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güüney sap gözlü -iensi

marywilliams:

Hey guys! Because of the great response I’ve gotten on this project, I wanted to make prints of the final available for everyone. If you’re interested, head over to my Society6 account and check it out! Here’s the link: http://society6.com/MaryWilliams.

(via scientificillustration)

smithsonianlibraries:

May 22 is the International Day for Biological Diversity. This year the theme is marine biodiversity.

International Day for Biological Diversity was created by the United Nations to increase the understanding and awareness of biodiversity issues. 

Images above from the Biodiversity Heritage Library (Smithsonian Libraries is just one of the many libraries that contribute to this collection, this item comes from our friends at the Museum of Comparative Zoology at Harvard.) The volume is entitled An attempt towards a natural history of the polype. Polyps belong to the phylum Cnidaria, which  includes

many charismatic organisms such as hydras, sea fans, jellyfishes, sea anemones, corals, and the Portuguese man-of-war. Cnidarians all have some type of specialized stinging cell organelle. Cnidarians’ bodies typically take one of two forms: the polyp or the medusa. While the polyp form is adapted for a sedentary or sessile lifestyle, the medusa form is adapted for floating or free-swimming. Sea anemones and corals (class Anthoza) are all polyps.  (quote from eol.org )

(Source: eskiesvaplarim)

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drawnblog:

These updated and animated archival photos are made by Kevin Weir over at Flux Machine. They remind me of Terry Gilliam’s animations for Monty Python, with a bit of the bizarre spookiness of Travis Louie.

(via stranger-than-kindness)

The Ancestral Genetic Code Cube from the Wolfram Demonstrations Project by Robersy Sánchez
scientificillustration:

Shoshonia arctopteryx gen. et sp. nov., an early coelacanth that preserves the oldest and most primitive paired fin skeleton known for that group. (A) Holotype (FMNH PF 15327) showing right flank scales and pectoral fin. Regions of the fish preserved in this specimen indicated by red area highlighted in hypothetical reconstruction. (B) Positive cast of the pectoral fin, including endoskeletal and dermal components. Fin endoskeleton has been false-color tinted for clarity. (C) Interpretive drawing of the pectoral fin endoskeleton. Abbreviations: l.sc, scales covering central lobe of pectoral fin; mes.III, mesomere three; mes.IV, mesomere four; mes.V, mesomere five; pr.v, ventral process of the mesomere; r.dst, distal radial; r.pst, postaxial radial; r.pre, preaxial radial.

Fig. 4. The evolution of pectoral appendages in early sarcopterygian fishes. Simplified cladogram adapted from that in Fig. 3 showing the distribution of major changes in pectoral appendage pattern in sarcopterygian fishes. This diagram encompasses the early diversity of pectoral appendages within crown-clade Sarcopterygii, and also illustrates selected patterns in proximal outgroups. Many previous depictions of sarcopterygian fin evolution (Coates et al. 2002; Long et al. 2006; Shubin et al. 2006) have been confined to the dipnomorph/tetrapodomorph clade, giving the misleading impression that the conditions found in dipnomorphs might be generalized. Bars representing character changes are color coded to indicate the aspects of morphology to which they refer, while the lengths of branches are scaled to the number of unambiguous character changes occurring along them. A key for these character changes is provided in supplementary material. Few changes separate Shoshonia and ‘osteolepiform’-grade tetrapodomorphs such as Gogonasus, Rhizodopsis, and Eusthenopteron from the base of Sarcopterygii as well as actinopterygian and acanthodian outgroups, but Latimeria and dipnomorphs are highly apomorphic, with many of their specializations arising in parallel.
First discovery of a primitive coelacanth fin fills a major gap in the evolution of lobed fins and limbs. Matt Friedman1,Michael I. Coates, Philip Anderson. Evolution & Development Volume 9, Issue 4, pages 329–337, July/August 2007 (pdf)

scientificillustration:

Shoshonia arctopteryx gen. et sp. nov., an early coelacanth that preserves the oldest and most primitive paired fin skeleton known for that group. (A) Holotype (FMNH PF 15327) showing right flank scales and pectoral fin. Regions of the fish preserved in this specimen indicated by red area highlighted in hypothetical reconstruction. (B) Positive cast of the pectoral fin, including endoskeletal and dermal components. Fin endoskeleton has been false-color tinted for clarity. (C) Interpretive drawing of the pectoral fin endoskeleton. Abbreviations: l.sc, scales covering central lobe of pectoral fin; mes.III, mesomere three; mes.IV, mesomere four; mes.V, mesomere five; pr.v, ventral process of the mesomere; r.dst, distal radial; r.pst, postaxial radial; r.pre, preaxial radial.

Fig. 4. The evolution of pectoral appendages in early sarcopterygian fishes. Simplified cladogram adapted from that in Fig. 3 showing the distribution of major changes in pectoral appendage pattern in sarcopterygian fishes. This diagram encompasses the early diversity of pectoral appendages within crown-clade Sarcopterygii, and also illustrates selected patterns in proximal outgroups. Many previous depictions of sarcopterygian fin evolution (Coates et al. 2002; Long et al. 2006; Shubin et al. 2006) have been confined to the dipnomorph/tetrapodomorph clade, giving the misleading impression that the conditions found in dipnomorphs might be generalized. Bars representing character changes are color coded to indicate the aspects of morphology to which they refer, while the lengths of branches are scaled to the number of unambiguous character changes occurring along them. A key for these character changes is provided in supplementary material. Few changes separate Shoshonia and ‘osteolepiform’-grade tetrapodomorphs such as Gogonasus, Rhizodopsis, and Eusthenopteron from the base of Sarcopterygii as well as actinopterygian and acanthodian outgroups, but Latimeria and dipnomorphs are highly apomorphic, with many of their specializations arising in parallel.

First discovery of a primitive coelacanth fin fills a major gap in the evolution of lobed fins and limbs. Matt Friedman1,Michael I. Coates, Philip Anderson. Evolution & Development Volume 9, Issue 4, pages 329–337, July/August 2007 (pdf)

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carlzimmer:

A hornbill from an 1882 monograph. I could look at this Flickr stream of old nature prints all day. (by BioDivLibrary)

carlzimmer:

A hornbill from an 1882 monograph. I could look at this Flickr stream of old nature prints all day. (by BioDivLibrary)

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