Professional Documents
Culture Documents
Group Members: Julia Luraguiz, Lubna Qutob, Megan Davis, Natasha Kelly
Section: 3
Title: The effects of weight on the dispersal distance and falling velocity of prototype seeds in
the presence and absence of wind
Pattern: Wind dispersed seeds have morphological features, such as weight, affecting falling
velocity and dispersal distance
Overall Research Question: How does weight affect the dispersal of red maple tree prototype
seeds?
Research Hypothesis 1: The lightest red maple prototype seed will have the greatest dispersal
distance inside.
Reasoning: Since seed weight and terminal velocity are directly correlated, decreasing
the weight will result in a decreased velocity, which results in an increase in travel time
inside
Null Hypothesis 1: The weight of the seed prototype will have no effect on the dispersal
distance inside.
Analytical Approach: ANOVA, Bar Graph
Independent Variable: Weight
Dependent Variable: Dispersal Distance
Research Hypothesis 2: The lightest seed prototype will have the greatest dispersal distance
outside.
Reasoning: Since seed weight and terminal velocity are directly correlated, decreasing
the weight will result in a decreased velocity, which results in an increase in travel time
outside
Null Hypothesis 2: The weight of the seed prototype will have no effect on the dispersal
distance outside.
Analytical Approach: ANOVA, Bar Graph
Independent Variable: Weight
Dependent Variable: Dispersal Distance
Research Hypothesis 3: The lightest seed prototype will have the slowest falling velocity inside.
Reasoning: Since seed weight and terminal velocity are directly proportional, decreasing
seed weight will lead to a slower falling velocity inside
Null Hypothesis 3: The weight of the seed prototype will have no effect on the falling
velocity inside.
Analytical Approach: ANOVA, Bar Graph
Independent Variable: Weight
Dependent Variable: Falling Velocity
Research Hypothesis 4: The lightest red maple prototype seed will have the slowest falling
velocity outside.
Reasoning: Since seed weight and terminal velocity are directly proportional, decreasing
seed weight will lead to a slower falling velocity outside
Null Hypothesis 4: The weight of the seed prototype will have no effect on the falling
velocity outside.
Analytical Approach: ANOVA, Bar Graph
Independent Variable: Weight
Dependent Variable: Falling Velocity
Research Hypothesis 5: All three red maple seed prototypes will travel farther outside than
inside.
Reasoning: The presence of wind outside will allow the seeds to travel farther
Null Hypothesis 5: The outside elements will have no effect on how far the seeds will
travel.
Analytical Approach: T-Test, Bar Graph
Independent Variable: Location (Wind Speed)
Dependent Variable: Dispersal Distance
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Abstract
Seed dispersal is a crucial component for plant survival and evolution. Without the ability
to disperse, plants face the serious risk of extinction. We focused on how varying seed weights
impact the plant’s dispersal ability. For our wind dispersed seed prototypes, we hypothesized that
the light seed prototypes will have the greatest dispersal distances and the slowest falling
velocities when dropped both indoors and outdoors. We also predicted that all three seed
prototypes would travel farther outside than inside. A series of experiments varying weight
among the artificial seeds were tested to determine how seed weight impacts the dispersal
distance and falling velocity in the presence and absence of wind. Our results suggest that lighter
seed weights have lower falling velocities and greater dispersal distance is the presence of wind.
However, our results showed a lack of variation among all the seeds dropped inside. These
results correlate to that of other studies on seed dispersal, which found that populations will
select against heavier seeds. We concluded that weight strongly influences seed dispersal and has
aid plant conservation. By reducing resource competition with the parent species as well as
establishing new habitats, dispersal enables seeds to increase their survival and productivity rates
(Ruxton and Schaefer 2012). Some seeds do not have the ability to self-distribute, and therefore
rely on external factors for transport. Dispersal distance distribution has been shown to have a
significant impact on recruitment patterns, genetic structure, and even community diversity
The spatial patterns of seedlings are heavily influenced by seed dispersal and predators,
and this causes changes in abiotic and biotic interactions. With the ability to connect populations
through dispersal, an increase in genetic variation can occur (Holt 1983). These changes could
have a significant impact on the distribution and diversity of plant populations (Beckman et al.
2012). Overall dispersal rates among local communities heavily depend on local competition and
the ability to migrate (Levin et al. 2003). While seed dispersal accelerates niche expansion, too
much dispersal as well as too little could lead to population extinction (Aguilée et al. 2013).
While some seeds can migrate on their own using active dispersal, many seeds travel
using a variety of different mechanisms. Since a great deal of plants are only mobile in the seed
stage, they require a vector for transport (Croteau 2010). When using animals as vectors for
dispersion, plants may produce fruit to be eaten and later defecated in a new location (Schupp
1993). For seeds that are prickly, animals can disperse seeds that stick to their fur or clothing. If
water serves as the primary vector, some plants produce floating seeds that rely on water currents
for dispersal (Nathan et al. 2008). Wind is commonly used for seed dispersal and can cause seeds
it falls (Greene and Johnson 1993). Based on the morphology of these seed types, the mass and
area have a significant impact on the seed’s falling velocity. This relationship can be explained
1/ 2
w
using the equation for terminal velocity, V f =( )
A
, where V f = terminal velocity of the seed, A
= area, and w = seed weight equal to mass x acceleration of gravity (9.8 m/ s2) (Norberg 1973).
Terminal velocity is a measurement in the absence of wind. As a result, windy habitats will result
in greater dispersal distances and lower falling velocities (Greene and Johnson 1993).
With wind dispersed seeds having morphological features that alter their falling velocity
and dispersal distances, we hypothesized that the light seed prototypes will have the greatest
dispersal distances and slowest falling velocities both inside and outside. We also predicted that
all three seed prototypes will have greater dispersal distances outside than inside. To test this
hypothesis using seed dropping experiments, we varied the weights of our artificial seeds and
controlled height as well as morphological traits such as shape and surface area.
Methods
Each seed prototype was constructed using a pipe cleaner, an index card, hot glue, a puff
ball, and foil. The index cards were cut down to the approximate shape of the wings for a red
maple seed (Figure 1). Three treatment groups were developed by manipulating the weights of
the seeds. The weight was altered by adding foil and hot glue to the prototypes: light seeds
(approx. 0.9 g), intermediate seeds (approx. 1.7 g), and heavy seeds (approx. 2.7 g). For the
of 12 m. Seeds were also dropped from the top of an outdoor staircase 7.7 m high. Falling time
was measured in seconds, while the dispersal distance was measured in meters. The average
Analysis of the raw data was done using JMP Pro 15 Software. Using an ANOVA, the
indoor dispersal distance, outdoor dispersal distance, indoor falling velocity, and outdoor falling
velocity were analyzed in relation to seed weight. A T-Test was used to analyze the impact of
wind speed on dispersal distance. Tukey letters were used to signify when a significant
inside than the light prototype (F2,27 = 8.880, p<0.0001, Figure 2).
3.5
2.5
1.5
0.5
Figure 2. Mean (± SE) falling velocity among differing Red Maple Prototypes indoors. Tukey
letters indicate differences (p<0.05) between groups.
When tested outside, the heavy prototype had a greater mean falling velocity than the
4.0
3.5 A
3.0
2.5
B
B
2.0
1.5
1.0
0.5
Outside
Figure 3. Mean (± SE) falling velocity among differing Red Maple Prototypes when outdoors.
Tukey letters indicate differences (p<0.05) between groups.
Overlapping errors bars for indoor dispersal distance indicates a lack of significant
variation between the three different prototypes (F2,27 = 0.5766, p<0.5686, Figure 4).
Figure 4. Mean (± SE) indoor dispersal distance among differing Red Maple Prototypes.
The dispersal distances of the prototypes tested outside were found to be greatest for the
5
A
AB
Outside
Figure 5. Mean (± SE) outdoor dispersal distance among differing Red Maple Prototypes. Tukey
letters indicate differences (p<0.05) between groups.
The light seed prototypes were found to travel a greater distance outside than inside (t18 =
Figure 6.
Mean (± SE)
1
dispersal
0 0.1 m/s (Inside) 0.9 m/s (Outside)
distances for indoor
light vs. outdoor light Red Wind speed (m/s) (light replicates)
Maple prototypes
The control seed prototypes also travelled a significantly greater distance outside than
4.0
3.5
3.0
2.5
2.0
1.5
1.0
0.5
Figure 7. Mean (± SE) dispersal distances for indoor control vs. outdoor control Red Maple
prototypes.
For the heavy seed prototype, there was a greater dispersal distance recorded outside than
3.0
2.5
2.0
1.5
1.0
0.5
Figure 8. Mean (± SE) dispersal distances for indoor heavy vs. outdoor heavy Red Maple
prototypes.
Discussion
The results for the falling velocities support our hypotheses that the light prototype seeds
have lower falling velocities than the heavy prototypes both inside and outside (Figure 2 and 3
respectively). The overlapping error bars for the indoor dispersal distance fail to confirm our
hypothesis that the lighter prototype seeds will travel the farthest inside (Figure 4). Our results
support our hypothesis that the lighter prototypes will have a greater dispersal distance outside
(Figure 5). The results for the indoor and outdoor dispersal distances for each weight confirmed
our hypothesis that all the prototypes will travel farther outside (Figure 6, 7, and 8).
Due to the lack of wind, it is not surprising that there was no significant difference
between the prototype indoor dispersal distances (Figure 4). Previous studies indicate that
external factors such as wind interact with plant traits to enable and increase movement of the
plant species (Wright et al. 2008). The presence of wind has been shown to create an effective
dispersal vector. In a study examining the behavior of a samara seed in the presence of wind, the
wings of the samara seed were shown to spin and generate lift, which then slowed the seed’s fall
and correspondingly increased the dispersal distance (Greene and Johnson 1993). The results of
this study directly correlate and support the results of our study. Longer dispersal distances have
also been shown reduce resource competition with the parent species and thus increase the
Our results suggest that lighter seeds have slower falling velocities, and previous studies
help explain why these prototypes dispersed farther. The structure of spinning samaras allows
them to fall slowly, which increases the likelihood they will get caught in a gust of wind and
travel a greater distance (Green 1980). According to the study, the samaras with lower terminal
velocity compensates for its low competitive ability by increasing the number of areas they can
compete for (Green 1980). Based on our results and that of the mentioned study, lighter seeds
will be able to provide genetic material to a population far away and allow for an increase in
genetic variation.
Corresponding with previous studies, our results indicate that the light prototype seeds
travel the farthest. Selection has shown it favors characteristics that will enhance dispersal
ability. During red maple succession, studies indicate heavy seeds will be selected against and
lighter seeds will be favored (Peroni 1994). As the generations progress, this selection for lighter
seeds remains present and thus indicates that the lighter seeds have an increased ability for
dispersal (Peroni 1994). From the data of previous studies as well as our own, we can infer that
Our study suggests that seed weight may help explain the dispersal patterns of wind
dispersed seeds, but further investigation is needed. A potential limitation in our experiment can
be attributed to water saturating the paper on our prototype seeds when outside and may have
impacted the dispersal distance and falling velocity values and caused a larger standard error.
Seeing how high winds speeds affect the dispersal ability of seeds with varying wingspans could
Literature Cited
Aguilée, R., Shaw, F., Rousset, F., Shaw, R., and Ronce, O. (2013). How does pollen
versus seed dispersal affect niche evolution? Evolution 67(3):792-805.
Beckman, N., Neuhauser, C., and Muller-Landau, H. 2012. The interacting effects of
clumped seed dispersal and distance- and density-dependent mortality on seedling
recruitment patterns. Journal of Ecology 100(4): 862-87
Croteau, E. K. 2010. Causes and consequences of dispersal in plants and animals. Nature
Education Knowledge 3(10):12.
Greene, D. F. and E. A. Johnson. 1993. Seed mass and dispersal capacity in wind-
dispersed diaspores. Oikos 67:69-74.
Green, D. S. 1980. The Terminal Velocity and Dispersal of Spinning Samaras.
American Journal of Botany 67:1218-1224.
Harms K.E., S.J. Wright, O. Calderón, A. Hernández, E.A. Herre. 2000. Pervasive density-
dependent recruitment enhances seedling diversity in a tropical forest. Nature 404: 493-
495.
Holt, R. D. 1983. Immigration and the dynamics of peripheral populations. In A. G. J. Rodin and
K. Miyata, eds. Advances in herpetology and evolutionary biology. Museum of
Comparative Zoology, Harvard University, Cambridge, Mass. 680-694.
Levin, S., Muller-Landau, H., Nathan, R., & Chave, J. 2003. The Ecology and Evolution of Seed
Dispersal: A Theoretical Perspective. Annual Review of Ecology, Evolution, and
Systematics 34:575-604.
Nathan, R., F. M. Schurr, O. Spiegel, O. Steinitz, A. Trakhtenbrot, and A. Tsoar. 2008. Review:
Mechanisms of long-distance seed dispersal. Trends in Ecology & Evolution 23:638-647.
Norberg, R. A. 1973. Auto rotation, self-stability, and structure of single-winged fruits and seeds
(samaras). Biological Review, 98:561-596.
Peroni, P.A., 1994. Seed Size and Dispersal Potential of Acer Rubrum (Aceraceae) Samaras
produced by populations in early and late successional environments. American Journal
of Botany 81: 1428–1434.
Ruxton, G. D. and H. M. Schaefer. 2012. The conservation physiology of seed
dispersal. Philosophical transactions of the Royal Society of London. Series B, Biological
sciences 367(1596): 1708-18.
Schupp, E. W. 1993. Quantity, quality, and effectiveness of seed dispersal by animals.
Vegetation 107(1):15-29.
Wright S. J., A. Trakhtenbrot, G. Bohrer, M. Detto, G. G. Katul, N. Horvitz, H. C. Muller-
Landau, F.A. Jones, and R. Nathan. 2008. Understanding strategies for seed dispersal by
wind under contrasting atmospheric conditions. PNAS 105: 19084-19089.