Do chitons have a compass? Evidence for magnetic sensitivity in Polyplacophora

Several animals and microbes have been shown to be sensitive to magnetic fields, though the exact mechanisms of this ability remain unclear in many animals. Chitons are marine molluscs which have high levels of biomineralised magnetite coating their radulae. This discovery led to persistent anecdotal suggestions that they too may be able to navigationally respond to magnetic fields. Several researchers have attempted to test this, but to date there have been no large-scale controlled empirical trials. In the current study, four chiton species (Katharina tunicata, Mopalia kennerleyi, Mopalia muscosa and Leptochiton rugatus, n=24 in each) were subjected to natural and artificially rotated magnetic fields while their movement through an arena was recorded over four hours. Field orientation did not influence the position of the chitons at the end of trials, possibly as a result of the primacy of other sensory cues (i.e. thigmotaxis). Under non-rotated magnetic field conditions, the orientation of subjects when they first reached the edge of an arena was clustered around 309-345 degrees (north-north-west) in all four species. However, orientations were random under the rotated magnetic field, which may indicate a disruptive effect of field rotation. This pattern suggests that chitons can detect and respond to magnetism.

Grazing under experimental hypercapnia and elevated temperature does not affect the radula of a chiton (Mollusca, Polyplacophora, Lepidopleurida)

Chitons (class Polyplacophora) are benthic grazing molluscs with an eight-part aragonitic shell armature. The radula, a serial tooth ribbon that extends internally more than half the length of the body, is mineralised on the active feeding teeth with iron magnetite apparently as an adaptation to constant grazing on rocky substrates. As the anterior feeding teeth are eroded they are shed and replaced with a new row. The efficient mineralisation and function of the radula could hypothetically be affected by changing oceans in two ways: changes in seawater chemistry (pH and pCO(2)) may impact the biomineralisation pathway, potentially leading to a weaker or altered density of the feeding teeth; rising temperatures could increase activity levels in these ectothermic animals, and higher feeding rates could increase wear on the feeding teeth beyond the animals' ability to synthesise, mineralise, and replace radular rows. We therefore examined the effects of pH and temperature on growth and integrity in the radula of the chiton Leptochiton asellus. Our experiment implemented three temperature (similar to 10, 15, 20 degrees C) and two pCO(2) treatments (similar to 400 mu atm, pH 8.0; similar to 2000 mu atm, pH 7.5) for six treatment groups. Animals (n = 50) were acclimated to the treatment conditions for a period of 4 weeks. This is sufficient time for growth of ca. 7-9 new tooth rows or 20% turnover of the mineralised portion. There was no significant difference in the number of new (non-mineralised) teeth or total tooth row count in any treatment. Examination of the radulae via SEM revealed no differences in microwear or breakage on the feeding cusps correlating to treatment groups. The shell valves also showed no signs of dissolution. As a lineage, chitons have survived repeated shifts in Earth's climate through geological time, and at least their radulae may be robust to future perturbations.

Biodiversidad marina en la isla Lobos de Tierra, Perú. 2011

Entre el 29 de setiembre y 3 de octubre 2011, se determinó la estructura de las comunidades, en términos de abundancia relativa, riqueza y diversidad y relación con el medio ambiente de la isla Lobos de Tierra (noreste de isla Rata, El Ñopo y La Grama). En los cálculos de diversidad específi ca se usó métodos uni y multivariados para hacer comparaciones en los lugares estudiados. En la zona mesolitoral se registró alta riqueza específi ca asociada a comunidades de fondos duros destacando el noreste de isla Rata con 58 especies. El grupo dominante fue moluscos en todas las zonas de estudio, sobresaliendo Tegula corvus y Acanthopleura echinata con mayores niveles de abundancia (296 a 412 ind.m-2). El índice de diversidad (H’) promedio por estación mostró valores >1,5 bits/ind en todas las zonas, con valores de dominancia y equitatividad <1,0. En el submareal, la riqueza fue de 124 especies. Los crustáceos y poliquetos tuvieron la mayor riqueza de especies y densidad. Los principales representantes fueron Gammarus sp. (26.607 ind.m-2), Spionidae (2.227 ind.m-2) y Diopatra rhizoicola (2.073 ind.m-2). El índice de diversidad promedio fue 2,2 bits, valor considerado de alta diversidad. La fauna íctica submareal estuvo conformada por 16 especies, destacando los géneros Auchenionchus y Labrisomus y en el intermareal se registraron 7 especies destacando Tomicodon chilensis. Se detectaron 24 especies de macroalgas: Rhodophyta (16 especies), Chlorophyta (5 especies) y Phaeophyta (3 especies), predominó Caulerpa fi liformis (submareal) y Gymnogongrus furcellatus (intermareal).