Fine root isotropy in Eucalyptus grandis plantations. Towards the prediction of root length densities from root counts on trench walls

The objectives of the study were to assess changes in fine root anisotropy and specific root lengths throughout the development of Eucalyptus grandis ( W. Hill ex Maiden) plantations and to establish a predictive model of root length density (RLD) from root intercept counts on trench walls. Fine root densities (<1 mm in diameter) were studied in 6-, 12-, 22-, 28-, 54-, 68- and 72-month-old E. grandis plantations established on deep Ferralsols in southern Brazil. Fine root intercepts were counted on 3 faces of 90-198 soil cubes (1 dm(3) in volume) in each stand and fine root lengths (L) were measured inside 576 soil cubes, sampled between the depths of 10 cm and 290 cm. The number of fine root intercepts was counted on one vertical face perpendicular to the planting row (N(t)), one vertical face parallel to the planting row (N(l)) and one horizontal face (N(h)), for each soil cube sampled. An overall isotropy of fine roots was shown by paired Student's t-tests between the numbers of fine roots intersecting each face of soil cubes at most stand ages and soil depths. Specific root lengths decreased with stand age in the upper soil layers and tended to increase in deep soil layers at the end of the rotation. A linear regression established between N(t) and L for all the soil cubes sampled accounted for 36% of the variability of L. Such a regression computed for mean Nt and L values at each sampling depth and stand age explained only 55% of the variability, as a result of large differences in the relationship between L and Nt depending on stand productivity. The equation RLD=1.89*LAI*N(t), where LAI was the stand leaf area index (m(2) m(-2)) and Nt was expressed as the number of root intercepts per cm(2), made it possible to predict accurately (R(2)=0.84) and without bias the mean RLDs (cm cm(-3)) per depth in each stand, for the whole data set of 576 soil cubes sampled between 2 years of age and the end of the rotation.

Corn root length density and root diameter as affected by soil compaction and soil water content

Negative effects of soil compaction have been recognized as one of the problems restricting the root system and consequently impairing yields, especially in the Southern Coastal Plain of the USA. Simulations of the root restricting layers in green house studies are necessary for the development of mechanism which alleviates soil compaction problems in these soils. The selection of three distinct bulk densities based on the standard proctor test is also an important factor to determine which bulk density restricts the root layer. The experiment was conducted to assess the root length density and root diameter of the corn (Zea mays L.) crop as a function of bulk density and water stress, characterized by the soil density (1.2; 1.4, and 1.6 g cm -3), and two levels of the water content, approximately (70 and 90% field capacity). The statistical design adopted was completely randomized design, with four replicates in a factorial pattern of (3 × 2). The PVC tubes were superimposed with an internal diameter of 20 cm with a height of 40 cm (the upper tube 20 cm, compacted and inferior tube 10 cm), the hardpan with different levels of soil compaction were located between 20 and 30 cm of the depth of the pot. Results showed that: the main effects of subsoil mechanical impedance were observed on the top layer indicating that the plants had to penetrate beyond the favorable soil conditions before root growth was affected from 3.16; 2.41 to 1.37 cm cm -3 (P<0.005). There was a significant difference at the hardpan layer for the two levels of water and 90% field capacity reduced the root growth from 0.91 to 0.60 cm cm -3 (P<0.005). The root length density and root diameter were affected by increasing soil bulk density from 1.2 to 1.6 g cm -3 which caused penetration resistance to increase to 1.4 MPa. Soil water content of 70% field capacity furnished better root growth in all the layers studied. The increase in root length density resulted in increased root volume. It can also be concluded that the effect of soil compaction impaired the root diameter mostly at the hardpan layer. Soil temperature had detrimental effect on the root growth mostly with higher bulk densities.

Changes of Root Length and Root-to-Crown Ratio after Apical Surgery: An Analysis by Using Cone-beam Computed Tomography

INTRODUCTION Apical surgery is an important treatment option for teeth with post-treatment periodontitis. Although apical surgery involves root-end resection, no morphometric data are yet available about root-end resection and its impact on the root-to-crown ratio (RCR). The present study assessed the length of apicectomy and calculated the loss of root length and changes of RCR after apical surgery. METHODS In a prospective clinical study, cone-beam computed tomography scans were taken preoperatively and postoperatively. From these images, the crown and root lengths of 61 roots (54 teeth in 47 patients) were measured before and after apical surgery. Data were collected relative to the cementoenamel junction (CEJ) as well as to the crestal bone level (CBL). One observer took all measurements twice (to calculate the intraobserver variability), and the means were used for further analysis. The following parameters were assessed for all treated teeth as well as for specific tooth groups: length of root-end resection and percentage change of root length, preoperative and postoperative RCRs, and percentage change of RCR after apical surgery. RESULTS The mean length of root-end resection was 3.58 ± 1.43 mm (relative to the CBL). This amounted to a loss of 33.2% of clinical and 26% of anatomic root length. There was an overall significant difference between the tooth groups (P < .05). There was also a statistically significant difference comparing mandibular and maxillary teeth (P < .05), but not for incisors/canines versus premolars/molars (P = .125). The mean preoperative and postoperative RCRs (relative to CEJ) were 1.83 and 1.35, respectively (P < .001). With regard to the CBL reference, the mean preoperative and postoperative RCRs were 1.08 and 0.71 (CBL), respectively (P < .001). The calculated changes of RCR after apical surgery were 24.8% relative to CEJ and 33.3% relative to CBL (P < .001). Across the different tooth groups, the mean RCR was not significantly different (P = .244 for CEJ and 0.114 for CBL). CONCLUSIONS This CBCT-based study demonstrated that the RCR is significantly changed after root-end resection in apical surgery irrespective of the clinical (CBL) or anatomic (CEJ) reference levels. The lowest, and thus clinically most critical, postoperative RCR was observed in maxillary incisors. Future clinical studies need to show the impact of resection length and RCR changes on the outcome of apical surgery.

Root system traits of Norway spruce, Scots pine, and silver birch in mixed boreal forests: an analysis of root architecture, morphology, and anatomy

The aim of this thesis was to unravel the functional-structural characteristics of root systems of Betula pendula Roth., Picea abies (L.) Karst., and Pinus sylvestris L. in mixed boreal forest stands differing in their developmental stage and site fertility. The root systems of these species had similar structural regularities: horizontally-oriented shallow roots defined the horizontal area of influence, and within this area, each species placed fine roots in the uppermost soil layers, while sinker roots defined the maximum rooting depth. Large radial spread and high ramification of coarse roots, and the high specific root length (SRL) and root length density (RLD) of fine roots indicated the high belowground competitiveness and root plasticity of B. pendula. Smaller radial root spread and sparser branching of coarse roots, and low SRL and RLD of fine roots of the conifers could indicate their more conservative resource use and high association with and dependence on ectomycorrhiza-forming fungi. The vertical fine root distributions of the species were mostly overlapping, implying the possibility for intense belowground competition for nutrients. In each species, conduits tapered and their frequency increased from distal roots to the stem, from the stem to the branches, and to leaf petioles in B. pendula. Conduit tapering was organ-specific in each species violating the assumptions of the general vascular scaling model (WBE). This reflects the hierarchical organization of a tree and differences between organs in the relative importance of transport, safety, and mechanical demands. The applied root model was capable of depicting the mass, length and spread of coarse roots of B. pendula and P. abies, and to the lesser extent in P. sylvestris. The roots did not follow self-similar fractal branching, because the parameter values varied within the root systems. Model parameters indicate differences in rooting behavior, and therefore different ecophysiological adaptations between species.

Fine root condition relates to visible crown damage in Norway spruce on acidified soils

Allochthonous Norway spruce stands in the Kysucké Beskydy Mts. (north-western Slovakia) have been exposed to substantial acid deposition in the recent past and grow in acidified soil conditions with mean pH of about 4.0 in the topsoil. We selected 90 spruce trees representing 30 triples of different crown status: healthy, stressed and declining to assess the relationship between crown and fine root status. Sequential coring and in-growth bags were applied to each triplet to investigate fine root biomass and growth in the soil depths of 0-10 and 10-20 cm. Fine root quantity (biomass and necromass), turnover (production over standing stock), morphological features (specific root length, root tip density) and chemical properties (Ca:Al molar ratio) were compared among the abovementioned health status categories. Living fine root biomass decreased with increasing stress, while the ratio of living to dead biomass increased. Annual fine root production decreased and specific root length increased in stressed trees when compared to healthy or declining trees, a situation which may be related to the position of trees in the canopy (healthy and declining – dominant, stressed – co-dominant). The Ca:Al ratio decreased with increasing crown damage, indicating a decreased ability to filter out aluminium. In conclusion, fine root status appears to be linked to visible crown damage and can be used as a tree health indicator.

Measuring variation in potato roots in both field and glasshouse: the search for useful yield predictors and a simple screen for root traits

Aims Potatoes have an inadequate rooting system for efficient acquisition of water and minerals and use disproportionate amounts of irrigation and fertilizer. This research determines whether significant variation in rooting characteristics of potato exists, which characters correlate with final yield and whether a simple screen for rooting traits could be developed. Methods Twenty-eight genotypes of Solanum tuberosum groups Tuberosum and Phureja were grown in the field; eight replicate blocks to final harvest, while entire root systems were excavated from four blocks. Root classes were categorised and measured. The same measurements were made on these genotypes in the glasshouse, 2 weeks post emergence. Results In the field, total root length varied from 40 m to 112 m per plant. Final yield was correlated negatively with basal root specific root length and weakly but positively with total root weight. Solanum tuberosum group Phureja genotypes had more numerous roots and proportionally more basal than stolon roots compared with Solanum tuberosum, group Tuberosum genotypes. There were significant correlations between glasshouse and field measurements. Conclusions Our data demonstrate that variability in rooting traits amongst commercially available potato genotypes exists and a robust glasshouse screen has been developed. By measuring potato roots as described in this study, it is now possible to assess rooting traits of large populations of potato genotypes.

Herbaceous plant species invading natural areas tend to have stronger adaptive root foraging than other naturalized species

Although plastic root-foraging responses are thought to be adaptive, as they may optimize nutrient capture of plants, this has rarely been tested. We investigated whether nutrient-foraging responses are adaptive, and whether they pre-adapt alien species to become natural-area invaders. We grew 12 pairs of congeneric species (i.e., 24 species) native to Europe in heterogeneous and homogeneous nutrient environments, and compared their foraging responses and performance. One species in each pair is a USA natural-area invader, and the other one is not. Within species, individuals with strong foraging responses, measured as plasticity in root diameter and specific root length, had a higher biomass. Among species, the ones with strong foraging responses, measured as plasticity in root length and root biomass, had a higher biomass. Our results therefore suggest that root foraging is an adaptive trait. Invasive species showed significantly stronger root-foraging responses than non-invasive species when measured as root diameter. Biomass accumulation was decreased in the heterogeneous vs. the homogeneous environment. In aboveground, but not belowground and total biomass, this decrease was smaller in invasive than in non-invasive species. Our results show that strong plastic root-foraging responses are adaptive, and suggest that it might aid in pre-adapting species to becoming natural-area invaders.

克氏针茅草原植物根与叶形态特性及其相互关系对氮素添加的响应

为了探究草原植物生长策略及其对养分变化的响应，本文比较分析了克氏针茅（Stipa krylovii)、冷蒿（Artemisia frigida)和糙隐子草（Cleistogenes squarrosa)根与叶的形态特性及其对氮素添加的响应。结果表明不同植物具有不同的生长策略，糙隐子草主要采取快速获取资源的生长策略，表现为具有高的比根长和比叶面积；冷蒿则主要采取保存资源的生长策略，表现为具有较高的根组织密度和较低的比根长；克氏针茅对资源的获取和保存能力都相对较强，表现为具有较大的比根长、较小的比叶面积和中等大小的根与叶组织密度。氮素添加主要影响克氏针茅和冷蒿的根特性，随着氮素添加量的增加，克氏针茅比根长显著增加，根组织密度显著降低，说明随着氮素添加量的增多克氏针茅根系对氮素的获取能力增强，从而导致其在群落中的生物量比例显著增加。冷蒿根表面积随着氮素添加量的增多显著降低，说明随着氮素添加量的增加冷蒿根系对氮素的吸收能力下降，导致其在群落中的生物量比例随着氮素添加量的增大而减少。氮素添加没有显著地影响糙隐子草根和叶特性，它在群落中的生物量比例也没有明显规律。因此，我们研究结果证明通过植物根和叶形态特性的变化能够预测植物在群落中地位的改变。 根与叶特性之间的关系可以进一步反映植物对资源获取和保存的权衡能力，研究植物根与叶特性的内在关系有助于更全面地理解植物的生存对策，更好地预测植物对环境变化的反应。我们通过简单相关分析和典型相关分析研究了克氏针茅草原植物的根与叶特性之间的关系及其对氮素添加的响应和根与叶总体关系。简单相关分析结果表明根特性之间、叶特性之间以及根与叶特性之间均存在相关性，植物特性之间的相互关系在根与叶中是相似的，且体现了植物对资源的获取与保存的权衡关系，如根组织密度与比根长负相关，叶组织密度与比叶面积负相关等，根与叶对应指标之间没有必然的联系。施氮肥使根与叶特性之间的相关性及其强弱发生变化，表明氮素添加是影响植物根与叶特性之间关系的因素之一。典型相关分析表明不同物种根与叶关系密切程度存在差异，不同根与叶特性之间的关系对根与叶总体的关系贡献程度也有所不同。

黄土丘陵区退耕地先锋群落演替过程中细根特征的变化

采用空间序列取代时间序列的方法,对退耕时间分别为2、4、6和8年的退耕地群落细根特征进行了分析,以探讨退耕地植被演替过程中细根特征在土壤剖面上的变化及其在演替过程中的作用.结果表明:(1)群落细根根长密度和根面积密度随植被演替显著增加;比根长、比根面积和地下/地上生物量也有增加趋势;细根平均直径随植被演替波动,但有减少趋势;(2)在土壤剖面上根长密度、根面积密度和根系生物量均随土壤深度的增加而降低.其中超过63%的根长、61%的根面积和72%的生物量分布在0～20cm的表层土壤中;(3)根径级统计表明,多数细根直径在0～0.5和0.5～1.0mm之间,这两级细根长度占细根总长度的80%以上;(4)逐步回归分析表明,植被演替过程中细根特征的变化主要与土壤有效氮(第2年)、有效磷(第2～8年)和土壤水分(第8年)的含量有关,且随着植被演替,2～6年退耕地中细根特征与土壤资源正相关,而第8年中二者呈负相关.这可能与植物生长对资源的需求与土壤提供资源的能力之间的平衡有关.研究表明,退耕地植被演替过程对土壤资源有一定影响,尤其是土壤水分含量显著减少;而土壤水分等土壤资源的变化又对群落产生影响,导致茵陈蒿先锋群落向地带性...

云雾山本氏针茅群落根系分布特征

为揭示本氏针茅(Stipa bungeana Trin.)群落的生理生态适应机制,采用根系取样器(Φ=9 cm)对宁夏云雾山本氏针茅群落根系分布特征和土壤含水量进行研究。结果表明:本氏针茅群落地下生物量、根长密度、根表面积、比根长均随土壤深度增加而减少,均表现出向表层(0~20 cm)集聚的趋势,且集中分布于0~40 cm土层,最大值均分布在0~20 cm土层,而底层(80~100 cm)最小;所有主要根系分布参数在0~20 cm和20~40 cm土层之间差异显著,以下各层差异不显著;土壤含水量与根生物量和比根长相关性达显著水平(P<0.05),与根表面积、根长密度均呈成正相关;根表面积、根生物量、根长密度和比根长间相关性均达极显著水平(P<0.01)。

黄土丘陵区油松人工林和白桦天然林细根垂直分布及其与土壤养分的关系

在黄土高原子午岭林区,对油松人工林、白桦天然林细根生物量、比根长、根长密度和细根表面积的垂直分布特征,以及这些根系指标与土壤水分、土壤容重、氮素和有机质的关系进行了研究。结果表明,油松人工林细根生物量随土壤深度增加呈单峰曲线,白桦林细根生物量随土壤深度增加呈减少趋势;油松林大部分根系生物量集中分布在0—40 cm土层中,其中0—20 cm土层占37%以上,20—40 cm集中了41%以上;表层土壤(0—20 cm)具有较高的比根长、根长密度和细根表面积,而底层(40—60 cm)的比根长、根长密度和细根表面积最低。油松林土壤全氮和有机质含量垂直变化趋势相似,随土壤深度的增加而降低;硝态氮(NO3--N)均随土壤深度的增加呈单峰曲线变化趋势,而铵态氮(NH4+-N)随土壤深度增加呈先降低后增加的抛物线趋势。白桦林75%的细根生物量集中在0—20 cm土层,比根长、根长密度和细根表面积的垂直分布规律与油松林相似,表层土壤白桦林细根表面积是油松人工林的3.91倍,而20—40 cm土层白桦林细根表面积比油松人工林降低了33%。白桦林土壤全氮、有机质含量、NO3--N和NH4+-N垂直变化趋势与油松林相似。土壤水分、...

黄土高原白羊草、沙棘和辽东栎细根比根长特性

以黄土高原地区典型草本(白羊草)、灌木(沙棘)和乔木(辽东栎)为对象,研究了3种植物细根比根长在不同土层的分布状况以及与其它细根参数和土壤物理因子之间的相关性。结果表明,3种植物细根比根长的变化范围为6~55 mm/mg。在0~80cm土层,白羊草、沙棘和辽东栎细根比根长变化范围分别为18~55 mm/mg,14~40 mm/mg,6~33 mm/mg。3种植物0~80cm土层平均细根比根长从大到小依次为白羊草>沙棘>辽东栎。3种植物0~10cm土层细根比根长依次为沙棘>辽东栎>白羊草,10~80cm依次为白羊草>辽东栎>沙棘,表明3种植物细根比根长不仅在这两土层中的分布不具一致性,而且与0~80cm土层平均比根长也不具有一致性,进一步说明3种植物沿土壤剖面的生物量分配策略不同。相关分析表明,3种植物细根比根长与其它细根参数之间的相互关系各不相同,制约程度存在差异。与土壤物理因子的相关分析表明,3种植物细根比根长均随土壤含水量的增加而减少。土壤各级水稳性团聚体和土壤颗粒对3种植物细根比根长并无一致的影响。

Effects of plant functional traits on soil stability: intraspecific variability matters

This data set describes different vegetation, soil and plant functional traits (PFTs) of 15 plant species in 30 sampling plots of an agricultural landscape in the Haean-myun catchment in South Korea. We divided the data set into two main tables, the first one includes the PFTs data of the 15 studied plant species, and the second one includes the soil and vegetation characteristics of the 30 sampling plots. For a total of 150 individuals, we measures the maximum plant height (cm) and leaf size (cm**2), which means the leaf surface area for the aboveground compartment of each individual. For the belowground compartment, we measured root horizontal width, which is the maximum horizontal spread of the root, rooting length, which is the maximum rooting depth, root diameter, which is the average root diameter of a the whole root, specific root length (SRL), which is the root length divided by the root dry mass, and root/shoot ratio, which is the root dry mass divided by the shoot dry mass. At each of the 30 studied plots, we estimated three different variables describing the vegetation characteristics: vegetation cover (i.e. the percentage of ground covered by vegetation), species richness (i.e. the number of observed species) and root density (estimated using a 30 cm x 30 cm metallic frame divided into nine 10 cm x 10 cm grids placed on the soil profile), as we calculated the total number of roots that appear in each of the nine grids and then we converted it into percentage based on the root count, following. Moreover, in each plot we estimated six different soil variables: Bulk density (g/cm**3), clay % (i.e. percentage of clay), silt % (i.e. percentage of silt), soil aggregate stability, using mean weight diameter (MWD), penetration resistance (kg/cm**2), using pocket penetrometer and soil shear vane strength (kPa).