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561 results for “rico”
Data from: Population connectivity of the plating coral Agaricia lamarcki from southwest Puerto Rico
Identifying genetic connectivity and discrete population boundaries is an important objective for man- agement of declining Caribbean reef-building corals. A double digest restriction-associated DNA sequencing pro- tocol was utilized to generate 321 single nucleotide poly- morphisms to estimate patterns of horizontal and vertical gene flow in the brooding Caribbean plate coral, Agaricia lamarcki. Individual colonies (n = 59) were sampled from eight locations throughout southwestern Puerto Rico from six shallow (* 10–20 m) and two mesophotic habitats (* 30–40 m). Descriptive summary statistics (Fixation index, FST), analysis of molecular variance, and analysis through landscape and ecological associations and dis- criminant analysis of principal components estimated high population connectivity with subtle subpopulation structure among all sampling localities.
FIGURE 3 in Resurrection of Dendropemon sintenisii (Loranthaceae): an endemic mistletoe from Puerto Rico
FIGURE 3. Map of Puerto Rico showing the locations (circles) where Dendropemon sintenisii has been collected.
FIGURE 2 in Resurrection of Dendropemon sintenisii (Loranthaceae): an endemic mistletoe from Puerto Rico
FIGURE 2. Dendropemon bicolor (Loranthaceae): A. fruiting branch. B. flower buds and flower at anthesis. C. leaves, inflorescences and infructescences. D. twig and young inflorescences. E. plant habit. F. ripe fruits. Photographs by T.A. Carlo.
FIGURE 1 in Resurrection of Dendropemon sintenisii (Loranthaceae): an endemic mistletoe from Puerto Rico
FIGURE 1. Dendropemon sintenisii (Loranthaceae): A. leaves and infructescences. B. ripe fruits. C. habit. D. inflorescence with flower buds. E. detail of inflorescence. F. flower at anthesis. Photographs by T.A. Carlo.
FIGURE 8 in A new species of Pronura (Neanuridae: Paleonurini) from the Luquillo Mountains Puerto Rico with a key to American poorly tuberculated Paleonurini
FIGURE 8. Dorsal abdominal chaetotaxy for some genera of Paleonurini, showing the position of setae in Abd IV and V. A. Paleonura bilinskii (Paśnik & Weiner, 2013), B. Paleonura nuda, C. Paramanura najtae, D. Pronura amazonica (Cassagnau & Oliveira, 1990).
FIGURE 2–6 in A new species of Pronura (Neanuridae: Paleonurini) from the Luquillo Mountains Puerto Rico with a key to American poorly tuberculated Paleonurini
FIGURE 2–6. Pronura yunquensis sp. nov. 2 Antenna dorsal chaetotaxy; 3. Antenna ventral chaetotaxy; 4. Labrum; 5. Labium; 6. Leg I.
FIGURES 5–9. 5 in Stictodora cablei n. sp. (Digenea: Heterophyidae) from the royal tern, Sterna maxima (Laridae: Sterninae) from Puerto Rico and the Brazos County area of the Texas Gulf coast, U.S.A., with a list of other endohelminths recovered in Texas
FIGURES 5–9. 5. Angularella sp., Scolex. 6. Angularella sp., rostellum. 7. Angularella sp., dorsal view of mature proglottid. 8. Unknown genus & species of Dilepididae, scolex without rostellar hooks. 9. Unknown genus & species of Dilepididae, dorsal view of mature proglottid. Abbreviations N, neck; O, ovary; R, rostellum; RG rostellar gland; S, seminal receptacle; T, testis; V, vitellarium. Scale bars: 5, 230µm; 6, 60µm; 7, 180µm; 8, 340 µm; 9, 38 µm.
FIGURES 1–4. 1. Stictodora cablei n in Stictodora cablei n. sp. (Digenea: Heterophyidae) from the royal tern, Sterna maxima (Laridae: Sterninae) from Puerto Rico and the Brazos County area of the Texas Gulf coast, U.S.A., with a list of other endohelminths recovered in Texas
FIGURES 1–4. 1. Stictodora cablei n. sp., ventral view of adult. 2. Stictodora cablei n. sp., composite drawing of terminal genitalia and acetabulogenital complex; 3. Stictodora cablei n. sp., photograph of the acetabulum; 4. Stictodora acanthotrema, photograph of the acetabulum. Abbreviations: A, acetabulum; GA, genital atrium; GP, genital pore; LP, large pad; O, ovary; PA, papilliform arm-like structures; SP, small pad; SV, seminal vesicle; T, testis; U, uterus. Scale bars: 1, 170µm; 2, 50µm.
FIGURE 10 in Stictodora cablei n. sp. (Digenea: Heterophyidae) from the royal tern, Sterna maxima (Laridae: Sterninae) from Puerto Rico and the Brazos County area of the Texas Gulf coast, U.S.A., with a list of other endohelminths recovered in Texas
FIGURE 10. Cercarioides cochleariformes, ventral view of adult. A, acetabulum; O, ovary; T, testis; U, uterus; W, lateral wing-like expansions of forebody. Scale bar: 10, 580µm.
FIGURE 1 in Rediscovery of Arrabidaea chica (Bignoniaceae) and Entada polystachya var. polyphylla (Fabaceae) in Puerto Rico
FIGURE 1. Map of the island of Puerto Rico showing the localities where the lianas Arrabidaea chica (circle) and Entada polystachya var. polyphylla (triangle) were rediscovered. The historical localities where E. polystachya var. polyphylla was collected during the 19th Century includes the municipality of Fajardo (rhombus) and the area between the municipalities of Manatí and Vega Baja (square). All the historical records of A. chica are from unspecified localities within the municipality of Bayamón.
Data from: The assembly and importance of a novel ecosystem: the ant community of coffee farms in Puerto Rico
<p>Agricultural ecosystems are, by their very nature novel, and, by definition, the more general biodiversity associated with them must likewise constitute a novel community. Here we examine the community of arboreally foraging ants in the coffee agroecosystem of Puerto Rico. We surveyed 20 coffee plants in 25 farms three times in a period of one year. We also conducted a more spatially explicit sampling in two of the farms and conducted a species interaction study between the two most abundant species, Wasmannia auropunctata and Solenopsis invicta in the laboratory. We find that the majority of the most common species are well-known invasive ants and that there is a highly variable pattern of dominance that varies considerably over the main coffee producing region of Puerto Rico, suggesting an unusual modality of community structure. The distribution pattern of the two most common species, W. auropunctata and S. invicta, suggests strong competitive exclusion. However, they also have opposite relationships with the percent of shade cover, with W. auropunctata showing a positive relationship with shade, while S. invicta has a negative relationship. The spatial distribution of these two dominant species in the two more intensively studied farms suggests that young colonies of S. invicta can displace W. auropunctata. Laboratory experiments confirm this. These results suggest the existence of a spatially explicit intransitive loop that includes these two species and is mediated by a phorid fly parasitoid that attack the larger workers of S. invicta. In addition to the elaboration of the nature and extent of this novel ant community, we speculate on the possibilities of its active inclusion as part of a biological control system dealing with several coffee pests, including one of the ants itself, W. auropunctata.</p>
Fig. 1. Leptostylopsis grandis. A in A New Species ofLeptostylopsisDillon (Coleoptera: Cerambycidae: Lamiinae) from Puerto Rico
Fig. 1. Leptostylopsis grandis. A) Dorsal view of holotype, B) Ventral view of holotype, C) Frontal view of holotype, D) Apical third of elytra of holotype, E) Lateral view of holotype, F) Type series showing the variation in elytral coloration (1= holotype, 2–5 = paratypes), G) Comparison of L. grandis holotype with L. argentatus.
NLL-SSST-coherence earthquake relocation catalog for the 2019-2020 Southwest Puerto Rico earthquake sequence.
<p>CSV table of the NLL-SSST-coherence earthquake relocation catalog for the 2019-2020 Southwest Puerto Rico earthquake sequence.</p> <p>This dataset is from relocations presented in the article:<br> The 2019-2020 Southwest Puerto Rico earthquake sequence: seismicity and faulting<br> by Blaž Vičič, Seyyedmaalek Momeni, Alessandra Borghi, Anthony Lomax, and Abdelkrim Aoudia<br> published in Seismological Research Letters</p>
FIGURE 2a–b in A new species of Pontarachna (Acari, Hydrachnidia, Pontarachnidae) from a mesophotic coral ecosystem off Vieques Island, Puerto Rico, Caribbean Sea
FIGURE 2a–b. Pontarachna nemethi sp. nov., female: a = idiosoma, ventral view; b = detail of postgenital sclerite illustrating one of the wheel-like acetabula and two pores. Scale bar = 100 µm (a), 40 µm (b).
FIGURE 1a–k in A new species of Pontarachna (Acari, Hydrachnidia, Pontarachnidae) from a mesophotic coral ecosystem off Vieques Island, Puerto Rico, Caribbean Sea
FIGURE 1a–k. Pontarachna nemethi sp. nov. (a–h—male [a, d–h—holotype, c – paratype]; i—female; j–k—deutonymph): a, j = idiosoma, ventral view; b = semidiagramatic illustration of a wheel-like acetabulum; c = genital field; d = ejaculatory complex; e = I-Leg-5-6; f = chelicera; g = palp and capitulum; h, k = palp; i = I-Leg-4-6. Scale bar = 100 µm (a, c–k), 40 µm (b).
Species of Acantholichen occurring only in the Neotropics show a high degree of endemism (Dal Forno et al. 2016). Of the seven species now recognized in this genus (Table 2), 71.4% (5) are known only from South America. As with Dictyonema, Acantholichen seem to be specific to substrate type and appears in the Andean small forest occurring on mosses in tree bark inhabiting mostly exposed habitats. Cyphellostereum is also represented by a high number of species restricted to the Neotropics [6 (66.6%)], while one is known only from North America, one from Southeastern United States and Puerto Rico, and another species is known only from Borneo and Fiji (Table 2). It is probably due to their unusual appearance that these lichens are getting confused with free-living cyanobacteria colonies, and that there are still undescribed species in the Neotropics. in Eight new species of lichenized Basidiomycota in the genera Acantholichen, Cyphellostereum and Dictyonema s.str. (Agaricales, Hygrophoraceae) from northern South America
Species of Acantholichen occurring only in the Neotropics show a high degree of endemism (Dal Forno et al. 2016). Of the seven species now recognized in this genus (Table 2), 71.4% (5) are known only from South America. As with Dictyonema, Acantholichen seem to be specific to substrate type and appears in the Andean small forest occurring on mosses in tree bark inhabiting mostly exposed habitats. Cyphellostereum is also represented by a high number of species restricted to the Neotropics [6 (66.6%)], while one is known only from North America, one from Southeastern United States and Puerto Rico, and another species is known only from Borneo and Fiji (Table 2). It is probably due to their unusual appearance that these lichens are getting confused with free-living cyanobacteria colonies, and that there are still undescribed species in the Neotropics.
FIGURE 5. Emerita portoricensis Schmitt, 1935 in Redescription of the mole crab Emerita portoricensis Schmitt, 1935 (Crustacea: Decapoda: Hippidae), based on Caribbean populations from Puerto Rico, Belize, Costa Rica, and Panama
FIGURE 5. Emerita portoricensis Schmitt, 1935: A, B, ovigerous female holotype, cl 17.5 mm, Mayaguez, Puerto Rico, USNM 65731; C, ovigerous female, cl 14.7 mm, San Juan Harbor, Puerto Rico, USNM 42209.
FIGURE 3. Emerita portoricensis Schmitt, 1935 in Redescription of the mole crab Emerita portoricensis Schmitt, 1935 (Crustacea: Decapoda: Hippidae), based on Caribbean populations from Puerto Rico, Belize, Costa Rica, and Panama
FIGURE 3. Emerita portoricensis Schmitt, 1935: ovigerous female paratype, cl 13.7 mm, Boca del Drago, Panama, USNM 1546925 (= ULLZ 13456): A, right lateral surface of carapace, eyestalk, and anterior appendages; B, right mandible, external surface; C, right first maxilla, external surface; D, right second maxilla, external surface; E, right first maxilliped, external surface; F, right second maxilliped, external surface; G, right third maxilliped, external surface; H, right third maxilliped, internal surface. Scale bars = 1 mm (A, C); 2 mm (D–F); 3 mm (G, H).
FIGURE 2. Emerita portoricensis Schmitt, 1935 in Redescription of the mole crab Emerita portoricensis Schmitt, 1935 (Crustacea: Decapoda: Hippidae), based on Caribbean populations from Puerto Rico, Belize, Costa Rica, and Panama
FIGURE 2. Emerita portoricensis Schmitt, 1935: A–C, ovigerous female holotype, cl 17.5 mm, Mayaguez, Puerto Rico, USNM 65731; D–F, ovigerous female, cl 11.5 mm, Dangriga, Belize, USNM 1545049 (= ULLZ 10465). A, carapace, eyestalk, and anterior appendages, right lateral surface; B, carapace front, eyestalks and anterior appendages, dorsal surface; C, G, terminus, dactylus of right first pereopod, lateral surface; D, right lateral surface of carapace, eyestalk, and anterior appendages; E, dorsal surface of carapace front, eyestalks, and anterior appendages; F, right first pereopod, lateral surface. Scale bars = 3 mm (A, B); 2 mm (D–E); 1 mm (C, G).
FIGURE 4. Emerita portoricensis Schmitt, 1935 in Redescription of the mole crab Emerita portoricensis Schmitt, 1935 (Crustacea: Decapoda: Hippidae), based on Caribbean populations from Puerto Rico, Belize, Costa Rica, and Panama
FIGURE 4. Emerita portoricensis Schmitt, 1935: A–D, ovigerous female, cl 14.7 mm, San Juan Harbor Puerto Rico, USNM 42209; E, female, cl 12.8 mm, same lot as previous; F, ovigerous female, cl 15.0 mm, same lot as previous; G–M, ovigerous female, cl 13.7 mm, Boca del Drago, Panama, USNM 1546925 (= ULLZ 13456). Emerita benedicti Schmitt, 1935: N, ovigerous female, cl 13.3 mm, Tampa, Florida; O, Emerita talpoida (Say, 1817): O, ovigerous female, cl 15.5 mm, Padre Island, Texas, TAMU/TCWC 2-8703. Emerita brasiliensis Schmitt, 1935: P, ovigerous female, cl 11.4 mm, Urbatuba, Laxaro Beach, Brazil, ULLZ 15981; Q, ovigerous female, cl 19.4 mm, Rio de Janeiro, Brazil, USNM 50674. A, right lateral habitus; B, right third maxilliped, external surface; C, G, right first pereopod, lateral surface; D–F, H, N–Q, terminus, dactylus of right first pereopod, lateral surface; I, lateral surface of right second pereopod; J, lateral surface of right third pereopod; K, mesial surface of right fourth pereopod; L, lateral surface of right fifth pereopod; M, external surfaces of telson and uropods. Scale bars = 12 mm (A); 8 mm (B, C, G); 2 mm (D–F, N, O–Q); 4 mm (H–L); 10 mm (M).
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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
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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
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