CD studies of double-stranded polydeoxynucleotides composed of repeating units of contiguous homopurine residues

Double-stranded synthetic polydeoxynucleotides of the general form poly[d(G_nC_n)] · poly[d(G_nC_n)], poly[d(G_nC)] · poly[d(GC_n)], and poly[d(A_nT_n)] · poly[d(A_nT_n)] have been synthesized. When n = 4 or larger, the CD spectra of polymers of the form poly[d(G_nC_n)] · poly[d(G_nC_n)] or poly[d(G_nC)] · poly[d(GC_n)] closely resemble the spectrum of poly[dG] · poly[dC], suggesting that a string of four continguous guanosine residues is sufficient to induce a conformation resembling that of the polypurine · polypyrimidine. With polymers of the form poly[d(A_nT_n)] · poly[d(A_nT_n)], however, the CD spectrum only gradually approaches that of poly[dA] · poly[dT].     

Muscle growth in juvenile Atlantic salmon as influenced by temperature in the egg and yolk sac stages and diet protein level

Atlantic salmon Salmo salar eggs derived from a single family were incubated at two different water temperature regimes, with a mean temperature between fertilization and first feeding differing between 6 and 10° C (HT) and 2–6° C (LT). From first feed the fry were kept under the same rearing conditions and fed either high (50%) or low (45%) protein diet level of equivalent energy content until smoltification. All treatments were carried out in duplicate tanks. At first feeding the groups were similar in mass, but thereafter the HT‐fish were heavier and longer compared to the LT‐fish throughout the experiment. The groups fed the high protein diet were significantly heavier and longer compared with the corresponding low protein diet. A strong positive relationship was observed between L_F and total white muscle cross‐sectional area (CSA), white muscle fibre diameter and fibre number. There were also equivalent relationships with body mass. There were no significant differences in CSA, the mean diameter or the number of white muscle fibres per CSA between groups at first feed. Muscle fibre number and CSA increased in all groups during the experiment, whereas fibre diameter reached a plateau when the fish reached > 9 cm L_F. There were only minor effects of pre‐hatch and yolk sac stage temperature on CSA and fibre number per CSA during the juvenile stage. In short periods the LT‐group had larger CSA and higher fibre number than the HT‐groups, but this differences had disappeared by the end of the juvenile stage. No differences in mean fibre diameter were found between groups, except at the time of smoltification. When the fish approached smoltification a decrease in mean fibre diameter and an increase in muscle fibres <25 µm was seen and taken as an indication of recruitment of new fibres (hyperplasia). Only minor differences in CSA, fibre number or fibre diameter was observed between high and low protein diet groups.     

Muscle fibre types and size distribution in sub-antarctic notothenioid fishes

The presumptive tonic muscles fibres of Cottoperca gobio, Champsocephalus esox, Harpagifer bispinis, Eleginops maclovinus, Patagontothen tessellata, P. cornucola and Paranotothenia magellanica stained weakly or were unstained for glycogen, lipid, succinic dehydrogenase (SDHase) and myosin ATPase (mATPase) activity. Slow, intermediate and fast twitch muscle fibres, distinguished on the basis of the pH stability of their mATPases, showed intense, moderate and low staining activity for SDHase, respectively. Slow fibres were the major component of the pectoral fin adductor profundis muscle. The proportion of different muscle fibre types varied from the proximal to distal end of the muscle, but showed relatively little variation between species. The myotomes contained a lateral superficial strip of red muscle composed of presumptive tonic, slow twitch and intermediate fibres, thickening to a major wedge at the horizontal septum. All species also had characteristic secondary dorsal and ventral wedges of red muscle. The relative abundance and localization of muscle fibre types in the red muscle varied between species and with body size in the protandric hermaphrodite E. maclovinus. The frequency distribution of diameters for fast twitch muscle fibres, the major component of deep white muscle, was determined in fish of a range of body sizes. The absence of fibres <20 μm diameter was used as a criterion for the cessation of muscle fibre recruitment. Fibre recruitment had stopped in P. tessellata of 13·8 cm L_T and E. maclovinus of 32·8 cm L_T, equivalent to 49 and 36·5% of their recorded maximum sizes respectively. As a result in 20‐cm P. tessellata, the maximum fibre diameter was 300 μm and 36% of fibres were in excess of 200 μm. The unusually large maximum fibre diameter, the general arrangement of the red muscle layer and the extreme pH lability of the mATPase of fast twitch fibres are all common characters of the sub‐Antarctic and Antarctic Notothenioids, including Cottoperca gobio, the suggested sister group to the Notothenidae.     

Morphological and histochemical characterization of the pectoral fin muscle of the stripped weakfish,Cynoscion guatucupa

The fibres of superficial and deep abductor muscles of the pectoral fins of the stripped weakfish, Cynoscion guatucupa have been studied using histochemical techniques: succinic dehydrogenase (SDH) for mitochondria, periodic acid–Schiff (PAS) for glycogen, myosin‐adenosintriphosphatase (mATPase) to identify different fibre types based on the contraction speed and modified ATPase to identify capillaries. The fibre diameters were measured, and the capillaries of the main fibre types – red, pink and white— were counted. The two muscles showed both macroscopically and microscopically two well‐differentiated zones with predominant white fibres. The area of insertion of muscles into the fin rays had red, pink and white fibres. The origin zone of the muscle into the bone was composed by white fibres only. Both zones of white muscle evidenced a mosaic of small, medium and large polygonal white fibres. Red, pink and white muscles showed a wide histochemical diversity of fibre subtypes. The area per peripheral capillary increased from the red to the white muscles. Due to the predominance of white fibres, the pectoral fins of C. guatucupa were mainly involved in rapid movements to stop/discontinue and stabilize the body during swimming.     

Computer simulation for effect of Pr(III) on Ca(II) speciation in human interstitial fluid

A mutiphase model of metal ion speciation in human interstitial fluid was constructed and the effect of Pr(III) on Ca(II) speciation was studied. Results show that Ca(II) mainly distributes in free Ca²⁺, [Ca(HCO₃)], and [Ca(Lac)]. Because of the competition of Pr(III) for ligands with Ca(II), with the total concentration of Pr(III) rising, the percentages of free Ca²⁺, [Ca(Lac)] and [Ca(His)(Thr)H₃], gradually increase and the percentages of CaHPO₄(aq) and [Ca(Cit)(His)H₂] gradually decrease. However, the percentages of [Ca(HCO₃)] and CaCO₃(aq) first increase, and then begin to decrease when the total concentration of Pr(III) exceeds 6.070×10⁻⁴ M.     

Organotin(IV) derivatives containing bis(diphenylphosphine)- and bis(diphenylphosphineoxo)alkanes

Di-organotin(IV)halides R₂SnCl₂ (R=Me or Ph) react with bis(diphenylphosphine)methane (DPPM) and bis(diphenylphosphine)ethane (DPPE) in ethanol in aerobic conditions yielding 1:1 adducts [R₂SnCl₂(DPPM–O₂)] and [R₂SnCl₂(DPPE–O₂)], respectively, containing the bis(diphenylphosphine) in oxidized form. The 1:1 adduct [SnMe₂Cl₂(DPPM–O₂)] is composed of separate molecules containing six-coordinate tin, with the ligands coordinated in the bidentate O₂-fashion, whereas [SnMe₂Cl₂(DPPE–O₂)] is polymeric, with octahedral and centrosymmetric (all trans) tin atoms. In inert atmosphere, the interaction between R₂SnCl₂ and DPPM or DPPE does not take place. Mono-organotin halides RSnCl₃ (R=Me, Buⁿ or Ph) react with DPPM and DPPE yielding 1:1 adducts [RSnCl₃(DPPM)] (R=Me, Buⁿ or Ph) and [RSnCl₃(DPPE)] (R=Buⁿ or Ph).     

Computer simulation for effect of Pr(III) on Ca(II) speciation in human interstitial fluid

A multiphase model of metal ion speciation in human interstitial fluid was constructed and the effect of Pr(III) on Ca(II) speciation was studied. Results show that free Ca²⁺, [Ca(HCO₃)], and [Ca(Lac)] are the main species of Ca(II). Because of the competition of Pr(III) for ligands with Ca(II), the percentages of free Ca²⁺, [Ca(Lac)], and [Ca(His)(Thr)H₃] increase gradually and the percentages of CaHPO₄(aq) and [Ca(Cit)(His)H₂] decrease gradually with the increase in the total concentration of Pr(III). However, the percentages of [Ca(HCO₃)] and CaCO₃(aq) first increase and then begin to decrease when the total concentration of Pr(III) exceeds 6.070×10⁻⁴ M.     

AMP-deaminase in elasmobranch fish: a comparative histochemical and enzymatic study

AMP-deaminase activity was measured in white muscle from a wide range of fish, including one cyclostome, 13 chondrosteans, and one teleost to elucidate the pattern of the AMP-deaminase activity in white muscle of fish. Compared to a mammalian (rat) muscle extract, low enzyme activities are found in the cyclostome and two elasmobranchs from two families (Scyliorhinidae, Hexanchidae). In contrast, higher AMP-deaminase activities, similar to mammals, are expressed in Squalidae, all families of skates, Chimaeridae and in the teleostean fish. We then compared AMP-deaminase activities in red and white muscles from two representative elasmobranch fish, the dogfish (Scyliorhinus canicula) and the thornback ray (Raja clavata). The fibre type composition and distribution of the locomotory musculature were determined in these two elasmobranchs to establish a relationship between the morphology, the type of fibres of the locomotion-implicated muscles and the AMP-deaminase activity. Experimental data are discussed with respect to the layout of fibres in the myotome. In both species, three fibre types were identified. In the two fish myotomes, most of the axial muscles are white fibres while red fibres constitute a thin sheet. Some differences were observed between the two species in the distribution of intermediate fibres: in dogfish, these are located between the red and white fibres; in thornback ray, some are dispersed within the white fibre region, while others form an intermediary layer like in dogfish. These results suggest that in the course of evolution, an amplification of the AMP-deaminase activity in muscle was coupled with increase of complexity of the muscular structure.     

Red muscle fibre and capillary dimensions in different sizes of a tilapia, Oreochromis niloticus (Trewavas)

Measurements of muscle dimensions that affect respiration in relation to body weight were carried out in a tilapia, Oreochromis niloticus . The fish used in all measurements weighed 0.65–812.3 g. The data were analysed with respect to body weight using logarithmic transformations (log Y=log a + b log W ).
The slopes (b) of the log/log regression lines for weight of body trunk red muscle, average cross-sectional area of muscle fibre, average number of capillaries in direct contact with a muscle fibre, average capillary contact length with a fibre as a fraction of average fibre circumference and number of capillaries mm² of fibre cross-sectional area [N_A(cƒ)] were 1.16, 0.221, 0.084, 0.015, and −0.137 respectively.
These results show that there is an increase in muscle cross-sectional fibre area and number of capillaries in contact with muscle fibres whereas number of capillaries supplying a unit area of muscle fibre decreases during development. There is development of new capillaries with increase in cross-sectional area of red muscle fibres.     

Hyperplasia and hypertrophy in the growth of skeletal muscle in juvenile Atlantic salmon, Salmo salar L.

Both red and white muscle fibre numbers in juvenile Atlantic salmon increased gradually with fish length throughout the freshwater growth period. Mean fibre area increased as fish grew to 6.5 cm f.l. , but thereafter was unrelated to fish length. Hyperplasia was most obvious when fish were growing fastest, and was the dominant growth process in fish over 6.5 cm f.l. Hypertrophy was most important when growth was slow, as in autumn and winter.
Mean white fibre area was significantly smaller in deep muscle than at medial and superficial sites. Total cross-sectional area of red, white and total trunk muscle increased with fish length. The ratio of red: white cross-sectional area increased with fish length to a plateau at about 10% after 6.5 cm f.l.     

Aurophilic interaction in gold(I) thiosaccharinates: Synthesis, characterization, crystal structures and DFT theoretical study

The reaction of gold with thiosaccharin ligand and additional phosphorous coligands is studied. Four new Au(I) complexes with thiosaccharinate as coordinating counteranion: [Au(tsac)(PPh₃)], [Au₂(tsac)₂(dppm)]·EtOH, Au₂(tsac)₂(dppe)·EtOH, and Au(tsac)(Htsac)₂·0.25 EtOH (tsac: thiosaccharinate, C₆H₄C(S)NSO₂⁻, dppm: bis(diphenylphosphino)methane, dppe: bis(diphenylphosphino)ethane) were synthesized and characterized by means of spectroscopic techniques (IR, UV-Vis, and ¹H, ¹³C and ¹³P NMR). The crystal structure of two of them, [Au(tsac)(PPh₃)] and [Au₂(tsac)₂(dppm)]·EtOH, were solved applying single crystal X-ray diffraction and studied using the density functional theory (DFT) formalism. In the latter, the aurophilic interaction between the two gold centers was analyzed and theoretically confirmed.     

On the interaction of compounds of chromium(VI) with hydrogen peroxide. A study of chromium(VI) and (V) peroxides in the acid-basic pH range

A computational study of chromium(VI) and (V) peroxides, which exhibit important genotoxic and mutagenic activity, is reported. Energies and equilibrium geometries for [Cr^VI(O)(O₂)₂(OH)]⁻, [Cr^VI(O)(O₂)₂(OH₂)], [Cr^VI(O)(O₂)₂(py)], [Cr^VI(OH)(O₂)₂(OH₂)]⁺, [Cr^V(O)(O₂)₂(OH₂)]⁻ and species were calculated using molecular mechanics calculations (MMFF94 and MM⁺), quantum calculations with semi-empirical methods (RHF and UHF/PM3) and density functional theory (pBP86/DN* or pBP/DN* and B3LYP/6-31G(d). Equilibrium geometries for the compounds [Cr^V(O₂)₃(OH)]²⁻ and [Cr^V(O₂)₄]³⁻ were determined by molecular mechanics. Vibrational frequencies, standard thermodynamic quantities and electronic spectra were calculated using B3LYP/6-31G(d). The structural relationship between all these species and an explanation of the formation of peroxo species in the acid-basic pH range are given. An experimental study of peroxo species in basic medium was also performed (synthesis, X-ray powder diffraction patterns and infrared spectra of the peroxo complexes isolated) but did not confirm the existence of a tri-peroxo complex in the solid phase.     

Lipid acquisition and retention in tissues of spawning adult paddlefish Polyodon spathula (Walbaum, 1792) in relation to extended and compressed life history patterns in two river‐reservoir systems

Data from recreationally caught adult paddlefish from North Dakota and Oklahoma, USA, was used in an initial attempt to explain variation in lipid content in adult wild paddlefish Polyodon spathula (Walbaum, 1792) by stock and by sex. The objectives of this study were to describe the relative importance of three distinct paddlefish tissues [white muscle, red muscle, and gonadal fat body (GFB)] for lipid storage, and compare lipid content of these tissues between stock and sex. It was hypothesized that lipid content of the three tissue types would be related to each other within individual fish; and that, consistent with previously documented life history differences, lipid concentrations for all tissues would be sex‐ and stock‐specific. Paddlefish were sampled in April and May 2012 from the Grand Lake, Oklahoma, USA (GL) and Yellowstone‐Sakakawea, North Dakota (SAK) stocks. Three tissue types were collected from SAK fish, including white muscle (N = 137; 83M, 54F), red muscle (N = 74; 36M, 38F), and GFB (N = 164; 105M, 59F). Samples from GL fish included white muscle (N = 60; 36M, 24F), and GFB (N = 42; 41M, 1F). Proximate analysis was used to quantify the percentage of lipid, water, ash, and protein in tissue samples. The lipid component of proximate analysis was completed using the ANKOM method of lipid extraction which uses heated petroleum ether to extract lipid. Also investigated were lipid accumulation and storage in adult paddlefish in relation to tissue type: white muscle, red muscle, gonadal fat bodies (GFB) within individual fish, between the sexes, and between the two different stocks. White muscle was significantly correlated with both red muscle and GFB lipid, but red muscle lipid was not significantly correlated with GFB lipid. White muscle lipid content differed by stock and sex, with the more northerly stock having higher lipid content than the more southerly stock. Females had higher white muscle lipid content (SAK F = 17.18, M = 9.09; GL F = 6.74, M = 4.99) and red muscle (SAK F = 47.72, M = 30.93) than males. In contrast, GFB lipid differed by sex but not stock, with females having lower lipid content (SAK = 79.79, GL = 89.08) than males (SAK = 89.08; GL = 91.72). Life history differences, growing season, and the role of metabolism may help explain the differences in concentrations of lipids observed between stocks and between the sexes for all three tissues. It was hypothesized that different tissues may be used for different metabolic processes and that although metabolism likely strongly influences muscle tissue lipid, GFB lipid is probably linked more closely to reproductive demands associated with gonad development.     

Myotube production in fast myotomal muscle is switched-off at shorter body lengths in male than female Atlantic halibut Hippoglossus hippoglossus (L.) resulting in a lower final fibre number

A sampling method is described to determine accurately the number of fast myotomal muscle fibres (N_F) in a large flatfish species, the Atlantic halibut Hippoglossus hippoglossus. An unusual feature of the fast myotomal muscle is the presence of internalized strips of slow muscle fibres. In fish of 1·5–3·5 kg (n = 24), the total cross‐sectional area (A_TC) of fast muscle was 18% greater in the dorsal than ventral myotomal compartments (P < 0·05), whereas there was no significant difference between left‐ and right‐hand sides of the body. Due the bilateral asymmetry, muscle blocks (5 × 5 × 5 mm) were prepared to systematically sample each myotomal quadrant (dorsal, ventral, left‐ and right‐side) and the diameters of 150 fast fibres measured per block. Smooth non‐parametric probability functions were fitted to a minimum of 800 measurements of fibre diameter per quadrant (n = 5). There were no significant differences in the distribution of muscle fibre diameters between myotomal compartments and therefore N_F could be estimated from a single quadrant. The number of blocks required to estimate N_F with a repeatability of ±2·5% increased from six at 300 g body mass to 17 at 96·5 kg, caused by variation within and between blocks. Gompertz curves were fitted to measurements of fibre number and fork length (L_F). The estimated final fibre number was 8·96 × 10⁵ (7·99–9·94 × 10⁵, 95% CI) for males and 1·73 × 10⁶ (1·56–1·90 × 10⁶, 95% CI) for female fish. The estimated L_F for cessation of fibre recruitment in the fast muscle of female fish (1775 mm) was almost twice that in males (810 mm), reflecting their greater ultimate body size.     

Electronic Effect of Substituents on the DNA Intercalation of Ruthenium(II)?Polypyridyl Complexes

Five ruthenium(II) complexes, i.e., [Ru(bpy)₂(TIP)]²⁺ (bpy=2,2′‐bipyridine; TIP=2‐thiophenimidazo[4,5‐f] [1,10]phenanthroline; 1 ), [Ru(bpy)₂(5‐NTIP)]²⁺ (5‐NTIP=2‐(5‐nitrothiophen)imidazo[4,5‐f] [1,10]phenanthroline; 2 ), [Ru(bpy)₂(5‐MOTIP)]²⁺ (5‐MOTIP=2‐(5‐methoxythiophen)imidazo[4,5‐f] [1,10]phenanthroline; 3 ), [Ru(bpy)₂(5‐BTIP)]²⁺ (5‐BTIP=2‐(5‐bromothiophen)imidazo[4,5‐f] [1,10]phenanthroline; 4 ), and [Ru(bpy)₂(4‐BTIP)]²⁺ (4‐BTIP=2‐(4‐bromothiophen)imidazo[4,5‐f] [1,10]phenanthroline; 5 ), were synthesized and characterized by elemental analysis and UV/VIS, IR, and ¹H‐NMR spectroscopic methods. The photophysical and DNA‐binding properties were investigated by means of UV and fluorescence spectroscopic methods and viscosity measurements, respectively. The results suggest that all five complexes can bind to CT‐DNA with various binding strength. Complexes 2 and 3 showed the strongest and the weakest binding affinity, respectively, among these five complexes. Due to the substituent position of the Br‐atom in the ligand, complex 5 interacted stronger with CT‐DNA than complex 4 . The binding affinities of the complexes decreased in the order 2, 5, 4, 1 , and 3 .     

Differences in protein mobilization between ventral and dorsal parts of white epaxial muscle from fed, fasted and refed white sturgeon (Acipenser transmontanus)

The effect of starvation-refeeding on protein mobilization in the lateral line, lateral (midway between lateral line and dorsum) and dorsal parts of white sturgeon ( Acipenser transmonlanus ) white epaxial muscle (type IIB) were compared by measuring muscle cross-sectional fibre areas. Effects on red (type I) and pink (type IIA) muscle were also studied. Fish starved throughout the experiment (5 weeks) showed a uniform response, i.e. the cross-sectional fibre area decreased at all sampled locations in the white muscle as well as in red and pink muscle. Fibre size in fish refed for 3 weeks after 2 weeks of fasting (S/F) was reduced mainly in the dorsal region of the white muscle. Starvation for 3 weeks after 2 weeks of initial feeding (F/S) also reduced fibre size mainly in the dorsal regions of the white muscle and in the pink muscle. The results indicate that in sturgeon exposed to short periods of low food availability, protein is utilized preferentially from trie more dorsal regions of the white epaxial muscle and from pink muscle. Protein in white muscle located closer to the lateral line and in red muscle seems to be spared. With the onset of refeeding, protein deposition occurred rapidly in pink muscle, but was delayed significantly in the dorsal part of the white muscle.     

Antibacterial,antifungal and in vitro antileukaemia activity of metal complexes with thiosemicarbazones

1‐phenyl‐3‐methyl‐4‐benzoyl‐5‐pyrazolone 4‐ethyl‐thiosemicarbazone (HL) and its copper(II), vanadium(V) and nickel(II) complexes: [Cu(L)(Cl)]·C₂H₅OH·( 1 ), [Cu(L)₂]·H₂O ( 2 ), [Cu(L)(Br)]·H₂O·CH₃OH ( 3 ), [Cu(L)(NO₃)]·2C₂H₅OH ( 4 ), [VO₂(L)]·2H₂O ( 5 ), [Ni(L)₂]·H₂O ( 6 ), were synthesized and characterized. The ligand has been characterized by elemental analyses, IR, ¹H NMR and ¹³C NMR spectroscopy. The tridentate nature of the ligand is evident from the IR spectra. The copper(II), vanadium(V) and nickel(II) complexes have been characterized by different physico‐chemical techniques such as molar conductivity, magnetic susceptibility measurements and electronic, infrared and electron paramagnetic resonance spectral studies. The structures of the ligand and its copper(II) ( 2 , 4 ), and vanadium(V) ( 5 ) complexes have been determined by single‐crystal X‐ray diffraction. The composition of the coordination polyhedron of the central atom in 2 , 4 and 5 is different. The tetrahedral coordination geometry of Cu was found in complex 2 while in complex 4 , it is square planar, in complex 5 the coordination polyhedron of the central ion is distorted square pyramid. The in vitro antibacterial activity of the complexes against Escherichia coli, Salmonella abony, Staphylococcus aureus, Bacillus cereus and the antifungal activity against Candida albicans strains was higher for the metal complexes than for free ligand. The effect of the free ligand and its metal complexes on the proliferation of HL‐60 cells was tested.     

Diversity of native myosin and myosin heavy chain in fish skeletal muscles

• 1.1. Polymorphism of native myosin and myosin heavy chain (MHC) of fish skeletal muscles was analysed by pyrophosphate and SDS-gel electrophoreses.
• 2.2. Depending on the species, three or four myosin isoforms were detected in the white muscle, one or two isoforms in the pure red muscle, and four isomyosins were found in the red muscle composed of red and pink (intermediate) fibres.
• 3.3. It is suggested that all main types of fish muscle fibre (red, intermediate and white) differ in myosin isoform content.
• 4.4. Myosin heavy chain of the red muscle is a distinct protein from that of the white muscle. However, structural differences between these proteins vary among species.

     

Genetic effects on wood quality traits of plantation-grown white spruce (Picea glauca) and their relationships with growth

Clonal repeatabilities on individual tree (H_i² H_i^2 ) and clonal mean (H_{[`(C)]</sub> <sup>2</sup> H_{{\overline C }}^2 ) bases for growth (14-year height and volume), wood quality traits (latewood proportion, wood density, fiber length, and microfibril angle), and genotypic correlations among the traits were estimated, using 30 white spruce (Picea glauca [Moench] Voss) clones from six full-sib families (five per family). These families were selected from a clonally replicated test to represent different early growth categories: fast, moderate, and slow. Wood increment cores of the 30 clones were collected from two contrasting sites at age 19 years. For growth traits, in contrast to most wood quality traits, more genetic variation was accounted for by clone within family than by family within growth category. Both growth and wood quality traits appear to be under moderate genetic control, with [^(H)]<sub>i</sub><sup>2</sup> = 0.20 - 0.36 \widehat{H}_i^2 = 0.20 - 0.36 and [^(H)]<sub>[`(C)]} ² = 0.70 - 0.83 \widehat{H}_{{\overline C }}^2 = 0.70 - 0.83 . The only exception was microfibril angle ( [^(H)]_i² = 0.10  \textand  [^(H)]_[`(C)] ² = 0.34 \widehat{H}_i^2 = 0.10\;{\text{and}}\;\widehat{H}_{{\overline C }}^2 = 0.34 ). Generally, faster growth resulted in a significantly lower latewood proportion and lower overall wood density. Selection for faster growth does not appear to impact on either fiber length or microfibril angle. Among the wood quality traits, significant genotypic association was observed only between latewood proportion and wood density. Despite the generally negative association between growth and wood density among families, several fast-growing clones maintained above-average density. This implies that, by adopting multiclonal forestry, one can simultaneously improve growth and wood density.