Academic literature on the topic 'Seeds – Dispersal – Longitudinal studies'

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Journal articles on the topic "Seeds – Dispersal – Longitudinal studies"

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Baskin, Jerry M., Juan J. Lu, Carol C. Baskin, and Dun Y. Tan. "The necessity for testing germination of fresh seeds in studies on diaspore heteromorphism as a life-history strategy." Seed Science Research 23, no. 2 (May 10, 2013): 83–88. http://dx.doi.org/10.1017/s096025851300010x.

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AbstractMany studies have compared diaspore dispersal ability and degree of dormancy in the two diaspores of dimorphic plant species. A primary goal of these studies was to determine if germination and dispersal characteristics of the two morphs fit within a high risk–low risk (bet-hedging) life-history strategy, i.e. high dispersal/low dormancy in one morph versus low dispersal/high dormancy in the other one. In a survey of 26 papers on 28 diaspore dimorphic species, we found that in 12 of the studies, which were published between 1978 and 2008, seeds were stored, and thus possibly afterripened, before they were tested for germination. The 14 papers that tested fresh seeds were published between 1963 and 2010. Failure to test fresh seeds likely resulted in misinterpretation of the diaspore dispersal/dormancy strategy in some of the species investigated. We conclude that it is imperative that fresh seeds be tested for germination in order to be certain that the correct relationship between dispersal and dormancy is elucidated, and thus that the correct interpretation is made concerning life-history strategy and bet-hedging, in dimorphic species.
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Wichmann, Matthias C., Matt J. Alexander, Merel B. Soons, Stephen Galsworthy, Laura Dunne, Robert Gould, Christina Fairfax, Marc Niggemann, Rosie S. Hails, and James M. Bullock. "Human-mediated dispersal of seeds over long distances." Proceedings of the Royal Society B: Biological Sciences 276, no. 1656 (September 30, 2008): 523–32. http://dx.doi.org/10.1098/rspb.2008.1131.

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Human activities have fundamental impacts on the distribution of species through altered land use, but also directly by dispersal of propagules. Rare long-distance dispersal events have a disproportionate importance for the spread of species including invasions. While it is widely accepted that humans may act as vectors of long-distance dispersal, there are few studies that quantify this process. We studied in detail a mechanism of human-mediated dispersal (HMD). For two plant species we measured, over a wide range of distances, how many seeds are carried by humans on shoes. While over half of the seeds fell off within 5 m, seeds were regularly still attached to shoes after 5 km. Semi-mechanistic models were fitted, and these suggested that long-distance dispersal on shoes is facilitated by decreasing seed detachment probability with distance. Mechanistic modelling showed that the primary vector, wind, was less important as an agent of long-distance dispersal, dispersing seeds less than 250 m. Full dispersal kernels were derived by combining the models for primary dispersal by wind and secondary dispersal by humans. These suggest that walking humans can disperse seeds to very long distances, up to at least 10 km, and provide some of the first quantified dispersal kernels for HMD.
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Tsuji, Yamato, Kumugo Yangozene, and Tetsuya Sakamaki. "Estimation of seed dispersal distance by the bonobo, Pan paniscus, in a tropical forest in Democratic Republic of Congo." Journal of Tropical Ecology 26, no. 1 (December 8, 2009): 115–18. http://dx.doi.org/10.1017/s0266467409990290.

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Great apes are considered to be important seed dispersers in palaeotropical habitats due to their large body size (this would be reflected in the amount of foods consumed) and large home ranges (Poulsen et al. 2001, Wrangham et al. 1994). Furthermore, the great apes might process seeds in a way that maintains their viability (Lambert 1999). Previous studies of seed dispersal by great apes have generally taken the form of lists of seeds found in their faeces (Voysey et al. 1999a, Wrangham et al. 1994), effects of passage through their guts on seed germination (Idani 1986, Wrangham et al. 1994), and effects of dispersal location on germination/seedling survival (Gross-Camp & Kaplin 2005, Rogers et al. 1998, Voysey et al. 1999b). In contrast with the richness of reports about aspects of seeds after their dispersal, few studies have investigated the dispersal pattern of seeds. In this study, we report on the estimated distances of seed dispersal by the wild bonobo (Pan paniscus Schwartz), a species of great ape.
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Liu, Xiaoguang, Yuhong Zeng, Gabriel Katul, Wenxin Huai, and Yu Bai. "Longitudinal dispersal properties of floating seeds within open-channel flows covered by emergent vegetation." Advances in Water Resources 144 (October 2020): 103705. http://dx.doi.org/10.1016/j.advwatres.2020.103705.

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Loebach, Christopher A., and Roger C. Anderson. "Measuring short distance dispersal of Alliaria petiolata and determining potential long distance dispersal mechanisms." PeerJ 6 (March 15, 2018): e4477. http://dx.doi.org/10.7717/peerj.4477.

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Introduction Alliaria petiolata, an herbaceous plant, has invaded woodlands in North America. Its ecology has been thoroughly studied, but an overlooked aspect of its biology is seed dispersal distances and mechanisms. We measured seed dispersal distances in the field and tested if epizoochory is a potential mechanism for long-distance seed dispersal. Methods Dispersal distances were measured by placing seed traps in a sector design around three seed point sources, which consisted of 15 second-year plants transplanted within a 0.25 m radius circle. Traps were placed at intervals ranging from 0.25–3.25 m from the point source. Traps remained in the field until a majority of seeds were dispersed. Eight probability density functions were fitted to seed trap counts via maximum likelihood. Epizoochory was tested as a potential seed dispersal mechanism for A. petiolata through a combination of field and laboratory experiments. To test if small mammals transport A. petiolata seeds in their fur, experimental blocks were placed around dense A. petiolata patches. Each block contained a mammal inclusion treatment (MIT) and control. The MIT consisted of a wood-frame (31 × 61× 31 cm) covered in wire mesh, except for the two 31 × 31 cm ends, placed over a germination tray filled with potting soil. A pan filled with bait was placed in the center of the tray. The control frame (11 × 31 × 61 cm) was placed over a germination tray and completely covered in wire mesh to exclude animal activity. Treatments were in the field for peak seed dispersal. In March, trays were moved to a greenhouse and A. petiolata seedlings were counted and then compared between treatments. To determine if A. petiolata seeds attach to raccoon (Procyon lotor) and white-tailed deer (Odocoileus virginianus) fur, wet and dry seeds were dropped onto wet and dry fur. Furs were rotated 180 degrees and the seeds that remained attached were counted. To measure seed retention, seeds were dropped on furs and rotated as before, then the furs were agitated for one hour. The seeds retained in the fur were counted. Results For the seed dispersal experiment, the 2Dt function provided the best fit and was the most biologically meaningful. It predicted that seed density rapidly declined with distance from the point source. Mean dispersal distance was 0.52 m and 95% of seeds dispersed within 1.14 m. The epizoochory field experiment showed increased mammal activity and A. petiolata seedlings in germination trays of the MIT compared to control. Laboratory studies showed 3–26% of seeds were attached and retained by raccoon and deer fur. Retention significantly increased if either seed or fur were wet (57–98%). Discussion Without animal seed vectors, most seeds fall within a short distance of the seed source; however, long distance dispersal may be accomplished by epizoochory. Our data are consistent with A. petiolata’s widespread distribution and development of dense clusters of the species in invaded areas.
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Hanson, Thor, Steven Brunsfeld, Bryan Finegan, and Lisette Waits. "Conventional and genetic measures of seed dispersal for Dipteryx panamensis (Fabaceae) in continuous and fragmented Costa Rican rain forest." Journal of Tropical Ecology 23, no. 6 (October 29, 2007): 635–42. http://dx.doi.org/10.1017/s0266467407004488.

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The effects of habitat fragmentation on seed dispersal can strongly influence the evolutionary potential of tropical forest plant communities. Few studies have combined traditional methods and molecular tools for the analysis of dispersal in fragmented landscapes. Here seed dispersal distances were documented for the tree Dipteryx panamensis in continuous forest and two forest fragments in Costa Rica, Central America. Distance matrices were calculated between adult trees (n = 283) and the locations of seeds (n = 3016) encountered along 100 × 4-m transects (n = 77). There was no significant difference in the density of seeds dispersed > 25 m from the nearest adult (n = 253) among sites. There was a strong correlation between the locations of dispersed seeds and the locations of overstorey palms favoured as bat feeding roosts in continuous forest and both fragments. Exact dispersal distances were determined for a subset of seeds (n = 14) from which maternal endocarp DNA could be extracted and matched to maternal trees using microsatellite analysis. Dispersal within fragments and from pasture trees into adjacent fragments was documented, at a maximum distance of 853 m. Results show no evidence of a fragmentation effect on D. panamensis seed dispersal in this landscape and strongly suggest bat-mediated dispersal at all sites.
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O'Connor, Julie M., David M. Burrows, Benjamin L. Allen, and Scott E. Burnett. "Is the European red fox a vector of the invasive basket asparagus (Asparagus aethiopicus) in eastern Australia?" Australian Mammalogy 42, no. 2 (2020): 204. http://dx.doi.org/10.1071/am19001.

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Basket asparagus (Asparagus aethiopicus) has become a naturalised invasive plant in some coastal areas of Australia since its introduction in the late 19th century. Its spread through garden waste dumping and avian seed dispersal has been well documented and both are considered to be the primary means of dispersal. While a small number of avian vectors have been identified, no Australian studies have investigated the potential of mammals to disperse basket asparagus seeds. We collected basket asparagus seeds from fox (Vulpes vulpes) scats collected in the field, confirmed the viability of these seeds in germination trials, and further documented the germination of basket asparagus seeds from an undisturbed fox scat in situ. These results demonstrate that foxes consume and disperse basket asparagus seeds, and that these seeds are viable and germinate under field conditions. Foxes not only use basket asparagus stands as harbour, but can also facilitate the plant’s dispersal in coastal ecosystems.
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Vanderhoff, Elizabeth Natasha, and Brian Grafton. "Behavior of tamarins, tanagers and manakins foraging in a strangler fig (Ficus sp.) in Suriname, South America: implications for seed dispersal." Biota Neotropica 9, no. 3 (September 2009): 419–23. http://dx.doi.org/10.1590/s1676-06032009000300039.

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The behavior of foragers can directly affect the dispersal of seeds. Strangler figs are keystone resources throughout the tropics and are important resources for both primates and birds. We examined the foraging behavior of golden-handed tamarins and four bird species in a strangler fig to see how these behaviors might affect the dispersal of fig seeds. Tamarins removed fruit at a faster rate than did any of the bird species examined. Additionally, tamarins tended to swallow figs whole whereas birds tended to drop figs once they were processed. Tamarins visiting fig trees ingest large quantities of fig seeds that may be deposited throughout the forest. Birds on the other hand tended to slowly process fruits near the fig tree and drop processed fruit containing large quantities of seeds. Future studies need to be conducted to ascertain differences in post dispersal seed fate.
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Black, Michael. "Darwin and seeds." Seed Science Research 19, no. 4 (December 2009): 193–99. http://dx.doi.org/10.1017/s0960258509990171.

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AbstractIn 2009, the bicentenary of Charles Darwin's birth on 12 February 1809 is being celebrated. For seed scientists, celebrations of the contributions of the great biologist should also mark his involvement with seeds. Darwin was interested in seeds, particularly in their role in dispersal and distribution of plant species over long distances. His studies of seeds, laid down in several books and articles, contributed to the development of his ideas on evolution and the distribution of living organisms on the planet. In this review, the place of seeds in Darwin's work is surveyed and it is shown how he referred to them to support and illustrate some of his most important ideas.
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Reiserer, Randall S., Gordon W. Schuett, and Harry W. Greene. "Seed ingestion and germination in rattlesnakes: overlooked agents of rescue and secondary dispersal." Proceedings of the Royal Society B: Biological Sciences 285, no. 1872 (February 7, 2018): 20172755. http://dx.doi.org/10.1098/rspb.2017.2755.

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Seed dispersal is a key evolutionary process and a central theme in the population ecology of terrestrial plants. The primary producers of most land-based ecosystems are propagated by and maintained through various mechanisms of seed dispersal that involve both abiotic and biotic modes of transportation. By far the most common biotic seed transport mechanism is zoochory, whereby seeds, or fruits containing them, are dispersed through the activities of animals. Rodents are one group of mammals that commonly prey on seeds (granivores) and play a critical, often destructive, role in primary dispersal and the dynamics of plant communities. In North America, geomyid, heteromyid and some sciurid rodents have specialized cheek pouches for transporting seeds from plant source to larder, where they are often eliminated from the pool of plant propagules by consumption. These seed-laden rodents are commonly consumed by snakes as they forage, but unlike raptors, coyotes, bobcats, and other endothermic predators which eat rodents and are known or implicated to be secondary seed dispersers, the role of snakes in seed dispersal remains unexplored. Here, using museum-preserved specimens, we show that in nature three desert-dwelling rattlesnake species consumed heteromyids with seeds in their cheek pouches. By examining the entire gut we discovered, furthermore, that secondarily ingested seeds can germinate in rattlesnake colons. In terms of secondary dispersal, rattlesnakes are best described as diplochorous. Because seed rescue and secondary dispersal in snakes has yet to be investigated, and because numerous other snake species consume granivorous and frugivorous birds and mammals, our observations offer direction for further empirical studies of this unusual but potentially important channel for seed dispersal.
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Dissertations / Theses on the topic "Seeds – Dispersal – Longitudinal studies"

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Pacey, Carol. "Fruiting strategies of the woody vine Parthenocissus quinquefolia." 1985. http://hdl.handle.net/2097/27516.

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Books on the topic "Seeds – Dispersal – Longitudinal studies"

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GUTSHOP '84 (1984 Pacific Grove, Calif.). Contemporary studies on fish feeding: The proceedings of GUTSHOP '84 : papers from the fourth workshop on fish food habits held at the Asilomar Conference Center, Pacific Grove, California, U.S.A., December 2-6, 1984. Dordrecht: W. Junk Publishers, 1986.

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Taylor, Clark. Seeds of Freedom: Liberating Education in Guatemala. Routledge, 2014.

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Feather, N. T. Historical Background to Research on Job Loss, Unemployment, and Job Search. Edited by Ute-Christine Klehe and Edwin van Hooft. Oxford University Press, 2014. http://dx.doi.org/10.1093/oxfordhb/9780199764921.013.001.

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This chapter provides a selective review of past research on job loss, unemployment, and job search up to the beginning of the 1990s. The Great Depression studies in the 1930s at Marienthal by Jahoda and colleagues and by Bakke at Greenwich and New Haven are described, along with other research at the time. These early studies sowed the seeds for subsequent research programs in England, Europe, and Australia; the theories that emerged from this early and later research are described. They include stage theory, deprivation theory, agency theory, and vitamin theory. Other more general approaches—such as stress and coping models and expectancy-value theory—are also described as relevant to the unemployment experience. The historical review provides lessons about the importance of using a variety of methodologies that include descriptive field research, survey and questionnaire studies, longitudinal research, and research across cultures. It also suggests that progress will involve the application of midrange theories about work, paid employment, and unemployment targeted to particular issues such as psychological well-being, health-related problems, social and family effects, and job-search behavior.
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Book chapters on the topic "Seeds – Dispersal – Longitudinal studies"

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Greg Murray, K., and Sharon Kinsman. "Plant-Animal Interactions." In Monteverde. Oxford University Press, 2000. http://dx.doi.org/10.1093/oso/9780195095609.003.0014.

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The term “plant-animal interactions” includes a diverse array of biologically important relationships. Plant-herbivore relationships (in which an animal feeds on whole plants or parts of them) are examples of exploitation, because one species benefits from the interaction while the other suffers. Plant-pollinator and plant-seed disperser relationships (in which animals disperse pollen or seeds, usually in return for a food reward) are examples of mutualisms because they are beneficial to both parties. Another class of plant-animal mutualisms involves plants that provide nesting sites and/or food rewards to ants, which often protect the plant from herbivores or competing plants. Plantpollinator and plant-seed disperser mutualisms probably originated as cases of exploitation of plants by animals (Thompson 1982, Crepet 1983, Tiffney 1986). Many of the distinctive plant structures associated with animal-mediated pollen and seed dispersal (e.g., flowers, nectaries, attractive odors, fleshy fruit pulp, and thickened seed coats) presumably evolved to attract consumers of floral or seed resources while preventing them from digesting the pollen or seeds. mutualisms in structuring ecological communities. Competition and predator-prey interactions were more common subjects. Botanists had described the characteristics of the plant and animal players in pollination and seed dispersal mutualisms (Knuth 1906, 1908, 1909, Ridley 1930, van der Pijl 1969, Faegri and van der Pijl 1979), but these descriptive works did not fully examine plant-animal mutualisms in the context of communities. The opportunity to work in the neotropics, facilitated by the Organization for Tropical Studies (OTS), the Smithsonian Tropical Research Institute (STRI), and other institutions, attracted the attention of temperate-zone ecologists to the mutualisms that are much more conspicuous components of tropical systems than of temperate ones (Wheelwright 1988b). Plant-pollinator interactions have attracted more attention in Monteverde than plant-frugivore interactions, and plant-herbivore interactions remain conspicuously understudied. This imbalance probably reflects the interests of those who first worked at Monteverde and later returned with their own students, rather than differences in the significance of the interactions at Monteverde or elsewhere. Aside from a few studies of herbivory in particular species (e.g., Peck, “Agroecology of Prosapia,”), even basic surveys remain to be done.
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