Phenotypic and Genotypic Variation and Covariation of Some Quantitative Turf Characters of Poa pratensis L. 1

Crop Science ◽  
1969 ◽  
Vol 9 (4) ◽  
pp. 470-473 ◽  
Author(s):  
C. D. Berry ◽  
D. V. Glover ◽  
W. H. Daniel
2010 ◽  
Vol 59 (2) ◽  
pp. 255-268
Author(s):  
István Harmati

Sekély humuszos szintű, erősen karbonátos réti talajon kialakult természetes (Achilleo-Festucetum pseudovinae) gyepen beállított tartamkísérletekben vizsgáltuk a műtrágyázás kérdéseit a gyep növényi összetételének megjavítása, termésének növelése és minősége javítása céljából. A kísérlet humuszban gazdag, nitrogénnel és káliummal igen jól ellátott, de foszforban szegény talaján az N- és P-műtrágya 2-2 adagját szólóban és kombinációikban alkalmaztuk. Az öntözetlen kísérletet 28, az öntözöttet 14 éven át folyamatosan, széleskörűen vizsgáltuk. Megállapításainkat a következőkben foglaljuk össze. – A gyep növényi összetételét a N- és a P-műtrágyák adagjaiktól és kombinációiktól függően megváltoztatták. A nitrogén a füvek, a foszfor a pillangósok versenyképességét fokozta és segítette elő növekedését. Az önmagában alkalmazott N-műtrágya a talaj nagyfokú P-szegénysége miatt nem gyakorolt pozitív hatást a gyepre. A P-műtrágya viszont kedvező változásokat okozott: a füvek fejlődésének elősegítése mellett nagymértékben növelte a pillangósok borítási értékét és tömegarányát, különösen az öntözött parcellákon. Öntözetlen viszonyok között a réti perje (Poa pratensis), a sovány csenkesz (Festuca pseudovina) és a komlós lucerna (Medicago lupulina) alkotta a gyep termésének túlnyomó részét, néhány egyéb fű- és pillangósvirágú komponens társaságában. Az öntözött kísérletben a pillangósok abszolút uralma mellett gyakran a réti perje jutott vezető szerephez. A pillangósok közül az eperhere (Trifolium fragiferum), a komlós lucerna (Medicago lupulina) és a vörös here (Trifolium pratense) váltakozva jutott uralomra. Az időjárás nagyban befolyásolta a gyep pillangós komponenseinek tömegarányát. Az NP kombinációkban a pillangósok tömegaránya erősen lecsökkent, különösen a nagyobb N-adag használata esetén. Öntözetlen területen a sovány csenkesz és a réti perje változó arányban alkotta a gyep termésének túlnyomó részét. Az öntözött parcellákon azonban a réti perje abszolút uralkodóvá vált és az egyre jobban előretörő tarackbúza (Agropyron repens) is jelentősen részt vett a termés kialakításában, elsősorban a nagyobb N-dózisú kombinációkban. A kísérlet 3. évtizedében a csapadékos években megjelent a francia perje (Arrhenatherum elatius) és a réti csenkesz (Festuca pratensis) is. – A gyep termését az önmagában alkalmazott N-műtrágya nem növelte jelentősen. Ezzel szemben a P-műtrágya nagy hatékonysággal 2–4-szeresére (3–5 t·ha–1-ra) növelte a gyep szénatermését, elsősorban a pillangósok nagyarányú térhódítása révén. 1 kg P2O5 öntözetlen körülmények között 43, míg öntözöttben 68 kg szénaterméstöbbletet eredményezett, sokévi átlagban. A 90 kg P2O5·ha–1 adag néhány év után soknak bizonyult. A legjobb eredményt a 200 kg N·ha–1 + 60 kg P2O5·ha–1 adaggal értük el, amellyel az öntözetlen területen – 28 év átlagában – 7,87, öntözötten – 14 év átlagában – 7,12 t·ha–1 szénatermést kaptunk. Az időjárás nagymértékben befolyásolta a termés mennyiségét és minőségét, legfőképpen a pillangósok tömegarányának változása révén, különösen az öntözetlen kísérletben. A három növedék tömegének aránya 7 évi átlagban, az öntözetlen kísérletben a szóló foszforkezeléseknél 48:37:15%, míg az NP kombinációknál 56:35:9% volt. Az öntözött területen ezek az arányok az előbbi sorrendben: 39:49:12, illetve 43:41:16%. A nitrogénből számított nyersfehérjehozam sokévi átlagban az öntözetlen kísérletben 428–550, míg az öntözöttben 560–760 kg·ha–1 volt. – A talaj felvehető tápanyagtartalma az évek során jelentősen megváltozott, különösen a talaj 0–10 cm-es rétegében. A P-trágyázás önmagában, de az NP kombinációiban is az adagoktól, illetve az ezek hatására kialakult termések mennyiségétől függő mértékben növelte a talaj P-tartalmát. A legjobbnak a 200 kg N·ha–1 + 60 kg P2O5·ha–1 kezelésű parcellákban bizonyult: a kísérlet 22. évében a talaj 0–10 cm-es rétegében a P-tartalom 260 mg P2O5·kg–1 lett, ami az erősen karbonátos talajok esetében igen jó P-ellátottságnak mondható. A K-ellátottság azonban az NP-kezeléseknél az optimális szint alá csökkent (172 mg K2O·kg–1) a termések nagyarányú K-kivonása következtében. Ezért néhány évi NP-trágyázás után K-pótlásra is szükség van.


2020 ◽  
pp. 13-26
Author(s):  
Ya. M. Golovanov ◽  
L. M. Abramova

The synthaxonomy and ecology of communities with predominance of Hordeum jubatum L., included in the «black list» of the Republic of Bashkortostan (Abramova, Golovanov, 2016a), the preliminary «black list» of the Orenburg Region (Abramova et al., 2017) and the «Black book of flora of Middle Russia» (Vinogradova et al., 2010), are discussed in the article, which continues a series of publications on the classification of communities with alien species in the South Urals (Abramova, 2011, 2016; Abramova, Golovanov, 2016b). H. jubatum was first found in the South Urals in 1984 as an adventive plant occurring along streets in the town of Beloretsk, as well as in gardens where it was grown as an ornamental plant. During the 1980s, it was met also at some railway stations and in several rural localities. Its active distribution throughout the South Urals started in XXI century (Muldashev et al., 2017). Currently, H. jubatum, most naturalized in the native salted habitats of the steppe zone, is often found in disturbed habitats in all natural zones within the region. The short vegetating period and resistance to drought allowed it to be naturalized also in dry steppes, where it increasingly acts as the main weed on broken pastures. The aim of the work, conducted during 2011–2017, was further finding the centers of H. jubatum invasion in 3 regions adjacent to the South Urals — the Republic of Bashkortostan and the Chelyabinsk and Orenburg Regions (Fig. 1). In the main sites of H. jubatum invasion 71 relevès were performed on 10–100 m² sample plots with the information of location, date, the plot size, the total cover, average and maximum height of herb layer. Classification was carried out following the Braun-Blanquet method (Braun-Blanquet, 1964) with using the Kopecký–Hejný approach (Kopecký, Hejný, 1974). The community ecology was assessed by weighted average values according to the optimal ecological scales by E. Landolt with usfge of the software of IBIS (Zverev, 2007). PCA-ordination method with usage CANOCO 4.5 software package was applied to identify patterns of environmental differentiation of invasive communities. The current wide distribution area of H. jubatum and its naturalization in synanthropic, meadow and saline communities in the South Urals, as well as its occurrence within mountain-forest belt, forest-steppe and steppe zones both in the Cis- and Trans-Urals, indicates species wide ecological amplitude, high adaptive capability and invasive potential. Its vast thickets are known in the steppe zone, both in disturbed steppes around settlements and along the banks of water bodies. The invasion sites are smaller in the northern regions and mountain forest belt, where these are located in settlements or along communication lines. Therefore, the steppe zone is more favorable for invasive populations, and their distribution will continue from the south to the north. Communities with predominance of H. jubatum, described earlier (Abramova, Golovanov, 2016b) in the Cis-Urals as two derivative communities (associations Hordeum jubatum [Scorzonero–Juncetea gerardii], Hordeum jubatum [Artemisietea]) and Polygono avicularis–Hordeetum jubati, were met in other regions of the South Urals. Also a new derivative community Hordeum jubatum–Poa pratensis [Cynosurion cristati], occuring in the northern part of the Cis-Urals and Trans-Urals, was established. In new habitats this species forms three types of communities: ass. Polygono avicularis–Hordeetum jubati (Fig. 2) the most widespread in anthropogenic habitats throughout the South Urals; derivative community Hordeum jubatum–Juncus gerardii [Scorzonero–Juncetalia gerardii] (Fig. 5) which replaces saline meadows mainly in the steppe zone of the region; derivative community Hordeum jubatum–Poa pratensis [Cynosurion cristati] (Fig. 4) which y replaces low-herb meadows in the forest-steppe zone and mountain-forest belt. PCA ordination (Fig. 6) shows that moisture (H) and soil richness-salinization (S) factors are in priority in differentiation of communities with predominance H. jubatum. The first axis is mainly related to the salinization and soil richness. The community pattern along the second axis is associated with wetting factor. The cenoses of the derivative community Hordeum jubatum–Poa pratensis [Cynosurion cristati] (less salted substrates in drier conditions in the northern part of the forest-steppe zone and the mountain forest belt) are grouped in the upper part of the ordination diagram, while communities of ass. Polygono avicularis–Hordeetum jubati (drier conditions in settlements, the steppe zone) in its low left part. Thus, axis 1 also reflects the intensity of trampling. Another group is formed by cenoses of the derivate community Hordeum jubatum–Juncus gerardii [Scorzonero–Juncetalia gerardii], (salt substrates with a high level of moisturization, on not very damaged water body banks). All communities with H. jubatum are well differentiated in the space of the main ordination axes that indirectly confirms the correctness of our syntaxonomic decision. Undoubted is further expansion of H. jubatum with its entering both anthropogenic and natural plant communities within the South Urals that suggests a constant monitoring in centers of species invasion.


2020 ◽  
Vol 51 (4) ◽  
pp. 1038-1047
Author(s):  
Mawia & et al.

This study had as principal objective identification of osmotic-tolerant potato genotypes by using "in vitro" tissue culture and sorbitol as a stimulating agent, to induce water stress, which was added to the  culture nutritive medium in different concentration (0,50, 110, 220, 330 and 440 mM).  The starting point was represented by plantlets culture collection, belonging to eleven potato genotypes: Barcelona, Nectar, Alison, Jelly, Malice, Nazca, Toronto, Farida, Fabulla, Colomba and Spunta. Plantlets were multiplied between two internodes to obtain microcuttings (in sterile condition), which were inoculated on medium. Sorbitol-induced osmotic stress caused a significant reduction in the ascorbic acid, while the concentration of proline, H2O2 and solutes leakage increased compared with the control. Increased the proline content prevented lipid peroxidation, which played a pivotal role in the maintenance of membrane integrity under osmotic stress conditions. The extent of the cytoplasmic membrane damage depends on osmotic stress severity and the genotypic variation in the maintenance of membranes stability was highly associated with the ability of producing more amounts of osmoprotectants (proline) and the non-enzymic antioxidant ascorbic acid in response to osmotic stress level. The results showed that the genotypes Jelly, Nectar, Allison, Toronto, and Colomba are classified as highly osmotic stress tolerant genotypes, while the genotypes Nazca and Farida are classified as osmotic stress susceptible ones.


Author(s):  
V.V. Tanyukevich ◽  
◽  
S.V. Tyurin ◽  
D.V. Khmeleva ◽  
A.A. Kvasha ◽  
...  

Works on protective afforestation are carried out in order to protect agricultural land from degradation processes, as well as to improve the microclimate of land. The research purpose is to study the bioproductivity and environmental role of Robinia pseudoacacia L. forest shelterbelts in the conditions of the Kuban lowland. The approved and generally accepted methods of forest valuation, forest land reclamation, botany, and mathematical statistics were applied. Plantings were created according to the standard technology for the steppe zone of the Russian Federation. The area of forest shelterbelts is 62.4 ths ha, including 5 % of the young growth (I state class), 80 % of middle-aged forest plantings (II state class), 10 % of maturing plantings (II state class), 5 % of mature and overmature plantings (III state class). Living ground cover is formed by the following species: Koeleria pyramidata L., Poa pratensis L., Festuca pratensis H., Elytrígia repens L., Dactylis glomerata L., and Phlum pratense L. Aboveground phytomass is 100–300 g/m2; height is 25–32 cm. Plantings are characterized by the quality classes: young growth – I and II; middle-aged and maturing – III; mature and overmature – IV. At the age of natural maturity (70 years), the Robinia trunk reaches the average height of 15.1 m with the average diameter of 22.1 cm. The total stock of wood reaches 18, (ths m3), including (ths m3): young growth – 68 (ths m3); middleaged plantings – 14,871 (ths m3); maturing plantings – 2,187 (ths m3); mature and overmature plantings – 1,314 (ths m3). Aboveground phytomass in young growth is 20.2 t/ha; in mature and overmature plantings it is 391.2 t/ha. In the region it is estimated at 17,070 ths t, including (ths t): young growth – 64; middle-aged plantings – 13,753; maturing plantings – 2,032; mature and overmature plantings – 1,221. The share of stem mass reaches 84.5–80.8 %; woody greenery – 4.2–1.5 %; branches – 11.3–17.7 %. Recalculation coefficients of the stock into aboveground phytomass are the following for: young growth – 0.936; mature and overmature forest shelterbelts – 0.929. Phytosaturation of forest shelterbelts varies within 0.314–2.474 kg/m3. Forest shelterbelts have accumulated 8,534 ths t of carbon, which is estimated at 145.1 mln dollars. The sphere of application of the research results is the Krasnodar Krai forestry, which is recommended to create an additional 60 ths ha of forest shelterbelts, which will provide a normative protective forest cover of arable land of 5 % and annual carbon sequestration up to 3.4 t/ha.


HortScience ◽  
1997 ◽  
Vol 32 (2) ◽  
pp. 296-300 ◽  
Author(s):  
M.R. Foolad ◽  
G.Y. Lin

Seed of 42 wild accessions (Plant Introductions) of Lycopersicon pimpinellifolium Jusl., 11 cultigens (cultivated accessions) of L. esculentum Mill., and three control genotypes [LA716 (a salt-tolerant wild accession of L. pennellii Corr.), PI 174263 (a salt-tolerant cultigen), and UCT5 (a salt-sensitive breeding line)] were evaluated for germination in either 0 mm (control) or 100 mm synthetic sea salt (SSS, Na+/Ca2+ molar ratio equal to 5). Germination time increased in response to salt-stress in all genotypes, however, genotypic variation was observed. One accession of L. pimpinellifolium, LA1578, germinated as rapidly as LA716, and both germinated more rapidly than any other genotype under salt-stress. Ten accessions of L. pimpinellifolium germinated more rapidly than PI 174263 and 35 accessions germinated more rapidly than UCT5 under salt-stress. The results indicate a strong genetic potential for salt tolerance during germination within L. pimpinellifolium. Across genotypes, germination under salt-stress was positively correlated (r = 0.62, P < 0.01) with germination in the control treatment. The stability of germination response at diverse salt-stress levels was determined by evaluating germination of a subset of wild, cultivated accessions and the three control genotypes at 75, 150, and 200 mm SSS. Seeds that germinated rapidly at 75 mm also germinated rapidly at 150 mm salt. A strong correlation (r = 0.90, P < 0.01) existed between the speed of germination at these two salt-stress levels. At 200 mm salt, most accessions (76%) did not reach 50% germination by 38 days, demonstrating limited genetic potential within Lycopersicon for salt tolerance during germination at this high salinity.


Author(s):  
Philippe Huneman

Considering challenges to the modern synthesis (MS), this chapter reconstructs an explanatory scheme proper to the MS. It contrasts it with the explanatory scheme proper to some alternatives to the MS. It considers which empirical facts should compel us to adopt the alternative scheme, or stand with the MS, or consider a weakly attenuated form of its explanatory scheme. Hence the last section focuses on the form of variation: Given that many findings are accumulating concerning the not purely random nature of variation, it asks which specific patterns of variation would be likely to support an alternative explanatory scheme. It argues that neither biased variation nor random genotypic variation is likely to vindicate a specific explanatory scheme.


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