Capillary trapping of buoyant particles within regions of emergent vegetation

Authors


Abstract

[1] The seeds of many aquatic plants are buoyant and thus transported at the water surface, where they are subject to surface tension that may enhance their retention within emergent vegetation. Specifically, seeds may be trapped by surface tension (i.e., by the Cheerios effect) at the surface-piercing interface of the vegetation. In this work we develop a physical model that predicts this mechanism of seed trapping, advancing the model proposed by Defina and Peruzzo (2010) that describes the propagation of floating particles through emergent vegetation. The emergent vegetation is simulated as an array of cylinders, randomly arranged, with the mean gap between cylinders far greater than the particle size, which prevents the trapping of particles between pairs of cylinders, referred to as net trapping. Laboratory experiments are used to guide and validate the model. The model also has good agreement with experimental data available in the literature for real seeds and more complex plant morphology.

1. Introduction

[2] Seed dispersal can play an important role in structuring aquatic habitat. The seeds of many aquatic plants are buoyant, which enhances their dispersal by keeping the seeds afloat for longer advection times [e.g., Nilsson and Danvind, 1997; Van den Broek et al., 2005; Nilsson et al., 2010]. The fate of these seeds within a region of vegetation is mainly controlled by the flow velocity and by the efficiency of a variety of seed-plant interaction mechanisms that trap the seeds [Chambert and James, 2009; Defina and Peruzzo, 2010]. The main mechanisms responsible for temporary or permanent trapping of particles are (1) inertial impaction [Palmer et al., 2004], which occurs when a particle deviates from a streamline because of its inertia and collides with a stem; (2) wake trapping, which occurs when a particle enters the unsteady recirculation zone behind a stem [e.g., White and Nepf, 2003]; (3) trapping due to surface tension, i.e., the Cheerios effect, in which floating particles are attracted toward stems by the rising meniscus [e.g., Vella and Mahadeven, 2005]; and (4) net trapping, which occurs where leaves and/or stems overlap enough to form a netlike structure that intercepts the floating particle [Defina and Peruzzo, 2010]. When the mean gap between leaves or stems is comparable to the particle size, then net trapping is the most efficient trapping mechanism [Defina and Peruzzo, 2010, 2012]. Alternatively, when the mean gap between plant elements is large compared to the particle size, and flow velocity is moderately slow, then the Cheerios effect is the main, if not the only, mechanism impacting seed propagation, capture and diffusion [Chambert and James, 2009]. The present study considers the latter flow condition and develops a physically based model to predict the impact of surface tension (Cheerios effect) on the fate of floating particles within a region of emergent vegetation.

2. Model and Experimental Methods

[3] The emergent vegetation is simulated as an array of randomly arranged cylinders, each with diameter d. The array density is described by the cylinders per unit bed area, n. The cylinder spacing is assumed to be far greater than the particle size, which eliminates net trapping, i.e., the trapping of particles between a pair of cylinders. In this case the capture of floating particles by the cylinders is dominated by inertial impaction [Palmer et al., 2004] and by the attraction due to the surface tension (i.e., the Cheerios effect).

2.1. Model

[4] As a particle advects through the array of cylinders, it passes, on average, one cylinder within each longitudinal distance, inline image, as shown in the work of White and Nepf [2003]. As each cylinder is passed, the particle has some probability of colliding with it, Pi, so that on average a particle will interact (collide) with a cylinder once per distance

display math

[5] Except for the extreme cases (i.e., for high cylinder density or very low flow velocity) we expect that the probability Pi does not depend on n. Preliminary experiments, discussed in section 3, confirm this.

[6] Observations have shown that particles may collide (interact) with several cylinders, before being captured by, i.e., permanently attaching to, a specific cylinder [Defina and Peruzzo, 2010]. Based on this, we separately define the process of interaction (collision followed by release) and the process of capture (permanent trapping). Below, the subscripts “i” and “c” will be used to denote parameters associated with interaction and capture, respectively.

[7] Following Defina and Peruzzo [2010], we define the probability inline image that a particle travels a distance X greater than L before being captured, as

display math

where Pc is the capture probability (i.e., the probability that a particle, which interacts with a cylinder, is permanently captured), and Ni is the number of interactions between a particle and the cylinders within the distance L, which we approximate as inline image. We can rewrite equation (2) as

display math

in which

display math

is the mean distance traveled by a particle before it is permanently captured.

[8] In order to estimate Pi, and thus inline image, we consider the trajectory of individual particles as they pass an individual cylinder (Figure 1). For example, to describe inertial impaction, previous authors assumed that the particle trajectory was set by the fluid drag and particle inertia. A set of trajectories associated with these assumptions is shown in Figure 1a. The length-scale b is the distance between the outermost trajectories that lead to collision. Geometrically, inline image (Figure 1). Models to predict b, and thus Pi, for inertial impaction are described in Shimeta and Jumars [1991] and Palmer et al. [2004].

Figure 1.

Definition sketch for the probability of particle collision (interaction) with a cylinder of diameter d. Solid lines indicate particle trajectories that lead to collision. The outermost trajectories that lead to collision are separated by distance b. The collision probability is inline image. (a) Inertial impaction occurs when the forces of drag and inertia dominate the particle trajectory approaching the cylinder. (b) For floating particles, the Cheerios effect adds to inertia and drag in controlling the particle trajectory, thus affecting the size of b.

[9] However, in this paper we focus on floating particles at low-flow velocity, for which the acceleration caused by surface tension (i.e., by the Cheerios effect) may be important drawing particles toward the cylinder from distances greater than d. An example of trajectories for surface particles influenced by surface tension is shown in the Figure 1b. Because it is possible for inline image, the probability of collision Pi can be greater than one. While this sounds contradictory, it is physically sound. It characterizes the fact that the influence of surface tension can generate more frequent cylinder collisions than would be predicted from the mean spacing, i.e., inline image. In section 2.2 we develop a model to predict b, and thus Pi, for floating particles influenced by surface tension.

2.2. Theoretical Prediction of Pi for Floating Particles Under the Influence of Surface Tension

[10] The Cheerios effect is influenced by the relative importance of inertial forces and surface tension. However, these two forces act on the particle in different directions, so that Pi cannot be parameterized simply by the ratio of the force magnitudes. Instead, we use a kinematic approach for defining Pi. For this description x and z are the streamwise and transverse coordinate directions, respectively (Figure 2). We define a rectangular area of influence, centered at the cylinder, whose edge in the x direction is the capillary length, 1/q, which is the characteristic length scale of the meniscus. In the z direction the edge has an infinite length. We assume that a particle crossing this area is attracted toward the cylinder through the Cheerios effect. If we assume that the particles move, on average, at the velocity inline image in the streamwise direction, with U the bulk flow velocity and inline image a correction factor, then, on average, a particle will spend time inline image, within the zone of influence. Tq is also the time available for the Cheerios effect to draw a particle to the cylinder, before it leaves the influence of the cylinder. From this time-scale we can estimate the maximum distance from the cylinder, H0, from which a particle can be drawn to collide with the cylinder by the action of surface tension (Figure 2).

Figure 2.

A particle trajectory influenced by surface tension which leads to collision with the cylinder. H0 represents the maximum distance from the cylinder from which a particle can be drawn to collide with the cylinder by the action of surface tension. inline image, with b defined in Figure 1.

[11] This maximum distance corresponds to inline image of Figure 1, i.e., inline image and

display math

[12] The distance H0 is computed, as a first approximation, by assuming that only the capillary force acts on both the particle and the cylinder. The particle is assumed to be spherical. The capillary force, Fc, is given by [Dushkin et al., 1996]

display math

[13] In (6)dp is the particle diameter, inline image is the particle-water contact angle, inline image and inline image are the meniscus slope angles at the particle and cylinder contact line, respectively (defined in Appendix A), inline image = 0.073 N m−1 is the surface tension, inline image = 0.0027 m is the capillary length and inline image is the modified Bessel function of the first kind, with z the transverse distance of the particle from the cylinder.

[14] The following differential equation governs the particle position, z,

display math

with

display math

and inline image the particle density. We assume that the particle starts from rest at position inline image, i.e., boundary conditions

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[15] We approximate the Bessel function in equation (7) as inline image for inline image, and find the solution as

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[16] The maximum distance, H0, will be that associated with the maximum time available for lateral transport driven by surface tension, that is Tq. For simplicity, we assume that the particle collides with the cylinder at z = 0, i.e., neglecting the radius of both the cylinder and the particle (Figure 2). The impact of this assumption on the time-scale for the particle to reach the stem is absorbed into the scale constant within Tq, i.e., inline image. Then, setting z = 0 and inline image, we solve (10) for H0

display math

[17] Using (5), (8), and (11) we find

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[18] Since inline image is the Weber number, equation (12) can be rewritten as

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where inline image and inline image is the water density. Experiments described in section 3 suggest inline image, such that inline image, which is close to unity, as expected.

2.3. Capture Probability Pc

[19] After a particle collides with a cylinder, it may become permanently attached, or it may be pulled away from the cylinder by the action of fluid drag. The probability of remaining permanently attached, Pc, depends on the ratio between the capillary force acting when the particle is stuck to the cylinder and the drag force due to the local mean flow, to turbulence and to vortex shedding. We assume that this drag force Fd, is proportional to the bulk velocity, U

display math

where kd is a scale factor, Ap is the projected area of the submerged part of the particle and CD is the particle drag coefficient.

[20] When the ratio of capillary force (6) to drag force (14) is large, the particle remains attached to the cylinder, i.e., Pc = 1.0. We define Ecr as the critical value of this force ratio above which the probability of capture becomes unity, i.e.,

display math

in which we define Ue as the escape velocity, i.e., the velocity above which particles may escape from the cylinder. We introduce the shape factor, kp, which depends on the particle draft (see Appendix A), such that inline image, then rearrange (15) to describe the escape velocity, to

display math

with

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which we will use as a calibration parameter. Experimental investigations described and discussed in section 3 suggest inline image = 1.26.

[21] The escape velocity Ue is the scale velocity of the problem. When inline image the capillary force is greater than the drag force no matter the position (with respect to the mean flow) at which the particle is stuck to the cylinder, therefore the probability of permanent capture is Pc = 1. When inline image, drag forces may locally and temporarily exceed the attraction force due to capillarity, and the particle may escape from the cylinder. Increasing of the ratio inline image reduces the probability Pc.

[22] The measurements, discussed below, suggest that the probability of capture Pc decays exponentially with inline image, specifically

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[23] From the models developed above we can now predict the following from the particle characteristics (dp, inline image), the contact angles ( inline image, inline image), the cylinder diameter (d), the stem density (n), and the bulk flow velocity (U): (i) the mean spacing between two interactions inline image from equations (1) and (13), (ii) the escape velocity Ue from equation (16), the capture probability Pc from equation (18), (iii) the mean distance a particle travels before it is permanently captured, from equation (4), and (iv) the path length distribution inline image from equation (3). In section 3 we use experimental observations to evaluate the two model parameters, inline image = 2.46 and inline image = 1.26.

2.4. Experiments

[24] To cover a wider range of flow conditions, two flumes are used in this investigation. The small flume has a channel width of 40 cm and length of 2.8 m, the large flume has a width of 120 cm and length of 13 m. In both flumes the water is recirculated by a pump that maintains steady flow. In both flumes the bottom is horizontal and the water depth is adjusted by a downstream weir. In the small flume the bulk flow velocity U is measured with an ADV (U is averaged over 33 points per cross section), while in the large flume U is estimated through a calibrated relationship between the pump frequency and the flowrate. The bulk velocity was varied between 0.7 and 5 cm s−1. Seven of the velocity experiments were carried out in the small flume (U = 0.007 – 0.032 m s−1), while higher velocity experiments (U = 0.04 and U = 0.05 m s−1) were carried out in the large flume. In both flumes, a random array of cylinders was constructed on three boards to create a total test section length of 1.80 m. The array filled the flume width. We constructed six different arrays, with n = 299 m−2 to 1780 m−2. The cylinders used in the experiments are wooden dowels with a diameter d of 6.0 mm, fitted into holes drilled into the boards.

[25] The model floating particles were cut from wood cylinders to have equal diameter and height of 3 mm (Figure 3). The relative density inline image = inline image was inline image0.7. These are the same as particle C used by Defina and Peruzzo [2012].

Figure 3.

Snapshots of particles trapped against the cylinders through the Cheerios effect.

[26] In the experiments, we release one particle at a time just upstream of the test section and at random positions in the transverse direction. For each experiment we released 200 particles. We observed the particle trajectory and measured the distance traveled by each particle, before it was permanently captured by a cylinder. We assumed a particle was permanently captured if it stayed stuck to one cylinder for more than 10 min, a time interval that was more than 1 order of magnitude longer than the mean time a particle took to travel the whole test section.

3. Results and Discussion

[27] We first consider the impact of cylinder density, n, while holding the bulk velocity constant (U = 2.5 cm s−1). In all cases the exponential distribution given by (3) could be fit to experimental data with inline image 0.95. From this fit we extracted the mean path length, inline image, for each stem density. From our theory, we expected that inline image would have a dependence on the stem spacing, inline image (see equation (4)). This relationship is observed in the measured inline image (Figure 4). Since we use a single value of cylinder diameter, d, these graphs are plotted with inline image alone. The data indicate a constant relationship between inline image and inline image, specifically inline image = 230/n for the present data (Figure 4, black circles). Since n is a constant, from (1) and (3) together, we can infer that the product inline image is also a constant. Consistent with the derivation above, we expect that the probability Pc is only a function of the flow near an individual cylinder, and that it does not depend on cylinder density, n. Then, Pi must also be independent of n.

Figure 4.

Mean path length as a function 1/n. Present experimental results (U = 0.025 m s−1, black circles aligned along the curve inline image = 230/n); Defina and Peruzzo [2012] experimental results with particle C and U = 0.033 m s−1 (white circles, inline image = 3600/n); and (half-full symbols) experimental data for Nasturtium ( inline image = 3.5 × inline image) and Sunflower seeds ( inline image = 1.5 × inline image) [Chambert and James, 2009].

[28] Further experiments were carried out with the aim of investigating how the model parameters change with the bulk flow velocity, U. The distance traveled by 200 particles is measured for n = 968 m−2 and seven different flow velocities (Table 1). In each case, the probability distribution of distances traveled by a particle before permanent capture followed an exponential law with inline image 0.95, except for the data with U = 0.040 m s−1 where, possibly because of the presence of a weak transverse seiche in the channel, the determination coefficient was lower (R2 = 0.90), but still highly significant. Again, the exponential fit was used to determine the mean path length, inline image, and to observe how this parameter varied with bulk flow velocity (see Table 1 and Figure 5). The dependence of inline image on velocity comes through both Pi and Pc: notice that inline image (from equation (12)) and Pc is also inversely proportional to U (equation (18)), so that inline image increases with increasing U (Figure 5). The behavior is consistent with physical reasoning: as velocity increases, the inertial forces become stronger relative to the capillary forces, leading to reduced interaction and capture by stems.

Figure 5.

Mean path length as a function flow velocity in log linear scale (present experiments).

Table 1. Summary of Present Experimental Data and Model Parametersa
U (m s−1)We (102)RePiΔsi (m)λ (m)Pc
  • a

    The observed travel distances for 200 particles are fit to (3) to find inline image. Pi is predicted from (13). inline image is predicted from (1). The experimental estimates of Pc are based on (4), inline image, and Pi predicted from (13).

0.0070.403422.320.0740.0210.971
0.0090.666542.050.0840.0250.965
0.0172.3801021.490.1160.0860.739
0.0203.2901201.370.1250.1100.680
0.0255.1401501.230.1400.2340.451
0.0286.4401681.160.1480.3530.343
0.0328.4201921.090.1590.6420.219
0.04013.2002400.970.1771.3570.122
0.05020.5003000.870.1983.5490.054

[29] Using the set of nine (U, inline image) pairs, we calibrated the model parameters inline image and inline image. First, we used the following trial and error procedure to find inline image. We fixed a tentative value for inline image and used it to compute the probability of interaction, Pi, from equation (13), which in turn is used to find the mean spacing between interactions inline image from (1) and (13). Together with the observed inline image, we find the capture probability Pc from equation (4). With nine pairs of (Pc, U), we find Ue by fitting equation (18). The value for inline image is then tuned to until we find the best fit to (18).

[30] Second, using the best-fit value for inline image, inline image is computed from (16). In this computation we used dp = 0.003 m, inline image = 0.7, and the measured contact angles inline image = 60° and inline image = 55° for the particle and the cylinder, respectively. We computed inline image = 1.55. (see Appendix A) and inline image = 90° − inline image = 35°. Through this procedure we find Ue = 0.013 m s−1, inline image = 2.46 and inline image = 1.26.

[31] With these values, the interaction probability Pi, the mean spacing inline image, and the probability Pc are computed as given in Table 1. The theoretical model for Pc (equation (18)) is shown as a solid line in Figure 6. The values of Pc estimated for individual cases are shown by symbols. The experimental estimates of Pc are based on (4), inline image, using the measured value of inline image, and Pi predicted from (13).

Figure 6.

Comparison between theoretical and experimental probability of capture as it varies with inline image. The capture probability is plotted both in (top) natural scale and (bottom) logarithmic scale.

[32] We now use experimental results from previous studies, Defina and Peruzzo [2010, 2012] and by Chambert and James [2009], to validate the model. These studies consider particle sizes and stem diameters which are different from those in the present study.

[33] Defina and Peruzzo's [2010, 2012] experiments were carried out in a 6 m long, 0.3 m wide tilting flume. The bed slope and a downstream weir were adjusted to achieve uniform flow conditions with a water depth of inline image0.1 m. The model plant canopy consisted of plastic plants inserted into a perforated Plexiglas board covering the middle 3 m length of the flume. The plants were arranged either randomly or in a staggered pattern. The plastic plants, which resemble Spartina Maritima, were 0.15 m high and composed of approximately 120 leaves per model plant. Here, we tentatively assume that each leaf piercing the free surface can be represented as a cylinder having a diameter of 2 mm, which corresponds to the larger dimension of the leaf, which has an elliptical cross-section. This leaf diameter is smaller than the particle diameter, dp (see Figure 7). Three different particles were used in the experiments to mimic different buoyant seeds: particle A was a wood particle with diameter of inline image mm and a relative density of 0.95, particle B (see Figure 7) was a smooth spherical berry with a mean diameter of 3.7 mm and a relative density of 0.83, and particle C was the same particle used in the present experiments.

Figure 7.

Particle B attached to a leaf through the Cheerios effect.

[34] For particle C, Defina and Peruzzo [2012] showed that the mean path length inline image varied inversely with the number of plants per unit area np, i.e., inline image = const. Since each plant had the same number of leaves, the mean path length also varies inversely with the number of leaves (i.e., cylinders) per unit area, as shown in Figure 4.

[35] From equations (1) and (4) we have inline image. The constant value inline image differs, in the different experiments by orders of magnitude (see Figure 4). For example, compare the present study ( inline image) with the Defina and Peruzzo [2012] experiments ( inline image), which use the same particle, but different stem diameter and velocity. The difference in inline image is explained in part by the difference in velocity. Using the data in Table 1, we can see that an increase in velocity from 0.025 m s−1 to 0.033 m s−1 increases inline image by a factor of 2.7. The remaining difference (an additional factor of about 5.7) can be attributed to the difference in stem diameter which affects Pi and Pc through Ue. On comparing the present study with the Chambert [2006] experiments, which use the same cylinder diameter, the differences can be ascribed to the different particle diameter, which affects both Pi and Pc and, mainly, to the different flow velocity: in the Chambert [2006] experiments velocity is 6.4 times the present velocity; as such both Pi and Pc reduces dramatically.

[36] In the study from the work of Defina and Peruzzo [2010], individual leaves were, in some places, spaced closely enough to create net trapping, so that the probability of capture, Pc, measured in those studies reflects both the net trapping and the trapping associated with the Cheerios effect. The theory presented here only accounts for the Cheerios effect, and so we must isolate that mechanism from the data reported by Defina and Peruzzo [2010]. We assume that the probability of capture due solely to the Cheerios effect is given by the measured total probability of capture (which includes the net trapping mechanism) times the measured percentage of captures due to the Cheerios effect, which is reported in the work of Defina and Peruzzo [2010]. Moreover, for the plastic leaves we measured a contact angle inline image 30° so that inline image. Experimental data as well as the results of the computations are given in Table 2.

Table 2. Summary of Experimental Conditions and the Results of Present Computationsa
Particledp (mm)ρp/ραp (deg)ψp (deg)U (m s−1)Ue (m s−1)Pc
A2.50.950.073
A2.50.950.081
B3.70.83353.550.0730.0200.13
C3.00.70601.550.0330.0160.24
C3.00.70601.550.0500.0160.16
C3.00.70601.550.1330.0160.02

[37] The values of Pc and inline image reported in Table 2 are included in Figure 6. The Defina and Peruzzo [2010] data points are consistent with the model curve (solid line) developed for an array of cylinders. This agreement is encouraging, especially given the rather different experimental conditions and possible uncertainties, e.g., Spartina leaves are not cylinders, some of the net-trapping captures may actually have been through the Cheerios effect, i.e., net trapping may mask some of the captures through the Cheerios effect. These experimental results suggest that the relationships proposed in the present paper to estimate the model parameters when the Cheerios effect is the dominant capture mechanism can be extended, with due care, to real plants. In this connection, an allometric study to establish the equivalence between real plant morphologies and the diameter and density of a group of cylinders could be of use.

[38] Chambert and James [2009] experiments were conducted in a 20 m long and 0.38 m wide flume. The model vegetation comprised an array of cylinders with a diameter of 0.006 m, arranged across the full width of the flume in staggered pattern. The total array length was 1.88 m, and the array began 1 m downstream from the seed feeder. Three sets of experiments were carried out with the three different stem densities given in Table 3 and the same mean flow velocity, U = 0.16 m s−1. Five types of natural, buoyant seeds were used for the experiments: African Daisy, Nasturtium, Rhubarb, Sunflowers, and Marigold. The flume was fed with 300 seeds during 4 min, and the flow was stopped after a total duration of 8 min. The number of seeds retained (i.e., permanently captured) was then counted visually (see Table 3).

Table 3. Number of Captured Seeds Nc and Mean Path Length inline image Between Brackets, for the Three Different Stem Densities na
Seed Typen = 431 (m−2)n = 1251 (m−2)n = 1681 (m−2)CSF
  • a

    The Corey Shape Factor (CSF), which measures the seed roundness, is also given as reported by Chambert [2006]. Nc is out of 300. inline image is in meters and n is in m−2.

Sunflower20;(27.2)44;(11.9)51;(10.1)0.43
African Daisy194;(1.8)204;(1.6)215;(1.5)0.19
Marigold134;(3.2)155;(2.6)162;(2.4)0.15
Rhubarb137;(3.1)141;(3.0)149;(2.7)0.54
Nasturtium5;(111.9)21;(25.9)29;(25.9)0.87

[39] The mean path length given in Table 3 was calculated from (3), specifically

display math

where we take L = 1.88 m, and inline image is the percentage of noncaptured seeds, i.e., inline image. Please note that the estimation of inline image is rather uncertain, because it uses data for a single value of L, rather than a large set of data inline image to fit inline image, as in the present experiments.

[40] In addition, the experimental procedure adopted by Chambert and James [2009] is different from the present experiments. We follow the trajectory and fate of one particle at a time, whereas Chambert and James [2009] release all the 300 seeds in 4 min, allowing the seeds to accumulate within the array. As a result, when the number of captured seeds is large, seeds released near the end of the run find little or no room to interact with the cylinders, and may instead attach, to previously captured seeds (see, e.g., their Figure 14), forming clusters of seeds within the array. The clustering likely increases the probability of capture for seeds released later in the run, a behavior that is not included in the present model. As a consequence the mean path length inline image of the lighter seeds (i.e., African Daisy, Marigold, and Rhubarb), which are more easily trapped and thus exhibited more clustering, does not follow inline image, as observed in the present study. However, the heavier seeds, Nasturtium and Sunflower, which did not form clusters, exhibit the relationship inline image consistent with the model developed in this paper (Figure 4).

[41] We use data for Nasturtium and Sunflowers seeds to compute Pc as it varies with inline image. We assume a contact angle inline image in the range 15°–35° for Sunflowers seeds, whereas for Nasturtium seeds we measured a contact angle inline image = 17.5°. In both cases we assume, for the cylinder, a contact angle inline image = 55° (i.e., the same contact angle for the cylinders used in the present experiments). We then compute the meniscus slope angle at the particle contact line inline image, the escape velocity Ue and the interaction probability Pi (see Table 4).

Table 4. Summary of Seed Characteristics and Computed Model Parametersa
Seed TypeAverage Diameter (mm)Mass (g/seed)ρp/ρndλαp (deg)ψp (deg)Ue (m s−1)PiPc
  • a

    The average seed diameter is computed as the geometric average of the three axes reported in the work of Chambert [2006]: orthogonal long d1, intermediate d2 and short axes d3. The seed density is computed as the ratio of seed mass [Chambert, 2006] to the volume of a sphere having the average diameter.

Sunflower6.20.05760.467715–3521.0–29.50.035–0.0321.11–1.150.011–0.012
Nasturtium7.00.13200.7322712–1918.8–23.50.021–0.0220.98–1.000.004–0.005
Rhubarb4.70.01690.328; 22; 2838–4614.7–16.9≈0.0391.19–1.210.099–0.100: ≈0.037; ≈0.030

[42] Combining equations (4) with (1) we have

display math

[43] We use d = 0.006 m and the mean experimental value for inline image ( inline image m−1 for Nasturtium seeds and inline image m−1 for Sunflowers seeds, Figure 4) in the above equation to compute the probability of capture Pc (shown in Table 4). These values are also plotted in Figure 6, and they compare favorably with the theoretical curve. It is interesting to observe in Table 4 that the capture probability is not very sensitive to the contact angle inline image so that uncertainties in evaluating inline image have a minor impact on the estimation of Pc. For example, for the Sunflowers seeds a inline image change in inline image ( inline image = 25° inline image 10°) leads to only a minor (2.2 inline image) change in Pc (Pc = 0.01135 inline image 0.00025); for the Rhubarb seeds a inline image change in inline image ( inline image = 15.5° inline image 3.5°) leads to a inline image change in Pc (Pc = 0.0048 inline image 0.0004). Finally, we also computed the capture probability for Rhubarb seed, which, among the three lighter seeds, has the greatest roundness (CSF), and thus comes closest to fitting the assumptions of the theoretical equations used to predict meniscus slope angle inline image (see Appendix A). Since the product inline image is not constant in this case, we computed three different values for Pc using the mean path lengths given in Table 3 for the three different cylinder densities. Results are plotted in Figure 6 and again a good agreement with the theory is found.

4. Conclusions

[44] In this work we improve upon the model developed by Defina and Peruzzo [2010] by reducing model complexity and by developing a physically based prediction for model parameters. We focused on the role of surface tension in capturing floating seeds within emergent vegetation. Two scaling parameters within the model were estimated using data from the present study of floating particles within an array of cylinders. Observations from Defina and Peruzzo [2010, 2012], which consider a different morphology of model plant, and from Chambert and James [2009], which considers real floating seeds, compare favorably with the model predictions, validating the model and confirming that it can be extended to other plant and seed morphologies. Indeed, the good agreement between model predictions and experimental results by Defina and Peruzzo [2012], with plants having a moderately complex geometry, suggests that the model can be used, with due care, with natural vegetation, provided that stem density is relatively small so that net trapping can be neglected, and that flow velocity is sufficiently slow so that the Cheerios effect is comparable to inertia.

Appendix A:: Evaluation of the Meniscus Slope Angle ψp

[45] The meniscus slope angle at the particle contact line inline image is estimated by the dynamic analysis of vertical forces acting on a floating sphere (see Figure 8). For light particle ( inline image) the equilibrium position is reached when the weight of the sphere and the surface tension in the vertical direction are balanced by the pressure force acting on the sphere

display math
Figure 8.

Forces acting on floating particle with density inline image; inline image is the surface tension acting along the wetted perimeter.

[46] Because of elementary geometric considerations the contact radius is

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with inline image and inline image the contact angle of the particle. Equation (A1) can be rewritten as

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[47] The contact radius ri can also be written as

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[48] From equations (A2) and (A4) the sphere immersion h can be expressed as a function of inline image

display math

[49] Replacing (A5) In (A3) and rearranging, the equilibrium position of the sphere is given by

display math

where inline image = inline image is the relative density of the sphere and inline image is the Bond number that represents the ratio between gravitational force and surface tension.

[50] According to Kralchevsky and Nagayama [2000] the shape of the meniscus wetting the sphere (see Figure 8) is given as

display math

where inline image is the capillary length and K0 is the modified Bessel function of order 0.

[51] Replacing (A2) in equation (A7) we obtain the rise of the meniscus with respect to the undisturbed free surface

display math

[52] By replacing (A8) in (A6) the equilibrium condition becomes

display math

which can be used to compute the meniscus slope angle inline image.

Acknowledgment

[53] We gratefully acknowledge Chris James for his helpful comments. This research has been partially supported by the Fondazione Aldo Gini, Padova, Italy.

Ancillary