Sequent periderm formation and changes in the cellular contents of phloem parenchyma during rhytidome development in Cryptomeria japonica

The outer bark that includes sequent periderms is referred to as rhytidome. The defense and physiological functions of rhytidome are maintained by the continuous formation of sequent periderms. To understand the mechanisms of rhytidome growth, we examined the development of sequent periderms and the corresponding changes in the cellular contents of phloem parenchyma cells in Cryptomeria japonica . New layers of rhytidome were formed in the studied trees during the two-year course of the study. Our records showed that a new layer of periderm forms annually, and therefore, rhytidome development in C . japonica can be studied by sequential sample collection in any given year. Formation of new periderm and initiation of nuclei disappearance in phloem parenchyma in the outer layers of the developing outer bark occurred simultaneously. The early disappearance of nuclei indicates that some parenchyma cells might have been in a stage of preparation for cell death before the formation of new periderm. Four developmental stages of annual rhytidome growth were identified by structural and physiological changes of the outer layers of phloem parenchyma and the growth of the new periderm.


Introduction
Bark includes all tissues outside the vascular cambium [1][2][3]. Bark tissues can be divided into inner bark and outer bark. The inner bark, which consists of secondary phloem, plays important roles in transportation and storage of photosynthetic products. In contrast, the outer bark, which consists of periderms and the tissues isolated by them, functions to protect from abiotic and biotic stresses. The periderm is a secondary protective tissue that is produced by phellogen (cork cambium) and contains phellem (cork), phellogen, and phelloderm. The innermost periderm is part of the outer bark and constitutes the boundary between the inner and outer bark [3]. The outer bark that includes sequent periderms is referred to as rhytidome [3]. In species that form rhytidome, sequent periderms arise at varying intervals of time in successively deeper layers of bark [4]. During rhytidome formation, color changes of cell walls and cell death of parenchyma cells occur in the secondary phloem, which is isolated between the new periderm and the previous periderm. Because older layers of rhytidome can gradually fall off the tree, the defense and physiological functions of the outer bark are maintained by formation of new rhytidome layers. Therefore, elucidation of the mechanism of sequent periderm formation and the corresponding physiological and morphological changes of the phloem cells located between the new and previous periderms is important for understanding the details of bark physiology and the defense mechanisms of trees.
The first periderm and sequent periderms differ with regard to the origin of the phellogen and the timing of their appearance [2]. The epidermis, the first protective layer in plants, is strained tangentially by radial growth, eventually leading to its collapse. Prior to the destruction of the epidermis, phellogen is formed from epidermal or cortical parenchyma cells, and produces the first periderm to protect the inner living tissue [2,4]. The first periderm that replaces the epidermis is formed in the first year of stem and root growth [2,4]. In contrast, sequent periderms may be initiated later the same year as or many years after the formation of the first periderm or may never appear [2]. Sequent periderms originate in deeper tissue than the first periderm, usually in nonconducting phloem [3]. In addition, Mullick and Jensen [5] and Mullick [6] proposed that periderms could be classified into two categories, namely necrophylactic and exophylactic, depending on the site of periderm formation and the coloration of phellem cells. Thus, as mentioned above, periderms have been categorized according to their origin, timing of appearance, and site of formation.
Research on periderm formation has been performed, for the most part, with the first periderm. Previous studies have identified factors that might affect the formation of the first periderm, such as light intensity [7,8], photoperiod [9,10], temperature [9,11], position of leaves and buds [8,12] and plant hormones [8,9]. In contrast, limited information is available on the mechanism of sequent periderm formation. Mullick [6] suggested that sequent periderm formation might be induced whenever the previous phellogen becomes non-functional. However, the cellular and molecular mechanisms of sequent periderm formation remain to be clarified.
In terms of periderm development during rhytidome formation, the characteristics and formation of phellem have been widely studied due to its economic importance in cork products [13]. The cell wall microstructure and chemical composition of phellem and its cellular and molecular mechanisms of formation have been reported in various tree species such as Betula, Populus and Quercus [14][15][16][17][18][19][20]. However, information about other phenomena during rhytidome formation such as changes in cellular contents in secondary phloem tissue that is isolated by periderms, and the seasonal development of sequent periderms, remains limited.
The main goal of the present study was to investigate the histological process of rhytidome formation in Cryptomeria japonica. Cryptomeria japonica is the dominant tree species for plantation in Japan, and has relatively simple xylem and phloem structure [21]. Therefore, C. japonica has been effectively used as a model in ecophysiological studies [22][23][24][25]. We studied the formation of sequent periderms leading to rhytidome development. In addition, we monitored changes in the cellular contents of parenchyma cells during the death of parenchyma cells.

Plant materials and sample collection
In the present study, we used five Cryptomeria japonica trees. Sample collection date, age, tree height, diameter at breast height (DBH) and location information is shown in Table 1.
Block samples containing phloem, cambium and xylem were collected from the main stems at breast height during an active season of vascular cambium growth. To minimize the effect of wounding, samples were collected in different positions at the almost same height. Samples were fixed overnight at room temperature in a 5% (w/v) solution of glutaraldehyde in 0.1 M phosphate buffer (pH 7.2), and then the samples were washed with the same buffer.

Microscopy
Transverse and radial sections of approximately 40 µm thickness were cut on the freezing stage of a sliding microtome (Yamatokohki, Saitama, Japan). Unstained sections were mounted on glass slides in aqueous glycerol. To observe tissue and cell structure in secondary phloem and periderms, sections were examined under a light microscope (Axioscop.A1; Carl Zeiss, Oberkochen, Germany). After the light microscopic observations, the same sections were washed with distilled water and double-stained with fluorol yellow 088 (FY) and Congo red (CR) to detect suberized, lignified and non-lignified cell walls [26]. The FY was used for staining of suberized walls [27]. The CR was used for the staining of non-lignified walls [28]. Furthermore, lignified walls were detected using blue autofluorescence under ultra-violet excitation. Stained sections were observed under a confocal laser scanning microscope (LSM 710; Carl Zeiss; excitation/ emission combination for detection of autofluorescence of lignin, 405 nm/BP 427-480; for detection of suberin stained with FY, 488 nm/BP 495-553 nm; and for detection of non-lignified walls stained with CR, 561 nm/BP 566-690 nm).
To record the emission spectra of the autofluorescence of cell walls of periderms, we examined sections in the ''lambda scanning'' mode with single-photon excitation under the confocal laser scanning microscope, which was equipped with a Plan Apochromat 20×/0.8 objective lens (Carl Zeiss), as described by Nakaba et al. [24]. Sequential single-plane images (1024 × 1024 pixels) were obtained at wavelengths from 417 to 727.4 nm and from 563 to 727.9 nm in steps of 9.7 nm with excitation at 405 nm and 561 nm, respectively. These obtained images were used to generate the lambda stack images with color using the ZEN 2010 software (Carl Zeiss). The relative intensity of autofluorescence as the brightness of captured digital images at each wavelength was recorded from ten randomly chosen pixels (0.415 × 0.415 μm 2 ) that distributed in the cell wall areas of periderms. Then, the average of values from the ten pixels was calculated.

Results
We observed the process of rhytidome formation in five individual trees collected from 2016 to 2018. Although there were differences in the progress of rhytidome formation among sample trees and positions within each individual tree, all sample trees showed sequential changes in rhytidome formation from May to August. We classified the process of rhytidome formation into four stages based on the morphology as follows: just before the formation of new periderm (Stage 0); formation of new periderm (Stage 1); development of the new periderm (Stage 2); and maturation of new rhytidome (Stage 3). Figure 1 shows the bark structure in transverse and radial plains in the stem of Cryptomeria japonica. The bark can be divided into two parts, namely inner bark and outer bark (rhytidome). The inner bark was observed as a pale-yellow area in unstained sections ( Fig. 1a, b, e, f). In this area, it was easy to distinguish individual secondary phloem cells, such as sieve cells (S), phloem axial parenchyma cells (axial parenchyma cells, AP), phloem ray parenchyma cells (ray parenchyma cells, RP) and phloem fibers (F). These secondary phloem cells were arranged in a well-ordered manner. In contrast, the rhytidome was observed as a dark-brown area located outside the pale-yellow area in unstained sections ( Fig. 1a, b, e, f). Under a confocal laser scanning microscope, the signals of FY were detected in one or two cell layers as shown by white arrows in Fig. 1. The cell layers stained with FY were considered to be phellem. Furthermore, the blue autofluorescence of phloem fibers with lignified walls was observed ( Fig. 1c, d, g, h). In addition, several periderm layers that formed before the current year were observed in the rhytidome (Fig. 1c).

Stage 0: just before the formation of new periderm
In radial sections, the axial and ray parenchyma cells in the inner bark and the phelloderm of the innermost periderm contained nuclei that were stained with acetocarmine (black arrowheads in Fig. 2b). In addition, large amounts of starch grains stained with I 2 -KI were observed in these parenchyma cells (white arrowheads in Fig. 2d). No clear difference in cell shape was observed in the phloem tissue around the innermost periderm that included no conducting phloem (Fig. 1a, b). In contrast, in the rhytidome, phloem and periderm cells contained no nuclei or starch grains and had brown cell walls (Figs. 1 and 2).

Stage 1: formation of new periderm
In transverse sections of the outer region of the inner bark, radially flattened cells were observed among the axial and ray parenchyma (white arrows in Fig. 3a, c). The meristematic appearance of such cells indicates that cell division occurred in axial and ray parenchyma leading to the formation of new periderm. The new periderm consisted of two to three cell layers in the radial direction. In these cells, no suberin signal by the FY staining in the cell walls was observed (Fig. 3b, d and Additional file 1: Fig.  S1). Development of phellem and phelloderm was not yet distinguishable. The cell walls of the phloem cells located outside the new periderm showed no dark-brown coloration as seen in the rhytidome. In radial sections, nuclei were distributed with high density in the new periderm in unstained sections (black arrowheads in Fig. 3f ). In addition, sporadic disappearance of nuclei in axial and ray parenchyma was first observed in cell layers outside the new periderm (black arrows in Fig. 3f ). In contrast, most of the phelloderm of the innermost periderm contained nuclei (Fig. 3f ). Almost no starch grains were observed in the new periderm (white arrowheads in Fig. 3g). In addition, smaller amounts of starch grains were detected in axial and ray parenchyma cells outside the new periderm than in the cell layers on the inside of the new periderm (Fig. 3g).

Stage 2: development of the new periderm
An increased number of cells with the typical phellem cell shape could be seen in the new periderm (white arrows in Fig. 4c, d and Additional file 1: Fig.  S2). Suberin signal by FY staining was detected in the thin cell walls of the outer 1-2 cell layers in this area (white arrows in Fig. 4b, d and Additional file 1: Fig.  S2). Therefore, we identified these cell layers as new phellem that was produced by the new phellogen. On the other hand, FY signals from cell walls was not observed in the inner 1-2 cell layers (a yellow arrowhead in Fig. 4d). Therefore, these cells were distinguished as the phelloderm.
In the secondary phloem outside the new periderm, the cell walls were brighter colored compared with the cell walls of the rhytidome in unstained sections (Fig. 4a). In addition, the proportion of axial parenchyma cells without nuclei increased in the outer region of the new periderm in radial sections compared with Stage 1 (Fig. 4e, f ). Decreased amounts of starch grains were observed across the entire inner bark and the new rhytidome, particularly in parenchyma cells outside the new periderm (white arrowheads in Fig. 4g, h). The phelloderm of the previous periderm had more nuclei and starch grains than the axial and ray parenchyma located between the new periderm and the previous periderm (Fig. 4e-h).

Stage 3: maturation of new rhytidome
The number of cells and the morphology of the new periderm in Stage 3 were similar to those of the new periderm in Stage 2. However, the phloem cells outside the new periderm had acquired brown cell walls that were strongly stained with FY (Fig. 5a-d and Additional file 1: Fig. S3). On the outer side of the new periderm, no cellular contents were observed in the axial parenchyma, making it indistinguishable from rhytidome (Fig. 5c, d).
In radial sections, axial and ray parenchyma cells outside the new periderm had no nuclei or starch grains (Fig. 5e-h). Figure 6 shows differences in the spectrum of autofluorescence between new and previous periderms in the transverse section in Stage 3. The emission spectrum under excitation at 561 nm of new periderm peaked at approximately 597 nm, while that of previous periderm peaked at approximately 636 nm (Fig. 6d). In addition, the relative intensity of fluorescence under excitation at 561 nm from previous periderm was higher than that from new periderm (Fig. 6d). Figure 7 shows schematic diagrams describing the four stages of the new rhytidome formation. In addition, Table 2 shows the stages of rhytidome formation that were observed in each sample. There was no clear relationship between tree age and periderm formation among sample trees used in the present study. New rhytidome layers were formed during two consecutive years in trees C and D ( Table 2).

Timing of new rhytidome formation
In species that form rhytidome, the timing of sequent periderm formation varies depending on the tree species [2]. Mullick [30] pointed out that sequent periderms form at unpredictable intervals of time, making it inherently difficult to collect samples for developmental studies. This characteristic of sequent periderms has prevented  (Table 2). In addition, new rhytidome formation was observed during two consecutive years in trees C and D ( Table 2). These results indicate that new rhytidome formation occurs annually in C. japonica. Furthermore, new periderm formation and development were observed during May to July and June to August, respectively ( Table 2). Our observations suggest that new periderm formation in C. japonica has seasonality. These characteristics of rhytidome formation indicate that we can follow the process of rhytidome formation in C. japonica by sequential sample collection in any given year. Therefore, we have confirmed that C. japonica is a suitable model species for analysis of the mechanism of periderm and rhytidome formation.

Process of new periderm and rhytidome formation
The process of rhytidome development in other conifer species was described by Mullick [6] using fluorescence microscopy with a cryofixation technique. In that study, the author focused on changes in pigment localization and the morphology and autofluorescence of cells. The present study enables us to discuss the timing of depletion of storage materials and cell death during new rhytidome formation.
The formation of new rhytidome proceeded in the order of Stages 0-3 as follows (Figs. 1, 2, 3 We observed the same processes in all studied individual trees of different ages and sizes. At Stage 3, the peak of the emission spectrum, under excitation at 561 nm, from previous periderms occurred at a longer wavelength than that from new periderms (Fig. 6d). In addition, the intensity of autofluorescence, under excitation at 561 nm, from previous periderm was higher than that from new periderms (Fig. 6d). The peak shift from 597 to 636 nm and higher intensity of fluorescence indicate that some additional substances, which emitted autofluorescence with longer wavelength, have been accumulated in the cell walls of periderms. In Quercus suber, it has been reported that phenolic compounds accumulated in periderm and that genes involved in phenolic biosynthesis expressed in phellogen cells [19,31]. Similarly, the biosynthesis of phenolic compounds might proceed in the phellogen cells in Cryptomeria japonica. Mullick [6] reported that dedifferentiating cells were significantly enlarged at the beginning of sequent periderm formation in young stems of Tsuga heterophylla. In transverse and radial sections, we detected no enlargement of parenchyma cells before new periderm formation at Stage 0 in the outer region of the inner bark of C. japonica (Figs. 1  and 2). The enlargement of cells prior to new periderm formation during sequent periderm formation might occur depending on the species and/or growth stage of the tree. Sequent periderms have been classified as necrophylactic periderm that is formed on the inner side of necrotic tissue [5,32]. Mullick [6] hypothesized that non-functionality of phellogen is the trigger for necrophylactic periderm formation and cell death itself is not the cause of rhytidome formation. However, the mechanism and function of the cell death that occurs outside the sequent periderm have not been discussed. In the present study, disappearance of nuclei was first observed in the phloem outside the newly formed periderm in radial sections of Stage 1 (Figs. 3 and 7). This observation indicates that the parenchyma cells in the outer layers of the inner bark might have already been in a stage of preparation for cell death before the formation of the new periderm. Wunderling et al. [33] suggested that first periderm growth in the root and hypocotyl of Arabidopsis thaliana is tightly connected to the development of outside tissues and particularly to endodermal programmed cell death. Similarly, the death of parenchyma cells outside the new periderm might have an important role in periderm development.
When the periderm had developed with phelloderm and phellem (Stage 2), fewer starch grains were observed in the parenchyma cells outside the new periderm in radial sections (Figs. 4 and 7). Furthermore, after the formation of the new periderm was complete (Stage 3), the cellular contents of the parenchyma cells outside the new periderm disappeared, and the color of cell walls became brown and indistinguishable from the rhytidome that had been formed in the previous year (Figs. 5 and 7). O'Gara et al. [34] suggested that starch grains in the primary cortex adjacent to the region of periderm formation in Eucalyptus marginata seedlings might be used as a raw material for new cell production in the phellogen or as a precursor for phenolic compounds deposited in the periderm, including lignification of the thick-walled phellem. It is possible that starch in parenchyma cells outside the new periderm is used as an energy source and raw material for new cell production in the phellogen, or as a precursor for the biosynthesis of secondary metabolites such as suberin and phenolic compounds.

Conclusion
In the present study, we examined the histology of sequent periderm formation and the corresponding changes in the cellular contents of phloem parenchyma cells in C. japonica. We determined the following two characteristics of rhytidome formation: (1) periderm forms annually; therefore, it is possible to investigate the process of rhytidome formation in C. japonica by sequential sample collection in any given year; and (2) formation of new periderm and initiation of nuclei disappearance in phloem parenchyma outside the newly formed periderm appear to occur simultaneously. Four distinct stages of growth of the annual periderm and rhytidome were identified by histological observations. It is important to further investigate the changes of structure and vital state of the phloem parenchyma cells during rhytidome formation. Future studies should also add ultrastructural and molecular information to further elucidate the mechanism of rhytidome formation.