Effects of weevil parasitismo n a Cecropia-Azteca mutualism


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Effects of weevil parasitismo n a Cecropia-Azteca mutualism

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Effects of weevil parasitismo n a Cecropia-Azteca mutualism
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Edmundson, Scott J.
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Mutualisms, beneficial interactions between organisms, are complex and often involve many species. Parasites on mutualisms disrupt the energy exchange and recycling between the mutually benefited species. This experiment explores the mutualism between Cecropia obtusifolia and Azteca xanthacroa and the effects of a parasitic disruption. Levels of fitness were estimated for sapling C. obtusifolia by measuring Müllerian body production and leaf herbivory. In addition, fitness levels of ants were ascertained by using the number of ants actively patrolling the top four nodes of the sapling as an estimation of the colony number. Results demonstrated that the Müllerian body production rate is significantly positively correlated with the number of ants actively patrolling (regression analysis, R2 = 0.530, p-value = 0.0003, n = 20). The number of ants did not significantly correspond with increased percent leaf herbivory, although a trend that an increase in ants conferred a decrease in herbivory was noticed (regression analysis, R2 = 0.093, p-value = 0.205, n = 20). The percent of trichilia infected by a petiole weevil (Curculionidae: Zygopinae), corresponded negatively with the rate of Müllerian body production (regression analysis, R2 = 0.492, pvalue = 0.0006, n = 20). Saplings that had any amount of infested trichilia had significantly less ants patrolling (Mann- Whitney U test: U = 13.5, p-value = 0.0055, n = 20). I also found the greater the degree of trichilia infestation, the higher the levels of herbivory (regression analysis, R2 = 0.286, p-value = 0.015, n = 20). These results suggest that this parasitic interference may reduce the fitness of one or both of the partners in the mutualism. ( ,, )
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Los mutualismos son las interacciones beneficiosas entre organismos que son complejas y a menudo incluyen a muchas especies. Los parásitos en los mutualismos interrumpen el intercambio de energía y el reciclaje entre las especies mutuamente beneficiadas. Este estudio explora el mutualismo entre Cecropia obtusifolia (guarumo) y Azteca xanthacroa (hormiga del guarumo) y los efectos de una interrupción parasitaria. Los niveles de salud de los árboles se estimaron con plántulas de C. obtusifolia midiendo la producción de cuerpos de Müller y la herbivoría de las hojas. Además, los niveles de salud de las hormigas fueron determinados utilizando el número de hormigas que patrullaban activamente los primeros cuatro nódulos de la plántula como una estimación del número de miembros de la colonia. Los resultados demostraron que la tasa de la producción de los cuerpos de Müller está positiva y significativamente correlacionada con el número de hormigas en patrulla (Regresión simple, R2 = 0,530, el P-valor = 0,0003, N = 20). El número de hormigas no correspondió significativamente con el porcentaje del incremento de herbivoría de las hojas, aunque se notó una tendencia sugiriendo que un aumento en el número de hormigas correspondía a una disminución en la herbivoría (Regresión simple, R2 = 0,093, el P-valor = 0,205, N = 20). El porcentaje de triquilia infectado por un gorgojo del pecíolo (Curculionidae: Zygopinae), correspondió negativamente con la tasa de la producción de cuerpos de Müller (Regresión simple, R2 = 0,492, el P-valor = 0,0006, N = 20). Las plántulas que tuvieron cualquier cantidad de triquilia infectadas mostraron significativamente menos hormigas en patrulla (Mann- Whitney U test: U = 13,5, el P-valor = 0,0055, N = 20). También descubrí que entre más grande el grado de infestación de triquilia, más altos los niveles de herbivoría (Regresión simple, R2 = 0,286, el P-valor = 0,015, N = 20). Estos resultados sugieren que esta interferencia parasitaria puede reducir la salud de uno o de ambos socios en el mutualismo.
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Testing the U nified Neutral Theory using the epiphylls of Geonoma spp. Arecaceae as model communities Caroline E. Farrior Department of Biology, University of Pennsylvania ABSTRACT Th is experiment test s the predictions of the Unified Neutral Theory of E cology Hubbell 2001 using epiphylls on leaves of the palm tree Geonoma spp. Arecaceae as local communities. The metacommunity is defined as the collection of leaves of one palm tree. The UNT assumes all species to be competitively equivalent and population sizes to remain constant overtime . It also asserts that community drift is strong and that for diversity to exist there must be factors that slow its progress. The UNT predicts that increases in connectivity of the metacommunity, community a rea , population size of local and metacommunities, as well as metacommunity area should slow the rate of community drift and favor increased species richness. The UNT also predicts that Dominance Diversity relationships of each metacommunity will form a f amily of curves that will differ in slope in relation to differences in community richness, rates of immigration between communities , and community sizes. Data taken on the epiphyll richness of different Geonoma spp. leaves support predictions that commun ity and me tacommunity size are positively correlate d with species richness. The data shows n o evidence of the effects of connectivity or population size on species richness. The model communities provided Dominance Diversity curves of which the slopes we re negatively correlated with species richness, but community size had no significant effect. I found Hubbell s Unified Neutral Theory to be an insufficient model of epiphyll community richness and dominance on Geonoma spp. leaves in the cloud forest of M onteverde, Costa Rica . RESUMEN E sta investigaci ó n es un exam e n de la s predicciones de la T eo r í a Neutral Unificada UNT de la Ecolog í a Hubbell 2001 usando ep í filas en las hojas de l a palma Geonoma spp. Arecaceae como com unidades locales. Se defin e metacomunidad como la colección de hojas de un a palma . La UNT asume que todas la s especies son competitivamente equivalentes y que el tamaño de la población permanece constante. También asume que la deriva de las com unidades es fuerte y que para que la diversidad sea posible deben existir factores que reduzcan su progreso . La UNT predice que los aumentos en las conexi o n es de la meta co munidad, el área de la comunidad, el tamaño de la poblac i ó n local y de las metacomunidades y el área de la metacom unidad debería reducir la tasa de deriva de communidades y favorecer el incremento de la riqueza de especies. La UNT también predice que las relaciones entre la dominancia y la diversidad d e cada meta com unidad formará una familia de curvas que diferirá en pendi ente en relació n con las differencias en la riqueza de las especies, la tasa de in migración entre las comunidades y el tamaño de las co munidades. Los d atos sobre la riqueza de especies en diferentes hojas de Geonoma spp. apoya ron la s predicciones de que e l tamaño de las comunidades y de las metacomunidades está positivamente relacionado con la riqueza de especies . Los datos no muestan ninguna evidencía de los efectos ni de las conexi o n es ni del tamaño de la población sobre la riqueza de especies. Las com unidades modelo produjeron curvas de dominancia contra diversidad cuyas pendientes fueron negativamente correlacionadas con la riqueza de especies, pero el tamaño de la comunidad no tuvo un efecto significativo . Se concluye que la Teo r í a Neutral Unificada de Hubbell es un modelo insu ficiente para describir la riqueza de especies y domina n cia de epífilas en las hojas de Geonoma spp. en el bosque nuboso de Monteverde, Costa Rica.

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INTRODUCTION Biodiversity is regarded as one of the most valuable resources t he natural world has to offer, a fact that is reflected in the choice and defense of conservation areas Myers et al. 2000, Orme et al. 2005. B iodiversity has been shown to increase stability th r ough its effect on productivity Tilman, et al. 1996, Hecto r, et al. 1999 and protection against invaders Naeem et al. 2000, Symstad et al. 2000 . It is important to know how biodiversity is created and mainta ined in order to preserve it effectively . Hubbell 2001 po sed an important stochastic theory , the Uni fied Neutral Theory, to explain patterns of biodiversity and community ass embly . To test the UNT , I examined epiphyll communities on lea ves of the palm Geonoma spp. Arecaceae . I defined epiph ylls as my ecological community. I delineated epiphylls on i ndividual leaves of Geonoma spp. as local communities, and the collection epiphylls on an entire palm as a metacommunity. The Unified Neutral Theory UNT assum es that all spec ies have equal competitive abilities . This is an unrealistic assumption, and t here have been many criticisms of this model with supporting data Chave 2004, Harpole and Tilman 2006 , Assaf 2005. However, in spite of its assumption, the model has successfully explained extensive experimental results Hubbell 2001, Brown 2001. Thi s disagreement in the literature provides reason for a small scale , straightforward test of the predictions of the UNT. The UNT presumes that j and J, the total number of individuals in the local and metacommunity, respectively, never changes. That is , t he birth rate plus immigration rate must equal the death rate plus emigration rate on both the local and community levels . From this, Hubbell 2001 states that every time an individual dies exactly one must replace it, and by competitive equivalence of s pecies, it follows that chance will tend to choose a member of the abundant species to fill the hole more often than those of rare species. T his leads, over time, to a new community where the abundant species are become increasingly abundant and the rare species become rarer. Continuing this pattern without allowing any immigration , emigration or speciation events, communities drift will cause communities to become monodominant, which is, composed of only one species. Hubbell 2001 terms this process th e random walk to extinction. In fact, natural communities hardly ever consist of one single species. To explain this apparent paradox, the UNT proposes that areas that have levels of high diversity must have mechanisms to slow down or counter the rand om walk to extinction. Specifically, the UNT makes five predictions for community assembly and diversity trends. 1 A higher level of connectivity between local communities will lead to greater local community species richness because of greater immig ration rates, which counter the random walk b y rescue effects. 2 A local community of greater area will provide room for more individuals, which slows the walk down and fa vors diversity . 3 A greater j or J , number of individuals in the local and meta communities respectively will also decrease demographic stochasticity, thus reducing the rate of drift and favor diversity. 4 A larger metacommunity area will provide more opportunities for immigration and favor diversity. 5 The Dominance Diversity c urves produced from t he collection of metacommunities will form a family of curves that will differ in slope . T he slope of these curves should depend on rates of immigration, local community size , and metacommunity size . It is superficially predicted tha t these curves will have shallower slopes with increases in any one of these three factors.

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I tested t hese five predictions of Hubbell s Unified Neutral Theory 2001 by examining the community of epiphylls on the leaves of individuals of the understory p alm Geonoma spp. Arecaceae. Epiphylls are photosynthetic organisms , usually bryophytes or lichens, which inhabit leaf surfaces Zartman 2003. To e piphylls the forest is a sea of uninhabitable area with habitable leaves interspersed as islands of habit at . Epiphylls are dispersed by wind and wat er, and have no known herbivores or pathogens . The fact that their dispersal, colonization, survival and reproduction rely more heavily on chance than species interactions, like most plants and animals, makes ep iphylls a good model community to test the effects of stochastic factors. Geonoma spp. provides a good substrate on which to observe patterns of epiphyll community composition because of the abundance of epiphylls, epiphyll diversity, and clearly defined and separated leaves that serve as convenient local communities Figure 2 Hooker 2002, Zuchowski 2005. For purposes here, t he collection of leaves on one Geonoma spp. plant makes up a single metacommunity Figure 1. METHODS Study Site and Samplin g Criteria To control potentially compounding environmental variables that may affect epiphyll communities , I sampled plants that were located , within a 200 meter radius, under approximately identical light conditions, and at the same elevation. I sampled t he oldest two photosynthetically active leaves on each plant , because the UNT makes predictions about stable communities, not those going through succession . Older leaves were more likely to have older communities of epiphylls and thus more equilibrated communities. The oldest two leaves are the two leaves closes t to the base of the tree. I used palms from the Cerro Chomongo 1725 m behind the Estación Biológica Monteverde, Monteverde, Costa Rica. The sample size included 42 leaves from 21 plants. Data Collection Local community species richness and diversity : Local community species richness of each leaf was calculated by subsampling an area of 20 cm 2 from one leaflet Figure 2 . I sampled the leaflet closest to the tip of the leaf that had a wi dth between 1.6 and 3.2 cm at the base of the leaflet . The 20 cm 2 grid was located four centimeters from the base of the leaflet. I checked the 480 crosshairs of the grid for epiphyll presence and determined their morphospecies. Prediction 1: Highe r levels of community connectivity should lead to greater local community species richness. I measured the distance from the sampled leaves to their closest neighboring leaves. Specifically, I measured from the base of the sampled leaf blade to the base of the nearest leaf blade See Figure 1 . Prediction 2: Increased local community area should increase local community richness. I made two measure of local community area. I measured both the length of the leaf blade, and also the area of the leaflet that was sampled to check for even finer scale effects Figure 2 . Leaf length is an approximation for area of the local community. This seems reasonable because most Geonoma spp. leaves have similar widths. Leaflet area is a measure of the microcommuni ty from which the diversity was sampled. It is an

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approximation, using the length of the leaflet multiplied by its width at the point of attachment, because Geonoma spp. leaflets are sigmoid shaped, this is most certainly an overestimate , but it is consis tently so . Prediction 3: Greater j and J should both independently lead to increases in local community species richness. J and j are the number of individuals in the local and metacommunities, respectively. I t is difficult and time consuming both to det ermine individuals of epiphylls as well as count them on a plant that must support thousands . Instead, area was used as a proxy for number of individuals. Area of the epiphylls was estimated for each leaf on the plant. I used a scale of 1 unit = 5 cm 2 an d took squares of 1, 5, and 10 units to help visually approximate the area of epiphylls on the leaves in the field. Prediction 4: The area of the metacommunity should lead to an increase in species richness. To approximate metacommunity area, I measured both the plant height from the base of the tree to the apical meristem and counted th e number of leaves on the plant Figure 1 . Prediction 5 : Dominance of a community should be negatively correlated with species richness, local and metacommunity area, a nd immigration. I analyzed the slopes of the Dominance Diversit y Curves produced by the species compositions and abundances of the 42 leaves sampled during the experiment. Only the effects of species richness and community size were tested because rates of immigration were too difficult to obtain in such a short term study . RESULTS I sampled 42 leaves from 21 plants of Geonoma spp. I found 27 morphospecies of epiphylls. The local community richness ranged from 2 to 14 species per 20 cm 2 X = 8.4 , S.D . = 2.6 . The results of the specific tests of each of the predictions of the UNT are as follows: Prediction 1: Nearest neighbor distance, a measure of the connectance of the metacommunity , does not correlate significantly with species richness of the lo cal community R 2 = 0.06, P = 0.12 , N = 42. In fact, nearest neighbor distance produced a positive t r end the opposite of that expected when p lotted against species richness Figure 3a . This result could be contributed to the close correlation between connected ness and metacommunity size R 2 = 0.23, P < 0.0001, N = 42 and R 2 = 0.20, P = 0.0003, N =42 for plant height and number of leaves respectively . Both plant height and number of leaves are shown to have significant or marginally significant posit ive effects on the local community species richness , and could be producing this same trend for connectivity . Prediction 2: The area of the local community positively correlates with local community species richness. Both leaf length and leaflet area ar e marginally significant and significant predictors of the species richness of a local community respectively R 2 = 0.08 , P = 0.06 , N = 42 and R 2 = 0.10 , P = 0.03 , N = 42 respectively Figure 3b, c. Prediction 3: The estimates of local and meta community size j and J do not significantly predict the species richness of the local community of epiphylls R 2 = 0.04 , P = 0.23, N = 42, and R 2 = 0.01, P = 0.62 , N = 42 respectively F igure 3d, e.

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Prediction 4: The n umber of leaves on a plant a measure of the size of the metacommunity significantly positively correlates with local community species richness R 2 = 0.14 , P = 0.01 , N = 42 See Figure 3f. Plant height showed no significant effect on l ocal community species richness R 2 = 0.05 , P = 0.1 5 , N = 42. Prediction 5: The Dominance Diversity C urves, shown together in Figure 4, seem to fit a family o f curves. These curves all have different slopes, which serve as measure s of dominance of the community. All the slopes are negative; a slope that is more negative has greater dominance. The UNT predicts that dominance will decrease with species richness, immigration and community size. Species richness is highly correlated with the dominance of the epiphyll communities R 2 = 0.41 , P < 0.0001 , N = 42 ; Figure 5a . But, community size was unable to explain variation in dominance R 2 = 0. 04, p value = 0.23 , N = 42 , R 2 = 0. 03, P = 0.28 , N = 42 ; Figure 5b, c . DISCUSSION In this investigation of epiphyll communities, I tested five predictions of Hubbell s Unified Neutral Theory. I found support for only two of the five predictions tested . Species richness of local communities was significantly explained by measures of the size of the local and metacommunities. However, m easures of connectivity, and to tal population were insufficient in explaining local community species richness. The nearest neighbor distance produces a nonsignificant positive trend with species richness, the opposite trend as expected from the UNT. My measure of community connectiv ity may not be a good measure of the actual connectivity of the metacommunity . When inspected, the distance of the nearest neighbor on a Geonoma spp. plant correlates closely with plant height and number of leaves , two factors which were shown to produce positive trends with species richness. The UNT predicts that Dominance Diversity Curves of communities of differing diversity will follow a family of curves that differ in slope . The differences in slope of the graphs are predicted to be a function of di fferent rates of immigration and local community size. The Dominance Diversity Curves of epiphyll communities on Geonoma spp. do belong to a family of curves with different slopes. The slope of these lines, or the community dominance, can be predicted by the species richness of a community, a result consistent with the UNT. However, local and metacommunity size were unable to predict the dominance slope of the Dominance Diversity curve of a community, a result inconsistent with the UNT. T he role of a stochastic model is to t ry to explain a community with the least amount of knowledge possible Hubbell 2005 . The Unified Neutral Theory proposes that a small number of fact ors will be able to predict community richness. In this examination of 42 local c ommunities, it seems that the information was not enough. O nly the leaf length and community size helped to predict 10% and 14% of the variation in local community species richness, respectively not necessarily independent of one another . T hese two sig nifica nt factors can account for at most 24% of the variation in species richness . It seems the Unified Neutral Theory of ecology does not provide enough parameters to sufficiently predict the dominance or diversity of the epiphyll community as it is orga nized on islands of palm leaves .

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This evidence corroborates findings of many other studies Chave 2004, Harpole and Tilman 2006, Assaf 2005 . The failure of Unified Neutral Theory to predict the dominance and diversity of local communities could be due to the role of many disregarded factors in community composition. The basic assumptions of competitive equivalence and constant population size could be wrong. Also mechanisms such as density dependent selection, dispersal limitations, and epiphyll species interactions could be important in these epiphyll communities. ACKNOWLEDGMENTS I appreciate the help of Karen Masters, Alan Mas ters, Maria Jost and Oliver Hyma n. Thanks also to Ellen Frondorf for collaborating in epiphyll identification and Kevi n Loope for his ever patient manner in helping with the infinitely enjoyable task of making Microsoft Word © diagrams . LITERATURE CITED Assaf, Z . 2005. A test of the Hubbell Theory using protist communities in bromeliad tanks as a model system. CIE E Tropical Ecology and Conservation Spring 2005. 20 33. Brown, J. H. 2001. Toward a general theory of biodiversity. Evolution 30 , 2137 2138. Chave, J. 2004. Neutral theory and community ecology. Ecology Letters 7 : 241 253. Harpole, W. S. and D. Tilman. 2006. Non neutral patterns of species abundance in grassland communities. Ecology Letters 9 : 15 23. Hector, A., B. Schmid, C Beirkuhnlein, M. C. Caldeira, M. Diemer, P. G. Dimitrakopoulos, J. A. Finn, H. Freitas, P. S. Giller, J. Good, R. Har ris, P. Hogberg, K. Huss Danell, J. Joshi, A Jumpponen, C. Kroner, P. W. Leadley, M. Loreau, A. Minns, C. P. H. Mulder, G. O Donovan, S. J. Otway, J. S. Pereira, A. Prinz, D. J. Read, M. Scherer Lorenzen, E. D. Shulze, A. S. D. Siamantziouras, E. M. Spehn, A. C. Terry, A. Y. Troumbis, F. I. Woodward, S. Yachi, and J. H. Lawton. 1999. Plant diversity and productivity experiments in European grasslands. Science 286 : 1123 1127. Hooker, A . 2002. The effects of northeast trade winds on epiphyll distributio n in a Monteverde cloud forest. CIEE Tropical Ecology and Conservation Fall 2002 . 12 23. Hubbell, S. P. 2001. The Unified Neutral Theory of Biodiversity and Biogeography. Princeton University Press, Princeton, New Jersey . Hubbell, S. P. 2005. N eutral theory in community ecology and the hypothesis of functional equivalence. Functional Ecology. 166 172. Myers, N., R. A. Mittermeier, C. G. Mittermeier, G. A. B. da Fonseca, and J. Kent. Biodiversity hotspots for conservation priorities. Nat ure 403 : 853 858. Naeem, S., J. M. H. Knops, D. Tilman, K. M. Howe, T. Kennedy and S. Gale . 2000. Plant diversity increases resistance to invasion in the absence of covarying extrinsic factors. Oikos 91 : 97 108. Orme, C. D. L., R. G. Davies, M. Bur gess, F. Eigenbrod, N. Pickup, V. A. Olson, A. J. Webster, T S Ding. P. C. Rasmussen, R. S. Ridgely, A. J. Stattersfield, P. M. Bennett, T. M. Blackburn, K. J. Gaston and I. P. F. Owens. 2005. Global hotspots of species richness are not congruent with e ndemism or threat. Nature 436 : 1016 1019. Symstad, A . J. 2000. A Test of the Effects of Functional Group Richness and Composition on Grassland Invasibility. Ecology 81 : 99 109. Tilman, D., D. Wedin, and J. Knops. 1996. Productivity and sustainabilit y influenced by biodiversity in grassland ecosystems. Nature 379 : 718 720. Zartman, C. E. 2003. Habitat fragmentation impacts on epiphyllous bryophyte communities in central Amazonia. Ecology 84 : 948 954. Zuchowski, Willow. 2005. A Guide to Tr opical Plants of Costa Rica. Zona Tropical, Miami, 390.

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Figure 1: Representation of one metacommunity. The epiphylls of each leaf is a local community. The epiphylls on all leaves of a Geonoma spp. palm are the met acommunity. The manner of collection of data taken from each metacommunity is shown here. Plant height was taken from the base of the plant to the apical meristem. The nearest neighbor distances were measured from the base of the leaf blade sampled to t he nearest leaf blade base. Also, the number of unfolded leaves was counted for each plant, here 6 leaves. Sampled Leaf #2 Nearest Neighbor Distances for Leaf #1, and #2 left and right arrows respectively. Sampled Leaf #1 Sampled Leaf #2 Plant Height

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Figure 2: T he local community and the sampling system. One local community is defined as one leaf blade in this experiment. The leaves of Geonoma spp. are split irregularly as is shown. To determine the diversity o f a leaf, I examined an area of constant size. The leaflet I chose to sample from the leaf was the one closest to the top of the leaf with a width ranging between 1.6 and 3.2 cm. The large oval is an enlargement of the sampled leaflet. A grid was place d four centimeters from the base of the leaflet. T his grid was 20cm 2 and contained 480 crosshairs. At each crosshair the presence and morphospecies of epiphyll was recorded. Leaflet width Leaflet Length 4cm Leaf Length

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Figure 3: The effect of six different parameters on local community species richness. All parameters , except for nearest neighbor distance are predicted by the UNT to correlate positively with local community species richness. A Local community species richness as predicted by nearest neighbor distance, a measure of connectivity , predicted to be a negative trend by the UNT but here is a positive trend R 2 = 0.06, P = 0.12 , N = 42. B Local community spe cies richness as predicted by the size of the local community. This trend is marginally significant and shows that greater community area could be effective 0 2 4 6 8 10 12 14 16 0 50 100 150 Leaf Length cm 0 2 4 6 8 10 12 14 16 2 4 6 8 10 12 14 Number of Leaves per Palm 0 2 4 6 8 10 12 14 16 0 10 20 30 40 50 Nearest Neighbor Distance 0 2 4 6 8 10 12 14 16 0 50 100 150 200 Local j 0 2 4 6 8 10 12 14 16 0 200 400 600 800 Metacommunity J 0 2 4 6 8 10 12 14 16 25 50 75 100 125 150 Leaflet Area cm^2 Local Community Species Richness B A C D F E

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as slowing community drift t o increase diversity R 2 = 0.08, P = 0.06 , N = 42. C The area of t he leaflet chosen to sample significantly correlates with local community species richness, again supporting t he second prediction of the UNT R 2 = 0.10 , P = 0.03, N = 42. D The population size of the local community, J does not significantly explain th e variation in local community species richness R 2 = 0.04 , P = 0.23 , N = 42. E The estimation of total population size for the metacommunity, total J, also does not significantly explain the variation in local community species richness R 2 = 0.0063, P = 0.6175, N = 42. F Number of leaves on the plant number of islands in the metacommunity significantly correlates with local community species richness R 2 = 0.14, P = 0.01, N = 42. Metacommunity size could also be an important factor in slowing community drift for the epiphyll communities. 0.1 1 10 100 0 5 10 15 Species Rank in Abundance Percent Relative Species Abundace Figure 4: The Dominance Diversity Curve s of all the epiphyll communities sampled. Each line represents one of the 42 communities leaves sampled in the experiment. The x axis, species rank in abundanc e, is the rank of abundance of each species in that community . The rank 1 species is the most abundant species in the community. The y axis is percent relative species abundance. This is the species percent of the tot al individuals in the community, re presented on a log 10 scale. The slope of the trendline is proportional to dominance of the community. The point at which the trendline stops on the x axis signifies the number of species in that community.

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Figure 5: T he relationship between dominance , as determined by the slopes of the dominance diversity curves s pecies richness and community size a measure of community size. Note that the slopes of the dominance diversity curves are all negative. A more negative slope corresponds to a community of greater levels of dominance. A This regression is a summary of Figure 4. The slopes of each of the lines represented there are plotted against species richness, where each of the lines stops on the x axis of Figure 4 R 2 = 0.41 , P < 0.0001 , N = 42 . Co mmunities of epiphylls with fewer species present have significantly greater dominance than those with high species richness. B a nd C Both graphs show dominance as predicted by community size. Leaflet area, and n umber of leaves were chosen because they were the only parameters that significantly affected the species richness. Neither is able to significantly predict the dominance of a community as was predicted by the UNT R 2 = 0. 04, p value = 0.23 , N = 42 and R 2 = 0. 03, P = 0.28 , N = 42 for B and C respectively. -0.8 -0.7 -0.6 -0.5 -0.4 -0.3 -0.2 -0.1 0 0 5 10 15 Species Richness -0.8 -0.7 -0.6 -0.5 -0.4 -0.3 -0.2 -0.1 0 0 50 100 150 Leaflet area cm 2 -0.8 -0.7 -0.6 -0.5 -0.4 -0.3 -0.2 -0.1 0 2 4 6 8 10 12 14 Number of Leaves Slope of Dominance Diversity Curve B A C


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