1. Introduction
Vegetation and debris function as ecosystem engineers, modifying river flow resistance and sediment transport. The distribution of vegetation is important in hydraulic and environmental engineering. An increase in flow resistance and a decrease in conveyance capacity are aquatic and riparian vegetation’s most apparent hydraulic effects [
1]. The hydraulic impact depends not only on the presence but also on its spatial distribution: vegetation location (e.g., atop a bar crest vs. channel edges) plays a determining role in bar asymmetry and channel evolution [
2].
Vegetation alters hydraulic geometry, influencing width-depth ratios and bank stability [
3]. Riparian vegetation significantly alters the riverbank strength and contributes to flow resistance, affecting the river’s physical structure. Numerous studies have linked riparian vegetation density to channel width, depth, and flow velocity [
2,
4]. Bank strength largely governs the channel pattern (e.g., meandering vs. braided), with vegetated banks promoting the development of alternate bars [
5]. Under weak banks, rivers both in nature and in laboratory experiments tend to widen and evolve into shallow braided rivers with disorganized bar patterns. In contrast, when a bank is strong, rivers tend to be smaller and deeper and often exhibit alternating bars [
6]. Pools forming between alternating bars can cause continuous bank erosion [
7], ultimately promoting the evolution of a meandering channel.
Floods are key natural disturbances that significantly shape riparian ecosystems by influencing species diversity, richness, and spatial structure [
8]. Riparian vegetation on sandbars is significantly impacted by inundation, as it is established along rivers [
9]. Vegetation zonation patterns influence where patches are established. Frequent inundation and strong shear stress at bar heads and outer banks hinder vegetation survival and promote erosion, whereas bar margins and apexes provide more stable conditions that facilitate colonization [
10]. As a result, riparian vegetation is established in distinct zones across the floodplain: vertically, with flood-tolerant species colonizing lower, frequently inundated surfaces and less tolerant species restricted to higher elevations; and laterally, with denser growth along bar margins and apexes compared to sparsely vegetated bar heads and outer banks [
3]. In Japanese rivers, the native willow (
Salix spp.) often colonizes lower bars in patchy formations, whereas the invasive black locust (
Robinia pseudoacacia) tends to form dense stands on elevated gravel zones [
11].
A vegetation distribution results from flow conditions, elevation, and climatic variables [
12]. Vegetation may establish itself on a stable riverbed when the water allows for its development [
13]. Preliminary numerical modeling found that the uneven distribution of vegetation on a floodplain influenced the planform of meandering rivers [
14]. A field study conducted along the Tagliamento River in Italy concluded that the median elevation of the vegetation patch is correlated with the statistical properties of an island interweaving the river [
15]. However, investigating the morphodynamic influence of vegetation arrangements on river morphology through controlled flume experiments presents notable challenges. Nevertheless, understanding how vegetation patch placement and density influence flow and bed evolution is critical for effective channel restoration and revegetation planning. Under ice-covered conditions, leafless bed vegetation systematically alters pool–riffle hydraulics and local scour, extending vegetation structure insights beyond open-channel settings [
16].
In recent decades, forest coverage of Japan’s hillslopes and riparian corridors has increased due to effective land management, leading to reduced sediment production rates [
17]. However, intense rainfall events can trigger debris flows that introduce large woody materials into channels, thereby influencing bedform development and altering hydraulic conditions [
18]. Large woody debris (LWD), logs, branches, and coarse wood > 10 cm in diameter and >1 m in length, promote pool–riffle and step–pool sequences, especially in steep, confined valleys [
19]. By increasing flow resistance and inducing flow separation zones, LWD also contributes to sediment sorting and bar stabilization. A prior field study evaluated the effects of LWD on braided or single-threaded rivers [
20]. A field study in the Queets River basin (Washington) observed that in narrow streams, floating wood often becomes trapped between the bed and channel margins, leading to rapid wood accumulation [
21]. In these river sections, bedforms such as sandbars create favorable conditions for trapping driftwood, as evidenced by frequent post-flood wood deposits. Local hydraulic changes near debris jams can induce erosion and sedimentation, but quantitative analyses of these effects remain limited.
Debris accumulation in front of vegetation patches can increase patch density, creating significant flow obstructions. Empirical and field studies show that debris jams influence river morphology and have led to models clarifying debris effects on upstream water levels [
22,
23,
24]. A field study [
25] reported that the presence of woody debris increased the mean Manning’s
n by 39%, altering channel morphology. An experimental study [
26] on bridge pier scour with wood debris introduced the driftwood Richardson number (
DRI) to categorize driftwood movement around blockages, concluding that the presence of driftwood alters flow patterns. A numerical model for simulating driftwood motion concluded that the existence of driftwood surrounding the blockage affects the flow pattern, ultimately changing the bed topography [
27].
A field survey [
28] after Typhoon Hagibis (2019), in the upper Arakawa River, classified trapped debris as grasses, roots, small branches, and trees, based on material and resistance. Tree destruction on gravel bars formed downstream debris dams, which reduced the maximum flow velocity on bars but increased it in low channel areas, altering the flood propagation. An experimental study examined how different floating debris trapping patterns affect flood resistance in forested areas, classifying debris as I-type (wall-like at a forest front) or U-type (horseshoe-shaped jams around trees) [
29].
Although many studies have explored the effects of wooden log debris on river morphology, particularly in braided or multi-threaded systems, few have examined how debris interacts with different vegetation layouts in shaping an alternate bar morphology. In particular, the joint influence of the vegetation spatial distribution and debris entrapment and its geometry on hybrid alternate bars under a steady flow remains underexplored. Therefore, key research aims are to (1) examine how vegetation patch layout (river line vs. upstream), and debris configuration (I-type and U-type) influence the morphology of non-migrating alternate sandbars in a straight flume under steady subcritical flow conditions and (2) quantify how vegetation density (G/D = 2.2 vs. 4.2, here, G = inter-trunk spacing, and D = trunk diameter) and debris geometry affect scour and deposition patterns and to assess their combined role in amplifying morphodynamic responses.
A regression model is provided to predict the normalized scour/deposition magnitude from vegetation density, spatial placement (upstream vs. river-line), and debris geometry (I-type and U-type). Dense upstream patches with I-type debris are expected to yield concentrated frontal scouring and focused wake deposition (bar anchoring), whereas river-line patches with U-type debris favor distributed deposition with milder scour (edge stabilization). Model skill was ~±20% over the tested conditions.
2. Methodology
2.1. Experimental Setup and Flow Conditions
Experiments were performed in a 15 m × 0.5 m × 0.5 m straight rectangular flume with glass sides and a movable bed (
Figure 1a,b) at Saitama University, Japan. The flume included a recirculating pump, an upstream manual sediment feeder, and a downstream reservoir with a triangular V-notch for energy dissipation and flow measurement. Water from the downstream reservoir was recirculated to the upstream end.
This study focused on the formation of hybrid alternate bars, which differ from free bars by being stabilized in position by external influences such as upstream blocks. These bars can arise from intrinsic riverbed instabilities, but external forcing, such as an upstream block, prevents their migration, resulting in non-migrating but morphodynamically active features [
30].
Figure 1c illustrates the alternating sandbar formation. Alternate bars arise from fundamental riverbed instabilities when the width-to-depth ratio exceeds a threshold, producing a repeating sequence of bars and pools [
31]. Stability analyses and laboratory experiments show that bar formation depends on two factors:
β (the channel half-width to water depth ratio) and the Shields number (
θ), both of which are determined by dimensional analysis [
32,
33]. The resonance between flow depth and channel width determines the dominant bar wavelength, while vegetation and local forcing can further stabilize these features into non-migrating hybrid bars. Equation (1) defines the threshold for sediment motion. Sediment motion occurs when the bed shear stress exceeds the critical Shields parameter (
θ >
θc) [
32].
Here, τ = ρghi = bed shear stress (N/m2), ∆ρ = (ρs − ρw) the difference in density between sediment, ρs (kg/m3), and water, ρw (kg/m3), i = longitudinal bed slope, g: acceleration due to gravity (9.81 m/s2), and d = median sand grain size (mm), which was d50 in this equation.
The bar formation regime map [
32] defines alternate bar formation domains in terms of the Shields number and aspect ratio. In this study, a discharge rate of
Q = 0.003 m
3/s and a slope of
i = 1/200 were selected, based on bar regime stability frameworks, to ensure alternating bar development under a steady, subcritical flow. The experimental hydraulic parameters are summarized in
Table 1. A steady, subcritical flow condition was maintained throughout the experiment (Froude number
Fr =
U/
√(
gh) < 1), where U is the flow velocity (m/s) and
h is the flow depth (m) to simulate early-stage channel adjustments following flood recession, conducive to vegetation colonization and debris deposition on stable alternate bars. All experiments started with a flatbed slope of 1/200 and used uniform, cohesionless sand (
d50), ensuring bedload-dominated transport. The sediment feed (only for alternate bar formation) and the fixed bed slope were selected to maintain equilibrium bar formation, ensuring nonmigrating alternate sandbars [
19,
34].
2.2. Sediment Characteristics and Flow Duration
The sediment transport mode was jointly controlled by the median grain size (
d50) and prevailing hydrodynamic boundary conditions. In the present experiments, the selected
d50 = 0.875 mm, under the applied flow depth and shear stress, favored predominant bedload transport, which minimized ripple formation and ensured representative sediment dynamics in the flume [
35]. The sediment used was a uniform, cohesionless sand with a
d50 of 0.875 mm and a dry density (
ρs) of 2650 kg/m
3. The grain size distribution is shown in
Figure 2a. The same sand was used as an inlet for sediment input upstream. The sediments had a sorting index
I = 0.5 (
d84/d50 +
d50/
d16) = 1.27, indicating a relatively broad range of particle sizes. The grain specific gravity (
Sg) was 2.65, while the sediment in the water had a specific gravity of 1.65. Here,
d50,
d84, and
d16 represent the particle sizes at which 50%, 84%, and 16% of the sediment grains are smaller, respectively.
The sand bed was manually compacted to achieve a flat bed. Layers of sand were evenly packed between two small, identical weirs (~0.1 m high), with one at the upstream inlet and the other 0.5 m upstream of the downstream outlet. Each experiment was concluded once the sediment outflow rate and sandbar topography exhibited no significant changes, indicating that equilibrium conditions were achieved when the bed slope equaled the water surface slope [
33,
36]. Subsequently, less than 5% of additional scouring occurred during alternate bar formation. Each vegetation and debris experiment was conducted for an additional four hours after equilibrium was achieved.
2.3. Vegetation and Debris Model Configuration
The spatial arrangement of vegetation is fundamental to modifying flow resistance and sediment transport in straight single-thread channels. A comparable arrangement and density-controlled shifts in flow structure have been reported for submerged canopies as well [
37], reinforcing the need to treat layout and blockage jointly. Vegetation along the sandbar margins enhances sediment retention and deflects flow laterally, thereby influencing bar stability and channel asymmetry [
21,
38]. Field studies report riparian vegetation widths ranging from 1.5 to 10.7 m, with an average of 3 m [
39]. With a geometric scale ratio of 1:50, this range corresponds to 0.03–0.21 m [
40]. A representative vegetation width of 0.064 m (6.4 cm) was used for river line vegetation. Field observations from the Arakawa River (
Figure 2b) show that vegetation often establishes along the margins of alternate sandbars. A germination experiment further confirmed that vegetation tends to establish along sandbar margins [
40]. Based on these observations, the river line vegetation configuration in this study was implemented to represent edge-focused vegetation development. In addition, prior studies have shown that vegetation positioned at the upstream bar boundary can significantly alter flow contraction, enhance turbulence intensity, and trigger localized sediment mobilization that stabilizes channel morphology [
41,
42]. Therefore, an upstream vegetation layout was also selected to assess the role of patch position with debris accumulation in shaping sediment transport and morphological response.
The vegetation model design was based on field observations of
Salix exigua colonizing sandbars in the Arakawa River, providing reference parameters for trunk structure and spatial distribution [
43]. Emergent vegetation was simulated using rigid wooden cylinders with a diameter of 0.004 m and a height of 0.18 m. Rigid emergent wooden dowels were widely adopted in previous flume studies to model vegetation–flow interactions, including [
41,
44], due to their ability to replicate the bulk hydraulic resistance and spatial obstruction effects of natural plants. This corresponds to a 1:50 scale model of mature riparian trunks (~0.2 m diameter in the field), chosen based on equivalent drag characteristics [
45]. Two vegetation densities were tested in a staggered planting pattern (
Figure 2c): a dense configuration with inter-trunk spacing
G = 0.0088 m (
G/
D = 2.2), and a sparse configuration with
G = 0.0168 m (
G/
D = 4.2). Here,
G is the gap between trunks, and
D is the trunk diameter. These parameters (diameter and density) were derived from a field study [
46] in which values were calibrated to replicate the effective crown-projected area per unit ground surface observed in dense vegetation patches dominated by
Salix spp. and
Robinia pseudoacacia. By accounting for the plant crown effect in the blockage density, the chosen
G/
D values provided a hydraulically realistic obstruction ratio for analyzing sediment dynamics under dense riparian colonization scenarios.
After alternate bar formation, two spatial vegetation patterns were experimented with: (1) river-line vegetation, in which cylinders were placed parallel to the flow along the sandbar edge (
Figure 3a), and (2) upstream vegetation where patches were arranged in a semicircular the sandbar apex (
Figure 3b). To avoid disturbing the bed equilibrium, cylinders were gently inserted into the bar surface and stabilized under a short, low-flow run before the main discharge was applied. These layouts were designed to simulate vegetation colonization patterns observed in natural channels and their effects on bar–pool development.
After establishing the vegetation patches, two debris configurations were introduced: I-type (linear, wall-like) and U-type (horseshoe-shaped). The debris was placed at the upstream (leading) edge of vegetation to simulate flood-induced entrapment, following field observations of the Tokigawa River after high-magnitude flow events, with measured average debris thickness around 0.64 to 1.03 m [
28,
29,
47]. The I-type debris acted as a frontal barrier in front of the vegetated patch, while the U-type debris surrounded the upstream and downstream to simulate the accumulation of drift material around the vegetation cylinders.
The debris was constructed from coconut fiber mats with a density of 44.6 kg/m
3. This material was chosen because its drag coefficient and porosity (
Cd ≈ 8.7;
Pr ≈ 84%) closely replicates the hydraulic resistance and flow blockage behavior of woody debris [
47]. This material provided a realistic degree of flow obstruction and debris trapping effects under steady flume conditions. The debris elements were manually arranged with vegetation patches to replicate typical flood-induced accumulation patterns. The debris coverage lengths and spatial arrangements were derived from field-measured debris entrapment after flood events [
47] and are detailed in
Table 2.
In the vegetation-only trials (no debris), a scouring and deposition change in morphology was observed. In the runs with debris, I-type debris accumulated along the front row of the vegetation belt and in the narrow gap between the sandbar and the bank.
Figure 4 shows a schematic plan view of I-type debris with vegetation. In river line vegetation cases, the I-type debris was affixed not only to the frontal edge (
Figure 4a) of the vegetation but also along the curved sandbar margins, extending into the approach-flow zone of the vegetation patch up to an effective debris coverage length (
ld’) (
Figure 4b). This curved interface between sandbar margins and the adjacent pools often serves as a natural trap for floating debris [
28].
Figure 4c shows the I-type debris with upstream vegetation.
Figure 4e and
Figure 5a show the perspective view of I-type debris with the vegetation. U-type debris elements traps (schematic diagram,
Figure 5a were strategically placed to intercept simulated tree trunks in the fore section of the vegetation, corresponding to the highest scouring activity (
Figure 5c,d). Both the vegetation and debris were represented using a 1:50 physical scale model, as illustrated in
Figure 4d and
Figure 5e. Primes denote model dimensions (
d′w,
d′h,
l′d); prototype values are 50× the model (1:50), e.g., a model debris width
d′w corresponds to a field width 50·
d′w.
Table 2 above summarizes the vegetation and debris geometric parameters.
Vegetation-only experimental results revealed that pronounced scour consistently occurred at the upstream edge of a patch [
44], where the approaching flow directly impinged and was deflected, leading to enhanced local near-bed scour. In contrast, the wake region behind the vegetation experienced significant flow deceleration, resulting in minimal erosion and predominantly sediment deposition [
41]. Accordingly, U-type debris was installed up to an effective debris coverage length (
ld’) in the upstream zones in both river line (
Figure 5c) and upstream vegetation (
Figure 5d) configurations, as preliminary tests showed major hydraulic effects in those areas. This strategic placement of U-type debris at the flow-facing edge simulated natural flood entanglement patterns, effectively increasing resistance and modifying bar-edge morphology without disturbing the bar interior.
2.4. Experimental Methodology and Measurements
A stilling basin with a flow stabilizer and an upstream weir was installed 0.5 m downstream of the reservoir to ensure uniform flow distribution. The initial longitudinal bed slope of the flume was set to 1/200 (0.005). A mechanical control system at the upstream tank maintained a constant flow rate of 0.003 m
3/s, selected based on bar regime criteria [
32]. With observed Stage I, depth
h, gives bed shear (
τ) =
pghi ≈ 0.8–1.0 N/m
2 and Shields number (
θ)≈0.05–0.07 for mean diameter (
d50) ≈ 0.875 mm, above incipient motion yet below sheet flow, placing the sediment in the alternate-bar mobility window [
48]. The chosen constant flow rate ensured a fixed hydraulic regime [
33] over 4–5 h run, allowing bars to reach dynamic equilibrium within the flume length, keeping the discharge (
Q) constant, isolates vegetation–debris effects from hydrograph transients.
To initiate a repeatable hybrid alternate bar pattern, a 0.1 m-wide cubic block was placed against the left channel wall upstream of the weir, which helped prevent bar migration in the downstream reach [
49]. The upstream sediment supply rate was calculated using an empirical formula (Equation (2)) to maintain sediment continuity and achieve equilibrium conditions [
50]. Each experimental run continued until the alternate sandbars reached equilibrium, defined as the bed slope matching the water surface slope [
36].
Here, Qs is the sediment transport rate (kg/h), and c is the critical Shields parameter for incipient sand motion, taken as 0.047.
After the equilibrium sandbars were developed in Stage I, two experimental scenarios were investigated in Stage II: (1) vegetated sandbars (river line vs. upstream configurations), and (2) vegetated sandbars with debris added (I-type and U-type). Two vegetation densities were tested: dense (
G/
D = 2.2,
ρv = 1630 stems/m
2) and sparse (
G/
D = 4.2,
ρv = 815 stems/m
2). In Stage II, scenario 1, wooden cylinders representing vegetation were installed on sandbars, and a steady flow was maintained for 4 h until equilibrium. In Stage II, scenario 2, debris was manually introduced and trapped with vegetation to assess its combined effect on morphology over the same 4 h period. No sediment was supplied during Stage II to avoid introducing external effects on local scour and deposition patterns. All the experimental cases (vegetation and debris combinations) are summarized in
Table 3. A concise workflow from Stage I to Stage II, including the scenario matrix, measurements, and Δ
z/
h processing, is shown in
Figure 5f, and the geometric-scale context (1:50) is illustrated in
Figure 4d and
Figure 5e.
After each run, the flume was gradually drained, and the bed surface was scanned using a laser displacement meter (LJ-V-7000, Keyence Corporation, Osaka, Japan, 2020). Bed scanning was conducted at 1 h intervals, with measurements taken every 10 cm streamwise and every 2.56 cm cross-stream interval (accuracy ± 0.2 mm). Bed elevation was analyzed from 2 m to 14 m along the flume, excluding regions affected by the inlet zone (where the inflow structure caused initial bed disturbances) and outlet zones (affected by the downstream weir), so that only the region with fully developed bedforms was considered. The water surface profiles and bed slopes were recorded hourly using a point gauge (accuracy ± 0.1 mm) on the flume carriage, with readings at 0.5 m in the longitudinal direction.
Scour and deposition were quantified as the bed-elevation changes (∆
z) observed within the bar pool region of the flume before and after experimental cases. These values were then expressed in dimensionless form (∆
z/
h) to ensure the scalability of the results, allowing lab-derived insights to predict morphodynamic responses in natural rivers. Accordingly, a dimensionless relationship (Equation (3)) was employed to generalize the complex interactions between vegetation, debris, and flow dynamics by eliminating scale dependency.
Here, ∆z/h is the scour depth or deposition normalized by water depth (h), G/D is the vegetation density, Ad is debris geometry (frontal area), Av is the vegetation blockage area, and Fr is the Froude number.
Scour depth (Δz < 0) and deposition height (Δz > 0) were computed as the difference between the equilibrium bed and the initial flat surface and normalized by water depth (Δz/h). For each patch (P1–P3), we recorded maximum scour and deposition, as well as downstream decay ratios (P1–P3).
4. Discussion
4.1. G/D = 2.2 (Dense Vegetation and Debris)
In the dense vegetation scenario (G/D = 2.2), vegetation strongly modulated both flow structure and sediment dynamics. River line vegetation patches arranged parallel to the flow (e.g., Case DV
RL;
Figure 6c) formed elongated obstructions that decelerated lateral inflow. This effect is consistent with previous experimental and empirical studies on vegetation–flow interaction, which showed that vegetation placement reshapes bar geometry [
3,
12]. This leads to moderate sediment deposition along the bar margin, particularly upstream of the patch at location L1–L2 +1.5 cm, consistent with observations from debris–vegetation interaction experiments under flood conditions [
52]. In contrast, curved river line patches (P2 and P3 on downstream bars S2, S3;
Figure 6c) deflected the main flow toward the opposite bank, producing localized scour (~−2.0 cm at L5) and focusing deposition at the downstream bar arc (L3–L4). These observations are consistent with the experimental patch tests, which demonstrated that curved vegetation zones enhance off-center bar–pool patterns and asymmetrical sedimentation accumulation [
44]. Mechanistically, increased frontal blockage causes flow contraction and impingement at the patch front, producing localized scour at the nose, while lee deceleration favors bar-crest deposition; stronger blockage (dense vegetation with I-type debris) intensifies this front–lee contrast and amplifies bar–pool asymmetry [
46].
When debris became trapped in these dense patches, the effects were intensified. In DV
RL_I (dense river line vegetation with I-type debris at Patch P1), it resulted in −2.7 cm scour (L1–L2) and crest deposition of +2.2 cm (
Figure 7a. This outcome confirms that debris structures act as concentrated obstacles: they increase local downflow (
Figure 9a) but have diminishing effects downstream, as evidenced by Patch 3 experiencing only −1.7 cm scour and +1.4 cm deposition (~37% reduction in morphodynamic amplitude) (maximum scour–deposition, Δ
z/
h) [
29,
52]. By contrast, in the DV
RL_U case, scour was limited to −1.8 cm and manifested as a broad erosional zone at the patch base (L5). Sedimentation was spread across the front patch and sides (
Figure 9b, consistent with field observation of woody debris accumulation) [
22,
53].
Among upstream vegetation with debris, the I-type debris configuration (DV
US_I) produced the most pronounced scour and deposition pattern. Placing I-type debris directly upstream of the patch (aligned it with the main current) greatly increased local flow constriction, generating approximately −3.5 cm of scour (L1–L2) and +2.8 cm of bar crest buildup (L2–L3), as seen in
Figure 8a and
Figure 9c. This finding is consistent with the previous experimental flume results, which showed that upstream debris jams caused an abrupt flow constriction and localized erosion, especially when the blockage-to-channel width ratio was high [
54,
55]. The scour was much deeper than in the river line case because upstream debris placement aligns the patch more directly with the main flow.
In the DV
US_U case, scour was more widely distributed (−2.1 cm at
Figure 8c, L5), and an erosion pattern formed at the base of the patch was observed, while deposition remained lower (+1.8 cm) and concentrated at the patch front (L1–L3) (
Figure 9d). These results indicate that I-type debris created a stronger blockage and local downflow (and thus deeper scour) than U-type debris. These trends support previous findings: denser, more obstructive patches (especially with I-type debris) cause stronger local acceleration and scour, and upstream debris placement increases both hydraulic pressure and turbulence intensity [
1]. Thus, patch placement and debris shape together determine the magnitude and location of sediment redistribution.
In upstream vegetation cases (DV
US_I and DV
US_U), Patch 2 exhibited stronger frontal scour (−3.0 to −4.0 cm) and narrower deposition peaks (+2.4 to +3.1 cm); dense upstream vegetation intensified the wake, increasing bar offset and promoting P2 crest migration. These effects affirm the role of frontal constriction and vegetation density in driving localized turbulence structures, as previously modeled and supported in field analogs [
41].
4.2. G/D = 4.2 (Sparse Vegetation and Debris)
In sparse vegetation (
G/
D = 4.2), wider cylinder spacing permitted flow-through, yielding smaller, more diffuse morphological changes. In the SV
RL_I case, weak scour at L1 (−0.8 cm) and minimal deposition developed (~+0.5 cm,
Figure 9a).
Figure 7b shows that localized L2 deposition reflected front-induced deceleration and obstruction. These patterns reflect the low hydraulic resistance of sparsely spaced trunks (even with debris present) [
23,
24]. Similarly, SV
RL_U case produced weak scour (~−0.6 cm at L1) and minimal deposition (+0.4 cm at L2) (
Figure 9b); shallow magnitudes are consistent with higher patch permeability. Field studies indicate that channels with sparse bank vegetation are about 25% wider and 25% shallower than those with dense vegetation, implying lower velocities and weaker scour under sparse conditions [
2].
Downstream attenuation in SVRL_I, P2 ≈ −1.0/+0.6 cm, responses were further diminished by P3, indicating weak continuation. A similar trend occurred in SVRL_U, where minor topographic differences leveled out after the first bar, suggesting minimal influence on further bar development.
SV
US_I, produced moderate scour (−3.0 cm at L5,
Figure 8b), but only negligible deposition (≈+2 cm at L2) (
Figure 9c). SV
US_U yielded only about −1.9 cm of scour at L5 with negligible deposition (
Figure 9d). Across sparse cases, scour remained localized at L1/L5 and was weaker than dense configurations. This pattern aligns with findings from an experimental study with wooden debris [
52]. That study found that increasing vegetation density diverted flow from the floodplain into the main channel, thereby increasing velocity and scour. By contrast, sparse vegetation allowed flow to spill over, which extended wake recirculation farther downstream and resulted in a mild sediment deposit behind the patch [
56,
57]. Finally, bar and bed morphology adjusted in response to the altered flow patterns. The combined presence of vegetation and debris modified the flow and promoted sediment deposition in sheltered zones (e.g., behind the patch or debris). Our observations of deposition at locations L2–L4 reflect this pattern, and the trend is further evident by the declining intensity of morphological features across successive downstream bars. In SV
US_I (
Figure 9c) and SV
US_U (
Figure 9d), the elevation variation at Patch 2 rarely exceeds 2.5 cm. By Patch 3, maximum changes are marginal (~1.5 cm), demonstrating that sparse vegetation, regardless of debris type, cannot sustain significant sediment redistribution through successive bar sequences.
A comparative analysis of scour and deposition depths was conducted against the respective upstream vegetation-only baselines (DVUS and SVUS) to quantify the effects of debris placement and type. In the dense case, DVRL_I showed a ~55% increase in scour and a ~31% increase in deposition relative to the DVUS, while DVRL_U showed smaller increases (~3% in scour, ~7% in deposition). In case DVUS_I, scour is enhanced by 70% and deposition by ~50%. For sparse vegetation, SVRL_I and SVRL_U each showed minimal scour increase (≥10%), confirming a low effect under permeable conditions. However, SVUS_I showed a 70% increase in scour and a 78% increase in deposition compared to SVUS_U. These results affirm that vegetation density and upstream debris geometry together determine the extent of morphodynamic intensification. While sparse vegetation reduces the overall magnitude of change, adding debris, especially I-type forms in upstream positions, can still significantly affect sediment transport and flow structure.
4.3. Interaction of Vegetation, Debris, and Flow Dynamics
Our results demonstrated that sandbar morphology is governed by the combined effects of vegetation density, patch placement, and debris geometry. Patch position further influenced flow paths and erosion patterns. River line vegetation tends to shield a bank uniformly, limiting erosion along the vegetated edge. This behavior is consistent with previous experimental studies of riparian vegetation-flow interactions [
3]. In contrast, upstream vegetation deflects the flow laterally into the main channel, shifting the scour zone toward the inner bank and intensifying erosion action at the patch front.
Figure 10 presents the dimensionless bed elevation changes (Δ
z/
h), providing a normalized comparison across all configurations. For each case, the values correspond to the maximum scour and deposition measured in the local bar pool domain surrounding the frontal areas of P1, P2, and P3, as shown in
Figure 6,
Figure 7 and
Figure 8. Among Patch 1 results, the upstream vegetation with I-type debris cases, such as DV
US_I and SV
US_I, exhibited the highest morphological response, with normalized scour reaching −1.55 and deposition exceeding +1.05. River line vegetation with I-type debris (DV
RL_I) also had a strong impact (approximate scour −1.30, deposition +0.95), whereas U-type debris led to slightly lower responses (for example, DV
US_U has −1.0 scour and +0.8 deposition).
By contrast, sparse river line configurations (e.g., SVRL_I and SVRL_U) exhibited limited morphodynamic influence, with normalized scour around −0.3 and deposition under +0.7. These results reinforce that both upstream vegetation placement and density play dominant roles in amplifying morphodynamic effects, particularly when paired with obstructive debris types like the I-type.
On average, morphodynamic intensity decayed from P1 to P3 by roughly 28.3% for scour and 24.7% for deposition. I-type configurations (DVUS_I and DVRL_I) retained 71% (scour) and ~86% (deposition), and ~65% (scour) and ~74% (deposition) of their initial impacts at P3, respectively. U-type cases (DVUS_U and DVRL_U) retained ~80% and ~88%, and ~85% and ~74%. SVUS_I also showed relatively high persistence (~68% scour, ~81% deposition), whereas SVUS_U and SVRL_U retained ~71% and ~67% (scour) and ~71% and ~67% (deposition), confirming the importance of patch density and debris geometry in sustaining bar morphology.
The morphodynamic responses observed under high vegetation density (
G/
D = 2.2) closely resemble field conditions in reaches dominated by dense stands of
Robinia pseudoacacia [
11]. These configurations concentrated flow and sediment around patch edges, generating pronounced bar–pool asymmetry and localized scour, similar to patterns observed in invaded gravel-bed rivers. In contrast, native
Salix species typically colonize lower, moist bar areas with sparse, patchy growth, leading to more diffuse morphodynamic signatures [
3]. These species-specific traits (such as tree density, trunk rigidity, and habitat preference) can shift erosion patterns toward side banks and influence bar stability [
11].
The intensified frontal scour for dense upstream + I-type configurations and the more distributed deposition for river-line + U-type are consistent with field observations of bar-head wood jams that focus scour and wake deposition on alternate bars [
18,
21]. These patterns align with finite-patch hydrodynamics in which the blockage ratio governs the wake strength and footprint: higher blockage focuses the response near the bar head, whereas partial blockage spreads it along bar edges [
41,
44]. In addition, bar theory and morphodynamic modeling indicate that enhanced lateral resistance/obstruction can locally increase bar amplitude and modulate downstream attenuation [
58]. These findings highlight the importance of understanding vegetation–debris–flow interactions in predicting channel responses to biophysical structures and in designing nature-based hydraulic interventions.
4.4. Empirical Relationship for Vegetation–Debris Synergy
In the present study, a multiple linear regression was used to develop an empirical equation for predicting normalized bed-level changes (Δ
z/
h) from vegetation density, spatial layout, and debris geometry. The categorical predictors (dense vs. sparse vegetation, upstream vs. river line placement, and debris type I vs. U) were encoded and combined with a geometry correction term to capture their morphodynamic effects. To create an interpretable model, a composite obstruction index (
CI) was formulated to combine the parameters describing the total flow obstruction effect. This reduces collinearity and yields moderate elasticities at the expense of some accuracy. The resulting empirical relationships, expressed in Equations (4) and (5), provide a framework for predicting the bed deformation patterns under different vegetation–debris configurations.
where
G/
D is the vegetation density index,
Vdis is a placement factor (upstream = 2.0, river line = 1.0,
df is (
wb/W) (debris geometry factor) the fraction of the channel width, W, that is continuously blocked,
wb, by the patch + debris at the front (across-stream):
df = 1.0 if
wb/W < 0.1 (vegetation only),
df = 1.2 if
wb/W < 0.3 (U-type), and
df = 1.4 if
wb/
W > 0.3 (I-type). Values reflect the relative increase in frontal blockage and wake intensity (I > U > none),
CI obstruction effects defined in Equation (5), and
Br (
Ac/
Av) is a blockage ratio representing the frontal obstruction area. This model applies to the alternate-bar regime under steady, subcritical flows (
Fr < 1) at constant discharge (
Q = 0.002–0.004 m
3 s
−1) in a narrow, straight channel with emergent rigid vegetation surrogates, with patch densities spanning sparse to dense.
Figure 11a,b plot experimental versus predicted non-dimensional magnitudes (Δ
z/
h) using Equation (4),
p-values for
G/
D and
CI are 8.0 × 10
−3 and 2.0 × 10
−3, respectively. The decision coefficient of determination (R
2) value for the predicted results obtained by Equation (4) was 0.921. These outcomes match the findings of a previous study, which emphasized wake-driven deposition in vegetated flows [
59]. Empirical theories highlighted how added roughness elements shift bar amplitude [
60] and scour location, which is evident in the displacement of scour zones observed here under debris-modified flows. Recent experimental findings [
47] confirm that vegetation–debris synergy amplifies flow heterogeneity, driving scour–deposition coupling. This predictive accuracy is comparable to the results of a laboratory study [
61] that found bar amplitudes within ±15%. Thus, the present regression model provides a tool for predicting bed responses under nature-based vegetation–debris interactions.
As shown in
Figure 11a (scour) and
Figure 11b (deposition), the empirical relationship reproduces results within the ±20% corridor, deposition is essentially unbiased, while scour is slightly under-predicted. The small offsets are consistent with (i) metric differences (bar-scale amplitude vs. local scour), (ii) depth normalization (very shallow h in [
61] vs. deep
h in [
52], and (iii) blockage definition (frontal-density or length-based measures mapped to our area-based
Br).
While our experimental design provided controlled conditions to isolate vegetation–debris interactions under equilibrium bar formation, several limitations must be acknowledged. The 1:50 geometric scale introduces disparities in Reynolds and Froude numbers that may affect the reproduction of turbulence structures and sediment transport thresholds, thereby limiting the transferability to natural river systems [
31]. Specifically, the Reynolds numbers (
Re)/
Fr mismatch shortens wake-recovery lengths relative to prototype, the operative mobility window (Shields number
θ) and the width–depth ratio in our flume fell within a non-migrating alternate-bar regime but may shift under field hydrographs, and sediment-transport thresholds for
d50 ≈ 0.875 mm at laboratory Reynolds numbers can underrepresent incipient-motion variability at full scale. Vegetation was represented by rigid cylinders, thus excluding effects such as trunk flexibility, anisotropic drag, and root-induced substrate reinforcement [
41]. Flexibility typically reduces the effective frontal area and dampens turbulence at higher velocities, while root networks can increase substrate cohesion.
Accordingly, the rigid-stem surrogate may slightly overestimate local scour and underestimate the spatial spread of deposition under the same hydraulic force. Debris was arranged in static I- and U-type configurations, whereas in natural channels, it accumulates stochastically as a function of discharge variability and channel morphology [
28]. Field jams recruit, rotate, and evolve in porosity during events, so our predicted Δ
z/
h should be interpreted as conditional on a given jam state rather than time-varying accumulation cycles. Additionally, using a uniformly graded cohesionless sediment (
d50 = 0.875 mm) neglects the grain-size diversity and cohesive properties of natural fluvial substrates [
35]. Mixed/cohesive beds can shift thresholds and bar mobility, altering the balance of scour and deposition relative to the tested sand. While these simplifications enhance experimental reproducibility, they limit the representation of complex feedback processes. Future investigations should incorporate variable sediment compositions, deformable vegetation models, and unsteady hydrographs to improve the ecological and morphodynamic realism.
5. Conclusions
This study demonstrated that vegetation and debris act as key eco-hydraulic drivers of sandbar morphology. When aligned with the flow and positioned upstream, these elements amplify or alter sediment redistribution, with the magnitude of their impact depending on their type, density, and spatial configuration. The key findings are summarized as follows:
Dense upstream vegetation with I-type debris produced the most intense morphodynamic effects, yielding up to 82% deeper scour and 50% greater deposition than the corresponding vegetation-only cases, due to rigid frontal obstruction and concentrated flow reattachment zones. U-type debris configurations induced less intense, more distributed effects, typically leading to only 20–35% increases in scour and deposition, or negligible changes in some sparse cases, due to the weaker blockage and less directed flow control associated with the U-type debris. These impacts attenuated downstream from P1 but remained measurable at P3, especially for I-type, indicating persistence of wake-driven morphodynamics.
Using experimental data, an empirical relationship was developed to predict the normalized bed change (∆z/h). The model achieved high accuracy (R2 ≈ 0.92), and the residual biases largely reflect differences in depth normalization, response metric (bar amplitude vs. local scour), and temporal sampling. Among the parameters in the Composite Obstruction Index (CI), the blockage ratio (Br), together with debris geometry (df) with upstream placement (Vdis), exerted the greatest influence, identifying these as the most effective levers for managing scour and deposition.
This experimental study advances the understanding of bio-geomorphic feedback in sand–gravel bed rivers by isolating the synergistic roles of vegetation structure and debris type. Field analogs in Japanese gravel-bed rivers—dense Robinia pseudoacacia stands that trap large pieces of wood—amplify local scour/deposition and persist downstream. These insights translate directly into a nature-based, flood-resilient design: debris jams at bar heads and strategic planting (e.g., willows) to deflect currents, protect banks, and stabilize bar crests. It also underscores the importance of species selection, patch design, and patch placement in sustainable river management.
Within the tested conditions, dense upstream vegetation with I-type debris produced the strongest bar anchoring but concentrated scouring at the patch nose; river-line vegetation with U-type debris yielded distributed deposition and a smaller peak scour. These outcomes frame nature-based choices—anchoring versus edge protection—according to scour tolerance and conveyance goals. The Δz/h relationship, summarized by the Composite Obstruction Index (CI), offers a screening-level comparison of alternatives within the study’s parameter space.