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Journal articles on the topic 'Biotic and abiotc'

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1

OLIVEIRA, FÁBIO H. P. C. DE, ANDRÉ L. S. CAPELA E. ARA, CESAR H. P. MOREIRA, OSMAN O. LIRA, MARIA DO ROSÁRIO F. PADILHA, and NEIDE K. S. SHINOHARA. "Seasonal changes of water quality in a tropical shallow and eutrophic reservoir in the metropolitan region of Recife (Pernambuco-Brazil)." Anais da Academia Brasileira de Ciências 86, no. 4 (December 2014): 1863–72. http://dx.doi.org/10.1590/0001-3765201420140128.

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This study investigated the water quality in an urban eutrophic reservoir in Northeastern Brazil, considering the influence of seasonality. Monthly, samples were collected in the sub-surface reservoir. The following abiotic variables were analyzed: temperature, pH, dissolved oxygen, apparent color, turbidity, conductivity, fluoride, total nitrogen, chlorides, total dissolved solids, total hardness, iron, copper, manganese, aluminum, chlorophyll-a and phaeophytin. Total and thermotolerant coliforms were analyzed according to APHA (2012). Cyanobacteria density was quantified through its biomass. The data were analyzed using one- way ANOVA and Pearson correlation test. Higher values mean phytoplankton biomass (26.3mm3.L–1) occurred in the dry season, especially Planktothrix agardhii and Geiterinema amphibium, which occurred in 100% of samples. High trophic state index was detected throughout the year. Seasonality exerted some influence on both biotic and abiotc variables, leading to changes in water quality of the reservoir.
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Kumari, Diksha, and Dipjyoti Chakraborty. "Drought stress mitigation in Vigna radiata by the application of root-nodulating bacteria." Plant Science Today 4, no. 4 (December 4, 2017): 209–12. http://dx.doi.org/10.14719/pst.2017.4.4.343.

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Plant growth promoting rhizobacteria (PGPR) facilitates plant growth and are of potential use as bio-fertilizer. Pulses are an important protein source in the vegetarian diet and being legumes harbour members of the Rhizobiaceae that form symbiotic relationships and nodules involved in nitrogen fixation. Vigna radiata is one such pulse crop popular in India. Nodulating bacteria were also found to mitigate biotic and abiotc stress and may be used as an alternative to chemical fertilizer for a sustainable agriculture. Here, we review rhizobial species isolated from V. radiata that have offered an efficient drought stress tolerance.
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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 (February 26, 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 menentukan tumbuhan-tumbuhan dan hewan-hewan yang mampu berada disuatu tempat tertentu sesuai dengan habitatnya. Metode yang digunakan dalam kajian ini adalah berupa kajian kualitatif. Artikel ini dikaji dengan menyatukn referensi dari berbagai sumber diantaranya berasal dari jurnal, buku, arsip dokumen pekon Gisting Permai, dan internet. Pengumpulan data diperoleh dengan menggunakan berbagai referensi yang dikumpulkan sebanyak mungkin yang berkaitan dengn faktor biotik dan abiotik pertumbuhan tumbuhan paku. Kata kunci: Biotik, Abiotik, Pteridophyta. ABSTRACT: The growth of Pteridophyta in the Permai Gisting Forest Area, Gisting Sub-District Tanggamus Regency was strongly influenced by biotic and abiotic factors. Biotic factors include all the life of living things on earth both individuals, populations and communities which include a large number of Pteridophyta hosts, while abiotic factors include all non-living factors of an environmental condition such as sunlight, temperature, water, and soil, height. These abiotic factors not only provide important energy and material, but also had a role in determining plants and animals that which are able to be in a certain place according to their habitat. The method used in this study is a qualitative study. This article was reviewed by citing references from various sources including journals, books, Gisting Permai archive documents, and the internet. The data collection was obtained by using as many references as possible related to biotic and abiotic factors for fern growth. Key word: biotic, abiotic, Pteridophyta.
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Aryanti, Nirmala Ayu, Febri Arif Cahyo Wibowo, Mahidi Mahidi, Frita Kusuma Wardhani, and I. Komang Tri Wijaya Kusuma. "Hubungan Faktor Biotik dan Abiotik Terhadap Keanekaragaman Makrobentos di Hutan Mangrove Kabupaten Lombok Barat." Jurnal Kelautan Tropis 24, no. 2 (May 19, 2021): 185–94. http://dx.doi.org/10.14710/jkt.v24i2.10044.

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High human activity around the coastal area will affect the mangrove ecosystem and the biota such as macrobenthos. Benthic diversity can reflect conditions of mangrove ecosystem, that slow growth and sensitive to environmental changes. This study aims to determine the influence of biotic and abiotic environments on the macrobenthos in Cendi Manik Village, Sekotong District, West Lombok Regency, West Nusa Tenggara. Data collection of macrobenthos, biotic and abiotic environments in natural and rehabilitation mangrove, then the diversity species of macrobenthos with biotic and abiotic environmental variables were analyzed multiple regression. The most dominant vegetations are Rhizophora mucronata Lam and Avicennia marina Forssk. The diversity index for macrobenthos is low (H’ 1,207) in natural and rehabilitation mangrove. Macrobenthos between two location have high similarity with 84,6%. The result of multiple regression test showed that most influencing of macrobenthos were mud thickness and brightness. Aktivitas manusia yang tinggi sekitar kawasan pesisir akan mempengaruhi ekosistem mangrove dan biota di dalamnya seperti makrobentos. Keanekaragaman bentos dapat mampu mencerminkan kondisi ekosistem mangrove, pertumbuhan yang lambat dan sensitif terhadap perubahan lingkungan. Penelitian ini bertujuan untuk mengetahui hubungan lingkungan biotik dan abiotik terhadap makrobentos yang ada di Desa Cendi Manik Kecamatan Sekotong Kabupaten Lombok Barat Nusa Tenggara Barat. Pengumpulan data makrobentos, biotik dan abiotik lingkungan pada hutan mangrove alam dan rehabilitasi, kemudian keanekaragaman jenis makrobentos dengan variabel lingkungan biotik dan abiotik dianalisis regresi berganda. Jenis vegetasi yang paling mendominasi adalah jenis Rhizophora mucronata Lam dan Avicennia marina Forssk. Keanekaragaman jenis makrobentos termasuk dalam kategori rendah (H’ 1,207) di hutan mangrove alam dan rehabilitasi. Jenis makrobentos antara dua lokasi tersebut memiliki kemiripan yang tinggi yaitu 84,6 %. Uji regresi berganda diperoleh variabel lingkungan yang paling berpengaruh pada keanekaragaman jenis makrobentos adalah ketebalan lumpur dan kedalaman kecerahan air.
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5

Demaria, D., D. Valentino, A. Matta, and F. Cardinale. "Cross-protection mechanisms between biotic and abiotic stresses in plants." Plant Protection Science 38, SI 2 - 6th Conf EFPP 2002 (December 31, 2017): 490–93. http://dx.doi.org/10.17221/10532-pps.

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In order to investigate cross-protection mechanisms between stresses of different origins, greenhouse experiments were conducted to determine whether resistance levels to the fungal pathogen P. capsici were affected on wounded plants. To this purpose, tomato roots were wounded at 24h-intervals and allowed to age for up to 7 days before inoculation. Data from preliminary experiments indicate first (0–48 h old wounds) an increase in disease severity in wounded as compared to unwounded tomato plants infected with P. capsici. Then, as the wounds age, disease severity decreases to the point that plants wounded 3 days before inoculation are less susceptible than nonwounded plants. Here, with the use of tomato mutant lines, we suggest the involvement of ethylene (C<sub>2</sub>H<sub>4</sub>) and jasmonates (Ja) in the development of these responses towards P. capsici upon wounding of tomato plants.
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6

Lytle, David A. "Biotic and abiotic effects of flash flooding in a montane desert stream." Fundamental and Applied Limnology 150, no. 1 (November 23, 2000): 85–100. http://dx.doi.org/10.1127/archiv-hydrobiol/150/2000/85.

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7

Sugisaki, Ryuichi, and Koichi Mimura. "Mantle hydrocarbons: Abiotic or biotic?" Geochimica et Cosmochimica Acta 58, no. 11 (June 1994): 2527–42. http://dx.doi.org/10.1016/0016-7037(94)90029-9.

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8

Suzuki, Nobuhiro, Rosa M. Rivero, Vladimir Shulaev, Eduardo Blumwald, and Ron Mittler. "Abiotic and biotic stress combinations." New Phytologist 203, no. 1 (April 11, 2014): 32–43. http://dx.doi.org/10.1111/nph.12797.

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9

Rema, I. Nyoman, and Ida Bagus Rai Putra. "SUMBER DAYA ALAM SEBAGAI MEDIA LITERASI DI BALI." Forum Arkeologi 31, no. 1 (June 29, 2018): 1. http://dx.doi.org/10.24832/fa.v31i1.462.

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Bali has an abundant cultural heritage, one of which is a literary culture of ancient manuscripts, written on media taken from nature, preserved, shaped, to a script. The purpose of this research is to understand the utilization of natural resources as media literacy in Bali. The data of this research were collected through direct observation, interview, and literature study. The result of this research is the utilization of biotic resources such as palm leaves, intaran tree bark, yam gadung, spices of isin rong wayah, coconut base bark, aubergine leaf, and candlenut. In addition to the utilization of biotic resources are also utilized abiotic resources such as clean water, sunlight, salt, wind and soot. Based on the results of the analysis it can be seen that the media literacy in Bali is very dependent on nature, because this function will affect the environmental sustainability, and grow a sense of appreciation, then trying to create harmony to nature. Bali memiliki warisan budaya yang melimpah, salah satunya adalah budaya literasi berupa naskah kuno, ditulis pada media dari alam, diawetkan, dibentuk, hingga menjadi naskah. Tujuan penelitian ini adalah untuk mengetahui pemanfaatan sumber daya alam daun lontar dan prosesnya sebagai bahan pembuatan media literasi serta proses penulisan literasi di Bali. Data penelitian dikumpulkan melalui observasi langsung, wawancara, dan studi pustaka. Hasil penelitian berupa pemanfaatan sumber daya biotik; daun lontar, kulit pohon intaran, ubi gadung, rempah-rempah yakni isin rong wayah, kulit pangkal pohon kelapa, daun terong, dan kemiri. Selain pemanfaatan sumber daya biotik juga dimanfaatkan sumber daya abiotik; air bersih, sinar matahari, garam, angin dan jelaga. Kesimpulan penelitian ini menunjukkan bahwa media literasi di Bali sangat bergantung kepada alam, karena fungsi ini berdampak kepada kelestarian lingkungan, dan tumbuh rasa menghargai untuk menciptakan keharmonisan terhadap alam. Kata kunci: sumber daya alam, media literasi, bali.
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10

Antonyak, H. L., N. E. Panas, O. I. Pershyn, A. I. Polishchuk, and N. K. Hoyvanovych. "Iodine in abiotic and biotic environments." Studia Biologica 12, no. 2 (2018): 117–34. http://dx.doi.org/10.30970/sbi.1202.567.

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11

Kuznetsov, Yuriy. "A GREEN LIGHT FOR MARINE BIOTECHNOLOGY IN FISHERIES." Fisheries 2020, no. 3 (June 16, 2020): 19–25. http://dx.doi.org/10.37663/0131-6184-2020-3-19-25.

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Bionic principles of technologies invention copying the organization of living systems on different levels give a good example of cognitive science application for nature management to achieve the synergistic effect. The fisheries still uses the mechanistic approach and extensive principles to problem solving what is leading to the deep technological crisis. To change the existing catches methodology a modern hydrobionics means are proposed. They allow to explain relations between biotic and abiotic factors in catches dynamics, the nature of problems and stacks in numerous prospective themes in fisheries.
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12

Schwarz, Christian, Joost Brinkkemper, and Gerben Ruessink. "Feedbacks between Biotic and Abiotic Processes Governing the Development of Foredune Blowouts: A Review." Journal of Marine Science and Engineering 7, no. 1 (December 28, 2018): 2. http://dx.doi.org/10.3390/jmse7010002.

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This paper reviews the initiation, development, and closure of foredune blowouts with focus on biotic-abiotic interactions. There is a rich body of literature describing field measurements and model simulations in and around foredune blowouts. Despite this abundance of data there is no conceptual framework available linking biotic and abiotic observations to pathways of blowout development (e.g., erosional blowout growth or vegetation induced blowout closure). This review identifies morphological and ecological processes facilitating the transition between blowout development stages and sets them in the context of existing conceptual frameworks describing biotic-abiotic systems. By doing so we are able to develop a new conceptual model linking blowout development to the dominance of its governing processes. More specifically we link blowout initiation to the dominance of abiotic (physical) processes, blowout development to the dominance of biotic-abiotic (bio-geomorphological) processes and blowout closure to the dominance of biotic (ecological) processes. Subsequently we identify further steps to test the proposed conceptual model against existing observations and show possibilities to include it in numerical models able to predict blowout development for various abiotic and biotic conditions.
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13

McNab, W. Henry, and Tara L. Keyser. "A vegetative index of stand productivity based on tree inventory for predicting oak site index in the Central Hardwood Region." Canadian Journal of Forest Research 50, no. 8 (August 2020): 760–73. http://dx.doi.org/10.1139/cjfr-2019-0412.

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Models for prediction of site index (SI) typically include only abiotic causal variables (e.g., soil) and lack biotic response variables (e.g., vegetation), which could exhibit greater sensitivity to important environmental factors affecting tree height growth. Our study objective was to evaluate Whittaker’s moisture condition index (MCI) (R.H. Whittaker. 1956. Ecol. Monogr. 26: 1–80) as a potential biotic variable for inclusion with conventional abiotic variables in oak (Quercus L.) SI prediction models. The MCI is the sum of relative abundances of inventoried plot tree species weighted by their moisture affinity classification. We compared regression parameters of conventional base models including only abiotic variables with exploratory models configured with abiotic variables and MCI for explaining variation of SI. The best abiotic model included only aspect. When MCI was included in the abiotic model, aspect became insignificant, resulting in a single-variable biotic model that accounted for increased SI variation. The MCI biotic model remained significant when tested with independent data from a distant location. The MCI is easily calculated using plot inventory data, and with further evaluation, it may be confirmed as a useful biotic variable in combination with abiotic soil and topographic variables for prediction of oak SI.
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Riedler, Patricia, Christian Baranyi, Thomas Hein, Susanne Keckeis, and Michael Schagerl. "Abiotic and biotic control of phytoplankton development in dynamic side-arms of the River Danube." River Systems 16, no. 4 (October 10, 2006): 577–94. http://dx.doi.org/10.1127/lr/16/2006/577.

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Margalef-Marti, Rosanna, Raul Carrey, Albert Soler, and Neus Otero. "Isotopic fractionation associated to nitrate attenuation by ferrous iron containing minerals." E3S Web of Conferences 98 (2019): 12013. http://dx.doi.org/10.1051/e3sconf/20199812013.

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Biotic and abiotic laboratory experiments of nitrate and nitrite reduction by Fe-containing minerals were performed and the isotopic fractionation of the different reactions was calculated in order to determine whether it is possible to distinguish biotic and abiotic reactions involving N compounds. Results of biotic experiments showed nitrate reduction up to 96 % with transient NO2- accumulation and no significant N2O production. No significant nitrate attenuation was observed in abiotic nitrate reduction experiments. Abiotic experiments of nitrite reduction showed a rapid decrease in nitrite concentrations in those experiments with added Fe2+ coupled with a significant N2O production. Preliminary results of the N and O isotopic fractionation of the biotic experiments of nitrate reduction show differences in the ε15NNO3 and ε18ONO3 when different minerals were added. The abiotic experiments of nitrite reduction contrarily, showed similar ε15NNO2 in all the experiments.
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Kapoor, Rahul, and Tarvinder Pal Singh. "Breeding Oats for Biotic and Abiotic Stresses." International Journal of Current Microbiology and Applied Sciences 9, no. 1 (January 10, 2020): 274–83. http://dx.doi.org/10.20546/ijcmas.2020.901.032.

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17

Main, Christopher L., Lawrence E. Steckel, Robert M. Hayes, and Thomas C. Mueller. "Biotic and abiotic factors influence horseweed emergence." Weed Science 54, no. 6 (November 2006): 1101–5. http://dx.doi.org/10.1614/ws-06-026r1.1.

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18

Radulovic, Zlatan, Dragan Karadzic, Ivan Milenkovic, Aleksandar Lucic, Ljubinko Rakonjac, Zoran Miletic, and Radojica Pizurica. "Declining of forests - biotic and abiotic stress." Bulletin of the Faculty of Forestry, suppl. (2014): 71–88. http://dx.doi.org/10.2298/gsf14s1071r.

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During the last several years, a significant decline of different forests in Serbia was recorded. The decline is more widespread in conifer stands, but occurence of decline was recorded in broadleaved forest stands as well. These declines are the result of abiotic, biotic and anthropogenic factors. According to the studies performed so far in Serbia, the predisposing factor were droughts during the 2012 and 2013 vegetation periods that caused physiological weakness of the trees. Among the biotic factors, the most important are fungi (mainly root rot, but rot fungi, and needle diseases) and insects (bark beetles in conifer species) and defoliators in broadleaved species).
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19

Decker, Kimberly H., Donald W. Duszynski, and Michael J. Patrick. "BIOTIC AND ABIOTIC EFFECTS ON ENDOPARASITES INFECTINGDIPODOMYSANDPEROGNATHUSSPECIES." Journal of Parasitology 87, no. 2 (April 2001): 300–307. http://dx.doi.org/10.1645/0022-3395(2001)087[0300:baaeoe]2.0.co;2.

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Peck, Scott, and Ron Mittler. "Plant signaling in biotic and abiotic stress." Journal of Experimental Botany 71, no. 5 (March 12, 2020): 1649–51. http://dx.doi.org/10.1093/jxb/eraa051.

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Heinz, Jacob, and Dirk Schulze-Makuch. "Thiophenes on Mars: Biotic or Abiotic Origin?" Astrobiology 20, no. 4 (April 1, 2020): 552–61. http://dx.doi.org/10.1089/ast.2019.2139.

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22

Jiang, Chao, Xinyue Zhang, Peng Gao, Qiong Chen, and Michael Snyder. "Decoding personal biotic and abiotic airborne exposome." Nature Protocols 16, no. 2 (January 13, 2021): 1129–51. http://dx.doi.org/10.1038/s41596-020-00451-8.

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23

Raška, Pavel, Jiří Riezner, Richard Pokorný, Michal Holec, and Martin Raška. "Relations between Biotic and Abiotic Diversity in Abandoned Basalt Quarry and Its Relevance for Ecological Restoration (Radobýl Hill, Northern Czechia)." Acta Universitatis Agriculturae et Silviculturae Mendelianae Brunensis 65, no. 1 (2017): 151–66. http://dx.doi.org/10.11118/actaun201765010151.

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The ecological value of abandoned quarries has gained increasing scientific attention in the last few decades, resulting in a paradigm shift in restoration programs regarding the use of natural processes. The linkages between biotic and abiotic diversity, such as landform and microclimatic diversity have been analyzed only slightly, however. In this paper, we use an interdisciplinary approach that includes vegetation mapping, geomorphological mapping, microclimatic measurements and modeling to reveal the specific two‑way linkages between abiotoc and biotic diversity. The present case study shows that in only 60 years landform diversity allowed the development of nine distinct biotopes with 134 identified species. At the same time, the vegetation diversity at these human‑induced biotopes is of high ecological value as it displays significant similarities with natural biotopes in the region (e.g., scree slope and rock cliff biotopes). Based on the results presented, the paper aims to contribute to current restoration programs involving processes of spontaneous succession and landforming.
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Wang, TsingHai, Cheng-Di Dong, Jui-Yen Lin, Chiu-Wen Chen, Jo-Shu Chang, Hyunook Kim, Chin-Pao Huang, and Chang-Mao Hung. "Recent Advances in Carbon Dioxide Conversion: A Circular Bioeconomy Perspective." Sustainability 13, no. 12 (June 21, 2021): 6962. http://dx.doi.org/10.3390/su13126962.

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Managing the concentration of atmospheric CO2 requires a multifaceted engineering strategy, which remains a highly challenging task. Reducing atmospheric CO2 (CO2R) by converting it to value-added chemicals in a carbon neutral footprint manner must be the ultimate goal. The latest progress in CO2R through either abiotic (artificial catalysts) or biotic (natural enzymes) processes is reviewed herein. Abiotic CO2R can be conducted in the aqueous phase that usually leads to the formation of a mixture of CO, formic acid, and hydrogen. By contrast, a wide spectrum of hydrocarbon species is often observed by abiotic CO2R in the gaseous phase. On the other hand, biotic CO2R is often conducted in the aqueous phase and a wide spectrum of value-added chemicals are obtained. Key to the success of the abiotic process is understanding the surface chemistry of catalysts, which significantly governs the reactivity and selectivity of CO2R. However, in biotic CO2R, operation conditions and reactor design are crucial to reaching a neutral carbon footprint. Future research needs to look toward neutral or even negative carbon footprint CO2R processes. Having a deep insight into the scientific and technological aspect of both abiotic and biotic CO2R would advance in designing efficient catalysts and microalgae farming systems. Integrating the abiotic and biotic CO2R such as microbial fuel cells further diversifies the spectrum of CO2R.
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Labbate, Maurizio, Hua Zhu, Leena Thung, Rani Bandara, Martin R. Larsen, Mark D. P. Willcox, Michael Givskov, Scott A. Rice, and Staffan Kjelleberg. "Quorum-Sensing Regulation of Adhesion in Serratia marcescens MG1 Is Surface Dependent." Journal of Bacteriology 189, no. 7 (January 19, 2007): 2702–11. http://dx.doi.org/10.1128/jb.01582-06.

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ABSTRACT Serratia marcescens is an opportunistic pathogen and a major cause of ocular infections. In previous studies of S. marcescens MG1, we showed that biofilm maturation and sloughing were regulated by N-acyl homoserine lactone (AHL)-based quorum sensing (QS). Because of the importance of adhesion in initiating biofilm formation and infection, the primary goal of this study was to determine whether QS is important in adhesion to both abiotic and biotic surfaces, as assessed by determining the degree of attachment to hydrophilic tissue culture plates and human corneal epithelial (HCE) cells. Our results demonstrate that while adhesion to the abiotic surface was AHL regulated, adhesion to the HCE cell biotic surface was not. Type I fimbriae were identified as the critical adhesin for non-QS-mediated attachment to the biotic HCE cell surface but played no role in adhesion to the abiotic surface. While we were not able to identify a single QS-regulated adhesin essential for attachment to the abiotic surface, four AHL-regulated genes involved in adhesion to the abiotic surface were identified. Interestingly, two of these genes, bsmA and bsmB, were also shown to be involved in adhesion to the biotic surface in a non-QS-controlled fashion. Therefore, the expression of these two genes appears to be cocontrolled by regulators other than the QS system for mediation of attachment to HCE cells. We also found that QS in S. marcescens regulates other potential cell surface adhesins, including exopolysaccharide and the outer membrane protein OmpX. We concluded that S. marcescens MG1 utilizes different regulatory systems and adhesins in attachment to biotic and abiotic surfaces and that QS is a main regulatory pathway in adhesion to an abiotic surface but not in adhesion to a biotic surface.
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Глушко, Sergey Glushko, Прохоренко, and Nina Prokhorenko. "Silvicultural properties of forest forming species." Vestnik of Kazan State Agrarian University 9, no. 3 (December 14, 2014): 120–22. http://dx.doi.org/10.12737/6541.

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The article concerns the process of silvicultural characteristics formation and features of their manifestation of tree species. Properties of species should be taken as information potential, formed during the interaction of biotic and abiotic (geo) components of natural systems. The strategy of species is a manifestation of silvicultural properties in specific forest site conditions. The nature of the strategy is defined in the process of adaptation to biotic and abiotic components of forest site conditions. The evolution of adaptations is due to the implementation of life strategy types, adaptive display of properties. The species are differentiated by membership in a particular strategy, split on the adaptation line to biotic and abiotic environment. The similarity of biotic, abiotic (geo) components, forming forest site properties and silvicultural forest conditions, gives a hope for the development of biogeocenology, geosistematic analysis of forests. Systematization of devices should consider the development of silvicultural properties, needed for the manifestation of the adaptive strategy in specific circumstances.
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Berens, Matthias L., Katarzyna W. Wolinska, Stijn Spaepen, Jörg Ziegler, Tatsuya Nobori, Aswin Nair, Verena Krüler, et al. "Balancing trade-offs between biotic and abiotic stress responses through leaf age-dependent variation in stress hormone cross-talk." Proceedings of the National Academy of Sciences 116, no. 6 (January 23, 2019): 2364–73. http://dx.doi.org/10.1073/pnas.1817233116.

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In nature, plants must respond to multiple stresses simultaneously, which likely demands cross-talk between stress-response pathways to minimize fitness costs. Here we provide genetic evidence that biotic and abiotic stress responses are differentially prioritized inArabidopsis thalianaleaves of different ages to maintain growth and reproduction under combined biotic and abiotic stresses. Abiotic stresses, such as high salinity and drought, blunted immune responses in older rosette leaves through the phytohormone abscisic acid signaling, whereas this antagonistic effect was blocked in younger rosette leaves byPBS3, a signaling component of the defense phytohormone salicylic acid. Plants lackingPBS3exhibited enhanced abiotic stress tolerance at the cost of decreased fitness under combined biotic and abiotic stresses. Together with this role,PBS3is also indispensable for the establishment of salt stress- and leaf age-dependent phyllosphere bacterial communities. Collectively, our work reveals a mechanism that balances trade-offs upon conflicting stresses at the organism level and identifies a genetic intersection among plant immunity, leaf microbiota, and abiotic stress tolerance.
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Lestari, Puji, Sutrisno Sutrisno, and I. Made Tasma. "QTL Study to Reveal Soybean Response on Abiotic and Biotic Stresses." Jurnal AgroBiogen 10, no. 3 (August 23, 2016): 109. http://dx.doi.org/10.21082/jbio.v10n3.2014.p109-114.

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<p>As an important grain legume, the improved soybean<br />(Glycine max [L.] Merr.) adaptive to environmental changes<br />is a valuable genetic resource. Strategy to minimize the<br />impact of climate effects should be underlined on soybean<br />production encompassing advanced genomics and well<br />predicted future climate. Crops including soybean respond<br />to climate change in the aspect of abiotic and biotic<br />environmental factors. To predict soybean response to<br />abiotic and biotic stresses, current progress of quantitative<br />trait loci (QTL) for abiotic and biotic stresses and flowering<br />and related genomic resources could be accessed at<br />SoyBase (http://www.soybase.org) and Phytozome<br />(http://www.phytozome.net). As the involvement of abiotic<br />and biotic stresses modulating flowering in soybean, genes<br />linked to QTL for abiotic/biotic stress and flowering/maturity<br />were also potential for resisting the environmental changes.<br />By mapping QTLs for flowering using one population in<br />different locations (Korea and China) with distinctive<br />longitude, latitude, and altitude, syntenic correlation<br />between these two QTLs on soybean chromosomes 6 and<br />13 indicates the environmental specific role of syntenic<br />regions. The information on QTL and related candidate<br />genes may assist marker-assisted breeding and enact<br />soybean as a model of adaptive legume crop under abiotic/<br />biotic stress.</p>
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29

THIELTGES, D. W., K. T. JENSEN, and R. POULIN. "The role of biotic factors in the transmission of free-living endohelminth stages." Parasitology 135, no. 4 (January 22, 2008): 407–26. http://dx.doi.org/10.1017/s0031182007000248.

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SUMMARYThe transmission success of free-living larval stages of endohelminths is generally modulated by a variety of abiotic and biotic environmental factors. Whereas the role of abiotic factors (including anthropogenic pollutants) has been in focus in numerous studies and summarized in reviews, the role of biotic factors has received much less attention. Here, we review the existing body of literature from the fields of parasitology and ecology and recognize 6 different types of biotic factors with the potential to alter larval transmission processes. We found that experimental studies generally indicate strong effects of biotic factors, and the latter emerge as potentially important, underestimated determinants in the transmission ecology of free-living endohelminth stages. This implies that biodiversity, in general, should have significant effects on parasite transmission and population dynamics. These effects are likely to interact with natural abiotic factors and anthropogenic pollutants. Investigating the interplay of abiotic and biotic factors will not only be crucial for a thorough understanding of parasite transmission processes, but will also be a prerequisite to anticipate the effects of climate and other global changes on helminth parasites and their host communities.
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30

Morris, William F., Johan Ehrlén, Johan P. Dahlgren, Alexander K. Loomis, and Allison M. Louthan. "Biotic and anthropogenic forces rival climatic/abiotic factors in determining global plant population growth and fitness." Proceedings of the National Academy of Sciences 117, no. 2 (December 30, 2019): 1107–12. http://dx.doi.org/10.1073/pnas.1918363117.

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Multiple, simultaneous environmental changes, in climatic/abiotic factors, interacting species, and direct human influences, are impacting natural populations and thus biodiversity, ecosystem services, and evolutionary trajectories. Determining whether the magnitudes of the population impacts of abiotic, biotic, and anthropogenic drivers differ, accounting for their direct effects and effects mediated through other drivers, would allow us to better predict population fates and design mitigation strategies. We compiled 644 paired values of the population growth rate (λ) from high and low levels of an identified driver from demographic studies of terrestrial plants. Among abiotic drivers, natural disturbance (not climate), and among biotic drivers, interactions with neighboring plants had the strongest effects on λ. However, when drivers were combined into the 3 main types, their average effects on λ did not differ. For the subset of studies that measured both the average and variability of the driver, λ was marginally more sensitive to 1 SD of change in abiotic drivers relative to biotic drivers, but sensitivity to biotic drivers was still substantial. Similar impact magnitudes for abiotic/biotic/anthropogenic drivers hold for plants of different growth forms, for different latitudinal zones, and for biomes characterized by harsher or milder abiotic conditions, suggesting that all 3 drivers have equivalent impacts across a variety of contexts. Thus, the best available information about the integrated effects of drivers on all demographic rates provides no justification for ignoring drivers of any of these 3 types when projecting ecological and evolutionary responses of populations and of biodiversity to environmental changes.
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31

Dresselhaus, Thomas, and Ralph Hückelhoven. "Biotic and Abiotic Stress Responses in Crop Plants." Agronomy 8, no. 11 (November 19, 2018): 267. http://dx.doi.org/10.3390/agronomy8110267.

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Agricultural productivity depends on increasingly extreme weather phenomena, and the use of germplasm that has to be continuously improved by plant breeders to become tolerant to various biotic and abiotic stresses. Molecular plant biologists try to understand the mechanisms associated with stress responses and provide knowledge that could be used in breeding programs. To provide a partial overview about our current understanding about molecular and physiological stress responses, and how this knowledge can be used in agriculture, we have edited a special issue on “Biotic and Abiotic Stress Responses in Crop Plants”. Contributions are from different fields including heat stress responses, stress responses during drought and salinity, as well as during flooding, and resistance and susceptibility to pathogenetic stresses and about the role of plant functional metabolites in biotic stress responses. Future research demand in particular areas of crop stress physiology is discussed, as well as the importance of translational research and investigations directly in elite crop plants and in the genetic resources available for breeding.
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32

Kurikesu, Irin, T. J. Anuja, A. Gangaprasad, and A. Jayakumaran Nair. "Regulation of micrornas during biotic and abiotic stress." Bulletin of Pure & Applied Sciences- Botany 37b, no. 1 (2018): 49. http://dx.doi.org/10.5958/2320-3196.2018.00007.1.

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33

Harikumar, Puthenveedu S. P., Kottekottil Jesitha, and Mannodi Sreechithra. "Remediation of Endosulfan by Biotic and Abiotic Methods." Journal of Environmental Protection 04, no. 05 (2013): 418–25. http://dx.doi.org/10.4236/jep.2013.45050.

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34

Signorelli, Santiago, Łukasz Paweł Tarkowski, Wim Van den Ende, and Diane C. Bassham. "Linking Autophagy to Abiotic and Biotic Stress Responses." Trends in Plant Science 24, no. 5 (May 2019): 413–30. http://dx.doi.org/10.1016/j.tplants.2019.02.001.

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35

Ojeda, Telmo F. M., Emilene Dalmolin, Maria M. C. Forte, Rodrigo J. S. Jacques, Fátima M. Bento, and Flávio A. O. Camargo. "Abiotic and biotic degradation of oxo-biodegradable polyethylenes." Polymer Degradation and Stability 94, no. 6 (June 2009): 965–70. http://dx.doi.org/10.1016/j.polymdegradstab.2009.03.011.

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36

Saratovsky, Ian, Peter G. Wightman, Pablo A. Pastén, Jean-François Gaillard, and Kenneth R. Poeppelmeier. "Manganese Oxides: Parallels between Abiotic and Biotic Structures." Journal of the American Chemical Society 128, no. 34 (August 2006): 11188–98. http://dx.doi.org/10.1021/ja062097g.

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37

Kumar, Rakesh, and Vinod Kumar. "A review of phylogeography: biotic and abiotic factors." Geology, Ecology, and Landscapes 2, no. 4 (March 29, 2018): 268–74. http://dx.doi.org/10.1080/24749508.2018.1452486.

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38

Zareeipolgardani, Bahareh, Agnès Piednoir, and Jean Colombani. "Tuning Biotic and Abiotic Calcite Growth by Stress." Crystal Growth & Design 19, no. 10 (August 2, 2019): 5923–28. http://dx.doi.org/10.1021/acs.cgd.9b00944.

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39

Hess, Thomas F., and Paul S. Schrader. "Coupled Abiotic–Biotic Mineralization of 2,4,6-Trinitrotoluene (TNT)." Journal of Environment Quality 31, no. 3 (2002): 736. http://dx.doi.org/10.2134/jeq2002.0736.

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40

Hess, Thomas F., and Paul S. Schrader. "Coupled Abiotic-Biotic Mineralization of 2,4,6-Trinitrotoluene (TNT)." Journal of Environmental Quality 31, no. 3 (May 2002): 736–44. http://dx.doi.org/10.2134/jeq2002.7360.

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41

Gassmann, Walter, Heidi M. Appel, and Melvin J. Oliver. "The interface between abiotic and biotic stress responses." Journal of Experimental Botany 67, no. 7 (March 2016): 2023–24. http://dx.doi.org/10.1093/jxb/erw110.

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42

Debona, Daniel, Fabrício A. Rodrigues, and Lawrence E. Datnoff. "Silicon's Role in Abiotic and Biotic Plant Stresses." Annual Review of Phytopathology 55, no. 1 (August 4, 2017): 85–107. http://dx.doi.org/10.1146/annurev-phyto-080516-035312.

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43

Collins, Daniel J. "Biotic and Abiotic Stressors of the Urban Forest." Journal of Horticultural Science and Biotechnology 82, no. 6 (January 2007): 1. http://dx.doi.org/10.1080/14620316.2007.11512312.

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44

Bareither, Christopher A., Craig H. Benson, Tuncer B. Edil, and Morton A. Barlaz. "Abiotic and Biotic Compression of Municipal Solid Waste." Journal of Geotechnical and Geoenvironmental Engineering 138, no. 8 (August 2012): 877–88. http://dx.doi.org/10.1061/(asce)gt.1943-5606.0000660.

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45

Jackson, R. D. "Remote Sensing of Biotic and Abiotic Plant Stress." Annual Review of Phytopathology 24, no. 1 (September 1986): 265–87. http://dx.doi.org/10.1146/annurev.py.24.090186.001405.

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46

Azevedo, R. A., and P. J. Lea. "Research on abiotic and biotic stress - what next?" Annals of Applied Biology 159, no. 3 (October 18, 2011): 317–19. http://dx.doi.org/10.1111/j.1744-7348.2011.00500.x.

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47

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

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48

Kissoudis, Christos, Rawnaq Chowdhury, Sjaak van Heusden, Clemens van de Wiel, Richard Finkers, Richard G. F. Visser, Yuling Bai, and Gerard van der Linden. "Combined biotic and abiotic stress resistance in tomato." Euphytica 202, no. 2 (January 30, 2015): 317–32. http://dx.doi.org/10.1007/s10681-015-1363-x.

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49

Martínez-Álvarez, Rosa M., Amalia E. Morales, and Ana Sanz. "Antioxidant Defenses in Fish: Biotic and Abiotic Factors." Reviews in Fish Biology and Fisheries 15, no. 1-2 (February 2005): 75–88. http://dx.doi.org/10.1007/s11160-005-7846-4.

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50

Ludovisi, Alessandro. "Biotic and abiotic entropy production in lake ecosystems." Ecological Modelling 179, no. 1 (November 2004): 145–47. http://dx.doi.org/10.1016/j.ecolmodel.2004.02.018.

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