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72 results for “Breeding System”

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dryad32/100

Data from: Mating system and genetic composition of the macaw palm (Acrocomia aculeata): implications for breeding and genetic conservation programs

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publicJun 2016View details →
dryad32/100

Breeding system of diploid sexuals within the Ranunculus auricomus complex and its role in a geographical parthenogenesis scenario

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publicMay 2021View details →
dryad32/100

Data from: Breeding system and geospatial variation shape the population genetics of Triodanis perfoliata

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publicSep 2022View details →
dryad32/100

Data from: Breeding system, shell size and age at sexual maturity affect sperm length in stylommatophoran gastropods

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publicApr 2016View details →
dryad32/100

Breeding system data for populations of T. perfoliata

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publicSep 2022View details →
zenodo28/100

Figure 5 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 5 Poa nemoralis. A whole plant B close-up of inflorescence with spikelets in mostly lateral view. Image A of S.P. Sylvester et al. 3555 (US) B of S.P. Sylvester et al. 3555 (PRE).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 1 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 1 Poa binata. A whole plants B basal part of plant showing fibrous basal sheaths C, D portions of inflorescence. Image A of S.P. Sylvester et al. 3489 (US) B of S.P. Sylvester et al. 3412 (US) C of S.P. Sylvester et al. 3518 (US) D of S.P. Sylvester et al. 3677 (US).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 4 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 4 Poa infirma. A whole plants B–D close-up of inflorescence showing spikelets generally in lateral view and miniscule anthers (a). Image A, B of Smook 3576 (PRE0652756-0) C, D of Smook 3672 (PRE).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 7 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 7 Poa pratensis subsp. pratensis. A whole plant B junction of sheath and blade of tiller leaf showing glabrous collar C spikelet, lateral view D part of inflorescence with spikelets mostly in lateral view. Images of R.J. Soreng et al. ZA-33 (US).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 8 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 8 Poa trivialis. A whole plant B part of inflorescence with spikelets mostly in lateral view. Images of Meredith s.n. (PRE0021311-0).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 6 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 6 Poa pratensis subsp. irrigata. A whole plant B junction of sheath and blade of tiller leaf showing collar with ciliolate margin C part of inflorescence with spikelets in lateral view. Images of S.P. Sylvester et al. 3437 (US).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 2 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 2 Poa compressa. A whole plant B spikelets, lateral view C portion of inflorescence and leaf blade. Image A of S.P. Sylvester et al. 3439 (US) B of S.P. Sylvester et al. 3439 (PRE) C of J.P.H. Acocks 20227 (PRE).

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 3 from: Soreng RJ, Sylvester SP, Sylvester MDPV, Clark VR (2020) New records and key to Poa (Pooideae, Poaceae) from the Flora of Southern Africa region and notes on taxa including a diclinous breeding system in Poa binata. PhytoKeys 165: 27-50. https://doi.org/10.3897/phytokeys.165.55948

Figure 3 Poa iconia var. iconia. A whole plant B spikelet, lateral view C close-up of inflorescence. Images A, C of V.R. Clark & C. Kelly 269 (GRA0009104) B of V.R. Clark & C. Kelly 269 (PRE).

opencc-by-4.0Nov 2020View details →
dryad28/100

Data from: Breeding system evolution influenced the geographic expansion and diversification of the core Corvoidea (Aves: Passeriformes)

Birds vary greatly in their life-history strategies, including their breeding systems, which range from brood parasitism to a system with multiple non-breeding helpers at the nest. By far the most common arrangement, however, is where both parents participate in raising the young. The traits associated with parental care have been suggested to affect dispersal propensity and lineage diversification, but to date tests of this potential relationship at broad temporal and spatial scales have been limited. Here, using data from a globally distributed group of corvoid birds in concordance with state-dependent speciation and extinction models, we suggest that pair breeding is associated with elevated speciation rates. Estimates of transition between breeding systems imply that cooperative lineages frequently evolve biparental care, whereas pair breeders rarely become cooperative. We further highlight that these groups have differences in their spatial distributions, with pair breeders over-represented on islands, and cooperative breeders mainly found on continents. Finally, we find that speciation rates appear to be significantly higher on islands compared to continents. These results imply that the transition from cooperative breeding to pair breeding was likely a significant contributing factor facilitating dispersal across tropical archipelagos, and subsequent world-wide phylogenetic expansion among the core Corvoidea.

opencc-zeroDec 2014View details →
zenodo28/100

Interactions between breeding system and ploidy affect niche breadth in Solanum

<p>As climate changes understanding what drives the way plants evolve to exist in new ecological niches becomes increasingly important. Here we find that in Solanum section Petota that specific breeding system and ploidy combinations increase niche divergence through the decoupling of geographical range and niche diversity. This allows for more targeted use for plant breeding and plant conservation. This is the data and code associated with the manuscript that describes these results.&nbsp;</p>

opencc-by-4.0Dec 2021View details →
zenodo28/100

Figure 1. A in Pollination and breeding system in two sympatric Fuchsia (Onagraceae) species at the Parque Nacional do Itatiaia (Brazil): Hummingbirds, insects and facultative self-pollination

Figure 1. A. Flowers of Fuchsia regia in female (left) and male phases (right). B. Flowers of F. campos-portoi. C. Possible hybrid (F. regia x F. campos-portoi) photographed in 2009, near the IBAMA base ao the Itatiaia National Park.

opencc-by-4.0Mar 2021View details →
zenodo28/100

Figure 3 in Effect of season and housing systems on various physiobehavioral attributes of local breed of rabbits (Oryctolagus cuniculus) in Southern Punjab, Pakistan

Figure 3. Effect of housing systems on various behavioral attributes of rabbits. Data is mean (± SE). Similar letters on the bars indicate non-significant (p ≥ 0.05) difference within caged and colony reared rabbits for sitting. Different letters on the bars indicate significant (p ≤ 0.05) difference within caged and colony reared rabbits for standing and walking.

opencc-by-4.0Dec 2022View details →
zenodo28/100

Figure 4 from: McDonnell AJ, Wetreich HB, Cantley JT, Jobson P, Martine CT (2019) Solanum plastisexum, an enigmatic new bush tomato from the Australian Monsoon Tropics exhibiting breeding system fluidity. PhytoKeys 124: 39-55. https://doi.org/10.3897/phytokeys.124.33526

Figure 4 Map showing geographic distribution of all taxa compared in this study. red points = S.jobsonii, blue points = S.diversiflorum, black points = S.eburneum, pink points = S.watneyi, yellow points = S.succosum and purple asterisk = S.plastisexum. All points are based on specimens databased in the Australasian Virtual Herbarium (https://avh.chah.org.au/) and specimens held at BUPL.

opencc-by-4.0Jun 2019View details →
zenodo28/100

Figure 1 from: McDonnell AJ, Wetreich HB, Cantley JT, Jobson P, Martine CT (2019) Solanum plastisexum, an enigmatic new bush tomato from the Australian Monsoon Tropics exhibiting breeding system fluidity. PhytoKeys 124: 39-55. https://doi.org/10.3897/phytokeys.124.33526

Figure 1 Morphology and the earliest-known herbarium specimen of Solanumplastisexum. A Flowering stem with a single staminate flower in 2016 B Mature fruit C Erect inflorescences bearing staminate flowers in 2018 and D Specimen collected by P. Latz in 1974, held at DNA and annotated by D. Symon with an annotation indicating his confusion about the reproductive morphology of the specimen (male rachis visible above fruit on far left).

opencc-by-4.0Jun 2019View details →
zenodo28/100

Figure 3 from: McDonnell AJ, Wetreich HB, Cantley JT, Jobson P, Martine CT (2019) Solanum plastisexum, an enigmatic new bush tomato from the Australian Monsoon Tropics exhibiting breeding system fluidity. PhytoKeys 124: 39-55. https://doi.org/10.3897/phytokeys.124.33526

Figure 3 Principal components analysis score plot with eigenvalues and the contribution of each PC displayed (left) and loading plot (right) of characters and species in Table 1. Left, red triangles = S.jobsonii, blue circles = S.diversiflorum, black crosses = S.eburneum, pink triangles = S.watneyi, yellow squares = S.succosum and purple asterisks = S.plastisexum. Right, weighted characters labelled and indicated with red arrows. A Seed length B Fruit width C Number of seeds per fruit D Fruit length E Depth of lobing on apical leaves F Depth of lobing on basal leaves G Fruit wall width H Width of basal leaves I Surface area of basal leaves J Calyx lobe length, hermaphrodite flowers K Internode length L Width of apical leaves, M Surface area of apical leaves N Petiole length O Pedicel length in fruit P Corolla diameter, hermaphrodite flowers Q Length of basal leaves R Corolla diameter, male flowers S Length of apical leaves T Plant height U Stem prickle length V Trichome density, abaxial surface of apical leaves W Trichome density, adaxial surface of apical leaves X Calyx lobe length, male flowers. Colours associated with each taxon also used in Figs 2, 3.

opencc-by-4.0Jun 2019View details →

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DANDI Archive for NWB datasets

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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OpenNeuro

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