THE POSTCRANIUM OF ARCHEGOSAURUS DECHENI, AND A PHYLOGENETIC ANALYSIS OF TEMNOSPONDYL POSTCRANIA

Abstract:  The gharial-like Archegosaurus decheni from the Permian/Carboniferous boundary of south-west Germany is one of the best known temnospondyls. Based largely on new material, we restudied the postcranial anatomy of this species, including ontogenetic aspects. A. decheni has 24 presacral vertebrae, and the length of the deep tail exceeds the length of the rest of the body. Neural spines are moderately high and slowly become differentiated during ontogeny. The intercentra start to ossify very late. Distal uncinate processes are developed on the anterior ribs in adult specimens. Only the ventral portion of the scapula is ossified. The slender ilium and the ischium are not co-ossified, and the pubis remained cartilaginous. Among stereospondylomorph temnospondyls, the very short and rudimentarily developed humerus exhibits a unique morphology. Carpals and tarsals start to ossify only in the largest specimens. The poorly ossified postcranium indicates that A. decheni was primarily an aquatic temnospondyl. We undertook a phylogenetic study of A. decheni and 16 other temnospondyls, based exclusively on postcranial characters. We analysed 52 characters, obtaining a single most parsimonious tree that agrees in many aspects with cranium-based analyses: Trimerorhachis and Dvinosaurus form a basal clade (Dvinosauria), followed by monophyletic euskelians (dissorophoids plus eryopids) and finally the stereospondylomorphs, within which A. decheni is nested above Sclerocephalus . Among stereospondyls, trematosaurids and metoposaurids form a clade, whereas the chigutisaurid Siderops is nested with capitosauroids. The primitive condition of Temnospondyli is still not adequately understood, especially the degree of terrestriality of the earliest temnospondyls.     

REVISION OF THE TYPE MATERIAL AND NOMENCLATURE OF MASTODONSAURUS GIGANTEUS (JAEGER) (TEMNOSPONDYLI) FROM THE MIDDLE TRIASSIC OF GERMANY

Abstract: The type material of Mastodonsaurus is revised and its complicated taxonomic history resolved. The genus was erected by Jaeger in 1828 without a species name, which was added subsequently by Holl (1829) who named the type species Mastodonsaurus jaegeri. The large tooth on which Jaeger based his Mastodonsaurus is chosen herein as lectotype of the type species. A smaller second individual, represented by a piece of an occiput, was also named by Jaeger in 1828 as Salamandroides giganteus and, owing to the find of a complete skull, was recognized in 1833 by the same author as belonging to the same species as the Mastodonsaurus. Therefore, Mastodonsaurus giganteus (Jaeger, 1828) is a senior subjective synonym of the type species M. jaegeri Holl, 1829. The precedence of the two generic names was chosen in 1834 by the first reviser, von Alberti, in favour of Salamandroides, but all later authors, including von Alberti himself, followed Jaeger, who decided in 1837 to retain the name Mastodonsaurus. The established usage of Mastodonsaurus is preserved formally herein (nomen protectum). The names Batrachosaurus Fitzinger, 1837, and Labyrinthodon Owen, 1841 are unjustified replacement names of Mastodonsaurus. The names M. jaegeri von Meyer, 1832, S. jaegeri von Alberti, 1834 and M. salamandroides Jaeger, 1837 are junior homonyms and synonyms of M. jaegeri Holl, 1829, and M. giganteus (Jaeger, 1828), respectively. A recent attempt to replace the universally used Capitosauroidea Watson, 1919 by the unused and newly elevated Mastodonsauroidea Lydekker, 1885 is rejected. Two older synonyms of Mastodonsauridae Lydekker, 1885 (nomen protectum) are rejected as unavailable (Labyrinthodontidae von Meyer, 1842 ) and nomen oblitum (Batrachosauridae Fitzinger, 1843), respectively. The holotype of Mastodonsaurus giganteus is reinstated and valid on the basis of three diagnostic features present: the tripartite posterior rim of the parasphenoid, a laterally pushed suture between the parasphenoid and basipterygoid, and a wide slit‐like eustachian tube opening. Mastodonsaurus is known from specimens representing a continuous growth series, now also encompassing the lectotype of Mastodonsaurus jaegeri, which until rather recently stood isolated from other specimens as the largest find by far.     

Involvement of respiratory processes in the transient knockout of net CO2 uptake in Mimosa pudica upon heat stimulation

Leaf photosynthesis of the sensitive plant Mimosa pudica displays a transient knockout in response to electrical signals induced by heat stimulation. This study aims at clarifying the underlying mechanisms, in particular, the involvement of respiration. To this end, leaf gas exchange and light reactions of photosynthesis were assessed under atmospheric conditions largely eliminating photorespiration by either elevated atmospheric CO₂ or lowered O₂ concentration (i.e. 2000 μmol mol^?1 or 1%, respectively). In addition, leaf gas exchange was studied in the absence of light. Under darkness, heat stimulation caused a transient increase of respiratory CO₂ release simultaneously with stomatal opening, hence reflecting direct involvement of respiratory stimulation in the drop of the net CO₂ uptake rate. However, persistence of the transient decline in net CO₂ uptake rate under illumination and elevated CO₂ or 1% O₂ makes it unlikely that photorespiration is the metabolic origin of the respiratory CO₂ release. In conclusion, the transient knockout of net CO₂ uptake is at least partially attributed to an increased CO₂ release through mitochondrial respiration as stimulated by electrical signals. Putative CO₂ limitation of Rubisco due to decreased activity of carbonic anhydrase was ruled out as the photosynthesis effect was not prevented by elevated CO₂.     

A chroniosuchid from the Triassic of Kyrgyzstan and analysis of chroniosuchian relationships

A nearly complete skull and associated osteoderms from the Middle/Upper Triassic Madygen Formation of Kyrgyzstan are referred to a new chroniosuchid genus and species. The new taxon is characterized by a parabolic skull outline, pustular ornamentation, tabular‐squamosal contact, marked postparietal embayments, and the lack of an antorbital fontanelle. The palate is only preserved in part, showing broad palatines and ectopterygoids. Presence of a preorbital fenestra and characteristic osteoderm morphology are synapomorphies shared with all other chroniosuchids. According to the phylogenetic analysis performed, the new chroniosuchid nests with Chroniosaurus, with which it shares the wide, transversely extended osteoderms and pustular ornamentation. The chroniosuchians are robustly supported as a natural group, but their position within the reptiliomorph (stem‐amniote) clade is not adequately understood. Whereas the parasphenoid is similar to that of anthracosaurs, most other characters support a higher nesting of chroniosuchians within the stem‐amniotes. © 2010 The Linnean Society of London, Zoological Journal of the Linnean Society, 2010, 160 , 515–530.     

Lake responses to reduced nutrient loading – an analysis of contemporary long-term data from 35 case studies

1. This synthesis examines 35 long‐term (5–35 years, mean: 16 years) lake re‐oligotrophication studies. It covers lakes ranging from shallow (mean depth <5 m and/or polymictic) to deep (mean depth up to 177 m), oligotrophic to hypertrophic (summer mean total phosphorus concentration from 7.5 to 3500 μg L^?1 before loading reduction), subtropical to temperate (latitude: 28–65°), and lowland to upland (altitude: 0–481 m). Shallow north‐temperate lakes were most abundant. 2. Reduction of external total phosphorus (TP) loading resulted in lower in‐lake TP concentration, lower chlorophyll a (chl a) concentration and higher Secchi depth in most lakes. Internal loading delayed the recovery, but in most lakes a new equilibrium for TP was reached after 10–15 years, which was only marginally influenced by the hydraulic retention time of the lakes. With decreasing TP concentration, the concentration of soluble reactive phosphorus (SRP) also declined substantially. 3. Decreases (if any) in total nitrogen (TN) loading were lower than for TP in most lakes. As a result, the TN : TP ratio in lake water increased in 80% of the lakes. In lakes where the TN loading was reduced, the annual mean in‐lake TN concentration responded rapidly. Concentrations largely followed predictions derived from an empirical model developed earlier for Danish lakes, which includes external TN loading, hydraulic retention time and mean depth as explanatory variables. 4. Phytoplankton clearly responded to reduced nutrient loading, mainly reflecting declining TP concentrations. Declines in phytoplankton biomass were accompanied by shifts in community structure. In deep lakes, chrysophytes and dinophytes assumed greater importance at the expense of cyanobacteria. Diatoms, cryptophytes and chrysophytes became more dominant in shallow lakes, while no significant change was seen for cyanobacteria. 5. The observed declines in phytoplankton biomass and chl a may have been further augmented by enhanced zooplankton grazing, as indicated by increases in the zooplankton : phytoplankton biomass ratio and declines in the chl a : TP ratio at a summer mean TP concentration of <100–150 μg L^?1. This effect was strongest in shallow lakes. This implies potentially higher rates of zooplankton grazing and may be ascribed to the observed large changes in fish community structure and biomass with decreasing TP contribution. In 82% of the lakes for which data on fish are available, fish biomass declined with TP. The percentage of piscivores increased in 80% of those lakes and often a shift occurred towards dominance by fish species characteristic of less eutrophic waters. 6. Data on macrophytes were available only for a small subsample of lakes. In several of those lakes, abundance, coverage, plant volume inhabited or depth distribution of submerged macrophytes increased during oligotrophication, but in others no changes were observed despite greater water clarity. 7. Recovery of lakes after nutrient loading reduction may be confounded by concomitant environmental changes such as global warming. However, effects of global change are likely to run counter to reductions in nutrient loading rather than reinforcing re‐oligotrophication.     

A new stereospondyl from the German Middle Triassic, and the origin of the Metoposauridae

Recent finds of well-preserved temnospondyl skeletons from the Lower Keuper (Ladinian, Middle Triassic) in southern Germany are assigned to a new genus and species, Callistomordax kugleri . This taxon is characterized by the following autapomorphies: (1) wide unpaired frontal; (2) vomerine fangs greatly enlarged to occupy entire width of element; (3) intercentra elongated and massive, anterior face being convex; (4) humerus semilunar with enlarged deltopectoral crest; (5) cleithrum strongly curved and bow-shaped; (6) trunk extremely elongated to reach three times the length of the skull. Callistomordax shares with the Metoposauridae the pattern of dermal ornamentation, the proportion of both posterior skull table and snout, the position of the lacrimal, the morphology of the basicranial region, and the structure of the clavicle and interclavicle. Phylogenetic analysis suggests Callistomordax to be the sister taxon of the Metoposauridae, nested within a grade formed by various trematosaurian taxa. In this assemblage, Lyrocephaliscus and a clade formed by Almasaurus , Rileymillerus , Callistomordax , and the Metoposauridae are sister taxa. In all variants of the cladistic analysis, Callistomordax and the Metoposauridae form immediate sister groups. According to the present findings, neither plagiosaurids nor brachyopoids and rhytidosteids are closely related to this 'trematosaurian' monophylum, although these taxa share a range of homoplasies.  © 2008 The Linnean Society of London, Zoological Journal of the Linnean Society , 2008, 152 , 79–113.     

Heat-induced electrical signals affect cytoplasmic and apoplastic pH as well as photosynthesis during propagation through the maize leaf

Combining measurements of electric potential and pH with such of chlorophyll fluorescence and leaf gas exchange showed heat stimulation to evoke an electrical signal (propagation speed: 3–5 mm s⁻¹) that travelled through the leaf while reducing the net CO₂ uptake rate and the photochemical quantum yield of both photosystems (PS). Two-dimensional imaging analysis of the chlorophyll fluorescence signal of PS II revealed that the yield reduction spread basipetally via the veins through the leaf at a speed of 1.6 ± 0.3 mm s⁻¹ while the propagation speed in the intervein region was c. 50 times slower. Propagation of the signal through the veins was confirmed because PS I, which is present in the bundle sheath cells around the leaf vessels, was affected first. Hence, spreading of the signal along the veins represents a path with higher travelling speed than within the intervein region of the leaf lamina. Upon the electrical signal, cytoplasmic pH decreased transiently from 7.0 to 6.4, while apoplastic pH increased transiently from 4.5 to 5.2. Moreover, photochemical quantum yield of isolated chloroplasts was strongly affected by pH changes in the surrounding medium, indicating a putative direct influence of electrical signalling via changes of cytosolic pH on leaf photosynthesis.     

Analysis of cytosolic and plastidic serine acetyltransferase mutants and subcellular metabolite distributions suggests interplay of the cellular compartments for cysteine biosynthesis in Arabidopsis

In plants, the enzymes for cysteine synthesis serine acetyltransferase (SAT) and O-acetylserine-(thiol)-lyase (OASTL) are present in the cytosol, plastids and mitochondria. However, it is still not clearly resolved to what extent the different compartments are involved in cysteine biosynthesis and how compartmentation influences the regulation of this biosynthetic pathway. To address these questions, we analysed Arabidopsis thaliana T-DNA insertion mutants for cytosolic and plastidic SAT isoforms. In addition, the subcellular distribution of enzyme activities and metabolite concentrations implicated in cysteine and glutathione biosynthesis were revealed by non-aqueous fractionation (NAF). We demonstrate that cytosolic SERAT1.1 and plastidic SERAT2.1 do not contribute to cysteine biosynthesis to a major extent, but may function to overcome transport limitations of O-acetylserine (OAS) from mitochondria. Substantiated by predominantly cytosolic cysteine pools, considerable amounts of sulphide and presence of OAS in the cytosol, our results suggest that the cytosol is the principal site for cysteine biosynthesis. Subcellular metabolite analysis further indicated efficient transport of cysteine, γ -glutamylcysteine and glutathione between the compartments. With respect to regulation of cysteine biosynthesis, estimation of subcellular OAS and sulphide concentrations established that OAS is limiting for cysteine biosynthesis and that SAT is mainly present bound in the cysteine–synthase complex.