107 research outputs found
The 10k zCOSMOS: Morphological Transformation of Galaxies in the Group Environment Since z ~1
We study the evolution of galaxies inside and outside of the group environment since z = 1 using a large well-defined set of groups and galaxies from the zCOSMOS-bright redshift survey in the COSMOS field. The fraction of galaxies with early-type morphologies increases monotonically with M_B luminosity and stellar mass and with cosmic epoch. It is higher in the groups than elsewhere, especially at later epochs. The emerging environmental effect is superposed on a strong global mass-driven evolution, and at z ~ 0.5 and log(M _*/M_⊙) ~ 10.2, the "effect" of the group environment is equivalent to (only) about 0.2 dex in stellar mass or 2 Gyr in time. The stellar mass function of galaxies in groups is enriched in massive galaxies. We directly determine the transformation rates from late to early morphologies, and for transformations involving color and star formation indicators. The transformation rates are systematically about twice as high in the groups as outside, or up to three to four times higher correcting for infall and the appearance of new groups. The rates reach values as high as 0.3-0.7 Gyr^(–1) in the groups (for masses around the crossing mass 10^(10.5) M_⊙), implying transformation timescales of 1.4-3 Gyr, compared with less than 0.2 Gyr^(–1), i.e., timescales >5 Gyr, outside of groups. All three transformation rates decrease at higher stellar masses, and must also decrease at lower masses below 10^(10) M _⊙ which we cannot probe well. The rates involving color and star formation are consistently higher than those for morphology, by a factor of about 50%. Our conclusion is that the transformations that drive the evolution of the overall galaxy population since z ~ 1 must occur at a rate two to four times higher in groups than outside of them
Smanjenje količine kalcija u mlijeku neutralnom ionskom izmjenom
Mlijeko spada među takve životne namirnice u kojima su u vrlo usklađenim proporcijama zastupani pojedini hranjivi sastojci: mast, bjelančevine, ugljikohidrati, mineralne tvari, vitamini. Svojim harmoničnim sastavom ono može podmiriti gotovo sve hranidbene i biološke potrebe mladog organizma - potomaka
Kemijska kvaliteta vode u proizvodnji maslaca
Kod planiranja mljekara, uključivo i izgradnju sabirališta za mlijeko, mora se kao prvo riješiti besprijekorna opskrba vodom
Kineziographic Research of Patients with Cross Bite
The paper describes the use of an objective method for the quantitative analysis of the
relationship between the posterior cross-bite and the occurrence of occlusive interferences
and damages to the mandible muscle elevator. Two groups of subjects were selected
for the analysis: 10 patients with unilateral cross-bite and 10 students without
any symptoms of temporomandibular disorders (TMD). By means of the Robert Jenkelson
K5A kinesiograph we measured maximal – opening velocity of the mandible
(mm/s), maximal- closing velocity (mm/s), first tooth contact velocity and displacement
in the vertical plane at the maximal intercuspidation (mm). The following values were
obtained: maximal-opening velocity in the first group was 349 mm/s and 380 mm/s in
the control group. This difference was incidental. The maximal closing velocity in the
study group was 204.9 and 345.2 in the control group (p < 0.05). The first tooth contact
velocity in the study group was 75.93 and 325 in the control group (p < 0.01). Displacements
in the vertical plane at the maximal intercuspidation in the investigated group
was 0.240.01 mm, while in control group that value was 0120.012 mm
Prosthetic Therapy of a Seven Year Old Patient with Oligodontia
A seven year old male patient was referred by his dentist to a specialist in dental prothetics with a diagnosis of oligodontia. Examination of the orthopantomogram showed germs of only eight teeth. No teeth were present in the oral cavity. The first permanent molars had been esctracted because of caries. From the case history and a clinical examination, it was established that the boy had craniofacial dysmorphosis/ dysostosis and hypertelorizm with lower positioned and poorly formed ears. He had diagnosis of thickening
of the right ventriculus. Kariotype normal. Also presented adactyly of digits II and III manus et pedis, clinodactyly of digit I, and syndactyly of digits IV and V was surgically treated. By examining the oral cavity, angulus infectiosus oris was diagnosed caused by lowered vertical dimension of occlusion and candidiasis lingue, and consequently the boy was referred to an oral pathologist for appropriate therapy. Special attention is required when fabricating a complete denture in a child\u27s mouth in orded not to comprome
any prosthetic principle. Thus, we were faced with several problems including how to find impression trays of adequate size, and how to explain to the patient the procedure of functional movements, achievement of rest position, and the artificial teeth selection.
Because of the small and narrow dental arches we decided for the smallest size of artificial teeth (D28) and reduced occlusion. The artificial teeth were modified and reduced. The second molar took the place of the first molar. With color and shape we tried to imitate deciduous teeth. After insertion of the complete dentures and control
examination, the patient was given an appointment for making new dentures in six months, because of the growth and development of the maxilla and mandible
Investigations of Tll Suspensions
Thallous iodide suspensions were obtained by direct mixing
of TlN03 and Na! solutions. The amount of TH was kept constant
in the systems, while the concentrations of Na! (in excess), laurylamine
nitrate (LAN) or myristylamine nitrate (MAN) were varied.
Tyndallometric values were recorded as the function of Na!, LAN,
and MAN concentrations respectively, for suspensions aged for
various times. Particle sizes of differently aged TH in \u27Suspensions
containing Na! and Eu(N03)a in solution were determined. Tyndal.:.
lometry and electronmicroscopy showed fast particle growth of
TH in suspension. After about 10 minutes the TH particle grew up
to 1.3 μ. The zero point of charge, determined by microelectrophoresis,
was attained at 0.001-0.005 M Na! and 0.0001-0.0005 M
LAN depending on the conditions under which the system had
been prepared. The results of radiometrically recorded adsorption-
desorption equilibria show a constant increase of the adsorption
capacity as the electrolyte concentration increases
Synthesis and structural characterization of microporous arsenates and phosphates
Predmet rada i istraživanja ove doktorske disertacije su sinteza i strukturne
karakteristike novih kristalnih arsenata i fosfata koji sadrže Mg, K, Ca, Mn, Fe, Co, Ni,
Cu, Zn, Sr, Ba i druge katjone. U strukturama arsenata i fosfata, AsO4- i PO4-tetraedri
najčešće se vezuju sa tetraedarski ili oktaedarski koordinisanim katjonima prelaznih
metala formirajući otvorene strukture (slojeve ili 3D mreže) sa širokim opsegom
različitih topologija. U šupljinama ili porama u obliku povezanih ili nepovezanih
kanala, tunela, kaveza i međuslojnog prostora mogu se ugraditi različiti vanmrežni joni
(obično alkalni i zemnoalkalni katjoni) ili molekuli (najčešće mali organski molekuli),
što čini ova jedinjenja veoma interesantnim zbog njihovih fizičkih i hemijskih osobina i
potencijalne primene.
U okviru ispitivanja sistema T1O–T2O–X2O5–(H2O)–Y, gde je T1 dvovalentni ili
jednovalentni (K+, Ca2+, Zn2+, Sr2+, Ba2+), T2 dvovalentni ili trovalentni (Mg2+, Mn2+,
Fe2+, Co2+, Ni2+, Cu2+, Zn2+, Fe3+, Co3+), X petovalentni (P5+, As5+) katjon, a Y je
vanmrežni katjon H2(C2H8N2)2+ ili NH4
+ sintetisana su nova jedinjenja metodom
niskotemperaturne hidrotermalne sinteze i određene njihove kristalne strukture. Cilj je
bio da se u okviru ovog sistema sintetišu monokristali koji u mikroporama ili
međuslojnom prostoru sadrže različite jone i molekule kao što je etilendiamin,
C2H4(NH2)2, ili odgovarajuća protonovana forma.
Kvalitet dobijenih monokristala proveravan je pomoću optičkog mikroskopa ili
binokularne lupe i strukture kristala određene su metodom rendgenske difrakcije na
monokristalu. Za morfološku i hemijsku karakterizaciju korišćena je metoda skenirajuće
elektronske mikroskopije (SEM) dopunjena energetsko-disperzivnim sistemom (EDS).
Kod kristala koji su zahtevali preciznu kvantitativnu hemijsku analizu korišćena je
elektronska mikrosonda, a metoda ramanske spektroskopije korišćena je za određivanje
prisustva H2O, (OH)−, (NH4)+ i NH3.
Pokazano je da četiri sintetisana kristala imaju zeolitski DFT-tip strukture. To su
(H2en)[ZnAsO4]2 (ZnAs), (H2en)[Co0,1Zn0,9AsO4]2 (ZnCoAs),...The doctoral dissertation research subjects are the synthesis and structural
investigation of new arsenate and phosphate containing Mg, K, Ca, Mn, Fe, Co, Ni, Cu,
Zn, Sr, Ba and other cations. In the structures of arsenates and phosphates, AsO4- and
PO4-tetrahedra are usually linked with tetrahedrally and octahedrally coordinated
cations of transition metals forming open structures (layers or 3D frameworks) with a
wide range of different topologies. In the holes, or pores, which are in the form of a
connected or unconnected channels, tunnels, cages and the interlayered space, various
non-framework ions (usually alkaline and earth alkaline cations) or molecules (usually
small organic molecules) can be incorporated. Therefore these compounds are very
interesting due to their physical and chemical properties and potential applications.
In the course of the investigation of the T1O–T2O–X2O5–(H2O)–Y system,
where T1 is a divalent or monovalent (K+, Ca2+, Zn2+, Sr2+, Ba2+), T2 divalent or
trivalent (Mg2+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Zn2+, Fe3+, Co3+), X pentavalent (P5+,
As5+) cation, and Y is non-framework cation H2(C2H8N2)2+ or NH4
+, several novel
compounds have been synthesized using the low temperature hydrothermal synthesis
method, and their crystal structures have been determined. The aim was to synthesize
single crystals with micropores or interlayer space containing different ions and
molecules like the ethylenediamine, C2H4(NH2)2, or the corresponding protonated
forms.
The quality of the obtained single crystals was evaluated using an optical or
binocular microscope, and the crystal structure was solved using single-crystal X-ray
diffraction data. For the morphological and chemical characterization the scanning
electron microscopy (SEM), coupled with energy-dispersive system (EDS) was used.
The electron microprobe provide precise quantitative chemical analysis, and the Raman
spectroscopy method was used for the determination of the presence of H2O, (OH)−,
(NH4)+ and NH3..
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