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1.
The molecular composition of fossil resins from early to middle Eocene coal from northeast India, has been analyzed for the first time to infer their paleobotanical source. The soluble component of fossil resin was analyzed using gas chromatography–mass spectrometry (GC–MS). The resin extracts are composed of cadalene-based C15 sesquiterpenoids and diagenetically altered triterpenoids. The macromolecular composition was investigated using pyrolysis gas chromatography-mass spectrometry (Py-GC–MS) and Fourier transform infrared (FTIR) spectroscopy. The major pyrolysis products are C15 bicyclic sesquiterpenoids, alkylated naphthalenes, benzenes and a series of C17–C34 n-alkene-n-alkane pairs. Spectroscopic analysis revealed the dominance of aliphatic components. The presence of cadalene-based sequiterpenoids confirms the resin to be Class II or dammar resin, derived from angiosperms of Dipterocarpaceae family. These sesquiterpenoids are often detected in many SE Asian fluvio-deltaic oils. Dipterocarpaceae are characteristic of warm tropical climate suggesting the prevalence of such climate during early Eocene in northeast India.  相似文献   

2.
Several samples of peat from 6 bogs located in southern Poland were investigated for occurrence and distribution types of biomarkers present in their extractable organic matter fraction. It was found that there are inputs from two different sources of organic compounds differing in their characteristics and origin: (1) recent immature peat organic matter deposited in situ which is the source of all polar functionalized compounds, most of n-alkanes, and acyclic isoprenoids, and (2) mature fossil fuels, most probably bituminous coals from the Upper Silesia Coal Basin of vitrinite reflectance equivalent values of 0.9–1.1%. The latter compounds were most probably transported with fly ash to bogs from nearby settlements utilizing such fuel in domestic ovens. This group includes pentacyclic triterpenoids (hopanes and moretanes), minor amounts of n-alkanes, and numerous alkyl naphthalenes and alkyl phenanthrenes. All these compounds show distributions and values of geochemical ratios characteristic for mature organic matter confirming there ex situ origin.  相似文献   

3.
Aliphatic and aromatic hydrocarbons in sediments of the middle and lower Mississippi Fan and two intraslope basins in the Gulf of Mexico are derived from terrestrial organic matter and thermogenic, mature hydrocarbons. The terrestrial hydrocarbon component consists primarily of terrigenous, plant biowaxes (n-alkanes with 21 to 33 carbons). The occurrence of thermogenic hydrocarbons in immature near-surface sediments, their molecular distributions and concentration variations with depth suggest that the majority of these mature hydrocarbons have migrated from a source much deeper in the sediment column. A portion of the thermogenic hydrocarbons may be derived from recycled material and includes phenanthrene, methyl phenanthrenes, chrysene and benzopyrenes. The migrated, thermogenic hydrocarbons include normal and isoprenoid alkanes with less than 21 carbons, naphthalene, methyl naphthalenes, ethyl naphthalenes and other aromatics of similar volatility (i.e., biphenyl, acenaphthene and fluorene). Triterpane, sterane and aromatized sterane distributions suggest that the thermogenic hydrocarbons at both sites have a common source and are overprinted with immature sediment hydrocarbons. The biomarker distributions and carbon isotopic compositions of the thermogenic hydrocarbons are atypical for petroleum produced in the Gulf of Mexico. Molecular distributions of the hydrocarbons are constant, regardless of the present depth of occurrence, suggesting that they have migrated in a separate phase. The upward migration of hydrocarbons from deeper sources is a wide-spread phenomenon in the Gulf of Mexico with several documented cases of massive seepage (visible oil) as well as the more diffuse permeation of Pleistocene sediments of the Mississippi Fan and two intraslopes reported here.  相似文献   

4.
The stable hydrogen isotopic compositions (δD) of selected aliphatic hydrocarbons (n-alkanes and isoprenoids) in eight crude oils of similar source and thermal maturity from the Upper Indus Basin (Pakistan) were measured. The oils are derived from a source rock deposited in a shallow marine environment. The low level of biodegradation under natural reservoir conditions was established on the basis of biomarker and aromatic hydrocarbon distributions. A plot of pristane/n-C17 alkane (Pr/n-C17) and/or phytane/n-C18 alkane (Ph/n-C18) ratios against American Petroleum Institute (API) gravity shows an inverse correlation. High Pr/n-C17 and Ph/n-C18 values and low API gravity values in some of the oils are consistent with relatively low levels of biodegradation. For the same oils, δD values for the n-alkanes relative to the isoprenoids are enriched in deuterium (D). The data are consistent with the removal of D-depleted low molecular weight (LMW) n-alkanes (C14–C22) from the oils. The δD values of isoprenoids do not change with progressive biodegradation and are similar for all the samples. The average D enrichment for n-alkanes with respect to the isoprenoids is found to be as much as 35‰ for the most biodegraded sample. For example, the moderately biodegraded oils show an unresolved complex mixture (UCM), loss of LMW n-alkanes (<C15) and moderate changes in the alkyl naphthalene distributions. The relative susceptibility of alkyl naphthalenes at low levels of biodegradation is discussed. The alkyl naphthalene biodegradation ratios were determined to assess the effect of biodegradation. The dimethyl, trimethyl and tetramethyl naphthalene biodegradation ratios show significant differences with increasing extent of biodegradation.  相似文献   

5.
This paper interprets the mass spectrometric, i.r. absorption and NMR data for 22 compounds obtained from a polar fraction of Green River shale. The major constituents analyzed are believed to be of the following compositional types: CnH2nO (cyclohexanols and chain isoprenoid ketones), CnH2n?10O (tetralones and indanones), CnH2n?7N (tetrahydroquinolines), CnH2n?11N (quinolines), CnH2n?1NO (alkoxypyrrolines), CnH2n?5NO2 (maleimides), CnH2n?8 (tetralins), CnH2n?12 (naphthalenes) and CnH2n?14 (benzylbenzenes). This work expands the present information about nitrogen, oxygen and aromatic constituents indigenous to Green River shale.  相似文献   

6.
Helium, neon, argon, krypton and xenon data are presented from stepwise heating of samples of the mineral whitlockite from the chondritic meteorite St. Severin. The xenon is shown to be a uniform mixture derived from 244Pu fission and rare-earth element spallation. The krypton similarly contains spallation products and 86Kr from 244Pu fission. Plutonium-244 fission yields of 86Kr/129Xe/131Xe/132Xe/134Xe/136Xe = 1.9 ± 0.5/4.8 ± 5.5/24.6 ± 2.0/88.5 ±3.0/93.9 ± 0.8/  100 are obtained. The helium, neon and argon are dominated by spallation and radiogenic 4He and 40Ar. A pile neutron irradiation experiment does not yield a unique Pu/U ratio for this mineral but yields ratios varying from 0.045 down to 0.017. Both the high concentration of 244Pu fission xenon and the high ratio of Pu/U previously reported by Wasserburget al. (J. Oeophys. Res. 74, 4221–4232, 1969) are thus confirmed.  相似文献   

7.
The molecular distributions of homologous aliphatic lipid compounds (n-alkanes, n-alkanoic acids, n-alkanols, n-alkanals and n-alkan-2-ones) were investigated in sediments of Lake Bera, Malaysia as well as in plant waxes from the vicinity using gas chromatography-mass spectrometry. In addition, triterpenoids of the oleanane, ursane, lupane and friedelane series, and their diagenetic products were also identified. Using the aquatic proxy Paq, it was found that the n-alkanes present in surface sediments S1, S5 and S6 correspond to an input from emergent macrophytes, whereas in sediments collected from open water (S2, S3 and S4) they correspond to input from submerged/floating macrophytes. The presence of n-alkan-2-ols, a commonly found homologous series in the sediments as well as in the plant wax, is novel here. In addition, the presence of 24-methylcycloart-22-enol and 24-ethylcycloart-22-enol in sediments as well as the plant wax of Pandanus helicopus, a dominant reed around the lake, also supports the input of plant biomarkers to the sediments. The occurrence of 5-membered ring triterpenoid derivatives as major diagenetic products of the triterpenoids identified (e.g. friedelan-2,3-dione) shows that the degradation of the organic matter in the sediments occurs mainly under oxic conditions. Also, the presence of ring-A degraded triterpenoids (dihydroputranjivic acid, 3-nor-2,4-seco-friedelane, 4α- and 4β-3-norfriedelanes, A-norfriedel-10-one, and A-norfriedel-8-en-10-one) and the aromatized triterpenoid hydrocarbons (mono- and triaromatic derivatives) as minor diagenetic products indicates photochemical and microorganism-mediated alteration reactions of natural products in the sediments. Additional novel polyfunctional friedelane derivatives, namely friedelane-2,3-dione, friedelane-1,3-diol-2-one and friedel-1(10)-ene-1,3-diol-2-one were identified for the first time in this study. These novel polyfunctional triterpenoids were inferred to derive from the oxidation of the triterpenoids from higher plants in this oxic tropical environment. For future reference purposes, the mass spectra of the identified polar triterpenoids are also presented here. This study provides important data on the biogeochemistry of organic matter in a tropical lake of SE Asia.  相似文献   

8.
Potassium permanganate oxidative degradations were conducted for kerogens isolated from Cretaceous black shales (DSDP Leg 41, Site 368), thermally altered during the Miocene by diabase intrusions and from unaltered samples heated under laboratory conditions (250–500°C).Degradation products of less altered kerogens are dominated by normal C4–C15 α,ω-dicarboxylic acids, with lesser amounts of n-C16 and n-C18 monocarboxylic acids, and benzene mono-to-tetracarboxylic acids. On the other hand, thermally altered kerogens show benzene di-to-tetracarboxylic acids as dominant degradation products, with lesser or no amounts (variable depending on the degree of thermal alteration) of α,ω-dicarboxylic acids. Essentially no differences between the oxidative degradation products of naturally- and artificially-altered kerogens are observed.As a result of this study, five indices of aromatization (total aromatic acids/kerogen; apparent aromaticity; benzenetetracarboxylic acids/total aromatic acids; benzene-1,2-dicarboxylic acid/benzenedicarboxylic acids; benzene-1,2,3-tricarboxylic acid/benzenetricarboxylic acids) and two indices of aliphatic character (Total aliphatic acids/kerogen; Aliphaticity) are proposed to characterize the degree of thermal alteration of kerogens.Furthermore, a good correlation is observed between apparent aromaticity estimated by the present KMnO4 oxidation method and that from the 13C NMR method (DENNIS et al., 1982).  相似文献   

9.
Previous studies have suggested that coal from the 1891 shipwreck of a collier off Victoria, BC, Canada is responsible for elevated parent (unsubstituted) PAH concentrations in sediments near deep marine outfalls from Esquimalt and Victoria in the Strait of Juan de Fuca. To resolve this question, we analysed a comprehensive suite of resolved and unresolved complex mixture (UCM) alkanes, tricyclic terpane, hopane and sterane biomarkers, and parent and alkyl polycyclic aromatic hydrocarbons (PAHs) in samples of coal, wastewater and sediments. Composition patterns, principal components analysis (PCA) models and PAH and biomarker ratios all indicate that coal from the collier does not make a dominant contribution to any sediment sample. Mass balance calculations based on the n-C24 content and 24/4 tetracyclic terpane to 26/3R tricyclic terpane ratio in coal provide a particularly good match between predicted and observed alkyl PAH concentrations for sediments with high alkyl naphthalenes and phenanthrene/anthracenes and low UCM, but the predicted coal contribution substantially underestimates the measured parent PAHs for all sediment samples. Methylbenz[a]anthracene/chrysene profiles for sediments with a dominance of parent PAHs are very close to coal tar, with a marked predominance of methylbenz[a]anthracenes and the possible 10-methylbenz[a]anthracene as a major constituent, while the methylchrysenes predominate in coal. Hence, coal from the collier could account for most alkyl PAHs in the sediments, but dredged sediment containing pyrolised coal waste from a former coal gas plant in Victoria Harbour is a more likely source for the samples with elevated parent PAHs. PAH ratios indicate that these sources are superimposed on combustion PAHs introduced by a combination of atmospheric deposition and delivery via stormwater and the outfalls. Parent PAH distributions also suggest that PAHs in wastewater that originate from oils and soot in liquid fossil fuel combustion are dispersed and degraded, while the larger wood char particles (containing PAHs more protected from degradation) settle closer to the outfalls. Overall, results suggest that PAHs have predominant sources in wood combustion, coal and possibly coke, with a likelihood of much lower bioavailability than would be expected from wastewater dominated by oils and soot from vehicle combustion.  相似文献   

10.
The solubilities of several medium molecular weight aromatic hydrocarbons were determined at 25°C in aqueous binary, ternary, and quaternary systems. The binary systems consisted of distilled water plus one each of the following: naphthalene, 1-methylnaphthalene, 2-methylnaphthalene, biphenyl, 2-ethylnaphthalene, 1,5-dimethylnaphthalene, 2,3-dimethylnaphthalene, 2,6-dimethylnaphthalene, acenaphthene and phenanthrene. The ternary systems consisted of distilled water plus one of the following hydrocarbon pairs: naphthalene/biphenyl, naphthalene/acenaphthene, naphthalene/phenanthrene, biphenyl/phenanthrene, biphenyl/2-methylnaphthalene, acenaphthene/phenanthrene and 2-methylnaph-thalene/phenanthrene. Quaternary systems consisted of distilled water and one of the following hydrocarbon mixtures: naphthalene/biphenyl/phenanthrene, 2-methylnaphthalene/biphenyl/phenanthrene and naphthalene/acenaphthene/phenanthrene. In binary systems at S%. = 0, solubilities ranged from 31.3 ppm for naphthalene to 1.07 ppm for phenanthrene. The alkyl naphthalenes exhibited solubilities which were a function of molar volume and substituent size and position. In ternary and quaternary systems, solubilities often deviated from values obtained in binary systems presumably due to solute-solute interactions and/or formation of solid solutions. Aromatic hydrocarbons are ‘salted out’ by increasing concentrations of inorganic salts. At S%. = 35, the solubility of naphthalene is 22.0 ppm and of phenanthrene, 0.71 ppm. The empirical salting parameters are identical in both binary and quaternary systems.  相似文献   

11.
《China Geology》2018,1(3):374-391
Numerous dark enclaves with different shapes are found in Jiuling Neoproterozoic granitoids. Precise LA-ICP-MS U-Pb dating was conducted on zircons extracted from two microcrystalline enclave samples, yielding crystallization ages of 822.6±5.8 Ma and 822.2±6.2 Ma, respectively. The consistent ages within analytical errors with the host granitoids suggested that they were the products of the same magmatism. The microcrystalline-dioritic enclaves commonly show plastic forms and contain similar plagioclase megacrysts to the host rocks, and both of the enclaves and host granitoids showed a complex composition and structural imbalance in plagioclases. Furthermore, the apatites with a euhedral acicular shape occurred widely in the microcrystalline-dioritic enclaves. All of these petrographic features above imply magma mixing is involved in their diagenesis. The enclaves and host granitoids show a marked zircon trace element difference and Hf isotopic signatures without correlation in zircon trace element pairs but form their own system between enclaves and host granitoids. Additionally, most of the zircons show extremely high εHf (t) with εHf (t) =3.54–11.94 from the southern samples, and εHf (t) =1.0–9.09 from the central region. Some zircons with the higher εHf (t) are similar to the zircons from the juvenile island arc in the eastern segment of Jiangnan Orogen. Integrated geological and Hf isotopic characteristics suggest microcrystalline-dioritic enclaves were derived from the partial melting process of the Mesoproterozoic crust which enriched juvenile island arc materials and mixed with the granitic magma that remelted from the Mesoproterozoic continental crust which relatively enriched ancient sediments and mixed with the host granitoid in diagenesis.  相似文献   

12.
The aliphatic hydrocarbon composition (acyclic isoprenoids, hopanoids and steroids) of oils from the most productive fields in the southern geological Province of Cuba have been studied. This province is defined by its position with respect to the Cretaceous overthrust belt generated during the formation of oceanic crust along the axis of the proto-Caribbean Basin. The relative abundances of 18α(H)-22,29,30-trisnorneohopane, gammacerane and diasteranes suggest that Pina oils are related to the carbonate oils from the Placetas Unit in the northern province (low Ts/(Ts+Tm) and C27,29 rr/(rr+sd) ratios). The Cristales and Jatibonico oils exhibit some differentiating features such as higher Ts/(Ts+Tm) and absence of gammacerane. The oils from this province do not exhibit significant differences in either hopane, C32 22S/(S+R) and C30 αβ/(αβ+βα), or sterane, C29 αα 20S/(S+R), maturity ratios. However, the relative content of 5α(H),14β(H),17β(H)-cholestanes (C29 ββ/(ββ+αα) ratio) indicates that Pina oils are more mature than Cristales and Jatibonico oils. Several of these oils (Cristales, Jatibonico and Pina 26) are heavily biodegraded, lacking n-alkanes, norpristane, pristane and phytane (the two former oils do not contain acyclic isoprenoid hydrocarbons). Other biodegradation products, the 25-norhopanes, are found in all the oils. Their occurrence is probably due to mixing of severely biodegraded oil residues with undegraded crude oils during accumulation in the reservoir.  相似文献   

13.
Lignin oxidation products and stable carbon isotope distributions are used to investigate the sources, transport, and chemical stability of land-derived organic matter in dated cores of modern sediment from the southern Washington State continental shelf and slope. There is no evidence for significant chemical alteration of lignin compounds in these sediments for time periods of up to 400 yr. Gymnosperm woods and nonwoody angiosperm tissues account for most of the land-derived organic matter in the deposits. These land plant remains have an average δ13C of approximately ?25.5% and are concentrated in a narrow band of silty sediment which extends northward from the Columbia River mouth along the mid-shelf. Marine organic matter having an approximate δ13C of ?21.5%, strongly predominates in most other shelf and slope environments. Net fluxes of land-derived organic matter into the surface 5 cm of the cores vary directly with sediment accumulation rates. Net fluxes of marine organic material into the surface sediments are highest in environments which favor the preservation of organic matter, but correspond to less than 1% of the primary productivity in the overlying waters.  相似文献   

14.
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15.
《Applied Geochemistry》2006,21(6):919-940
Smoke particulate matter from grasses (Gramineae, temperate, tropical and arctic) subjected to controlled burning, both under smoldering and flaming conditions, was sampled by high volume air filtration on pre-cleaned quartz fiber filters. The filtered particles were extracted with dichloromethane/methanol and the crude extracts were methylated for separation by thin layer chromatography into hydrocarbon, carbonyl, carboxylic acid ester and polar fractions. Then, the total extract and individual fractions were analyzed by GC–MS. The major organic components directly emitted in grass smoke particles were the homologous series of n-alkanoic acids from plant lipids, n-alkanes from epicuticular wax, and sterols and triterpenols. The major natural products altered by combustion included pyrolysis products from cellulose and lignin biopolymers, and oxidation products from triterpenoids and sterols. Polycyclic aromatic hydrocarbons (PAH) were also present; however, only as minor components. Although the concentrations of organic compounds in smoke aerosols are highly variable and dependent on combustion temperature, the biomarkers and their combustion alteration products are in these cases source specific. The major components are adsorbed on or trapped in smoke particulate matter and thus may be utilized as molecular tracers in the atmosphere for determining fuel type and source contributions from grass burning.  相似文献   

16.
Two hydrogen-rich lithobodies of highly alipathic character from a coal occurring in southwest Utah, have been studied. Bituminite (>50%), vitrinite (25–30%) and liptodetrinite (7–12%) are the principal macerals. The hexane-soluble products of hydrogenating the lithotypes at 400° with tetralin and hydrogen have been analyzed by GC-MS. Products identified include homologous series of alkylated naphthalenes, phenols, furans, cyclohexenones and hydroxy-pyridines. In the case of furans, the alkyl groups extend beyond C30. Materials released by Soxhlet extraction with pyridine consist chiefly of homologous series of fatty acids and their methyl esters and of methyl alkyl ketones, which were not found in the hydrogenation products. The long alkyl chains in these substances can account for about 75% of the alkanes found in the hydrogenation products but not in the extracts. Most of the compounds mentioned in the foregoing are thought to be physically held or trapped in the coal, rather than chemically combined in its macromolecular network. Except for the fatty acids, the origins of these substances are difficult to identify.  相似文献   

17.
《Applied Geochemistry》2001,16(9-10):1021-1031
A set of chlorinated hydrocarbons (TCE, PCE, DCM, 1,1,1-TCA, chloroform) provided by four manufacturers has been isotopically characterised for both C and Cl, using a new sensitive method. A very large range of δ13C (from −51.66 to −24.07‰/PDB) associated with a very large range of δ37Cl (from −2.7 to +3.4‰/SMOC) was obtained. This range of δ37Cl is much larger than that of inorganic Cl (±1‰ SMOC) and most individual solvents show a very distinct δ37Cl compared to inorganic Cl isotopic signatures. Moreover, δ37Cl/δ13C pairs are distinct from one solvent/manufacturer to another. In a δ13C versus δ37Cl diagram, δ37Cl / δ13C pairs show different trends for the products of a single manufacturer compared to another. This suggests that Cl isotopic compositions are probably highly fractionated during organic synthesis. The δ37Cl values can be interpreted in terms of the probable manufacturing processes. Unlike the data published previously, with one exception, all the new results for samples reported here have positive δ37Cl values which might differentiate natural Cl from that derived from degradation. This method has significant potential as a tool for investigating environmental pollution problems; in particular, it offers the possibility for validating models of transport and fate of pollutants.  相似文献   

18.
The surface sediments collected from the southern Mariana Trench at water depths between ca. 4900 m and 7068 m were studied using lipid biomarker analyses to reveal the origin and distribution of organic matters. For all samples, an unresolved complex mixture (UCM) was present in the hydrocarbon fractions, wherein resistant component tricyclic terpanes were detected but C27–C29 regular steranes and hopanes indicative of a higher molecular weight range of petroleum were almost absent. This biomarker distribution patterns suggested that the UCM and tricyclic terpanes may be introduced by contamination of diesel fuels or shipping activities and oil seepage elsewhere. The well-developed faults and strike-slip faults in the Mariana subduction zone may serve as passages for the petroleum hydrocarbons. In addition, the relative high contents of even n-alkanes and low Carbon Preference Indices indicated that the n-alkanes were mainly derived from bacteria or algae. For GDGTs, the predominance of GDGT-0 and crenarchaeol, together with low GDGT-0/Crenarchaeol ratios (ranging from 0.86 to 1.64), suggests that the GDGTs in samples from the southern Mariana Trench were mainly derived from planktic Thaumarchaeota. However, the high GDGT-0/crenarchaeol ratio (10.5) in sample BC07 suggests that the GDGTs probably were introduced by methanogens in a more anoxic environment. Furthermore, the n-alkanes C19–C22 and the n-fatty acids C20:0–C22:0 were depleted in 13C by 3‰ compared to n-alkanes C16–C18 and the n-fatty acids C14:0–C18:0, respectively, which was interpreted to result from the preferential reaction of fatty acid fragments with carbon “lighter” terminal carboxyl groups during carbon chain elongation from the precursors to products. The abundance of total alkanes, carboxylic acids, alcohols and total lipids were generally increased along the down-going seaward plate, suggesting the lateral organic matter inputs play an important role in organic matter accumulation in hadal trenches. The extremely high contents of biomarkers in sample BC11 were most likely related to trench topography and current dynamics, since the lower steepness caused by graben texture and proximity to the trench axis may result in higher sedimentation rate. This paper, for the first time, showed the biomarker patterns in surface sediments of the Mariana Trench and shed light on biogeochemistry of the hardly reached trench environment.  相似文献   

19.
Labradorite was altered artificially by HC1 solution ranging from M = 1 to M = 0.003 at 245 and 230°C. The products of alteration were examined by X-ray diffraction, electron microscopy, electron diffraction, infrared spectroscopy and the electron microprobe and the solution was analyzed chemically.Amorphous silica only was formed in solutions with MHCl = 1 and MHCl = 0.3. In a solution with MHCl = 0.2, amorphous silica was initially formed, later dissolved and replaced by kaolinite. A mixture of microcrystalline boehmite and amorphous aluminosilicate was formed, altering to kaolinite in solutions with MHCl = 0.1 and 0.3. Small amounts of kaolinite were initially formed but the alteration soon stopped in solution with MHCl = 0.003. Relationships between the alteration processes and pH of the solutions can be roughly explained by using solubility diagrams assuming the congruent dissolution of labradorite and precipitation of the products in partial equilibrium. However, these assumptions are not valid with strongly acid solutions.The rate of dissolution of labradorite is controlled not only by its surface area, but also by the diffusion of matter through the layer of alteration products.  相似文献   

20.
Microalgal culture experiments to track chlorophyll-a (chl-a) transformation during senescence were characterised by the production of demetallated Type I chl-a transformation products in Pavlova gyrans and by the production of oxidative Type I transformation products in Isochrysis galbana. Dark-induced senescence in I. galbana produced a different distribution of Type I products from nutrient depletion induced senescence. Several novel Type I compounds were detected, including a chl-d like compound in I. galbana and a chl-a precursor like compound in P. gyrans. Type II chl-a transformation products were detected in the dissolved phase of I. galbana cultures; this is the first report of such compounds associated with marine algae.  相似文献   

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