"Gastropoda" - Books

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Results: 14 books (32 items)

Select item 14152801.

Madame Curie Bioscience Database [Internet].

Austin (TX): Landes Bioscience; 2000-2013.

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Select item 31050562.

In the Light of Evolution: Volume VI: Brain and Behavior.

National Academy of Sciences; Striedter GF, Avise JC, Ayala FJ, editors.

Washington (DC): National Academies Press (US); 2013 Jan 25.

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Select item 31318243.

In the Light of Evolution: Volume II: Biodiversity and Extinction.

National Research Council (US); Avise JC, Hubbell SP, Ayala FJ, editors.

Washington (DC): National Academies Press (US); 2008.

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Select item 16072124.

Developmental Biology. 6th edition.

Gilbert SF.

Sunderland (MA): Sinauer Associates; 2000.

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Select item 31129085.

50 Years of Ocean Discovery: National Science Foundation 1950—2000.

National Research Council (US) Ocean Studies Board.

Washington (DC): National Academies Press (US); 2000.

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Select item 44036686.

StatPearls [Internet].

Treasure Island (FL): StatPearls Publishing; 2026 Jan-.

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Select item 57441727.

Anthracene, 2-Bromopropane, Butyl Methacrylate, and Dimethyl Hydrogen Phosphite.

IARC Working Group on the Identification of Carcinogenic Hazards to Humans.

Lyon (FR): International Agency for Research on Cancer; 2024. (IARC Monographs on the Identification of Carcinogenic Hazards to Humans, No. 133.)

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Select item 14447648.

Ecology, Epidemiology, and Evolution of Parasitism in Daphnia [Internet].

Ebert D.

Bethesda (MD): National Center for Biotechnology Information (US); 2005.

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Select item 19508929.

Entrez® Programming Utilities Help [Internet].

Bethesda (MD): National Center for Biotechnology Information (US); 2010-.

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Select item 323422410.

Molecular Biology in Marine Science: Scientific Questions, Technological Approaches, and Practical Implications.

National Research Council (US) Committee on Molecular Marine Biology.

Washington (DC): National Academies Press (US); 1994.

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Select item 326611811.

Neem: A Tree For Solving Global Problems.

National Research Council (US) Panel on Neem.

Washington (DC): National Academies Press (US); 1992.

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Select item 327192012.

Animals for Research: A Directory of Sources. 10th edition.

National Research Council (US) Institute for Laboratory Animal Research.

Washington (DC): National Academies Press (US); 1979.

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Select item 425362813.

Polychlorinated Biphenyls and Polybrominated Biphenyls.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 2016. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 107.)

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Select item 553632614.

Toxicological Profile for Atrazine.

Atlanta (GA): Agency for Toxic Substances and Disease Registry (US); 2003 Sep.

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FIGURE 9.6

Homologues of the Tritonia DV swim CPG neurons are not rhythmically active during LR swim motor patterns. (A) In Melibe, the C2 and DSI homologues do not display any rhythmic bursting in phase with the swim motor pattern reflected in the alternating firing pattern of the left and right Si. (B) In Dendronotus, a contralateral pair of DSI homologues exhibit synchronous irregular spiking that shows no relation to the ongoing LR swim motor pattern displayed by two contralateral pedal motor neurons (L-Pd and R-Pd).

Homology and Homoplasy of Swimming Behaviors and Neural Circuits in the Nudipleura (Mollusca, Gastropoda, Opisthobranchia).

National Academy of Sciences; Striedter GF, Avise JC, Ayala FJ, editors. In the Light of Evolution: Volume VI: Brain and Behavior. Washington (DC): National Academies Press (US); 2013 Jan 25.
FIGURE 9.2

Two examples of swimming behaviors. (A) LR swimming exhibited by M. leonina. The ventral side of the animal is shown with the mouth at the top of the image. During swimming, the foot is narrowed to a strip and the animal rhythmically flexes its body leftward and rightward, bending at a point midway along the body axis. (B) DV swimming exhibited by T. diomedea. The animal starts on the substrate, shown at the bottom with its head to the right. It launches with a ventral flexion, where the head and tail meet under the foot. Then, it flexes so that the head and tail meet above the dorsal body surface. The foot is flattened and expanded to the width of the body. A, anterior; P, posterior.

Homology and Homoplasy of Swimming Behaviors and Neural Circuits in the Nudipleura (Mollusca, Gastropoda, Opisthobranchia).

National Academy of Sciences; Striedter GF, Avise JC, Ayala FJ, editors. In the Light of Evolution: Volume VI: Brain and Behavior. Washington (DC): National Academies Press (US); 2013 Jan 25.
FIGURE 9.1

An abbreviated phylogeny of the Nudipleura with reference to their behavior. Only the genera of the species listed in Table 9.1 are shown here unless species differences exist within the genus. The phylogenic relationships are based on Thollesson (1999), Waegele and Willan (2000), Wollscheid-Lengeling et al. (2001), Vonnemann et al. (2005), Göbbeler and Klussmann-Kolb (2010), and Pola and Gosliner (2010). The references for the behavior are listed in Table 9.1. Note that this figure represents all the known swimming species and only a tiny fraction of the more than 2,000 species that are not capable of swimming or for which there are no published reports of swimming. LR, left–right flexion; NS, nonswimmer; DV, dorsal–ventral flexion; LU, left–right undulation; BS, breaststroke; DU, dorsal–ventral undulation; AU, asymmetric undulation; F, flapping.

Homology and Homoplasy of Swimming Behaviors and Neural Circuits in the Nudipleura (Mollusca, Gastropoda, Opisthobranchia).

National Academy of Sciences; Striedter GF, Avise JC, Ayala FJ, editors. In the Light of Evolution: Volume VI: Brain and Behavior. Washington (DC): National Academies Press (US); 2013 Jan 25.
FIGURE 9.3

Possible evolutionary scenarios explaining the phylogenetic distribution of swimming behaviors. Just the families of the DV and LR swimming animals are shown. (A) In scenario 1, DV swimming is a synapomorphy of the Nudipleura that was lost and replaced six times by LR swimming. (B) In scenario 2, LR swimming is a synapomorphy of the Nudibranchia. DV swimming then reappears four times in different nudibranch lineages. (C) For scenario 3, the phylogenetic tree of Dendronotida is altered to group LR swimmers together. Goniodorididae (asterisk), which includes T. velox, is switched from LR to DV (as discussed in the text). This reduces the number of transitions to LR from six in scenario 1 to four. (D) Scenario 4 is similar to scenario 2, with Goniodorididae (asterisk) switched to DV. This represents the most parsimonious explanation if DV swimming is ancestral, with just three transitions from the basal DV state.

Homology and Homoplasy of Swimming Behaviors and Neural Circuits in the Nudipleura (Mollusca, Gastropoda, Opisthobranchia).

National Academy of Sciences; Striedter GF, Avise JC, Ayala FJ, editors. In the Light of Evolution: Volume VI: Brain and Behavior. Washington (DC): National Academies Press (US); 2013 Jan 25.