Fresh Cattle Faeces Research Articles

Assessment of Contamination Risk from Fecal Matter Presence on Fruit and Mulch in the tomato fields based on generic Escherichia coli population

The purpose of this study was to evaluate the fate of generic Escherichia coli in fecal pats under different field conditions and to predict Salmonella and Shiga toxin-producing E. coli (STEC) survival dynamics based on developed models. Eight trials were conducted during spring and fall in both North and Central Florida. Fresh cattle feces (1g) was placed on mature green round tomatoes located inside (TIP) and outside (TOP) of the plant canopy. Fecal pats (10 g) were placed under (MUP) and distant (MDP) to tomato plants on plastic mulch. Pathogen populations were predicted based on developed models. Declines in generic E. coli populations over 7 days (Log CFU/g) in fecal pats were between 0.9 and 2.7 on TIP, 1.2 and 3.0 on TOP, 0.2 and 1.2 on MUP, and 0.4 and 1.5 on MDP in the Central Florida fall and spring trials, respectively. E. coli populations remained stable at ≤4.2 and ≤ 6.5 Log CFU/g during all North Florida trials. The concentration changes in predicted Salmonella and STEC population were less than 2.1 Log CFU/g in fecal pats for all conditions. Developed models predicted similar pathogen survival trends to generic E. coli with no dramatical impact under the field conditions.

Evaluation of pyriproxyfen in cattle by oral treatment: An alternative to control Haematobia irritans

The horn fly, Haematobia irritans, is a bovine ectoparasite that causes large losses to cattle breeders, through lower meat and milk production and hide damage. Currently, the control of this parasite is mainly through chemicals. However, the indiscriminate use of these substances generates resistance. Pyriproxyfen belongs to an insect growth disruptors class with mechanisms of action for the control of immature forms of the insect. The aim of this study was to investigate the potential of pyriproxyfen administered orally to cattle for the control of the horn fly. In vitro bioassays were carried out by evaluating the number of adults emerged from 30 eggs per replicate, in triplicate, added in a substrate (fresh cattle feces) spiked with pyriproxyfen solutions in the concentration range of 2–130 ppb (ng.g−1). Probit analysis estimated LC50 value of 7.89 ppb and LC90 value of 70.08 ppb. The doses used in the in vivo evaluation were established based on the LC90 values and the anatomical and physiological aspects of the bovine digestive tract. Capsules containing pyriproxyfen at doses of 2.5 mg (G2.5) and 40 mg (G40) were produced and administered orally by bolus applicator for 12 days. The efficacy of pyriproxyfen against the immature forms of H. irritans was determined by incubating eggs in vitro in the feces collected on days 0, +3, +6, +10 and +13. Quantification of pyriproxyfen in feces was performed by UPLC-MS/MS, finding concentrations ranging from 13.4 to 22.6 ppb for G2.5 and between 268.5 to 509.0 ppb for G40. Pyriproxyfen administered orally is eliminated in the active form in the fecal mass and at a dose of 40 mg.day−1 (0.1 mg/kg/day) generates fecal concentrations able to produce 100 % prevention of adults emergence of H. irritans.

The stable oxygen isotope ratio of resin extractable phosphate derived from fresh cattle faeces.

RationalePhosphorus losses from agriculture pose an environmental threat to watercourses. A new approach using the stable oxygen isotope ratio of oxygen in phosphate (δ18OPO4 value) may help elucidate some phosphorus sources and cycling. Accurately determined and isotopically distinct source values are essential for this process. The δ18OPO4 values of animal wastes have, up to now, received little attention.MethodsPhosphate (PO4) was extracted from cattle faeces using anion resins and the contribution of microbial PO4 was assessed. The δ18OPO4 value of the extracted PO4 was measured by precipitating silver phosphate and subsequent analysis on a thermal conversion elemental analyser at 1400°C, with the resultant carbon monoxide being mixed with a helium carrier gas passed through a gas chromatography (GC) column into a mass spectrometer. Faecal water oxygen isotope ratios (δ18OH2O values) were determined on a dual‐inlet mass spectrometer through a process of headspace carbon dioxide equilibration with water samples.ResultsMicrobiological results indicated that much of the extracted PO4 was not derived directly from the gut fauna lysed during the extraction of PO4 from the faeces. Assuming that the faecal δ18OH2O values represented cattle body water, the predicted pyrophosphatase equilibrium δ18OPO4 (Eδ18OPO4) values ranged between +17.9 and +19.9‰, while using groundwater δ18OH2O values gave a range of +13.1 to +14.0‰. The faecal δ18OPO4 values ranged between +13.2 and +15.3‰.ConclusionsThe fresh faecal δ18OPO4 values were equivalent to those reported elsewhere for agricultural animal slurry. However, they were different from the Eδ18OPO4 value calculated from the faecal δ18OH2O value. Our results indicate that slurry PO4 is, in the main, derived from animal faeces although an explanation for the observed value range could not be determined.

Assessment of the ability of five culture media for the detection of E scherichia coli O157

Summary Cattle are a common reservoir for Escherichia coli O157:H7. Prior to confirming its presence in a sample, proper isolation of E. coli O157 is necessary. Consequently, this study evaluated the ability of five commercial plating media to isolate E. coli O157 from 138 samples of fresh cattle faeces, water from water trough and pond, and surfaces of water trough and hay bunk. For the isolation of E. coli O157, samples were enriched in tryptic soya broth, followed by immunoseparation and then plating on SMAC, CT-SMAC, CHROMagar™ O157, Tellurite CHROMagar™ O157 and Vancomycin Cefixime Cefsoludin CHROMagar™ O157. Real-time PCR targeting genes stx1, stx2 and wzyO157 was used to confirm selected isolates. When analysed together, CT-SMAC and CHROMagar™ O157 were the best combination for isolating E. coli O157, giving 79% true-positive results and only 0.05% false-negative results.

Characterization of fibrolytic and lipid accumulating fungi isolated from fresh cattle feces

To characterize coprophilous fungi for converting lignocellulose into lipids, four fungal strains utilizing cellulose microcrystalline and xylan were screened. The fungi were identified as Cladosporium sp. F1, Circinella sp. F6, Mycocladus sp. F49, and Byssochlamys sp. F52 based on the ITS1-5.8S-ITS2 sequence similarity. The strain F52 accumulated 336.0 mg/L reducing sugars on cottonseed shells treated with ethanol. The combination of F1+F52 increased the reducing sugar accumulating rates. However, the activities of avicelase and xylanase were not correlated with the reducing sugars accumulated by the test strains. Strains F6 and F52 produced higher cellular lipids (above 530.7 mg/L) than other strains. However, the strain F52 could produce more cellular lipids with xylose and mannose as the sole carbon sources. The results indicated that the reducing sugar contents accumulated by the different strains were influenced by the fungal taxa and ligocellulosic types. With fibrolytic and lipid accumulating activities, diverse fungi harboring in herbivore feces need to be further characterized.

Absence of E coli O157:H7 in sheep and cattle faeces in North Wales

Escherichia coli O157:H7 is a human pathogen associated with haemolytic uraemic syndrome and haemorrhagic colitis cases throughout the developed world (Garcia and others 2010). The faeces of ruminant animals, in...

Chromogenic Agar Medium for Detection and Isolation of Escherichia coli Serogroups O26, O45, O103, O111, O121, and O145 from Fresh Beef and Cattle Feces

Non-O157 Shiga toxin-producing Escherichia coli (STEC) strains are clinically important foodborne pathogens. Unlike E. coli O157:H7, these foodborne pathogens have no unique biochemical characteristics to readily distinguish them from other E. coli strains growing on plating media. In this study, a chromogenic agar medium was developed in order to differentiate among non-O157 STEC strains of serogroups O26, O45, O103, O111, O121, and O145 on a single agar medium. The ability of this chromogenic agar medium to select and distinguish among these pathogens is based on a combination of utilization of carbohydrates, β-galactosidase activity, and resistance to selective agents. The agar medium in combination with immunomagnetic separation was evaluated and successfully allowed for the detection and isolation of these six serogroups from artificially contaminated fresh beef. The agar medium in combination with immunomagnetic separation also allowed successful detection and isolation of naturally occurring non-O157 STEC strains present in cattle feces. Thirty-five strains of the top six non-O157 STEC serogroups were isolated from 1,897 fecal samples collected from 271 feedlot cattle. This chromogenic agar medium could help significantly in routine screening for the top six non-O157 STEC serogroups from beef cattle and other food.

Estimated human health risks from exposure to recreational waters impacted by human and non-human sources of faecal contamination

This work was conducted to determine whether estimated risks following exposure to recreational waters impacted by gull, chicken, pig, or cattle faecal contamination are substantially different than those associated with waters impacted by human sources such as treated wastewater. Previously published Quantitative Microbial Risk Assessment (QMRA) methods were employed and extended to meet these objectives. Health outcomes used in the analyses were infection from reference waterborne pathogens via ingestion during recreation and subsequent gastrointestinal (GI) illness. Illness risks from these pathogens were calculated for exposure to faecally contaminated recreational water at the U.S. regulatory limits of 35 cfu 100 mL −1 enterococci and 126 cfu 100 mL −1 Escherichia coli. The probabilities of GI illness were calculated using pathogen dose-response relationships from the literature and Monte Carlo simulations. Three scenarios were simulated, representing a range of feasible interpretations of the available data. The primary findings are that: 1) GI illness risks associated with exposure to recreational waters impacted by fresh cattle faeces may not be substantially different from waters impacted by human sources; and 2) the risks associated with exposure to recreational waters impacted by fresh gull, chicken, or pig faeces appear substantially lower than waters impacted by human sources. These results suggest that careful consideration may be needed in the future for the management of recreational waters not impacted by human sources.

Survival and persistence of human and ruminant‐specific faecal Bacteroidales in freshwater microcosms

Amplification of host-specific markers from Bacteroidales faecal anaerobes can rapidly identify the source of faecal pollution. It is necessary to understand persistence and survival of these markers and marker cells, both to interpret quantitative source-tracking data, and to use such data to predict pathogen occurrence. We measured marker persistence and cell survival of two human (HF134, HF183) and two ruminant (CF128, CF193) faecal Bacteroidales markers, compared with Escherichia coli and enterococci. Freshwater microcosms were inoculated with fresh cattle or human faeces and incubated at 13 degrees C in natural light or darkness. Marker persistence was measured by polymerase chain reaction (PCR) and quantitative PCR. Survival of marker cells was measured by real-time quantitative PCR. There was no difference in persistence between the two human-specific Bacteroidales DNA markers in the light and dark microcosms. Cell survival profiles of the two human markers were also similar; both were significantly affected by light. Ruminant markers persisted and survived longer than human markers (14 versus 6 days respectively). CF193 decreased more rapidly than CF128, and light significantly affected CF128 but not CF193. These results support use of host-specific faecal Bacteroidales markers as indicators of recent faecal pollution, but suggest that caution is needed in interpreting quantitative results to indicate proportional contribution of different sources, as individual markers differ in their survival, persistence and response to environmental variables. The survival and persistence profiles for Bacteroidales markers are consistent with survival profiles for several faecal pathogens.

Potential To Reduce Escherichia coli Shedding in Cattle Feces by Using Sainfoin ( Onobrychis viciifolia ) Forage, Tested In Vitro and In Vivo

There is a growing concern about the presence of pathogens in cattle manure and its implications on human and environmental health. The phytochemical-rich forage sainfoin (Onobrychis viciifolia) and purified phenolics (trans-cinnamic acid, p-coumaric acid, and ferulic acid) were evaluated for their ability to reduce the viability of pathogenic Escherichia coli strains, including E. coli O157:H7. MICs were determined using purified phenolics and acetone extracts of sainfoin and alfalfa (Medicago sativa), a non-tannin-containing legume. Ground sainfoin or pure phenolics were mixed with fresh cattle feces and inoculated with a ciprofloxacin-resistant strain of E. coli, O157:H7, to assess its viability at -20 degrees C, 5 degrees C, or 37 degrees C over 14 days. Forty steers were fed either a sainfoin (hay or silage) or alfalfa (hay or silage) diet over a 9-week period. In the in vitro study, the MICs for coumaric (1.2 mg/ml) and cinnamic (1.4 mg/ml) acids were 10- to 20-fold lower than the MICs for sainfoin and alfalfa extracts. In the inoculated feces, the -20 degrees C treatment had death rates which were at least twice as high as those of the 5 degrees C treatment, irrespective of the additive used. Sainfoin was less effective than coumaric acid in reducing E. coli O157:H7 Cip(r) in the inoculated feces. During the animal trial, fecal E. coli numbers declined marginally in the presence of sainfoin (silage and hay) and alfalfa silage but not in the presence of hay, indicating the presence of other phenolics in alfalfa. In conclusion, phenolic-containing forages can be used as a means of minimally reducing E. coli shedding in cattle without affecting animal production.

Survival of Indicator and Pathogenic Bacteria in Bovine Feces on Pasture

The survival of enteric bacteria was measured in bovine feces on pasture. In each season, 11 cow pats were prepared from a mixture of fresh dairy cattle feces and sampled for up to 150 days. Four pats were analyzed for Escherichia coli, fecal streptococci, and enterococci, and four inoculated pats were analyzed for Campylobacter jejuni and Salmonella enterica. Two pats were placed on drainage collectors, and another pat was fitted with a temperature probe. In the first 1 to 3 weeks, there were increases (up to 1.5 orders of magnitude) in the counts of enterococci (in four seasons), E. coli (three seasons), fecal streptococci (three seasons), and S. enterica (two seasons), but there was no increase in the counts of C. jejuni. Thereafter, the counts decreased, giving an average ranking of the times necessary for 90% inactivation of C. jejuni (6.2 days from deposition) < fecal streptococci (35 days) < S. enterica (38 days) < E. coli (48 days) < enterococci (56 days). The pat temperature probably influenced bacterial growth, but the pattern of increases and decreases was primarily determined by desiccation; growth occurred when the water content was greater than 80%, but at a water content of 70 to 75% counts decreased. E. coli and enterococcus regrowth appeared to result from pat rehydration. Of 20 monthly leaching losses of E. coli, 16 were <10% of the total counts in the pat, and 12 were <1%. Drainage losses of C. jejuni (generally <1%) were detected for only 1 to 2 months. Although enterococci exhibited the best survival rate, higher final counts suggested that E. coli is the more practical indicator of bovine fecal pollution.

Transmission of Escherichia coli O157:H7 to cattle by house flies

The main reservoir of Escherichia coli O157:H7 is the digestive tract of cattle; however, the ecology of this food-borne pathogen is poorly understood. House flies ( Musca domestica L.) might play a role in dissemination of this pathogen in the cattle environment. In our study, eight calves were individually exposed to house flies that were orally inoculated with a mixture of four strains of nalidixic acid-resistant E. coli O157:H7 ( Nal REcO157) for 48 h. Another eight calves were individually exposed to uninoculated flies and served as the control. Fresh cattle feces (rectal sampling) and drinking water were periodically sampled and screened for Nal REcO157 up to 19 days after the exposure. At the end of the experiment, all calves were euthanized and the lumen contents of rumen, cecum, colon, and rectum as well as swab samples of gall-bladder mucosa and the recto-anal mucosa were screened for Nal REcO157. On day 1 after the exposure, fecal samples of all eight calves and drinking-water samples of five of eight calves exposed to inoculated flies tested positive for Nal REcO157. The concentration of Nal REcO157 in feces ranged over time from detectable only by enrichment (<10 2) to up to 1.1 × 10 6 CFU/g. Feces of all calves remained positive for Nal REcO157 up to 11 days after the exposure and 62% were positive until the end of experiment. Contamination of drinking water was more variable and all samples were negative on day 19. At necropsy, the highest prevalence of Nal REcO157 was in the recto-anal mucosa region, followed by rectal and colonic contents.

Persistence of Escherichia coli O157 on farm surfaces under different environmental conditions

To compare the persistence of Escherichia coli O157 on a variety of common faecally contaminated farmyard material surfaces (wood and steel) under different moisture and temperature regimes. Samples of field-conditioned farmyard materials (galvanized steel and wood) were cut into pieces and contaminated with fresh cattle faeces inoculated with nontoxigenic E. coli O157 (strain 3704). Thereafter, they were stored at four different environmental conditions; with temperature (5 and 20 degrees C) and moisture (moist or dry) as variables. Transfer of the pathogen to hands from the surfaces was also evaluated. Escherichia coli O157 numbers declined over time on all surfaces albeit at different rates according to the sample material and environmental conditions. Persistence was greatest on moist wood samples under cooler temperatures with large population numbers remaining after 28 days. Desiccation of surfaces resulted in a more rapid decline in E. coli O157 populations under both temperature regimes. Substantial numbers of colonies may also potentially be transferred to human hands from the surfaces during brief contact. When environmental conditions are favourable, E. coli O157 may persist for considerable times on a range of surfaces. However, when exposed to higher temperatures and dehydration, survival is notably decreased. Overall, bacterial persistence was significantly greater on wood samples relative to steel. Escherichia coli O157 is a prevalent pathogen, common in ruminant faeces. Contact with contaminated faeces may lead to human infection, resulting in possible severe illness. Although our study used only one strain of bacteria, our findings indicates that E. coli O157 has the potential to persist for long periods of time on gates, stiles and other farmyard surfaces under a range of environmental conditions. These farmyard surfaces therefore pose a potential infection pathway particularly where there is a high risk of direct human contact (e.g. child petting zoos, open farms).

Cyllamyces aberensis gen.nov. sp.nov., a new anaerobic gut fungus with branched sporangiophores isolated from cattle

A new genus of the anaerobic gut fungi (Neocallimastigales), Cyllamyces aberensis gen.nov. sp.nov., with bulbous holdfast, branched sporangiophores and limited polycentric thallus development is described. The fungus was isolated from fresh cattle faeces. Free-swimming zoospores were spherical, uninucleate, and uniflagellate. After encystment, zoospores germinated and gave rise to a single, bulbous holdfast. One or several branched sporangiophores were produced from different locations on the holdfast, each bearing several spherical sporangia. DAPI staining of thalli indicated that nuclei were present in the holdfast, sporangiophores, and sporangia. As many as 12 sporangia were observed per thallus on up to 5 sporangiophores, with zoosporogenesis beginning 16–18 h after encystment. Zoospore ultrastructure was examined by transmission electron microscopy and found to be similar to that reported for other anaerobic chytrid fungi. Organelles were evenly distributed throughout the cell, except for the posteriorly attached flagellum and associated attachment apparatus, the hydrogenosomes, which were mainly situated in the posterior parts of the cell and a posteriorly directed, beak-shaped nucleus. Limited polycentric thallus development (including branched sporangiophores), the possession of a single bulbous holdfast and the absence of rhizoids were stable features of this fungus that distinguished it from the other five genera of gut fungi. Therefore, we have used these characteristics to assign the fungus to a new genus, Cyllamyces, with the specific name C. aberensis.Key words: rumen, fungal taxonomy, Neocallimastigales, chytrid, zoospore ultrastructure.

&lt;i&gt;Cyllamyces aberensis&lt;/i&gt; gen.nov. sp.nov., a new anaerobic gut fungus with branched sporangiophores isolated from cattle

A new genus of the anaerobic gut fungi (Neocallimastigales), Cyllamyces aberensis gen.nov. sp.nov., with bulbous holdfast, branched sporangiophores and limited polycentric thallus development is described. The fungus was isolated from fresh cattle faeces. Free-swimming zoospores were spherical, uninucleate, and uniflagellate. After encyst - ment, zoospores germinated and gave rise to a single, bulbous holdfast. One or several branched sporangiophores were produced from different locations on the holdfast, each bearing several spherical sporangia. DAPI staining of thalli in - dicated that nuclei were present in the holdfast, sporangiophores, and sporangia. As many as 12 sporangia were ob- served per thallus on up to 5 sporangiophores, with zoosporogenesis beginning 16-18 h after encystment. Zoospore ultrastructure was examined by transmission electron microscopy and found to be similar to that reported for other an - aerobic chytrid fungi. Organelles were evenly distributed throughout the cell, except for the posteriorly attached flagellum and associated attachment apparatus, the hydrogenosomes, which were mainly situated in the posterior parts of the cell and a posteriorly directed, beak-shaped nucleus. Limited polycentric thallus development (including branched sporangiophores), the possession of a single bulbous holdfast and the absence of rhizoids were stable features of this fungus that distinguished it from the other five genera of gut fungi. Therefore, we have used these characteris- tics to assign the fungus to a new genus, Cyllamyces, with the specific name C. aberensis.

The use of herbal preparations for tick control in western Ethiopia.

Information on the traditional tick control methods used in Keffa, Illubabor and Wellega Provinces in western Ethiopia was obtained from 86 veterinary clinics and 865 peasant farmers through a questionnaire survey. Latexes of Euphorbia obovalifolia and Ficus brachypoda, juice of crushed leaves of Phytolaca dodecandra and Vernonia amygdalina, fruit juice of Solanum incanum, crushed seeds of Lepidium sativum mixed with fresh cattle faeces, juice of crushed leaves and bark of Calpurnea aurea and commercially available spice of Capsicum spp. mixed with butter, were used by peasant farmers to control ticks. Preliminary in vitro efficacy tests of these plant preparations were performed on engorged female Boophilus decoloratus. Preparations of Capsicum spp., E. obovalifolia, S. incanum and F. brachypoda were found to have 30-100% killing effects. Subsequently, in vivo treatment trials of these preparations were conducted using indigenous Bos indicus cattle naturally infested with ticks. Results indicate that treatments at the rate of once per day for 5 consecutive days with the latexes of E. obovalifolia and F. brachypoda can reduce tick burdens by up to 70% on cattle.

Annual and spatial activity of dung flies and carrion in a Mediterranean holm-oak pasture ecosystem.

The annual activity and spatial distribution of Muscidae and Calliphoridae were investigated in a holm-oak ('dehesa') ecosystem in western Spain over two years in pasture and woodland habitats, using wind-orientated traps baited with a mixture of fresh cattle faeces, liver and sodium sulphide solution. Lucilia sericata (Meigen) was always the dominant species and, with Chrysomya albiceps (Weidemann), Hydrotaea ignava (Harris), Muscina levida (Harris) and Muscina prolapsa (Harris), was more abundant during the second than the first year. By contrast, Calliphora vicina Robineau-Desvoidy, Calliphora vomitoria (L.), Hydrotaea armipes (Fallén), Hydrotaea penicillata (Rondani) and Hydrotaea dentipes (Fabricius) were more numerous during the first than the second year of the study. In summer, the Diptera sampled were significantly more abundant in a wooded than a pasture area. However, in autumn, while H. penicillata remained significantly more abundant in woodland, L. sericata became more abundant in the pasture, whereas C. vicina was captured in open and wooded areas in similar proportions. During winter and spring the populations sampled were relatively small. The changing patterns of abundance are discussed in relation to differences in climate within and between years.

Dissolved and particulate phosphorus in leachate from structured soil amended with fresh cattle faeces

Substantial transfer of phosphorus from land to aquatic environments has been observed in regions supporting intensive animal husbandry. We characterised leaching of P derived from fresh cattle faeces located at the surface of a structured clayey soil. Fresh cattle faeces were placed on top of an undisturbed column of structured soil (diam. and height 0.5 m) subjected to steady, saturated flow (1 mm h-1) with a synthetic rain solution. After 0.01 pore volumes (PV, 1PV = 46.5 1) or 2.5 h of flow the effluent concentrations of both dissolved and particulate P forms increased rapidly, and after 0.15 PV (37 h) a maximum of 12 mg P l-1 was observed for total P. This rapid, strong and permanent leaching of P from applied faeces was ascribed to preferential flow through continuous macropores. Dye tracing showed that especially earthworm burrows were active flow paths. Of the faeces derived P observed in the effluent, dissolved inorganic P (DIP, measured as molybdate reactive P) constituted the largest fraction (37%) followed by particulate organic P (POP, 33%) and particulate inorganic P (PIP, 22%) while dissolved organic P (DOP) accounted for the remaining 8%. Leaching of IP from faeces appeared to be greater than from inorganic sources. This may be ascribed to co-leaching of P complexating compounds, or compounds that compete with faeces derived P for sorption sites. When the flow regime was shifted from saturated to unsaturated conditions (after 5 days), DIP temporarily became undetectable in the effluent, and the concentration of PIP and POP decreased markedly, while DOP remained almost unchanged and became the main P fraction leached. Average effluent concentration of total P for the whole 12 day leaching period was 4.1 mg P l-1. This high concentration suggests well-drained soils with high animal densities to constitute future field research targets.

Effect of volumetric water content on thermal properties of dairy cattle feces mixed with sawdust

This paper describes the thermal properties (effective thermal conductivity and thermal diffusivity) of an organic waste used to model the composting process in relation to volumetric water content at 20°C. The organic waste was a mixture of fresh dairy cattle feces and sawdust with a ratio of one-to-one on a dry weight basis. The thermal probe method was used to determine the effective thermal conductivity and diffusivity. The effective thermal conductivities were found to increase with volumetric water content, and ranged from 0.0500 to 0.202 W m −1 K −1 at volumetric water contents of 0% and 44.2%, respectively. The thermal diffusivity was not affected by the volumetric water content, and was found to have a mean value of 1.08 × 10 −7 m 2 s −1.

Development of the gas production technique to assay for anti-nutritive compounds in temperate tree fodders with polyphenol adsorbents using inoculum based on fresh cattle faeces

The polyphenol concentration in various tree fodders has been assayed by the gas production technique using rumen fluid inoculum either by fermentation of whole samples +/- a polyphenol adsorbent (Khazaal et al., 1994) or simply by the reduction of gas production caused by acetone extracts of the fodders (Wood and Plumb, 1995). Successful replacement of rumen fluid as a source of anaerobic bacteria by faeces from ruminant animals has been reported both for two-stage Tilley and Terry dry-matter digestibility (DMD) (El Shaer et al., 1987) and for the gas production technique (Davies, 1991). The use of faeces based inoculum +/- polyphenol adsorbents was therefore tested and optimized for fallen paulownia and poplar leaves using the gas production technique (the trees were commercial hybrids of Paulownia and Populus species respectively). A series of trials was carried out to: develop the use of preliminary incubation of the faeces inoculum; optimize the adsorbent type, molecular weight (MW) and quantity; optimize the faeces concentration in the inoculum and the use of glucose as a pre-incubation stimulant; and evaluate the use of differences in Tl /2 for gas production and end DMD +/- adsorbent to assess the effect of anti-nutritive compounds (ANCs) on the relative rate and extent of fermentation.All trials were carried out using 100 ml plastic vaccine flexibottles as containers maintained at 39°C in water baths. Gas was manually extracted with disposable syringes, generally at 3, 6, 9,12,15,18, 21, 24, 30, 36, 42, 48, 60, 72 h and bottles were well shaken at these times.