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Journal articles on the topic 'Biotic communites'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

NINGSIH, SRI WAHYU, Achyani Achyani, and Handoko Santoso. "FAKTOR BIOTIK DAN ABIOTIK YANG MENDUKUNG KERAGAMAN TUMBUHAN PAKU(Pteridophyta) DI KAWASAN HUTAN GISTING PERMAI KABUPATEN TANGGAMUS LAMPUNG." BIOLOVA 2, no. 1 (2021): 64–71. http://dx.doi.org/10.24127/biolova.v2i1.293.

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ABSTRACT: Tumbuh suburnya Pteridophyta di Kawasan Hutan Gisting Permai Kecamatan Gisting Kabupaten Tanggamus sangat dipengaruhi oleh faktor biotik dan abiotik. Faktor biotik meliputi semua kehidupan makhluk hidup di bumi baik individu, populasi dan komunitas yang di dalamnya termasuk jumlah inang Pteridophyta yang banyak, sedangkan faktor abiotik meliputi seluruh faktor-faktor non hidup dari suatu kondisi lingkungan seperti cahaya matahari, suhu, air, dan tanah, ketinggian. Faktor-faktor abiotik ini tidak hanya menyediakan energi dan materi penting, tetapi juga mempunyai peranan dalam menentuk

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2

Bennett, Bradley C., S. Kawano, J. H. Connell, and T. Hidaka. "Evolution and Coadaptation in Biotic Communities." Brittonia 42, no. 1 (1990): 11. http://dx.doi.org/10.2307/2807020.

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3

Permogorskiy, M. S. "Competitive intransitivity among species in biotic communities." Biology Bulletin Reviews 5, no. 3 (2015): 213–19. http://dx.doi.org/10.1134/s2079086415030068.

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4

Stepniewska, S., and M. Mańka. "Biotic relations between Rhizoctonia solani (damping-off pathogen) and soil fungal communities from forest nursery." Plant Protection Science 38, SI 1 - 6th Conf EFPP 2002 (2002): 235–38. http://dx.doi.org/10.17221/10456-pps.

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In forest nursery Wronczyn (central-west Poland) the occurrence of Scots pine (Pinus sylvestris L.) seedlings damping-off<br />caused by Rhizoctonia solani Kühn is connected with a strong supporting effect of soil fungi community on R. solani.<br />Both the soil fungi community isolated in June and in October 1999 supported the pathogen growth to considerable extent.<br />In both months the support was bigger in the case of more severe isolate of the pathogen.

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5

Schmid, Rudolf, David E. Brown, and Charles H. Lowe. "Biotic Communities: Southwestern United States and Northwestern Mexico." Taxon 44, no. 4 (1995): 659. http://dx.doi.org/10.2307/1223522.

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6

Warwick, R., M. J. S. Tevesz, and P. L. McCall. "Biotic Interactions in Recent and Fossil Benthic Communities." Journal of Applied Ecology 22, no. 1 (1985): 293. http://dx.doi.org/10.2307/2403353.

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7

Fraser, Danielle, and S. Kathleen Lyons. "Biotic interchange has structured Western Hemisphere mammal communities." Global Ecology and Biogeography 26, no. 12 (2017): 1408–22. http://dx.doi.org/10.1111/geb.12667.

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8

Hagberg, Jacob, Niclas Jonzén, Per Lundberg, and Jörgen Ripa. "Uncertain biotic and abiotic interactions in benthic communities." Oikos 100, no. 2 (2003): 353–61. http://dx.doi.org/10.1034/j.1600-0706.2003.12138.x.

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9

Semenchenko, Vitaliy P., Vladimir I. Razlutskij, Irina Yu Feniova, and Denis N. Aibulatov. "Biotic relations affecting species structure in zooplankton communities." Hydrobiologia 579, no. 1 (2006): 219–31. http://dx.doi.org/10.1007/s10750-006-0411-x.

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10

Wang, Yonghui, Xiaxia Niu, Liqing Zhao, et al. "Biotic stability mechanisms in Inner Mongolian grassland." Proceedings of the Royal Society B: Biological Sciences 287, no. 1928 (2020): 20200675. http://dx.doi.org/10.1098/rspb.2020.0675.

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Biotic mechanisms associated with species diversity are expected to stabilize communities in theoretical and experimental studies but may be difficult to detect in natural communities exposed to large environmental variation. We investigated biotic stability mechanisms in a multi-site study across Inner Mongolian grassland characterized by large spatial variations in species richness and composition and temporal fluctuations in precipitation. We used a new additive-partitioning method to separate species synchrony and population dynamics within communities into different species-abundance grou

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11

Tóth, Anikó B., S. Kathleen Lyons, W. Andrew Barr, et al. "Reorganization of surviving mammal communities after the end-Pleistocene megafaunal extinction." Science 365, no. 6459 (2019): 1305–8. http://dx.doi.org/10.1126/science.aaw1605.

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Large mammals are at high risk of extinction globally. To understand the consequences of their demise for community assembly, we tracked community structure through the end-Pleistocene megafaunal extinction in North America. We decomposed the effects of biotic and abiotic factors by analyzing co-occurrence within the mutual ranges of species pairs. Although shifting climate drove an increase in niche overlap, co-occurrence decreased, signaling shifts in biotic interactions. Furthermore, the effect of abiotic factors on co-occurrence remained constant over time while the effect of biotic factor

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12

Devictor, Vincent, Romain Julliard, Joanne Clavel, Frédéric Jiguet, Alexandre Lee, and Denis Couvet. "Functional biotic homogenization of bird communities in disturbed landscapes." Global Ecology and Biogeography 17, no. 2 (2008): 252–61. http://dx.doi.org/10.1111/j.1466-8238.2007.00364.x.

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13

ROONEY, THOMAS P., SHANNON M. WIEGMANN, DAVID A. ROGERS, and D. M. WALLER. "Biotic Impoverishment and Homogenization in Unfragmented Forest Understory Communities." Conservation Biology 18, no. 3 (2004): 787–98. http://dx.doi.org/10.1111/j.1523-1739.2004.00515.x.

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14

Piehler, Michael F. "Pollution Impacts on Marine Biotic Communities. Michael J. Kennish." Quarterly Review of Biology 75, no. 3 (2000): 333. http://dx.doi.org/10.1086/393559.

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15

Power, Mary E., R. Jean Stout, Colbert E. Cushing, et al. "Biotic and Abiotic Controls in River and Stream Communities." Journal of the North American Benthological Society 7, no. 4 (1988): 456–79. http://dx.doi.org/10.2307/1467301.

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16

Kratina, Pavel, and Monika Winder. "Biotic invasions can alter nutritional composition of zooplankton communities." Oikos 124, no. 10 (2015): 1337–45. http://dx.doi.org/10.1111/oik.02240.

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17

Ricks, Kevin D., and Roger T. Koide. "Biotic filtering of endophytic fungal communities in Bromus tectorum." Oecologia 189, no. 4 (2019): 993–1003. http://dx.doi.org/10.1007/s00442-019-04388-y.

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18

Rozenberg, G. S. "ONCE AGAIN ABOUT THE BIOTIC COMMUNITY." ÈKOBIOTEH 3, no. 3 (2020): 472–77. http://dx.doi.org/10.31163/2618-964x-2020-3-3-472-477.

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Community ecology studies the patterns of changes in biodiversity, species structure, and the number of individual populations in a spatial and temporal aspect. The article discusses some modern theories of community ecology (neutral theory, patch dynamics, M. Vellend's ideas about four basic processes in communities similar to processes of population genetics [selection, drift, dispersal, selection], etc.).

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19

BRASHER, ANNE M. D. "Impacts of Human Disturbances on Biotic Communities in Hawaiian Streams." BioScience 53, no. 11 (2003): 1052. http://dx.doi.org/10.1641/0006-3568(2003)053[1052:iohdob]2.0.co;2.

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20

Muthukrishnan, Ranjan, and Daniel J. Larkin. "Invasive species and biotic homogenization in temperate aquatic plant communities." Global Ecology and Biogeography 29, no. 4 (2020): 656–67. http://dx.doi.org/10.1111/geb.13053.

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21

Houle, Gilles, and Donald L. Phillips. "Seed Availability and Biotic Interactions in Granite Outcrop Plant Communities." Ecology 70, no. 5 (1989): 1307–16. http://dx.doi.org/10.2307/1938190.

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22

Helmens, Karin F., Christos Katrantsiotis, J. Sakari Salonen, et al. "Warm summers and rich biotic communities during N-Hemisphere deglaciation." Global and Planetary Change 167 (August 2018): 61–73. http://dx.doi.org/10.1016/j.gloplacha.2018.05.004.

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23

Liu, Ping, Shaolin Xu, Jianhao Lin, Huiming Li, Qiuqi Lin, and Bo-Ping Han. "Urbanization increases biotic homogenization of zooplankton communities in tropical reservoirs." Ecological Indicators 110 (March 2020): 105899. http://dx.doi.org/10.1016/j.ecolind.2019.105899.

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24

Kremer, Laura Pioli, and Rosana Moreira da Rocha. "The biotic resistance role of fish predation in fouling communities." Biological Invasions 18, no. 11 (2016): 3223–37. http://dx.doi.org/10.1007/s10530-016-1210-6.

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25

Zhang, Youzheng, Steven C. Pennings, Bo Li, and Jihua Wu. "Biotic homogenization of wetland nematode communities by exoticSpartina alterniflorain China." Ecology 100, no. 4 (2019): e02596. http://dx.doi.org/10.1002/ecy.2596.

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26

Iannone III, Basil V., Kevin M. Potter, Qinfeng Guo, Insu Jo, Christopher M. Oswalt, and Songlin Fei. "Environmental harshness drives spatial heterogeneity in biotic resistance." NeoBiota 40 (December 4, 2018): 87–105. http://dx.doi.org/10.3897/neobiota.40.28558.

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Ecological communities often exhibit greater resistance to biological invasions when these communities consist of species that are not closely related. The effective size of this resistance, however, varies geographically. Here we investigate the drivers of this heterogeneity in the context of known contributions of native trees to the resistance of forests in the eastern United States of America to plant invasions. Using 42,626 spatially referenced forest community observations, we quantified spatial heterogeneity in relationships between evolutionary relatedness amongst native trees and both

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27

Lawrey, James D. "Biotic Interactions in Lichen Community Development: A Review." Lichenologist 23, no. 3 (1991): 205–14. http://dx.doi.org/10.1017/s0024282991000373.

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AbstractThe extent to which biotic factors (competition, predation/disease, longevity) regulate lichen community development can be addressed by considering a number of general trends expected in higher plant successions and searching for supporting evidence from lichen studies. Four of the most frequently observed (or predicted) trends during succession are that: (1) superior competitors replace poor competitors; (2) ecologically specialized species replace generalists; (3) chemically well-defended species replace poorly-defended species; (4) long-lived species replace ephemeral species. Avai

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28

Hofmann, Richard, Melanie Tietje, and Martin Aberhan. "Diversity partitioning in Phanerozoic benthic marine communities." Proceedings of the National Academy of Sciences 116, no. 1 (2018): 79–83. http://dx.doi.org/10.1073/pnas.1814487116.

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Biotic interactions such as competition, predation, and niche construction are fundamental drivers of biodiversity at the local scale, yet their long-term effect during earth history remains controversial. To test their role and explore potential limits to biodiversity, we determine within-habitat (alpha), between-habitat (beta), and overall (gamma) diversity of benthic marine invertebrates for Phanerozoic geological formations. We show that an increase in gamma diversity is consistently generated by an increase in alpha diversity throughout the Phanerozoic. Beta diversity drives gamma diversi

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29

Morel, Jean Daniel, Rubens Manoel dos Santos, Marco Aurélio Leite Fontes, Paulo Oswaldo Garcia, and Fernanda Maria de Souza. "FLORISTIC COMPARISON BETWEEN TWO TREE COMMUNITIES ASSOCIATED WITH HABITAT DESCRIPTOR VARIABLES." CERNE 21, no. 4 (2015): 601–16. http://dx.doi.org/10.1590/01047760201521041934.

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ABSTRACT The knowledge about the influence of habitat variables is essential to understand the underlying ecological patterns in vegetation. This study compared the floristic composition of two forest communities located in different altitudes. Associated with this comparison, we used a methodology where habitat descriptor variables were scaled and interpreted by the biotic set sampled. We constructed one matrix with scores given to physical, biotic, vegetation, and anthropogenic variables in the field and one matrix with the species sampled and performed multivariate analyses. We found that t

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30

Keehn, Jade E., and Chris R. Feldman. "Disturbance affects biotic community composition at desert wind farms." Wildlife Research 45, no. 5 (2018): 383. http://dx.doi.org/10.1071/wr17059.

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Context The global benefits of increased renewable energy production may come at a cost to local biotic communities and even regional ecosystems. Wind energy developments, in particular, are known to cause bird and bat mortalities, and to fragment habitat for terrestrial vertebrates within developed project areas. Effects on species sensitive to wind turbines (and increased prevalence of species tolerant to this disturbance) might alter community-level patterns of occurrence, with potentially detrimental changes to wildlife habitat and ecosystem health. Aims The present study assessed whether

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31

Beard, Jason M., Natalie A. Moltschaniwskyj, Christine M. Crawford, John A. E. Gibson, and D. Jeff Ross. "Using macrofaunal communities to inform estuarine classification." Marine and Freshwater Research 70, no. 3 (2019): 371. http://dx.doi.org/10.1071/mf17372.

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Worldwide, geomorphological classifications of estuaries are often used to guide the design of monitoring programs and management strategies. However, if classifications do not reflect biotic patterns, the effectiveness of monitoring and management is potentially reduced. In this study, we consider the effectiveness of one classification scheme in describing biotic patterns by examining and comparing spatial variation of macrofaunal assemblages and their relationship with the environment in 12 estuaries of 2 geomorphological types (mesotidal river dominated and permanently open barrier estuari

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32

O'Brien, W. John, Michael Barfield, Neil D. Bettez, et al. "Physical, chemical, and biotic effects on arctic zooplankton communities and diversity." Limnology and Oceanography 49, no. 4part2 (2004): 1250–61. http://dx.doi.org/10.4319/lo.2004.49.4_part_2.1250.

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33

Turner, Kelsey L., Erin F. Abernethy, L. Mike Conner, Olin E. Rhodes, and James C. Beasley. "Abiotic and biotic factors modulate carrion fate and vertebrate scavenging communities." Ecology 98, no. 9 (2017): 2413–24. http://dx.doi.org/10.1002/ecy.1930.

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34

Zhao, Xin-Feng, Yi-Qi Hao, Da-Yong Zhang, and Quan-Guo Zhang. "Local biotic interactions drive species-specific divergence in soil bacterial communities." ISME Journal 13, no. 11 (2019): 2846–55. http://dx.doi.org/10.1038/s41396-019-0477-x.

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35

Dziallas, Claudia, and Hans-Peter Grossart. "Temperature and biotic factors influence bacterial communities associated with the cyanobacteriumMicrocystissp." Environmental Microbiology 13, no. 6 (2011): 1632–41. http://dx.doi.org/10.1111/j.1462-2920.2011.02479.x.

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36

L., K. "Some Other Books of Interest: Evolution and Coadaptation in Biotic Communities." Science 241, no. 4865 (1988): 605–6. http://dx.doi.org/10.1126/science.241.4865.605-b.

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37

Smith, Alexander J., Robert W. Bode, and Gary S. Kleppel. "A nutrient biotic index (NBI) for use with benthic macroinvertebrate communities." Ecological Indicators 7, no. 2 (2007): 371–86. http://dx.doi.org/10.1016/j.ecolind.2006.03.001.

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38

Jones, Devin K., Brian M. Mattes, William D. Hintz, et al. "Investigation of road salts and biotic stressors on freshwater wetland communities." Environmental Pollution 221 (February 2017): 159–67. http://dx.doi.org/10.1016/j.envpol.2016.11.060.

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39

Clarke, J. E., and R. H. V. Bell. "Representation of biotic communities in protected areas: A Malawian case study." Biological Conservation 35, no. 4 (1986): 293–311. http://dx.doi.org/10.1016/0006-3207(86)90091-1.

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40

Fayle, Tom M., and Andrea Manica. "Reducing over-reporting of deterministic co-occurrence patterns in biotic communities." Ecological Modelling 221, no. 19 (2010): 2237–42. http://dx.doi.org/10.1016/j.ecolmodel.2010.06.013.

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41

Avanesyan, Alina. "Should I Eat or Should I Go? Acridid Grasshoppers and Their Novel Host Plants: Potential for Biotic Resistance." Plants 7, no. 4 (2018): 83. http://dx.doi.org/10.3390/plants7040083.

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Novel, non-coevolved associations between introduced plants and native insect herbivores may lead to changes in trophic interactions in native communities, as well as to substantial economic problems. Although some studies in invasion ecology demonstrated that native herbivores can preferentially feed on introduced plants and therefore contribute to the biotic resistance of native communities to plant invasions, the role of acridid grasshoppers as native generalist insect herbivores is largely overlooked. This systematic review aimed to identify patterns of grasshopper feeding preferences for

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42

Espinosa-Reyes, Guillermo, Donaji J. González-Mille, César A. Ilizaliturri-Hernández, et al. "Effect of Mining Activities in Biotic Communities of Villa de la Paz, San Luis Potosi, Mexico." BioMed Research International 2014 (2014): 1–13. http://dx.doi.org/10.1155/2014/165046.

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Mining is one of the most important industrial activities worldwide. During its different stages numerous impacts are generated to the environment. The activities in the region have generated a great amount of mining residues, which have caused severe pollution and health effects in both human population and biotic components. The aim of this paper was to assess the impact of mining activities on biotic communities within the district of Villa de la Paz. The results showed that the concentrations of As and Pb in soil were higher than the national regulations for urban or agricultural areas. Th

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43

Herren, Cristina M. "Disruption of cross-feeding interactions by invading taxa can cause invasional meltdown in microbial communities." Proceedings of the Royal Society B: Biological Sciences 287, no. 1927 (2020): 20192945. http://dx.doi.org/10.1098/rspb.2019.2945.

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The strength of biotic interactions within an ecological community affects the susceptibility of the community to invasion by introduced taxa. In microbial communities, cross-feeding is a widespread type of biotic interaction that has the potential to affect community assembly and stability. Yet, there is little understanding of how the presence of cross-feeding within a community affects invasion risk. Here, I develop a metabolite-explicit model where native microbial taxa interact through both cross-feeding and competition for metabolites. I use this model to study how the strength of biotic

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44

Malanson, George P., Lynn M. Resler, David R. Butler, and Daniel B. Fagre. "Mountain plant communities: Uncertain sentinels?" Progress in Physical Geography: Earth and Environment 43, no. 4 (2019): 521–43. http://dx.doi.org/10.1177/0309133319843873.

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Mountain plant communities are thought to be sensitive to climate change and, thus, able to reveal its effects sooner than others. The status as sentinels of two plant communities are reviewed. Alpine treeline ecotones and alpine vegetation have been observed to respond to climate change in recent decades. The treeline has moved upslope and alpine communities have had some species increase and others decrease. The response for both, however, has been inconsistent if taken as a whole. Problematic factors for this response are outlined for both: abiotic and biotic interactions partially decouple

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45

Darroch, Simon A. F., Erik A. Sperling, Thomas H. Boag, et al. "Biotic replacement and mass extinction of the Ediacara biota." Proceedings of the Royal Society B: Biological Sciences 282, no. 1814 (2015): 20151003. http://dx.doi.org/10.1098/rspb.2015.1003.

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The latest Neoproterozoic extinction of the Ediacara biota has been variously attributed to catastrophic removal by perturbations to global geochemical cycles, ‘biotic replacement’ by Cambrian-type ecosystem engineers, and a taphonomic artefact. We perform the first critical test of the ‘biotic replacement’ hypothesis using combined palaeoecological and geochemical data collected from the youngest Ediacaran strata in southern Namibia. We find that, even after accounting for a variety of potential sampling and taphonomic biases, the Ediacaran assemblage preserved at Farm Swartpunt has significa

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46

Srinivasan, Umesh, Paul R. Elsen, Morgan W. Tingley, and David S. Wilcove. "Temperature and competition interact to structure Himalayan bird communities." Proceedings of the Royal Society B: Biological Sciences 285, no. 1874 (2018): 20172593. http://dx.doi.org/10.1098/rspb.2017.2593.

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Longstanding theory predicts that competitive interactions set species' range limits in relatively aseasonal, species-rich regions, while temperature limits distributions in more seasonal, species-poor areas. More recent theory holds that species evolve narrow physiological tolerances in aseasonal regions, with temperature being an important determining factor in such zones. We tested how abiotic (temperature) and biotic (competition) factors set range limits and structure bird communities along strong, opposing, temperature-seasonality and species-richness gradients in the Himalayas, in two r

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47

Wehenkel, Chr, F. Bergmann, and H. R. Gregorius. "Genotype-Species Interactions in Neighbourhoods of Forest Tree Communities." Silvae Genetica 56, no. 1-6 (2007): 101–10. http://dx.doi.org/10.1515/sg-2007-0016.

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Abstract Studies on plant communities of various annual species suggest that there are particular biotic interactions among individuals from different species which could be the basis for long-term species coexistence. In the course of a large survey on species-genetic diversity relationships in several forest tree communities, it was found that statistically significant differences exist among isozyme genotype frequencies of conspecific tree groups, which differ only by species identity of their neighbours. Based on a specific measure, the association of the neighbouring species with the geno

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48

Vázquez-Reyes, Leopoldo D., María del Coro Arizmendi, Héctor O. Godínez-Álvarez, and Adolfo G. Navarro-Sigüenza. "Directional effects of biotic homogenization of bird communities in Mexican seasonal forests." Condor 119, no. 2 (2017): 275–88. http://dx.doi.org/10.1650/condor-16-116.1.

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49

Dinara, Dairova, Ostrovskaya Elena, Kurapov Aleksei, and Umerbaeva Roza. "CHANGES IN BIOTIC COMMUNITIES OF THE NORTHERN CASPIAN IN A CHANGING CLIMATE." Астраханский вестник экологического образования 19, no. 6 (2020): 97–107. http://dx.doi.org/10.36698/2304-5957-2020-19-6-97-107.

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50

Worthen, Wade B., Sara Mayrose, and R. Gayle Wilson. "Complex Interactions between Biotic and Abiotic Factors: Effects on Mycophagous Fly Communities." Oikos 69, no. 2 (1994): 277. http://dx.doi.org/10.2307/3546148.

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