The Developing Understanding of Assessment for Learning (DUAL) programme was developed with the dual aims of improving both the quality and consistency of feedback students receive and the students' ability to use that feedback to improve. DUAL comprises a range of processes (including marking rubrics, sample reports, moderation discussions and peer-review activities) which support explicit knowledge exchange between staff, and between staff and students and the development of tacit knowledge of standards in all participants. This paper describes the study which quantified the extent to which the DUAL programme improved reliability and efficiency of marking of first year biology reports by a large team of laboratory demonstrators. Marker reliability increased after participation in DUAL, with demonstrators marking laboratory reports significantly closer to the marks awarded by an expert marker of the discipline. Efficiency was also improved since time taken to mark the reports did not increase significantly, despite the fact that demonstrators were adapting to a new system of marking. Demonstrators valued the programme and nominated the marking rubric, feedback code and moderation discussion as the most useful elements. The community of practice built through joint participation in the DUAL programme created a supportive working environment for demonstrators and strengthened the collaboration between the discipline and academic language and learning lecturers.
Biffarius arenosus had a mean δ13C of
–15·4 ± 0·2‰ and a mean
δ15N of 5·9 ± 0·1‰
(n = 38), and
Trypea australiensis had a mean
δ13C of –16·3 ± 0·3 and
a mean δ15N of 7·6 ± 0·1
(n = 20). The δ13C
signatures of the only mangrove species present
(Avicennia marina) and the most abundant saltmarsh plant
(Sarcocornia quinqueflora) indicated that they were not
major food sources. Seagrasses, predominantly
Heterozostera tasmanica, had mean
δ13C and δ15N values
of –11·7 ± 0·2‰ (n
= 65) and 3·9 ± 0·2‰
(n = 62), respectively. Seagrass epiphytes had
mean δ13C and δ15N
values of –17·9 ± 0·4‰ and 4·6
± 0·3‰ (n = 27),
respectively. A mixture of seagrasses and their epiphytes was the most likely
source of organic carbon for B. arenosus. Benthic
microalgae, such as diatoms, were a possible food source, but phospholipid
biomarkers indicated a meagre abundance of diatoms in the sediments, and
microscopy of shrimp guts revealed few or no diatom frustules. For
T. australiensis, food sources were less easily
distinguished than for B. arenosus, but they could
include seagrass epiphytes plus the green macroalgae
Enteromorpha spp. and/or the brown alga
Chordaria cladisiphon.
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