156.76 ± 9.28 a8.72 ± 1.89 a31.15 ± 2.97 a5.53 ± 1.56 a8258
SR211231308855.74 ± 7.95 a8.61 ± 1.78 a31.73 ± 3.47 a5.25 ± 1.43 a7664
SR221321409556.79 ± 7.74 a8.62 ± 2.03 a30.95 ± 2.99 a5.42 ± 1.39 a7759
SC1451459957.07 ± 6.89 a8.93 ± 2.11 a 31.09 ± 2.99 a5.66 ± 1.55 a7759
Total 55.58 ± 8.898.72 ± 1.8531.23 ± 1.345.47 ± 1.67
p-value. 0.103 ns0.473 ns0.564 ns0.271 ns
UR20Liquid1391429741.72 ± 8.44 f7.22 ± 1.10 e31.51 ± 2.74 e5.45 ± 0.89 e3232
UR211341409541.03 ± 8.26 f7.79 ± 1.22 e30.43 ± 2.55 e5.52 ± 0.92 e3541
UR221391449842.69 ± 9.67 f7.81 ± 1.54 e31.49 ± 2.86 e5.47 ± 0.95 e3643
UC1321389445.19 ± 9.93 e7.94 ± 1.44 e31.51 ± 3.02 e5.66 ± 0.96 e4340
Total 42.66 ± 9.087.69 ± 1.3231.23 ± 2.945.52 ± 0.94
p-value. 0.007 **0.978 ns0.305 ns0.231 ns
SPC—Number Seedlings in perfect condition, TSS–Total survived seedlings, RSS—rate of seedling survival. S—State Forests solid fertilization, U—University novel liquid fertilization, R—novel substrates, C—control substrate (peat−perlite) (N = 147). Letters with different alphabet indicate statistically significant differences between means (p < 0.05). Alphabets ‘a’ and ‘b’ denote homogeneous groups under solid fertilization and ‘e’ and ‘f’ denote homogeneous groups under liquid fertilization. ns = not significance, * = p < 0.05, ** = p < 0.01.
Table 5. Morphological parameters of root system of F. sylvatica and Q. robur seedlings under different substrate fertilizer treatment after one year in the forest.
Table 5. Morphological parameters of root system of F. sylvatica and Q. robur seedlings under different substrate fertilizer treatment after one year in the forest.
TreatmentFertilization TypeTRL (cm)RSA (cm2)ARD (mm)RV (cm3)
F. sylvatica
SR20Solid1673.27 ± 252.94 a171.66 ± 41.43 a0.85 ± 0.15 a3.59 ± 0.77 b
SR211265.52 ± 151.19 a168.37 ± 39.55 a0.82 ± 0.17 a3.51 ± 1.32 b
SR221424.69 ± 265.10 a182.79 ± 62.43 a0.72 ± 0.16 a3.37 ± 1.58 b
SC 1377.56 ± 104.39 a226.28 ± 48.05 a0.93 ± 0.19 a4.10 ± 1.59 a
Total1335.26 ± 207.75187.28 ± 52.15 a0.83 ± 0.18 a3.89 ± 1.48
p-value.0.285 ns0.061 ns0.087 ns0.035 *
UR20liquid1132.69 ± 130.54 e113.87 ± 19.61 e0.83 ± 0.10 e2.39 ± 0.89 e
UR211037.03 ± 92.90 e88.98 ± 14.17 f0.72 ± 0.08 f1.80 ± 0.26 f
UR221029.58 ± 88.39 e89.30 ± 6.50 f0.72 ± 0.09 f1.61 ± 0.56 f
UC1056.09 ± 98.93 e122.22 ± 10.22 e0.74 ± 0.06 f1.53 ± 0.42 f
Total1063.85 ± 107.7699.09 ± 16.650.75 ± 0.091.83 ± 0.65
p-value.0.157 ns0.001 **0.024 *0.015 **
Q. robur
SR20Solid1396.90 ± 81.03 a218.23 ± 38.22 a0.97 ± 0.12 a4.66 ± 0.56 b
SR211445.48 ± 83.89 a219.83 ± 30.32 a1.03 ± 0.13 a6.01 ± 1.07 a
SR221443.91 ± 95.26 a189.41 ± 18.21 b0.79 ± 0.14 b3.68 ± 0.48 c
SC 1386.20 ± 82.95 a187.28 ± 20.75 b1.03 ± 0.14 a4.24 ± 0.76 bc
Total1418.13 ± 86.59203.69 ± 31.000.95 ± 0.164.65 ± 1.13
p-value.0.336 ns0.024 *0.001 **0.000 **
UR20liquid1329.14 ± 59.57 f144.58 ± 19.36 f0.99 ± 0.32 ef3.41 ± 0.48 e
UR211345.08 ± 44.24 f125.69 ± 25.66 g0.81 ± 0.06 f2.44 ± 0.49 e
UR221248.43 ± 68.06 g109.37 ± 15.36 g1.07 ± 0.19 e2.99 ± 0.11 e
UC1453.88 ± 65.88 e164.48 ± 10.42 e0.87 ± 0.18 ef3.36 ± 1.19 e
Total1344.13 ± 93.91136.03 ± 27.420.94 ± 0.233.05 ± 1.43
p-value.0.000 **0.000 **0.051 *0.471 ns
TRL—Total root length, RSA—Root surface area, ARD—Average root diameter, RV—Root volume. Letters with different alphabet indicate statistically significant differences between means (p < 0.05). Alphabets ‘a, b’ and ‘c’ denote homogeneous groups under solid fertilization and ‘e, f’ and ‘g’ denote homogeneous groups under liquid fertilization. ns = not significance, * = p < 0.05, ** = p < 0.01.
Table 6. Root diameter classification of beech and oak seedlings under different treatments.
Table 6. Root diameter classification of beech and oak seedlings under different treatments.
TreatmentFertilization TypeLength < 0.5 mmLength 0.5–2.0 mmLength > 2.0 mmSurface Area < 0.5 mmSurface Area 0.5–2.0 mmSurface Area > 2.0 mmVolume < 0.5 mmVolume 0.5–2.0 mmVolume > 2.0 mm
Fagus sylvatica
SR20Solid465.22 ± 94.62 b144.40 ± 30.07 b36.04 ± 6.30 ab23.72 ± 6.32 a42.28 ± 9.08 b58.19 ± 11.61 b0.17 ± 0.02 a 1.13 ± 0.27 ab10.59 ± 2.31 b
SR21463.26 ± 99.38 b118.89 ± 41.23 b28.82 ± 8.58 b21.27 ± 8.28 a33.90 ± 11.14 b57.00 ± 16.68 b0.14 ± 0.06 a0.90 ± 0.35 b10.05 ± 3.55 b
SR22472.41 ± 109.16 ab133.92 ± 57.69 b30.40 ± 7.53 b24.48 ± 7.03 a39.49 ± 19.08 b59.43 ± 9.28 b0.15 ± 0.05 a0.97 ± 0.38 b10.89 ± 1.73 b
SC493.66 ± 109.71 a194.83 ± 67.13 a40.70 ± 9.64 a26.32 ± 5.46 a58.74 ± 20.40 a72.39 ± 15.11 a0.18 ± 0.04 a1.52 ± 0.39 a14.40 ± 4.54 a
Total471.14 ± 111.71148.01 ± 56.7633.99 ± 9.1123.19 ± 6.8743.60 ± 17.7160.75 ± 14.610.16 ± 0.041.13 ± 0.3511.38 ± 3.03
p-value0.048 *0.021 *0.015 *0.376 ns0.013 *0.043 *0.1236 ns0.045 *0.032 *
UR20Liquid325.34 ± 118.82 e88.38 ± 25.80 ef22.79 ± 7.43 e21.22 ± 6.78 ef23.21 ± 7.00 ef42.16 ± 8.81 e0.14 ± 0.04 e0.56 ± 0.20 f6.97 ± 1.40 f
UR21302.71 ± 94.01 e81.96 ± 30.18 f23.84 ± 7.70 e20.07 ± 5.66 f21.24 ± 8.24 ef40.79 ± 11.58 e0.13 ± 0.04 e0.50 ± 0.21 f6.31 ± 2.02 f
UR22360.41 ± 103.54 e112.89 ± 45.33 ef22.83 ± 3.78 e24.60 ± 7.39 ef29.68 ± 12.54 f39.07 ± 4.52 e0.17 ± 0.06 e0.71 ± 0.33 e7.13 ± 1.08 f
UC382.04 ± 101.77 e123.33 ± 41.95 e24.88 ± 5.05 e26.77 ± 5.66 e34.31 ± 17.49 e47.47 ± 8.63b e0.18 ± 0.05 e0.72 ± 0.35 e8.32 ± 1.66 e
Total342.62 ± 105.03101.63 ± 39.1223.58 ± 6.0023.16 ± 6.7027.11 ± 12.6642.36 ± 8.960.16 ± 0.040.62 ± 0.276.89 ± 1.54
p-value0.394 ns0.070 ns0.876 ns0.124 ns0.103 *0.222 ns0.285 ns0.022 *0.015 *
Quercus robur
SR20Solid597.88 ± 151.78 b130.18 ± 19.66 a37.64 ± 8.96 ab33.85 ± 2.83 b37.49 ± 4.85 a47.87 ± 5.43 a0.24 ± 0.07 a0.99 ± 0.15 a6.38 ± 0.48 a
SR21 664.72 ± 156.56 a145.75 ± 27.53 a34.94 ± 12.46 bc39.58 ± 3.23 a40.86 ± 3.84 a56.42 ± 16.35 a0.26 ± 0.06 a1.09 ± 0.21 a8.25 ± 1.81 a
SR22670.63 ± 193.31 a134.17 ± 48.93 a46.29 ± 5.92 a29.60 ± 6.76 b38.72 ± 3.33 a59.85 ± 13.16 a0.22 ± 0.09 a1.04 ± 0.36 a7.62 ± 1.46 a
SC672.41 ± 112.37 a152.96 ± 17.73 a36.57 ± 9.13 c31.33 ± 6.61 b41.46 ± 4.77 a48.78 ± 15.77 a0.22 ± 0.07 a1.03 ± 0.19 a8.69 ± 1.41 a
Total641.41 ± 157.42140.76 ± 31.0736.36 ± 11.4833.59 ± 6.2739.63 ± 7.5653.23 ± 13.810.23 ± 0.061.04 ± 0.227.74 ± 1.29
p-value0.012 *0.395 ns0.001 *0.002 *0.674 ns0.184 ns0.191 ns0.204 ns0.152 ns
UR20Liquid443.93 ± 225.91 e55.89 ± 29.77b ef12.29 ± 2.96 e25.54 ± 11.89 e15.28 ± 7.80 ef12.53 ± 3.73 f0.16 ± 0.07 e0.39 ± 0.21 f0.95 ± 0.51 e
UR21421.33 ± 202.95 e56.70 ± 28.37b ef13.08 ± 4.37 e17.63 ± 10.41 e13.71 ± 8.49 ef13.25 ± 4.45 ef0.11 ± 0.06 e0.38 ± 0.24 f1.12 ± 0.46 e
UR22474.44 ± 91.74 e71.06 ± 35.94 e13.49 ± 5.74 e24.22 ± 6.32 e21.22 ± 9.63 e11.91 ± 5.49 f0.15 ± 0.07 e0.59 ± 0.24 e1.24 ± 0.43 e
UC437.25 ± 94.64 e54.60 ± 18.55 f15.68 ± 2.94 e21.92 ± 4.97 e19.11 ± 5.25 f17.42 ± 4.45 e0.13 ± 0.06 e0.23 ± 0.15 f1.67 ± 0.58 e
Total444.24 ± 171.8852.06 ± 30.7113.54 ± 4.1922.33 ± 9.0114.83 ± 8.7813.78 ± 4.890.14 ± 0.060.40 ± 0.091.25 ± 0.49
p-value0.147 ns0.042 *0.349 ns0.267 ns0.025 *0.054 *0.062 ns0.042 *0.097 ns
S—State Forests Solid fertilization, U—University novel liquid fertilization, R—novel substrates, C—control substrate (peat−perlite). Letters with different alphabet indicate statistically significant differences between means (p < 0.05). Alphabets ‘a, b’ and ‘c’ denote homogeneous groups under state fertilization and ‘e’ and ‘f’ denote homogeneous groups under novel liquid fertilization. ns = not significance, * = p < 0.05.
Table 7. Model estimates for above ground parameters of F. sylvatica and Q.robur one year after planting in the forest.
Table 7. Model estimates for above ground parameters of F. sylvatica and Q.robur one year after planting in the forest.
Species/Dependent VariablePredictorCoefficientStd. Errorp-ValueCI LowerCI UpperAdjusted R2
F. sylvatica/Plant heightVFL0.0610.0170.0010.0270.0950.619
VFSA−3.1951.2130.011−5.623−0.7660.619
F. sylvatica/collar diameterVFL0.0110.0020.0000.0060.0160.644
VFSA−0.3510.1690.043−0.689−0.0110.644
Q. robur/Plant heightTRL−0.0340.0130.009−0.059−0.0090.530
TRL—Total Root Length (cm), VFL (≤0.50)—Very-fine length (cm), VFSA (VFSA.≤0.50)—Very fine surface area (cm2).
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Rotowa, O.J.; Małek, S.; Kupka, D.; Pach, M.; Banach, J. Innovative Peat-Free Organic Substrates and Fertilizers Influence Growth Dynamics and Root Morphology of Fagus sylvatica L. and Quercus robur L. Seedlings One Year After Planting. Forests 2025, 16, 800. https://doi.org/10.3390/f16050800

AMA Style

Rotowa OJ, Małek S, Kupka D, Pach M, Banach J. Innovative Peat-Free Organic Substrates and Fertilizers Influence Growth Dynamics and Root Morphology of Fagus sylvatica L. and Quercus robur L. Seedlings One Year After Planting. Forests. 2025; 16(5):800. https://doi.org/10.3390/f16050800

Chicago/Turabian Style

Rotowa, Odunayo James, Stanisław Małek, Dawid Kupka, Maciej Pach, and Jacek Banach. 2025. "Innovative Peat-Free Organic Substrates and Fertilizers Influence Growth Dynamics and Root Morphology of Fagus sylvatica L. and Quercus robur L. Seedlings One Year After Planting" Forests 16, no. 5: 800. https://doi.org/10.3390/f16050800

APA Style

Rotowa, O. J., Małek, S., Kupka, D., Pach, M., & Banach, J. (2025). Innovative Peat-Free Organic Substrates and Fertilizers Influence Growth Dynamics and Root Morphology of Fagus sylvatica L. and Quercus robur L. Seedlings One Year After Planting. Forests, 16(5), 800. https://doi.org/10.3390/f16050800

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