Results 31 to 40 of about 83,361 (251)

Host-related Morphological Variation of Dwellings Inhabited by the Crab Domecia acanthophora in the Corals Acropora palmata and Millepora complanata (Southern Caribbean)

Diversity, 2020
Brachyuran crabs of various families are known as obligate associates of stony corals, with many of these species living as endosymbionts inside the skeleton of their hosts [...]
Bert W. Hoeksema, Jaaziel E. García-Hernández   +1 more
doaj   +1 more source

Conserved organ-specific microbial assemblages in different populations of a terrestrial crab

Frontiers in Microbiology, 2023
Microorganisms are ubiquitous in the environment and provide genetic and physiological functions to multicellular organisms. Knowledge on the associated microbiota is becoming highly relevant to understand the host’s ecology and biology.
Giovanni Bacci, Sara Fratini, Sara Fratini, Niccolò Meriggi, Christine L. Y. Cheng, Ka Hei Ng, Massimo Pindo, Alessio Iannucci, Alessio Iannucci, Alessio Mengoni, Duccio Cavalieri, Duccio Cavalieri, Stefano Cannicci, Stefano Cannicci, Stefano Cannicci   +14 more
doaj   +1 more source

Brachyuran Crabs collected at Curaçao [PDF]

Bijdragen tot de Dierkunde, 1924
In 1920 a report ¹) on Dr. BOEKE’S collection of crabs and shrimps from Curaçao and other Dutch West Indian Islands was published. Dr. VAN DER HORST’S collection forms an important addition to the fauna of Curaçao, especially as to the Xanthids and Majids, or spider crabs.
openaire   +3 more sources

West African Brachyuran crabs

Smithsonian Contributions to Zoology, 1981
NH-Invertebrate Zoology ; si-staff ; NMNH ; SISP ; Peer ...
Manning, Raymond B., Holthuis, L. B.
openaire   +2 more sources

The highly rearranged mitochondrial genomes of the crabs Maja crispata and Maja squinado (Majidae) and gene order evolution in Brachyura [PDF]

, 2017
We sequenced the mitochondrial genomes of the spider crabs Maja crispata and Maja squinado (Majidae, Brachyura). Both genomes contain the whole set of 37 genes characteristic of Bilaterian genomes, encoded on both \u3b1- and \u3b2-strands.
AD Miller, AE Smith, AH Sahyoun, AT Beckenbach, BQ Minh, C Hahn, C Moritz, DR Wolstenholme, DV Lavrov, E Negrisolo, F Jühling, F Kilpert, FJ Lin, G Shi, G Shi, G Sotelo, G Tan, G Tang, H Ma, H Shen, H Shimodaira, H Sun, I Marcadé, IM Fearnley, J Yang, JD Thompson, JL Boore, JL Boore, JL Boore, JL Boore, JM Sung, JM Sung, JS Ki, K Strimmer, K Tamura, LM Tsang, LS Quang, LT Nguyen, M Babbucci, M Bernt, M Bernt, M Bernt, M Dowton, M Hui, MH Tan, MH Tan, MM Yamauchi, N Lartillot, NT Perna, O Rota-Stabelli, P Cantatore, P Salvato, R Lanfear, R Raimond, RD Segawa, S Grave De, S Montelli, S Saito, SF Altschul, SJ Kim, SL Cameron, TA Rawlings, TM Lowe, X Wang, Y Xing, YK Ji, YQ Yu, Z Yang   +67 more
core   +1 more source

Climate Change and invasibility of the Antarctic benthos [PDF]

, 2007
Benthic communities living in shallow-shelf habitats in Antarctica (<100-m depth) are archaic in their structure and function. Modern predators, including fast-moving, durophagous (skeleton-crushing) bony fish, sharks, and crabs, are rare or absent ...
A Brandt, A Brandt, A Brandt, A Brandt, A Clarke, A Clarke, A Clarke, A Clarke, A Clarke, AL Allcock, Andrew Clarke, BA Seibel, Brad A. Seibel, Cheryl D. Wilga, D Thies, DA Hodgson, Daniel B. Blake, DS Coombs, EW Dawson, G Chapelle, GA Knox, GA Lovrich, GE Hofmann, GJ Vermeij, JC Carrier, JE Werner, JH Lipps, JM Raguá-Gil, JP Kennett, JS Pearse, JT Eastman, JT Eastman, JW Wakeling, L Watling, LC Ivany, LI Comoglio, Lloyd S. Peck, LS Peck, M Klages, MA Bitner, P Huybrechts, PA Fields, PD Glorioso, PM Arnaud, Pörtner H-O, R Revelle, RB Aronson, Richard B. Aronson, RJ Menzies, RM Feldmann, S Thatje, S Thatje, SM Stanley, Snelgrove PVR, ST Ahyong, Sven Thatje, T Antezana, T Brey, TJ Page, U Piatkowski, WE Arntz, WE Arntz, WE Arntz   +62 more
core   +1 more source

Systematic assessment of the Panopeidae and broader Eubrachyura (Decapoda: Brachyura) using mitochondrial genomics [PDF]

Arthropod Systematics & Phylogeny, 2021
This study provides a broad phylogenetic analysis for the Eubrachyura, with the inclusion of three new Panopeidae mitochondrial genomes: Eurypanopeus depressus (flatback mud crab) (15,854bp), Panopeus herbstii (Atlantic mud crab) (15,812bp) and ...
Lucas A. Jennings, April M. H. Blakeslee, Krista A. McCoy, Donald C. Behringer, Jamie Bojko   +4 more
doaj   +3 more sources

Report of brachyuran crabs (Crustacea, Decapoda) from the Pliocene of Borgomanero, Novara (Piedmont, NW Italy)

Natural History Sciences, 2018
Some brachyuran crabs from the Pliocene of a new outcrop nearby Borgomanero (Novara, Piedmont, NW Italy) are reported. This study allows us to recognize a peculiar brachyuran crabs assemblage including: Macropipus cf. M.
Giovanni Pasini, Alessandro Garassino, Piero Damarco   +2 more
doaj   +1 more source

Global Distribution of Brachyuran Crabs in Mangroves

Sustainable Marine Structures, 2023
The present work has compiled a total of 389 brachyuran crab species belonging to 188 genera and 38 families to be present in mangrove forests across 122 countries/territories in 10 sub-regions of two global hemispheres viz., Indo-West Pacific (IWP) and Atlantic East Pacific (AEP).
Wah Wah Min, K. Kathiresan
openaire   +1 more source

Feeding spectra and activity of the freshwater crab Trichodactylus kensleyi (Decapoda: Brachyura: Trichodactylidae) at La Plata basin [PDF]

, 2014
Background: In inland water systems, it is important to characterize the trophic links in order to identify the ‘trophic species’ and, from the studies of functional diversity, understand the dynamics of matter and energy in these environments.
A Ruttner-Kolisko, AA Bonetto, AH Beltzer, AH Beltzer, AH Beltzer, B Hepher, BL Zimmermann, C Magalhães, C Sokolowicz, CE Cushing, CG Vélez, CP Balasubramanian, CS Pontes, DA Carvalho, DA Carvalho, DA Carvalho, E Massoia, EC Lopretto, ED Burress, F Fernandez de Miguel, FL Zilli, FLM Mantelatto, FLM Mantelatto, G Mancinelli, G Woodward, GAS Melo, H Aréchiga, HJ Dumont, I Ezcurra de Drago, I Nordhaus, II César, IJ McGaw, J Aguzzi, J Freire, J Josileen, JD Icely, JG Irons, JH Zar, JJ Bianchini, JJ Neiff, K Cheshire, KD Colpo, L Pinkas, LA López, M Devercelli, M Dobson, M Zimmer, MG Frick, N Kronfeld-Schor, N Lo, N Myers, P Kratina, PA Collins, PA Collins, PA Collins, PA Collins, R Pirela, RC Lajmanovich, RG Wear, RK Colwell, S Cannicci, S Daan, SM Linton, SM Linton, SP Hart, V Williner, V Williner, V Williner, WF Edmonson, WJ Mattson, ZT Long   +70 more
core   +1 more source