On Lower and Upper Jurassic dibranchiate cephalopods from Germany and England

Three dibranchiate cephalopod remains from different bituminous shales contribute to our knowledge of Jurassic representatives: 1. The recently re-discovered holotype ofLioteuthis problematica Naef, 1922, from the Lower Toarcian of southwestern Germany has been prepared and is found to be taxonomically and phylogenetically isolated of its strange morphology: 2. An exceptionally preserved ink sac of a Lower Toarcian squid [probablyBelopeltis aalensis (Zieten, 1832)] from southwestern Germany, shows the finest imprints of the blood vessels yet seen. 3. The Callovian speciesBelemnoteuthis antiqua Mantell, 1847, mentioned, but not figured from the middle Kimmeridge Clay of southern England, is figured here from these beds for the first time.     

The localization of enzyme activities in the pancreatic appendages of Sepia officinalis L. (Cephalopoda).

In this study, enzyme activities of the pancreatic appendages of the ductus hepatoPancreas (the so-called "pancreas") in Sepia officinalis L. have been demonstrated by light and electron micicroscopical methods: Malate dehydrogenase, monoamine oxidase, acid phosphatase, beta-glucuronidase, adenosine triphosphatase and carbonic anhydrase were shown by the former, and monoamine oxidase, catalase, glutamic oxalacetic transaminase, choline esterase (non-specific), alkaline phosphatase, acid phosphatase and carbonic anhydrase by the latter technique. The correlation between enzyme activity and distribution, and the presumed function of the two pancreatic epithelia is discussed.     

The localization of enzyme activities in the pancreatic appendages of Sepia officinalis L. (Cephalopoda)

Summary In this study, enzyme activities of the pancreatic appendages of the ductus hepatopancreas (the so-called Pancreas) in Sepia officinalis L. have been demonstrated by light and electron microscopical methods: Malate dehydrogenase, monoamine oxidase, acid phosphatase, -glucuronidase, adenosine triphosphatase and carbonic anhydrase were shown by the former, and monoamine oxidase, catalase, glutamic oxalacetic transaminase, choline esterase (non-specific), alkaline phosphatase, acid phosphatase and carbonic anhydrase by the latter technique.The correlation between enzyme activity and distribution, and the presumed function of the two pancreatic epithelia is discussed.This study was supported by the Deutsche Forschungsgemeinschaft     

Neurotransmitters of cephalopods

1. ACh, dopamine, noradrenaline, 5-HT,l-glutamate, and GABA are widely distributed in cephalopods and probably all function as neurotransmitters; octopamine also occurs and at one site is known to act as a neuromodulator.
2. Several peptides are also present, as well as nitric oxide synthase.
3. In the brain and sense organs cholinergic, aminergic, serotonergic and glutamatergic systems seem to be the most important.
4. ACh is also active in the gut, vascular system and some body muscles: it is generally inhibitory. The ACh receptors are similar to the vertebrate nicotinic type.
5. The catecholamines are important in the gut and vascular system: they are generally excitatory. The NA receptors are like the α-adrenergic subtype of vertebrates, but the nature of the DA and OA receptors is less certain.
6. 5-HT is important in the gut but is endogenous in some chromatophore nerves and acts on receptors that seem like the vertebrate 5-HT₁ type.
7. l-glutamate is an excitatory transmitter at the chromatophore (and probably at other) nerve-muscle junctions and is an extremely strong candidate for being the excitatory transmitter at the squid giant synapse. There are NMDA receptors on Schwann-cells but the receptors on neurons and muscles are like the vertebrate kainate type.
8. Little is known about the mode of action of cephalopod peptides; nor has it ever been shown that they co-exist with conventional transmitters in these animals.
9. The structure of one (FMRFamide) receptor has been elucidated, but apart from this nothing is known of the molecular biology of receptors in cephalopods.

     

The origin and evolution of appendages

Current awareness of gene expression patterns and developmental mechanisms involved in the outgrowth and patterning of animal appendages contributes to our understanding of the origin and evolution of these body parts. Nevertheless, this vision needs to be complemented by a new adequate comparative framework, in the context of a factorial notion of homology. It may even be profitable to categorize as appendages also gut diverticula, body ingrowths and 'virtual appendages' such as the eye spots on butterfly wings. Another unwarranted framework is the Cartesian co-ordinate system onto which the appendages are currently described and where it is supposed that one patterning system exists for each separate Cartesian axis. It may be justified, instead, to look for correspondences between the appendages and the main body axis of the same animal, as the latter might be the source of the growth and patterning mechanisms which gave rise to the former. This hypothesis of axis paramorphisms is contrasted with the current hypothesis of gene co-option. Recapitulationism is a common fault in current Evo-Devo perspectives concerning the origin of the appendages, in that the evolutionary origin of appendages is often expected to be the same as one of the key mechanisms involved in the ontogenetic inception of appendage formation. This unwarranted perspective is also evident in the current debate on the nature of the default arthropod appendage. Most likely, a default arthropod appendage never did exist, as the first appendages probably developed along the trunk of an animal already patterned extensively along the antero-posterior body axis.     

Cannibalism in cephalopods

Cannibalism refers to the action of consuming a member of the same species and is common in many taxa. This paper reviews the available literature on cannibalism in cephalopods. All species of the class Cephalopoda are predators and cannibalism is common in most species whose diet has been studied. Cannibalism in cephalopods is density-dependent due to their aggressive predatory and in case of the octopuses territorial nature. It also depends upon local and temporal food availability and of the reproductive season. Cannibalistic behaviour is positively related to the size of both cannibal and victim. It can affect population dynamics of cephalopods in periods of low food availability and/or high population abundance. Cephalopods are generally restricted in their ability to store energy. It is thus assumed that cannibalism is part of a population energy storage strategy enabling cephalopod populations to react to favourable and adverse environmental conditions by increasing and reducing their number. Finally, we propose five orientation points for future research on cannibalism in cephalopods.     

Host defense mechanisms of cephalopods

Humoral and cellular mechanisms of defense have been described for cephalopods, a relatively advanced group of mollusks. Typical of other mollusks, cephalopod agglutinins are the most documented component of humoral immunity. Lectins, which have agglutinating properties, have been described and characterized from octopuses. Agglutinins from cephalopod hemolymph have also been shown to agglutinate a variety of vertebrate red blood cells, as well as potential bacterial pathogens. Hemocytes are the primary component of cellular immunity. Although the hemocyte role in phagocytosis has been extensively studied in other mollusks, the mechanisms of phagocytosis have not been described extensively for cephalopods. Cephalopod hemocytes have phagocytic capabilities and may function in encapsulation and neutralization of foreign substances; however, the effects of environmental factors and the full extent of phagocytic capabilities of cephalopod hemocytes have not been reported. Hemocytes from cephalopods have a role in wound healing and inflammation which have been reported in detail by several investigators.     

The siphuncle in Georginidae and other Ordovician actinoceroid cephalopods

The lower Middle Ordovician carbonate sediments of the Georgina Basin in Australia contain many and varied Actinoceratida, including an endemic family, Georginidae Wade (1977), with siphuncular calcification consisting of radial lamellae separated by spaces (now sediment-filled) enclosed within calcified annulus walls. In each segment a distinct series of more massive calcareous engrafts grows inward from the inside of the connecting ring and is engrafted into adjacent annuli across the interannulus; this divides the perispatium into longitudinal perispatial sinuses. At each extremity each perispatial sinus is connected with passages leading through the segments to the axial space and, nearer to, or at the interannulus, with radial canals. Axial canals are few, but more than one is normal. Good preservation of Armenoceras and Actinoceras allows recognition of similar structures in the annuli of normal Actinoceratida.     

Trilobites within nautiloid cephalopods

'Sheltered preservation' of the remains of trilobites within the shells of nautiloid cephalopods is not especially uncommon. In most cases, of course, both the trilobites and the nautiloids were dead, and the association, merely due to post-mortem happenstance. However, on the basis of state of preservation and occurrence, a number of live individuals of the trilobite genera Acidaspis, Flexicalymene, and Isotelus from the Ordovician of the United States and of Alcymene and Encrinuraspis from the Silurian of Wales and the Czech Republic seem to have entered conchs of dead cephalopods, presumably for refuge.     

Phospholipids in Mediterranean cephalopods

Polar lipids of the cephalopods Eledone moschata, Sepia officinalis and Todarodes sagittatus mantle, represent 50.5%, 66.1% and 74.2% of wet tissue respectively. On the other hand the polar lipids of these three species of cephalopods constitute of 80.8%, 94.8% and 93.7% of phospholipids, respectively. The main phospholipids identified were phosphatidylcholine (52.2, 51.3 and 58.4% of total phospholipids respectively in the above mentioned species), phosphatidylethanolamine (18.1, 19.7 and 23.9%), sphingomyelin (10.7, 15.2 and 6.7%), lyso-phosphatidylcholine (3.1, 3.8 and 1.8%) and the unusual lipid ceramide aminoethylphosphonic acid (15.9, 10 and 9.2%). The 56.8% of phosphatidylcholine in Eledone moschata, the 46% in Sepia officinalis and the 74.1% in Todarodes sagittatus refer to the structure of 1,2-diacyl-glycerocholine and the remaining percentage refer to the structure of 1-o-alkyl-2-acyl-glycerocholine or 1-o-alkyl-1-enyl-2-acyl-glycerocholine. The 87.2% of phosphatidylethanolamine in Eledone moschata, the 81% in Sepia officinalis and the 90.7% in Todarodes sagittatus refer to the structure of 1,2-diacyl-glyceroethanolamine and the remaining percentage refer to the structure of 1-o-alkyl-2-acyl-glyceroethanolamine or 1-o-alkyl-1-enyl-2-acyl-glyceroethanolamine. The major saturated fatty acids in phosphatidylcholine and phosphatidylethanolamine were C16:0 (30.3-67.5% and 23.2-54.5%) and C18:0 (3.6-17% and 15.4-28%), respectively, while the major unsaturated fatty acids in these lipids were C18:1n-9, n-7 (1.0-7.3% and 5.3-10.5%), C20:5n-3 (1.5-9.8% and 4,5-15.8%) and C22:6n-3 (12.5-42.0% and 7.0-11.3%), respectively.     

Integumentary appendages of chelonians

The head and neck of four families of turtles, the Chelydridae, Kinosternidae, Pelomedusidae, and Chelidae, possess a diverse assemblage of skin appendages. Appendages are termed barbels when they occur in the gular region and tubercles when they occur other places. The appendages consist of protrusions of the dermis and epidermis and are devoid of such specializations as taste buds or neuromasts. They lack skeletal tissue, muscle, or erectile tissue. Methylene blue and silver staining techniques reveal a high density of nerves. The occurrence and morphology of barbels and tubercles suggest that they function as mechanoreceptors. Skin appendages are most elaborate in carnivorous species and reach maximum development in two distantly related convergent species: Macroclemys temmincki (Chelydridae) and Chelus fimbriatus (Chelidae). Skin appendages also help provide camouflage and disruptive effects on the head. The increase in surface area produced by the appendages may be important in aquatic respiratory gas exchange in some species within the Kinosternidae.