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.
113
datasets available to search
ShareScore release 0.9.0
Dataset results
113 results for “pipefish”
Figure 7 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 7 Stigmatopora harastii in situ, male, The Leap, Kurnell, Botany Bay, NSW, Australia, 12 meters depth, 03 October 2018 (photograph: Andrew Trevor-Jones).
Figure 6 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 6 Aerial view of the scuba dive site The Steps, Kurnell, Botany Bay, NSW, Australia A shore and entrance B inshore boulders (photographs: Michael McFadyen).
Figure 4 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 4 Stigmatopora harastii in situ, ASM I.47267 paratypes, female, The Steps, Kurnell, Botany Bay, NSW, Australia at 11–12 meters depth, 06 June 2017 (photographs: David Harasti).
Figure 3 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 3 Stigmatopora harastii in situ, ASM I. 49510-001, holotype, male A (right individual) B (left individual); The Steps, Kurnell, Botany Bay, NSW, Australia, 13.5 meters depth, 18 June 2020. The male holotype was photographed with a paired female individual, which was not collected. Note the large cluster of distinct red spots extending posteriad on venter of anterior trunk rings in the male (photographs: Andrew Trevor-Jones).
Figure 2 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 2 Stigmatopora harastii, preserved directly after collection, paratypes, female A ASM I.47267-001, 136.3 mm SLB ASM I.47267-002, 138.2 mm SL; Australia: NSW, Botany Bay, Kurnell (photograph: Kerryn Parkinson).
Figure 11 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 11 Fucoid algae and seagrass associating members of Stigmatoporain situAS. nigra, male, Nelson Bay, NSW (photograph: David Harasti) BS. nigra, female, Port Hughes, Gulf St Vincent, South Australia (photograph: David Muirhead) CS. argus, Port Hughes, Gulf St Vincent, South Australia (photograph: Graham Short) DS. narinosa, Port Hughes, Gulf St Vincent, South Australia (photograph: Graham Short) ES. macropterygia, Winstones Cove, North Island, New Zealand (photograph: Nick Shears).
Figure 1 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 1 Stigmatopora harastii, preserved directly after collection, ASM I. 49510-001, holotype male, 145.5 mm SLA dorsal view B lateral view C ventral view; Australia: NSW, Botany Bay, Kurnell (photograph: Kerryn Parkinson).
Figure 10 from: Short G, Trevor-Jones A (2020) Stigmatopora harastii, a new species of pipefish in facultative associations with finger sponges and red algae from New South Wales, Australia (Teleostei, Syngnathidae). ZooKeys 994: 105-123. https://doi.org/10.3897/zookeys.994.57160
Figure 10 Comparison of the dorsal median ridge present on the head and first trunk ring in: AS. harastii and BS. nigra, ASM I.42611-009. Note the dorsal median ridge (DMR) extending into the first trunk ring in S. nigra versus ending on the posterior nuchal plate in S. harastii. Abbreviations: ANP, anterior nuchal plate; DMR, dorsal median ridge; Fr, frontal; PNP, posterior nuchal plate; SOC, supraoccipital; first TnR, first trunk ring (illustration by Kent Sorgon).
Data from: Effects of mating order and male size on embryo survival in a pipefish
In species that provide parental care, individuals should invest adaptively in their offspring in relation to the pre- and post-zygotic care provided by their partners. In the broad-nosed pipefish, Syngnathus typhle L., females transfer large, nutrient-rich eggs into the male brood pouch during mating. The male broods and nourishes the embryos for several weeks before independent juveniles emerge at parturition. Given a choice, females clearly prefer large partners. Yet, females provide protein-richer eggs when the same individual mates with a smaller than a larger male. In the present study, we allowed each female to mate with one small and one large male, in alternated order. We found a strong effect of female mating order, with larger clutches and higher embryo mortality in first- than second-laid broods, which may suggest that eggs over-ripen in the ovaries or reflect the negative effects of high embryo density in the brood pouch. In either case, this effect should put constraints on the possibility of a female being selective in mate choice. We also found that small and large males produced embryos of similar size and survival, consistent with the reproductive compensation hypothesis, suggesting that, in this species, larger males provide better nourishment to the embryos than smaller males.
Data from: Baltic pipefish females need twice as many males as they get
Sex role reversal in 2 pipefish species, Syngnathus typhle and Nerophis ophidion, is potentially explained by females reproducing twice as fast as males. Moreover, in oceanic populations from the Swedish west coast, females compete for males with males preferring to mate with larger females. However, in a brackish Baltic population of S. typhle, males do not prefer larger mates, whereas choosiness remains in the local N. ophidion population. We explore whether this absence of male choice in brackish S. typhle can be explained by males and females having more similar potential reproductive rates here, whereas the sex difference may remain in the local N. ophidion population. Contrary to our expectations, in both species, females out-reproduced males by a factor of more than 2, just as in the oceanic populations. We measured this experimentally as the number of males a female potentially could fill with eggs within the time span of 1 male pregnancy, in relation to males available in nature. Thus, we conclude that sexual selection on females is as strong in brackish as in oceanic populations of both species but that targets of selection via male choice are shifted to traits other than body size in S. typhle. Hence, costs and benefits of choice are probably more important than potential reproductive rates to understand mate choice. We suggest that it may be misleading to use targets of sexual selection, such as choice for large body size, as an indicator of the strength of sexual selection.
FIGURE 3 in Syngnathus chihiroe, a new species of pipefish (Syngnathidae) from southern Japan
FIGURE 3. Type locality of Syngnathus chihiroe sp. nov. (red star).
Fig. 2 in First Confirmed Record of the Samoan Pipefish Halicampus mataafae (Perciformes: Syngnathidae) from Japan
Fig. 2. Lateral views of head of Halicampus mataafae. KAUM–I. 104496, 135.5 mm SL. A, fresh specimen; B, sketch (dermal flaps, pectoral fin and scutellum not illustrated). Bar indicates 1 mm.
Figure 6 in Pebbled places preferred by people and pipefish in a World Heritage protected area
Figure 6. – Human activities that are potentially pulse disturbances to SSCSs. A: Post-dredging of a lowland reach of Teima Stream, Okinawa Island (Photo: KM); B: Gravel extraction from stream Waimaro River, Viti Levu Island in Fiji (Photo: LC); C: Water transport truck pumping from an instream pit in lower Emmagen Creek, Australia, late in the dry season (Photo: BE); and D: Signage aimed at preventing pebble removal from beachside resort are 'Pebble Beach' north of Cairns, Australia (Photo: BE).
Figure 5. – A in Pebbled places preferred by people and pipefish in a World Heritage protected area
Figure 5. – A selection of makeshift human modifications to streams in north Queensland. A: A recreational weir at Emmagen Creek bifurcating habitat of M. leiaspis; B: A recreational spa on Magnetic Island; C: Rock stacking in Thompson Creek within M. leiaspis habitat; D: A recreational weir at low water at Rollingstone Creek in the southern AWT (Photos: JD & BE).
Figure 3 in Pebbled places preferred by people and pipefish in a World Heritage protected area
Figure 3. – Microphis leiaspis feeding at Cape Tribulation, Australia. A: Front view revealing the small open mouth of an adult female; B: Posturing and sideways glance prior to striking small benthic prey from a cobble surface; C: The forward-facing foraging technique (Photos: BE).
Figure 3. – Coelonotus kaipuae n in A new species of freshwater pipefish (Teleostei: Syngnathidae: Coelonotus) from Papua New Guinea
Figure 3. – Coelonotus kaipuae n. sp. Up: Holotype, MNHN IC-2021-0306 (tag 19161), male, 86.22 mm SL. Gavuvu river, New Britain (Papua New Guinea), 28 Oct. 2018, Keith coll. Down: Paratype, in MNHN IC-2021-0307 (tag 19167), female, 83.87 mm SL. Gavuvu river, New Britain (Papua New Guinea), 28 Oct. 2018, Keith coll.
FIGURE 2 in Partial characterization of digestive proteases in juveniles of Microphis brachyurus (short-tailed pipefish) (Syngnathiformes: Syngnathidae)
FIGURE 2 | Effect of temperature on digestive proteases of juvenile of short-tailed pipefish (Microphis brachyurus): A. optimum temperature of acidic proteases; B. thermal stability of acidic proteases; C. optimum temperature of alkaline proteases; and D. thermal stability of alkaline proteases (mean ± SD, n = 3). Mean values denoted with different letters are statistically different, p <0.05.
FIGURE 1 in Partial characterization of digestive proteases in juveniles of Microphis brachyurus (short-tailed pipefish) (Syngnathiformes: Syngnathidae)
FIGURE 1 | Effect of pH on the enzymatic activity of digestive proteases of short-tailed pipefish (Microphis brachyurus) juveniles for the determination of: A. optimal pH of acidic proteases; B. optimal pH of alkaline proteases; C. pH stability of acidic proteases; and D. pH stability of alkaline proteases (mean ± SD, n = 3). Mean values denoted with different letters are statistically different, p <0.05.
TABLE 1 in A new freshwater pipefish species (Syngnathidae: Microphis) from the Sunda shelf islands, Indonesia
<p><b>TABLE 1.</b> Samples for morphomeristic and molecular analyses. Type specimens: (●) Holotype; (■) Syntypes. MNHN: Muséum national d’Histoire Naturelle, Paris, France; USNM: Smithonian Institute, National Museum of Natural History, Washington D.C, USA; BMNH: British Museum of Natural History, London, UK; MZB: Indonesian Institute of Science, Research Center for Biology, Cibinong, Indonesia.</p><table><tbody><tr><th><b>Species</b></th><th><b>Catalog Number</b></th><th><b>Genbank/</b></th><th><b>Tag</b></th><th><b>Country</b></th><th><b>Island</b></th><th><b>Genetic</b></th><th><b>Morphomeristic</b></th></tr></tbody><tbody><tr><th></th><td></td><td><b>bold ID</b></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis retzii ■</i></th><td>BMNH-1867-11-28-350</td><td><b>-</b></td><td>1</td><td>Indonesia</td><td>Sulawesi</td><td>✕</td><td>✓</td></tr><tr><th><i>Microphis retzii ■</i></th><td>BMNH-1867-11-28-350</td><td><b>-</b></td><td>2</td><td>Indonesia</td><td>Sulawesi</td><td>✕</td><td>✓</td></tr><tr><th><i>Microphis retzii</i></th><td>-</td><td>BOLD:</td><td>BIF5345</td><td>Indonesia</td><td>Ceram</td><td>✓</td><td>✕</td></tr><tr><th></th><td></td><td>ADO3837</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis retzii</i></th><td>MZB-BIF-3193</td><td>BOLD:</td><td>BIF3193</td><td>Indonesia</td><td>Papua</td><td>✓</td><td>✕</td></tr><tr><th></th><td></td><td>ADO3837</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis retzii</i></th><td>MZB-BIF-3198</td><td>BOLD:</td><td>BIF3198</td><td>Indonesia</td><td>Papua</td><td>✓</td><td>✕</td></tr><tr><th></th><td></td><td>ADO3837</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis retzii</i></th><td>MZB-BIF-3199</td><td>BOLD:</td><td>BIF3199</td><td>Indonesia</td><td>Papua</td><td>✓</td><td>✕</td></tr><tr><th></th><td></td><td>ADO3837</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis retzii</i></th><td>-</td><td>BOLD:</td><td>BIF10261</td><td>Indonesia</td><td>Sulawesi</td><td>✓</td><td>✕</td></tr><tr><th></th><td></td><td>ADO3837</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis retzii</i></th><td>-</td><td>BOLD:</td><td>BIF10266</td><td>Indonesia</td><td>Sulawesi</td><td>✓</td><td>✕</td></tr><tr><th></th><td></td><td>ADO3837</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis retzii</i></th><td>MNHN-IC-2021-0332</td><td>OQ221650.1</td><td>14953</td><td>Indonesia</td><td>Ceram</td><td>✓</td><td>✓</td></tr><tr><th><i>Microphis retzii</i></th><td>MNHN-IC-2024-0058</td><td>PQ352220</td><td>14969</td><td>Indonesia</td><td>Ambon</td><td>✓</td><td>✓</td></tr><tr><th><i>Microphis retzii</i></th><td>MNHN-IC-2021-0333</td><td>OQ221649.1</td><td>14973</td><td>Indonesia</td><td>Ambon</td><td>✓</td><td>✓</td></tr><tr><th><i>Microphis retzii</i></th><td>MNHN-IC-2021-0333</td><td>OQ220383.1</td><td>14974</td><td>Indonesia</td><td>Ambon</td><td>✓</td><td>✓</td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2023-0318</td><td>BOLD:</td><td>BIF3775</td><td>Indonesia</td><td>Lombok</td><td>✓</td><td>✓</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td>ACT8563</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2023-0318</td><td>BOLD:</td><td>BIF3776</td><td>Indonesia</td><td>Lombok</td><td>✓</td><td>✓</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td>ACT8563</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB.26974</td><td>PQ352218</td><td>BIF4073</td><td>Indonesia</td><td>Lombok</td><td>✓</td><td>✓</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB.26973</td><td>PQ352219</td><td>BIF4074</td><td>Indonesia</td><td>Lombok</td><td>✓</td><td>✓</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>-</td><td>KU692624</td><td>-</td><td>Indonesia</td><td>Java</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-1939</td><td>BOLD:</td><td>BIF1939</td><td>Indonesia</td><td>Java</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td>ACT8563</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-1940</td><td>KU692625.1</td><td>BIF1940</td><td>Indonesia</td><td>Java</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-1942</td><td>KU692628.1</td><td>BIF1942</td><td>Indonesia</td><td>Java</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> sp. nov.</th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td><b>bold ID</b></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-2809</td><td>KU692621.1</td><td>BIF2809</td><td>Indonesia</td><td>Bali</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-2811</td><td>KU692622.1</td><td>BIF2811</td><td>Indonesia</td><td>Bali</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-2812</td><td>KU692626.1</td><td>BIF2812</td><td>Indonesia</td><td>Bali</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-2814</td><td>KU692627.1</td><td>BIF2814</td><td>Indonesia</td><td>Bali</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-2815</td><td>KU692629.1</td><td>BIF2815</td><td>Indonesia</td><td>Bali</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-2817</td><td>KU692623.1</td><td>BIF2817</td><td>Indonesia</td><td>Bali</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MZB-BIF-2818</td><td>KU692630.1</td><td>BIF2818</td><td>Indonesia</td><td>Bali</td><td>✓</td><td>✕</td></tr><tr><th><i>arrakisae</i> <b>sp. nov.</b></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>USNM 51725</td><td>-</td><td>-</td><td>Samoa</td><td>Upolu</td><td>✕</td><td>✓</td></tr><tr><th><i>torrentius ●</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0334</td><td>OQ221631.1</td><td>RTNC114_A</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0334</td><td>OQ221635.1</td><td>RTNC114_B</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0334</td><td>OQ221632.1</td><td>RTNC114_C</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0334</td><td>OQ221634.1</td><td>RTNC114_D</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0335</td><td>OQ221636.1</td><td>RTNC118</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0335</td><td>OQ221633.1</td><td>RTNC119</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2005-1902</td><td>OQ221736.1</td><td>1</td><td>Vanuatu</td><td>Santo</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2005-1902</td><td>OQ221735.1</td><td>2</td><td>Vanuatu</td><td>Santo</td><td>✓</td><td>✓</td></tr><tr><th><i>torrentius</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2019-0082</td><td>OQ221638.1</td><td>19193</td><td>Solomon</td><td>Kolombangara</td><td>✓</td><td>✓</td></tr><tr><th><i>nicoleae ●</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0337</td><td>OQ221637.1</td><td>19199</td><td>Solomon</td><td>Kolombangara</td><td>✓</td><td>✓</td></tr><tr><th><i>nicoleae ■</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0336</td><td>OQ221639.1</td><td>14961</td><td>Solomon</td><td>Ranongga</td><td>✓</td><td>✓</td></tr><tr><th><i>nicoleae ■</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0336</td><td>OQ221647.1</td><td>14962</td><td>Solomon</td><td>Ranongga</td><td>✓</td><td>✓</td></tr><tr><th><i>nicoleae ■</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0338</td><td>OQ221644.1</td><td>17692</td><td>Papua New</td><td>New Britain</td><td>✓</td><td>✓</td></tr><tr><th><i>nicoleae ■</i></th><td></td><td></td><td></td><td>Guinea</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0339</td><td>OQ221640.1</td><td>19071</td><td>Papua New</td><td>New Britain</td><td>✓</td><td>✓</td></tr><tr><th><i>nicoleae ■</i></th><td></td><td></td><td></td><td>Guinea</td><td></td><td></td><td></td></tr><tr><th><i>Microphis</i></th><td>MNHN-IC-2021-0340</td><td>OQ221641.1</td><td>19174</td><td>Papua New</td><td>New Britain</td><td>✓</td><td>✓</td></tr><tr><th><i>nicoleae ■</i></th><td></td><td></td><td></td><td>Guinea</td><td></td><td></td><td></td></tr><tr><th></th><td></td><td><b>bold ID</b></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Hippichthys</i></th><td>MNHN-IC-2021-0315</td><td>OQ221729.1</td><td>18257</td><td>Solomon</td><td>Santa Isabel</td><td>✓</td><td>✓</td></tr><tr><th><i>heptagonus</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Hippichthys</i></th><td>MNHN-IC-2021-0316</td><td>OQ221728.1</td><td>18273</td><td>Solomon</td><td>Santa Isabel</td><td>✓</td><td>✓</td></tr><tr><th><i>heptagonus</i></th><td></td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th><i>Hippichthys</i></th><td>MNHN-IC-2022-0001</td><td>OQ221732.1</td><td>RTNC372</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>albomaculosus</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr><tr><th><i>Hippichthys</i></th><td>MNHN-IC-2022-0001</td><td>OQ221730.1</td><td>RTNC373</td><td>New</td><td>Grande Terre</td><td>✓</td><td>✓</td></tr><tr><th><i>albomaculosus</i></th><td></td><td></td><td></td><td>Caledonia</td><td></td><td></td><td></td></tr></tbody></table><p>......continued on the next page</p><p>......continued on the next page</p>
Data from: Sexual selection on female ornaments in the sex-role-reversed Gulf pipefish (Syngnathus scovelli)
Understanding how selection acts on traits individually and in combination is an important step in deciphering the mechanisms driving evolutionary change, but for most species, and especially those in which sexual selection acts more strongly on females than on males, we have no estimates of selection coefficients pertaining to the multivariate sexually selected phenotype. Here, we use a laboratory-based mesocosm experiment to quantify pre- and post-mating selection on female secondary sexual traits in the Gulf pipefish (Syngnathus scovelli), a sexually dimorphic, sex-role-reversed species in which ornamented females compete for access to choosy males. We calculate selection differentials and gradients on female traits, including ornament area, ornament number and body size for three episodes of selection related to female reproductive success (number of mates, number of eggs transferred and number of surviving embryos). Selection is strong on both ornament area and ornament size, and the majority of selection occurs during the premating episode of selection. Interestingly, selection on female body size, which has been detected in previous studies of Gulf pipefish, appears to be indirect, as evidenced by a multivariate analysis of selection gradients. Our results show that sexual selection favours either many bands or larger bands in female Gulf pipefish.
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.