Choosing Crustaceans: All About Hermit Crabs
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Topazes and Hermits
Trochilidae I: Topazes and Hermits Fiery Topaz, Topaza pyra Topazini Crimson Topaz, Topaza pella Florisuginae White-necked Jacobin, Florisuga mellivora Florisugini Black Jacobin, Florisuga fusca White-tipped Sicklebill, Eutoxeres aquila Eutoxerini Buff-tailed Sicklebill, Eutoxeres condamini Saw-billed Hermit, Ramphodon naevius Bronzy Hermit, Glaucis aeneus Phaethornithinae Rufous-breasted Hermit, Glaucis hirsutus ?Hook-billed Hermit, Glaucis dohrnii Threnetes ruckeri Phaethornithini Band-tailed Barbthroat, Pale-tailed Barbthroat, Threnetes leucurus ?Sooty Barbthroat, Threnetes niger ?Broad-tipped Hermit, Anopetia gounellei White-bearded Hermit, Phaethornis hispidus Tawny-bellied Hermit, Phaethornis syrmatophorus Mexican Hermit, Phaethornis mexicanus Long-billed Hermit, Phaethornis longirostris Green Hermit, Phaethornis guy White-whiskered Hermit, Phaethornis yaruqui Great-billed Hermit, Phaethornis malaris Long-tailed Hermit, Phaethornis superciliosus Straight-billed Hermit, Phaethornis bourcieri Koepcke’s Hermit, Phaethornis koepckeae Needle-billed Hermit, Phaethornis philippii Buff-bellied Hermit, Phaethornis subochraceus Scale-throated Hermit, Phaethornis eurynome Sooty-capped Hermit, Phaethornis augusti Planalto Hermit, Phaethornis pretrei Pale-bellied Hermit, Phaethornis anthophilus Stripe-throated Hermit, Phaethornis striigularis Gray-chinned Hermit, Phaethornis griseogularis Black-throated Hermit, Phaethornis atrimentalis Reddish Hermit, Phaethornis ruber ?White-browed Hermit, Phaethornis stuarti ?Dusky-throated Hermit, Phaethornis squalidus Streak-throated Hermit, Phaethornis rupurumii Cinnamon-throated Hermit, Phaethornis nattereri Little Hermit, Phaethornis longuemareus ?Tapajos Hermit, Phaethornis aethopygus ?Minute Hermit, Phaethornis idaliae Polytminae: Mangos Lesbiini: Coquettes Lesbiinae Coeligenini: Brilliants Patagonini: Giant Hummingbird Lampornithini: Mountain-Gems Tro chilinae Mellisugini: Bees Cynanthini: Emeralds Trochilini: Amazilias Source: McGuire et al. (2014).. -
Observations on the Biology of the Hermit Crab, Coenobita Compressus H
Rev. Bio!' Tl'Op.. 20(2). 265-273. 1972 Observations on the biology of the hermit crab, Coenobita compressus H. Milne Edwards (Decapoda; Anomura) on the west coast of the Americas* by Eldon E. BaU" t, (Received for pubJi(ation )uly 5, 1972) AnSTRACT: The 5emi·terre,t¡ial hwnit rompl'eJ!llf, IS one erab, Cut/wbitll of tbe most conspicuous supra-littoral invertcbrates on the \Vest coast of the Amtrican UOpiC5. During Stanfvrcl Qctanographic Expeditivn lS. which 5�mplcd lhe intenidal Hora anJ fau"" al variouó points betwc�n Peru ami California, information \Vas (ollcctcd on lhe nahlral history of this species over a \Vide ran,¡;c oí lalitudes and habitatl, Thi5 information, whieh i, sumo mari!�d here, includes detJils on color, distribution, local names, type of .\ hell oc�\lpied, pcrccntage of fcm�k, ovigerous al \'ariou, localities, food and \'JriOllS a:;pteb oi beha,'i()!'. 111e semi·terrcstrial hcrmit crab H. MiJl1C Edwards CQ(J10bit" compl'l'JJtti IS a conspicuous and frcqucntly abundant iohabitant of the supra.Jittoral zone of thc castcrn tropical Pacific fl'OlTI Mcxico to Pcru. However, aside fmm brid mentions in the papers of (2), BRlGHT (1), and I-IAIG, el al. (3), GLASSELL there is little information available 00 the natural histo¡y of this species. ConsiderabJe mformation on the biology of was Coellohifa wmpreJJtiJ obtained as part of a survey oE the hermit crab fauna o[ the castern tropical Pa· cific during Stanford Oceanogra hlC Expcditioo 18 from l\pril to June p 1968. 11115 cxpcdition, abüard lhe RV Te Vega, sampled lhc mteríldal fauna and Íiora from Paila, Perú (50S) to Bahía Magdalena, Ba¡a California (24"N), A mal.' of this cruisc and a station list are prcscnted in Fi¡z.urc 1 ;tnd TabIe 1, rcspcctively. -
Reappraisal of Hermit Crab Species (Crustacea: Anomura: Paguridea) Reported by Camill Heller in 1861, 1862 and 1865
Ann. Naturhist. Mus. Wien 103 B 135 - 176 Wien, Dezember 2001 Reappraisal of hermit crab species (Crustacea: Anomura: Paguridea) reported by Camill Heller in 1861, 1862 and 1865 P.A. McLaughlin1 & P.C. Dworschak2 Abstract Redescriptions based on the type material are presented for 11 species of hermit crabs described as new by Camill Heller (HELLER 1861a, c, 1862, 1865): Coenobita violascens HELLER, 1862, Diogenes avarus HELLER, 1865 - for which a lectotype is designated, Diogenes senex HELLER, 1865, Pagurus varipes HELLER, 1861 [= Dardanus tinctor (FORSKÅL, 1775)], Pagurus depressus HELLER, 1861 [= Dardanus lago- podos (FORSKÅL, 1775)], Calcinus rosaceus HELLER, 1861, Calcinus nitidus HELLER, 1865, Clibanarius carnifex HELLER, 1861, Clibanarius signatus HELLER, 1861, Paguristes barbatus (HELLER, 1862) and Paguristes ciliatus HELLER, 1862. For 7 of those, detailed figures are provided. In addition, the material from the Red Sea along with the hermit crabs obtained during the circumnavigation of the earth by the fri- gate 'Novara' and identified by him have been reevaluated and necessary corrections made. Keywords: Crustacea, Anomura, Paguridea, Camill Heller, Novara, lectotype designation Zusammenfassung Elf Arten von Einsiedlerkrebsen, die Camill Heller als neue Arten beschrieb (HELLER 1861a, c, 1862, 1865), werden hier anhand des Typenmaterials wiederbeschrieben: Coenobita violascens HELLER, 1862, Diogenes avarus HELLER, 1865 - für die ein Lectotypus designiert wird, Diogenes senex HELLER, 1865, Pagurus varipes HELLER, 1861 [= Dardanus tinctor (FORSKÅL, 1775)], Pagurus depressus HELLER, 1861 [= Dardanus lago- podos (FORSKÅL, 1775)], Calcinus rosaceus HELLER, 1861, Calcinus nitidus HELLER, 1865, Clibanarius carnifex HELLER, 1861, Clibanarius signatus HELLER, 1861, Paguristes barbatus (HELLER, 1862) und Paguristes ciliatus HELLER, 1862. Zu sieben Arten davon werden detailierte Zeichnungen präsentiert. -
Ecography ECOG-01538 Maglianesi, M
Ecography ECOG-01538 Maglianesi, M. A., Blüthgen, N., Böhning-Gaese, K. and Schleuning, M. 2015. Topographic microclimates drive microhabitat associations at the range margin of a butterfly. – Ecography doi: 10.1111/ecog.01538 Supplementary material Appendix 1 Table A1. List of families, genera and species of plants recorded by identification of pollen loads carried by hummingbird individuals at three elevations in northeastern Costa Rica. Only plant morphotypes that could be identified to species, genus or family level are given. The proportion of pollen identified to species level was 43% and that identified to a higher taxonomic level was 10%; 47% of pollen grains were categorized into pollen morphotypes (not shown here). Plant families are ordered alphabetically within each elevation. Elevation Family Genus Species Low Bromeliaceae Aechmea Aechmea mariareginae Low Acanthaceae Aphelandra Aphelandra storkii Low Bignoniaceae Arrabidaea Arrabidaea verrucosa Low Gesneraciae Besleria Besleria columnoides Low Alstroemeriaceae Bomarea Bomarea obovata Low Gesneriaceae Columnea Columnea linearis Low Gesneraceae Columnea Columnea nicaraguensis Low Gesneraceae Columnea Columnea purpurata Low Gesneraceae Columnea Columnea querceti Low Costaceae Costus Costus pulverulentus Low Costaceae Costus Costus scaber Low Costaceae Costus Costus sp 1 Low Gesneriaceae Drymonia Drymonia macrophylla Low Ericaceae Ericaceae Ericaceae 1 Low Ericaceae Ericaceae Ericaceae 2 Low Bromeliaceae Guzmania Guzmania monostachia Low Rubiaceae Hamelia Hamelia patens Low Heliconiaceae -
Nesting Behavior of Reddish Hermits (Phaethornis Ruber) and Occurrence of Wasp Cells in Nests
NESTING BEHAVIOR OF REDDISH HERMITS (PHAETHORNIS RUBER) AND OCCURRENCE OF WASP CELLS IN NESTS YOSHIKA ONIKI REDraSHHermits (Phaethornisruber) are small hummingbirdsof the forested tropical lowlands east of the Andes and south of the Orinoco (Meyer de Schauensee,1966: 161). Five birds mist-nettedat Belem (1 ø 28' S, 48ø 27' W, altitude 13 m) weighed2.0 to 2.5 g (average2.24 g). I studiedtheir nestingfrom 14 October1966 to October1967 at Belem, Brazil, in the Area de PesquisasEco16gicas do Guam•t (APEG) and MocamboForest reserves,in the Instituto de Pesquisase Experimentaqfio Agropecu•triasdo Norte (IPEAN). Names of forest types used and the Portugueseequivalents are: tidal swamp forest (vdrze'a), mature upland forest (terra-/irme) and secondgrowth (capoeira). In all casescapo.eira has been in mature upland situations. At Belem Phaethornisruber is commonall year in the lower levels of secondgrowth (capoeira) where thin branchesare plentiful. Isolated males call frequently from thin horizontal branches,never higher than 2.5-3.0 m. The male sits erect and wags his tail forward and backward as he squeaksa seriesof insectlike"pi-pi-pipipipipipi" notes, 18-20 times per minute; the first two or three notesare short and separated,the rest are run togetherrapidly. The bird sometimesstops calling for someseconds and flasheshis tongue in and out several times during the interval. I foundno singingassemblies of malehermits such as Davis (1934) describes for both the Reddishand Long-tailedHermits (Phaethornissuperciliosus). and Snow (1968) for the Little Hermit (P. longuemareus). Breeding season.--The monthly rainfall at Belem in the year of the study was 350 to 550 mm from January to May and 25 to 200 mm from June to December,with lows in October and November and highs in March and April. -
Land Hermit Crab (Coenobita Clypeatus) Densities and Patterns Of
Journal of Biogeography (J. Biogeogr.) (2006) 33, 314–322 ORIGINAL Land hermit crab (Coenobita clypeatus) ARTICLE densities and patterns of gastropod shell use on small Bahamian islands Lloyd W. Morrison1* and David A. Spiller2 1Department of Biology, Missouri State ABSTRACT University, Springfield, MO, USA and 2Center Aim To examine patterns of abundance, density, size and shell use in land hermit for Population Biology and Section of Evolution and Ecology, University of California, Davis, crabs, Coenobita clypeatus (Herbst), occurring on three groups of small islands, CA, USA and to determine how these variables change among islands. Location Small islands in the Central Exuma Cays and near Great Exuma, Bahamas. Methods Land hermit crabs were captured in baited pitfall traps and were separately attracted to baits. A mark–recapture technique was used in conjunction with some pitfall traps monitored for three consecutive days. The size of each crab and the type of adopted gastropod shell were recorded, along with physical island variables such as total island area, vegetated area, island perimeter, elevation and distance to the nearest mainland island. Results Relative abundances, densities and sizes of crabs differed significantly among the three island groups. Densities of land hermit crabs were as high as ) 46 m 2 of vegetated island area. In simple and multiple linear regressions, the only variable that was a significant predictor of the abundance of hermit crabs was the perimeter to area ratio of the island. Patterns of gastropod shell use varied significantly among the island groups, and the vast majority of adopted shells originated from gastropod species that inhabit the high intertidal and supratidal shorelines of the islands. -
Hermit Crabs. During the Hottest Times of the Day They'll Hide to Avoid the Heat, So Look for Them Under Flotsam and Jetsam and Sea Shore Plants
HERMIT CRABS Hermit crabs are unusual because they use sea snail shells for their homes. Recycling shells has helped hermit crabs wander where their crab cousins fear to tread. HOME SWEET HOME To hermit crabs, snail shells are everything! If startled, they use their snail shells for protection. They tuck neatly into a ball, using strong front legs and nippers to block the entrance from intruders. The shell also keeps them wet when they venture onto land, shields them from the sun's rays and is a protected place for them to lay their eggs. Some hermit crabs allow other marine life to piggy-back on their snail shells. The sea anemone is a welcome hitch-hiker as it stings predators. The anemone benefits from the ride by feeding on tiny particles of food as it is moved around. This arrangement, which benefits both creatures, is known as A marine hermit crab with symbiosis. a sea anemone attached to its shell. Shaped to fit! Hermit crabs are arthropods and therefore have an exoskeleton (a hard shell-like covering). The original crab body shape has changed to fit the shape of snail shells, making them look more like a crayfish. The soft abdomen is shaped to curl inside the shell opening. Their four rear legs hang tightly onto the inside of the shell. Their four front legs are used for walking and must be powerful to be able to pull a house along! They have two front nippers used to cut up their food and defend themselves. WARNING: never try to pull a hermit crab from a shell; they hang on so well that they may be torn apart! Close up of Hermit crab habitat baby hermit crab Cheliped (zooplankton). -
Observations of Hummingbird Feeding Behavior at Flowers of Heliconia Beckneri and H
SHORT COMMUNICATIONS ORNITOLOGIA NEOTROPICAL 18: 133–138, 2007 © The Neotropical Ornithological Society OBSERVATIONS OF HUMMINGBIRD FEEDING BEHAVIOR AT FLOWERS OF HELICONIA BECKNERI AND H. TORTUOSA IN SOUTHERN COSTA RICA Joseph Taylor1 & Stewart A. White Division of Environmental and Evolutionary Biology, Graham Kerr Building, University of Glasgow, Glasgow, CB23 6DH, UK. Observaciones de la conducta de alimentación de colibríes con flores de Heliconia beckneri y H. tortuosa en El Sur de Costa Rica. Key words: Pollination, sympatric, cloud forest, Cloudbridge Nature Reserve, Green Hermit, Phaethornis guy, Violet Sabrewing, Campylopterus hemileucurus, Green-crowned Brilliant, Heliodoxa jacula. INTRODUCTION sources in a single foraging bout (Stiles 1978). Interactions between closely related sympatric The flower preferences shown by humming- flowering plants may involve competition for birds (Trochilidae) are influenced by a com- pollinators, interspecific pollen loss and plex array of factors including their bill hybridization (e.g., Feinsinger 1987). These dimensions, body size, habitat preference and processes drive the divergence of genetically relative dominance, as influenced by age and based floral phenotypes that influence polli- sex, and how these interact with the morpho- nator assemblages and behavior. However, logical, caloric and visual properties of flow- floral convergence may be favored if the ers (e.g., Stiles 1976). increased nectar supplies and flower densities, Hummingbirds are the primary pollina- for example, increase the regularity and rate tors of most Heliconia species (Heliconiaceae) of flower visitation for all species concerned (Linhart 1973), which are medium to large (Schemske 1981). Sympatric hummingbird- clone-forming herbs that usually produce pollinated plants probably face strong selec- brightly colored floral bracts (Stiles 1975). -
Basic Crab Care
BASIC CRAB CARE Blondie the Ecuadorian crab Just the Basics To live comfortably in captivity, hermit crabs require the following: • Temperature no lower than 72°F. Consistent low temperatures can kill a hermit crab. Don't allow them to bake in a window, either. If they get too hot they will die, and overheating causes irreversible damage and a slow, painful death. Signs of overheating are a musty smell and discharge of brown liquid • A constant humidity level of at LEAST 70% humidity. Try to remember that you want the inside of your crabitat to have a moist, "tropical" feel to it • Substrate deep enough that the crabs can bury but not so deep that it negates the effects of your under-tank heater. If you are having trouble keeping your crabitat warm, try moving some substrate from over the heater. If you are having trouble getting the crabitat to cool down, turn off the heater. See the molting page if you need information on heating a molter's isolation tank • Food, water, shells and other tank decorations to keep the crabs engaged and active. Friends! I'm sure you've heard this before, but you really shouldn't keep only one hermit crab alone as a pet. The name 'hermit' is misapplied to our little friends -- they are quite gregarious and like to be around their own kind. In the wild, they travel in packs of up to 100 crabs, scavenging the beach for food and shells. The reason they travel in packs is simple: Where there are more crabs, there are more shells. -
The Behavior and Ecology of Hermit Hummingbirds in the Kanaku Mountains, Guyana
THE BEHAVIOR AND ECOLOGY OF HERMIT HUMMINGBIRDS IN THE KANAKU MOUNTAINS, GUYANA. BARBARA K. SNOW OR nearly three months, 17 January to 5 April 1970, my husband and I F camped at the foot of the Kanaku Mountains in southern Guyana. Our camp was situated just inside the forest beside Karusu Creek, a tributary of Moco Moco Creek, at approximately 80 m above sea level. The period of our visit was the end of the main dry season which in this part of Guyana lasts approximately from September or October to April or May. Although we were both mainly occupied with other observations we hoped to accumulate as much information as possible on the hermit hummingbirds of the area, particularly their feeding niches, nesting and social organization. Previously, while living in Trinidad, we had studied various aspects of the behavior and biology of the three hermit hummingbirds resident there: the breeding season (D. W. Snow and B. K. Snow, 1964)) the behavior at singing assemblies of the Little Hermit (Phaethornis Zonguemareus) (D. W. Snow, 1968)) the feeding niches (B. K. Snow and D. W. Snow, 1972)) the social organization of the Hairy Hermit (Glaucis hirsuta) (B. K. Snow, 1973) and its breeding biology (D. W. Snow and B. K. Snow, 1973)) and the be- havior and breeding of the Guys’ Hermit (Phuethornis guy) (B. K. Snow, in press). A total of six hermit hummingbirds were seen in the Karusu Creek study area. Two species, Phuethornis uugusti and Phaethornis longuemureus, were extremely scarce. P. uugusti was seen feeding once, and what was presumably the same individual was trapped shortly afterwards. -
How to Become a Crab: Phenotypic Constraints on a Recurring Body Plan
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 25 December 2020 doi:10.20944/preprints202012.0664.v1 How to become a crab: Phenotypic constraints on a recurring body plan Joanna M. Wolfe1*, Javier Luque1,2,3, Heather D. Bracken-Grissom4 1 Museum of Comparative Zoology and Department of Organismic & Evolutionary Biology, Harvard University, 26 Oxford St, Cambridge, MA 02138, USA 2 Smithsonian Tropical Research Institute, Balboa–Ancon, 0843–03092, Panama, Panama 3 Department of Earth and Planetary Sciences, Yale University, New Haven, CT 06520-8109, USA 4 Institute of Environment and Department of Biological Sciences, Florida International University, Biscayne Bay Campus, 3000 NE 151 Street, North Miami, FL 33181, USA * E-mail: [email protected] Summary: A fundamental question in biology is whether phenotypes can be predicted by ecological or genomic rules. For over 140 years, convergent evolution of the crab-like body plan (with a wide and flattened shape, and a bent abdomen) at least five times in decapod crustaceans has been known as ‘carcinization’. The repeated loss of this body plan has been identified as ‘decarcinization’. We offer phylogenetic strategies to include poorly known groups, and direct evidence from fossils, that will resolve the pattern of crab evolution and the degree of phenotypic variation within crabs. Proposed ecological advantages of the crab body are summarized into a hypothesis of phenotypic integration suggesting correlated evolution of the carapace shape and abdomen. Our premise provides fertile ground for future studies of the genomic and developmental basis, and the predictability, of the crab-like body form. Keywords: Crustacea, Anomura, Brachyura, Carcinization, Phylogeny, Convergent evolution, Morphological integration 1 © 2020 by the author(s). -
Ga7459. B) Polyonyx Pedalis, 1 Female 4.56×4.73 Mm, Mayotte, St
23 Figure 11. A) Polyonyx biunguiculatus, 1 male 2.68×3.23 mm, Mayotte, St. 23, MNHN- Ga7459. B) Polyonyx pedalis, 1 female 4.56×4.73 mm, Mayotte, St. 19, MNHN-Ga7464 (coloration altered by preservative). C) Polyonyx triunguiculatus, 1 male 3.69×4.37, Mayotte, St. 23, MNHN-Ga7438. D) Polyonyx aff. boucheti, 1 ovigerous female 2.20×3.24 mm, Mayotte, St. 12, MNHN-Ga7465. Polyonyx triunguiculatus Zehntner, 1894 Polyonyx triunguiculatus (Figure 11 C) - Haig, 1966: 44 (Mayotte, lagoon, small blocks and coarse sands, coll. A. Crosnier, September 1959, 2 males 2.7 and 3.2 mm, 1 female 1.9 mm, 2 ovigerous females 3.1 and 3.2 mm; same, coarse sands, 50 m, 1 male 3.7 mm, 1 female 3.3 mm, MNHN). - BIOTAS collections, Glorioso, 3-7 May 2009, det. J. Poupin from photo, St. GLOR-2, reef platform and shallow canyons with dead Acropora digitifera head, 7-14 m, specimen MEPA 948; St. GLOR-5, reef slope East side, 17 m, specimen MEPA 1045. - Mayotte, KUW fieldwork November 2009, St. 14, La Prudente bank, 15-17 m, 2 males 3.38×4.13 and 3.31×3.79 mm, 1 ovigerous female 3.29×4.20, 1 juvenile broken, MNHN-Ga7436; St. 17, North reef, 22 m, 1 male 3.43×3.94, 1 ovigerous female 3.10×3.97 mm, MNHN-Ga7437; St. 23, Choizil pass ‘Patate à Teddy’, 15-30 m, 1 male 3.69×4.37, 1 female 2.72×3.12 mm, MNHN-Ga7438; St. 25, islet M'tzamboro, 15-20 m, 1 ovigerous female 3.46×4.45 mm, 1 female 2.74×3.06 mm, 2 ovigerous females 2.89×3.44 and 3.40×3.99 mm, 1 female not measured, MNHN-Ga7439; St.