Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
157
datasets available to search
ShareScore release 0.9.0
Dataset results
157 results for “Sapotaceae”
The complete chloroplast genome of Mimusops elengi (Sapotaceae)
<p><span>The first complete chloroplast genome sequences of <i><span>Mimusops elengi</span></i> (Sapotaceae) were reported in this study. The cpDNA of <i><span>M</span></i><i><span>.</span></i><i><span> elengi</span></i> is 159,719 bp in length, contains a large single-copy region (LSC) of 88,935 bp and a small single-copy region (SSC) of 18,606 bp, which were separated by a pair of inverted repeat (IR) regions of 26,089 bp. The genome contains 132 genes, including 87 protein-coding genes, 8 ribosomal RNA genes, and 37 transfer RNA genes. The overall GC content of the whole genome is 36.8%. Phylogenetic analysis of 12 chloroplast genomes within the family Sapotaceae suggests that the sister relationship of <i><span>Autranella</span></i> and <i><span>Tieghemella</span></i><span> is strongly supported. </span><i><span>Minusops</span></i> genus is close to <i><span>Autranella</span></i> and <i><span>Tieghemella</span></i>, although the support value is still low.</span></p>
Fig. 4 in Pichonia munzingeri (Sapotaceae), a new and rare micro-endemic species from New Caledonia
Fig. 4. – Geographic distribution of Pichonia munzingeri Gâteblé & Swenson.
Table 3 in One in, one out: Generic circumscription within subtribe Manilkarinae (Sapotaceae)
<p><b>Table 3.</b> Divergence time estimations.</p><table><tbody><tr><th>Node</th><th>Mean age BEAST (mya)</th><th>95% HPD BEAST (mya)</th></tr></tbody><tbody><tr><th>Crown of Manilkarinae subtribe</th><td>37.65</td><td>33.13–42.37</td></tr><tr><th><i>Labramia</i> A.DC. – <i>Manilkara</i> Adans. s.str. divergence</th><td>33.86</td><td>30.34–37.97</td></tr><tr><th><i>Labourdonnaisia</i> Bojer – <i>Abebaia</i> Baehni divergence</th><td>30.33</td><td>24.24–36.42</td></tr><tr><th>Crown of <i>Labramia</i></th><td>10.72</td><td>8.6–12.83</td></tr><tr><th>Crown of <i>Manilkara</i> s.str.</th><td>29.38</td><td>28.08–31.57</td></tr><tr><th>Crown of <i>Labourdonnaisia</i></th><td>17.29</td><td>13.85–20.75</td></tr><tr><th>Crown of <i>Abebaia</i> clade</th><td>13.96</td><td>8.54–19.91</td></tr><tr><th>Crown of <i>Labramia mayottensis</i> Labat & al.</th><td>4.63</td><td>2.82–6.6</td></tr><tr><th>Crown of Mascarene <i>Labourdonnaisia</i></th><td>6.00</td><td>3.38–8.98</td></tr></tbody></table><p>mya: million years ago; HPD: highest posterior density.</p>
Table 1 in One in, one out: Generic circumscription within subtribe Manilkarinae (Sapotaceae)
<p><b>Table 1.</b> Ingroup genera with distribution and described species included in this study.</p><table><tbody><tr><th>Genus, with number of accepted species</th><th>Distribution</th><th>Species included in this study</th></tr></tbody><tbody><tr><th><i>Faucherea</i> Lecomte 11 species</th><td>Madagascar</td><td><i>Faucherea ambrensis</i> Aubrév.</td></tr><tr><td><i>Faucherea glutinosa</i> Aubrév.</td></tr><tr><td><b><i>Faucherea hexandra</i> (Lecomte) Lecomte</b></td></tr><tr><td><i>Faucherea laciniata</i> Lecomte</td></tr><tr><td><i>Faucherea manongarivensis</i> Aubrév.</td></tr><tr><td><i>Faucherea parvifolia</i> Lecomte</td></tr><tr><td><i>Faucherea tampoloensis</i> Aubrév.</td></tr><tr><td><i>Faucherea thouvenotii</i> Lecomte</td></tr><tr><td><i>Faucherea urschii</i> Capuron ex Aubrév.</td></tr><tr><th><i>Labourdonnaisia</i> Bojer 6 species</th><td>Mascarenes Islands and Madagascar</td><td><b><i>Labourdonnaisia calophylloides</i> Bojer</b></td></tr><tr><td><i>Labourdonnaisia glauca</i> Bojer</td></tr><tr><td><i>Labourdonnaisia lecomtei</i> Aubrév.</td></tr><tr><td><i>Labourdonnaisia madagascariensis</i> Pierre ex Baill.</td></tr><tr><td><i>Labourdonnaisia revoluta</i> Bojer</td></tr><tr><th><i>Labramia</i> A.DC. 10 species</th><td>Madagascar and Comoros</td><td><i>Labramia ankaranaensis</i> Aubrév.</td></tr><tr><td><i>Labramia ankaranaensis</i> var. <i>antsingensis</i> Aubrév.</td></tr><tr><td><i>Labramia boivinii</i> (Pierre) Aubrév.</td></tr><tr><td><b><i>Labramia bojeri</i> A.DC.</b></td></tr><tr><td><i>Labramia capuronii</i> Aubrév.</td></tr><tr><td><i>Labramia costata</i> (M.M.Hartog ex Baill.) Aubrév.</td></tr><tr><td><i>Labramia louvelii</i> Aubrév.</td></tr><tr><td><i>Labramia mayottensis</i> Labat, Pignal & O.Pascal</td></tr><tr><td><i>Labramia platanoides</i> Capuron ex Aubrév.</td></tr><tr><td><i>Labramia sambiranensis</i> Aubrév.</td></tr><tr><th><i>Manilkara</i> Adans. s.str. 78 species</th><td>Pantropical (Africa, America, Asia, Pacific Asia)</td><td><i>Manilkara bidentata</i> (A.DC.) A.Chev.</td></tr><tr><td><i>Manilkara boivinii</i> Aubrév.</td></tr><tr><td><i>Manilkara cuneifolia</i> (Baker) Dubard</td></tr><tr><td><i>Manilkara dissecta</i> (L.f.) Dubard</td></tr><tr><td><i>Manilkara fasciculata</i> (Warb.) H.J.Lam & Maas Geest</td></tr><tr><td><b>(type species of the genus <i>Abebaia</i>)</b></td></tr><tr><td><i>Manilkara hexandra</i> (Roxb.) Kuntze</td></tr><tr><td><i>Manilkara lacera</i> (Baker) Dubard</td></tr><tr><td><i>Manilkara longifolia</i> (A.DC.) Dubard</td></tr><tr><td><i>Manilkara multinervis</i> (Baker) Dubard</td></tr><tr><td><i>Manilkara obovata</i> (Sabine & G.Don) J.H.Hemsl.</td></tr><tr><td><i>Manilkara sansibarensis</i> (Engl.) Dubard</td></tr><tr><td><i>Manilkara udoido</i> Kaneh.</td></tr><tr><td><i>Manilkara zapota</i> (L.) P.Royen</td></tr></tbody></table>
Fig. 2 in Présence du genre Pradosia (Sapotaceae) en Afrique: description d'une nouvelle espèce, P. spinosa
Fig. 2. — Distribution de Pradosia spinosa Ewango & Breteler.
The complete chloroplast genome of Mimusops elengi (Sapotaceae)
Open the record for dataset details and reuse information.
Figure 9 in Ceropsylla pouteriae Burckhardt sp. nov. (Hemiptera: Psylloidea: Triozidae)ı a new species of jumping plant-louse inducing galls on the leaves of Pouteria ramiflora (Mart.) Radlk. (Sapotaceae): taxonomyı gall structure and histochemistry
Figure 9. Histochemical positive results in C. pouteriae gall. (a) starch in abaxial cortex and near to vascular bundles; (b) reducing sugars detected mainly in the adaxial cortex; (c) proteins in adaxial and abaxial cortex cells; (d) lipids in the cortex; (e) proanthocyanidins detected in cells adjacent to pit and in the adaxial cortex; (f) auxins in the adaxial cortex and in the cells around the pit. Pi = pit.
Figure 4 in Ceropsylla pouteriae Burckhardt sp. nov. (Hemiptera: Psylloidea: Triozidae)ı a new species of jumping plant-louse inducing galls on the leaves of Pouteria ramiflora (Mart.) Radlk. (Sapotaceae): taxonomyı gall structure and histochemistry
Figure 4. Ceropsylla spp., male terminalia. (a, b) male proctiger, in profile; (c, d) inner face of paramere, in profile; (e) paramere, rear view; (f, g) distal portion of aedeagus. ‒ (a, c, f) C. pouteriae Burckhardt, sp. nov.; (b, d, e, g) C. sideroxyli Riley.
Figure 6 in Ceropsylla pouteriae Burckhardt sp. nov. (Hemiptera: Psylloidea: Triozidae)ı a new species of jumping plant-louse inducing galls on the leaves of Pouteria ramiflora (Mart.) Radlk. (Sapotaceae): taxonomyı gall structure and histochemistry
Figure 6. Ceropsylla sideroxyli Riley, immature. (a) habitus, left side, dorsal view; (b) habitus, right side, ventral view; (c) marginal sectasetae; (d) antenna; (e) dorsal sectasetae; (f) circumanal ring; (g) tip of tarsus with tarsal arolium.
Figure 7 in Ceropsylla pouteriae Burckhardt sp. nov. (Hemiptera: Psylloidea: Triozidae)ı a new species of jumping plant-louse inducing galls on the leaves of Pouteria ramiflora (Mart.) Radlk. (Sapotaceae): taxonomyı gall structure and histochemistry
Figure 7. Anatomical structure of Ceropsylla pouteriae gall and Pouteria ramiflora leaf. (a, b) leaf; (c, d) gall; (a) midrib with bicollateral vascular bundle surrounded by fibres and laticifers; (b) intercostal region with dorsiventral mesophyll; (c) cortex with three zonation: adaxial cortex, median cortex and abaxial cortex; (d) vascular bundles in median cortex. Xy = xylem; Ph = phloem; Col = collenchyma; Lac = laticifer; AdE = adaxial surface of epidermis; PP = palisade parenchyma; SP = spongy parenchyma; VB = vascular bundles; AbE = adaxial surface of epidermis; Co = cortex; AdC = adaxial cortex; MD = medium cortex; AbC = abaxial cortex; Pi = pit.
Figure 5 in Ceropsylla pouteriae Burckhardt sp. nov. (Hemiptera: Psylloidea: Triozidae)ı a new species of jumping plant-louse inducing galls on the leaves of Pouteria ramiflora (Mart.) Radlk. (Sapotaceae): taxonomyı gall structure and histochemistry
Figure 5. Ceropsylla pouteriae Burckhardt, sp. nov., immature. (a) habitus, left side, dorsal view; (b) habitus, right side, ventral view (vp = ventral process); (c) marginal sectasetae; (d) antenna; (e) dorsal sectasetae; (f) circumanal ring; (g) tip of tarsus with tarsal arolium.
Data from: Forest degradation and invasive species synergistically impact Mimusops andongensis (Sapotaceae) in Lama Forest Reserve, Benin
Harvesting of Non-Timber Forest Products (NTFPs) can threaten target species, especially those with limited distribution and density. Exploited species also face threats from habitat fragmentation, fire, and invasive species. We assessed the impact of human disturbances and invasive species on the population of a key multipurpose NTFP species, Mimusops andongensis, in Lama Forest reserve (Benin). The densities of adult trees and regenerative stems decreased with increasing degradation. Mimusops andongensis contributed less to total tree density with increasing human disturbance. There were significantly fewer M. andongensis recruits with increasing cover of invasive Chromolaena odorata. Smaller diameter individuals predominated in non-degraded and moderately degraded sites while in degraded sites, the structure showed a negative exponential trend with the density of small diameter individuals being less than two trees/ha. Larger individuals were also rare in degraded sites. The low density of both mature trees and seedlings in degraded sites may undermine the long-term viability of M. andongensis, despite existing protection against NTFP harvesting and other anthropogenic pressures. Management should emphasize facilitating recruitment subsidies and limiting the presence of C. odorata.
Fig. 3 in A new species, genus and tribe of Sapotaceae, endemic to Madagascar
Fig. 3. Line drawing of the type collection of Bemangidia lowryi L. Gaut. (Lowry & al. 6657; P). A, flowering branch; B, flower with corolla and 3 calyx lobes removed, showing gynoecium; C, flower with corolla removed; D, two cross-sections of ovary; E, staminode; F, corolla opened; G, fruit; H, seed. — A–F drawn from P.P. Lowry II & al. 6657; G–H drawn from L. Gautier & al. 5789. — Drawing: C. Chatelain.
Fig. 1. Bemangidia lowryi L. Gaut., a in A new species, genus and tribe of Sapotaceae, endemic to Madagascar
Fig. 1. Bemangidia lowryi L. Gaut., a new species of a new genus from Madagascar. A, Bemangidy Forest, SE Madagascar; B, flowers of the type specimen; C, branch with fruit; D, secondary leaf venation (upper surface); E, cross-section of a pre-anthesis flower from the type collection; F, longitudinal section of a fruit; G, seed. — Photos: A, C, D, F, G by Ulf Swenson; B by Pete Lowry (MO); E by Laurent Gautier.
FIGURES 113–117. 113–114 in Description of five new eulophid species (Hymenoptera: Eulophidae) associated with leaf vein galls of Madhuca longifolia (J. Koenig) (Sapotaceae) in India
FIGURES 113–117. 113–114, biology of Aprostocetus madhucae Singh sp. nov.: 113, 114, dissected gall of Madhuca longifolia showing pupae inside the pupal skin of Selitrichodes madhucae Singh & Kaneria, sp. nov.. 115–117, biology of Chrysonotomyia madhucae Singh, sp. nov.: 115, gall dissected to show pupa in dorsal view; 116, dissected out pupa in ventral view; 117, pupa with larva of an unidentified ectoparasitoid.
FIGURES 108–112 in Description of five new eulophid species (Hymenoptera: Eulophidae) associated with leaf vein galls of Madhuca longifolia (J. Koenig) (Sapotaceae) in India
FIGURES 108–112. Biology of Selitrichodes madhucae Singh sp. nov.: 108, dissected gall of Madhuca longifolia showing larvae; 109, male pupa; 110, female pupa in ventral view; 111, female pupa in dorso-lateral view; 112, some emerged males and females in pre-mating courtship.
FIGURES 90–96 in Description of five new eulophid species (Hymenoptera: Eulophidae) associated with leaf vein galls of Madhuca longifolia (J. Koenig) (Sapotaceae) in India
FIGURES 90–96. Chrysonotomyia madhucae Singh sp. nov., female: 90, body in lateral view; 91, body in dorsal view; 92, head in dorsal view; 93, antenna; 94, mesosoma in dorsal view; 95, forewing; 96, ovipositor.
FIGURES 83–89 in Description of five new eulophid species (Hymenoptera: Eulophidae) associated with leaf vein galls of Madhuca longifolia (J. Koenig) (Sapotaceae) in India
FIGURES 83–89. Quadrastichus manmohani Singh, sp. nov., 83–84, female: 83, ovipositor; 84, distal part of ovipositor enlarged to show cercal setae. 85–89, male: 85, body in dorso-lateral view; 86, body in lateral view; 87, antenna; 88, mesosoma in dorsal view; 89, forewing.
FIGURES 74–82 in Description of five new eulophid species (Hymenoptera: Eulophidae) associated with leaf vein galls of Madhuca longifolia (J. Koenig) (Sapotaceae) in India
FIGURES 74–82. Quadrastichus manmohani Singh sp. nov., female: 74, body in dorsal view; 75, body in lateral view; 76, antenna; 77, part of antenna showing anelli; 78, distal segments of club showing apical spine; 79, mesosoma in dorsal view; 80, forewing; 81, part of forewing showing dorsal seta on SMV; 82, part of forewing venation showing postmarginal and stigmal veins.
FIGURES 103–107 in Description of five new eulophid species (Hymenoptera: Eulophidae) associated with leaf vein galls of Madhuca longifolia (J. Koenig) (Sapotaceae) in India
FIGURES 103–107. Chrysonotomyia madhucae Singh sp. nov., male: 103, body in dorsal view; 104, antenna; 105, forewing; 106; genitalia; 107, distal part of genitalia showing digitus spines.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.